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Disease on EC 1.4.1.2 - glutamate dehydrogenase

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DISEASE
TITLE OF PUBLICATION
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3-hydroxy-2-methylbutyryl-coa dehydrogenase deficiency
Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.
Two genetic forms of hyperinsulinemic hypoglycemia caused by dysregulation of glutamate dehydrogenase.
3-hydroxyacyl-coa dehydrogenase deficiency
Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.
Abscess
Protease-Mediated Growth of Staphylococcus aureus on Host Proteins Is opp3 Dependent.
[Application of serum glutamic dehydrogenase for the diagnosis of hepatic carcinoma and abscess and for the evaluation of their treatment (author's transl)]
Acidosis
Activation of oxoglutarate dehydrogenase in the kidney in response to acute acidosis.
Adaptation of renal tricarboxylic acid cycle metabolism to various acid-base states: study with [3-13C,5-15N]glutamine.
Ammoniagenesis by cultured human renal cortical epithelial cells: study with 15N.
Biochemical and histocytochemical studies on response of ammonia-producing enzymes for nh4cl-induced acidosis.
Biochemical pathways and modulators of renal ammoniagenesis.
Changes in the profile of liver enzymes in newborn calves induced by experimental, subclinical acidosis in pregnant cows and osmotic diarrhoea.
Effect of acute metabolic acidosis on ammonia metabolism in kidney.
Effect of altered acid-base balance and of various agonists on levels of renal glutamate dehydrogenase mRNA.
Evidence of activation of the renal glutamate dehydrogenase pathway in intact acidotic dogs.
Hormonal regulation of glutamine metabolism by OK cells.
Inhibition of glutamine synthetase in the mouse kidney: a novel mechanism of adaptation to metabolic acidosis.
Metabolism and transport of L-glutamine and L-alanine by renal tubules of chickens.
Metabolism of glutamine and glutamate by rat renal tubules. Study with 15N and gas chromatography-mass spectrometry.
Metabolism of [2-13C]succinate in renal cells determined by 13C NMR.
Newer aspects of glutamine/glutamate metabolism: the role of acute pH changes.
pH-responsive stabilization of glutamate dehydrogenase mRNA in LLC-PK1-F+ cells.
Plasma amino acid concentrations and mRNA expression of components related to protein degradation in lambs with nutritionally induced metabolic acidosis.
Regulation of glutamate dehydrogenase by branched-chain amino acids in skeletal muscle from rats and chicks.
Renal metabolite concentrations and the activities of glutaminase and glutamate dehydrogenase during recovery from metabolic acidosis in the rat.
The kidney of chicken adapts to chronic metabolic acidosis: in vivo and in vitro studies.
The role of glutamate dehydrogenase in mammalian ammonia metabolism.
[Interrelation of fetal metabolism and late pregnancy in animals]
Acquired Immunodeficiency Syndrome
Chronic subclinical ovine fascioliasis: plasma glutamate dehydrogenase, gamma-glutamyl transpeptidase and aspartate aminotransferase activities and their significance as diagnostic aids.
Acrodynia
gdhB, a gene encoding a second quinoprotein glucose dehydrogenase in Pantoea citrea, is required for pink disease of pineapple.
Identification and characterization of a Pantoea citrea gene encoding glucose dehydrogenase that is essential for causing pink disease of pineapple.
Adenocarcinoma
Hyperthermia potentiates cisplatin cytotoxicity and negative effects on mitochondrial functions in OVCAR-3 cells.
[Oxidoreductase activity in the cells of stomach cancer]
Adrenocortical Hyperfunction
Effect of serum storage, anti-inflammatory oral doses of prednisone, and spontaneous hyperadrenocorticism on serum glutamate dehydrogenase activity in dogs.
Alzheimer Disease
Glutamate Dehydrogenase as a Neuroprotective Target Against Neurodegeneration.
Glutamate metabolizing enzymes in prefrontal cortex of Alzheimer's disease patients.
Implications for altered glutamate and GABA metabolism in the dorsolateral prefrontal cortex of aged schizophrenic patients.
Lymphocyte glutamate dehydrogenase activity in normal aging and neurological diseases.
Plasma concentrations of glutamate and its metabolites in patients with Alzheimer's disease.
[Impaired cerebral glutamate metabolism in mental diseases (Alzheimer's disease, schizophrenia]
Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis: glutamate dehydrogenase and transmitter amino acids in the spinal cord.
Glutamate dehydrogenase activity in amyotrophic lateral sclerosis.
Anemia
NTP Toxicology and Carcinogenesis Studies of Chloroprene (CAS No. 126-99-8) in F344/N Rats and B6C3F1 Mice (Inhalation Studies).
Arthritis
Oxidative state and oxidative metabolism of the heart from rats with adjuvant-induced arthritis.
Asbestosis
Biochemical mechanisms in asbestos toxicity.
Astrocytoma
Glutaminolysis dynamics during astrocytoma progression correlates with tumor aggressiveness.
Asymptomatic Infections
Detection of Clostridium difficile in Feces of Asymptomatic Patients Admitted to the Hospital.
Ataxia
Cryo-EM structures of the ionotropic glutamate receptor GluD1 reveal a non-swapped architecture.
Glutamate dehydrogenase deficiency in Machado-Joseph disease.
Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy.
Leucocyte glutamate dehydrogenase in various hereditary ataxias.
Leukocyte glutamate dehydrogenase and CSF amino acids in late onset ataxias.
Basal Ganglia Diseases
Degenerative neurological disorders associated with deficiency of glutamate dehydrogenase.
beta-Thalassemia
Glycerol-3-phosphate dehydrogenase activity in the red cells of patients with thalassemia.
Brain Concussion
[Changes in the activities of oxidoreductases, content of malondialdehyde and medium weight molecules in the blood of patients with craniocerebral injuries of different severity]
Brain Diseases
Histochemical studies in experimental portal-systemic encephalopathy.
Brain Diseases, Metabolic
Differential effects of fatty acyl coenzyme A derivatives on citrate synthase and glutamate dehydrogenase.
Brain Ischemia
Glutamate dehydrogenase as a neuroprotective target against brain ischemia and reperfusion.
Brain Neoplasms
[Activities of glutamate dehydrogenase and aspartate aminotransferase in human brain tumors]
Breast Neoplasms
Allosteric regulation of glutamate dehydrogenase deamination activity.
Blood and Tissue Enzymatic Activities of GDH and LDH, Index of Glutathione, and Oxidative Stress among Breast Cancer Patients Attending Referral Hospitals of Addis Ababa, Ethiopia: Hospital-Based Comparative Cross-Sectional Study.
Expression of glutamine metabolism-related proteins according to molecular subtype of breast cancer.
Glutamate dehydrogenase (GLUD1) expression in breast cancer.
Metabolic recycling of ammonia via glutamate dehydrogenase supports breast cancer biomass.
[Correlation of glutamate dehydrogenase with several tumors].
Carcinogenesis
Effects of low-dose radiation on glutamate dehydrogenase activity in tissues of rats with transplanted Guerin's carcinoma.
Glutaminolysis and glycolysis regulation by troglitazone in breast cancer cells: relationship to mitochondrial membrane potential.
Carcinoma
Effects of low-dose radiation on glutamate dehydrogenase activity in tissues of rats with transplanted Guerin's carcinoma.
Enzyme activities and level of SH groups in breast carcinomas.
Enzyme activities in human breast tumours.
Flow-cytometric determination of dehydrogenase activities in primary human gastrointestinal tumor cell lines.
[Application of serum glutamic dehydrogenase for the diagnosis of hepatic carcinoma and abscess and for the evaluation of their treatment (author's transl)]
[Glutamate dehydrogenase from human liver. VI. Glutamate dehydrogenase in primary liver cell carcinomas]
[Laboratory tests in the diagnosis of stomach cancer]
Carcinoma, Ehrlich Tumor
Changes in enzyme pattern of Ehrlich ascites tumor cells following serial cultivation in media with increased (hypertonic) NaCl content.
Enzyme activities of six different dehydrogenases in Ehrlich ascites cells measured by flow cytometry.
Carcinoma, Hepatocellular
Characterization of glutamate dehydrogenase isoproteins purified from the cerebellum of normal subjects and patients with degenerative neurological disorders, and from human neoplastic cell lines.
Effects of glutamate dehydrogenase, choline oxidase, and glucose-6-phosphatase on 67Ga accumulation in lysosome.
Glutamate dehydrogenase activity related to histopathological grade of hepatocellular carcinoma in man.
Glutamate dehydrogenase and alkaline phosphatase as very early predictors of hepatocellular carcinoma recurrence after liver transplantation.
Physiological Role of Glutamate Dehydrogenase in Cancer Cells.
Proceedings: Grade of histological differentiation, glutamate dehydrogenase activity and alphafetoprotein production in human hepatocellular carcinoma.
Serum level of ornithine carbamoyltransferase is influenced by the state of Kupffer cells.
The comparative enzymology and cell origin of rat hepatomas. II. Glutamate dehydrogenase, choline oxidase, and glucose-6-phosphatase.
[Evaluation of serum glutamic dehydrogenase activity in the diagnosis and treatment of hepatocellular carcinoma and liver metastasis]
[Glutamate dehydrogenase from human liver. VI. Glutamate dehydrogenase in primary liver cell carcinomas]
Cerebellar Ataxia
Glutamate dehydrogenase (GDH) deficiency in different types of progressive hereditary cerebellar ataxia.
Leukocyte glutamate dehydrogenase and CSF amino acids in late onset ataxias.
Chagas Disease
Comparative study of enzymes in testes and ovaries from adult Dipetalogaster maximus (Uhler) and triatoma infestans (Klug) (Hemiptera: Reduviidae). correlation with fine structural organization.
Cholangiocarcinoma
Expression and prognostic value of glutamate dehydrogenase in extrahepatic cholangiocarcinoma patients.
Cholestasis
Activities of APh, gamma-GT, GlDH and GPT and bile acid concentrations in serum after bile duct obstruction and cycloheximide in the rat.
Value of so called cholestasis markers in the dog: an experimental study.
Clostridium Infections
Algorithm combining toxin immunoassay and stool culture for diagnosis of Clostridium difficile infection.
Clinical significance of a positive Clostridioides difficile glutamate dehydrogenase test on the outcomes of hospitalized older patients.
Clostridium difficile infection diagnostics - evaluation of the C. DIFF Quik Chek Complete assay, a rapid enzyme immunoassay for detection of toxigenic C. difficile in clinical stool samples.
Detection of nosocomial Clostridium difficile infections with toxigenic strains despite negative toxin A/B testing on stool samples.
Diagnostic test accuracy of glutamate dehydrogenase for Clostridium difficile: Systematic review and meta-analysis.
Does my patient have Clostridium difficile infection?
Evaluation of a rapid membrane enzyme immunoassay for the simultaneous detection of glutamate dehydrogenase and toxin for the diagnosis of Clostridium difficile infection.
Evaluation of a simultaneous detection kit for the glutamate dehydrogenase antigen and toxin A/B in feces for diagnosis of Clostridium difficile infection.
Evaluation of risk factors for Clostridium difficile infection based on immunochromatography testing and toxigenic culture assay.
Glutamate dehydrogenase for laboratory diagnosis of Clostridium difficile infection.
In Vitro Selection of Circular DNA Aptamers for Biosensing Applications.
Laboratory diagnosis of clostridium difficile infection. An evaluation of tests for faecal toxin, glutamate dehydrogenase, lactoferrin and toxigenic culture in the diagnostic laboratory.
Simultaneous Detection of Clostridioides difficile Glutamate Dehydrogenase and Toxin A/B: Comparison of the C. DIFF QUIK CHEK COMPLETE and RIDASCREEN Assays.
The Role of Glutamate Dehydrogenase (GDH) Testing Assay in the Diagnosis of Clostridium difficile Infections: A High Sensitive Screening Test and an Essential Step in the Proposed Laboratory Diagnosis Workflow for Developing Countries like China.
Coccidiosis
[Alteration of enzyme activities in serum of Eimeria stiedai infected rabbits (author's transl)]
Coinfection
Dominance of Giardia assemblage B in León, Nicaragua.
First genetic characterisation of Giardia in human isolates from Jordan.
Giardia and Cryptosporidium infections in Danish cats: risk factors and zoonotic potential.
High genetic polymorphism among Giardia duodenalis isolates from Sahrawi children.
Multilocus genotyping of Giardia duodenalis isolated from patients in Egypt.
Multiple-subgenotype infections of Giardia intestinalis detected in Palestinian clinical cases using a subcloning approach.
Prevalence and mulilocus genotypes of Giardia duodenalis infecting pigs in Ogun state, Nigeria.
Subclass profile of specific IgG antibodies in rats challenged during acute and chronic primary infection with Fasciola hepatica.
Colonic Neoplasms
Emergency presentation of colon cancer is most frequent during summer.
Colorectal Neoplasms
Glutamate dehydrogenase is a novel prognostic marker and predicts metastases in colorectal cancer patients.
Metabolic Adaptation to Nutritional Stress in Human Colorectal Cancer.
[Correlation of glutamate dehydrogenase with several tumors].
Coma
Acute metabolic effects of ammonia on the enzymes of glutamate metabolism in isolated astroglial cells.
Effect of total hepatectomy on selected cerebral substrates and enzymes of the glycolytic pathways and Krebs cycle.
Communicable Diseases
Performance of laboratory tests for detection for Clostridioides difficile: A multicenter prospective study in Japan.
Congenital Hyperinsulinism
A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene.
Biochemical evaluation of an infant with hypoglycemia resulting from a novel de novo mutation of the GLUD1 gene and hyperinsulinism-hyperammonemia syndrome.
Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism.
Clinical and Molecular Spectrum of Glutamate Dehydrogenase Gene Defects in 26 Chinese Congenital Hyperinsulinemia Patients.
Disorders of glutamate metabolism.
Functional evaluation of 16 SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss-of-function phenotypes in vitro.
Glutaminolysis and insulin secretion: from bedside to bench and back.
Hyperinsulinism in infancy and childhood: when an insulin level is not always enough.
Hyperinsulinism-hyperammonemia syndrome: a de novo mutation of the GLUD1 gene in twins and a review of the literature.
Hyperinsulinism/hyperammonemia syndrome: insights into the regulatory role of glutamate dehydrogenase in ammonia metabolism.
Mechanisms of amino acid-stimulated insulin secretion in congenital hyperinsulinism.
Mechanisms of Disease: advances in diagnosis and treatment of hyperinsulinism in neonates.
Molecular characterisation of glutamate dehydrogenase gene defects in Japanese patients with congenital hyperinsulinism/hyperammonaemia.
Mutational analysis of ABCC8, KCNJ11, GLUD1, HNF4A and GCK genes in 30 Chinese patients with congenital hyperinsulinism.
Neurological aspects of hyperinsulinism-hyperammonaemia syndrome.
Rare forms of congenital hyperinsulinism.
Spectrum of glutamate dehydrogenase mutations in Japanese patients with congenital hyperinsulinism and hyperammonemia syndrome.
Unregulated elevation of glutamate dehydrogenase activity induces glutamine-stimulated insulin secretion: identification and characterization of a GLUD1 gene mutation and insulin secretion studies with MIN6 cells overexpressing the mutant glutamate dehydrogenase.
[ABCC8, KCNJ11 and GLUD1 gene mutation analysis in congenital hyperinsulinism pedigree].
[Hyperinsulinism in infancy and childhood: when an insulin level is not always enough.]
[Mutation analysis of the GLUD1 gene in patients with glutamate dehydrogenase congenital hyperinsulinism.]
Cystic Fibrosis
Timing and sequence of differentiation of embryonic rat hepatocytes along the biliary epithelial lineage.
Cysts
A natural zoonotic giardiasis: Infection of a child via Giardia cysts in pet chinchilla droppings.
Comparison of two target genes for detection and genotyping of Giardia lamblia in human feces by PCR and PCR-restriction fragment length polymorphism.
Cryptosporidium and Giardia in Danish organic pig farms: Seasonal and age-related variation in prevalence, infection intensity and species/genotypes.
Discrimination of all genotypes of Giardia duodenalis at the glutamate dehydrogenase locus using PCR-RFLP.
Genotyping of Giardia lamblia isolates from human in southern Iran.
Giardia duodenalis assemblages in cats from Virginia, USA.
Giardia duodenalis in small animals and their owners in Germany: A pilot study.
Giardia intestinalis in Thailand: identification of genotypes.
Giardia lamblia subtypes and their relationship with clinical symptoms in patients with giardiasis.
High genetic polymorphism among Giardia duodenalis isolates from Sahrawi children.
Histoenzymological study of selected dehydrogenase enzymes in Pneumocystis carinii.
Improved sensitivity of PCR amplification of glutamate dehydrogenase gene for detection and genotyping of Giardia duodenalis in stool specimen.
Improvement in cyst recovery and molecular detection of Giardia duodenalis from stool samples.
Intestinal parasites and genotyping of Giardia duodenalis in children: first report of genotype B in isolates from human clinical samples in Mexico.
Molecular characterisation of Giardia isolates from clinical infections following a waterborne outbreak.
Molecular identification of Giardia duodenalis isolates from humans, dogs, cats and cattle from the state of São Paulo, Brazil, by sequence analysis of fragments of glutamate dehydrogenase (gdh) coding gene.
Molecular typing of canine Giardia duodenalis isolates from Minas Gerais, Brazil.
Multilocus sequence typing of canine Giardia duodenalis from South Eastern European countries.
Performance of glutamate dehydrogenase and triose phosphate isomerase genes in the analysis of genotypic variability of isolates of Giardia duodenalis from livestocks.
Quantification of viable Giardia cysts and Cryptosporidium oocysts in wastewater using propidium monoazide quantitative real-time PCR.
Sarcocystis fusiformis: some protein metabolic enzymes in various fractions of sarcocysts of buffalo (Bubalus bubalis).
Synthesis of pyruvate: ferredoxin oxidoreductase and alcohol dehydrogenase E enzymes during Giardia intestinalis excystation.
The mixed AII and BIII genotypes of human Giardia lamblia isolates circulating in Mazandaran Province, northern Iran.
Transcription of metabolic enzyme genes during the excystation of Giardia lamblia.
Understanding Giardia infections among rural communities using the one health approach.
[Comparison of methods of DNA extraction from Giardia spp. measured by conventional PCR].
Dehydration
Ammonium metabolism in Selaginella bryopteris in response to dehydration-rehydration and characterisation of desiccation tolerant, thermostable, cytosolic glutamine synthetase from plant.
Comparative study of enzymes related to proline metabolism in tepary bean (Phaseolus acutifolius) and common bean (Phaseolus vulgaris) under drought and irrigated conditions, and various urea concentrations.
Corrigendum to: Ammonium metabolism in Selaginella bryopteris in response to dehydration-rehydration and characterisation of desiccation tolerant, thermostable, cytosolic glutamine synthetase from plant.
Effect of water stress on growth and proline metabolism of Phaseolus vulgaris L.
Nitric Oxide Signal, Nitrogen Metabolism, and Water Balance Affected by ?-Aminobutyric Acid (GABA) in Relation to Enhanced Tolerance to Water Stress in Creeping Bentgrass.
Nitrogen Metabolism in Adaptation of Photosynthesis to Water Stress in Rice Grown under Different Nitrogen Levels.
Over-expression of a glutamate dehydrogenase gene, MgGDH, from Magnaporthe grisea confers tolerance to dehydration stress in transgenic rice.
Ten-Step Minimally Invasive Treatment of Lumbar Giant Disc Herniation via Unilateral Tubular Laminotomy for Bilateral Decompression: 2-Dimensional Operative Video.
Dementia
[Geriatric day hospital: what evidence? A systematic review].
Dental Plaque
[Biochemical studies of glutamate dehydrogenase in fusobacterium from human dental plaque (author's transl)]
Diabetes Mellitus, Experimental
[Changes of some energy exchange parameters in the rat heart under insulin hypoglycemia]
Diabetes Mellitus, Type 2
Glutamate dehydrogenase, insulin secretion, and type 2 diabetes: a new means to protect the pancreatic ?-cell?
Diabetes, Gestational
Low mitochondrial glycerophosphate dehydrogenase activity in lymphocytes of women with gestational diabetes.
Digestive System Diseases
[Diagnostic significance of serum glutamate dehydrogenase in hepatobiliary diseases]
Diphtheria
Folding funnels and conformational transitions via hinge-bending motions.
Down Syndrome
Mitochondrial enzyme deficiencies in Down's syndrome.
Drug Resistant Epilepsy
Differential glutamate dehydrogenase (GDH) activity profile in patients with temporal lobe epilepsy.
Dysentery
[Findings concerning characteristics of responses to administration of vaccines containing antigenic complexes of enteric bacteria and tetanus toxoid]
Dystonia
Deregulation of glutamate dehydrogenase in human neurologic disorders.
Generalized dystonia in a patient with a novel mutation in the GLUD1 gene.
Eczema
Bile Duct Lesions Associated With Turnip (Brassica rapa) Photosensitization Compared With Those Due to Sporidesmin Toxicosis in Dairy Cows.
Could Nitrile Derivatives of Turnip (Brassica rapa) Glucosinolates Be Hepato- or Cholangiotoxic in Cattle?
Endocarditis
Streptococcus tigurinus is frequent among gtfR-negative Streptococcus oralis isolates and in the human oral cavity, but highly virulent strains are uncommon.
Endometriosis
A potential role of Sirtuin3 and its target enzyme activities in patients with ovarian endometrioma.
Endotoxemia
[The effect of triamcinolone acetonide on the liver mitochondria in endotoxemia]
Epilepsies, Myoclonic
Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase.
Epilepsies, Partial
Enzyme changes in actively spiking areas of human epileptic cerebral cortex.
Familial increase in plasma glutamic acid in epilepsy.
Epilepsy
Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations.
Differential glutamate dehydrogenase (GDH) activity profile in patients with temporal lobe epilepsy.
Expression of glutamine synthetase and glutamate dehydrogenase in the latent phase and chronic phase in the kainate model of temporal lobe epilepsy.
Glutamate Dehydrogenase as a Neuroprotective Target Against Neurodegeneration.
Hyperinsulinism-hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype-phenotype correlations.
Modulation of brain glutamate dehydrogenase as a tool for controlling seizures.
Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase.
Neurological aspects of hyperinsulinism-hyperammonaemia syndrome.
The Glutamate-Glutamine Cycle in Epilepsy.
[Glutamate dehydrogenase determination in epilepsy]
Epilepsy, Absence
Specific alteration in the expression of glial fibrillary acidic protein, glutamate dehydrogenase, and glutamine synthetase in rats with genetic absence epilepsy.
Epilepsy, Generalized
Familial increase in plasma glutamic acid in epilepsy.
Two genetic forms of hyperinsulinemic hypoglycemia caused by dysregulation of glutamate dehydrogenase.
Epilepsy, Temporal Lobe
Differential glutamate dehydrogenase (GDH) activity profile in patients with temporal lobe epilepsy.
Expression of glutamine synthetase and glutamate dehydrogenase in the latent phase and chronic phase in the kainate model of temporal lobe epilepsy.
Glutamate Dehydrogenase as a Neuroprotective Target Against Neurodegeneration.
Fascioliasis
Biochemical indicators of liver injury in calves with experimental fascioliasis.
Chronic subclinical ovine fascioliasis: plasma glutamate dehydrogenase, gamma-glutamyl transpeptidase and aspartate aminotransferase activities and their significance as diagnostic aids.
Response of goats to repeated infections with Fasciola gigantica.
Fatty Liver
Biochemical changes associated with the fatty liver syndrome in cows.
Clinicopathological evaluation of downer dairy cows with fatty liver.
Evaluation of ornithine carbamoyl transferase and other serum and liver-derived analytes in diagnosis of fatty liver and postsurgical outcome of left-displaced abomasum in dairy cows.
Glucose and insulin responses to glucagon injection in dairy cows with ketosis and fatty liver.
Glutamate dehydrogenase activator BCH stimulating reductive amination prevents high fat/high fructose diet-induced steatohepatitis and hyperglycemia in C57BL/6J mice.
Impaired hepatic autophagic activity in dairy cows with severe fatty liver is associated with inflammation and reduced liver function.
Polyenylphosphatidylcholine attenuates alcohol-induced fatty liver and hyperlipemia in rats.
Fatty Liver, Alcoholic
Hepatic gamma-glutamyltransferase activity in alcoholic fatty liver: comparison with other liver enzymes in man and rats.
Favism
Serum glutamic oxalacetic transaminase, glutamic pyruvic transaminase, gamma-glutamyl transpeptidase and glutamic dehydrogenase levels in favism.
Fibrosarcoma
Glutamate dehydrogenase activity in subcellular fractions of mouse fibrosarcoma.
Friedreich Ataxia
Abnormalities of mitochondrial enzymes in hereditary ataxias.
fumarate hydratase deficiency
Combined metabolomic and correlation networks analyses reveal fumarase insufficiency altered amino acid metabolism.
Gallstones
Clinical and pathological studies in cattle with hepatic disease.
Gastrointestinal Diseases
Malnutrition and related risk factors in older adults from different health-care settings: an enable study.
Genetic Diseases, Inborn
Two genetic forms of hyperinsulinemic hypoglycemia caused by dysregulation of glutamate dehydrogenase.
Giardiasis
A natural zoonotic giardiasis: Infection of a child via Giardia cysts in pet chinchilla droppings.
Comparison of ELISA, nested PCR and sequencing and a novel qPCR for detection of Giardia isolates from Jordan.
Comparison of two target genes for detection and genotyping of Giardia lamblia in human feces by PCR and PCR-restriction fragment length polymorphism.
First genetic characterisation of Giardia in human isolates from Jordan.
Genotyping of Giardia lamblia isolates from human in southern Iran.
High prevalence Giardia duodenalis assemblage B and potentially zoonotic subtypes in sporadic human cases in Western Australia.
Molecular Genotyping of Giardia duodenalis Isolates from Symptomatic Individuals Attending Two Major Public Hospitals in Madrid, Spain.
Multilocus genotyping and risk factor analysis of Giardia duodenalis in dogs in Korea.
Gingivitis
[Activity of glutamate dehydrogenase, gamma-glutamyltranspeptidase and creatine kinase in saliva in gingivitis]
Glioblastoma
Glioblastoma cells require glutamate dehydrogenase to survive impairments of glucose metabolism or akt signaling.
Glutaminolysis dynamics during astrocytoma progression correlates with tumor aggressiveness.
[Primary and secondary glioblastoma. Distinction by glutamate dehydrogenase activity]
Glioma
Characterization of glutamate dehydrogenase isoproteins purified from the cerebellum of normal subjects and patients with degenerative neurological disorders, and from human neoplastic cell lines.
Diagnostic value of glutamate with 2-hydroxyglutarate in magnetic resonance spectroscopy for IDH1 mutant glioma.
Glutamate dehydrogenase (GDH) regulates bioenergetics and redox homeostasis in human glioma.
[Correlation of glutamate dehydrogenase with several tumors].
glutamate dehydrogenase deficiency
Clinical expression of glutamate dehydrogenase deficiency.
Decreased glutamate dehydrogenase protein in spinocerebellar degeneration.
Decreased viability of skin fibroblasts from patients with glutamate dehydrogenase deficiency.
Glutamate dehydrogenase (GDH) deficiency in different types of progressive hereditary cerebellar ataxia.
Glutamate dehydrogenase and aspartate aminotransferase in leukocytes of patients with motor neuron disease.
Glutamate dehydrogenase and its isozyme activity in olivopontocerebellar atrophy.
Glutamate dehydrogenase deficiency disrupts glutamate homeostasis in hippocampus and prefrontal cortex and impairs recognition memory.
Glutamate dehydrogenase deficiency in cerebellar degenerations: clinical, biochemical and molecular genetic aspects.
Glutamate dehydrogenase deficiency in Machado-Joseph disease.
Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy.
Glutamate dehydrogenase deficiency in spinocerebellar degenerations.
Glutamate dehydrogenase deficiency in three patients with spinocerebellar ataxia: a new enzymatic defect?
Glutamate dehydrogenase deficiency in three patients with spinocerebellar syndrome.
Glutamate dehydrogenase isoenzymes in the bovine retina and human leukocyte.
Glutamate Dehydrogenase-Deficient Mice Display Schizophrenia-Like Behavioral Abnormalities and CA1-Specific Hippocampal Dysfunction.
Multiple system degeneration with glutamate dehydrogenase deficiency: pathology and biochemistry.
Mutation analysis in glutaric aciduria type I.
Neonatal hyperinsulinemic hypoglycemia. Two case reports.
Neurological disorders associated with deficiency of glutamate dehydrogenase.
Neurophysiologic study of olivopontocerebellar atrophy with or without glutamate dehydrogenase deficiency.
Pathology of olivopontocerebellar atrophy with glutamate dehydrogenase deficiency.
The natural history of hyperuricemia among asymptomatic relatives of patients with gout.
Heart Failure
The diagnostic significance of liver cell inhomogeneity: serum enzymes in patients with central liver necrosis and the distribution of glutamate dehydrogenase in normal human liver.
[Fibrosing reaction of nutmeg liver]
Hepatic Encephalopathy
Effects of acute hepatic encephalopathy and in vitro treatment with ammonia on glutamate oxidation in bulk-isolated astrocytes and mitochondria of the rat brain.
Histochemical studies in experimental portal-systemic encephalopathy.
Hyperammonemia and hepatic encephalopathy stimulate rat cerebral synaptic mitochondrial glutamate dehydrogenase activity specifically in the direction of glutamate oxidation.
[Changes of glutamic dehydrogenase and ornithine carbamyl transferase activities in sera in patients with hepatic encephalopathy]
[The enzymatic activity of ammonia metabolism in the liver during the parenteral nitrogen feeding of animals with experimental liver failure]
Hepatic Insufficiency
[The enzymatic activity of ammonia metabolism in the liver during the parenteral nitrogen feeding of animals with experimental liver failure]
Hepatitis
A diagnostic approach to different types of non-A non-B acute hepatitis through the evaluation of the lobular distribution of hepatocytic damage.
Glutamate dehydrogenase: a reliable marker of liver cell necrosis in the alcoholic.
Multivariate analysis of an enzymic profile for the differential diagnosis of viral hepatitis.
T cell-mediated hepatitis in mice infected with lymphocytic choriomeningitis virus. Liver cell destruction by H-2 class I-restricted virus-specific cytotoxic T cells as a physiological correlate of the 51Cr-release assay?
[Clinical evaluation of glutamate dehydrogenase in viral hepatitis and jaundice of other origins]
[Comparative studies on vitamin B 12 and glutamic dehydrogenase serum levels in children with acute viral hepatitis]
[Glutamate dehydrogenase activity in the blood serum in viral hepatitis and other liver diseases]
[Glutamate dehydrogenase in the course of viral hepatitis]
[Glutamate dehydrogenase in viral hepatitis]
[Glutamic dehydrogenase and alcohol dehydrogenase of blood in various conditions of experimental hepatic necrosis: hepatitis due to MHV-3 virus, acute poisoning due to carbon tetrachloride.]
[Research on the diagnostic value of some enzyme activities in icteric hepatitis in childhood. I. Ornithine carbamoyltransferase and glutamate dehydrogenase]
[Significance of the determination of glutamate dehydrogenase (GLDH) in viral hepatitis in childhood]
[Significance of the proteinogram and the determination of glutamate dehydrogenase in atypical forms of viral hepatitis]
Hepatitis A
[Drug-induced hepatitis]
Hepatitis, Alcoholic
Serum glutamate dehydrogenase is not a reliable marker of liver cell necrosis in alcoholics.
[Glutamate dehydrogenase and acute alcoholic hepatitis]
Hepatitis, Chronic
Chronic hepatitis induced by alcohol.
Hepatic activity and mRNA expression of aspartate aminotransferase isoenzymes in alcoholic and nonalcoholic liver disease.
Multivariate analysis of an enzymic profile for the differential diagnosis of viral hepatitis.
Hyperalgesia
Intraplantar injection of gangliosides produces nociceptive behavior and hyperalgesia via a glutamate signaling mechanism.
Hypercholesterolemia
The influence of fluoride ions upon selected enzymes of protein metabolism in blood plasma of rabbits with hypercholesterolemia.
Hyperglycemia
Effects of sodium nitroprusside on blood glucose concentration, B-cell morphology and islet glutamate dehydrogenase activity in mice.
Glutamate dehydrogenase activator BCH stimulating reductive amination prevents high fat/high fructose diet-induced steatohepatitis and hyperglycemia in C57BL/6J mice.
Hyperinsulinism
A severe case of hyperinsulinism due to hemizygous activating mutation of glutamate dehydrogenase.
Allosteric discrimination at the NADH/ADP regulatory site of glutamate dehydrogenase.
Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism.
Clinical and Molecular Spectrum of Glutamate Dehydrogenase Gene Defects in 26 Chinese Congenital Hyperinsulinemia Patients.
Clinical features and insulin regulation in infants with a syndrome of prolonged neonatal hyperinsulinism.
Congenital hyperinsulinism: molecular basis of a heterogeneous disease.
Correction to: Hyperinsulinism associated with GLUD1 mutation: allosteric regulation and functional characterization of p.G446V glutamate dehydrogenase.
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations.
Dominantly inherited hyperinsulinaemic hypoglycaemia.
From pancreatic islets to central nervous system, the importance of glutamate dehydrogenase for the control of energy homeostasis.
Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment.
Glutamate Dehydrogenase as a Promising Target for Hyperinsulinism Hyperammonemia Syndrome Therapy.
Glutamate dehydrogenase: Structure of a hyperinsulinism mutant, corrections to the atomic model, and insights into a regulatory site.
Hunting for a hypoglycemia gene: severe neonatal hypoglycemia in a consanguineous family.
Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.
Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene.
Hyperinsulinism associated with GLUD1 mutation: allosteric regulation and functional characterization of p.G446V glutamate dehydrogenase.
Hyperinsulinism hyperammonaemia (HI/HA) syndrome due to GLUD1 mutation: phenotypic variations ranging from late presentation to spontaneous resolution.
Hyperinsulinism of the newborn.
Impaired FAD-glycerophosphate dehydrogenase activity in islet and liver homogenates of fa/fa rats.
Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.
Mitochondrial GTP insensitivity contributes to hypoglycemia in Hyperinsulinemia Hyperammonemia (HI/HA) by inhibiting glucagon release.
Mitochondrial signals in glucose-stimulated insulin secretion in the beta cell.
Monogenic hyperinsulinemic hypoglycemia: current insights into the pathogenesis and management.
Protein causes hyperinsulinemia: a Chinese patient with hyperinsulinism/hyperammonaemia syndrome due to a glutamate dehydrogenase gene mutation.
Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with hyperinsulinism: a novel glucose-fatty acid cycle?
Short-chain 3-hydroxyacyl-coenzyme A dehydrogenase associates with a protein super-complex integrating multiple metabolic pathways.
Stimulatory effects of malathion on the key enzymes activities of insulin secretion in langerhans islets, glutamate dehydrogenase and glucokinase.
The genetics of neonatal hyperinsulinism.
Two genetic forms of hyperinsulinemic hypoglycemia caused by dysregulation of glutamate dehydrogenase.
Two unrelated Chinese patients with hyperinsulinism /hyperammonemia (HI/HA) syndrome due to mutations in glutamate dehydrogenase gene.
Hyperkalemia
Comparison of classic hypoadrenocorticism with glucocorticoid-deficient hypoadrenocorticism in dogs: 46 cases (1985-2005).
Hyperlipidemias
Polyenylphosphatidylcholine attenuates alcohol-induced fatty liver and hyperlipemia in rats.
Hyperoxaluria, Primary
Enzymological characterization of a feline analogue of primary hyperoxaluria type 2: a model for the human disease.
Hypersensitivity
Glutaminolysis and insulin secretion: from bedside to bench and back.
Hyperthyroidism
[Effect of experimental changes in thyroid function on oxidative metabolism and glutamate dehydrogenase activity in the limbic system of the rat]
Hypoglycemia
A severe case of hyperinsulinism due to hemizygous activating mutation of glutamate dehydrogenase.
Biochemical evaluation of an infant with hypoglycemia resulting from a novel de novo mutation of the GLUD1 gene and hyperinsulinism-hyperammonemia syndrome.
Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations.
Congenital Hyperinsulinemic Hypoglycemia and Hyperammonemia due to Pathogenic Variants in GLUD1.
Effects of a GTP-insensitive mutation of glutamate dehydrogenase on insulin secretion in transgenic mice.
Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor.
Glutamate dehydrogenase: role in regulating metabolism and insulin release in pancreatic ?-cells.
Glutaminolysis and insulin secretion: from bedside to bench and back.
GREEN TEA POLYPHENOLS CONTROL DYSREGULATED GLUTAMATE DEHYDROGENASE IN TRANSGENIC MICE BY HIJACKING THE ADP ACTIVATION SITE.
Hyperinsulinemic hypoglycemia: think of hyperinsulinism/hyperammonemia (HI/HA) syndrome caused by mutations in the GLUD1 gene.
Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene.
Mitochondrial GTP insensitivity contributes to hypoglycemia in Hyperinsulinemia Hyperammonemia (HI/HA) by inhibiting glucagon release.
Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase.
Overexpression of constitutively activated glutamate dehydrogenase induces insulin secretion through enhanced glutamate oxidation.
Propylselen inhibits cancer cell growth by targeting glutamate dehydrogenase at the NADP+ binding site.
Protein-sensitive hypoglycemia without leucine sensitivity in hyperinsulinism caused by K(ATP) channel mutations.
Regulation of leucine-stimulated insulin secretion and glutamine metabolism in isolated rat islets.
Two genetic forms of hyperinsulinemic hypoglycemia caused by dysregulation of glutamate dehydrogenase.
Unregulated elevation of glutamate dehydrogenase activity induces glutamine-stimulated insulin secretion: identification and characterization of a GLUD1 gene mutation and insulin secretion studies with MIN6 cells overexpressing the mutant glutamate dehydrogenase.
[Parameters of energy and nitrogen metabolism in rats under insulin-induced hypoglycemia]
Hypokinesia
[Activity of various oxidases and transaminases in the rat liver in the readaptation period after hypokinesia up to 30 days]
Hyponatremia
Comparison of classic hypoadrenocorticism with glucocorticoid-deficient hypoadrenocorticism in dogs: 46 cases (1985-2005).
Hypothyroidism
[Effect of experimental changes in thyroid function on oxidative metabolism and glutamate dehydrogenase activity in the limbic system of the rat]
Infections
A Clostridium difficile outbreak in an Italian hospital: the efficacy of the multi-disciplinary and multifaceted approach.
A novel high-resolution multilocus sequence typing of Giardia intestinalis Assemblage A isolates reveals zoonotic transmission, clonal outbreaks and recombination.
Active equine parvovirus-hepatitis infection is most frequently detected in Austrian horses of advanced age.
Algorithm combining toxin immunoassay and stool culture for diagnosis of Clostridium difficile infection.
Algorithm proposal based on the C. Diff Quik Chek Complete ICT device for detecting Clostridium difficile infection.
An integrated analysis of enzyme activities, cofactor pools and metabolic fluxes in baculovirus-infected Spodoptera frugiperda Sf9 cells.
Cadazolid for the treatment of Clostridium difficile infection: results of two double-blind, placebo-controlled, non-inferiority, randomised phase 3 trials.
Characterization of Streptococcus suis serotype 2 blood infections using RT-qPCR to quantify glutamate dehydrogenase copy numbers.
Chronic subclinical ovine fascioliasis: plasma glutamate dehydrogenase, gamma-glutamyl transpeptidase and aspartate aminotransferase activities and their significance as diagnostic aids.
Clinical significance of a positive Clostridioides difficile glutamate dehydrogenase test on the outcomes of hospitalized older patients.
Clostridioides difficile in Outpatients: Application of a Diagnostic Algorithm Recommended by the European Society of Clinical Microbiology and Infectious Diseases.
Clostridium difficile glutamate dehydrogenase is a secreted enzyme that confers resistance to H2O2.
Clostridium difficile infection diagnostics - evaluation of the C. DIFF Quik Chek Complete assay, a rapid enzyme immunoassay for detection of toxigenic C. difficile in clinical stool samples.
Combination of culture, antigen and toxin detection, and cytotoxin neutralization assay for optimal Clostridium difficile diagnostic testing.
Comprehensive evaluation of chemiluminescent immunoassays for the laboratory diagnosis of Clostridium difficile infection.
Defining the Metabolic Pathways and Host-Derived Carbon Substrates Required for Francisella tularensis Intracellular Growth.
Detection of glutamate dehydrogenase enzyme activity in Plasmodium falciparum infection.
Detection of nosocomial Clostridium difficile infections with toxigenic strains despite negative toxin A/B testing on stool samples.
Diagnostic test accuracy of glutamate dehydrogenase for Clostridium difficile: Systematic review and meta-analysis.
Does my patient have Clostridium difficile infection?
Efficacy of an injectable combination anthelmintic (nitroxynil+clorsulon+ivermectin) against early immature Fasciola hepatica compared to triclabendazole combination flukicides given orally or topically to cattle.
Engineering Bacillus velezensis with high production of acetoin primes strong induced systemic resistance in Arabidopsis thaliana.
Evaluation of a rapid membrane enzyme immunoassay for the simultaneous detection of glutamate dehydrogenase and toxin for the diagnosis of Clostridium difficile infection.
Evaluation of a simultaneous detection kit for the glutamate dehydrogenase antigen and toxin A/B in feces for diagnosis of Clostridium difficile infection.
Evaluation of risk factors for Clostridium difficile infection based on immunochromatography testing and toxigenic culture assay.
Evolution of Testing Algorithms at a University Hospital for Detection of Clostridium difficile Infections.
GDH and toxin immunoassay for the diagnosis of Clostridioides (Clostridium) difficile infection is not a 'one size fit all' screening test.
Giardiasis in NSW: Identification of Giardia duodenalis assemblages contributing to human and cattle cases, and an epidemiological assessment of sporadic human giardiasis.
Glutamate dehydrogenase antigen detection in Plasmodium falciparum infections.
Glutamate dehydrogenase for laboratory diagnosis of Clostridium difficile infection.
Glutamate Dehydrogenase Is Required by Mycobacterium bovis BCG for Resistance to Cellular Stress.
Hepatitis E in blood donors: investigation of the natural course of asymptomatic infection, Germany, 2011.
Immunochromatographic test and ELISA for the detection of glutamate dehydrogenase (GDH) and A/B toxins as an alternative for the diagnosis of Clostridioides (Clostridium) difficile-associated diarrhea in foals and neonatal piglets.
In Vitro Selection of Circular DNA Aptamers for Biosensing Applications.
Infection rate and genetic diversity of Giardia duodenalis assemblage C in Iranian stray dogs, targeting the glutamate dehydrogenase gene.
Is Clostridioides difficile toxins detection necessary when the glutamate dehydrogenase enzyme is detected?
Laboratory diagnosis of clostridium difficile infection. An evaluation of tests for faecal toxin, glutamate dehydrogenase, lactoferrin and toxigenic culture in the diagnostic laboratory.
Metabolic adjustments during compatible interaction between barley genotypes and stripe rust pathogen.
Metabolic Reprogramming of Host Cells in Response to Enteroviral Infection.
Mixed Giardia duodenalis assemblage infections in children and adults in South India.
Molecular diversity and frequency of the diarrheagenic enteric protozoan Giardia duodenalis and Cryptosporidium spp. in a hospital setting in Northern Spain.
Molecular test to determine toxigenic capabilities in GDH-positive, toxin-negative samples: evaluation of the Portrait toxigenic C. difficile assay.
Occurrence and multilocus genotyping of Giardia duodenalis from post-weaned dairy calves in Sichuan province, China.
Plasma aspartate aminotransferase (AST), glutamate dehydrogenase (GLDH) and gamma-glutamyl transpeptidase (GGT) activities in water buffaloes with experimental subclinical fasciolosis.
Prospective Evaluation of the mariPOC® Test for the Detection of Clostridioides difficile GDH and Toxins A/B.
Proteome analysis reveals translational inhibition of Caenorhabditis elegans enhances susceptibility to Pseudomonas aeruginosa PAO1 pathogenesis.
Rapid identification of Giardia duodenalis assemblages in NSW using terminal-restriction fragment length polymorphism.
Recirculation of Giardia lamblia Assemblage A After Metronidazole Treatment in an Area With Assemblages A, B, and E Sympatric Circulation.
Response of goats to repeated infections with Fasciola gigantica.
Serum and bile antibody responses (IgG and IgA) during subclinical Fasciola hepatica infection in sheep.
Serum enzyme tests in hepatosplenic schistosomiasis.
Simultaneous Detection of Clostridioides difficile Glutamate Dehydrogenase and Toxin A/B: Comparison of the C. DIFF QUIK CHEK COMPLETE and RIDASCREEN Assays.
Stool antigen immunodetection for diagnosis of Giardia duodenalis infection in human subjects with HIV and cancer.
Susceptibility to homologous reinfection with Fasciola gigantica in goats.
The effect of experimental fascioliasis on the pharmacokinetics of antipyrine and sulphadimidine in desert sheep.
The effects of fascioliasis on the activities of some drug-metabolizing enzymes in desert sheep liver.
The fate of glutamate in different brain regions of the chick during Newcastle disease virus infection.
The predominance and clustering of Clostridioides (Clostridium) difficile PCR ribotype 001 isolates in three hospitals in Eastern Slovakia, 2017.
The resistance of sheep to Fasciola hepatica: studies on the pathophysiology of challenge infections.
The Role of Glutamate Dehydrogenase (GDH) Testing Assay in the Diagnosis of Clostridium difficile Infections: A High Sensitive Screening Test and an Essential Step in the Proposed Laboratory Diagnosis Workflow for Developing Countries like China.
The zoonotic potential of Giardia and Cryptosporidium in Norwegian sheep: A longitudinal investigation of 6 flocks of lambs.
Trends in Healthcare Facility-Onset Clostridioides difficile Infection and the Impact of Testing Schemes in an Acute Care Hospital System in New York City, 2016-2019.
Use of culture- and ELISA-based toxin assay for detecting
[Alteration of enzyme activities in serum of Eimeria stiedai infected rabbits (author's transl)]
Infectious Mononucleosis
Glutamate dehydrogenase activity in lymphocytes of B-cell chronic lymphocytic leukaemia patients.
Infertility, Male
Testis-Specific Bb8 Is Essential in the Development of Spermatid Mitochondria.
Inflammatory Bowel Diseases
Low glutamate dehydrogenase levels are associated with colonization in Clostridium difficile PCR-only positive patients with inflammatory bowel disease.
Insulin Resistance
Blood profiles in dairy cows with displaced abomasum.
Insulinoma
Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism.
Overexpression of constitutively activated glutamate dehydrogenase induces insulin secretion through enhanced glutamate oxidation.
SIRT4 inhibits glutamate dehydrogenase and opposes the effects of calorie restriction in pancreatic beta cells.
Unregulated elevation of glutamate dehydrogenase activity induces glutamine-stimulated insulin secretion: identification and characterization of a GLUD1 gene mutation and insulin secretion studies with MIN6 cells overexpressing the mutant glutamate dehydrogenase.
Intellectual Disability
Deregulation of glutamate dehydrogenase in human neurologic disorders.
Intervertebral Disc Displacement
Ten-Step Minimally Invasive Treatment of Lumbar Giant Disc Herniation via Unilateral Tubular Laminotomy for Bilateral Decompression: 2-Dimensional Operative Video.
Intestinal Diseases
[Alanine aminotransferase (ALT), aspartate aminotransferase (AST), glutamate dehydrogenase (GLDH), alkaline phosphatase (AP) and gamma-glutamyltransferase (GGP) in intestinal diseases of dogs]
Iron Deficiencies
Effect of iron deficiency on developing rat brain.
The pleiotropic effects of the glutamate dehydrogenase (GDH) pathway in Saccharomyces cerevisiae.
Ketosis
Glucose and insulin responses to glucagon injection in dairy cows with ketosis and fatty liver.
Leptospirosis
Clinical and pathological studies in cattle with hepatic disease.
Leukemia
Glutamic acid dehydrogenase and glutamic-oxalacetic transaminase of blood in leukemia and cancer.
High-resolution Antibody Array Analysis of Childhood Acute Leukemia Cells.
[Characteristics of leukemic blood cells. V. Glutamic acid dehydrogenase in leukemias and summary.]
Leukemia, Lymphoid
Glutamate dehydrogenase activity in lymphocytes of B-cell chronic lymphocytic leukaemia patients.
Leukemia, Myeloid, Acute
High-resolution Antibody Array Analysis of Childhood Acute Leukemia Cells.
Lipidoses
Clinical and pathological studies in cattle with hepatic disease.
Clinical and pathological studies in horses with hepatic disease.
Effect on liver function of acetonaemia and the fat cow syndrome in cattle.
Liver Cirrhosis
[Assessment of glutamic dehydrogenase activity in liver cirrhosis]
[Glutamate dehydrogenase in liver cirrhosis and liver stasis]
Liver Cirrhosis, Alcoholic
Hepatic activity and mRNA expression of aspartate aminotransferase isoenzymes in alcoholic and nonalcoholic liver disease.
Liver Diseases
Adaptation of methods for glutamate dehydrogenase and alcohol dehydrogenase activities to a centrifugal analyser: assessment of their clinical use in anoxic states of the liver.
Biochemical markers of chronic alcoholism.
Field study of dairy cows with reduced appetite in early lactation: clinical examinations, blood and rumen fluid analyses.
Ischemic preconditioning protects from hepatic ischemia/reperfusion-injury by preservation of microcirculation and mitochondrial redox-state.
Masking by enzyme inhibitor of raised serum glutamate dehydrogenase activity in Reye's syndrome.
Mitochondrial enzyme activities in liver biopsies from patients with alcoholic liver disease.
Mitochondrial enzymes in human serum: comparative determinations of glutamate dehydrogenase and mitochondrial aspartate aminotransferase in healthy persons and patients with chronic liver diseases.
Multivariate analysis of an enzymic profile for the differential diagnosis of viral hepatitis.
Nephrotoxicity and hepatotoxicity in calves apparently caused by experimental feeding with Narthecium ossifragum.
Serum mitochondrial biomarkers and damage-associated molecular patterns are higher in acetaminophen overdose patients with poor outcome.
The diagnostic significance of liver cell inhomogeneity: serum enzymes in patients with central liver necrosis and the distribution of glutamate dehydrogenase in normal human liver.
The effect of thioacetamide on urea cycle enzymes of rat liver.
The mechanism of release of hepatic enzymes in various liver diseases. II. Altered activity ratios of GOT to GPT in serum and liver of patients with liver diseases.
The mechanism of the release of hepatic enzymes in various liver diseases. 1. Alterations in cytoplasmic and mitochondrial enzyme activities in serum.
[Activity of glutamic acid dehydrogenase in serum of patients with liver diseases]
[Glutamate dehydrogenase activity in the blood serum in viral hepatitis and other liver diseases]
[On the influence of surgery on the biliary system, especially in liver diseases, on the serum level of the enzymes sorbitol dehydrogenase, glutamic-pyruvic transaminase, lactate dehydrogenase and glutamic dehydrogenase.]
Liver Diseases, Alcoholic
Adaptation of methods for glutamate dehydrogenase and alcohol dehydrogenase activities to a centrifugal analyser: assessment of their clinical use in anoxic states of the liver.
Biochemical markers of chronic alcoholism.
Plasma glutamate dehydrogenase: clinical application in patients with alcoholic liver disease.
Serum glutamate dehydrogenase as a marker of hepatocyte necrosis in alcoholic liver disease.
Serum glutamate dehydrogenase in alcoholic liver disease.
Serum level of ornithine carbamoyltransferase is influenced by the state of Kupffer cells.
Liver Failure
Hyperammonemia and hepatic encephalopathy stimulate rat cerebral synaptic mitochondrial glutamate dehydrogenase activity specifically in the direction of glutamate oxidation.
miR?30a?5p inhibits hypoxia/reoxygenation?induced oxidative stress and apoptosis in HK?2 renal tubular epithelial cells by targeting glutamate dehydrogenase 1 (GLUD1).
Liver Neoplasms
[On the practical utility of determining in conjunction with transaminases the values of glutamate dehydrogenase in the blood of patients with cholostatic jaundice and primary or metastatic hepatic neoplasm]
Lung Neoplasms
Hypoxia promotes mitochondrial glutamine metabolism through HIF1?-GDH pathway in human lung cancer cells.
Lymphatic Metastasis
Expression and prognostic value of glutamate dehydrogenase in extrahepatic cholangiocarcinoma patients.
Lymphoma
SIRT4 protein suppresses tumor formation in genetic models of Myc-induced B cell lymphoma.
Lymphoma, B-Cell
SIRT4 protein suppresses tumor formation in genetic models of Myc-induced B cell lymphoma.
Machado-Joseph Disease
Glutamate and malate dehydrogenase activities in Joseph disease and olivopontocerebellar atrophy.
Glutamate dehydrogenase deficiency in Machado-Joseph disease.
Malaria
Absence of alpha-ketoglutarate dehydrogenase activity and presence of CO2-fixing activity in Plasmodium falciparum grown in vitro in human erythrocytes.
Capacitive malaria aptasensor using Plasmodium falciparum glutamate dehydrogenase as target antigen in undiluted human serum.
Chloroquine is a potent inhibitor of glutamate dehydrogenase in liver and kidney-cortex of rabbit.
Detection of glutamate dehydrogenase enzyme activity in Plasmodium falciparum infection.
Development of an aptamer-based field effect transistor biosensor for quantitative detection of Plasmodium falciparum glutamate dehydrogenase in serum samples.
Dye coupled aptamer-captured enzyme catalysed reaction for detection of pan malaria and P. falciparum species in laboratory settings and instrument-free paper based platform.
Glutamate dehydrogenase antigen detection in Plasmodium falciparum infections.
Glutamate dehydrogenase, the marker protein of Plasmodium falciparum--cloning, expression and characterization of the malarial enzyme.
Glutamate dehydrogenase: a novel candidate to diagnose Plasmodium falciparum through rapid diagnostic test in blood specimen from fever patients.
Glutathione reductase and glutamate dehydrogenase of Plasmodium falciparum, the causative agent of tropical malaria.
Plasmodium falciparum glutamate dehydrogenase is genetically conserved across eight malaria endemic states of India: Exploring new avenues of malaria elimination.
Recent Advances in the Development of Biosensors for Malaria Diagnosis.
Sequence conservation of Plasmodium vivax glutamate dehydrogenase among Korean isolates and its application in seroepidemiology.
Studies on enzyme variation in the murine malaria parasites Plasmodium berghei, P. yoelii, P. vinckei and P. chabaudi by starch gel electrophoresis.
[Preparation of a monoclonal antibodies against Plasmodium falciparum glutamate dehydrogenase and establishment of colloidal gold-immunochromatographic assay]
Malaria, Falciparum
[Preparation of a monoclonal antibodies against Plasmodium falciparum glutamate dehydrogenase and establishment of colloidal gold-immunochromatographic assay]
Malnutrition
Effects of undernutrition and protein deficiency on glutamate dehydrogenase and decarboxylase in rat brain.
Expression of a bacterial aspartase gene in Aspergillus nidulans: an efficient system for selecting multicopy transformants.
Malnutrition and related risk factors in older adults from different health-care settings: an enable study.
Protein malnutrition potentiates the amplifying pathway of insulin secretion in adult obese mice.
The Physical Functional Capacity of Frail Elderly Persons Undergoing Ambulatory Rehabilitation is Related to Their Nutritional Status.
Maple Syrup Urine Disease
Enzymatic method for branched chain alpha-ketoacid determination: application to rapid analysis of urine and plasma samples from maple syrup urine disease patients.
Metabolic Syndrome
PREVALENCE OF THE METABOLIC SYNDROME IN MODERATELY-SEVERELY OBESE SUBJECTS WITH AND WITHOUT GROWTH HORMONE DEFICIENCY.
Motor Neuron Disease
Glutamate dehydrogenase and aspartate aminotransferase in leukocytes of patients with motor neuron disease.
Lymphocyte glutamate dehydrogenase activity in normal aging and neurological diseases.
Movement Disorders
Deregulation of glutamate dehydrogenase in human neurologic disorders.
Multiple Sclerosis
[Cerebral form of glutamate dehydrogenase activity in autonomic paroxysms (attacks of panic)]
Multiple System Atrophy
Characterization of glutamate dehydrogenase isoproteins purified from the cerebellum of normal subjects and patients with degenerative neurological disorders, and from human neoplastic cell lines.
Glutamate dehydrogenase deficiency in cerebellar degenerations: clinical, biochemical and molecular genetic aspects.
Glutamate dehydrogenase deficiency in Machado-Joseph disease.
Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disorders.
Low leukocyte glutamate dehydrogenase activity does not correlate with a particular type of multiple system atrophy.
Novel human glutamate dehydrogenase expressed in neural and testicular tissues and encoded by an X-linked intronless gene.
Muscular Dystrophy, Duchenne
Safety and disease monitoring biomarkers in Duchenne muscular dystrophy: results from a Phase II trial.
Myocardial Infarction
Systemic short-term fibrinolysis with high-dose streptokinase in acute myocardial infarction: time course of biochemical parameters.
[Enzyme diagnosis of liver dysfunction in acute myocardial infarct and its complications]
Neoplasm Metastasis
Expression and prognostic value of glutamate dehydrogenase in extrahepatic cholangiocarcinoma patients.
Glutamate dehydrogenase is a novel prognostic marker and predicts metastases in colorectal cancer patients.
Glutamate Dehydrogenase to the Rescue.
Value of alkaline phosphatase, 5'-nucleotidase, gamma-glutamyltransferase, and glutamate dehydrogenase activity measurements (single and combined) in serum in diagnosis of metastasis to the liver.
[Evaluation of serum glutamic dehydrogenase activity in the diagnosis and treatment of hepatocellular carcinoma and liver metastasis]
Neoplasms
Biomolecular Interaction Assays Identified Dual Inhibitors of Glutaminase and Glutamate Dehydrogenase That Disrupt Mitochondrial Function and Prevent Growth of Cancer Cells.
Both-In-One Hybrid Bacteria Suppress the Tumor Metastasis and Relapse via Tandem-Amplifying Reactive Oxygen Species-Immunity Responses.
Changes in enzyme pattern of Ehrlich ascites tumor cells following serial cultivation in media with increased (hypertonic) NaCl content.
Clinical and pathological studies in horses with hepatic disease.
Crystal structure of glutamate dehydrogenase 2, a positively selected novel human enzyme involved in brain biology and cancer pathophysiology.
CtBP maintains cancer cell growth and metabolic homeostasis via regulating SIRT4.
Ebselen Reversibly Inhibits Human Glutamate Dehydrogenase at the Catalytic Site.
Enhanced mitochondrial glutamine anaplerosis suppresses pancreatic cancer growth through autophagy inhibition.
Enzyme activities of six different dehydrogenases in Ehrlich ascites cells measured by flow cytometry.
Enzyme pathology of the liver in patients with and without nonhepatic cancer.
Expression and prognostic value of glutamate dehydrogenase in extrahepatic cholangiocarcinoma patients.
Expression of glutamine metabolism-related proteins according to molecular subtype of breast cancer.
Expression of glutamine metabolism-related proteins in thyroid cancer.
Expression of metabolism-related proteins in invasive lobular carcinoma: comparison to invasive ductal carcinoma.
Expression of the glutamine metabolism-related proteins glutaminase 1 and glutamate dehydrogenase in canine mammary tumours.
Flow-cytometric determination of dehydrogenase activities in primary human gastrointestinal tumor cell lines.
Glutamate dehydrogenase (GDH) regulates bioenergetics and redox homeostasis in human glioma.
Glutamate dehydrogenase (GLUD1) expression in breast cancer.
Glutamate dehydrogenase inhibits tumor growth in gastric cancer through the Notch signaling pathway.
Glutamate dehydrogenase is a novel prognostic marker and predicts metastases in colorectal cancer patients.
Glutamate Dehydrogenase to the Rescue.
Glutamate Dehydrogenase, a Complex Enzyme at a Crucial Metabolic Branch Point.
Glutamate production from ammonia via glutamate dehydrogenase 2 activity supports cancer cell proliferation under glutamine depletion.
Glutamic acid dehydrogenase and glutamic-oxalacetic transaminase of blood in leukemia and cancer.
Glutamine oxidation maintains the TCA cycle and cell survival during impaired mitochondrial pyruvate transport.
Glutaminolysis and carcinogenesis of oral squamous cell carcinoma.
Glutaminolysis dynamics during astrocytoma progression correlates with tumor aggressiveness.
GREEN TEA POLYPHENOLS CONTROL DYSREGULATED GLUTAMATE DEHYDROGENASE IN TRANSGENIC MICE BY HIJACKING THE ADP ACTIVATION SITE.
Hepatic mitochondrial enzyme activity and serum amino acid composition in rats treated with tumor necrosis factor.
Increased susceptibility of carbamylated glutamate dehydrogenase to proteolysis.
Influence of formulation parameters on gadolinium entrapment and tumor cell uptake using folate-coated nanoparticles.
Isocitrate dehydrogenase 1-mutated cancers are sensitive to the green tea polyphenol epigallocatechin-3-gallate.
L-carnitine could not improve hepatic warm ischemia-reperfusion injury despite ameliorated blood flow.
Mapping the Intramolecular Communications among Different Glutamate Dehydrogenase States Using Molecular Dynamics.
Metabolic Adaptation to Nutritional Stress in Human Colorectal Cancer.
Metabolic recycling of ammonia via glutamate dehydrogenase supports breast cancer biomass.
Oncogenes and tumor suppressors regulate glutamine metabolism in cancer cells.
PDHA1 gene knockout in prostate cancer cells results in metabolic reprogramming towards greater glutamine dependence.
Physiological Role of Glutamate Dehydrogenase in Cancer Cells.
Prominent glutamine oxidation activity in mitochondria of avian transplantable hepatoma induced by MC-29 virus.
Propylselen inhibits cancer cell growth by targeting glutamate dehydrogenase at the NADP+ binding site.
Short-term metabolic fate of L-[13N]glutamate in the Walker 256 carcinosarcoma in vivo.
Silibinin protects OTA-mediated TNF-alpha release from perfused rat livers and isolated rat Kupffer cells.
The pathway of glutamate oxidation in isolated mitochondria from the avian hepatomatous growth induced by MC-29 virus.
Upregulation of GLS1 Isoforms KGA and GAC Facilitates Mitochondrial Metabolism and Cell Proliferation in Epstein-Barr Virus Infected Cells.
Value of alkaline phosphatase, 5'-nucleotidase, gamma-glutamyltransferase, and glutamate dehydrogenase activity measurements (single and combined) in serum in diagnosis of metastasis to the liver.
[Correlation of glutamate dehydrogenase with several tumors].
[Oxidoreductase activity in the cells of stomach cancer]
[Studies of glutamate dehydrogenase activity in normal tissues and in malignant tumors]
Nervous System Diseases
Characterization of glutamate dehydrogenase isoproteins purified from the cerebellum of normal subjects and patients with degenerative neurological disorders, and from human neoplastic cell lines.
Degenerative neurological disorders associated with deficiency of glutamate dehydrogenase.
Deregulation of glutamate dehydrogenase in human neurologic disorders.
Fitting neurological protein aggregation kinetic data via a 2-step, minimal/"Ockham's razor" model: the Finke-Watzky mechanism of nucleation followed by autocatalytic surface growth.
Glutamate Dehydrogenase as a Neuroprotective Target Against Neurodegeneration.
Glutamate dehydrogenase deficiency disrupts glutamate homeostasis in hippocampus and prefrontal cortex and impairs recognition memory.
Glutamate dehydrogenase deficiency in cerebellar degenerations: clinical, biochemical and molecular genetic aspects.
Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disorders.
Leukocyte glutamate dehydrogenase in patients with degenerative neurological disorders.
Levels of glutamic acid decarboxylase (GAD), gamma amino butyric acid transaminase (GABA-T), glutamic acid dehydrogenase (GLDH) and proteins in cerebrospinal fluid of certain neurological disorders.
Neurological aspects of hyperinsulinism-hyperammonaemia syndrome.
Neurological disorders associated with deficiency of glutamate dehydrogenase.
Novel human glutamate dehydrogenase expressed in neural and testicular tissues and encoded by an X-linked intronless gene.
Using cryo-EM to map small ligands on dynamic metabolic enzymes: Studies with glutamate dehydrogenase.
Neuroblastoma
Human GLUD1 and GLUD2 glutamate dehydrogenase localize to mitochondria and endoplasmic reticulum.
Small-interfering-RNA-mediated silencing of human glutamate dehydrogenase induces apoptosis in neuroblastoma cells.
Neurodegenerative Diseases
Activation of two types of brain glutamate dehydrogenase isoproteins by gabapentin.
Allosteric regulation of glutamate dehydrogenase deamination activity.
Cellular and regional expression of glutamate dehydrogenase in the rat nervous system: non-radioactive in situ hybridization and comparative immunocytochemistry.
Differential Levels of Glutamate Dehydrogenase 1 (GLUD1) in BALB/c and C57BL/6 Mice and the Effects of Over-Expression of Glud1 Gene on Glutamate Release in Striatum.
Glutamate Dehydrogenase as a Neuroprotective Target Against Neurodegeneration.
Regional distribution of astrocytes with intense immunoreactivity for glutamate dehydrogenase in rat brain: implications for neuron-glia interactions in glutamate transmission.
The human GLUD2 glutamate dehydrogenase and its regulation in health and disease.
Unaltered cytochrome oxidase, glutamate dehydrogenase and glutaminase activities in platelets from patients with sporadic amyotrophic lateral sclerosis--a study of potential pathogenetic mechanisms in neurodegenerative diseases.
Non-alcoholic Fatty Liver Disease
Glutamate dehydrogenase activator BCH stimulating reductive amination prevents high fat/high fructose diet-induced steatohepatitis and hyperglycemia in C57BL/6J mice.
Obesity
Differential representation of liver proteins in obese human subjects suggests novel biomarkers and promising targets for drug development in obesity.
Odontogenic Cysts
Odontogenic keratocysts: a clinical and histological study with special reference to enzyme histochemistry.
Olivopontocerebellar Atrophies
Abnormal glutamate metabolism in an adult-onset degenerative neurological disorder.
Abnormal platelet glutamate dehydrogenase activity and activation in dominant and nondominant olivopontocerebellar atrophy.
Abnormalities of mitochondrial enzymes in hereditary ataxias.
Cerebellar glutamate metabolizing enzymes in spinocerebellar ataxia type I.
Degenerative neurological disorders associated with deficiency of glutamate dehydrogenase.
Glutamate and malate dehydrogenase activities in Joseph disease and olivopontocerebellar atrophy.
Glutamate dehydrogenase and its isozyme activity in olivopontocerebellar atrophy.
Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy.
Glutamate dehydrogenase deficiency in spinocerebellar degenerations.
Glutamate dehydrogenase in olivopontocerebellar atrophies: leukocytes, fibroblasts, and muscle mitochondria.
Low leukocyte glutamate dehydrogenase activity does not correlate with a particular type of multiple system atrophy.
Lymphocyte glutamate dehydrogenase activity in normal aging and neurological diseases.
Multiple system degeneration with glutamate dehydrogenase deficiency: pathology and biochemistry.
Neurological disorders associated with deficiency of glutamate dehydrogenase.
Neurophysiologic study of olivopontocerebellar atrophy with or without glutamate dehydrogenase deficiency.
Olivopontocerebellar atrophy with retinal degeneration. An electroretinographic and histopathologic investigation.
Oral glutamate loading in disorders with spinocerebellar and extrapyramidal involvement: effect on plasma glutamate, aspartate and taurine.
Pathology of olivopontocerebellar atrophy with glutamate dehydrogenase deficiency.
Osteoarthritis, Hip
Protein metabolism in the synovial membrane in the hip osteoarthritis.
Ovarian Neoplasms
[Correlation of glutamate dehydrogenase with several tumors].
Pancreatic Neoplasms
Flow-cytometric determination of dehydrogenase activities in primary human gastrointestinal tumor cell lines.
Pancreatitis
[Glutamate dehydrogenase activity in the pancreatic tissue in acute experimental pancreatitis and under the action of sodium thiosulphate]
Paralysis
Glutamate dehydrogenase (GDH) deficiency in different types of progressive hereditary cerebellar ataxia.
Parasitic Diseases
Development of Molecular Diagnosis Using Multiplex Real-Time PCR and T4 Phage Internal Control to Simultaneously Detect Cryptosporidium parvum, Giardia lamblia, and Cyclospora cayetanensis from Human Stool Samples.
Exploring alterations in hematological and biochemical parameters, enzyme activities and serum cortisol in Besnoitia besnoiti naturally infected dairy cattle.
Studies on ammonia-metabolizing enzymes during Plasmodium yoelii infection and pyrimethamine treatment in mice.
Parkinson Disease
Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset.
Glutamate Dehydrogenase as a Neuroprotective Target Against Neurodegeneration.
Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disorders.
Lymphocyte glutamate dehydrogenase activity in normal aging and neurological diseases.
Propylselen inhibits cancer cell growth by targeting glutamate dehydrogenase at the NADP+ binding site.
The human GLUD2 glutamate dehydrogenase and its regulation in health and disease.
[Cytochemical activity of mitochondrial enzymes in Parkinson's disease]
Parkinsonian Disorders
Decreased glutamate dehydrogenase protein in spinocerebellar degeneration.
Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy.
Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disorders.
Rehabilitation outcomes of older patients at 6 months follow-up after discharged from a geriatric day hospital (GDH).
Periodontitis
[Activity of glutamate dehydrogenase, gamma-glutamyltranspeptidase and creatine kinase in saliva in gingivitis]
Peripheral Nervous System Diseases
Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy.
Photosensitivity Disorders
Bile Duct Lesions Associated With Turnip (Brassica rapa) Photosensitization Compared With Those Due to Sporidesmin Toxicosis in Dairy Cows.
Could Nitrile Derivatives of Turnip (Brassica rapa) Glucosinolates Be Hepato- or Cholangiotoxic in Cattle?
Prostatic Neoplasms
PDHA1 gene knockout in prostate cancer cells results in metabolic reprogramming towards greater glutamine dependence.
Protein Deficiency
Effects of undernutrition and protein deficiency on glutamate dehydrogenase and decarboxylase in rat brain.
Pyelonephritis
[Glutamic dehydrogenase activities in renal tissue during experimental and human ehronie pyelonephritis (author's transl)]
Renal Insufficiency, Chronic
Canagliflozin mediated dual inhibition of mitochondrial glutamate dehydrogenase and complex I: an off-target adverse effect.
Reye Syndrome
Absence of diffusible inhibitor of glutamate dehydrogenase in the hepatocytes of Reye syndrome patients.
Effects of peroxidized polyunsaturated fatty acids on mitochondrial function and structure: pathogenetic implications for Reye's syndrome.
Glutamate dehydrogenase in Reye's syndrome. Evidence for the presence of an altered enzyme in serum with increased susceptibility to inhibition by GTP.
Masking by enzyme inhibitor of raised serum glutamate dehydrogenase activity in Reye's syndrome.
Quantitative evaluation of the extent of hepatic enzyme changes in Reye syndrome compared with normal liver or with non-Reye liver disorders: objective criteria for animal models.
Serum glutamate dehydrogenase and ornithine carbamyl transferase in Reye's syndrome.
Sarcoidosis
Lactate, malate and glutamate dehydrogenase activity in mediastinal lymph nodes in sarcoidosis.
Sarcoma, Yoshida
Effects of glutamate dehydrogenase, choline oxidase, and glucose-6-phosphatase on 67Ga accumulation in lysosome.
Schistosomiasis
Serum isocitric dehydrogenase and glutamic dehydrogenase in schistosomiasis.
Schistosomiasis mansoni
Serum enzyme tests in hepatosplenic schistosomiasis.
Seizures
A severe case of hyperinsulinism due to hemizygous activating mutation of glutamate dehydrogenase.
Anticonvulsant drugs, brain glutamate dehydrogenase activity and oxygen consumption.
Biochemical evaluation of an infant with hypoglycemia resulting from a novel de novo mutation of the GLUD1 gene and hyperinsulinism-hyperammonemia syndrome.
Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations.
Deregulation of glutamate dehydrogenase in human neurologic disorders.
Differential glutamate dehydrogenase (GDH) activity profile in patients with temporal lobe epilepsy.
Effect of vigabatrin on glutamate dehydrogenase in the hippocampus of seizure prone gerbils.
Effects of acute hyperammonemia in vivo on oxidative metabolism in nonsynaptic rat brain mitochondria.
Modulation of brain glutamate dehydrogenase as a tool for controlling seizures.
Neurological aspects of hyperinsulinism-hyperammonaemia syndrome.
[Metabolic investigations of epileptic seizures: the role of aminotransferases and glutamate dehydrogenase in convulsions]
Sexually Transmitted Diseases
Population genetics of Neisseria gonorrhoeae in a high-prevalence community using a hypervariable outer membrane porB and 13 slowly evolving housekeeping genes.
Spinal Cord Ischemia
Preventive effects of intrathecal methylprednisolone administration on spinal cord ischemia in rats: the role of excitatory amino acid metabolizing systems.
Spinocerebellar Ataxias
Cerebellar glutamate metabolizing enzymes in spinocerebellar ataxia type I.
Decreased glutamate dehydrogenase protein in spinocerebellar degeneration.
Glutamate Dehydrogenase as a Neuroprotective Target Against Neurodegeneration.
Glutamate dehydrogenase deficiency in three patients with spinocerebellar ataxia: a new enzymatic defect?
Glutamate dehydrogenase deficiency in three patients with spinocerebellar syndrome.
Spinocerebellar Degenerations
Decreased glutamate dehydrogenase protein in spinocerebellar degeneration.
Glutamate dehydrogenase deficiency in Machado-Joseph disease.
Glutamate dehydrogenase deficiency in spinocerebellar degenerations.
Glutamate metabolism of leukocytes and skin fibroblasts in spinocerebellar degeneration with lowered glutamate dehydrogenase activity.
Leucocyte glutamate dehydrogenase in various hereditary ataxias.
Low leukocyte glutamate dehydrogenase activity does not correlate with a particular type of multiple system atrophy.
Normal cerebellar glutamate dehydrogenase protein in spinocerebellar degeneration.
Partially deficient glutamate dehydrogenase activity and attenuated oscillatory potentials in patients with spinocerebellar degeneration.
[Dual nature of excitatory amino acids in the vertebrate retina]
[Glutamate dehydrogenase and its isozyme activity in spinocerebellar degeneration]
Starvation
Amino-acid metabolism enzyme activities in rat white adipose tissue.
Asparagine metabolism and nitrogen distribution during protein degradation in sugar-starved maize root tips.
Changes in Viability, Cell Composition, and Enzyme Levels During Starvation of Continuously Cultured (Ammonia-Limited) Selenomonas ruminantium.
Distinctive properties and expression profiles of glutamine synthetase from a plant symbiotic fungus.
Dynamic transcriptome analysis of root nitrate starvation and re-supply provides insights into nitrogen metabolism in pear (Pyrus bretschneideri).
Effect of 24-hour starvation on amino acid pool composition and enzyme activities of rat brown adipose tissue.
Effect of glucose starvation on the nicotinamide adenine dinucleotide phosphate-dependent glutamate dehydrogenase of yeast.
Glutamate deamination by glutamate dehydrogenase plays a central role in amino acid catabolism in plants.
Long-term nutritional effects on the primary liver and kidney metabolism in rainbow trout. Adaptive response to starvation and a high-protein, carbohydrate-free diet on glutamate dehydrogenase and alanine aminotransferase kinetics.
Metabolic pathways of ammoniogenesis in the shrimp Crangon crangon L.: possible role of glutamate dehydrogenase.
Metabolic responses to short starvation and refeeding in Dicentrarchus labrax. Effect of dietary composition
Muliple sites of action of cycloheximide in addition to inhibition of protein synthesis in Physarum polycephalum.
Multiple Forms of Glutamate Dehydrogenase in Animals: Structural Determinants and Physiological Implications.
Mutation-induced metabolite pool alterations in Corynebacterium glutamicum: towards the identification of nitrogen control signals.
NAD(H)-dependent glutamate dehydrogenase is essential for the survival of Arabidopsis thaliana during dark-induced carbon starvation.
New insights towards the function of glutamate dehydrogenase revealed during source-sink transition of tobacco (Nicotiana tabacum) plants grown under different nitrogen regimes.
Phosphorylation of NAD-dependent glutamate dehydrogenase from yeast.
Physiological role and regulation of glutamate dehydrogenase in Prochlorococcus sp. strain MIT9313.
Regulation of Saccharomyces cerevisiae nicotinamide adenine dinucleotide phosphate-dependent glutamate dehydrogenase by proteolysis during carbon starvation.
Screening, morphological and molecular characterization of fungi producing cystathionine ?-lyase.
Stress-induced changes in glutamate dehydrogenase activity imply its role in adaptation to C and N metabolism in lupine embryos.
The dynamics of local kinetic parameters of glutamate dehydrogenase in rat liver.
The influence of high dietary protein, energy and mineral intake on deficient young camel (Camelus dromedarius)--I. Changes in metabolic profiles and growth performance.
The two-component, ATP-dependent Clp protease of Escherichia coli. Purification, cloning, and mutational analysis of the ATP-binding component.
Stomach Neoplasms
Flow-cytometric determination of dehydrogenase activities in primary human gastrointestinal tumor cell lines.
Glutamate dehydrogenase inhibits tumor growth in gastric cancer through the Notch signaling pathway.
Striatonigral Degeneration
Low leukocyte glutamate dehydrogenase activity does not correlate with a particular type of multiple system atrophy.
Stroke
Glutamate Dehydrogenase as a Neuroprotective Target Against Neurodegeneration.
[Geriatric day hospital: what evidence? A systematic review].
Subacute Sclerosing Panencephalitis
Promoter specificity of sigma G-containing RNA polymerase from sporulating cells of Bacillus subtilis: identification of a group of forespore-specific promoters.
sulfite oxidase deficiency
A mechanism of sulfite neurotoxicity: direct inhibition of glutamate dehydrogenase.
Supranuclear Palsy, Progressive
Leukocyte glutamate dehydrogenase activity in patients with degenerative neurological disorders.
Tauopathies
Identification of non-Alzheimer's disease tauopathies-related proteins by proteomic analysis.
Thiamine Deficiency
Interplay Between Thiamine and p53/p21 Axes Affects Antiproliferative Action of Cisplatin in Lung Adenocarcinoma Cells by Changing Metabolism of 2-Oxoglutarate/Glutamate.
Physiological studies on the effects of nutritional imbalance on the central nervous system. II. Effects of thiamine deficiency on oxidative enzymes in the brain of chicken, Gallus domesticus.
Thrombocytopenia
NTP Toxicology and Carcinogenesis Studies of Chloroprene (CAS No. 126-99-8) in F344/N Rats and B6C3F1 Mice (Inhalation Studies).
Thyrotoxicosis
[Effect of experimental changes in thyroid function on oxidative metabolism and glutamate dehydrogenase activity in the limbic system of the rat]
Tuberculosis
Glutamate Dehydrogenase Is Required by Mycobacterium bovis BCG for Resistance to Cellular Stress.
The gdhB gene of Pseudomonas aeruginosa encodes an arginine-inducible NAD(+)-dependent glutamate dehydrogenase which is subject to allosteric regulation.
Typhoid Fever
[Enzymatic activity in the lung cells to the intrapulmonary administration of antigen]
[The effect of lipids from typhoid endotoxin on the activity of some liver enzymes]
Vitamin E Deficiency
Combined vitamin E deficiency and ethanol pretreatment: liver glutathione and enzyme changes.