Disease on EC 1.1.1.26 - glyoxylate reductase
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Carcinoma, Hepatocellular
Glyoxylate Reductase/Hydroxypyruvate Reductase: A Novel Prognostic Marker for Hepatocellular Carcinoma Patients after Curative Resection.
Colitis
Up regulation of glyoxylate reductase/hydroxypyruvate reductase (GRHPR) is associated with intestinal epithelial cells apoptosis in TNBS-induced experimental colitis.
Colorectal Neoplasms
Correction to: Downregulation of GLYR1 contributes to microsatellite instability colorectal cancer by targeting p21 via the p38MAPK and PI3K/AKT pathways.
Colorectal Neoplasms
Downregulation of GLYR1 contributes to microsatellite instability colorectal cancer by targeting p21 via the p38MAPK and PI3K/AKT pathways.
Crohn Disease
Up regulation of glyoxylate reductase/hydroxypyruvate reductase (GRHPR) is associated with intestinal epithelial cells apoptosis in TNBS-induced experimental colitis.
Genetic Diseases, Inborn
A mutation creating an out-of-frame alternative translation initiation site in the GRHPR 5'UTR causing primary hyperoxaluria type II.
glyoxylate reductase deficiency
Combined Liver-Kidney Transplantation for Primary Hyperoxaluria Type 2: A Case Report.
glyoxylate reductase deficiency
Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2.
glyoxylate reductase deficiency
Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report.
glyoxylate reductase deficiency
Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism.
glyoxylate reductase deficiency
[Primary hiperoxaluria: a new mutation in gen AGXT (R197Q) cause of neonatal convulsions]
Hyperoxaluria
Failure of isolated kidney transplantation in a pediatric patient with primary hyperoxaluria type 2.
Hyperoxaluria
Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association.
Hyperoxaluria
Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis.
Hyperoxaluria
[Primary hiperoxaluria: a new mutation in gen AGXT (R197Q) cause of neonatal convulsions]
Hyperoxaluria, Primary
4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition.
Hyperoxaluria, Primary
A mutation creating an out-of-frame alternative translation initiation site in the GRHPR 5'UTR causing primary hyperoxaluria type II.
Hyperoxaluria, Primary
A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2.
Hyperoxaluria, Primary
Biochemical and genetic diagnosis of the primary hyperoxalurias: a review.
Hyperoxaluria, Primary
Combined Liver-Kidney Transplantation for Primary Hyperoxaluria Type 2: A Case Report.
Hyperoxaluria, Primary
Enzymological characterization of a feline analogue of primary hyperoxaluria type 2: a model for the human disease.
Hyperoxaluria, Primary
Ethnic differences in GRHPR mutations in patients with primary hyperoxaluria type 2.
Hyperoxaluria, Primary
Etiological Profile of Nephrocalcinosis in Children from Southern India.
Hyperoxaluria, Primary
Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxalurias.
Hyperoxaluria, Primary
Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2.
Hyperoxaluria, Primary
Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association.
Hyperoxaluria, Primary
Identification of missense, nonsense, and deletion mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2).
Hyperoxaluria, Primary
Kinetic analysis and tissue distribution of human D-glycerate dehydrogenase/glyoxylate reductase and its relevance to the diagnosis of primary hyperoxaluria type 2.
Hyperoxaluria, Primary
Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling.
Hyperoxaluria, Primary
Metabolism of Oxalate in Humans: A Potential Role Kynurenine Aminotransferase/Glutamine Transaminase/Cysteine Conjugate Beta-lyase Plays in Hyperoxaluria.
Hyperoxaluria, Primary
Modification of primers for GRHPR genotyping: avoiding allele dropout by single nucleotide polymorphisms and homology sequence.
Hyperoxaluria, Primary
Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2.
Hyperoxaluria, Primary
Novel mutation in the GRHPR gene in a Chinese patient with primary hyperoxaluria type 2 requiring renal transplantation from a living related donor.
Hyperoxaluria, Primary
Phenotypic and functional analysis of human SLC26A6 variants in patients with familial hyperoxaluria and calcium oxalate nephrolithiasis.
Hyperoxaluria, Primary
Primary cultures of renal proximal tubule cells derived from individuals with primary hyperoxaluria.
Hyperoxaluria, Primary
Promoter rearrangements cause species-specific hepatic regulation of the glyoxylate reductase/hydroxypyruvate reductase gene by the peroxisome proliferator-activated receptor alpha.
Hyperoxaluria, Primary
Recent developments in our understanding of primary hyperoxaluria type 2.
Hyperoxaluria, Primary
Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report.
Hyperoxaluria, Primary
Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism.
Hyperoxaluria, Primary
Tissue differences in the expression of mutations and polymorphisms in the GRHPR gene and implications for diagnosis of primary hyperoxaluria type 2.
Hyperoxaluria, Primary
Up regulation of glyoxylate reductase/hydroxypyruvate reductase (GRHPR) is associated with intestinal epithelial cells apoptosis in TNBS-induced experimental colitis.
Hyperoxaluria, Primary
[Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder].
Kidney Calculi
Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling.
Kidney Calculi
Promoter rearrangements cause species-specific hepatic regulation of the glyoxylate reductase/hydroxypyruvate reductase gene by the peroxisome proliferator-activated receptor alpha.
Kidney Failure, Chronic
Failure of isolated kidney transplantation in a pediatric patient with primary hyperoxaluria type 2.
Metabolic Diseases
Restrictive cardiomyopathy in a patient with primary hyperoxaluria type II.
Metabolism, Inborn Errors
Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism.
Neoplasms
Downregulation of GLYR1 contributes to microsatellite instability colorectal cancer by targeting p21 via the p38MAPK and PI3K/AKT pathways.
Neoplasms
Glyoxylate Reductase/Hydroxypyruvate Reductase: A Novel Prognostic Marker for Hepatocellular Carcinoma Patients after Curative Resection.
Neoplasms
Up regulation of glyoxylate reductase/hydroxypyruvate reductase (GRHPR) is associated with intestinal epithelial cells apoptosis in TNBS-induced experimental colitis.
Nephrocalcinosis
Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling.
Nephrocalcinosis
Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report.
Nephrolithiasis
Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report.
Obesity
Differential representation of liver proteins in obese human subjects suggests novel biomarkers and promising targets for drug development in obesity.
Renal Insufficiency
Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling.
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