Disease on EC 1.3.3.3 - coproporphyrinogen oxidase
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Anemia, Sideroblastic
Coproporphyrinogen oxidase activity and porphyrin concentrations in peripheral red blood cells in hereditary sideroblastic anaemia.
Brain Diseases
A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp).
Brain Neoplasms
Enhanced expression of coproporphyrinogen oxidase in malignant brain tumors: CPOX expression and 5-ALA-induced fluorescence.
Brain Neoplasms
Retraction of "Enhanced expression of coproporphyrinogen oxidase in malignant brain tumors: CPOX expression and 5-ALA-induced fluorescence". Neuro-Oncology 13(11):1234-1243.
Carcinoma
Expression of coproporphyrinogen oxidase is associated with detection of upper gastrointestinal carcinomas by 5-aminolevulinic acid-mediated photodynamic diagnosis.
Carcinoma, Hepatocellular
Effect of acute lead treatment on coproporphyrinogen oxidase activity in HepG2 cells.
Cataract
Hereditary cataract of the Nakano mouse: Involvement of a hypomorphic mutation in the coproporphyrinogen oxidase gene.
Coproporphyria, Hereditary
A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp).
Coproporphyria, Hereditary
A description of an HPLC assay of coproporphyrinogen III oxidase activity in mononuclear cells.
Coproporphyria, Hereditary
A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.
Coproporphyria, Hereditary
A novel missense mutation in exon 4 of the human coproporphyrinogen oxidase gene in two patients with hereditary coproporphyria.
Coproporphyria, Hereditary
A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family.
Coproporphyria, Hereditary
Alterations in the activity of enzymes of haem biosynthesis in lead poisoning and acute hepatic prophyria.
Coproporphyria, Hereditary
Analysis of porphyrins and enzymes in porphyrin synthesis in Taenia solium cysticercus from man and pig.
Coproporphyria, Hereditary
Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene.
Coproporphyria, Hereditary
Characterization and expression of cDNA encoding coproporphyrinogen oxidase from a patient with hereditary coproporphyria.
Coproporphyria, Hereditary
Co-existence of hereditary coproporphyria and porphyria cutanea tarda: The importance of genetic testing.
Coproporphyria, Hereditary
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.
Coproporphyria, Hereditary
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant.
Coproporphyria, Hereditary
Decreased lymphocyte coproporphyrinogen III oxidase activity in hereditary coproporphyria.
Coproporphyria, Hereditary
Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria.
Coproporphyria, Hereditary
DGGE analysis of the coproporphyrinogen oxidase gene: two new mutations in DNA from Danish patients with hereditary coproporphyria.
Coproporphyria, Hereditary
Four novel mutations of the coproporphyrinogen III oxidase gene.
Coproporphyria, Hereditary
Function and structure of rat hepatic coproporphyrinogen oxidase.
Coproporphyria, Hereditary
Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R.
Coproporphyria, Hereditary
Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene.
Coproporphyria, Hereditary
Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms.
Coproporphyria, Hereditary
Identification of a novel mutation of the CPO gene in a Japanese hereditary coproporphyria family.
Coproporphyria, Hereditary
Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyria.
Coproporphyria, Hereditary
International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias.
Coproporphyria, Hereditary
Investigation of the catalytic and structural roles of conserved histidines of human coproporphyrinogen oxidase using site-directed mutagenesis.
Coproporphyria, Hereditary
Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12.
Coproporphyria, Hereditary
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias.
Coproporphyria, Hereditary
Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria.
Coproporphyria, Hereditary
Molecular cloning, sequencing and expression of cDNA encoding human coproporphyrinogen oxidase.
Coproporphyria, Hereditary
Molecular defects of the coproporphyrinogen oxidase gene in hereditary coproporphyria.
Coproporphyria, Hereditary
Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
Coproporphyria, Hereditary
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria.
Coproporphyria, Hereditary
Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis.
Coproporphyria, Hereditary
Neonatal-Onset Hereditary Coproporphyria: A New Variant of Hereditary Coproporphyria.
Coproporphyria, Hereditary
Oxygen-dependent coproporphyrinogen-III oxidase from Escherichia coli: one-step purification and biochemical characterisation.
Coproporphyria, Hereditary
Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP).
Coproporphyria, Hereditary
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update.
Coproporphyria, Hereditary
The enzyme engineering of mutant homodimer and heterodimer of coproporphyinogen oxidase contributes to new insight into hereditary coproporphyria and harderoporphyria.
Coproporphyria, Hereditary
Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria.
Coproporphyria, Hereditary
[Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria]
coproporphyrinogen oxidase deficiency
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.
coproporphyrinogen oxidase deficiency
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant.
coproporphyrinogen oxidase deficiency
Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
Epilepsy
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.
Leukemia, Erythroblastic, Acute
Coproporphyrinogen oxidase. Purification, molecular cloning, and induction of mRNA during erythroid differentiation.
Leukemia, Erythroblastic, Acute
Expression of coproporphyrinogen oxidase and synthesis of hemoglobin in human erythroleukemia K562 cells.
Leukemia, Erythroblastic, Acute
Induction of terminal enzymes for heme biosynthesis during differentiation of mouse erythroleukemia cells.
Leukemia, Erythroblastic, Acute
Involvement of the transcriptional factor GATA-1 in regulation of expression of coproporphyrinogen oxidase in mouse erythroleukemia cells.
Leukemia, Erythroblastic, Acute
Mouse coproporphyrinogen oxidase is a copper-containing enzyme: expression in Escherichia coli and site-directed mutagenesis.
Leukemia, Feline
Comparison of protoporphyrin IX content and related gene expression in the tissues of chickens laying brown-shelled eggs.
Liver Diseases, Alcoholic
Coproporphyrinogen oxidase, protoporphyrinogen oxidase and ferrochelatase activities in human liver biopsies with special reference to alcoholic liver disease.
Neoplasms
Expression of coproporphyrinogen oxidase is associated with detection of upper gastrointestinal carcinomas by 5-aminolevulinic acid-mediated photodynamic diagnosis.
Neoplasms
Mechanism of differentiation-enhanced photodynamic therapy for cancer: upregulation of coproporphyrinogen oxidase by C/EBP transcription factors.
Photosensitivity Disorders
Antibacterial photosensitization through activation of coproporphyrinogen oxidase.
Porphyria Cutanea Tarda
Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda.
Porphyria Cutanea Tarda
[Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria]
Porphyria, Acute Intermittent
International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias.
Porphyria, Acute Intermittent
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias.
Porphyria, Acute Intermittent
Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP).
Porphyria, Erythropoietic
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant.
Porphyria, Variegate
International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias.
Porphyria, Variegate
Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP).
Porphyrias
Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda.
Porphyrias
Decreased activity of liver coproporphyrinogen oxidase in hexachlorobenzene-induced porphyria.
Porphyrias
Digenic Inheritance of Mutations in the Coproporphyrinogen Oxidase and Protoporphyrinogen Oxidase Genes in a Unique Type of Porphyria.
Porphyrias
Direct Assay of Enzymes in Heme Biosynthesis for the Detection of Porphyrias by Tandem Mass Spectrometry. Uroporphyrinogen Decarboxylase and Coproporphyrinogen III Oxidase.
Porphyrias
Dual gene defects involving delta-aminolaevulinate dehydratase and coproporphyrinogen oxidase in a porphyria patient.
Porphyrias
International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias.
Porphyrias
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias.
Porphyrias
Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria.
Porphyrias
Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP).
Porphyrias
Studies on the etiology of trace metal-induced porphyria: effects of porphyrinogenic metals on coproporphyrinogen oxidase in rat liver and kidney.
Porphyrias
Use of Di- and Tripropionate substrate analogs to probe the active site of human recombinant coproporphyrinogen oxidase.
Porphyrias
[Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria]
Porphyrias, Hepatic
Acute hepatic porphyrias: Identification of 46 hydroxymethylbilane synthase, 11 coproporphyrinogen oxidase, and 20 protoporphyrinogen oxidase novel mutations.
Porphyrias, Hepatic
Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R.
Porphyrias, Hepatic
Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyria.
Porphyrias, Hepatic
International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias.
Porphyrias, Hepatic
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria.
Porphyrias, Hepatic
Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis.
Porphyrias, Hepatic
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update.
Protoporphyria, Erythropoietic
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant.
protoporphyrin ferrochelatase deficiency
Elucidation of the mechanism of mitochondrial iron loading in Friedreich's ataxia by analysis of a mouse mutant.
Skin Neoplasms
Vitamin D3 enhances the apoptotic response of epithelial tumors to aminolevulinate-based photodynamic therapy.
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