Any feedback?
Please rate this page
(enzyme.php)
(0/150)

BRENDA support

Disease on EC 1.3.3.3 - coproporphyrinogen oxidase

Please use the Disease Search for a specific query.
Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Anemia
Adherence modifies the regulation of gene expression induced by interleukin-10.
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.
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).
A description of an HPLC assay of coproporphyrinogen III oxidase activity in mononuclear cells.
A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.
A novel missense mutation in exon 4 of the human coproporphyrinogen oxidase gene in two patients with hereditary coproporphyria.
A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family.
Alterations in the activity of enzymes of haem biosynthesis in lead poisoning and acute hepatic prophyria.
Analysis of porphyrins and enzymes in porphyrin synthesis in Taenia solium cysticercus from man and pig.
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.
Characterization and expression of cDNA encoding coproporphyrinogen oxidase from a patient with hereditary coproporphyria.
Co-existence of hereditary coproporphyria and porphyria cutanea tarda: The importance of genetic testing.
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant.
Decreased lymphocyte coproporphyrinogen III oxidase activity in hereditary coproporphyria.
Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria.
DGGE analysis of the coproporphyrinogen oxidase gene: two new mutations in DNA from Danish patients with hereditary coproporphyria.
Fecal coproporphyrin isomers in hereditary coproporphyria.
Four novel mutations of the coproporphyrinogen III oxidase gene.
Function and structure of rat hepatic coproporphyrinogen oxidase.
Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R.
Harderoporphyria: a variant hereditary coproporphyria.
Hereditary coproporphyria: an imitator of multiple sclerosis.
Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene.
Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms.
Identification of a novel mutation of the CPO gene in a Japanese hereditary coproporphyria family.
Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyria.
International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias.
Investigation of the catalytic and structural roles of conserved histidines of human coproporphyrinogen oxidase using site-directed mutagenesis.
Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12.
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias.
Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria.
Molecular cloning, sequencing and expression of cDNA encoding human coproporphyrinogen oxidase.
Molecular defects of the coproporphyrinogen oxidase gene in hereditary coproporphyria.
Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria.
Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis.
Neonatal-Onset Hereditary Coproporphyria: A New Variant of Hereditary Coproporphyria.
Oxygen-dependent coproporphyrinogen-III oxidase from Escherichia coli: one-step purification and biochemical characterisation.
Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP).
Structural basis of hereditary coproporphyria.
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update.
The enzyme engineering of mutant homodimer and heterodimer of coproporphyinogen oxidase contributes to new insight into hereditary coproporphyria and harderoporphyria.
The porphyrias.
The primary enzyme defect in hereditary coproporphyria.
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.
[Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria]
[Demonstration of hereditary enzyme defect in coproporphyria]
coproporphyrinogen oxidase deficiency
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant.
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.
Expression of coproporphyrinogen oxidase and synthesis of hemoglobin in human erythroleukemia K562 cells.
Induction of terminal enzymes for heme biosynthesis during differentiation of mouse erythroleukemia cells.
Involvement of the transcriptional factor GATA-1 in regulation of expression of coproporphyrinogen oxidase in mouse erythroleukemia cells.
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.
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.
[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.
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias.
Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP).
The porphyrias.
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.
Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP).
The porphyrias.
Porphyrias
Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda.
Decreased activity of liver coproporphyrinogen oxidase in hexachlorobenzene-induced porphyria.
Digenic Inheritance of Mutations in the Coproporphyrinogen Oxidase and Protoporphyrinogen Oxidase Genes in a Unique Type of Porphyria.
Direct Assay of Enzymes in Heme Biosynthesis for the Detection of Porphyrias by Tandem Mass Spectrometry. Uroporphyrinogen Decarboxylase and Coproporphyrinogen III Oxidase.
Dual gene defects involving delta-aminolaevulinate dehydratase and coproporphyrinogen oxidase in a porphyria patient.
International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias.
Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias.
Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria.
Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP).
Studies on the etiology of trace metal-induced porphyria: effects of porphyrinogenic metals on coproporphyrinogen oxidase in rat liver and kidney.
The porphyrias.
The primary enzyme defect in hereditary coproporphyria.
Use of Di- and Tripropionate substrate analogs to probe the active site of human recombinant coproporphyrinogen oxidase.
[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.
Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R.
Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyria.
International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias.
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria.
Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis.
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update.
The porphyrias.
Protoporphyria, Erythropoietic
Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant.
The porphyrias.
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.
Tics
Two proteins with different functions are derived from the KlHEM13 gene.