1.3.3.3 Anemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=15579372&form=6&db=m Adherence modifies the regulation of gene expression induced by interleukin-10. causal interaction,therapeutic application,unassigned 1,1,0 1.3.3.3 Anemia, Sideroblastic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3992190&form=6&db=m Coproporphyrinogen oxidase activity and porphyrin concentrations in peripheral red blood cells in hereditary sideroblastic anaemia. ongoing research,therapeutic application,unassigned 4,1,0 1.3.3.3 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29660996&form=6&db=m A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp). unassigned - 1.3.3.3 Brain Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21824890&form=6&db=m Enhanced expression of coproporphyrinogen oxidase in malignant brain tumors: CPOX expression and 5-ALA-induced fluorescence. causal interaction,diagnostic usage,ongoing research,unassigned 3,3,1,0 1.3.3.3 Brain Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23674837&form=6&db=m Retraction of "Enhanced expression of coproporphyrinogen oxidase in malignant brain tumors: CPOX expression and 5-ALA-induced fluorescence". Neuro-Oncology 13(11):1234-1243. unassigned - 1.3.3.3 Carcinoma http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28416355&form=6&db=m Expression of coproporphyrinogen oxidase is associated with detection of upper gastrointestinal carcinomas by 5-aminolevulinic acid-mediated photodynamic diagnosis. causal interaction,diagnostic usage,therapeutic application,unassigned 3,3,1,0 1.3.3.3 Carcinoma, Hepatocellular http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9674964&form=6&db=m Effect of acute lead treatment on coproporphyrinogen oxidase activity in HepG2 cells. ongoing research,unassigned 4,0 1.3.3.3 Cataract http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23631845&form=6&db=m Hereditary cataract of the Nakano mouse: Involvement of a hypomorphic mutation in the coproporphyrinogen oxidase gene. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=63041&form=6&db=m The primary enzyme defect in hereditary coproporphyria. causal interaction,ongoing research,unassigned 1,4,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=398301&form=6&db=m The porphyrias. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=712737&form=6&db=m Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria. causal interaction,unassigned 3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=843348&form=6&db=m Decreased lymphocyte coproporphyrinogen III oxidase activity in hereditary coproporphyria. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=866144&form=6&db=m [Demonstration of hereditary enzyme defect in coproporphyria] diagnostic usage,ongoing research,unassigned 2,3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=913057&form=6&db=m Alterations in the activity of enzymes of haem biosynthesis in lead poisoning and acute hepatic prophyria. causal interaction,unassigned 2,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1733615&form=6&db=m Fecal coproporphyrin isomers in hereditary coproporphyria. diagnostic usage,unassigned 2,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=1859268&form=6&db=m Hereditary coproporphyria: an imitator of multiple sclerosis. causal interaction,diagnostic usage,unassigned 3,4,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3574346&form=6&db=m Analysis of porphyrins and enzymes in porphyrin synthesis in Taenia solium cysticercus from man and pig. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6181213&form=6&db=m Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney. ongoing research,unassigned 2,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6886003&form=6&db=m Harderoporphyria: a variant hereditary coproporphyria. causal interaction,unassigned 4,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7592568&form=6&db=m Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria. causal interaction,diagnostic usage,unassigned 3,2,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7757079&form=6&db=m A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7849704&form=6&db=m Characterization and expression of cDNA encoding coproporphyrinogen oxidase from a patient with hereditary coproporphyria. ongoing research,unassigned 4,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7959694&form=6&db=m Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12. ongoing research,unassigned 2,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8012360&form=6&db=m Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms. causal interaction,unassigned 3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8286403&form=6&db=m Molecular cloning, sequencing and expression of cDNA encoding human coproporphyrinogen oxidase. diagnostic usage,ongoing research,unassigned 3,2,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8621830&form=6&db=m Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant. diagnostic usage,unassigned 1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9048920&form=6&db=m A novel missense mutation in exon 4 of the human coproporphyrinogen oxidase gene in two patients with hereditary coproporphyria. causal interaction,ongoing research,therapeutic application,unassigned 3,2,1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9074789&form=6&db=m Molecular defects of the coproporphyrinogen oxidase gene in hereditary coproporphyria. ongoing research,unassigned 2,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9298818&form=6&db=m Hereditary coproporphyria: exon screening by heteroduplex analysis detects three novel mutations in the coproporphyrinogen oxidase gene. causal interaction,diagnostic usage,ongoing research,unassigned 3,2,3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9454777&form=6&db=m Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis. causal interaction,unassigned 4,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9747031&form=6&db=m A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese family. causal interaction,unassigned 3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9843038&form=6&db=m Identification of a novel mutation of the CPO gene in a Japanese hereditary coproporphyria family. causal interaction,unassigned 3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9888388&form=6&db=m Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update. causal interaction,unassigned 3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11079369&form=6&db=m Function and structure of rat hepatic coproporphyrinogen oxidase. diagnostic usage,ongoing research,therapeutic application,unassigned 2,4,1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11202054&form=6&db=m DGGE analysis of the coproporphyrinogen oxidase gene: two new mutations in DNA from Danish patients with hereditary coproporphyria. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11831056&form=6&db=m [Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria] causal interaction,therapeutic application,unassigned 3,1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11929047&form=6&db=m Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria. therapeutic application,unassigned 1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=12181641&form=6&db=m 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. causal interaction,unassigned 3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=13129604&form=6&db=m Oxygen-dependent coproporphyrinogen-III oxidase from Escherichia coli: one-step purification and biochemical characterisation. causal interaction,unassigned 1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14605502&form=6&db=m A description of an HPLC assay of coproporphyrinogen III oxidase activity in mononuclear cells. causal interaction,unassigned 3,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14669009&form=6&db=m Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias. causal interaction,unassigned 1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16159891&form=6&db=m Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria. causal interaction,therapeutic application,unassigned 1,1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16176984&form=6&db=m Structural basis of hereditary coproporphyria. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=17179900&form=6&db=m Investigation of the catalytic and structural roles of conserved histidines of human coproporphyrinogen oxidase using site-directed mutagenesis. causal interaction,unassigned 4,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19267996&form=6&db=m Four novel mutations of the coproporphyrinogen III oxidase gene. ongoing research,unassigned 2,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21103937&form=6&db=m Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21231929&form=6&db=m Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyria. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23582006&form=6&db=m Co-existence of hereditary coproporphyria and porphyria cutanea tarda: The importance of genetic testing. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24078084&form=6&db=m The enzyme engineering of mutant homodimer and heterodimer of coproporphyinogen oxidase contributes to new insight into hereditary coproporphyria and harderoporphyria. causal interaction,ongoing research,unassigned 3,1,0 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24997713&form=6&db=m Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP). unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28349448&form=6&db=m Neonatal-Onset Hereditary Coproporphyria: A New Variant of Hereditary Coproporphyria. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29660996&form=6&db=m A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp). unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31073229&form=6&db=m International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias. unassigned - 1.3.3.3 Coproporphyria, Hereditary http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33008663&form=6&db=m 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. causal interaction,unassigned 3,0 1.3.3.3 coproporphyrinogen oxidase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6181213&form=6&db=m Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney. ongoing research,unassigned 2,0 1.3.3.3 coproporphyrinogen oxidase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8621830&form=6&db=m Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant. diagnostic usage,unassigned 1,0 1.3.3.3 coproporphyrinogen oxidase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11929047&form=6&db=m Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria. therapeutic application,unassigned 1,0 1.3.3.3 Epilepsy http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6181213&form=6&db=m Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney. ongoing research,unassigned 2,0 1.3.3.3 Leukemia, Erythroblastic, Acute http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7607249&form=6&db=m Induction of terminal enzymes for heme biosynthesis during differentiation of mouse erythroleukemia cells. unassigned - 1.3.3.3 Leukemia, Erythroblastic, Acute http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8407975&form=6&db=m Coproporphyrinogen oxidase. Purification, molecular cloning, and induction of mRNA during erythroid differentiation. ongoing research,unassigned 4,0 1.3.3.3 Leukemia, Erythroblastic, Acute http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8547339&form=6&db=m Mouse coproporphyrinogen oxidase is a copper-containing enzyme: expression in Escherichia coli and site-directed mutagenesis. ongoing research,unassigned 3,0 1.3.3.3 Leukemia, Erythroblastic, Acute http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9168923&form=6&db=m Involvement of the transcriptional factor GATA-1 in regulation of expression of coproporphyrinogen oxidase in mouse erythroleukemia cells. unassigned - 1.3.3.3 Leukemia, Erythroblastic, Acute http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11248690&form=6&db=m Expression of coproporphyrinogen oxidase and synthesis of hemoglobin in human erythroleukemia K562 cells. causal interaction,ongoing research,unassigned 1,4,0 1.3.3.3 Leukemia, Feline http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24235220&form=6&db=m Comparison of protoporphyrin IX content and related gene expression in the tissues of chickens laying brown-shelled eggs. unassigned - 1.3.3.3 Liver Diseases, Alcoholic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2921508&form=6&db=m Coproporphyrinogen oxidase, protoporphyrinogen oxidase and ferrochelatase activities in human liver biopsies with special reference to alcoholic liver disease. diagnostic usage,ongoing research,unassigned 1,3,0 1.3.3.3 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23686770&form=6&db=m Mechanism of differentiation-enhanced photodynamic therapy for cancer: upregulation of coproporphyrinogen oxidase by C/EBP transcription factors. ongoing research,unassigned 2,0 1.3.3.3 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28416355&form=6&db=m Expression of coproporphyrinogen oxidase is associated with detection of upper gastrointestinal carcinomas by 5-aminolevulinic acid-mediated photodynamic diagnosis. causal interaction,diagnostic usage,therapeutic application,unassigned 3,3,1,0 1.3.3.3 Photosensitivity Disorders http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28739897&form=6&db=m Antibacterial photosensitization through activation of coproporphyrinogen oxidase. causal interaction,therapeutic application,unassigned 1,1,0 1.3.3.3 Porphyria Cutanea Tarda http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=661926&form=6&db=m Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda. causal interaction,ongoing research,unassigned 2,4,0 1.3.3.3 Porphyria Cutanea Tarda http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11831056&form=6&db=m [Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria] causal interaction,therapeutic application,unassigned 3,1,0 1.3.3.3 Porphyria, Acute Intermittent http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=398301&form=6&db=m The porphyrias. unassigned - 1.3.3.3 Porphyria, Acute Intermittent http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14669009&form=6&db=m Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias. causal interaction,unassigned 1,0 1.3.3.3 Porphyria, Acute Intermittent http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24997713&form=6&db=m Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP). unassigned - 1.3.3.3 Porphyria, Acute Intermittent http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31073229&form=6&db=m International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias. unassigned - 1.3.3.3 Porphyria, Erythropoietic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8621830&form=6&db=m Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant. diagnostic usage,unassigned 1,0 1.3.3.3 Porphyria, Variegate http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=398301&form=6&db=m The porphyrias. unassigned - 1.3.3.3 Porphyria, Variegate http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24997713&form=6&db=m Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP). unassigned - 1.3.3.3 Porphyria, Variegate http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31073229&form=6&db=m International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias. unassigned - 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=63041&form=6&db=m The primary enzyme defect in hereditary coproporphyria. causal interaction,ongoing research,unassigned 1,4,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=398301&form=6&db=m The porphyrias. unassigned - 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=661926&form=6&db=m Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda. causal interaction,ongoing research,unassigned 2,4,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2079105&form=6&db=m Decreased activity of liver coproporphyrinogen oxidase in hexachlorobenzene-induced porphyria. unassigned - 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=2916235&form=6&db=m Studies on the etiology of trace metal-induced porphyria: effects of porphyrinogenic metals on coproporphyrinogen oxidase in rat liver and kidney. ongoing research,unassigned 4,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=7592568&form=6&db=m Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyria. causal interaction,diagnostic usage,unassigned 3,2,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=11831056&form=6&db=m [Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria] causal interaction,therapeutic application,unassigned 3,1,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=14669009&form=6&db=m Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias. causal interaction,unassigned 1,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16398658&form=6&db=m Dual gene defects involving delta-aminolaevulinate dehydratase and coproporphyrinogen oxidase in a porphyria patient. therapeutic application,unassigned 1,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18160932&form=6&db=m Use of Di- and Tripropionate substrate analogs to probe the active site of human recombinant coproporphyrinogen oxidase. causal interaction,unassigned 4,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=18294003&form=6&db=m Direct Assay of Enzymes in Heme Biosynthesis for the Detection of Porphyrias by Tandem Mass Spectrometry. Uroporphyrinogen Decarboxylase and Coproporphyrinogen III Oxidase. diagnostic usage,ongoing research,unassigned 3,1,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21734717&form=6&db=m Digenic Inheritance of Mutations in the Coproporphyrinogen Oxidase and Protoporphyrinogen Oxidase Genes in a Unique Type of Porphyria. causal interaction,unassigned 2,0 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24997713&form=6&db=m Seven Novel Mutations in Bulgarian Patients with Acute Hepatic Porphyrias (AHP). unassigned - 1.3.3.3 Porphyrias http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31073229&form=6&db=m International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias. unassigned - 1.3.3.3 Porphyrias, Hepatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=398301&form=6&db=m The porphyrias. unassigned - 1.3.3.3 Porphyrias, Hepatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9454777&form=6&db=m Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis. causal interaction,unassigned 4,0 1.3.3.3 Porphyrias, Hepatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9888388&form=6&db=m Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update. causal interaction,unassigned 3,0 1.3.3.3 Porphyrias, Hepatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=16159891&form=6&db=m Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria. causal interaction,therapeutic application,unassigned 1,1,0 1.3.3.3 Porphyrias, Hepatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21103937&form=6&db=m Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R. unassigned - 1.3.3.3 Porphyrias, Hepatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21231929&form=6&db=m Identification of an AluY-mediated deletion of exon 5 in the CPOX gene by MLPA analysis in patients with hereditary coproporphyria. unassigned - 1.3.3.3 Porphyrias, Hepatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30385147&form=6&db=m Acute hepatic porphyrias: Identification of 46 hydroxymethylbilane synthase, 11 coproporphyrinogen oxidase, and 20 protoporphyrinogen oxidase novel mutations. causal interaction,diagnostic usage,unassigned 1,1,0 1.3.3.3 Porphyrias, Hepatic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=31073229&form=6&db=m International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias. unassigned - 1.3.3.3 Protoporphyria, Erythropoietic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=398301&form=6&db=m The porphyrias. unassigned - 1.3.3.3 Protoporphyria, Erythropoietic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=8621830&form=6&db=m Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant. diagnostic usage,unassigned 1,0 1.3.3.3 protoporphyrin ferrochelatase deficiency http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=19805308&form=6&db=m Elucidation of the mechanism of mitochondrial iron loading in Friedreich's ataxia by analysis of a mouse mutant. causal interaction,unassigned 4,0 1.3.3.3 Skin Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21807844&form=6&db=m Vitamin D3 enhances the apoptotic response of epithelial tumors to aminolevulinate-based photodynamic therapy. causal interaction,therapeutic application,unassigned 3,3,0 1.3.3.3 Tics http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=21821717&form=6&db=m Two proteins with different functions are derived from the KlHEM13 gene. unassigned -