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humans (13) 13
index medicus (12) 12
coproporphyrinogen oxidase - genetics (11) 11
cpo (10) 10
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Journal Article
CANADIAN JOURNAL OF MICROBIOLOGY, ISSN 0008-4166, 03/2005, Volume 51, Issue 3, pp. 241 - 249
The KIHEM13 gene of Kluyveromyces lactis encoding the coproporphyrinogen oxidase (EC 1.3.3.3), an oxygen-requiring enzyme that catalyzes the sixth step of heme... 
HEM13 | hypoxic genes | MICROBIOLOGY | INDUCTION | SACCHAROMYCES-CEREVISIAE | YEAST | OXYGEN | ROX1 | HEM13 GENE | REPRESSION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | COPROPORPHYRINOGEN-III OXIDASE | SEQUENCE | Kluyveromyces lactis | coproporphyrinogen oxidase (CPO) | TRANSCRIPTIONAL REGULATION | Enzymes | Oxygen | Yeast | Microbiology | Genes | Cloning | Genetics
Journal Article
Biochemical Journal, ISSN 0264-6021, 04/2005, Volume 387, Issue 2, pp. 281 - 293
Phospholipids and sphingolipids play critical roles in signal transduction, intracellular membrane trafficking, and control of cell Growth and survival. We... 
Sphingomyelin synthase | Lipid phosphatase | Lysophosphatidic acid | Sphingolipid metabolism | Phospholipid metabolism | Sphingosine 1-phosphate | WNT SIGNALING PATHWAY | PHOSPHATIDIC-ACID PHOSPHATASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | phospholipid metabolism | sphingolipid metabolism | GERM-CELL MIGRATION | SACCHAROMYCES-CEREVISIAE | sphingomyelin synthase | lysophosphatidic acid | ACTIVE-SITE MUTANTS | DIACYLGLYCEROL PYROPHOSPHATE PHOSPHATASE | lipid phosphatase | FUNGUS CURVULARIA-INAEQUALIS | sphingosine 1-phosphate | SPHINGOSINE-1-PHOSPHATE PHOSPHOHYDROLASE | Phosphotransferases - chemistry | Cell Membrane - enzymology | Multigene Family | Animals | Cell Division | Humans | Membrane Lipids - metabolism | Signal Transduction - physiology | Gene Expression Profiling | Phosphoric Monoester Hydrolases - physiology | Phosphotransferases - physiology | Phosphoric Monoester Hydrolases - chemistry | DG, diacylglycerol | DPP, diacylglycerolpyrosphosphate phosphatase | LPP, lipid phosphate phosphatase | SM, sphingomyelin | Review | EST, expressed sequence tag | LPR | S1P, sphingosine 1-phosphate | SPP, sphingosine phosphate phosphatase | G6P, glucose 6-phosphatase | plasticity-related gene | phosphotransferase | PA, phosphatidic acid | PC, phosphatidylcholine | SMS, sphingomyelin synthase | CPO, chloroperoxidase | LPA, lysophosphatidic acid | C1P, ceramide 1-phosphate | PRG, lipid phosphatase-related protein | CSS2, type 2 candidate sphingomyelin synthase | PLD, phospholipase D | LPT, lipid phosphatase
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 05/2001, Volume 68, Issue 5, pp. 1130 - 1138
Hereditary coproporphyria (HCP) is the least common of the autosomal dominant acute hepatic porphyrias. It results from mutations in the CPO gene that encodes... 
CPO gene | coproporphyria | harderoporphyria
Journal Article
ASN Neuro, ISSN 1759-0914, 2013, Volume 5, Issue 1, pp. 27 - 42
Genetic and environmental factors are both likely to contribute to neurodevelopmental disorders, including ASDs (autism spectrum disorders). In this study, we... 
Cerebellum | Autism | Social interaction | Ultrasonic communication | Olfactory bulb | Reeler | Hippocampus | reeler | olfactory bulb | DEVELOPMENTAL NEUROTOXICITY | hippocampus | METALLOPROTEINASE | SCHIZOPHRENIA | AUTISM SPECTRUM DISORDERS | NEUROSCIENCES | autism | cerebellum | ultrasonic communication | SIGNALING PATHWAY | ULTRASONIC VOCALIZATIONS | DENDRITIC SPINE | social interaction | EXTRACELLULAR-MATRIX | MICE | MUTANT MOUSE | Age Factors | Embryo, Mammalian | Gene Expression Regulation, Developmental - genetics | Male | Colorimetry | RNA, Messenger - metabolism | Mice, Neurologic Mutants | Drug Delivery Systems | Exploratory Behavior - drug effects | Serine Endopeptidases - genetics | beta-Galactosidase - metabolism | Behavior, Animal - drug effects | Female | Vocalization, Animal - drug effects | Cell Adhesion Molecules, Neuronal - metabolism | Interpersonal Relations | Organophosphates - toxicity | Extracellular Matrix Proteins - metabolism | Animals, Newborn | Extracellular Matrix Proteins - genetics | Gene Expression Regulation, Developmental - drug effects | Mice, Transgenic | Nerve Tissue Proteins - genetics | Cell Adhesion Molecules, Neuronal - genetics | Brain - drug effects | Nerve Tissue Proteins - metabolism | Animals | Analysis of Variance | Behavioral Symptoms - chemically induced | Mice | Serine Endopeptidases - metabolism | Acetylcholinesterase - metabolism | Chlorpyrifos | Cortex (olfactory) | Vocalization behavior | Pesticides (organophosphorus) | Environmental factors | Cortex (piriform) | Neurodevelopmental disorders | Reelin protein | Social behavior | Social interactions | Extracellular matrix | Prenatal experience | Ultrasound | Open-field behavior
Journal Article
BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE, ISSN 0001-4079, 06/2014, Volume 198, Issue 6, pp. 1069 - 1093
Hereditary porphyrias comprise a group of eight metabolic disorders of the haem biosynthesis pathway, characterised by acute neurovisceral symptoms and/or skin... 
ACUTE INTERMITTENT PORPHYRIA | LOW EXPRESSION | 5-AMINOLEVULINATE | CPO GENE | PORPHYRIA ERYTHROPOIETIC | PHENOTYPE | HEREDITARY COPROPORPHYRIA | MEDICINE, GENERAL & INTERNAL | LINKED DOMINANT PROTOPORPHYRIA | CONGENITAL ERYTHROPOIETIC PORPHYRIA | HEME | METABOLISM | MUTATIONS | ANEMIA
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 08/2002, Volume 47, Issue 8, pp. 407 - 412
Hereditary coproporphyria (HCP) is an autosomal dominant disorder, resulting from a partial deficiency of the enzyme coproporphyrinogen oxidase (CPO). This... 
Hereditary coproporphyria | Coproporphyrinogen oxidase | DNA mutational analysis | Heme biosynthesis CPO mutations | Genetic research | Genetic aspects | Gene mutations | Analysis
Journal Article