Disease on EC 1.6.2.4 - NADPH-hemoprotein reductase
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3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency
Estimation of reference curves for the urinary steroid metabolome in the first year of life in healthy children: Tracing the complexity of human postnatal steroidogenesis.
3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency
Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS).
3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency
Novel insight into etiology, diagnosis and management of primary adrenal insufficiency.
3alpha(or 20beta)-hydroxysteroid dehydrogenase deficiency
Role of a Disordered Steroid Metabolome in the Elucidation of Sterol and Steroid Biosynthesis.
Aberrant Crypt Foci
Role of Hepatic and Intestinal P450 Enzymes in the Metabolic Activation of the Colon Carcinogen Azoxymethane in Mice.
Adenocarcinoma
DNA damage induced by NADPH cytochrome P450 reductase-activated idarubicin in sensitive and multidrug resistant MCF7 breast cancer cells.
Adenocarcinoma
Importance of P450 reductase activity in determining sensitivity of breast tumour cells to the bioreductive drug, tirapazamine (SR 4233).
Adenocarcinoma
Overexpression of cytochrome P450 NADPH reductase sensitises MDA 231 breast carcinoma cells to 5-fluorouracil: Possible mechanisms involved.
Adrenal Hyperplasia, Congenital
46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene.
Adrenal Hyperplasia, Congenital
A male twin infant with skull deformity and elevated neonatal 17-hydroxyprogesterone: a prismatic case of P450 oxidoreductase deficiency.
Adrenal Hyperplasia, Congenital
A rare cause of congenital adrenal hyperplasia: Antley-Bixler syndrome due to POR deficiency.
Adrenal Hyperplasia, Congenital
Alternative pathway androgen biosynthesis and human fetal female virilization.
Adrenal Hyperplasia, Congenital
Clinical implications of androgen synthesis via 5alpha-reduced precursors.
Adrenal Hyperplasia, Congenital
Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.
Adrenal Hyperplasia, Congenital
Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study.
Adrenal Hyperplasia, Congenital
Congenital adrenal hyperplasia owing to 17?-hydroxylase/17,20 lyase and p450 oxidoreductase deficiencies.
Adrenal Hyperplasia, Congenital
Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant.
Adrenal Hyperplasia, Congenital
Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review.
Adrenal Hyperplasia, Congenital
Disorders of sex development and female reproductive capacity: A literature review.
Adrenal Hyperplasia, Congenital
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.
Adrenal Hyperplasia, Congenital
Impact of molecular genetics on congenital adrenal hyperplasia management.
Adrenal Hyperplasia, Congenital
Impaired hepatic drug and steroid metabolism in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.
Adrenal Hyperplasia, Congenital
Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: a novel case of P450 oxidoreductase deficiency.
Adrenal Hyperplasia, Congenital
Long-term follow-up of a female with congenital adrenal hyperplasia due to P450-oxidoreductase deficiency.
Adrenal Hyperplasia, Congenital
MECHANISMS IN ENDOCRINOLOGY: Update on pathogenesis of primary adrenal insufficiency: beyond steroid enzyme deficiency and autoimmune adrenal destruction.
Adrenal Hyperplasia, Congenital
Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype.
Adrenal Hyperplasia, Congenital
Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children.
Adrenal Hyperplasia, Congenital
P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia.
Adrenal Hyperplasia, Congenital
P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.
Adrenal Hyperplasia, Congenital
P450 Oxidoreductase Deficiency: loss of activity caused by protein instability from a novel L374H mutation.
Adrenal Hyperplasia, Congenital
Prenatal diagnosis of congenital adrenal hyperplasia caused by p450 oxidoreductase deficiency.
Adrenal Hyperplasia, Congenital
Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency.
Adrenal Hyperplasia, Congenital
Successful live birth in a Chinese woman with P450 oxidoreductase deficiency through frozen-thawed embryo transfer: a case report with review of the literature.
Adrenal Insufficiency
Clinical and biochemical consequences of p450 oxidoreductase deficiency.
Adrenal Insufficiency
Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan.
Adrenal Insufficiency
P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia.
Adrenal Insufficiency
P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.
Androgen-Insensitivity Syndrome
Disorders of sex development and female reproductive capacity: A literature review.
Antley-Bixler Syndrome Phenotype
46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene.
Antley-Bixler Syndrome Phenotype
A case of Antley-Bixler syndrome caused by compound heterozygous mutations of the cytochrome P450 oxidoreductase gene.
Antley-Bixler Syndrome Phenotype
Altered Human CYP3A4 Activity Caused by Antley-Bixler Syndrome-Related Variants of NADPH-Cytochrome P450 Oxidoreductase Measured in a Robust In Vitro System.
Antley-Bixler Syndrome Phenotype
Ambiguous genitalia, impaired steroidogenesis, and Antley-Bixler syndrome in a patient with P450 oxidoreductase deficiency.
Antley-Bixler Syndrome Phenotype
Anorectal and urinary anomalies and aberrant retinoic acid metabolism in cytochrome P450 oxidoreductase deficiency.
Antley-Bixler Syndrome Phenotype
Backdoor pathway for dihydrotestosterone biosynthesis: Implications for normal and abnormal human sex development.
Antley-Bixler Syndrome Phenotype
Basic concepts and recent developments in human steroid hormone biosynthesis.
Antley-Bixler Syndrome Phenotype
Clinical and genetic analysis of cytochrome P450 oxidoreductase (POR) deficiency in a female and the analysis of a novel POR intron mutation causing alternative mRNA splicing : Overall analysis of a female with POR deficiency.
Antley-Bixler Syndrome Phenotype
Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan.
Antley-Bixler Syndrome Phenotype
Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency.
Antley-Bixler Syndrome Phenotype
Compound heterozygous mutations of cytochrome P450 oxidoreductase gene (POR) in two patients with Antley-Bixler syndrome.
Antley-Bixler Syndrome Phenotype
Compound heterozygous variants in POR gene identified by whole-exome sequencing in a Chinese pedigree with cytochrome P450 oxidoreductase deficiency.
Antley-Bixler Syndrome Phenotype
Conditional Deletion of Cytochrome P450 Reductase in Osteoprogenitor Cells Affects Long Bone and Skull Development in Mice Recapitulating Antley-Bixler Syndrome: Role of a Redox Enzyme in Development.
Antley-Bixler Syndrome Phenotype
Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review.
Antley-Bixler Syndrome Phenotype
Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysis.
Antley-Bixler Syndrome Phenotype
Cytochrome P450 oxidoreductase deficiency with Antley-Bixler syndrome: steroidogenic capacities.
Antley-Bixler Syndrome Phenotype
Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients.
Antley-Bixler Syndrome Phenotype
Cytochrome P450 Oxidoreductase Deficiency: Novel Cause of Ambiguity with Primary Amenorrhea.
Antley-Bixler Syndrome Phenotype
Cytochrome P450 oxidoreductase deficiency: rare congenital disorder leading to skeletal malformations and steroidogenic defects.
Antley-Bixler Syndrome Phenotype
Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.
Antley-Bixler Syndrome Phenotype
Cytochromes P450--a family of proteins and scientists-understanding their relationships.
Antley-Bixler Syndrome Phenotype
Diminished FAD binding in the Y459H and V492E Antley-Bixler syndrome mutants of human cytochrome P450 reductase.
Antley-Bixler Syndrome Phenotype
Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis.
Antley-Bixler Syndrome Phenotype
Establishment of an induced pluripotent stem cell line from a Antley-Bixler Syndrome (ABS) patient with the homozygote mutation p.R457H (c.1370G>A) in POR gene.
Antley-Bixler Syndrome Phenotype
Human cytochrome P450 oxidoreductase deficiency caused by the Y181D mutation: molecular consequences and rescue of defect.
Antley-Bixler Syndrome Phenotype
Impairment of human CYP1A2-mediated xenobiotic metabolism by Antley-Bixler syndrome variants of cytochrome P450 oxidoreductase.
Antley-Bixler Syndrome Phenotype
In vitro fertilization-frozen embryo transfer in a patient with cytochrome P450 oxidoreductase deficiency: a case report.
Antley-Bixler Syndrome Phenotype
Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: a novel case of P450 oxidoreductase deficiency.
Antley-Bixler Syndrome Phenotype
Mouse Knockout of the Cholesterogenic Cytochrome P450 Lanosterol 14{alpha}-Demethylase (Cyp51) Resembles Antley-Bixler Syndrome.
Antley-Bixler Syndrome Phenotype
Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome.
Antley-Bixler Syndrome Phenotype
Non-classic cytochrome P450 oxidoreductase deficiency strongly linked with menstrual cycle disorders and female infertility as primary manifestations.
Antley-Bixler Syndrome Phenotype
Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children.
Antley-Bixler Syndrome Phenotype
P450 oxidoreductase deficiency and Antley-Bixler syndrome.
Antley-Bixler Syndrome Phenotype
P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.
Antley-Bixler Syndrome Phenotype
P450 Oxidoreductase deficiency: Analysis of mutations and polymorphisms.
Antley-Bixler Syndrome Phenotype
Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): a disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotype.
Antley-Bixler Syndrome Phenotype
The mechanism of Psoralen and Isopsoralen hepatotoxicity as revealed by hepatic gene expression profiling in SD rats.
Antley-Bixler Syndrome Phenotype
Two cases of cytochrome P450 oxidoreductase deficiency with severe scoliosis and surgery requirement.
Antley-Bixler Syndrome Phenotype
Two-Step Biochemical Differential Diagnosis of Classic 21-Hydroxylase Deficiency and Cytochrome P450 Oxidoreductase Deficiency in Japanese Infants by GC-MS Measurement of Urinary Pregnanetriolone/ Tetrahydroxycortisone Ratio and 11?-Hydroxyandrosterone.
Antley-Bixler Syndrome Phenotype
Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone.
Antley-Bixler Syndrome Phenotype
[Clinical and genetic analysis of a pedigree affected with cytochrome P450 oxidoreductase deficiency].
aromatase deficiency
Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysis.
aromatase deficiency
Sex determination and disorders of sex development according to the revised nomenclature and classification in 46,XX individuals.
Ascorbic Acid Deficiency
The effect of certain vitamin deficiencies on hepatic drug metabolism.
Breast Neoplasms
A variant in the cytochrome p450 oxidoreductase gene is associated with breast cancer risk in African Americans.
Breast Neoplasms
Carbonyl reductase and NADPH cytochrome P450 reductase activities in human tumoral versus normal tissues.
Breast Neoplasms
CYPOR is a novel and independent prognostic biomarker of recurrence-free survival in triple-negative breast cancer patients.
Breast Neoplasms
Differentiation-associated staining with anti-pimonidazole antibodies in head and neck tumors.
Breast Neoplasms
Dissecting the role of multiple reductases in bioactivation and cytotoxicity of the antitumor agent 2,5-diaziridinyl-3-(hydroxymethyl)-6-methyl-1,4-benzoquinone (RH1).
Breast Neoplasms
Does reductive metabolism predict response to tirapazamine (SR 4233) in human non-small-cell lung cancer cell lines?
Breast Neoplasms
Importance of P450 reductase activity in determining sensitivity of breast tumour cells to the bioreductive drug, tirapazamine (SR 4233).
Breast Neoplasms
Overexpression of cytochrome P450 NADPH reductase sensitises MDA 231 breast carcinoma cells to 5-fluorouracil: Possible mechanisms involved.
Breast Neoplasms
Overexpression of human NADPH:cytochrome c (P450) reductase confers enhanced sensitivity to both tirapazamine (SR 4233) and RSU 1069.
Breast Neoplasms
Subcellular Location of Tirapazamine Reduction Dramatically Affects Aerobic but Not Anoxic Cytotoxicity.
Breast Neoplasms
Synthesis and cytotoxicity of pyranonaphthoquinone natural product analogues under bioreductive conditions.
Breast Neoplasms
The relative importance of NADPH: cytochrome c (P450) reductase for determining the sensitivity of human tumour cells to the indolequinone EO9 and related analogues lacking functionality at the C-2 and C-3 positions.
Breast Neoplasms
Viral delivery of P450 reductase recapitulates the ability of constitutive overexpression of reductase enzymes to potentiate the activity of mitomycin C in human breast cancer xenografts.
Carcinogenesis
Characterization of an acute molecular marker of nongenotoxic rodent hepatocarcinogenesis by gene expression profiling in a long term clofibric acid study.
Carcinoma
Catechol estrogen metabolites and conjugates in different regions of the prostate of Noble rats treated with 4-hydroxyestradiol: implications for estrogen-induced initiation of prostate cancer.
Carcinoma
Differentiation-associated staining with anti-pimonidazole antibodies in head and neck tumors.
Carcinoma
DT-diaphorase as a critical determinant of sensitivity to mitomycin C in human colon and gastric carcinoma cell lines.
Carcinoma
Nonenzymatic reductive activation of 7-N-((2-([2-(gamma-L-glutamylamino)ethyl]dithio)ethyl))mitomycin C by thiol molecules: a novel mitomycin C derivative effective on mitomycin C-resistant tumor cells.
Carcinoma, Hepatocellular
Characterization of NADPH-cytochrome P-450 reductase in a mouse hepatoma cell line.
Carcinoma, Hepatocellular
Drug metabolism in the Novikoff hepatoma: evidence for a mixed function oxidase system and partial purification of cytochrome P-450 reductase.
Carcinoma, Hepatocellular
G6PD inhibits ferroptosis in hepatocellular carcinoma by targeting cytochrome P450 oxidoreductase.
Carcinoma, Hepatocellular
Genetic variants and Expression of Cytochrome p450 Oxidoreductase Predict Postoperative Survival in Patients with Hepatitis B Virus-Related Hepatocellular Carcinoma.
Carcinoma, Hepatocellular
Mechanisms of NADPH-cytochrome P450 oxidoreductase induction by dexamethasone in the H4IIE rat hepatoma cell line.
Carcinoma, Hepatocellular
NADPH-cytochrome P-450 reductase is involved in flunitrazepam reductive metabolism in Hep G2 and Hep 3B cells.
Carcinoma, Hepatocellular
Nonenzymatic reductive activation of 7-N-((2-([2-(gamma-L-glutamylamino)ethyl]dithio)ethyl))mitomycin C by thiol molecules: a novel mitomycin C derivative effective on mitomycin C-resistant tumor cells.
Carcinoma, Hepatocellular
Preparation of homogeneous NADPH-cytochrome P-450 reductase from rat hepatoma.
Carcinoma, Hepatocellular
Suppression of cytochrome P450 reductase expression in hepatoma cells replicates the hepatic lipidosis observed in hepatic POR-null mice.
Carcinoma, Hepatocellular
The drug metabolism systems of liver and liver tumors: a comparison of activities and characteristics.
Carcinoma, Hepatocellular
Thyroid regulation of NADPH:cytochrome P450 oxidoreductase: identification of a thyroid-responsive element in the 5'-flank of the oxidoreductase gene.
Carcinoma, Non-Small-Cell Lung
NADPH:cytochrome c (P450) reductase activates tirapazamine (SR4233) to restore hypoxic and oxic cytotoxicity in an aerobic resistant derivative of the A549 lung cancer cell line.
Carcinoma, Ovarian Epithelial
Profiling cytochrome P450 expression in ovarian cancer: identification of prognostic markers.
Cardiotoxicity
A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor.
Chagas Disease
cDNA Isolation and Expression of Nicotinamide Adenine Dinucleotide Phosphate-Dependent Cytochrome P450 Reductase Gene in the Chagas Disease Vector
Cholestasis
Microsomal function in biliary obstructed rats: effects of S-adenosylmethionine.
Cholestasis, Intrahepatic
Selective reduction of hepatic cytochrome P450 content in patients with intrahepatic cholestasis. A mechanism for impairment of microsomal drug oxidation.
Coinfection
Co-expression of human cytochrome P4501A1 (CYP1A1) variants and human NADPH-cytochrome P450 reductase in the baculovirus/insect cell system.
Coinfection
Differential metabolism of benzo[a]pyrene and benzo[a]pyrene-7,8-dihydrodiol by human CYP1A1 variants.
Coinfection
Expression and coupling of human cytochrome P450 2E1 and NADPH-cytochrome P450 oxidoreductase in dual expression and co-infection systems with baculovirus in insect cells.
Colitis
Intestinal epithelium-specific knockout of the cytochrome P450 reductase gene exacerbates dextran sulfate sodium-induced colitis.
Colonic Neoplasms
The reductive activation of the antitumor drug RH1 to its semiquinone free radical by NADPH cytochrome P450 reductase and by HCT116 human colon cancer cells.
Congenital Abnormalities
A male twin infant with skull deformity and elevated neonatal 17-hydroxyprogesterone: a prismatic case of P450 oxidoreductase deficiency.
Congenital Abnormalities
Instability of the Human Cytochrome P450 Reductase A287P Variant Is the Major Contributor to its Antley-Bixler Syndrome-Like Phenotype.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Cytochrome P450 oxidoreductase deficiency: rare congenital disorder leading to skeletal malformations and steroidogenic defects.
Craniosynostoses
P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia.
Disorders of Sex Development
Ambiguous genitalia, impaired steroidogenesis, and Antley-Bixler syndrome in a patient with P450 oxidoreductase deficiency.
Disorders of Sex Development
Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan.
Disorders of Sex Development
Clinical, Genetic, and Enzymatic Characterization of P450 Oxidoreductase Deficiency in Four Patients.
Disorders of Sex Development
Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.
Disorders of Sex Development
Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients.
Disorders of Sex Development
Diminished FAD binding in the Y459H and V492E Antley-Bixler syndrome mutants of human cytochrome P450 reductase.
Disorders of Sex Development
Disorder of sex development as a diagnostic clue in the first Spanish known newborn with P450 oxidoreductase deficiency.
Disorders of Sex Development
Disorders of sex development and female reproductive capacity: A literature review.
Disorders of Sex Development
Epigenetic alterations in cytochrome P450 oxidoreductase (Por) in sperm of rats exposed to tetrahydrocannabinol (THC).
Disorders of Sex Development
P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.
Disorders of Sex Development
P450 Oxidoreductase deficiency: Analysis of mutations and polymorphisms.
Disorders of Sex Development
Successful live birth in a Chinese woman with P450 oxidoreductase deficiency through frozen-thawed embryo transfer: a case report with review of the literature.
Disorders of Sex Development
[Rare forms of female pseudohermaphroditism: when to investigate?]
Encephalitis
Distribution of hammerhead and hammerhead-like RNA motifs through the GenBank.
Encephalomyelitis
Quantifying immunohistochemical staining of phospho-eIF2alpha, heme oxygenase-2 and NADPH cytochrome P450 reductase in oligodendrocytes during experimental autoimmune encephalomyelitis.
Encephalomyelitis, Autoimmune, Experimental
Heme oxygenase-1 and NADPH cytochrome P450 reductase expression in experimental allergic encephalomyelitis: an expanded view of the stress response.
Encephalomyelitis, Autoimmune, Experimental
Quantifying immunohistochemical staining of phospho-eIF2alpha, heme oxygenase-2 and NADPH cytochrome P450 reductase in oligodendrocytes during experimental autoimmune encephalomyelitis.
Epilepsy
Effects of CYP2C19 and P450 Oxidoreductase Polymorphisms on the Population Pharmacokinetics of Clobazam and N-Desmethylclobazam in Japanese Patients With Epilepsy.
Fanconi Anemia
Abnormal microsomal detoxification implicated in Fanconi anemia group C by interaction of the FAC protein with NADPH cytochrome P450 reductase.
Fanconi Anemia
Do Fanconi anemia genes control cell response to cross-linking agents by modulating cytochrome P-450 reductase activity?
Fatty Liver
Defining a relationship between dietary fatty acids and the cytochrome P450 system in a mouse model of fatty liver disease.
Fatty Liver
Fatty liver and impaired hepatic metabolism alter the congener-specific distribution of polychlorinated biphenyls (PCBs) in mice with a liver-specific deletion of cytochrome P450 reductase.
Fetal Growth Retardation
Disorders of sex development and female reproductive capacity: A literature review.
Fibrosarcoma
Oxygen-sensitive enzyme-prodrug gene therapy for the eradication of radiation-resistant solid tumours.
Genetic Diseases, Inborn
P450 Oxidoreductase Deficiency: A Systematic Review and Meta-analysis of Genotypes, Phenotypes, and Their Relationships.
Glioma
Expression, induction and regulation of the cytochrome P450 monooxygenase system in the rat glioma C6 cell line.
Glioma
Glutathione S-transferases and cytochrome P450 detoxifying enzyme distribution in human cerebral glioma.
Glioma
Identification of inducible mixed function oxidase system in rat glioma C6 cell line.
Gliosarcoma
Combination of the bioreductive drug tirapazamine with the chemotherapeutic prodrug cyclophosphamide for P450/P450-reductase-based cancer gene therapy.
Gliosarcoma
Impact of liver P450 reductase suppression on cyclophosphamide activation, pharmacokinetics and antitumoral activity in a cytochrome P450-based cancer gene therapy model.
Gonadal Dysgenesis
Disorders of sex development and female reproductive capacity: A literature review.
Gonadal Dysgenesis
Sex determination and disorders of sex development according to the revised nomenclature and classification in 46,XX individuals.
Gonadal Dysgenesis, Mixed
Disorders of sex development and female reproductive capacity: A literature review.
Granulomatous Disease, Chronic
Subcellular localization of the human neutrophil NADPH oxidase. b-Cytochrome and associated flavoprotein.
Hepatitis B
Genetic variants and Expression of Cytochrome p450 Oxidoreductase Predict Postoperative Survival in Patients with Hepatitis B Virus-Related Hepatocellular Carcinoma.
Hepatitis C
Engineered retargeting of viral RNA replication complexes to an alternative intracellular membrane.
Herpes Zoster
Developmental changes in steroidogenic enzymes in human postnatal adrenal cortex: immunohistochemical studies.
Herpes Zoster
Levels of adrenodoxin, NADPH-cytochrome P-450 reductase and cytochromes P-45011 beta, P-45021, P-450scc, in adrenal zona fasciculata-reticularis tissue from androgen-treated rats.
Herpes Zoster
Relationships between NADPH diaphorase staining and neuronal, endothelial, and inducible nitric oxide synthase and cytochrome P450 reductase immunoreactivities in guinea-pig tissues.
Herpes Zoster
Zonal distribution of cytochromes P-450 and related enzymes of bovine adrenal cortex--quantitative assay of concentrations and total contents.
Huntington Disease
Preimplantation genetic diagnosis of P450 oxidoreductase deficiency and Huntington Disease using three different molecular approaches simultaneously.
Hypertension
Combined homozygous 21 hydroxylase with heterozygous P450 oxidoreductase mutation in a Saudi boy presented with hypertension.
Hyperthyroidism
Lipid peroxidation in rat liver microsomes. I. Stimulation of the NADPH-cytochrome P-450 reductase-dependent process in hyperthyroid state.
Hypoglycemia
TCF7L2 rs7903146 C>T gene polymorphism is not associated with hypoglycemia in sulfonylurea-treated type 2 diabetic patients.
Infections
An integrated in vitro model for simultaneous assessment of drug uptake, metabolism, and efflux.
Infections
[CYP2D6*1, CYP2D6*10 co-expressed with CYPOR in Bac-to-Bac expression system and activity determination].
Infertility
Clinical, Genetic, and Enzymatic Characterization of P450 Oxidoreductase Deficiency in Four Patients.
Infertility
Non-classic cytochrome P450 oxidoreductase deficiency strongly linked with menstrual cycle disorders and female infertility as primary manifestations.
Infertility
Successful live birth in a Chinese woman with P450 oxidoreductase deficiency through frozen-thawed embryo transfer: a case report with review of the literature.
Infertility, Female
Non-classic cytochrome P450 oxidoreductase deficiency strongly linked with menstrual cycle disorders and female infertility as primary manifestations.
Leukemia, Myeloid, Acute
A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor.
Lipidoses
Suppression of cytochrome P450 reductase expression in hepatoma cells replicates the hepatic lipidosis observed in hepatic POR-null mice.
Liver Neoplasms, Experimental
Drug metabolism in the Novikoff hepatoma: evidence for a mixed function oxidase system and partial purification of cytochrome P-450 reductase.
Liver Neoplasms, Experimental
The drug metabolism systems of liver and liver tumors: a comparison of activities and characteristics.
Lung Injury
Inhibition of NADPH cytochrome P450 reductase by the model sulfur mustard vesicant 2-chloroethyl ethyl sulfide is associated with increased production of reactive oxygen species.
Lung Injury
Lung injury induced by pyrrolizidine alkaloids depends on metabolism by hepatic cytochrome P450s and blood transport of reactive metabolites.
Lung Neoplasms
A virus-directed enzyme prodrug therapy (VDEPT) strategy for lung cancer using a CYP2B6/NADPH-cytochrome P450 reductase fusion protein.
Lung Neoplasms
Does reductive metabolism predict response to tirapazamine (SR 4233) in human non-small-cell lung cancer cell lines?
Lung Neoplasms
NADPH:cytochrome c (P450) reductase activates tirapazamine (SR4233) to restore hypoxic and oxic cytotoxicity in an aerobic resistant derivative of the A549 lung cancer cell line.
Lung Neoplasms
Quantification of CYP2B7, CYP4B1, and CYPOR messenger RNAs in normal human lung and lung tumors.
Malaria
Biochemical comparison of Anopheles gambiae and human NADPH P450 reductases reveals different 2'-5'-ADP and FMN binding traits.
Melanoma
A highly efficient tumor-infiltrating MDSC differentiation system for discovery of anti-neoplastic targets, which circumvents the need for tumor establishment in mice.
Melanoma
The effect of functional groups on reduction and activation of quinone bioreductive agents by DT-diaphorase.
nadph-hemoprotein reductase deficiency
A male twin infant with skull deformity and elevated neonatal 17-hydroxyprogesterone: a prismatic case of P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Age-specific changes in sex steroid biosynthesis and sex development.
nadph-hemoprotein reductase deficiency
Alternative pathway androgen biosynthesis and human fetal female virilization.
nadph-hemoprotein reductase deficiency
Ambiguous genitalia, impaired steroidogenesis, and Antley-Bixler syndrome in a patient with P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Anorectal and urinary anomalies and aberrant retinoic acid metabolism in cytochrome P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Apparent manifesting heterozygosity in P450 oxidoreductase deficiency and its effect on coexisting 21-hydroxylase deficiency.
nadph-hemoprotein reductase deficiency
Backdoor pathway for dihydrotestosterone biosynthesis: Implications for normal and abnormal human sex development.
nadph-hemoprotein reductase deficiency
Basic concepts and recent developments in human steroid hormone biosynthesis.
nadph-hemoprotein reductase deficiency
Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites.
nadph-hemoprotein reductase deficiency
Clinical and biochemical consequences of p450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan.
nadph-hemoprotein reductase deficiency
Clinical implications of androgen synthesis via 5alpha-reduced precursors.
nadph-hemoprotein reductase deficiency
Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Clinical, Genetic, and Enzymatic Characterization of P450 Oxidoreductase Deficiency in Four Patients.
nadph-hemoprotein reductase deficiency
Compound heterozygous variants in POR gene identified by whole-exome sequencing in a Chinese pedigree with cytochrome P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Congenital adrenal hyperplasia owing to 17?-hydroxylase/17,20 lyase and p450 oxidoreductase deficiencies.
nadph-hemoprotein reductase deficiency
Congenital adrenal hyperplasia: clinical symptoms and diagnostic methods.
nadph-hemoprotein reductase deficiency
Congenital Adrenal Hyperplasia: Time to Replace 17OHP with 21-Deoxycortisol.
nadph-hemoprotein reductase deficiency
Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review.
nadph-hemoprotein reductase deficiency
Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysis.
nadph-hemoprotein reductase deficiency
Cytochrome P450 oxidoreductase deficiency with Antley-Bixler syndrome: steroidogenic capacities.
nadph-hemoprotein reductase deficiency
Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients.
nadph-hemoprotein reductase deficiency
Cytochrome P450 Oxidoreductase Deficiency: Novel Cause of Ambiguity with Primary Amenorrhea.
nadph-hemoprotein reductase deficiency
Cytochrome P450 oxidoreductase deficiency: rare congenital disorder leading to skeletal malformations and steroidogenic defects.
nadph-hemoprotein reductase deficiency
Delayed diagnosis of disorder of sex development (DSD) due to P450 oxidoreductase (POR) deficiency.
nadph-hemoprotein reductase deficiency
Disorder of sex development as a diagnostic clue in the first Spanish known newborn with P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Disorders of sexual development in a cultural context.
nadph-hemoprotein reductase deficiency
Effect of Cytochrome P450 Reductase Deficiency on 2-Amino-9H-pyrido[2,3-b]indole Metabolism and DNA Adduct Formation in Liver and Extrahepatic Tissues of Mice.
nadph-hemoprotein reductase deficiency
Electron transfer by human wild-type and A287P mutant P450 oxidoreductase assessed by transient kinetics: Functional Basis of P450 Oxidoreductase Deficiency.
nadph-hemoprotein reductase deficiency
Estimation of reference curves for the urinary steroid metabolome in the first year of life in healthy children: Tracing the complexity of human postnatal steroidogenesis.
nadph-hemoprotein reductase deficiency
Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS).
nadph-hemoprotein reductase deficiency
Genetic and Clinical Features of P450 Oxidoreductase Deficiency.
nadph-hemoprotein reductase deficiency
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Human cytochrome P450 oxidoreductase deficiency caused by the Y181D mutation: molecular consequences and rescue of defect.
nadph-hemoprotein reductase deficiency
Impaired hepatic drug and steroid metabolism in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
In vitro fertilization-frozen embryo transfer in a patient with cytochrome P450 oxidoreductase deficiency: a case report.
nadph-hemoprotein reductase deficiency
Inhibition of placental CYP19A1 activity remains as a valid hypothesis for 46,XX virilization in P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: a novel case of P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Long-term follow-up of a female with congenital adrenal hyperplasia due to P450-oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Mutations of human cytochrome P450 reductase differentially modulate heme oxygenase-1 activity and oligomerization.
nadph-hemoprotein reductase deficiency
Non-classic cytochrome P450 oxidoreductase deficiency strongly linked with menstrual cycle disorders and female infertility as primary manifestations.
nadph-hemoprotein reductase deficiency
Novel insight into etiology, diagnosis and management of primary adrenal insufficiency.
nadph-hemoprotein reductase deficiency
Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children.
nadph-hemoprotein reductase deficiency
P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia.
nadph-hemoprotein reductase deficiency
P450 oxidoreductase deficiency and Antley-Bixler syndrome.
nadph-hemoprotein reductase deficiency
P450 oxidoreductase deficiency with maternal virilization during pregnancy.
nadph-hemoprotein reductase deficiency
P450 oxidoreductase deficiency: a disorder of steroidogenesis with multiple clinical manifestations.
nadph-hemoprotein reductase deficiency
P450 oxidoreductase deficiency: a new disorder of steroidogenesis affecting all microsomal P450 enzymes.
nadph-hemoprotein reductase deficiency
P450 oxidoreductase deficiency: a new disorder of steroidogenesis with multiple clinical manifestations.
nadph-hemoprotein reductase deficiency
P450 oxidoreductase deficiency: a new disorder of steroidogenesis.
nadph-hemoprotein reductase deficiency
P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.
nadph-hemoprotein reductase deficiency
P450 Oxidoreductase Deficiency: A Systematic Review and Meta-analysis of Genotypes, Phenotypes, and Their Relationships.
nadph-hemoprotein reductase deficiency
P450 Oxidoreductase deficiency: Analysis of mutations and polymorphisms.
nadph-hemoprotein reductase deficiency
P450 Oxidoreductase Deficiency: loss of activity caused by protein instability from a novel L374H mutation.
nadph-hemoprotein reductase deficiency
Preimplantation genetic diagnosis of P450 oxidoreductase deficiency and Huntington Disease using three different molecular approaches simultaneously.
nadph-hemoprotein reductase deficiency
Prenatal diagnosis of congenital adrenal hyperplasia caused by p450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): a disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotype.
nadph-hemoprotein reductase deficiency
Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency.
nadph-hemoprotein reductase deficiency
Reply to Flück et al.: Alternative androgen pathway biosynthesis drives fetal female virilization in P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Role of a Disordered Steroid Metabolome in the Elucidation of Sterol and Steroid Biosynthesis.
nadph-hemoprotein reductase deficiency
Structural basis for human NADPH-cytochrome P450 oxidoreductase deficiency.
nadph-hemoprotein reductase deficiency
Successful live birth in a Chinese woman with P450 oxidoreductase deficiency through frozen-thawed embryo transfer: a case report with review of the literature.
nadph-hemoprotein reductase deficiency
The mechanism of Psoralen and Isopsoralen hepatotoxicity as revealed by hepatic gene expression profiling in SD rats.
nadph-hemoprotein reductase deficiency
Two cases of cytochrome P450 oxidoreductase deficiency with severe scoliosis and surgery requirement.
nadph-hemoprotein reductase deficiency
Two-Step Biochemical Differential Diagnosis of Classic 21-Hydroxylase Deficiency and Cytochrome P450 Oxidoreductase Deficiency in Japanese Infants by GC-MS Measurement of Urinary Pregnanetriolone/ Tetrahydroxycortisone Ratio and 11?-Hydroxyandrosterone.
nadph-hemoprotein reductase deficiency
Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone.
nadph-hemoprotein reductase deficiency
[Clinical and genetic analysis of a pedigree affected with cytochrome P450 oxidoreductase deficiency].
Neoplasm Metastasis
CYPOR is a novel and independent prognostic biomarker of recurrence-free survival in triple-negative breast cancer patients.
Neoplasm Metastasis
Profiling cytochrome P450 expression in ovarian cancer: identification of prognostic markers.
Neoplasms
Activation of oxazaphosphorines by cytochrome P450: Application to gene-directed enzyme prodrug therapy for cancer.
Neoplasms
Biochemical characterization of in vivo alkylating agent resistance of a murine EMT-6 mammary carcinoma. Implication for systemic involvement in the resistance phenotype.
Neoplasms
Bioreductive metabolism of the novel fluorinated 2-nitroimidazole hypoxia probe N-(2-hydroxy-3,3,3-trifluoropropyl)-2-(2-nitroimidazolyl) acetamide (SR-4554).
Neoplasms
Capsaicin alleviates the imbalance in xenobiotic metabolizing enzymes and tumor markers during experimental lung tumorigenesis.
Neoplasms
Carbonyl reductase and NADPH cytochrome P450 reductase activities in human tumoral versus normal tissues.
Neoplasms
Catechol estrogen metabolites and conjugates in different regions of the prostate of Noble rats treated with 4-hydroxyestradiol: implications for estrogen-induced initiation of prostate cancer.
Neoplasms
Chemopreventive effect of Ginkgo biloba extract against benzo(a)pyrene-induced forestomach carcinogenesis in mice: amelioration of doxorubicin cardiotoxicity.
Neoplasms
Combination of the bioreductive drug tirapazamine with the chemotherapeutic prodrug cyclophosphamide for P450/P450-reductase-based cancer gene therapy.
Neoplasms
CYPOR is a novel and independent prognostic biomarker of recurrence-free survival in triple-negative breast cancer patients.
Neoplasms
Cytochrome P450 oxidoreductase contributes to phospholipid peroxidation in ferroptosis.
Neoplasms
Direct measurement of pO2 distribution and bioreductive enzymes in human malignant brain tumors.
Neoplasms
Dissecting the role of multiple reductases in bioactivation and cytotoxicity of the antitumor agent 2,5-diaziridinyl-3-(hydroxymethyl)-6-methyl-1,4-benzoquinone (RH1).
Neoplasms
Distinct roles of cytochrome P450 reductase in mitomycin C redox cycling and cytotoxicity.
Neoplasms
Distribution of DT-diaphorase and reduced nicotinamide adenine dinucleotide phosphate: cytochrome p450 oxidoreductase in bladder tissues and tumors.
Neoplasms
Does reductive metabolism predict response to tirapazamine (SR 4233) in human non-small-cell lung cancer cell lines?
Neoplasms
DT-diaphorase activity in normal and neoplastic human tissues; an indicator for sensitivity to bioreductive agents?
Neoplasms
DT-diaphorase as a critical determinant of sensitivity to mitomycin C in human colon and gastric carcinoma cell lines.
Neoplasms
Effects of phenobarbital and 3-methylcolanthrene treatment on microsomes of Morris hepatoma 3924-A, tumour-bearing and normal rat liver.
Neoplasms
Enhanced antitumor activity of P450 prodrug-based gene therapy using the low Km cyclophosphamide 4-hydroxylase P450 2B11.
Neoplasms
Enzymology of mitomycin C metabolic activation in tumour tissue. Characterization of a novel mitochondrial reductase.
Neoplasms
Enzymology of mitomycin C metabolic activation in tumour tissue: implications for enzyme-directed bioreductive drug development.
Neoplasms
Expression of DT-diaphorase and cytochrome P450 reductase correlates with mitomycin C activity in human bladder tumors.
Neoplasms
Expression of xenobiotic-metabolizing enzymes by primary and secondary hepatic tumors in man.
Neoplasms
Frequent, moderate-dose cyclophosphamide administration improves the efficacy of cytochrome P-450/cytochrome P-450 reductase-based cancer gene therapy.
Neoplasms
Genetically modified macrophages expressing hypoxia regulated cytochrome P450 and P450 reductase for the treatment of cancer.
Neoplasms
Human hepatic and renal microsomes, cytochromes P450 1A1/2, NADPH:cytochrome P450 reductase and prostaglandin H synthase mediate the formation of aristolochic acid-DNA adducts found in patients with urothelial cancer.
Neoplasms
Hypoxia targeted gene therapy to increase the efficacy of tirapazamine as an adjuvant to radiotherapy: reversing tumor radioresistance and effecting cure.
Neoplasms
Immunohistochemical analysis of NAD(P)H:quinone oxidoreductase and NADPH cytochrome P450 reductase in human superficial bladder tumours: relationship between tumour enzymology and clinical outcome following intravesical mitomycin C therapy.
Neoplasms
Impact of liver P450 reductase suppression on cyclophosphamide activation, pharmacokinetics and antitumoral activity in a cytochrome P450-based cancer gene therapy model.
Neoplasms
Involvement of NADPH: cytochrome P450 reductase in the activation of indoloquinone EO9 to free radical and DNA damaging species.
Neoplasms
KEMTUB012-NI2, a novel potent tubulysin analog that selectively targets hypoxic cancer cells and is potentiated by cytochrome p450 reductase downregulation.
Neoplasms
Localized aberrant expression of cytochrome P450 aromatase in primary and metastatic malignant tumors of human liver.
Neoplasms
Metabolic activation of adriamycin by NADPH-cytochrome P450 reductase; overview of its biological and biochemical effects.
Neoplasms
Modulation of cyclophosphamide-based cytochrome P450 gene therapy using liver P450 inhibitors.
Neoplasms
NAD(P)H:quinone oxidoreductase-1-dependent and -independent cytotoxicity of potent quinone Cdc25 phosphatase inhibitors.
Neoplasms
Non-nuclear localized human NOSII enhances the bioactivation and toxicity of tirapazamine (SR4233) in vitro.
Neoplasms
Nonenzymatic reductive activation of 7-N-((2-([2-(gamma-L-glutamylamino)ethyl]dithio)ethyl))mitomycin C by thiol molecules: a novel mitomycin C derivative effective on mitomycin C-resistant tumor cells.
Neoplasms
Overexpression of human NADPH:cytochrome c (P450) reductase confers enhanced sensitivity to both tirapazamine (SR 4233) and RSU 1069.
Neoplasms
Pharmacological and biochemical determinants of the antitumour activity of the indoloquinone EO9.
Neoplasms
Phenobarbital at low dose exerts hormesis in rat hepatocarcinogenesis by reducing oxidative DNA damage, altering cell proliferation, apoptosis and gene expression.
Neoplasms
Potentiation of cytochrome P450/cyclophosphamide-based cancer gene therapy by coexpression of the P450 reductase gene.
Neoplasms
Quantification of CYP2B7, CYP4B1, and CYPOR messenger RNAs in normal human lung and lung tumors.
Neoplasms
Reductase enzyme expression across the National Cancer Institute Tumor cell line panel: correlation with sensitivity to mitomycin C and EO9.
Neoplasms
Reduction of 3-amino-1,2,4-benzotriazine-1,4-di-N-oxide (tirapazamine, WIN 59075, SR 4233) to a DNA-damaging species: a direct role for NADPH:cytochrome P450 oxidoreductase.
Neoplasms
Retroviral transfer of human cytochrome P450 genes for oxazaphosphorine-based cancer gene therapy.
Neoplasms
Role of NADPH:cytochrome P450 reductase in the hypoxic accumulation and metabolism of BRU59-21, a technetium-99m-nitroimidazole for imaging tumor hypoxia.
Neoplasms
Role of structural factors of antitumour anthraquinone derivatives and analogues in the ability to undergo bioreductive activation by NADPH cytochrome P450 reductase. Implications for increasing the activity against sensitive and multidrug-resistant leukaemia HL60 cells.
Neoplasms
The drug metabolism systems of liver and liver tumors: a comparison of activities and characteristics.
Neoplasms
The hypoxia-activated prodrug evofosfamide in combination with multiple regimens of radiotherapy.
Neoplasms
The mechanism of Psoralen and Isopsoralen hepatotoxicity as revealed by hepatic gene expression profiling in SD rats.
Neoplasms
The overexpression of CPR and P450 3A4 in pancreatic cancer cells changes the metabolic profile and increases the cytotoxicity and pro-apoptotic activity of acridine antitumor agent, C-1748.
Neoplasms
The role of bioreductive activation of antitumour anthracycline drugs in cytotoxic activity against sensitive and multidrug resistant leukaemia HL60 cells.
Neoplasms
The role of bioreductive activation of doxorubicin in cytotoxic activity against leukaemia HL60-sensitive cell line and its multidrug-resistant sublines.
Neoplasms
The role of cytochrome P450 and cytochrome P450 reductase in the reductive bioactivation of the novel benzotriazine di-N-oxide hypoxic cytotoxin 3-amino-1,2,4-benzotriazine-1,4-dioxide (SR 4233, WIN 59075) by mouse liver.
Neoplasms
Viral delivery of P450 reductase recapitulates the ability of constitutive overexpression of reductase enzymes to potentiate the activity of mitomycin C in human breast cancer xenografts.
Neoplasms
Xenobiotic metabolizing enzymes in genetically and chemically initiated mouse liver tumors.
Neoplasms
Zinc finger nuclease knock-out of NADPH:cytochrome P450 oxidoreductase (POR) in human tumor cell lines demonstrates that hypoxia-activated prodrugs differ in POR dependence.
Neurodegenerative Diseases
Localization of NADPH cytochrome P450 oxidoreductase in rat brain by immunohistochemistry and in situ hybridization and a comparison with the distribution of neuronal NADPH-diaphorase staining.
Ovarian Diseases
Clinical implications of androgen synthesis via 5alpha-reduced precursors.
Ovarian Neoplasms
Profiling cytochrome P450 expression in ovarian cancer: identification of prognostic markers.
Ovotesticular Disorders of Sex Development
Sex determination and disorders of sex development according to the revised nomenclature and classification in 46,XX individuals.
Pancreatic Neoplasms
The overexpression of CPR and P450 3A4 in pancreatic cancer cells changes the metabolic profile and increases the cytotoxicity and pro-apoptotic activity of acridine antitumor agent, C-1748.
Polycystic Ovary Syndrome
P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.
Retinal Degeneration
[Changes in cytochrome P-450 and NADPH-cytochrome P-450 reductase in hereditary retinal degeneration in rats]
Riboflavin Deficiency
Lipid metabolism in riboflavin-deficient rats. 2. Mitochondrial fatty acid oxidation and the microsomal desaturation pathway.
Sarcoma
Effect of extra-hepatic Walker sarcoma 256 on the synthesis and degradation of liver cytochromes P-450 and b5.
Scoliosis
Two cases of cytochrome P450 oxidoreductase deficiency with severe scoliosis and surgery requirement.
Starvation
Induction and regulation of cytochrome P450 K-5 (lauric acid hydroxylase) in rat renal microsomes by starvation.
steroid 11beta-monooxygenase deficiency
Congenital Adrenal Hyperplasia: Time to Replace 17OHP with 21-Deoxycortisol.
steroid 17alpha-monooxygenase deficiency
Homozygous mutation G539R in the gene for P450 oxidoreductase in a family previously diagnosed as having 17,20-lyase deficiency.
steroid 21-monooxygenase deficiency
Apparent manifesting heterozygosity in P450 oxidoreductase deficiency and its effect on coexisting 21-hydroxylase deficiency.
steroid 21-monooxygenase deficiency
Backdoor pathway for dihydrotestosterone biosynthesis: Implications for normal and abnormal human sex development.
steroid 21-monooxygenase deficiency
Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites.
steroid 21-monooxygenase deficiency
Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.
steroid 21-monooxygenase deficiency
Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysis.
steroid 21-monooxygenase deficiency
Disorders of sex development and female reproductive capacity: A literature review.
steroid 21-monooxygenase deficiency
Prenatal diagnosis of congenital adrenal hyperplasia caused by p450 oxidoreductase deficiency.
steroid 21-monooxygenase deficiency
The common P450 oxidoreductase variant A503V is not a modifier gene for 21-hydroxylase deficiency.
steroid 21-monooxygenase deficiency
Two-Step Biochemical Differential Diagnosis of Classic 21-Hydroxylase Deficiency and Cytochrome P450 Oxidoreductase Deficiency in Japanese Infants by GC-MS Measurement of Urinary Pregnanetriolone/ Tetrahydroxycortisone Ratio and 11?-Hydroxyandrosterone.
Stroke
Variables in human liver microsome preparation: impact on the kinetics of l-alpha-acetylmethadol (LAAM) n-demethylation and dextromethorphan O-demethylation.
Synostosis
Regulation of gap junction function and Connexin 43 expression by cytochrome P450 oxidoreductase (CYPOR).
Thyroid Cancer, Papillary
Microsomal reductase activity in patients with thyroid neoplasms.
Triple Negative Breast Neoplasms
CYPOR is a novel and independent prognostic biomarker of recurrence-free survival in triple-negative breast cancer patients.
Turner Syndrome
Disorders of sex development and female reproductive capacity: A literature review.
Urinary Bladder Diseases
Distribution of DT-diaphorase and reduced nicotinamide adenine dinucleotide phosphate: cytochrome p450 oxidoreductase in bladder tissues and tumors.
Urinary Bladder Neoplasms
Differentiation-associated urothelial cytochrome P450 oxidoreductase predicates the xenobiotic-metabolizing activity of "luminal" muscle-invasive bladder cancers.
Urinary Bladder Neoplasms
Distribution of DT-diaphorase and reduced nicotinamide adenine dinucleotide phosphate: cytochrome p450 oxidoreductase in bladder tissues and tumors.
Urinary Bladder Neoplasms
Expression of DT-diaphorase and cytochrome P450 reductase correlates with mitomycin C activity in human bladder tumors.
Urinary Bladder Neoplasms
Immunohistochemical analysis of NAD(P)H:quinone oxidoreductase and NADPH cytochrome P450 reductase in human superficial bladder tumours: relationship between tumour enzymology and clinical outcome following intravesical mitomycin C therapy.
Urogenital Abnormalities
Mouse Knockout of the Cholesterogenic Cytochrome P450 Lanosterol 14{alpha}-Demethylase (Cyp51) Resembles Antley-Bixler Syndrome.
Vaccinia
Human NADPH-P450 oxidoreductase: complementary DNA cloning, sequence and vaccinia virus-mediated expression and localization of the CYPOR gene to chromosome 7.
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