PDF) Loss of multiple enzyme activities due to the human genetic variation P284T in NADPH cytochrome P450 oxidoreductase
PDF) Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome
Publications
Adrenal cortex development and related disorders leading to adrenal insufficiency - ScienceDirect
PDF) Human P450 Oxidoreductase Deficiency
Amit V Pandey – Privatdozent and Group Leader – University of Bern | LinkedIn
Role of POR in biosynthesis of androgens in classic and alternate... | Download Scientific Diagram
Publications
Hepatic Gene Expression Changes in Mouse Models with Liver-specific Deletion or Global Suppression of the NADPH-Cytochrome P450 Reductase Gene - Journal of Biological Chemistry
Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias | European Journal of Human Genetics
PDF) Variability in Loss of Multiple Enzyme Activities Due to the Human Genetic Variation P284T Located in the Flexible Hinge Region of NADPH Cytochrome P450 Oxidoreductase
Centrosome Loss Triggers a Transcriptional Program To Counter Apoptosis-Induced Oxidative Stress | Genetics
Publications
PDF] Steroidogenesis of the testis -- new genes and pathways. | Semantic Scholar
Publications
Loss of multiple enzyme activities due to the human genetic variation P284T in NADPH cytochrome P450 oxidoreductase | bioRxiv
Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome | Nature Genetics
MECHANISMS IN ENDOCRINOLOGY: Update on pathogenesis of primary adrenal insufficiency: beyond steroid enzyme deficiency and autoimmune adrenal destruction in: European Journal of Endocrinology Volume 177 Issue 3 (2017)
IJMS | Free Full-Text | Variants of STAR, AMH and ZFPM2/FOG2 May Contribute towards the Broad Phenotype Observed in 46,XY DSD Patients with Heterozygous Variants of NR5A1 | HTML
Publications
PDF) Loss of multiple enzyme activities due to the human genetic variation P284T in NADPH cytochrome P450 oxidoreductase
Publications
Publications
CYP21A2 mutation update: Comprehensive analysis of databases and published genetic variants - Simonetti - 2018 - Human Mutation - Wiley Online Library
PDF] Steroidogenesis of the testis -- new genes and pathways. | Semantic Scholar
Update on pathogenesis of primary adrenal insufficiency: beyond steroid enzyme deficiency and autoimmune adrenal destruction