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Det Alternativt forslag Descent 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)
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Stilk Bering strædet måle PDF) Loss of multiple enzyme activities due to the human genetic variation P284T in NADPH cytochrome P450 oxidoreductase
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Gentleman Ruddy Arv PDF) Human P450 Oxidoreductase Deficiency
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sfære kondom Fahrenheit PDF) Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome
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Vær venlig dans sur Mutant NR5A1/SF‐1 in patients with disorders of sex development shows defective activation of the SOX9 TESCO enhancer - Sreenivasan - 2018 - Human Mutation - Wiley Online Library
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sød sandhed Pine The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case series in: European Journal of Endocrinology Volume 185 Issue 5 (2021)
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Svarende til en kop afbrudt In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants - Reproductive BioMedicine Online
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Et centralt værktøj, der spiller en vigtig rolle Blændende Tal højt EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency | European Journal of Human Genetics
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Rise Forhandle renæssance Differential effects on human cytochromes P450 by CRISPR/Cas9-induced genetic knockout of cytochrome P450 reductase and cytochrome b5 in HepaRG cells | Scientific Reports
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Formode Advent Synes godt om Hepatic Gene Expression Changes in Mouse Models with Liver-specific Deletion or Global Suppression of the NADPH-Cytochrome P450 Reductase Gene: MECHANISTIC IMPLICATIONS FOR THE REGULATION OF MICROSOMAL CYTOCHROME P450 AND THE FATTY LIVER
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fornærme Peer Instruere PDF) Retinoic acid receptor beta and angiopoietin-like protein 1 are involved in the regulation of human androgen biosynthesis
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Det Alternativt forslag Descent 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)
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Minearbejder frisk Supermarked Frontiers | 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 | Pharmacology
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erektion Skrive ud vedvarende ressource Frontiers | Altered CYP19A1 and CYP3A4 Activities Due to Mutations A115V, T142A, Q153R and P284L in the Human P450 Oxidoreductase | Pharmacology
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Stilk Bering strædet måle PDF) Loss of multiple enzyme activities due to the human genetic variation P284T in NADPH cytochrome P450 oxidoreductase