Articles with public access mandates - Walter L MillerLearn more
Available somewhere: 57
The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders
WL Miller, RJ Auchus
Endocrine reviews 32 (1), 81-151, 2011
Mandates: US National Institutes of Health
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline
PW Speiser, R Azziz, LS Baskin, L Ghizzoni, TW Hensle, DP Merke, ...
The Journal of Clinical Endocrinology & Metabolism 95 (9), 4133-4160, 2010
Mandates: US National Institutes of Health
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an endocrine society clinical practice guideline
PW Speiser, W Arlt, RJ Auchus, LS Baskin, GS Conway, DP Merke, ...
The Journal of Clinical Endocrinology & Metabolism 103 (11), 4043-4088, 2018
Mandates: US National Institutes of Health, UK Medical Research Council
Human cytochromes P450 in health and disease
DW Nebert, K Wikvall, WL Miller
Philosophical Transactions of the Royal Society B: Biological Sciences 368 …, 2013
Mandates: US National Institutes of Health, Swedish Research Council
Early steps in steroidogenesis: intracellular cholesterol trafficking: thematic review series: genetics of human lipid diseases
WL Miller, HS Bose
Journal of lipid research 52 (12), 2111-2135, 2011
Mandates: US National Institutes of Health
Congenital adrenal hyperplasia—current insights in pathophysiology, diagnostics, and management
HL Claahsen-van der Grinten, PW Speiser, SF Ahmed, W Arlt, RJ Auchus, ...
Endocrine reviews 43 (1), 91-159, 2022
Mandates: US National Institutes of Health, German Research Foundation, UK …
Why boys will be boys: two pathways of fetal testicular androgen biosynthesis are needed for male sexual differentiation
CE Flück, M Meyer-Böni, AV Pandey, P Kempná, WL Miller, EJ Schoenle, ...
The American Journal of Human Genetics 89 (2), 201-218, 2011
Mandates: Swiss National Science Foundation
Steroidogenic enzymes
WL Miller
Disorders of the human Adrenal cortex 13, 1-18, 2008
Mandates: US National Institutes of Health
The serine phosphorylation hypothesis of polycystic ovary syndrome: a unifying mechanism for hyperandrogenemia and insulin resistance
AA Bremer, WL Miller
Fertility and sterility 89 (5), 1039-1048, 2008
Mandates: US National Institutes of Health
Androgen synthesis in adrenarche
WL Miller
Reviews in Endocrine and Metabolic Disorders 10 (1), 3-17, 2009
Mandates: US National Institutes of Health
Steroidogenic activity of StAR requires contact with mitochondrial VDAC1 and phosphate carrier protein
M Bose, RM Whittal, WL Miller, HS Bose
Journal of Biological Chemistry 283 (14), 8837-8845, 2008
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Pharmacogenetics of P450 oxidoreductase: effect of sequence variants on activities of CYP1A2 and CYP2C19
V Agrawal, N Huang, WL Miller
Pharmacogenetics and genomics 18 (7), 569-576, 2008
Mandates: US National Institutes of Health
Substrate-specific modulation of CYP3A4 activity by genetic variants of cytochrome P450 oxidoreductase
V Agrawal, JH Choi, KM Giacomini, WL Miller
Pharmacogenetics and genomics 20 (10), 611-618, 2010
Mandates: US National Institutes of Health
The syndrome of 17, 20 lyase deficiency
WL Miller
The Journal of Clinical Endocrinology & Metabolism 97 (1), 59-67, 2012
Mandates: US National Institutes of Health
FGF-23 regulates CYP27B1 transcription in the kidney and in extra-renal tissues
A Chanakul, MYH Zhang, A Louw, HJ Armbrecht, WL Miller, AA Portale, ...
PloS one 8 (9), e72816, 2013
Mandates: US National Institutes of Health
Considering sex as a biological variable in basic and clinical studies: an endocrine society scientific statement
A Bhargava, AP Arnold, DA Bangasser, KM Denton, A Gupta, ...
Endocrine reviews 42 (3), 219-258, 2021
Mandates: US National Institutes of Health
Consequences of POR mutations and polymorphisms
WL Miller, V Agrawal, D Sandee, MK Tee, N Huang, JH Choi, K Morrissey, ...
Molecular and cellular endocrinology 336 (1-2), 174-179, 2011
Mandates: US National Institutes of Health
Partial Defect in the Cholesterol Side-Chain Cleavage Enzyme P450scc (CYP11A1) Resembling Nonclassic Congenital Lipoid Adrenal Hyperplasia
T Sahakitrungruang, MK Tee, PR Blackett, WL Miller
The Journal of Clinical Endocrinology & Metabolism 96 (3), 792-798, 2011
Mandates: US National Institutes of Health
Homozygous mutation G539R in the gene for P450 oxidoreductase in a family previously diagnosed as having 17, 20-lyase deficiency
E Hershkovitz, R Parvari, SA Wudy, MF Hartmann, LG Gomes, ...
The Journal of Clinical Endocrinology & Metabolism 93 (9), 3584-3588, 2008
Mandates: US National Institutes of Health
Guidelines for the development of comprehensive care centers for congenital adrenal hyperplasia: guidance from the CARES Foundation initiative
RJ Auchus, SF Witchel, KR Leight, J Aisenberg, R Azziz, TA Bachega, ...
International journal of pediatric endocrinology 2010, 1-17, 2010
Mandates: US National Institutes of Health
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