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International Journal of Molecular Sciences|November 27, 2021
Transcriptome Analysis of Insulin Signaling-Associated Transcription Factors in C. elegans Reveal Their Genome-Wide Target Genes Specificity and ComplexityNeha Kaushik, Soumya Rastogi, Sonia Verma, et al.Journal of the Endocrine Society|April 23, 2020
Novel CYP19A1 Mutations Extend the Genotype-Phenotype Correlation and Reveal the Impact on Ovarian FunctionValiyaparambil Pavithran Praveen, Asmahane Ladjouze, Kay-Sara Sauter, et al.The Journal of Clinical Endocrinology and Metabolism|December 3, 2009
Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and actionVibor Petkovic, Michela Godi, Amit V Pandey, et al.Hormone Research in Paediatrics|July 1, 2019
HIV Drug Efavirenz Inhibits CYP21A2 Activity with Possible Clinical ImplicationsJana Malikova, Tanja Zingg, Ralph Fingerhut, et al.Clinical Endocrinology|July 18, 2013
STAR splicing mutations cause the severe phenotype of lipoid congenital adrenal hyperplasia: insights from a novel splice mutation and review of reported casesNúria Camats, Amit V Pandey, Mónica Fernández-Cancio, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|February 14, 2025
Pyridine indole hybrids as novel potent CYP17A1 inhibitorsTomasz M Wróbel, Angelika Grudzińska, Jibira Yakubu, et al.Plos One|June 8, 2011
Characterization of novel StAR (steroidogenic acute regulatory protein) mutations causing non-classic lipoid adrenal hyperplasiaChrista E Flück, Amit V Pandey, Bernhard Dick, et al.Pharmaceuticals (Basel, Switzerland)|May 2, 2018
Mechanism of the Dual Activities of Human CYP17A1 and Binding to Anti-Prostate Cancer Drug Abiraterone Revealed by a Novel V366M Mutation Causing 17,20 Lyase DeficiencyMónica Fernández-Cancio, Núria Camats, Christa E Flück, et al.Molecular Syndromology|September 28, 2023
Expanding the p.(Arg85Trp) Variant-Specific Phenotype of HNF4A: Features of Glycogen Storage Disease, Liver Cirrhosis, Impaired Mitochondrial Function, and Glomerular ChangesMara Grassi, Bernard Laubscher, Amit V Pandey, et al.European Journal of Endocrinology|February 19, 2013
Short stature in two siblings heterozygous for a novel bioinactive GH mutant (GH-P59S) suggesting that the mutant also affects secretion of the wild-type GHVibor Petkovic, Maria Consolata Miletta, Annemieke M Boot, et al.Pageof 14