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Molecular and Cellular Neurosciences|January 23, 2025
Identifying potential genes driving ferroptosis in the substantia nigra and dopaminergic neurons in Parkinson's diseaseArdra Chakrabarti, Sonia Verma
Frontiers in Pharmacology|October 4, 2017
Altered CYP19A1 and CYP3A4 Activities Due to Mutations A115V, T142A, Q153R and P284L in the Human P450 OxidoreductaseSameer S Udhane, Shaheena Parween, Norio Kagawa, et al.
Journal of the Endocrine Society|June 25, 2026
Integrated mapping resolves pathogenicity of 11 CYP21A2 variants in congenital adrenal hyperplasiaYingtong Xu, Anna Matveeva, Flemming Steen Jørgensen, et al.
Biomolecules|January 28, 2026
Dihydrotanshinone as a Natural Product-Based CYP17A1 Lyase Inhibitor for Hyperandrogenic DisordersKaige Li, Jibira Yakubu, Flemming Steen Jørgensen, et al.
Biochimica Et Biophysica Acta|May 31, 2015
Cell-cell fusion induced by the Ig3 domain of receptor FGFRL1 in CHO cellsLei Zhuang, Amit V Pandey, Peter M Villiger, et al.
The Journal of Steroid Biochemistry and Molecular Biology|February 1, 2019
In silico and functional studies reveal novel loss-of-function variants of SRD5A2, but no variants explaining excess 5α-reductase activityEfstathios Katharopoulos, Kay Sauter, Amit V Pandey, et al.
The Journal of Endocrinology|June 24, 2024
Clinical spectrum of human STAR variants and their genotype-phenotype correlationEmre Murat Altinkilic, Philipp Augsburger, Amit V Pandey, et al.
European Journal of Endocrinology|June 24, 2006
Clinical and biochemical description of a novel CYP21A2 gene mutation 962_963insA using a new 3D model for the P450c21 proteinMarco Janner, Amit V Pandey, Primus E Mullis, et al.
Molecular and Cellular Endocrinology|March 2, 2010
Restoration of mutant cytochrome P450 reductase activity by external flavinCatherine Nicolo, Christa E Flück, Primus E Mullis, et al.
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