PubMed (GeneRIF) for id: 1586

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Results by year

Year	Number of Results
1992	1
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521 results

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Proteomics, modeling, and fluorescence assays delineate cytochrome b₅ residues involved in binding and stimulation of cytochrome P450 17A1 17,20-lyase.

Tateishi Y, Webb SN, Li B, Liu L, Lindsey Rose K, Leser M, Patel P, Guengerich FP. Tateishi Y, et al. J Biol Chem. 2024 Mar;300(3):105688. doi: 10.1016/j.jbc.2024.105688. Epub 2024 Jan 26. J Biol Chem. 2024. PMID: 38280431 Free PMC article.

Prostate cancer androgen biosynthesis relies solely on CYP17A1 downstream metabolites.

Snaterse G, Taylor AE, Moll JM, O'Neil DM, Teubel WJ, van Weerden WM, Arlt W, Hofland J. Snaterse G, et al. J Steroid Biochem Mol Biol. 2024 Feb;236:106446. doi: 10.1016/j.jsbmb.2023.106446. Epub 2023 Dec 15. J Steroid Biochem Mol Biol. 2024. PMID: 38104728 Free article.

CYP17A1 (rs74357) polymorphism and polycystic ovary syndrome risk: a systemic review and meta-analysis.

Rezgoun ML, El Khour D, Bendaoud H, Chellat D. Rezgoun ML, et al. Acta Biomed. 2023 Aug 3;94(4):e2023167. doi: 10.23750/abm.v94i4.14229. Acta Biomed. 2023. PMID: 37539608 Free PMC article.

Mutated CYP17A1 promotes atherosclerosis and early-onset coronary artery disease.

Wu TT, Zheng YY, Ma X, Xiu WJ, Yang HT, Hou XG, Yang Y, Chen Y, Ma YT, Xie X. Wu TT, et al. Cell Commun Signal. 2023 Jun 27;21(1):155. doi: 10.1186/s12964-023-01061-z. Cell Commun Signal. 2023. PMID: 37370070 Free PMC article.

Clinical characteristics and molecular etiology of partial 17α-hydroxylase deficiency diagnosed in 46,XX patients.

Zhang D, Yao F, Luo M, Wang Y, Tian T, Deng S, Tian Q. Zhang D, et al. Front Endocrinol (Lausanne). 2022 Dec 15;13:978026. doi: 10.3389/fendo.2022.978026. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36589849 Free PMC article.

A Role of DNA Methylation within the CYP17A1 Gene in the Association of Genetic and Environmental Risk Factors with Stress-Related Manifestations of Schizophrenia.

Alfimova M, Kondratyev N, Korovaitseva G, Lezheiko T, Plakunova V, Gabaeva M, Golimbet V. Alfimova M, et al. Int J Mol Sci. 2022 Oct 20;23(20):12629. doi: 10.3390/ijms232012629. Int J Mol Sci. 2022. PMID: 36293479 Free PMC article.

Insights into Interactions of Human Cytochrome P450 17A1: A Review.

Singh H, Kumar R, Mazumder A, Salahuddin, Mazumder R, Abdullah MM. Singh H, et al. Curr Drug Metab. 2022;23(3):172-187. doi: 10.2174/1389200223666220401093833. Curr Drug Metab. 2022. PMID: 35366770 Review.

Importance of Asparagine 202 in Manipulating Active Site Structure and Substrate Preference for Human CYP17A1.

Liu Y, Denisov I, Gregory M, Sligar SG, Kincaid JR. Liu Y, et al. Biochemistry. 2022 Apr 5;61(7):583-594. doi: 10.1021/acs.biochem.2c00023. Epub 2022 Mar 15. Biochemistry. 2022. PMID: 35287432 Free PMC article.

A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency.

Beştaş A, Bolu S, Unal E, Aktar Karakaya A, Eröz R, Tekin M, Haspolat YK. Beştaş A, et al. Endocrine. 2022 Mar;75(3):927-933. doi: 10.1007/s12020-021-02914-8. Epub 2021 Nov 1. Endocrine. 2022. PMID: 34724156

Mechanism of the Clinically Relevant E305G Mutation in Human P450 CYP17A1.

Liu Y, Grinkova Y, Gregory MC, Denisov IG, Kincaid JR, Sligar SG. Liu Y, et al. Biochemistry. 2021 Nov 2;60(43):3262-3271. doi: 10.1021/acs.biochem.1c00282. Epub 2021 Oct 18. Biochemistry. 2021. PMID: 34662099 Free PMC article.

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