Chernykh V - Search Results

1

Pathogenic Variants and Genotypes of the CFTR Gene in Russian Men with Cystic Fibrosis and CBAVD Syndrome.

Chernykh V, Krasovsky S, Solovova O, Adyan T, Stepanova A, Marnat E, Shtaut M, Sedova A, Sorokina T, Beskorovainaya T, Kondratyeva E, Shchagina O, Polyakov A. Chernykh V, et al. Int J Mol Sci. 2023 Nov 14;24(22):16287. doi: 10.3390/ijms242216287. Int J Mol Sci. 2023. PMID: 38003474 Free PMC article.

2

L138ins Variant of the CFTR Gene in Russian Infertile Men.

Chernykh V, Sorokina T, Sedova A, Shtaut M, Solovova O, Marnat E, Adyan T, Beskorovaynaya T, Stepanova A, Shchagina O, Polyakov A. Chernykh V, et al. Genes (Basel). 2023 Jul 7;14(7):1407. doi: 10.3390/genes14071407. Genes (Basel). 2023. PMID: 37510311 Free PMC article.

3

Comprehensive semen examination in patients with pancreatic-sufficient and pancreatic-insufficient cystic fibrosis.

Sedova AO, Shtaut MI, Bragina EE, Sorokina TM, Shmarina GV, Andreeva MV, Kurilo LF, Krasovskiy SA, Polyakov AV, Chernykh VB. Sedova AO, et al. Among authors: chernykh vb. Asian J Androl. 2023 Mar 3;25(5):591-7. doi: 10.4103/aja2022115. Online ahead of print. Asian J Androl. 2023. PMID: 36891936 Free PMC article.

4

[The frequency and spectrum of mutations and the IVS8-T polymorphism of the CFTR gene in Russian infertile men].

Chernykh VB, Stepanova AA, Beskorovaĭnaia TS, Sorokina TM, Shileĭko LV, Kurilo LF, Poliakov AV. Chernykh VB, et al. Genetika. 2010 Jun;46(6):844-52. Genetika. 2010. PMID: 20734777 Russian.

5

A Mosaic Mutation in the LAMA2 Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy.

Chausova PA, Ryzhkova OP, Rudenskaya GE, Chernykh VB, Shchagina OA, Polyakov AV. Chausova PA, et al. Among authors: chernykh vb. Front Genet. 2021 Oct 29;12:686800. doi: 10.3389/fgene.2021.686800. eCollection 2021. Front Genet. 2021. PMID: 34777456 Free PMC article.

6

Unique mosaic X/Y translocation/insertion in infant 45,X male.

Chernykh VB, Vyatkina SV, Antonenko VG, Shilova NV, Zolotukhina TV, Kurilo LF, Chukhrova AL, Polyakov AV. Chernykh VB, et al. Am J Med Genet A. 2008 Dec 15;146A(24):3195-7. doi: 10.1002/ajmg.a.32578. Am J Med Genet A. 2008. PMID: 19012335

7

Hidden X chromosomal mosaicism in a 46,XX male.

Chernykh VB, Kurilo LF, Shilova NV, Zolotukhina TV, Ryzhkova OP, Bliznetz EA, Polyakov AV. Chernykh VB, et al. Sex Dev. 2009;3(4):183-7. doi: 10.1159/000228718. Epub 2009 Sep 11. Sex Dev. 2009. PMID: 19752597

8

Genes associated with testicular germ cell tumors and testicular dysgenesis in patients with testicular microlithiasis.

Dantsev IS, Ivkin EV, Tryakin AA, Godlevski DN, Latyshev OY, Rudenko VV, Mikhaylenko DS, Chernykh VB, Volodko EA, Okulov AB, Loran OB, Nemtsova MV. Dantsev IS, et al. Among authors: chernykh vb. Asian J Androl. 2018 Nov-Dec;20(6):593-599. doi: 10.4103/aja.aja_54_18. Asian J Androl. 2018. PMID: 30027931 Free PMC article.

9

[Polymorphisms of KITLG, SPRY4, and BAK1 genes in patients with testicular germ cell tumors and individuals with infertility associated with AZFc deletion of the Y chromosome].

Nemtsova MV, Ivkin EV, Simonova OA, Rudenko VV, Chernykh VB, Mikhaylenko DS, Loran OB. Nemtsova MV, et al. Among authors: chernykh vb. Mol Biol (Mosk). 2016 Nov-Dec;50(6):960-967. doi: 10.7868/S002689841605013X. Mol Biol (Mosk). 2016. PMID: 28064312 Free article. Russian.

10

The effect of Robertsonian translocations on the intranuclear positioning of NORs (nucleolar organizing regions) in human sperm cells.

Wiland E, Olszewska M, Huleyuk N, Chernykh VB, Kurpisz M. Wiland E, et al. Sci Rep. 2019 Feb 18;9(1):2213. doi: 10.1038/s41598-019-38478-x. Sci Rep. 2019. PMID: 30778082 Free PMC article.

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