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Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients.
Petrova NV, Kashirskaya NY, Vasilyeva TA, Kondratyeva EI, Zhekaite EK, Voronkova AY, Sherman VD, Galkina VA, Ginter EK, Kutsev SI, Marakhonov AV, Zinchenko RA. Petrova NV, et al. Among authors: sherman vd. Genes (Basel). 2020 May 15;11(5):554. doi: 10.3390/genes11050554. Genes (Basel). 2020. PMID: 32429104 Free PMC article.
Vitamin D Status in Russian Children and Adolescents: Contribution of Genetic and Exogenous Factors.
Kondratyeva EI, Zakharova IN, Ilenkova NA, Klimov LY, Petrova NV, Zodbinova AE, Zhekaite EK, Chikunov VV, Dolbnya SV, Voronkova AY, Sherman VD, Loshkova EV, Melyanovskaya YL, Budzinskiy RM, Kuryaninova VA, Kutsev SI. Kondratyeva EI, et al. Among authors: sherman vd. Front Pediatr. 2020 Nov 19;8:583206. doi: 10.3389/fped.2020.583206. eCollection 2020. Front Pediatr. 2020. PMID: 33330279 Free PMC article.
Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.
Petrova NV, Kashirskaya NY, Saydaeva DK, Polyakov AV, Adyan TA, Simonova OI, Gorinova YV, Kondratyeva EI, Sherman VD, Novoselova OG, Vasilyeva TA, Marakhonov AV, Macek M Jr, Ginter EK, Zinchenko RA. Petrova NV, et al. Among authors: sherman vd. BMC Med Genet. 2019 Mar 21;20(1):44. doi: 10.1186/s12881-019-0785-z. BMC Med Genet. 2019. PMID: 30898088 Free PMC article.
High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia.
Petrova NV, Kashirskaya NY, Vasilyeva TA, Timkovskaya EE, Voronkova AY, Shabalova LA, Kondratyeva EI, Sherman VD, Novoselova OG, Kapranov NI, Zinchenko RA, Ginter EK, Makaov AKh, Kerem B. Petrova NV, et al. Among authors: sherman vd. J Cyst Fibros. 2016 May;15(3):e28-32. doi: 10.1016/j.jcf.2016.02.003. J Cyst Fibros. 2016. PMID: 26948992 Free article.