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Clinical and Functional Characteristics of the E92K CFTR Gene Variant in the Russian and Turkish Population of People with Cystic Fibrosis.
Kondratyeva E, Melyanovskaya Y, Bulatenko N, Davydenko K, Filatova A, Efremova A, Skoblov M, Bukharova T, Sherman V, Voronkova A, Zhekaite E, Krasovskiy S, Amelina E, Petrova N, Polyakov A, Adyan T, Starinova M, Krasnova M, Vasilyev A, Makhnach O, Zinchenko R, Kutsev S, Gokdemir Y, Karadag B, Goldshtein D. Kondratyeva E, et al. Among authors: sherman v. Int J Mol Sci. 2023 Mar 28;24(7):6351. doi: 10.3390/ijms24076351. Int J Mol Sci. 2023. PMID: 37047318 Free PMC article.
Evaluation of the Complex p.[Leu467Phe;Phe508del] CFTR Allele in the Intestinal Organoids Model: Implications for Therapy.
Kondratyeva E, Efremova A, Melyanovskaya Y, Voronkova A, Polyakov A, Bulatenko N, Adyan T, Sherman V, Kovalskaia V, Petrova N, Starinova M, Bukharova T, Kutsev S, Goldshtein D. Kondratyeva E, et al. Among authors: sherman v. Int J Mol Sci. 2022 Sep 8;23(18):10377. doi: 10.3390/ijms231810377. Int J Mol Sci. 2022. PMID: 36142302 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.
Clinical and genetic characterization of patients with cystic fibrosis and functional assessment of the chloride channel with the pathogenic variant c.831G>A (p.Trp277*), described for the first time.
Kondratyeva E, Efremova A, Melyanovskaya Y, Petrova N, Satsuk N, Bulatenko N, Bukharova T, Zodbinova A, Sherman V, Kashirskaya N, Zinchenko R, Kutsev S, Goldshtein D. Kondratyeva E, et al. Among authors: sherman v. Gene. 2020 Nov 30;761:145023. doi: 10.1016/j.gene.2020.145023. Epub 2020 Aug 3. Gene. 2020. PMID: 32758581
Personalized Selection of a CFTR Modulator for a Patient with a Complex Allele [L467F;F508del].
Kondratyeva E, Bulatenko N, Melyanovskaya Y, Efremova A, Zhekaite E, Sherman V, Voronkova A, Asherova I, Polyakov A, Adyan T, Kovalskaia V, Bukharova T, Goldshtein D, Kutsev S. Kondratyeva E, et al. Among authors: sherman v. Curr Issues Mol Biol. 2022 Oct 21;44(10):5126-5138. doi: 10.3390/cimb44100349. Curr Issues Mol Biol. 2022. PMID: 36286063 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.
Multiparameter screen optimizes immunoprecipitation.
Xie S, Saba L, Jiang H, Bringas OR, Oghbaie M, Stefano LD, Sherman V, LaCava J. Xie S, et al. Among authors: sherman v. Biotechniques. 2024 Apr;76(4):145-152. doi: 10.2144/btn-2023-0051. Epub 2024 Feb 29. Biotechniques. 2024. PMID: 38425263 Free article.
Consensus-Based Evaluation of Outcome Measures in Pediatric Stroke Care: A Toolkit.
Feldman SJ, Beslow LA, Felling RJ, Malone LA, Waak M, Fraser S, Bakeer N, Lee JEM, Sherman V, Howard MM, Cavanaugh BA, Westmacott R, Jordan LC. Feldman SJ, et al. Among authors: sherman v. Pediatr Neurol. 2023 Apr;141:118-132. doi: 10.1016/j.pediatrneurol.2023.01.009. Epub 2023 Jan 19. Pediatr Neurol. 2023. PMID: 36812698 Free PMC article. Review.
109 results