Petrova NV - Search Results

1

Clinical Presentation of the c.3844T>C (p.Trp1282Arg, W1282R) Variant in Russian Cystic Fibrosis Patients.

Petrova NV, Kashirskaya NY, Krasovskiy SA, Amelina EL, Kondratyeva EI, Marakhonov AV, Vasilyeva TA, Voronkova AY, Sherman VD, Ginter EK, Kutsev SI, Zinchenko RA. Petrova NV, et al. Genes (Basel). 2020 Sep 27;11(10):1137. doi: 10.3390/genes11101137. Genes (Basel). 2020. PMID: 32992607 Free PMC article.

2

[Portion of certain cystic fibrosis gene mutations and linkage dysequilibrium between the CFTR-gene locus and two DNA marker loci in Russian populations].

Petrova NV, Ginter EK, Kapranov NI, El'chinova GI. Petrova NV, et al. Genetika. 1994 Jul;30(7):974-7. Genetika. 1994. PMID: 7525404 Russian.

3

Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel alleles.

Verlingue C, Kapranov NI, Mercier B, Ginter EK, Petrova NV, Audrezet MP, Férec C. Verlingue C, et al. Among authors: petrova nv. Hum Mutat. 1995;5(3):205-9. doi: 10.1002/humu.1380050304. Hum Mutat. 1995. PMID: 7541273

4

[Genetico-demographic characteristics of the population from three districts of the Bryansk region].

Kadoshnikova MIu, Brusintseva OV, Startseva EA, El'chinova GI, Petrova NV, Bukina AM, Mamedova RA, Ginter EK. Kadoshnikova MIu, et al. Among authors: petrova nv. Genetika. 1996 Aug;32(8):1142-7. Genetika. 1996. PMID: 8964485 Russian.

5

[Detection of frequent mutations of the CFTR gene in cystic fibrosis patients from Central Russia].

Petrova NV, Kapranov NI, Ginter EK. Petrova NV, et al. Genetika. 1997 Jan;33(1):106-9. Genetika. 1997. PMID: 9162681 Russian.

6

[Determination of the frequency of the deltaF508 mutation among newborns in the city of Moscow and evaluation of the frequency of cystic fibrosis in the European part of Russia].

Petrova NV, Ginter EK. Petrova NV, et al. Genetika. 1997 Sep;33(9):1326-8. Genetika. 1997. PMID: 9445828 Russian.

7

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.

Dörk T, Macek M Jr, Mekus F, Tümmler B, Tzountzouris J, Casals T, Krebsová A, Koudová M, Sakmaryová I, Macek M Sr, Vávrová V, Zemková D, Ginter E, Petrova NV, Ivaschenko T, Baranov V, Witt M, Pogorzelski A, Bal J, Zékanowsky C, Wagner K, Stuhrmann M, Bauer I, Seydewitz HH, Neumann T, Jakubiczka S. Dörk T, et al. Among authors: petrova nv. Hum Genet. 2000 Mar;106(3):259-68. doi: 10.1007/s004390000246. Hum Genet. 2000. PMID: 10798353

8

TNF gene polymorphisms in cystic fibrosis patients: contribution to the disease progression.

Shmarina G, Pukhalsky A, Petrova N, Zakharova E, Avakian L, Kapranov N, Alioshkin V. Shmarina G, et al. J Transl Med. 2013 Jan 23;11:19. doi: 10.1186/1479-5876-11-19. J Transl Med. 2013. PMID: 23343370 Free PMC article.

9

A clinical and molecular analysis of branchio-oculo-facial syndrome patients in Russia revealed new mutations in TFAP2A.

Meshcheryakova TI, Zinchenko RA, Vasilyeva TA, Marakhonov AV, Zhylina SS, Petrova NV, Kozhanova TV, Belenikin MS, Petrin AN, Mutovin GR. Meshcheryakova TI, et al. Among authors: petrova nv. Ann Hum Genet. 2015 Mar;79(2):148-52. doi: 10.1111/ahg.12098. Epub 2015 Jan 15. Ann Hum Genet. 2015. PMID: 25590586

10

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. 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.

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