Dzhemileva LU - Search Results

1

Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A).

Pshennikova VG, Barashkov NA, Romanov GP, Teryutin FM, Solov'ev AV, Gotovtsev NN, Nikanorova AA, Nakhodkin SS, Sazonov NN, Morozov IV, Bondar AA, Dzhemileva LU, Khusnutdinova EK, Posukh OL, Fedorova SA. Pshennikova VG, et al. Among authors: dzhemileva lu. ScientificWorldJournal. 2019 Mar 20;2019:5198931. doi: 10.1155/2019/5198931. eCollection 2019. ScientificWorldJournal. 2019. PMID: 31015822 Free PMC article.

2

[Frequency of the 35delG mutation of the connexin 26 gene (GJB2) in patients with non-syndromic autosome-recessive deafness from Bashkortostan and in ethnic groups of the Volga-Ural region].

Khidiiatova IM, Dzhemileva LU, Khabibulin RM, Khusnutdinova EK. Khidiiatova IM, et al. Among authors: dzhemileva lu. Mol Biol (Mosk). 2002 May-Jun;36(3):438-41. Mol Biol (Mosk). 2002. PMID: 12068628 Russian. No abstract available.

3

[Genes of connexin proteins participating in sound perception].

Dzhemileva LU, Grinberg ER, Khabibullin RM, Khusnutdinova EK. Dzhemileva LU, et al. Vestn Otorinolaringol. 2006;(4):15-20. Vestn Otorinolaringol. 2006. PMID: 17152467 Review. Russian.

4

[Molecular genetics of Usher syndrome].

Tazetdinov AM, Dzhemileva LU, Khusnutdinova EK. Tazetdinov AM, et al. Among authors: dzhemileva lu. Genetika. 2008 Jun;44(6):725-33. Genetika. 2008. PMID: 18727382 Review. Russian.

5

[Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia)].

Barashkov NA, Dzhemileva LU, Fedorova SA, Maksimova NR, Khusnutdinova EK. Barashkov NA, et al. Among authors: dzhemileva lu. Vestn Otorinolaringol. 2008;(5):23-8. Vestn Otorinolaringol. 2008. PMID: 19008837 Russian.

6

[Cochlear implantation in a child with congenital sensorineural deafness due to 35 DELG mutation in GJB2 (connexin 26) gene].

Teriutin FM, Barashkov NA, Dzhemileva LU, Posukh OL, Fedotova EE, Gurinova EE, Fedorova SA, Tavartkiladze GA, Khusnutdinova EK. Teriutin FM, et al. Among authors: dzhemileva lu. Vestn Otorinolaringol. 2009;(2):17-9. Vestn Otorinolaringol. 2009. PMID: 19491791 Russian.

7

[Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia].

Dzhemileva LU, Posukh OL, Tazetdinov AM, Barashkov NA, Zhuravskiĭ SG, Ponidelko SN, Markova TG, Tadinova VN, Fedorova SA, Maksimova NR, Khusnutdinova EK. Dzhemileva LU, et al. Genetika. 2009 Jul;45(7):982-91. Genetika. 2009. PMID: 19705751 Russian.

8

Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia.

Dzhemileva LU, Barashkov NA, Posukh OL, Khusainova RI, Akhmetova VL, Kutuev IA, Gilyazova IR, Tadinova VN, Fedorova SA, Khidiyatova IM, Lobov SL, Khusnutdinova EK. Dzhemileva LU, et al. J Hum Genet. 2010 Nov;55(11):749-54. doi: 10.1038/jhg.2010.101. Epub 2010 Aug 26. J Hum Genet. 2010. PMID: 20739944

9

Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect.

Barashkov NA, Dzhemileva LU, Fedorova SA, Teryutin FM, Posukh OL, Fedotova EE, Lobov SL, Khusnutdinova EK. Barashkov NA, et al. Among authors: dzhemileva lu. J Hum Genet. 2011 Sep;56(9):631-9. doi: 10.1038/jhg.2011.72. Epub 2011 Jul 21. J Hum Genet. 2011. PMID: 21776002

10

Haplotype Diversity and Reconstruction of Ancestral Haplotype Associated with the c.35delG Mutation in the GJB2 (Cx26) Gene among the Volgo-Ural Populations of Russia.

Dzhemileva LU, Posukh OL, Barashkov NA, Fedorova SA, Teryutin FM, Akhmetova VL, Khidiyatova IM, Khusainova RI, Lobov SL, Khusnutdinova EK. Dzhemileva LU, et al. Acta Naturae. 2011 Jul;3(3):52-63. Acta Naturae. 2011. PMID: 22649694 Free PMC article.

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