Search Results - "Barashkov, N. A"

Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A by Solovyev, A. V., Barashkov, N. A., Teryutin, F. M., Pshennikova, V. G., Romanov, G. P., Rafailov, A. M., Sazonov, N. N., Dzhemileva, L. U., Tomsky, M. I., Posukh, O. L., Khusnutdinova, E. K., Fedorova, S. A.

“…We present the results of analysis of skin epidermis thickness in individuals with recessive mutation c.-23+1G>A in the GJB2 gene in comparison with…”
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The Spectrum and Frequency of Inner Ear Anomalies in Patients with Congenital Hearing Impairment in Yakutia by Klarov, L. A., Barashkov, N. A., Teryutin, F. M., Romanov, G. P., Popov, M. M., Solov’ev, A. V., Luginov, N. V., Tobokhov, A. V., Kotlyarov, P. M.

“…Objective . To analyze the spectrum and frequency of inner ear anomalies in patients with congenital hearing impairment in Yakutia. Material and methods . A…”
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The audiological analysis in the patients homozygous for the c.-23+1G>A mutation in the GJB2 gene presenting with the loss of hearing in Yakutiya by Teryutin, F M, Barashkov, N A, Kunel'skaya, N L, Pshennikova, V G, Solov'ev, A V

“…In the course of previous investigations carried out in the Republic of Sakha (Yakutiya), we have identified the main molecular-genetic factor responsible for…”
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The impact of the sociodemographic structure of deaf people communities on the prevalence of hereditary hearing loss by Posukh, O. L., Bady-Khoo, M. S., Zytsar, M. V., Mikhalskaia, V. Yu, Lashin, S. A., Barashkov, N. A., Romanov, G. P.

“…Hearing loss caused by environmental or genetic factors concerns more than 10% of the world’s population, leading to disability and considerable deterioration…”
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Impact of socio-demographic structure of the deaf people communities in prevalence of hereditary hearing loss by O. L. Posukh, M. S. Bady-Khoo, M. V. Zytsar, V. Yu. Mikhalskaia, S. A. Lashin, N. A. Barashkov, G. P. Romanov

“…Hearing loss caused by environmental or genetic factors concerns more than 10 % of the world population. It leads to disability and considerably reduces the…”
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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 by Dzhemileva, L U, Posukh, O L, Barashkov, N A, Fedorova, S A, Teryutin, F M, Akhmetova, V L, Khidiyatova, I M, Khusainova, R I, Lobov, S L, Khusnutdinova, E K

“…The mutations in theGJB2(Сх26) gene make the biggest contribution to hereditary hearing loss. The spectrum and prevalence of theGJB2gene mutations are specific…”
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Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia by Dzhemileva, L U, Posukh, O L, Tazetdinov, A M, Barashkov, N A, Zhuravskiĭ, S G, Ponidelko, S N, Markova, T G, Tadinova, V N, Fedorova, S A, Maksimova, N R, Khusnutdinova, E K

“…Mitochondrial DNA (mtDNA) mutations play an important role in etiology of hereditary hearing loss. In various regions of the world, patients suffer from…”
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Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia) by Barashkov, N A, Dzhemileva, L U, Fedorova, S A, Maksimova, N R, Khusnutdinova, E K

“…The aim of the study was to elucidate the causes of hereditary non-syndromic loss of hearing, a frequent monogene pathology in the Republic of Sakha (Yakutia)…”
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Analysis of mitochondrial 12S rRNA and tRNASer(UCN) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia by Dzhemilova, L. U., Posukh, O. L., Tazetdinov, A. M., Barashkov, N. A., Zhuravskii, S. A., Ponidelko, S. N., Markova, T. G., Tadinova, V. N., Fedorova, S. A., Maksimova, N. R., Khusnutdinova, E. K.

“…Mitochondrial DNA (mtDNA) mutations play an important role in etiology of hereditary hearing loss. In various regions of the world, patients suffer from…”
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Cochlear implantation in a child with congenital sensorineural deafness due to 35 DELG mutation in GJB2 (connexin 26) gene by Teriutin, F M, Barashkov, N A, Dzhemileva, L U, Posukh, O L, Fedotova, E E, Gurinova, E E, Fedorova, S A, Tavartkiladze, G A, Khusnutdinova, E K

“…This paper reports the first case of cochlear implantation performed in this country in a child with congenital non-syndromic sensorineural loss of hearing…”
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Genetic History of Russian Old-Settlers of the Arctic Coast of Yakutia from the Settlement of Russkoe Ust’ye Inferred from Y Chromosome Data and Genome-Wide Analysis by Solovyev, A. V., Borisova, T. V., Romanov, G. P., Teryutin, F. M., Pshennikova, V. G., Nikitina, S. E., Alekseev, A. N., Barashkov, N. A., Fedorova, S. A.

“…There are different hypotheses on the origin and time of appearance of Russian settlements in the northeast of the Arctic. To study the history of the…”
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Analysis of GJB6 (Сx30) and GJB3 (Сx31) genes in deaf patients with monoallelic mutations in GJB2 (Сx26) gene in the Sakha Republic (Yakutia) by Pshennikova, V. G., Barashkov, N. A., Solovyev, A. V., Romanov, G. P., Diakonov, E. E., Sazonov, N. N., Morozov, I. V., Bondar, A. A., Posukh, O. L., Dzhemileva, L. U., Khusnutdinova, E. K., Tomsky, M. I., Fedorova, S. A.

“…Тhe DNA testing of autosomal recessive deafness type 1A (DFNB1A, MIM 220290) is complicated when deaf patients have only monoallelic (heterozygous) recessive…”
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Reconstruction of SNP haplotypes with mutation c.-23+1G>A in human gene GJB2 (Chromosome 13) in some populations of Eurasia by Solovyev, A. V., Barashkov, N. A., Bady-Khoo, M. S., Zytsar, M. V., Posukh, O. L., Romanov, G. P., Rafailov, A. M., Sazonov, N. N., Alexeev, A. N., Dzhemileva, L. U., Khusnutdinova, E. K., Fedorova, S. A.

“…The c.-23+1G>A splice site mutation is one of the most frequent mutations of gene GJB2 (Cx26, 13q11-q12) associated with congenital non-syndromic autosomal…”
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Marital Structure, Genetic Fitness, and the GJB2 Gene Mutations among Deaf People in Yakutia (Eastern Siberia, Russia) by Romanov, G. P., Barashkov, N. A., Teryutin, F. M., Lashin, S. A., Solovyev, A. V., Pshennikova, V. G., Bondar, A. A., Morozov, I. V., Sazonov, N. N., Tomsky, M. I., Dzhemileva, L. U., Khusnutdinova, E. K., Posukh, O. L., Fedorova, S. A.

“…Autosomal recessive deafness type 1A (DFNB1A) caused by mutations in the GJB2 gene (Cx26) is the main cause of nonsyndromic hearing impairment in many…”
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Analysis of mitochondrial 12S rRNA and tRNA Ser(UCN) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia by Dzhemilova, L. U., Posukh, O. L., Tazetdinov, A. M., Barashkov, N. A., Zhuravskii, S. A., Ponidelko, S. N., Markova, T. G., Tadinova, V. N., Fedorova, S. A., Maksimova, N. R., Khusnutdinova, E. K.

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Analysis of mitochondrial 12S rRNA and tRNA Ser⁽UCN⁾ genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia by Dzhemilova, L. U, Posukh, O. L, Tazetdinov, A. M, Barashkov, N. A, Zhuravskii, S. A, Ponidelko, S. N, Markova, T. G, Tadinova, V. N, Fedorova, S. A, Maksimova, N. R, Khusnutdinova, E. K

“…Mitochondrial DNA (mtDNA) mutations play an important role in etiology of hereditary hearing loss. In various regions of the world, patients suffer from…”
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Training of students for the performance of the duties of the troop physician by Barashkov, N A

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On the preliminary training of the military surgeon in the department of military medicine by Barashkov, N A

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On the method of teaching the subject "Organization of the work of the medico-sanitary battalion" by Barashkov, N A

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Optimizing the teaching of therapy in a military medicine department by Barashkov, N A, Kliachkin, L M

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