Search Results

Age-Related Hearing Impairment (ARHI) Associated with GJB2 Single Mutation IVS1+1G>A in the Yakut Population Isolate in Eastern Siberia

by Barashkov, Nikolay A., Teryutin, Fedor M., Pshennikova, Vera G., Solovyev, Aisen V., Klarov, Leonid A., Solovyeva, Natalya A., Kozhevnikov, Andrei A., Vasilyeva, Lena M., Fedotova, Elvira E., Pak, Maria V., Lekhanova, Sargylana N., Zakharova, Elena V., Savvinova, Kyunney E., Gotovtsev, Nyurgun N., Rafailo, Adyum M., Luginov, Nikolay V., Alexeev, Anatoliy N., Posukh, Olga L., Dzhemileva, Lilya U., Khusnutdinova, Elza K., Fedorova, Sardana A.
Published in PLoS ONE (2014)

Age-Related Hearing Impairment (ARHI) associated with GJB2 single mutation IVS1+1G>A in the Yakut population isolate in Eastern Siberia.

by Nikolay A Barashkov, Fedor M Teryutin, Vera G Pshennikova, Aisen V Solovyev, Leonid A Klarov, Natalya A Solovyeva, Andrei A Kozhevnikov, Lena M Vasilyeva, Elvira E Fedotova, Maria V Pak, Sargylana N Lekhanova, Elena V Zakharova, Kyunney E Savvinova, Nyurgun N Gotovtsev, Adyum M Rafailo, Nikolay V Luginov, Anatoliy N Alexeev, Olga L Posukh, Lilya U Dzhemileva, Elza K Khusnutdinova, Sardana A Fedorova
Published in PLoS ONE (2014)

Age-Related Hearing Impairment (ARHI) Associated with GJB2 Single Mutation IVS1+1G>A in the Yakut Population Isolate in Eastern Siberia

by Barashkov, Nikolay A., Teryutin, Fedor M., Pshennikova, Vera G., Solovyev, Aisen V., Klarov, Leonid A., Solovyeva, Natalya A., Kozhevnikov, Andrei A., Vasilyeva, Lena M., Fedotova, Elvira E., Pak, Maria V., Lekhanova, Sargylana N., Zakharova, Elena V., Savvinova, Kyunney E., Gotovtsev, Nyurgun N., Rafailo, Adyum M., Luginov, Nikolay V., Alexeev, Anatoliy N., Posukh, Olga L., Dzhemileva, Lilya U., Khusnutdinova, Elza K., Fedorova, Sardana A.
Published in PLoS ONE (2014)

A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C...

by Nikolay A. Barashkov, Georgii P. Romanov, Uigulaana P. Borisova, Aisen V. Solovyev, Vera G. Pshennikova, Fedor M. Teryutin, Alexander A. Bondar, Igor V. Morozov, Elza K. Khusnutdinova, Olga L. Posukh, Tatiana E. Burtseva, Jon Øyvind Odland, Sardana A. Fedorova
Published in International Journal of Circumpolar Health (2019)

A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C...

by Barashkov, Nikolay A., Romanov, Georgii P., Borisova, Uigulaana P., Solovyev, Aisen V., Pshennikova, Vera G., Teryutin, Fedor M., Bondar, Alexander A., Morozov, Igor V., Khusnutdinova, Elza K., Posukh, Olga L., Burtseva, Tatiana E., Odland, Jon Øyvind, Fedorova, Sardana A.
Published in International Journal of Circumpolar Health (2019)

Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies

by Leonid A. Klarov, Vera G. Pshennikova, Georgii P. Romanov, Aleksandra M. Cherdonova, Aisen V. Solovyev, Fedor M. Teryutin, Nikolay V. Luginov, Petr M. Kotlyarov, Nikolay A. Barashkov
Published in International Journal of Molecular Sciences (2022)

A rare case of Waardenburg syndrome with unilateral hearing loss caused by nonsense variant c.772C...

by Barashkov, Nikolay A., Romanov, Georgii P., Borisova, Uigulaana P., Solovyev, Aisen V., Pshennikova, Vera G., Teryutin, Fedor M., Bondar, Alexander A., Morozov, Igor V., Khusnutdinova, Elza K., Posukh, Olga L., Burtseva, Tatiana E., Odland, Jon Øyvind, Fedorova, Sardana A.
Published in International Journal of Circumpolar Health (2019)

Analysis of SLC26A4,FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies

by Leonid A. Klarov, Vera G. Pshennikova, Georgii P. Romanov, Aleksandra M. Cherdonova, Aisen V. Solovyev, Fedor M. Teryutin, Nikolay V. Luginov, Petr M. Kotlyarov, Nikolay A. Barashkov
Published in International Journal of Molecular Sciences (2022)

ВЛИЯНИЕ ТРЕВОЖНО-ДЕПРЕССИВНЫХ РАССТРОЙСТВ НА КАЧЕСТВО ЖИЗНИ СЛАБОСЛЫШАЩИХ МИГРАНТОВ КРАЙНЕГО СЕВЕРА В ПЕРИОД РЕАДАПТАЦИИ К НОВЫМ КЛИМАТИЧЕСКИМ УСЛОВИЯМ...

by ЯСКЕВИЧ Р.А., ИГНАТОВА И.А., ШИЛОВ С.Н., ПОКИДЫШЕВА Л.И., ДЕРЕВЯННЫХ Е.В., БАЛАШОВА Н.А.
Published 2014

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., Posukh, O., Barashkov, N., Fedorova, S., Teryutin, F., Akhmetova, V., Khidiyatova, I., Khusainova, R., Lobov, S., Khusnutdinova, E.
Published 2011

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.
Published 2011

ВЛИЯНИЕ ТРЕВОЖНО-ДЕПРЕССИВНЫХ РАССТРОЙСТВ НА КАЧЕСТВО ЖИЗНИ У МИГРАНТОВ КРАЙНЕГО СЕВЕРА С АРТЕРИАЛЬНОЙ ГИПЕРТОНИЕЙ...

by Яскевич, Р., Поликарпов, Л., Деревянных, Е., Харьков, Е., Балашова, Н.
Published 2014

Un front pionnier contemporain en Arctique (Sibérie occidentale).

by Vaguet, Yvette
Published 2019

Henri LECOMTE : Les esprits écoutent. Musiques des peuples autochtones de Sibérie

by Legrain, Laurent
Published 2014

Letter from John Muir to [Louie Strentzel Muir], 1881 Aug 16.

by Muir, John
Published 1881

Letter from John Muir to [Louie Strentzel Muir], 1881 Aug 16.

by Muir, John
Published 1881

Letter from John Muir to [Louie Strentzel Muir], 1881 Aug 16.

by Muir, John
Published 1881

Letter from John Muir to [Louie Strentzel Muir], 1881 Aug 16.

by Muir, John
Published 1881

Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies

by Klarov, Leonid A., Pshennikova, Vera G., Romanov, Georgii P., Cherdonova, Aleksandra M., Solovyev, Aisen V., Teryutin, Fedor M., Luginov, Nikolay V., Kotlyarov, Petr M., Barashkov, Nikolay A.
Published in International Journal of Molecular Sciences (2022)

Reconstruction of the founder haplotype with mutation c.644G>A p. (Trp215*) in the CLIC5 gene, leading to juvenile autosomal recessive deafness (DFNB103) in Yakutia

by N. Barashkov A., T. Borisova V., A. Gerasimova A., A. Solovyev V., F. Teryutin M., V. Pshennikova G., G. Romanov P., T. Burtseva E., S. Fedorova A., Н. Барашков А., Т. Борисова В., А. Герасимова А., А. Соловьев В., Ф. Терютин М., В. Пшенникова Г., Г. Романов П., Т. Бурцева Е., С. Федорова А.
Published in Nauchno-prakticheskii zhurnal «Medicinskaia genetika (2021)