Поиск

Автор

Ключевое слово

Коллекция

Дополнительно:

Период публикации

Научный руководитель

Оппонент

По вашему запросу найдено документов: 1667

Страница 1 из 167

Genetic Predictors of Antipsychotic Efflux Impairment via Blood-Brain Barrier: Role of Transport Proteins

Nasyrova, Regina F., Shnayder, Natalia A., Osipova, Sofia M., Khasanova, Aiperi K., Efremov, Ilya S., Al-Zamil, Mustafa, Petrova, Marina M., Narodova, Ekaterina A., Garganeeva, Natalia P., Shipulin, German A. (2023)

of 15 transport proteins involved in the efflux of drugs and other xenobiotics across cell membranes (P-gp

ФАКТОРЫ РИСКА РАЗВИТИЯ ОСЛОЖНЕНИЙ ОСТРОГО ПОСТИНФЕКЦИОННОГО ГЛОМЕРУЛОНЕФРИТА В ДЕБЮТЕ У ДЕТЕЙ

RISK FACTORS FOR THE DEVELOPMENT OF COMPLICATIONS IN THE ONSET OF ACUTE POSTINFECTIOUS GLOMERULONEPHRITIS IN CHILDREN

ИМАЕВА, Л.Р., АХМЕТШИН, Р.З., ШИРЯЕВА, Г.П., ШАГАРОВА, С.В., ХАЗИЕВА, Н.Е., IMAEVA, L.R., AKHMETSHIN, R.Z., SHIRYAEVA, G.P., SHAGAROVA, S.V., KHAZIEVA, N.E. (2021)

RECONSTRUCTION OF SNP HAPLOTYPES WITH MUTATION C.-23+1G>A IN HUMAN GENE GJB2 (CHROMOSOME 13) IN SOME POPULATIONS OF EURASIA

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. (2017)

COMPARISON OF PREDICTIVE IN SILICO TOOLS ON MISSENSE VARIANTS IN GJB2, GJB6, AND GJB3 GENES ASSOCIATED WITH AUTOSOMAL RECESSIVE DEAFNESS 1A (DFNB1A)

PSHENNIKOVA, V.G., BARASHKOV, N.A., ROMANOV, G.P., TERYUTIN, F.M., SOLOV'EV, A.V., GOTOVTSEV, N.N., NIKANOROVA, A.A., FEDOROVA, S.A., NAKHODKIN, S.S., SAZONOV, N.N., MOROZOV, I.V., BONDAR, A.A., POSUKH, O.L, DZHEMILEVA, L.U., KHUSNUTDINOVA, E.K. (2019)

the Sakha Republic (Eastern Siberia, Russia): Сх26: p.Val27Ile, p.Met34Thr, p.Val37Ile, p.Leu90Pro, p.Glu114

Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

Barashkov, N.A., Konovalov, F.A., Borisova, T.V., Teryutin, F.M., Solovyev, A.V., Pshennikova, V.G., Sapojnikova, N.V., Vychuzhina, L.S., Romanov, G.P., Gotovtsev, N.N., Morozov, I.V., Bondar, A.A., Platonov, F.A., Burtseva, T.E., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A. (2021)

. We have revealed the novel homozygous c.1621C>T transition leading to premature stop codon p.(Gln541

A NOVEL PATHOGENIC VARIANT C.975G>A (P.TRP325*) IN THE POU3F4 GENE IN YAKUT FAMILY (EASTERN SIBERIA, RUSSIA) WITH THE X-LINKED DEAFNESS-2 (DFNX2)

BARASHKOV, N.A., KLAROV, L.A., TERYUTIN, F.M., SOLOVYEV, A.V., PSHENNIKOVA, V.G., ROMANOV, G.P., TOMSKY, M.I., FEDOROVA, S.A., KONNIKOVA, E.E., TOBOKHOV, A.V., MOROZOV, I.V., BONDAR, A.A., POSUKH, O.L., DZHEMILEVA, L.U., KHUSNUTDINOVA, E.K. (2018)

Here, we report a novel hemizygous transition c.975G>A (p.Trp325*) in POU3F4 gene (Xq21) found

A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia

Romanov, G.P., Pshennikova, V.G., Lashin, S.A., Solovyev, A.V., Teryutin, F.M., Cherdonova, A.M., Borisova, T.V., Sazonov, N.N., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A., Barashkov, N.A. (2020)

ОСОБЕННОСТИ НУТРИТИВНОГО СТАТУСА ДЕТЕЙ С РЕЦИДИВИРУЮЩЕЙ РЕСПИРАТОРНОЙ ПАТОЛОГИЕЙ

FEATURES THE NUTRITIONAL STATUS OF CHILDREN WITH RELAPSING RESPIRATORY PATHOLOGY

ДРУЖИНИНА, Н. А., НАСИБУЛЛИНА, Л.М., МЕРЗЛЯКОВА, Д.Р., АХМЕТШИН, Р. З., ШИРЯЕВА, Г.П., ШАГАРОВА, С.В., Druzhinina, N.A., Nasibullina, L.M., Merzlyakova, D.R., Akhmetshin, R.Z., Shiryaeva, G.P., Shagarova, S.V. (2019)

СТРОМАЛЬНО-ВАСКУЛЯРНАЯ ФРАКЦИЯ И ВОЗМОЖНОСТИ ЕЕ ПРИМЕНЕНИЯ В РАДИАЦИОННОЙ МЕДИЦИНЕ И КОЛОПРОКТОЛОГИИ

STROMAL-VASCULAR FRACTION AND POSSIBILITY OF ITS APPLICATION IN RADIATION MEDICINE AND COLOPROCTOLOGY

Терюшкова, Ж.И., Важенин, А.В., Васильев, В.С., Васильев, С.А., Димов, Г.П., Teryushkova, Zh. I., Vazhenin, A.V., Vasilyev, V.S., Vasilyev, S.A., Dimov, G.P. (2020)

OPINIONS OF HEARING PARENTS ABOUT THE CAUSES OF HEARING IMPAIRMENT OF THEIR CHILDREN WITH BIALLELIC GJB2 MUTATIONS

Solovyev, A.V., Dzhemileva, L.U., Posukh, O.L., Barashkov, N.A., Bady-Khoo, M.S., Lobov, S.L., Popova, N.Y., Romanov, G.P., Sazonov, N.N., Bondar, A.A., Morozov, I.V., Tomsky, M.I., Fedorova, S.A., Khusnutdinova, E.K. (2017)

to Bnon-hereditary^ causes and 22% (CI 14.7–31.6%) to Bhereditary^ causes (p < 0.05). Therefore, the prior

Страница 1 из 167