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По вашему запросу найдено документов: 370

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Widespread natural selection on metabolite levels in humans

Timasheva, Yanina, Lepik, Kaido, Liska, Orsolya, Papp, Balázs, Kutalik, Zoltán (2024)

variants associated with traits under selection. The genetic signatures of such evolutionary events can

AVPR1A MAIN EFFECT AND OXTR-BY-ENVIRONMENT INTERPLAY IN INDIVIDUAL DIFFERENCES IN DEPRESSION LEVEL

KAZANTSEVA, A.V., DAVYDOVA, YU.D., ENIKEEVA, R.F., LOBASKOVA, M.M., MUSTAFIN, R.N., MALYKH, S.B., TAKHIROVA, Z.R., KHUSNUTDINOVA, E.K. (2020)

of genetic variants in a moderately large sample, was used. Conclusions: Our preliminary findings indicate

High-Tech Methods of Cytokine Imbalance Correction in Intervertebral Disc Degeneration

Shnayder, Natalia A., Ashhotov, Azamat V., Trefilova, Vera V., Novitsky, Maxim A., Medvedev, German V., Petrova, Marina M., Narodova, Ekaterina A., Kaskaeva, Daria S., Chumakova, Galina A., Garganeeva, Natalia P., Lareva, Natalia V., Al-Zamil, Mustafa, Asadullin, Azat R., Nasyrova, Regina F. (2023)

engineering); genetic technologies (gene modifications, microRNA, and molecular inducers of IDD); technologies

Поиск ассоциации полиморфных локусов генов HIF1A, VEGFA с риском развития рака яичников у женщин Республики Башкортостан

STUDY OF THE ASSOCIATION BETWEEN HIF1A AND VEGFA GENE POLYMORPHISMS AND OVARIAN CANCER RISK IN WOMEN FROM BASHKORTOSTAN

molecular genetic research

Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant

Elena, Merkuryeva, Tatiana, Markova, Anton, Tyurin, Diana, Valeeva, Vladimir, Kenis, Maria, Sumina, Igor, Sorokin, Olga, Shchagina, Mikhail, Skoblov, Maria, Nefedova, Rita, Khusainova, Ekaterina, Zakharova, Dadali, Elena, Kutsev, Sergey (2023)

of this variant will contribute to optimal molecular genetic diagnostics, which can reduce diagnostic costs

Exosomal non coding RNAs as a novel target for diabetes mellitus and its complications

Sufianov, A., Kostin, A., Begliarzade, S., Kudriashov, V., Ilyasova, T., Liang, Y., Mukhamedzyanov, A., Beylerli, O. (2023)

of the molecular genetic mechanisms of the pathogenesis of DM is of critical importance for the development of new

Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga–Ural Region

Khidiyatova, Irina, Khidiyatova, Indira, Zinchenko, Rena, Marakhonov, Andrey, Karunas, Alexandra, Avkhadeeva, Svetlana, Aznzbaev, Marat, Khusnutdinova, Elza (2023)

Hereditary cataracts are characterized by significant clinical and genetic heterogeneity, which can

Genetic Biomarkers of Antipsychotic-Induced Prolongation of the QT Interval in Patients with Schizophrenia

Vaiman, E.E., Shnayder, N.A., Zhuravlev, N.M., Petrova, M.M., Asadullin, A.R., Al-Zamil, M., Garganeeva, N.R., Shipulin, G.A., Cumming, G., Nasyrova, R.F. (2022)

, and monotherapy, etc.) and non-modifying factors (genetic predisposition, gender, age, etc.). The genetic

The use of bioinformatic analysis to study intracerebral hemorrhage

Gareev, Ilgiz, Beylerli, Ozal, Ilyasova, Tatiana, Mashkin, Andrey, Shi, Huaizhang (2024)

in elucidating the genetic, molecular, and environmental underpinnings of ICH. Through a detailed examination

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)

sensory disorder. The results of the molecular-based studies of HI are widely used in various genetic test

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