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По вашему запросу найдено документов: 61

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Genome-Wide Association Study: Analysis of Association of Polymorphic Loci in 4p15.2 and 20q13.31 Regions with Paranoid Schizophrenia

Gareeva, A.E. (2023)

million polymorphic risk markers for schizophrenia, significantly advancing our understanding

ANALYSIS OF ASSOCIATIONS OF ALLELES AND GENOTYPES OF POLYMORPHIC LOCI OF A RANGE OF CANDIDATE GENES WITH PHENOTYPIC VARIATIONS AT THE LEVEL OF INTELLIGENCE

Nurgalieva, A.Kh., Bashkatov, S.A., Volkova, E.V., Petrova, S.G., Takhirova, Z.R., Mustafin, R.N., Fedorova, Y.Y., Prokofyeva, D.S., Khusnutdinova, E.K. (2023)

of future endeavors. There has been conducted a molecular genetic study of the frequency distribution

Single-Nucleotide Polymorphisms as Biomarkers of Antipsychotic-Induced Akathisia: Systematic Review

Nasyrova, Regina F, Vaiman, Elena E, Repkina, Vera V, Khasanova, Aiperi K, Asadullin, Azat R, Shipulin, German A, Altynbekov, Kuanysh S, Al-Zamil, Mustafa, Petrova, Marina M, Shnayder, Natalia A (2023)

genetic studies of the predisposition to the development of AIA. Objective: The goal of our study

Ассоциации полиморфного варианта rs2072100 гена субстанции P-TAC 1 с тяжестью бронхиальной астмы

Associations of the rs2072100 polymorphic variant of the substance P-TAC 1 gene depending on the severity of bronchial asthma

Borisova, A.I., Galimova, E.S., Karimov, D.O., Kabirova, E.F., Nurtdinova, G.M., Борисова, А. И., Галимова, Е. С., Каримов, Д. О., Кабирова, Э. Ф., Нуртдинова, Г. М. (2023)

Associations of the rs2072100 polymorphic variant of the substance P-TAC 1 gene depending

Исследование полиморфизма генов фолатного цикла у женщин с бесплодием и невынашиванием беременности в программах вспомогательных репродуктивных технологий

Influence of polymorphism of folate cycle genes in assisted reproductive technologies programs in women with infertility and miscarriage

Sugurova, A.T., Yashchuk, A.G., Tyrina, A.A., Yalaev, B.I., Kharisova, Z.I., Khusainova, R.I., СУГУРОВА, А.Т., ЯЩУК, А.Г., ТЮРИНА, А.А., ЯЛАЕВ, Б.И., ХАРИСОВА, З.И., ХУСАИНОВА, Р.И. (2023)

Influence of polymorphism of folate cycle genes in assisted reproductive technologies programs

СОВРЕМЕННЫЙ ВЗГЛЯД НА ГЕНЕТИЧЕСКИЕ АСПЕКТЫ РАЗВИТИЯ ЯЗВЕННОЙ БОЛЕЗНИ

CONTEMPORARY VIEW OF THE GENETIC ASPECTS OF ULCER DISEASE DEVELOPMENT

Kuramshina, Olga,A., Batrakova, Ksenia, V., Tuvaleva, Lia,S., Shuvaeva, Lilia, G., Nigmatullin, Rustem, K., Kutuev, Zemfir, Z., Samsonova, Yanna, E., КУРАМШИНА, О.А., БАТРАКОВА, К.В., БАТРАКОВА, К.В., ШУВАЕВА, Л.Г., НИГМАТУЛЛИН, Р.Х., КУТУЕВ, З.З., САМСОНОВА, Я.Е. (2023)

CONTEMPORARY VIEW OF THE GENETIC ASPECTS OF ULCER DISEASE DEVELOPMENT

Integrating Common Risk Factors with Polygenic Scores Improves the Prediction of Type 2 Diabetes

Timasheva, Y., Balkhiyarova, Z., Avzaletdinova, D., Rassoleeva, I., Morugova, T.V., Korytina, G., Prokopenko, I., Kochetova, O. (2023)

We tested associations between 13 established genetic variants and type 2 diabetes (T2D) in 1371

Влияние однонуклеотидных полиморфизмов генов свертывающей системы крови и фолатного цикла на тяжесть течения и исходы COVID-19

The effect of single-nucleotide polymorphisms of the blood coagulation system and folate cycle genes on the severity of the duration and outcomes of COVID-19

The effect of single-nucleotide polymorphisms of the blood coagulation system and folate cycle

Polygenic Analysis of Cytokine and Inflammatory Gene Polymorphisms in Chronic Obstructive Pulmonary Disease

Korytina, G.F., Aznabaeva, Y.G., Kochetova, O.V., Nasibullin, T.R., Akhmadishina, L.Z., Khusnutdinova, N.N., Zagidullin, N. Sh., Victorova, T.V. (2023)

the association of cytokines and inflammatory genes polymorphisms and their combinations with COPD. SNPs

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 AP-induced ADRs is a genetically-determined impairment of AP efflux across the blood-brain barrier

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