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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.
National Library of Medicine; SNPedia; OMIM Online Mendelian Inheritance in Man; The PharmGKB. The role
Burials dating to the migration period in Western Siberia
Matveeva, N. P., Матвеева, Н. П.
in the funeral feast, and the addition of sand and grog to ceramic paste are elements inherited from the earlier
Association of the ACTN3 Gene’s Single-Nucleotide Variant Rs1815739 (R577X) with Sports Qualification and Competitive Distance in Caucasian Athletes of the Southern Urals
Balberova, Olga V., Shnayder, Natalia A., Bykov, Evgeny V., Zakaryukin, Yuri E., Petrova, Marina M., Soloveva, Irina A., Narodova, Ekaterina A., Chumakova, Galina A., Al-Zamil, Mustafa, Asadullin, Azat R., Vaiman, Elena E., Trefilova, Vera V., Nasyrova, Regina F.
and additive inheritance models demonstrated that high athletic performance for sprinters was associated
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
in an autosomal dominant pattern of inheritance. Two previously undescribed likely pathogenic missense variants
Genetic Predictors of Antipsychotic Efflux Impairment via Blood-Brain Barrier:Role of Transport Proteins
Nasyrova R.F., Shnayder N.A., Osipova S.M., Khasanova A.K., Efremov I.S., Al-Zamil Mustafa, Petrova M.M., Narodova E.A., Garganeeva N.P., Shipulin G.A.
National Library of Medicine; SNPedia; OMIM Online Mendelian Inheritance in Man; The PharmGKB. The role
Association of the ACTN3 Gene's Single-Nucleotide Variant Rs1815739 (R577X) with Sports Qualification and Competitive Distance in Caucasian Athletes of the Southern Urals
Balberova O.V., Shnayder N.A., Bykov E.V., Zakaryukin Y.E., Petrova M.M., Soloveva I.A., Narodova E.A., Chumakova G.A., Al-Zami Mustafa, Asadullin A.R., Vaiman E.E., Trefilova V.V., Nasyrova R.F.
and additive inheritance models demonstrated that high athletic performance for sprinters was associated
Идея справедливости как социальная "ловушка" для России
Черняк А.З., Ивлева М.Л., Орехов А.М.
not meet social expectations determined by the system of previous values or inherited from it. The authors
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.
National Library of Medicine; SNPedia; OMIM Online Mendelian Inheritance in Man; The PharmGKB. The role
Association of the ACTN3 Gene’s Single-Nucleotide Variant Rs1815739 (R577X) with Sports Qualification and Competitive Distance in Caucasian Athletes of the Southern Urals
Balberova Olga V., Shnayder Natalia A., Bykov Evgeny V., Zakaryukin Yuri E., Petrova Marina M., Soloveva Irina A., Narodova Ekaterina A., Chumakova Galina A., Al-Zamil Mustafa, Asadullin Azat R., Vaiman Elena E., Trefilova Vera V., Nasyrova Regina F.
and additive inheritance models demonstrated that high athletic performance for sprinters was associated
Синдром Пейтца-Егерса в детской дерматологической практике
Таганов А.В., Тамразова О.Б., Молочков А.В., Гончарова Л.В., Стадникова А.С., Глухова Е.А.
Peutz-Jeghers' syndrome is a rare hereditary disease inherited by an autosomal dominant type

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