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CHEMOKINE GENE POLYMORPHISMS ASSOCIATION WITH INCREASED RISK OF TYPE 2 DIABETES MELLITUS IN TATAR ETHNIC GROUP, RUSSIA
KOCHETOVA, O.V., MUSTAFINA, O.E., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2019)
inflammation in adipose tissue, obesity pathogenesis, glucose intolerance and type 2 diabetes. It has also been
CLINICAL CASE OF ADULT ONSET NIEMANN-PICK DISEASE TYPE C
Saifullina, E.V., Magzhanov, R.V., Mardanova, A.K., Proshlyakova, T.Yu., Zakharova, E.Yu., Klyushnikov, S.A., Illarioshkin, S.N. (2016)
–Pick disease type C (NPC), a rare neurovisceral lysosomal storage disease. It highlights the main clinical
Predicting Threat Degree for Onset of Type 2 Diabetes Mellitus Based on Machine Learning Methods
Shakhmametova, G., Vakkazov, N., Klimets, S. (2023)
for onset of type 2 diabetes mellitus in patients aged 25 years. Type 2 diabetes mellitus is a disease
The Expression of TP53TG1, LINC00342, MALAT1, H19, and MEG3 Long Noncoding RNAs in Type 2 diabetes mellitus
Kochetova, O.V., Avzaletdinova, D. Sh., Korytina, G.F. (2024)
Abstract—Type 2 diabetes is a complex and multifactorial metabolic disorder. The frequency of type
Does the c.-14C>T Mutation in the IFITM5 Gene Provide Identical Phenotypes for Osteogenesis Imperfecta Type V? Data from Russia and a Literature Review
Tyurin, Anton, Merkuryeva, Elena, Zaripova, Aliya, Markova, Tatyana, Nagornova, Tatyana, Dantsev, Ilya, Nadyrshina, Dina, Zakharova, Ekaterina, Khusainova, Rita (2022)
shown that a mutation (c.-14C>T) in the IFITM5 gene is responsible for autosomal dominant OI type V
MOLECULAR AND BIOCHEMICAL STUDY OF GLUTARIC ACIDURIA TYPE 1 IN 49 RUSSIAN FAMILIES: NINE NOVEL MUTATIONS IN THE GCDH GENE
KURKINA, M.V., MIHAYLOVA, S.V., BAIDAKOVA, G.V., SAIFULLINA, E.V., KOROSTELEV, S.A., PYANKOV, D.V., KANIVETS, I.V., YUNIN, M.A., PECHATNIKOVA, N.L., ZAKHAROVA, E.YU (2020)
Glutaric aciduria type 1 (GA1, deficiency of glutaryl CoA dehydrogenase, glutaric acidemia type 1
Osteogenesis Imperfecta: Search for Mutations in Patients from the Republic of Bashkortostan (Russia)
Nadyrshina, D., Zaripova, A., Tyurin, A., Minniakhmetov, I., Zakharova, E., Khusainova, R. (2022)
found combined mutations (c.2869C>T, p. Gln957* in COL1A1 and c.1197+5G>A in COL1A2; c.579delT, p. Gly
THE ASSOCIATION BETWEEN EATING BEHAVIOR AND POLYMORPHISMS IN GRIN2B, GRIK3, GRIA1 AND GRIN1 GENES IN PEOPLE WITH TYPE 2 DIABETES MELLITUS
KOCHETOVA, O.V., KORYTINA, G.F., MUSTAFINA, O.E., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2020)
Excess body weight is the main risk factor of type 2 diabetes. Recent studies have shown
СПОСОБ ПРОГНОЗИРОВАНИЯ ИСХОДА ОСТРОГО ПЕРИОДА ИШЕМИЧЕСКОГО ИНСУЛЬТА У БОЛЬНЫХ САХАРНЫМ ДИАБЕТОМ 2 ТИПА
METHOD FOR PREDICTING THE OUTCOME OF AN ACUTE PERIOD OF ISCHEMIC STROKE IN TYPE 2 DIABETES MELLITUS PATIENTS
Ижбульдина, Г.И., Новикова, Л.Б., IZHBULDINA, G.I., NOVIKOVA, L.B. (2020)
определение в первые трое суток заболевания содержания гликолизированного гемоглобина HbA1c и при уровне HbA1c
PATHOPHYSIOLOGY OF CALCIUM MEDIATED VENTRICULAR ARRHYTHMIAS AND NOVEL THERAPEUTIC OPTIONS WITH FOCUS ON GENE THERAPY
Paar, V., Jirak, P., Larbig, R., Zagidullin, N.S., Brandt, M.C., Lichtenauer, M., Hoppe, U.C., Motloch, L.J. (2019)
L-type calcium channel

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