Search Results - "Kuraeva, Tamara L"

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    The carriage of the type 1 diabetes-associated R262W variant of human LNK correlates with increased proliferation of peripheral blood monocytes in diabetic patients by Lavrikova, Elena Y, Nikitin, Alexey G, Kuraeva, Tamara L, Peterkova, Valentina A, Tsitlidze, Nina M, Chistiakov, Dimitry A, Nosikov, Valery V

    Published in Pediatric diabetes (01-03-2011)
    “…Lavrikova EY, Nikitin AG, Kuraeva TL, Peterkova VA, Tsitlidze NM, Chistiakov DA, Nosikov VV. The carriage of the type 1 diabetes‐associated R262W variant of…”
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    Journal Article
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    Studying progression from glucose intolerance to type 2 diabetes in obese children by Dubinina, Irina A, Chistiakov, Dimitry A, Eremina, Irina A, Brovkin, Alexei N, Zilberman, Lyubov I, Nikitin, Alexei G, Kuraeva, Tamara L, Nosikov, Valery V, Peterkova, Valentina A, Dedov, Ivan I

    “…Abstract Aim Identification of metabolic and genetic factors capable to mediate progression from normal glucose tolerance (NGT) through impaired glucose…”
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    Evaluation of IDDM8 susceptibility locus in a Russian simplex family data set by Chistiakov, Dimitry A., Seryogin, Yuri A., Turakulov, Rustam I., Savost'anov, Kirill V., Titovich, Elena V., Zilberman, Lyubov' I., Kuraeva, Tamara L., Dedov, Ivan I., Nosikov, Valery V.

    Published in Journal of autoimmunity (01-05-2005)
    “…Type 1 diabetes (T1D) susceptibility locus, IDDM8, has been accurately mapped to 200 kilobases at the terminal end of chromosome 6q27. This is within the…”
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    The TAF5L gene on chromosome 1q42 is associated with type 1 diabetes in Russian affected patients by Chistiakov, Dimitry A., Chernisheva, Ana, Savost'anov, Kirill V., Turakulov, Rustam I., Kuraeva, Tamara L., Dedov, Ivan I., Nosikov, Valery V.

    Published in Autoimmunity (Chur, Switzerland) (01-06-2005)
    “…Type 1 diabetes (T1D) is a multifactorial autoimmune disease, with strong genetic component. Several susceptibility loci contribute to genetic predisposition…”
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    Lack of association between genetic markers on chromosome 16q22-Q24 and type 1 diabetes in Russian affected families by Chistiakov, Dimitry A, Chernisheva, Ana, Savost'anov, Kirill V, Turakulov, Rustam I, Kuraeva, Tamara L, Dedov, Ivan I, Nosikov, Valery V

    Published in Croatian medical journal (01-08-2005)
    “…To evaluate whether the T1D susceptibility locus on chromosome 16q contributes to the genetic susceptibility to T1D in Russian patients. Thirteen…”
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    Diabetes mellitus associated with type A insulin resistance by Sechko, E. A., Kuraeva, T. L., Peterkova, V. A., Laptev, D. N.

    Published in Sakharnyĭ diabet (14-07-2023)
    “…Insulin resistance type A is a monogenic disorder with insulin action defect, observed in females with acanthosis nigricans (AN), hyperandrogenism,…”
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    Characteristics of patients with cystic fibrosis-dependent diabetes mellitus in childhood according to the register of patients with cystic fibrosis of the Russian Federation in 2021 by Kondratyeva, E. I., Tlif, A. I., Voronkova, A. Yu, Amelina, E. L., Kashirskaya, N. Yu, Krasovsky, S. A., Starinova, M. A., Kuraeva, T. L.

    Published in Sakharnyĭ diabet (01-11-2023)
    “…BACKGROUND : In recent decades, the life expectancy of patients with CF has increased, which leads to an increase in the frequency of conditions associated…”
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    Non-immune diabetes mellitus in children due to heterozygous mutations in the glucokinase gene (GCK-MODY): data of 144 patients by Sechko, E. A., Kuraeva, T. L., Zilberman, L. I., Laptev, D. N., Bezlepkina, O. B., Peterkova, V. A.

    Published in Sakharnyĭ diabet (01-05-2022)
    “…BACKGROUND: Monogenic diabetes mellitus (MDM) is a rare form of diabetes mellitus (DM) which caused by one or more mutations in one of the genes that cause…”
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    MODY caused by a mutation in the insulin gene by Sechko, E. A., Kuraeva, T. L., Andrianova, E. A., Zilberman, L. I., Emelyanov, A. O., Laptev, D. N., Bezlepkina, O. B.

    Published in Sakharnyĭ diabet (23-03-2022)
    “…MODY10 is a rare subtype of MODY diabetes, which caused by heterozygous mutations in the insulin gene INS. There are single descriptions of families with…”
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