Search Results - "Sherman, V.D"

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    High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia by Petrova, N.V, Kashirskaya, N.Yu, Vasilyeva, T.A, Timkovskaya, E.E, Voronkova, A.Yu, Shabalova, L.A, Kondratyeva, E.I, Sherman, V.D, Novoselova, O.G, Kapranov, N.I, Zinchenko, R.A, Ginter, E.K, Makaov, A.Kh-M, Kerem, B

    Published in Journal of cystic fibrosis (01-05-2016)
    “…Abstract Cystic fibrosis (CF; OMIM # 219700 ) is a common autosomal recessive disease. The spectrum and frequency of CFTR mutations vary significantly in…”
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    Journal Article
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    EXTRACELLULAR DNA AND PLASMA NUCLEASE ACTIVITY EFFECT ON THE COURSE OF THE MICROBIAL INFLAMMATORY PROCESS IN THE RESPIRATORY TRACT IN CYSTIC FIBROSIS by Kondratieva, E.I., Kondakova, Yu.A., Kostyuk, S.V., Ershova, E.V., Zyryanov, S.K., Melyanovskaya, Yu.L., Voronkova, A.Yu, Sherman, V.D., Shadrina, V.V.

    Published in Journal of bioinformatics and genomics (01-08-2018)
    “…Background. Cystic fibrosis is a hereditary multi-organ disease. The involvement of the respiratory system due to chronic inflammation and a chronic infectious…”
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    Journal Article
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