Перегляд за автором "Chernushyn, S.Yu."

Сортувати за: Порядок: Результатів:

  • Development of MLPA approach for SNP detection in MTHFR, F5 and F2 genes 
    Kravchenko, S.A.; Chernushyn, S.Yu.; Kucherenko, A.M.; Soloviov, O.O.; Livshits, L.A. (Вiopolymers and Cell, 2015)
    Single nucleotide polymorphism (SNP) is an important and valuable form of DNA variation among individuals. Various methods for SNP genotyping have been developed, but a few are suitable for the flexible and low-cost ...
  • Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis 
    Livshits, L.A.; Kravchenko, S.A.; Nechyporenko, M.V.; Pampukha, V.M.; Hryshchenko, N.V.; Livshyts, G.B.; Soloviov, O.O.; Tatarskyy, P.F.; Fesai, O.A.; Chernushyn, S.Yu.; Kucherenko, A.M.; Gulkovskyy, R.V. (Вiopolymers and Cell, 2013)
    The summarized results of 25-year studies of department of human genomics of IMBG NASU are presented. The investigations were focused on identification of molecular genetic nature of human genome coding and non-coding ...
  • Study of SNRPN genetic and epigenetic mutations in Prader-Willi and Angelman patients 
    Chernushyn, S.Yu.; Hryshchenko, N.V. (Вiopolymers and Cell, 2018)
    Prader-Willi (PWS) and Angelman (AS) syndromes are two clinically distinct genetic diseases associated with multiple physical and cognitive abnormalities. The genetic cause of PWS and AS is the alteration in the 15q11.2-q13 ...