Перегляд за автором "Hryshchenko, N.V."

Сортувати за: Порядок: Результатів:

  • Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine 
    Hryshchenko, N.V.; Livshits, L.A. (Цитология и генетика, 2009)
    Two intercomplementary methods of 17p11.2 duplication/deletion identification have been elaborated: STR allelic variants analysis and direct PMP22 gene dosage measuring by means of quantitative Real Time PCR. It has been ...
  • Expression of cancer-associated genes in prostate tumors 
    Rosenberg, E.E.; Gerashchenko, G.V.; Hryshchenko, N.V.; Mevs, L.V.; Nekrasov, K.A.; Lytvynenko, R.A.; Vitruk, Y.V.; Gryzodub, O.P.; Stakhovsky, E.A.; Kashuba, V.I. (Experimental Oncology, 2017)
    Background: Prostate cancer is one of the most common male cancers in Western countries and takes the third place in morbidity in Ukraine. It is a highly heterogeneous disease. Aim: To analyze relative expression levels ...
  • 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 ...
  • Polymorphic short tandem repeats for PCR-based diagnosis of the Charcot-Marie-Tooth 1A duplication in Ukraine 
    Hryshchenko, N.V.; Kravchenko, S.A.; Livshits, L.A. (Цитология и генетика, 2005)
    Charcot-Marie-Tooth neuropathy (CMT) is one of the most common hereditary disorders, affecting 1 : 2500 individuals. The major mutation – microduplication of 1.4 megabases in 17р11.2 region, which is responsible for 68–90 ...
  • 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 ...