Zobrazeno 1 - 10
of 16
pro vyhledávání: '"N. V. Hryshchenko"'
Autor:
S. M. Drohovoz, A. L. Shtroblia, V. V. Shtroblia, M. V. Shtroblia, К. H. Shchokina, K. V. Kalko, L. V. Derymedvid, V. M. Khomenko, I. V. Kireiev, V. D. Lykianchuk, O. Y. Hishchak, N. V. Hryshchenko
Publikováno v:
Likarska sprava. :5-13
Corona virus disease (COVID-19) is an infectious disease caused by the SARS-CoV-2 virus and its mutants. COVID-19 is often the cause of the development of pathologies on the part of the respiratory system against the background of hypoxia. One of the
Autor:
S. Yu. Chernushyn, Nataliia Melnichuk, N. V. Hryshchenko, M. A. Tukalo, L. M. Chernenko, Vladimir I. Kashuba, T. V. Marchishak, V. K. Liashko, G. V. Gerashchenko, Z. Yu. Tkachuk
Publikováno v:
Biopolymers and Cell. 37:117-124
Aim. To identify and characterize the SARS-CoV-2 variants, collected upon the new wave of COVID-19 outbreak in Ivano-Frankivs’k region of Ukraine, using the whole genome genotyping. Methods. The parallel whole genome sequencing was performed on the
Publikováno v:
Biopolymers and Cell. 37:105-116
Publikováno v:
Cytology and Genetics. 54:130-136
Proximal spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease caused by homozygous deletion in the seventh exon of the SMN1 gene. The aim of this work is to analyze the association of the allelic polymorphism of telomeric
Publikováno v:
Biopolymers and Cell. 35:333-339
Autor:
E E, Rosenberg, G V, Gerashchenko, N V, Hryshchenko, L V, Mevs, K A, Nekrasov, R A, Lytvynenko, Y V, Vitruk, O P, Gryzodub, E A, Stakhovsky, V I, Kashuba
Publikováno v:
Experimental oncology. 39(2)
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.To analyze relative expression levels of the TGFB1, IL1B, FOS, EFNA5, TAGLN, PLAU, and
Autor:
S. Yu. Chernushyn, N. V. Hryshchenko
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 chromosomal region; expres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::776258716931647a560a830e5d4da6cf
http://dspace.nbuv.gov.ua/handle/123456789/154359
http://dspace.nbuv.gov.ua/handle/123456789/154359
Autor:
E. A. Stakhovsky, K A Nekrasov, L. V. Mevs, Y V Vitruk, R A Lytvynenko, G. V. Gerashchenko, O. P. Gryzodub, E. E. Rosenberg, Vladimir I. Kashuba, N V Hryshchenko
Publikováno v:
Scopus-Elsevier
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 of the TGFB1, IL1B, FOS, EFNA5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c2b51905cb82214208ca0098b9d2c88
http://dspace.nbuv.gov.ua/handle/123456789/140088
http://dspace.nbuv.gov.ua/handle/123456789/140088
Autor:
S. Yu. Lohush, I. V. Dubrovska, T. V. Nikitchina, N. V. Hryshchenko, O. O. Soloviov, P. F. Tatarskyy, G. M. Bychkova, A. M. Kucherenko, G. B. Livshyts, V. M. Pampukha, N. O. Afanasieva, N. O. Zymak-Zakutnia, S. A. Kravchenko, E. J. Patskun, L. A. Livshits
Publikováno v:
Cytology and Genetics; Vol 46
The results of clinical, genealogical, cytogenetic, and molecular genetic studies of 113 patients from 96 families with different forms of mental retardation from Ukraine are presented. This study was held as part of the CHERISH project of the Sevent
Autor:
O. A. Fesai, G. B. Livshyts, A. M. Kucherenko, L. A. Livshits, V. M. Pampukha, M. V. Nechyporenko, S. A. Kravchenko, R. V. Gulkovskyy, O. O. Soloviov, N. V. Hryshchenko, S. Yu. Chernushyn, P. F. Tatarskyy
Publikováno v:
Biopolymers and Cell, Vol 29, Iss 4, Pp 330-338 (2013)
Scopus-Elsevier
Scopus-Elsevier
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 region mutations (genetic polymo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d07bd565bca06e9f912f6ca56f1df44
http://dspace.nbuv.gov.ua/handle/123456789/152994
http://dspace.nbuv.gov.ua/handle/123456789/152994