Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Y. M. Zgonnyk"'
Autor:
S. O. Vozianov, E. E. Rudenko, G. V. Gerashchenko, Vladimir I. Kashuba, Y. V. Lapska, Y. M. Zgonnyk
Publikováno v:
Biopolymers and Cell, Vol 30, Iss 3, Pp 229-233 (2014)
Aim. To investigate the expression levels of PPM1M and PRICKLE2 in clear-cell renal cell carcinomas (ccRCC) and propose a mechanism leading to the expression changes in tumor. Methods. Analysis of GEO data, quantitative PCR (Q-PCR), bisulfite sequenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ddb17cd625a86bd06357c0721c25d05
http://dspace.nbuv.gov.ua/handle/123456789/154299
http://dspace.nbuv.gov.ua/handle/123456789/154299
Autor:
Vladimir I. Kashuba, Y. M. Zgonnyk, Liubov A. Stoliar, Eugene R. Zabarovsky, V. V. Gordiyuk, Alina Romanenko, Aleksandr G. Kondratov, Alla Rynditch, Elena Kashuba, Sergiy M. Kvasha
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e47012 (2012)
PLoS ONE
PLoS ONE
WNT7A (wingless-type MMTV integration site family, member 7A) is a known tumor suppressor gene of non-small cell lung carcinomas (NSCLC) and is frequently inactivated due to CpG-island hypermethylation in human cancers. The members of WNT family are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fa27a649c2fa410f29630e95cc7c257
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-85296
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-85296
Autor:
A. F. Vozianov, A. V. Gerashchenko, Eugene R. Zabarovsky, V. V. Gordiyuk, Y. M. Zgonnyk, L. A. Stoliar, Vladimir I. Kashuba, Alla Rynditch, S. M. Kvasha, A. G. Kondratov
Publikováno v:
Molecular Medicine Reports.
The leucine rich repeat containing 3B (LRRC3B) gene is a putative tumor suppressor located on human chromosome 3 in the 3p24 region. LRRC3B is frequently altered in colon and gastric cancers and also in leukaemias. In this study we investigated the p
Autor:
Dmytro Ugryn, Alla Rynditch, V. V. Gordiyuk, Alexandr F. Vozianov, Sergiy M. Kvasha, A. G. Kondratov, Y. M. Zgonnyk
Publikováno v:
Cancer letters. 265(2)
FHIT is a tumour suppressor gene which is frequently inactivated in different types of cancer. Both genetic (mutations, deletions, chromosomal rearrangements) and epigenetic (aberrant methylation of the 5'CpG island) alterations of the FHIT gene have
Autor:
E. E. Rudenko, Kashuba, Y. M. Zgonnyk, Oleksandr Kondratov, G. V. Gerashchenko, S. A. Kravchenko, S. O. Vozianov, Koliada O, Y. V. Lapska
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Aim: To find putative diagnostic markers for clear cell renal cell carcinomas (ccRCC). Material and methods: Quantitative polymerase chain reaction (Q-PCR), bisulfite treatment, methylation-specific PCR, analysis on cBioPortal for Cancer Genomics. Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4ac9217ac5439a0b883514de1ee065e
http://www.scopus.com/inward/record.url?eid=2-s2.0-84933510136&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84933510136&partnerID=MN8TOARS