Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Erika Patskun"'
Autor:
Oksana Boyarchuk, Larysa Kostyuchenko, Hayane Akopyan, Anastasiia Bondarenko, Alla Volokha, Anna Hilfanova, Ihor Savchak, Liliia Nazarenko, Nataliia Yarema, Olha Urbas, Iryna Hrabovska, Oleksandr Lysytsia, Andrii Budzyn, Oksana Tykholaz, Mariana Ivanchuk, Olha Bastanohova, Erika Patskun, Nataliia Vasylenko, Yuriy Stepanovskyy, Liudmyla Chernyshova, Halyna Makukh
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionNijmegen breakage syndrome (NBS) is an autosomal recessive disorder, characterized by microcephaly, immunodeficiency, and impaired DNA repair. NBS is most prevalent among Slavic populations, including Ukraine. Our study aimed to comprehen
Externí odkaz:
https://doaj.org/article/8fb6ab1f5e0b463ebf94b246bec0cece
Autor:
Wladimir Wertelecki, Lyubov Yevtushok, Nataliia Zymak-Zakutnia, Serhiy Lapchenko, Erika Patskun, Diana Akhmedzhanova
Publikováno v:
Birth Defects Research. 113:1152-1155
Background Leading Teratology Information Systems (TIS) arose in major industrial nations and are mostly in English. The prevalence of anglophone speakers in Ukraine is among the lowest in Europe. A TIS in Ukrainian (UTIS) seeks to diminish an inform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f81f73d9a0ed616953cc3573874ee186
https://doi.org/10.1002/bdr2.1901
https://doi.org/10.1002/bdr2.1901
The rearrangements of the 15q11-q13 region such as deletions, duplications, uniparental disomies (UPDs), and translocations caused different neurodevelopment phenotypes including Prader-Willy and Angelman syndromes, 5q11-q13 duplication syndrome, aut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b061009cf170a41e4506c5cc3a4baa2
https://doi.org/10.21203/rs.3.rs-1598143/v1
https://doi.org/10.21203/rs.3.rs-1598143/v1
Autor:
Serhiy Lapchenko, Olga Tychkivska, Iryna Hohosha, Nataliya Kamut, Lyubov Ostapchuk, Serhiy Tkhorevskyy, Lyubov Yevtushok, Diana Akhmedzhanova, Nataliia Zymak-Zakutnia, Iryna Lastivka, Erika Patskun, Wladimir Wertelecki, Yuriy Korzhynskyy, Serhiy Liashenko
Publikováno v:
Reproductive Toxicology. 72:45-46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00f1ac11078f15e8855e62dea550f948
https://doi.org/10.1016/j.reprotox.2017.06.171
https://doi.org/10.1016/j.reprotox.2017.06.171
Autor:
Iryna Lastivka, Serhiy Lapchenko, Nataliia Zymak-Zakutnia, Erika Patskun, Wladimir Wertelecki, Lyubov Yevtushok, Diana Akhmedzhanova, Svitlana Kalynka, Yuriy Korzhynskyy
Publikováno v:
Reproductive Toxicology. 72:46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c01edf3027685e1d28a2934356ba11f
https://doi.org/10.1016/j.reprotox.2017.06.172
https://doi.org/10.1016/j.reprotox.2017.06.172
Autor:
Krzysztof Rębała, Zofia Szczerkowska, Erika Patskun, S. A. Kravchenko, Daniela Siváková, Igor Veselinović
Publikováno v:
Forensic science international. Genetics. 8(1)
Studies on Y-chromosomal markers revealed significant genetic differentiation between Southern and Northern (Western and Eastern) Slavic populations. The northern Serbian region of Vojvodina is inhabited by Southern Slavic Serbian majority and, inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18f5bd0b634bbbe2ec8e324db4f56576
https://pubmed.ncbi.nlm.nih.gov/24315599
https://pubmed.ncbi.nlm.nih.gov/24315599