Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sandra Krasucka"'
Autor:
Baiba Alksere, Dace Berzina, Alesja Dudorova, Una Conka, Santa Andersone, Evija Pimane, Sandra Krasucka, Arita Blumberga, Aigars Dzalbs, Ieva Grinfelde, Natalija Vedmedovska, Violeta Fodina, Juris Erenpreiss
Publikováno v:
Case Reports in Genetics, Vol 2019 (2019)
Male factor infertility accounts for 40–50% of all infertility cases. Deletions of one or more AZF region parts in chromosome Y are one of the most common genetic causes of male infertility. Usually full or partial AZF deletions, including genes in
Externí odkaz:
https://doaj.org/article/db4c77e2dfda4b958b187b17b56c0370
Autor:
Baiba Alksere, Sandra Krasucka, Una Conka, Irina Kovalova, Violeta Fodina, Ieva Grinfelde, Liene Kornejeva, Santa Andersone, Natalija Vedmedovska, Dace Berzina, Aigars Dzalbs, Arita Blumberga
Publikováno v:
Gynecological Endocrinology. 36:53-57
Aim: The aim of this study is to summarize the outcomes of transfers of mosaic embryos, which were classified according to guidelines and in strong collaboration of reproductologists, clinical geneticists and patients approved as suitable for transfe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa93a12eeb3f7535277673076c3ab6e9
https://doi.org/10.1080/09513590.2020.1816719
https://doi.org/10.1080/09513590.2020.1816719
Autor:
Natalija Vedmedovska, Arita Blumberga, Dace Berzina, Aigars Dzalbs, Ieva Grinfelde, Baiba Alksere, Alesja Dudorova, Evija Pimane, Santa Andersone, Violeta Fodina, Juris Erenpreiss, Una Conka, Sandra Krasucka
Publikováno v:
Case Reports in Genetics, Vol 2019 (2019)
Case Reports in Genetics
Case Reports in Genetics
Male factor infertility accounts for 40–50% of all infertility cases. Deletions of one or more AZF region parts in chromosome Y are one of the most common genetic causes of male infertility. Usually full or partial AZF deletions, including genes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58db52fb4505bf702c15d2ec777956a7
https://doaj.org/article/db4c77e2dfda4b958b187b17b56c0370
https://doaj.org/article/db4c77e2dfda4b958b187b17b56c0370
Autor:
Violeta Fodina, Ludmila Voložonoka, Liene Korņejeva, Dmitry Perminov, Evija Jokste-Pțmane, Arita Blumberga, Sandra Krasucka, Nellija Seimuškina, Irina Kovaļova
Publikováno v:
Gynecological Endocrinology. 33:47-49
Huntington's disease (HD) is fatal neurodegenerative disease caused by a (CAG) triplet repeat expansion in the Huntingtin (HTT) gene. Inheritance pattern of the disease is autosomal dominant and onset depending on triplet repeat count. Transgeneratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51e02709001dedc7d34c67925ad61c43
https://doi.org/10.1080/09513590.2017.1404239
https://doi.org/10.1080/09513590.2017.1404239