Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Aigars Dzalbs"'
Autor:
Caroline Küstermann, Karīna Narbute, Valērija Movčana, Vadims Parfejevs, Fēlikss Rūmnieks, Pauls Kauķis, Miks Priedols, Rihards Mikilps-Mikgelbs, Marija Mihailova, Santa Andersone, Aigars Dzalbs, Cristina Bajo-Santos, Alvils Krams, Arturs Abols
Publikováno v:
Stem Cell Research & Therapy, Vol 15, Iss 1, Pp 1-15 (2024)
Abstract Background Lung cancer remains a leading cause of cancer-related mortality globally. Although recent therapeutic advancements have provided targeted treatment approaches, the development of resistance and systemic toxicity remain primary con
Externí odkaz:
https://doaj.org/article/7d6dbadf88c142798cbad369128092d8
Autor:
Baiba Alksere, Liene Kornejeva, Ieva Grinfelde, Aigars Dzalbs, Dace Enkure, Una Conka, Santa Andersone, Arita Blumberga, Liene Nikitina-Zake, Liga Kangare, Ilze Radovica-Spalvina, Inta Vasiljeva, Linda Gailite, Juris Erenpreiss, Violeta Fodina
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss , Pp 100796- (2021)
Hereditary ectodermal dysplasias are a complex group of inherited disorders characterised by abnormalities in two or more ectodermal derivatives (skin, nails, sweat glands, etc.). There are two main types of these disorders – hidrotic and hypohidro
Externí odkaz:
https://doaj.org/article/78751b9f28d64b6cbcc1ed83c4ccf488
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
Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6)
Publikováno v:
The American journal of case reports. 23
BACKGROUND Parental chromosomal structural abnormalities can lead to diverse chromosomal imbalances at meiotic segregation during gametogenesis and subsequent early pregnancy loss or birth of a child with a chromosomal abnormality. The incidence of u
Autor:
Violeta Fodina, Linda Gailite, Inta Vasiljeva, Baiba Alksere, Liga Kangare, Juris Erenpreiss, Dace Enkure, Aigars Dzalbs, Liene Nikitina-Zake, Arita Blumberga, Liene Kornejeva, Ieva Grinfelde, Una Conka, Santa Andersone, Ilze Radovica-Spalvina
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss, Pp 100796-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Hereditary ectodermal dysplasias are a complex group of inherited disorders characterised by abnormalities in two or more ectodermal derivatives (skin, nails, sweat glands, etc.). There are two main types of these disorders – hidrotic and hypohidro
Autor:
Aigars Dzalbs, Violeta Fodina, Erenpreiss Juris, Baiba Alksere, Berzina Dace, Alesja Dudorova, Natalija Vedmedovska, Santa Andersone, Conka Una
Publikováno v:
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology. 35(sup1)
The aim of this study was to analyze differences in chromosomal aberrations and euploidy in embryos of each translocation type and gender of carrier in the case series of 10 couples with balanced translocations who underwent IVF with embryos trophect
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
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.