Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anna Maria Punab"'
Autor:
Triin Kikas, Anna Maria Punab, Laura Kasak, Olev Poolamets, Vladimir Vihljajev, Kristjan Pomm, Mario Reiman, Stanislav Tjagur, Paul Korrovits, Margus Punab, Maris Laan
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Data on the clinical validity of DNA copy number variants (CNVs) in spermatogenic failure (SPGF) is limited. This study analyzed the genome-wide CNV profile in 215 men with idiopathic SPGF and 62 normozoospermic fertile men, recruited at the
Externí odkaz:
https://doaj.org/article/9474f93be7174ceebcfd86f6f9a6c362
Autor:
Marina Grigorova, Margus Punab, Anna Maria Punab, Olev Poolamets, Vladimir Vihljajev, Birutė Zilaitienė, Juris Erenpreiss, Valentinas Matulevičius, Maris Laan
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94244 (2014)
Follicle-Stimulating Hormone Receptor (FSHR) -29G/A polymorphism (rs1394205) was reported to modulate gene expression and reproductive parameters in women, but data in men is limited. We aimed to bring evidence to the effect of FSHR -29G/A variants i
Externí odkaz:
https://doaj.org/article/67875be3c36d44ba9e5abc505a8ac31a
Autor:
Alexandra M. Lopes, Eve Laasik, Lee B. Smith, Donald F. Conrad, Margus Punab, Filipa Carvalho, Marina Grigorova, Kenneth I. Aston, Laura Kasak, Ave Minajeva, Anna Maria Punab, Maris Laan, Liina Nagirnaja
Publikováno v:
The American Journal of Human Genetics. 103:200-212
Infertility affects around 7% of men worldwide. Idiopathic non-obstructive azoospermia (NOA) is defined as the absence of spermatozoa in the ejaculate due to failed spermatogenesis. There is a high probability that NOA is caused by rare genetic defec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1db10f74b5bc21f03d4f3edb66ba35c8
https://doi.org/10.1016/j.ajhg.2018.07.005
https://doi.org/10.1016/j.ajhg.2018.07.005
Autor:
J. Erenpreiss, T. Kuura, Anna Maria Punab, Birutė Žilaitienė, Margus Punab, Maris Laan, Olev Poolamets, Mart Adler, Valentinas Matulevičius, Vladimir Vihljajev, Marina Grigorova
Publikováno v:
Andrology
Summary Luteinizing hormone (LH) is a pituitary heterodimeric glycoprotein essential in male and female reproduction. Its functional polymorphic variant (V-LH) is determined by two missense mutations (rs1800447, A/G, Trp8Arg; rs34349826, A/G, Ile15Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93c95942435a43fe3a6aac97c8cdc9a2
https://doi.org/10.1111/andr.12022
https://doi.org/10.1111/andr.12022
Autor:
Margus Punab, Olev Poolamets, Vladimir Vihljajev, Marina Grigorova, Maris Laan, Anna Maria Punab, Birutė Žilaitienė, Valentinas Matulevičius, Juris Erenpreiss
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94244 (2014)
PLoS ONE
PLoS ONE
Follicle-Stimulating Hormone Receptor (FSHR) -29G/A polymorphism (rs1394205) was reported to modulate gene expression and reproductive parameters in women, but data in men is limited. We aimed to bring evidence to the effect of FSHR -29G/A variants i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6a804b6d757c2b44d58c4e1b2502a3
http://europepmc.org/articles/PMC3981791?pdf=render
http://europepmc.org/articles/PMC3981791?pdf=render