Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Kinship Theory"'
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 15 (2021)
Angelman syndrome (AS) is caused by loss of information from the 15q11.2-13 region on the maternal chromosome with striking phenotypic difference from Prader–Willi syndrome in which information is lost from the same region on the paternal chromosom
Externí odkaz:
https://doaj.org/article/fdc814d52d894405addf199e6fda9d55
Autor:
Galbraith, David A., Kocher, Sarah D., Glenn, Tom, Albert, Istvan, Hunt, Greg J., Strassmann, Joan E., Queller, David C., Grozinger, Christina M.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2016 Jan . 113(4), 1020-1025.
Externí odkaz:
https://www.jstor.org/stable/26467527
Autor:
Paola Bressan, Peter Kramer
Publikováno v:
Biomedicines, Vol 9, Iss 2, p 116 (2021)
This paper presents a broad perspective on how mental disease relates to the different evolutionary strategies of men and women and to growth, metabolism, and mitochondria—the enslaved bacteria in our cells that enable it all. Several mental disord
Externí odkaz:
https://doaj.org/article/6fbef9efcd9f40d6a9820437f076fbbb
Akademický článek
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Autor:
Willi, Yvonne
Publikováno v:
The American Naturalist, 2013 Jun 01. 181(6), 787-798.
Externí odkaz:
https://www.jstor.org/stable/10.1086/670196
Publikováno v:
The American Naturalist, 2010 Oct . 176(4), 440-455.
Externí odkaz:
https://www.jstor.org/stable/10.1086/656277
Autor:
Li, Na, Dickinson, Hugh G.
Publikováno v:
Proceedings: Biological Sciences, 2010 Jan 01. 277(1678), 3-10.
Externí odkaz:
https://www.jstor.org/stable/40506081
Autor:
Rössler, Martin
Publikováno v:
Anthropos, 1998 Jan 01. 93(4/6), 437-454.
Externí odkaz:
https://www.jstor.org/stable/40464842
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 15 (2021)
Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience
Angelman syndrome (AS) is caused by loss of information from the 15q11.2-13 region on the maternal chromosome with striking phenotypic difference from Prader–Willi syndrome in which information is lost from the same region on the paternal chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fa7dd12ffab79928348e1c06298daf1
https://www.frontiersin.org/articles/10.3389/fnbeh.2021.618271/full
https://www.frontiersin.org/articles/10.3389/fnbeh.2021.618271/full