Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Andrea Slavney"'
Autor:
Takeshi Kawakami, Meghan K Jensen, Andrea Slavney, Petra E Deane, Ausra Milano, Vandana Raghavan, Brett Ford, Erin T Chu, Aaron J Sams, Adam R Boyko
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248233 (2021)
Structural variations (SVs) represent a large fraction of all genetic diversity, but how this genetic diversity is translated into phenotypic and organismal diversity is unclear. Explosive diversification of dog coat color and patterns after domestic
Externí odkaz:
https://doaj.org/article/12ff6d5a85ae4258afd0b97435c28b0c
Publikováno v:
PLoS Genetics, Vol 14, Iss 10, p e1007648 (2018)
Consumer genomics enables genetic discovery on an unprecedented scale by linking very large databases of personal genomic data with phenotype information voluntarily submitted via web-based surveys. These databases are having a transformative effect
Externí odkaz:
https://doaj.org/article/5356b6b20fb74e8da6c20f16e32335b3
Autor:
Diana Chang, Feng Gao, Andrea Slavney, Li Ma, Yedael Y Waldman, Aaron J Sams, Paul Billing-Ross, Aviv Madar, Richard Spritz, Alon Keinan
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e113684 (2014)
Many complex human diseases are highly sexually dimorphic, suggesting a potential contribution of the X chromosome to disease risk. However, the X chromosome has been neglected or incorrectly analyzed in most genome-wide association studies (GWAS). W
Externí odkaz:
https://doaj.org/article/2b6b7d9875d94e669bbf80e84b5feb1f
Autor:
Adam R. Boyko, Takeshi Kawakami, Thomas C. Nelson, Meghan K. Jensen, Aaron J. Sams, Andrea Slavney
Publikováno v:
PLoS ONE, Vol 16, Iss 5, p e0250579 (2021)
PLoS ONE
PLoS ONE
In mammals, the pigment molecule pheomelanin confers red and yellow color to hair, and the intensity of this coloration is caused by variation in the amount of pheomelanin. Domestic dogs exhibit a wide range of pheomelanin intensity, ranging from the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd0810cff3b22f7851efbe0f11901acc
https://doaj.org/article/3e82cc5dd1254c1ba7ce53d99ef7bbb4
https://doaj.org/article/3e82cc5dd1254c1ba7ce53d99ef7bbb4
Autor:
Brett Ford, Meghan K. Jensen, Vandana Raghavan, Petra E. Deane, Erin T. Chu, Adam R. Boyko, Takeshi Kawakami, Ausra Milano, Andrea Slavney, Aaron J. Sams
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248233 (2021)
PLoS ONE
PLoS ONE
Structural variations (SVs) represent a large fraction of all genetic diversity, but how this genetic diversity is translated into phenotypic and organismal diversity is unclear. Explosive diversification of dog coat color and patterns after domestic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d5428ac14c9af100b95d987c9107875
https://doaj.org/article/12ff6d5a85ae4258afd0b97435c28b0c
https://doaj.org/article/12ff6d5a85ae4258afd0b97435c28b0c
Publikováno v:
PLoS Genetics, Vol 14, Iss 10, p e1007648 (2018)
PLoS Genetics
PLoS Genetics
Consumer genomics enables genetic discovery on an unprecedented scale by linking very large databases of personal genomic data with phenotype information voluntarily submitted via web-based surveys. These databases are having a transformative effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa654f07debdeaa380626e977570d83
http://europepmc.org/articles/PMC6171790?pdf=render
http://europepmc.org/articles/PMC6171790?pdf=render
Publikováno v:
Molecular Biology and Evolution
In eutherian mammals, X-linked gene expression is normalized between XX females and XY males through the process of X chromosome inactivation (XCI). XCI results in silencing of transcription from one ChrX homolog per female cell. However, approximate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a074961a36fcc885aaeae479769b97ed
https://doi.org/10.1093/molbev/msv225
https://doi.org/10.1093/molbev/msv225
Autor:
Feng Gao, Li Ma, Aviv Madar, Paul Billing-Ross, Diana Chang, Aaron J. Sams, Alon Keinan, Yedael Y. Waldman, Andrea Slavney, Richard A. Spritz
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e113684 (2014)
PLoS ONE
PLoS ONE
Many complex human diseases are highly sexually dimorphic, suggesting a potential contribution of the X chromosome to disease risk. However, the X chromosome has been neglected or incorrectly analyzed in most genome-wide association studies (GWAS). W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1b151ee6d3c006ce91692040a8990c5
https://doi.org/10.1371/journal.pone.0113684
https://doi.org/10.1371/journal.pone.0113684