Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Amy S. Gates"'
Autor:
Rachel A. Watson, Amy S. Gates, Elizabeth H. Wynn, Fiona E. Calvert, Amandine Girousse, Christopher J. Lelliott, Inês Barroso
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 12, Pp 1481-1488 (2017)
Genome-wide association studies (GWAS) have detected association between variants in or near the Lysophospholipase-like 1 (LYPLAL1) locus and metabolic traits, including central obesity, fatty liver and waist-to-hip ratio. LYPLAL1 is also known to be
Externí odkaz:
https://doaj.org/article/0b780057b0ef4225a90afbbbcb228668
Autor:
Fiona Calvert, Elizabeth H. Wynn, Inês Barroso, Amandine Girousse, Christopher J. Lelliott, Rachel A. Watson, Amy S. Gates
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 10, Iss 12, Pp 1481-1488 (2017)
Disease Models & Mechanisms, Vol 10, Iss 12, Pp 1481-1488 (2017)
Genome-wide association studies (GWAS) have detected association between variants in or near the Lysophospholipase-like 1 (LYPLAL1) locus and metabolic traits, including central obesity, fatty liver and waist-to-hip ratio. LYPLAL1 is also known to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58a9abc53d1afbc438de7406d541e4bf
https://www.repository.cam.ac.uk/handle/1810/294958
https://www.repository.cam.ac.uk/handle/1810/294958
Autor:
Derek W. Morris, Gary W. Jones, Paul Cormican, Amy S Gates, Naushaba Hasin, Jennifer O'Brien, Elaine Kenny, David A. Fitzpatrick, Ciara Moran
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e28684 (2011)
PloS one
PLoS ONE
PloS one
PLoS ONE
The yeast prion [PSI(+)] has been implicated in the generation of novel phenotypes by a mechanism involving a reduction in translation fidelity causing readthrough of naturally occurring stop codons. Some [PSI(+)] associated phenotypes may also be ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d72f0b25767add1980510cfcc84656cc
https://doi.org/10.1371/journal.pone.0028684
https://doi.org/10.1371/journal.pone.0028684
Autor:
Damian Smedley, Colin McKerlie, Xiang Gao, Henrik Westerberg, Simon Greenaway, Monica J. Justice, Hiroshi Masuya, Elissa J. Chesler, Robert E. Braun, Mary E. Dickinson, Shay Yaacoby, Stephen A. Murray, Karen L. Svenson, Jeremy Mason, Martin Hrabé de Angelis, Luis Santos, Tania Sorg, Christopher J. Lelliott, Sara Wells, Ann M. Flenniken, Ruth Heller, Ann-Marie Mallon, Lynette Bower, Karen P. Steel, Helen Parkinson, Judith E. Mank, Arthur L. Beaudet, Kevin C K Lloyd, Richard Mott, Yann Herault, Yoav Benjamini, Jacqueline K. White, Steve D.M. Brown, Shiying Guo, John R. Seavitt, Helmut Fuchs, Natalja Kurbatova, Anneliese O. Speak, Natasha A. Karp, Ramiro Ramirez-Solis, Terrence F. Meehan, David B. West, Shigeharu Wakana
Publikováno v:
Nature Communications
Nature Communications, 2017, 8, ⟨10.1038/ncomms15475⟩
Nature communications, vol 8, iss 1
Nat. Commun. 8:15475 (2017)
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
Nature Communications, 2017, 8, ⟨10.1038/ncomms15475⟩
Nature communications, vol 8, iss 1
Nat. Commun. 8:15475 (2017)
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
The role of sex in biomedical studies has often been overlooked, despite evidence of sexually dimorphic effects in some biological studies. Here, we used high-throughput phenotype data from 14,250 wildtype and 40,192 mutant mice (representing 2,186 k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a22ff32917f16b5f536bab3a8bab6e17
https://hal.science/hal-03679179/file/islandora_77521.pdf
https://hal.science/hal-03679179/file/islandora_77521.pdf