Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kerrie Lashley"'
Autor:
Kerrie Lashley, Guinevere Granite
Publikováno v:
Reports, Vol 4, Iss 1, p 2 (2021)
Anatomical variation is defined as the normal range of possibilities in the topography and morphology of body structures. In contrast, an anomaly is any structural or functional anatomical finding beyond the normal range of possibilities. This case s
Externí odkaz:
https://doaj.org/article/e6df3808fc174655bb380a39073c09f5
Autor:
Adebowale Adeyemo, Norman Gerry, Guanjie Chen, Alan Herbert, Ayo Doumatey, Hanxia Huang, Jie Zhou, Kerrie Lashley, Yuanxiu Chen, Michael Christman, Charles Rotimi
Publikováno v:
PLoS Genetics, Vol 5, Iss 7, p e1000564 (2009)
The evidence for the existence of genetic susceptibility variants for the common form of hypertension ("essential hypertension") remains weak and inconsistent. We sought genetic variants underlying blood pressure (BP) by conducting a genome-wide asso
Externí odkaz:
https://doaj.org/article/20a7da60efcc42948501239fd86c819c
Vascular variations of the head and neck are common, but often go unnoticed because they generally do not present clear clinical symptoms. Lack of awareness of the presence and location of such variations may result in iatrogenic complications or eve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36f1a7ac56e4ba2c5c791a148a831292
https://doi.org/10.9734/bpi/hmms/v18/11507d
https://doi.org/10.9734/bpi/hmms/v18/11507d
Autor:
Guinevere Granite, Kerrie Lashley
Publikováno v:
Reports, Vol 4, Iss 2, p 2 (2021)
Anatomical variation is defined as the normal range of possibilities in the topography and morphology of body structures. In contrast, an anomaly is any structural or functional anatomical finding beyond the normal range of possibilities. This case s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91c22707a09b7d95e3d31d4d97250144
https://www.mdpi.com/2571-841X/4/1/2
https://www.mdpi.com/2571-841X/4/1/2
Autor:
Kerrie Lashley, Guinevere Granite‐Cohn
Publikováno v:
The FASEB Journal. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b39489e7ebaca64070f4195acee747a1
https://doi.org/10.1096/fasebj.2018.32.1_supplement.89.3
https://doi.org/10.1096/fasebj.2018.32.1_supplement.89.3
Autor:
Kerrie Lashley, Guinevere Granite
Publikováno v:
The FASEB Journal. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c25d56c056f6a3be860294d1bc5099
https://doi.org/10.1096/fasebj.2018.32.1_supplement.lb501
https://doi.org/10.1096/fasebj.2018.32.1_supplement.lb501
Publikováno v:
The Open Anatomy Journal. 3:21-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d08c1ab6f3f84fa3244a7939ccf960b
https://doi.org/10.2174/1877609401103010021
https://doi.org/10.2174/1877609401103010021
Autor:
Kofi Agyenim-Boateng, Adebowale Adeyemo, Jie Zhou, Clement Adebamowo, Olufemi Fasanmade, Albert G.B. Amoah, Charles N. Rotimi, Johnnie Oli, Ayo P. Doumatey, Kerrie Lashley, Guanjie Chen, Hanxia Huang
Publikováno v:
Obesity. 18:598-603
Several research studies in different populations indicate that inflammation may be the link between obesity and insulin resistance (IR). However, this relationship has not been adequately explored among African Americans, an ethnic group with dispro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc81285b7649c2f407c307edc5a07dd
https://doi.org/10.1038/oby.2009.322
https://doi.org/10.1038/oby.2009.322
Autor:
Valur Emilsson, Shyamali Ghosh, Yuanxiu Chen, Unnur Styrkarsdottir, Ayo Doumatey, Mark E. Gurney, Juliana C.N. Chan, Kerrie Lashley, Adebowale Adeyemo, Augustine Kong, Kari Stefansson, Inga Reynisdottir, Gunnar Sigurdsson, Marten H. Hofker, Jeffrey R. Gulcher, Oluf Pedersen, Cisca Wijmenga, Hjordis Bjarnason, Wing-Yee So, Torben Hansen, Daniel J. Rader, Thorbjorg Jonsdottir, Knut Borch-Johnsen, Valgerdur Steinthorsdottir, Claus Christiansen, Guanjie Chen, Charles N. Rotimi, Gudmar Thorleifsson, Rafn Benediktsson, Torben Jørgensen, Robert L. Wilensky, Vilmundur Gudnason, Hanxia Huang, Unnur Thorsteinsdottir, Muredach P. Reilly, Adam Baker, Yu Z. Bagger, Gitte Andersen, Steinunn Snorradottir, Jana V. van Vliet-Ostaptchouk, G. Bragi Walters, Ronald Ching-Wa Ma, Jie Zhou, Maggie C.Y. Ng, Solveig Gretarsdottir
Publikováno v:
Nature Genetics, 39(6), 770-775. Nature Publishing Group
We conducted a genome-wide association study for type 2 diabetes (T2D) in Icelandic cases and controls, and we found that a previously described variant in the transcription factor 7-like 2 gene (TCF7L2) gene conferred the most significant risk. In a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7f08f970e64f0526760d315bec751e
https://doi.org/10.1038/ng2043
https://doi.org/10.1038/ng2043
Autor:
Ashley M. Burris, Bari J. Ballew, Joshua B. Kentosh, Clesson E. Turner, Scott A. Norton, Neelam Giri, Blanche P. Alter, Anandani Nellan, Christopher Gamper, Kip R. Hartman, Sharon A. Savage, Sara Bass, Joseph Boland, Laurie Burdett, Salma Chowdhury, Michael Cullen, Casey Dagnall, Herbert Higson, Amy A. Hutchinson, Kristine Jones, Sally Larson, Kerrie Lashley, Hyo Jung Lee, Wen Luo, Michael Malasky, Jason Mitchell, David Roberson, Aurelie Vogt, Mingyi Wang, Meredith Yeager, Xijun Zhang, Neil E. Caporaso, Stephen J. Chanock, Mark H. Greene, Lynn R. Goldin, Alisa M. Goldstein, Allan Hildesheim, Nan Hu, Maria Teresa Landi, Jennifer T. Loud, Phuong L. Mai, Mary L. McMaster, Lisa Mirabello, Lindsay Morton, Melissa Rotunno, Douglas R. Stewart, Phil Taylor, Geoffrey S. Tobias, Margaret A. Tucker, Xiaohong R. Yang, Guoqin Yu
Publikováno v:
Pediatric Neurology. 56:62-68.e1
Background Hoyeraal-Hreidarsson syndrome is a dyskeratosis congenita–related telomere biology disorder that presents in infancy with intrauterine growth retardation, immunodeficiency, and cerebellar hypoplasia in addition to the triad of nail dyspl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::979563bcf1a6264edf21d3126a0925b4
https://doi.org/10.1016/j.pediatrneurol.2015.12.005
https://doi.org/10.1016/j.pediatrneurol.2015.12.005