Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Zachariah S. Demarais"'
Autor:
Gabrielle E. W. Giersch, Margaret C. Morrissey, Cody R. Butler, Abigail T. Colburn, Zachariah S. Demarais, Stavros A. Kavouras, Ollie Jay, Nisha Charkoudian, Douglas J. Casa
Publikováno v:
Physiological Reports, Vol 9, Iss 14, Pp n/a-n/a (2021)
Abstract Although it is well established that dehydration has a negative impact on thermoregulation during exercise in the heat, it is unclear whether this effect of dehydration is different between men and women, or across the phases of the menstrua
Externí odkaz:
https://doaj.org/article/90dceccb2720465cbd77d60b003a59fe
Autor:
Yuhan Xie, Julián N. Acosta, Yixuan Ye, Zachariah S. Demarais, Carolyn J. Conlon, Ming Chen, Hongyu Zhao, Guido J. Falcone
Publikováno v:
Stroke. 54:800-809
Background: Ischemic stroke (IS) is a highly heritable trait, and genome-wide association studies have identified several commonly occurring susceptibility risk loci for this condition. However, there are limited data on the contribution of rare gene
Autor:
Julián N. Acosta, Cameron P. Both, Zachariah S. Demarais, Carolyn J. Conlon, Audrey C. Leasure, Victor M. Torres-Lopez, Adam de Havenon, Nils H. Petersen, Thomas M. Gill, Lauren H. Sansing, Kevin N. Sheth, Guido J. Falcone
Publikováno v:
Neurology
Background and ObjectivesBlood pressure (BP) is often not at goal in stroke survivors, leaving individuals vulnerable to additional vascular events. Given that BP is a highly heritable trait, we hypothesize that a higher polygenic susceptibility to h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::720c20340b1bdceffd3695d0dcb12a21
https://europepmc.org/articles/PMC10103110/
https://europepmc.org/articles/PMC10103110/
Autor:
Yuhan Xie, Julián N. Acosta, Yixuan Ye, Zachariah S. Demarais, Carolyn J. Conlon, Ming Chen, Hongyu Zhao, Guido J. Falcone
Ischemic stroke (IS) is a highly heritable trait. Genome-wide association studies have identified several commonly occurring susceptibility risk loci for this condition. However, there are limited data on the contribution of rare genetic variation to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac6a2e958ee3005b55aff122a03c34ad
https://doi.org/10.1101/2022.05.31.22275825
https://doi.org/10.1101/2022.05.31.22275825