Zobrazeno 1 - 10
of 850
pro vyhledávání: '"V. Sun"'
Autor:
Junyu Chen, Qin Hui, Zeyuan Wang, Francis P. Wilson, Kaku So-Armah, Matthew S. Freiberg, Amy C. Justice, Ke Xu, Wei Zhao, Farah Ammous, Jennifer A. Smith, Sharon L.R. Kardia, Marta Gwinn, Vincent C. Marconi, Yan V. Sun
Publikováno v:
Kidney International Reports. 8:1076-1086
Autor:
Boghuma K. Titanji, Zeyuan Wang, Junyu Chen, Qin Hui, Kaku So-Armah, Matthew Freiberg, Amy C. Justice, Xu Ke, Vincent C. Marconi, Yan V. Sun
Publikováno v:
AIDS (London, England). 36(11)
Elevated plasma levels of sCD14 predict all-cause mortality in people with HIV (PWH). Epigenetic regulation plays a key role in infection and inflammation. To reveal the epigenetic relationships between sCD14, immune function and disease progression
Autor:
Nicole Beaulieu Perez, Gail D'Eramo Melkus, Fay Wright, Gary Yu, Allison A. Vorderstrasse, Yan V. Sun, Cindy A. Crusto, Jacquelyn Y. Taylor
Publikováno v:
Nursing Research. 72:93-102
Autor:
Jacquelyn Y. Taylor, Yunfeng Huang, Wei Zhao, Michelle L. Wright, Zeyuan Wang, Qin Hui, Stephanie Potts‐Thompson, Veronica Barcelona, Laura Prescott, Yutong Yao, Cindy Crusto, Sharon L. R. Kardia, Jennifer A. Smith, Yan V. Sun
Publikováno v:
Obesity. 31:243-255
Obesity is a significant public health concern across the globe. Research investigating epigenetic mechanisms related to obesity and obesity-associated conditions has identified differences that may contribute to cellular dysregulation that accelerat
Autor:
Krisann K Oursler, Vincent C Marconi, Zeyuan Wang, Ke Xu, Monty Montano, Kaku So-Armah, Amy C Justice, Yan V Sun
Publikováno v:
Clinical Infectious Diseases. 76:e638-e644
Background Biomarkers that provide insight into drivers of aging are needed for people with human immunodeficiency virus (PWH). The study objective was to determine if epigenetic age acceleration (EAA) markers are associated with physiologic frailty
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Jia-Xing Wu, Ming Shi, Bao-Ming Gong, Bao-Wei Ji, Cheng-Chen Hu, Gui-Cheng Wang, Lei Lei, Chao Tang, Ling V. Sun, Xiao-Hui Wu, Xue Wang
Publikováno v:
Frontiers in Bioengineering and Biotechnology. 11
Introduction: Functional disorder of the placenta is the principal cause of fetal growth restriction (FGR), usually cured with suitable clinical treatment and good nursing. However, some FGR mothers still give birth to small for gestational age (SGA)
Autor:
Jason L. Vassy, Daniel C. Posner, Yuk-Lam Ho, David R. Gagnon, Ashley Galloway, Vidisha Tanukonda, Serena C. Houghton, Ravi K. Madduri, Benjamin H. McMahon, Philip S. Tsao, Scott M. Damrauer, Christopher J. O’Donnell, Themistocles L. Assimes, Juan P. Casas, J. Michael Gaziano, Michael J. Pencina, Yan V. Sun, Kelly Cho, Peter W.F. Wilson
Publikováno v:
JAMA Cardiology.
ImportancePrimary prevention of atherosclerotic cardiovascular disease (ASCVD) relies on risk stratification. Genome-wide polygenic risk scores (PRSs) are proposed to improve ASCVD risk estimation.ObjectiveTo determine whether genome-wide PRSs for co
Publikováno v:
medRxiv
BackgroundHeart failure (HF) is a serious condition with increasing prevalence, high morbidity, and increased mortality. Obesity is an established risk factor for cardiovascular diseases, including HF. Fluctuation in body mass index (BMI) has shown a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27f661a7482ee3f748b9bb76624378f0
https://europepmc.org/articles/PMC10081412/
https://europepmc.org/articles/PMC10081412/
Autor:
Daniel, Hupalo, Christopher W, Forsberg, Jack, Goldberg, William S, Kremen, Michael J, Lyons, Anthony R, Soltis, Coralie, Viollet, Robert J, Ursano, Murray B, Stein, Carol E, Franz, Yan V, Sun, Viola, Vaccarino, Nicholas L, Smith, Clifton L, Dalgard, Matthew D, Wilkerson, Harvey B, Pollard
Publikováno v:
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry. 23(4)
Major Depressive Disorder (MDD) is a complex neuropsychiatric disease with known genetic associations, but without known links to rare variation in the human genome. Here we aim to identify rare genetic variants associated with MDD using deep whole-g