Zobrazeno 1 - 4
of 4
pro vyhledávání: '"William J. Jeong"'
Autor:
Joseph B. Lockridge, Mary L. Sailors, David J. Durgan, Oluwaseun Egbejimi, William J. Jeong, Molly S. Bray, William C. Stanley, Martin E. Young
Publikováno v:
Journal of Lipid Research, Vol 49, Iss 7, Pp 1395-1408 (2008)
Diabetes mellitus, obesity, and dyslipidemia increase risk for cardiovascular disease, and expose the heart to high plasma fatty acid (FA) levels. Recent studies suggestthat distinct FA species are cardiotoxic (e.g., palmitate), while others are card
Externí odkaz:
https://doaj.org/article/332d0fb77c93499380b045f0998e328e
Autor:
William C. Stanley, Mary L. Sailors, Martin E. Young, Oluwaseun Egbejimi, William J. Jeong, David J. Durgan, Joseph B. Lockridge, Molly S. Bray
Publikováno v:
Journal of Lipid Research, Vol 49, Iss 7, Pp 1395-1408 (2008)
Diabetes mellitus, obesity, and dyslipidemia increase risk for cardiovascular disease, and expose the heart to high plasma fatty acid (FA) levels. Recent studies suggestthat distinct FA species are cardiotoxic (e.g., palmitate), while others are card
Autor:
Martin E. Young, Chad A. Shaw, David J. Durgan, Heiko Bugger, William J. Jeong, Melissa M. Zanquetta, Jason R.B. Dyck, Michael W. S. Moore, Paul E. Hardin, E. Dale Abel, Ju Yun Tsai, Sheldon E. Litwin, Dongfang Zhang, Rodrigo Antonio Peliciari Garcia, Margaret P. Chandler, Andreas Rohrwasser, Julie H. Rennison, Chi Wing Chow, Molly S. Bray
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 294:H1036-H1047
Virtually every mammalian cell, including cardiomyocytes, possesses an intrinsic circadian clock. The role of this transcriptionally based molecular mechanism in cardiovascular biology is poorly understood. We hypothesized that the circadian clock wi
Autor:
Elizabeth A. Eckman, Rudolph E. Tanzi, Yang Chang, Giuseppina Tesco, William J. Jeong, Suzanne Y. Guénette, Loren Lindsley, Christopher B. Eckman
Publikováno v:
Journal of Biological Chemistry. 278:51100-51107
Members of the FE65 family of adaptor proteins, FE65, FE65L1, and FE65L2, bind the C-terminal region of the amyloid precursor protein (APP). Overexpression of FE65 and FE65L1 was previously reported to increase the levels of alpha-secretase-derived A