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Stephen G. Young
Stephen G. Young
Verified email at mednet.ucla.edu
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Cited by
Cited by
Year
MCP-1 deficiency reduces susceptibility to atherosclerosis in mice that overexpress human apolipoprotein B
J Gosling, S Slaymaker, L Gu, S Tseng, CH Zlot, SG Young, BJ Rollins, ...
The Journal of clinical investigation 103 (6), 773-778, 1999
9271999
Probucol inhibits oxidative modification of low density lipoprotein.
S Parthasarathy, SG Young, JL Witztum, RC Pittman, D Steinberg
The Journal of clinical investigation 77 (2), 641-644, 1986
8281986
The knockout mouse project
Nature genetics 36 (9), 921-924, 2004
7632004
Lamins A and C but not lamin B1 regulate nuclear mechanics
J Lammerding, LG Fong, JY Ji, K Reue, CL Stewart, SG Young, RT Lee
Journal of Biological Chemistry 281 (35), 25768-25780, 2006
7592006
Recent progress in understanding apolipoprotein B.
SG Young
Circulation 82 (5), 1574-1594, 1990
5641990
ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration
JA Lee, A Beigneux, ST Ahmad, SG Young, FB Gao
Current biology 17 (18), 1561-1567, 2007
5522007
Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect
MO Bergo, B Gavino, J Ross, WK Schmidt, C Hong, LV Kendall, A Mohr, ...
Proceedings of the National Academy of Sciences 99 (20), 13049-13054, 2002
5292002
Glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 plays a critical role in the lipolytic processing of chylomicrons
AP Beigneux, BSJ Davies, P Gin, MM Weinstein, E Farber, X Qiao, ...
Cell metabolism 5 (4), 279-291, 2007
5232007
Analysis of the role of microsomal triglyceride transfer protein in the liver of tissue-specific knockout mice
M Raabe, MM Véniant, MA Sullivan, CH Zlot, J Björkegren, LB Nielsen, ...
The Journal of clinical investigation 103 (9), 1287-1298, 1999
5071999
Lamin B1 is required for mouse development and nuclear integrity
L Vergnes, M Péterfy, MO Bergo, SG Young, K Reue
Proceedings of the National Academy of Sciences 101 (28), 10428-10433, 2004
4702004
Inactivation of the integrin beta 6 subunit gene reveals a role of epithelial integrins in regulating inflammation in the lung and skin.
XZ Huang, JF Wu, D Cass, DJ Erle, D Corry, SG Young, RV Farese Jr, ...
The Journal of cell biology 133 (4), 921-928, 1996
4081996
Phenotypes of apolipoprotein B and apolipoprotein E after liver transplantation.
MF Linton, R Gish, ST Hubl, E Bütler, C Esquivel, WI Bry, JK Boyles, ...
The Journal of clinical investigation 88 (1), 270-281, 1991
4041991
GPIHBP1 is responsible for the entry of lipoprotein lipase into capillaries
BSJ Davies, AP Beigneux, RH Barnes, Y Tu, P Gin, MM Weinstein, ...
Cell metabolism 12 (1), 42-52, 2010
3942010
Biochemistry and pathophysiology of intravascular and intracellular lipolysis
SG Young, R Zechner
Genes & development 27 (5), 459-484, 2013
3892013
A protein farnesyltransferase inhibitor ameliorates disease in a mouse model of progeria
LG Fong, D Frost, M Meta, X Qiao, SH Yang, C Coffinier, SG Young
Science 311 (5767), 1621-1623, 2006
3742006
Linking lipid metabolism to the innate immune response in macrophages through sterol regulatory element binding protein-1a
SS Im, L Yousef, C Blaschitz, JZ Liu, RA Edwards, SG Young, M Raffatellu, ...
Cell metabolism 13 (5), 540-549, 2011
3722011
Blocking protein farnesyltransferase improves nuclear blebbing in mouse fibroblasts with a targeted Hutchinson–Gilford progeria syndrome mutation
SH Yang, MO Bergo, JI Toth, X Qiao, Y Hu, S Sandoval, M Meta, ...
Proceedings of the National Academy of Sciences 102 (29), 10291-10296, 2005
3582005
Deficiency of a protein-repair enzyme results in the accumulation of altered proteins, retardation of growth, and fatal seizures in mice
E Kim, JD Lowenson, DC MacLaren, S Clarke, SG Young
Proceedings of the National Academy of Sciences 94 (12), 6132-6137, 1997
3481997
Familial hypobetalipoproteinemia.
MF Linton, RV Farese Jr, SG Young
Journal of lipid research 34 (4), 521-541, 1993
3391993
A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation
SH Yang, M Meta, X Qiao, D Frost, J Bauch, C Coffinier, S Majumdar, ...
The Journal of clinical investigation 116 (8), 2115-2121, 2006
3342006
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