Author
Listed:
- Joanne Hsieh
(Columbia University)
- Masahiro Koseki
(Columbia University
Cardiovascular Medicine, Osaka University Graduate School of Medicine)
- Matthew M. Molusky
(Columbia University)
- Emi Yakushiji
(Columbia University)
- Ikuyo Ichi
(Faculty of Core Research, Ochanomizu University)
- Marit Westerterp
(Columbia University)
- Jahangir Iqbal
(State University of New York Health Science Center at Brooklyn (SUNY Downstate Medical Center))
- Robin B. Chan
(Columbia University)
- Sandra Abramowicz
(Columbia University)
- Liana Tascau
(Columbia University)
- Shunichi Takiguchi
(Perelman School of Medicine, University of Pennsylvania
Perelman School of Medicine, University of Pennsylvania)
- Shizuya Yamashita
(Cardiovascular Medicine, Osaka University Graduate School of Medicine)
- Carrie L. Welch
(Columbia University)
- Gilbert Di Paolo
(Columbia University)
- M. Mahmood Hussain
(State University of New York Health Science Center at Brooklyn (SUNY Downstate Medical Center))
- Jay H. Lefkowitch
(Columbia University)
- Daniel J. Rader
(Perelman School of Medicine, University of Pennsylvania
Perelman School of Medicine, University of Pennsylvania)
- Alan R. Tall
(Columbia University)
Abstract
In mice, deficiency in the high-density lipoprotein gene T39 stabilizes liver X receptor (LXR), reducing both atherosclerosis and steatohepatitis, suggesting that T39 inhibition could be an effective strategy for reducing these diseases.
Suggested Citation
Joanne Hsieh & Masahiro Koseki & Matthew M. Molusky & Emi Yakushiji & Ikuyo Ichi & Marit Westerterp & Jahangir Iqbal & Robin B. Chan & Sandra Abramowicz & Liana Tascau & Shunichi Takiguchi & Shizuya Y, 2016.
"TTC39B deficiency stabilizes LXR reducing both atherosclerosis and steatohepatitis,"
Nature, Nature, vol. 535(7611), pages 303-307, July.
Handle:
RePEc:nat:nature:v:535:y:2016:i:7611:d:10.1038_nature18628
DOI: 10.1038/nature18628
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