337 related articles for article (PubMed ID: 19037247)
1. Nuclear receptor corepressor and histone deacetylase 3 govern circadian metabolic physiology.
Alenghat T; Meyers K; Mullican SE; Leitner K; Adeniji-Adele A; Avila J; Bućan M; Ahima RS; Kaestner KH; Lazar MA
Nature; 2008 Dec; 456(7224):997-1000. PubMed ID: 19037247
[TBL] [Abstract][Full Text] [Related]
2. Circadian clocks: tips from the tip of the iceberg.
Turek FW
Nature; 2008 Dec; 456(7224):881-3. PubMed ID: 19092918
[No Abstract] [Full Text] [Related]
3. The orphan nuclear receptor Rev-erbalpha recruits the N-CoR/histone deacetylase 3 corepressor to regulate the circadian Bmal1 gene.
Yin L; Lazar MA
Mol Endocrinol; 2005 Jun; 19(6):1452-9. PubMed ID: 15761026
[TBL] [Abstract][Full Text] [Related]
4. A circadian rhythm orchestrated by histone deacetylase 3 controls hepatic lipid metabolism.
Feng D; Liu T; Sun Z; Bugge A; Mullican SE; Alenghat T; Liu XS; Lazar MA
Science; 2011 Mar; 331(6022):1315-9. PubMed ID: 21393543
[TBL] [Abstract][Full Text] [Related]
5. Circadian and light-induced transcription of clock gene Per1 depends on histone acetylation and deacetylation.
Naruse Y; Oh-hashi K; Iijima N; Naruse M; Yoshioka H; Tanaka M
Mol Cell Biol; 2004 Jul; 24(14):6278-87. PubMed ID: 15226430
[TBL] [Abstract][Full Text] [Related]
6. Rev-erbα dynamically modulates chromatin looping to control circadian gene transcription.
Kim YH; Marhon SA; Zhang Y; Steger DJ; Won KJ; Lazar MA
Science; 2018 Mar; 359(6381):1274-1277. PubMed ID: 29439026
[TBL] [Abstract][Full Text] [Related]
7. Nuclear receptor co-repressors are required for the histone-deacetylase activity of HDAC3 in vivo.
You SH; Lim HW; Sun Z; Broache M; Won KJ; Lazar MA
Nat Struct Mol Biol; 2013 Feb; 20(2):182-7. PubMed ID: 23292142
[TBL] [Abstract][Full Text] [Related]
8. Deacetylase-independent function of HDAC3 in transcription and metabolism requires nuclear receptor corepressor.
Sun Z; Feng D; Fang B; Mullican SE; You SH; Lim HW; Everett LJ; Nabel CS; Li Y; Selvakumaran V; Won KJ; Lazar MA
Mol Cell; 2013 Dec; 52(6):769-82. PubMed ID: 24268577
[TBL] [Abstract][Full Text] [Related]
9. Balanced control of thermogenesis by nuclear receptor corepressors in brown adipose tissue.
Richter HJ; Hauck AK; Batmanov K; Inoue SI; So BN; Kim M; Emmett MJ; Cohen RN; Lazar MA
Proc Natl Acad Sci U S A; 2022 Aug; 119(33):e2205276119. PubMed ID: 35939699
[TBL] [Abstract][Full Text] [Related]
10. GR SUMOylation and formation of an SUMO-SMRT/NCoR1-HDAC3 repressing complex is mandatory for GC-induced IR nGRE-mediated transrepression.
Hua G; Paulen L; Chambon P
Proc Natl Acad Sci U S A; 2016 Feb; 113(5):E626-34. PubMed ID: 26712002
[TBL] [Abstract][Full Text] [Related]
11. System-driven and oscillator-dependent circadian transcription in mice with a conditionally active liver clock.
Kornmann B; Schaad O; Bujard H; Takahashi JS; Schibler U
PLoS Biol; 2007 Feb; 5(2):e34. PubMed ID: 17298173
[TBL] [Abstract][Full Text] [Related]
12. Histone deacetylase 1/mSin3A disrupts gamma interferon-induced CIITA function and major histocompatibility complex class II enhanceosome formation.
Zika E; Greer SF; Zhu XS; Ting JP
Mol Cell Biol; 2003 May; 23(9):3091-102. PubMed ID: 12697811
[TBL] [Abstract][Full Text] [Related]
13. Machine learning helps identify CHRONO as a circadian clock component.
Anafi RC; Lee Y; Sato TK; Venkataraman A; Ramanathan C; Kavakli IH; Hughes ME; Baggs JE; Growe J; Liu AC; Kim J; Hogenesch JB
PLoS Biol; 2014 Apr; 12(4):e1001840. PubMed ID: 24737000
[TBL] [Abstract][Full Text] [Related]
14. A novel protein, CHRONO, functions as a core component of the mammalian circadian clock.
Goriki A; Hatanaka F; Myung J; Kim JK; Yoritaka T; Tanoue S; Abe T; Kiyonari H; Fujimoto K; Kato Y; Todo T; Matsubara A; Forger D; Takumi T
PLoS Biol; 2014 Apr; 12(4):e1001839. PubMed ID: 24736997
[TBL] [Abstract][Full Text] [Related]
15. Loss of Nocturnin, a circadian deadenylase, confers resistance to hepatic steatosis and diet-induced obesity.
Green CB; Douris N; Kojima S; Strayer CA; Fogerty J; Lourim D; Keller SR; Besharse JC
Proc Natl Acad Sci U S A; 2007 Jun; 104(23):9888-93. PubMed ID: 17517647
[TBL] [Abstract][Full Text] [Related]
16. Ataxin-3 represses transcription via chromatin binding, interaction with histone deacetylase 3, and histone deacetylation.
Evert BO; Araujo J; Vieira-Saecker AM; de Vos RA; Harendza S; Klockgether T; Wüllner U
J Neurosci; 2006 Nov; 26(44):11474-86. PubMed ID: 17079677
[TBL] [Abstract][Full Text] [Related]
17. The N-CoR complex enables chromatin remodeler SNF2H to enhance repression by thyroid hormone receptor.
Alenghat T; Yu J; Lazar MA
EMBO J; 2006 Sep; 25(17):3966-74. PubMed ID: 16917504
[TBL] [Abstract][Full Text] [Related]
18. Dichotomous engagement of HDAC3 activity governs inflammatory responses.
Nguyen HCB; Adlanmerini M; Hauck AK; Lazar MA
Nature; 2020 Aug; 584(7820):286-290. PubMed ID: 32760002
[TBL] [Abstract][Full Text] [Related]
19. Rev-erbalpha, a heme sensor that coordinates metabolic and circadian pathways.
Yin L; Wu N; Curtin JC; Qatanani M; Szwergold NR; Reid RA; Waitt GM; Parks DJ; Pearce KH; Wisely GB; Lazar MA
Science; 2007 Dec; 318(5857):1786-9. PubMed ID: 18006707
[TBL] [Abstract][Full Text] [Related]
20. Toward construction of a self-sustained clock-like expression system based on the mammalian circadian clock.
Chilov D; Fussenegger M
Biotechnol Bioeng; 2004 Jul; 87(2):234-42. PubMed ID: 15236253
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
