Author(s) |
(Date) |
Paper Title |
Citation |
Model Type |
Applications |
Full Text |
| Méjat A, et al. Mouse over for full list Méjat A, Ramond F, Bassel-Duby R, Khochbin S, Olson EN, Schaeffer L |
(2005) | Histone deacetylase 9 couples neuronal activity to muscle chromatin acetylation and gene expression. | Nat. Neurosci. 8(3):313-21 | |||
| Vega RB, et al. Mouse over for full list Vega RB, Matsuda K, Oh J, Barbosa AC, Yang X, Meadows E, McAnally J, Pomajzl C, Shelton JM, Richardson JA, Karsenty G, Olson EN |
(2004) | Histone deacetylase 4 controls chondrocyte hypertrophy during skeletogenesis. | Cell 119(4):555-66 | |||
| Chang S, et al. Mouse over for full list Chang S, McKinsey TA, Zhang CL, Richardson JA, Hill JA, Olson EN |
(2004) | Histone deacetylases 5 and 9 govern responsiveness of the heart to a subset of stress signals and play redundant roles in heart development. | Mol. Cell. Biol. 24(19):8467-76 | |||
| Zhang CL, et al. Mouse over for full list Zhang CL, McKinsey TA, Olson EN |
(2001) | The transcriptional corepressor MITR is a signal-responsive inhibitor of myogenesis. | Proc. Natl. Acad. Sci. U.S.A. 98(13):7354-9 | |||
| Zhang CL, et al. Mouse over for full list Zhang CL, McKinsey TA, Lu JR, Olson EN |
(2001) | Association of COOH-terminal-binding protein (CtBP) and MEF2-interacting transcription repressor (MITR) contributes to transcriptional repression of the MEF2 transcription factor. | J. Biol. Chem. 276(1):35-9 |
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