Utrophin muscles in on the action

Author:

Karpati George

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference18 articles.

1. Koenig, M. et al. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50, 509–517 (1987).

2. Hoffman, E.P., Brown, R.H.J. & Kunkel, L.N. Dystrophin: the protein product of Duchenne muscular dystrophy locus. Cell 51, 919–928 (1987).

3. Dunnen, J. et al. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. Am. J. Hum. Genet. 45, 835–847 (1989).

4. Koenig, M. et al. The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion. Am. J. Hum. Genet. 45, 498–506 (1989).

5. Sunada, Y. & Campbell, K. Dystrophin-glycoprotein complex: Molecular organization and critical roles in skeletal muscle. Curr. Opin. Neurol. 8, 379–384 (1995).

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1. Targeting Artificial Transcription Factors to the Utrophin A Promoter;Journal of Biological Chemistry;2008-12

2. The Molecular Era of Myology;Journal of Neuropathology & Experimental Neurology;2003-12

3. Cell Cycle and Cancer;BMB Reports;2003-01-31

4. Sp1 and the ets-related transcription factor complex GABPα/β functionally cooperate to activate the utrophin promoter;Journal of the Neurological Sciences;2002-05

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