Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy-Reference-Cited by-同舟云学术

Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy

Published:2004-08-18 Issue:20 Volume:13 Page:2505-2518
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

O'Cochlain D. Fearghas,Perez-Terzic Carmen,Reyes Santiago,Kane Garvan C.,Behfar Atta,Hodgson Denice M.,Strommen Jeffrey A.,Liu Xiao-Ke,van den Broek Walther,Wansink Derick G.,Wieringa Bé,Terzic Andre

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/13/20/2505/1592022/ddh266.pdf

Reference64 articles.

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2. Harper, P.S. (2001) Myotonic Dystrophy. WB Saunders Co Ltd, London, UK.

3. Riento, K. and Ridley, A.J. (2003) Rocks: multifunctional kinases in cell behaviour. Nat. Rev. Mol. Cell. Biol., 4, 446–456.

4. Ueda, H., Ohno, S. and Kobayashi T. (2000) Myotonic dystrophy and myotonic dystrophy protein kinase. Prog. Histochem. Cytochem., 35, 187–251.

5. Wansink, D.G., van Herpen, R.E.M.A., Coerwinkel-Driessen, M.M., Groenen, P.J.T.A., Hemmings, B.A. and Wieringa, B. (2003) Alternative splicing controls myotonic dystrophy protein kinase structure, enzymatic activity and subcellular localization. Mol. Cell. Biol., 23, 5489–5501.

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