A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice-Reference-Cited by-同舟云学术

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A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice

Published:2005-01-20 Issue:5 Volume:14 Page:667-677
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Herron Bruce J.,Rao Cherie,Liu Shanming,Laprade Lisa,Richardson James A.,Olivieri Emily,Semsarian Chris,Millar Sarah E.,Stubbs Lisa,Beier David R.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/14/5/667/6949769/ddi063.pdf

Reference33 articles.

1. Semsarian, C., Healey, M.J., Fatkin, D., Giewat, M., Duffy, C., Seidman, C.E. and Seidman, J.G. ( 2001 ) A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol. , 33 , 2055 –2060.

2. Crew, F. ( 1933 ) Waved: an autosomal recessive coat form character in the mouse. J. Genet. , 27 , 95 –96.

3. Keeler, C. ( 1935 ) A second rexoid coat character in the house mouse. J. Hered. , 26 , 189 –191.

4. Neuhaus, I.M. and Beier, D.R. ( 1998 ) Efficient localization of mutations by interval haplotype analysis. Mamm. Genome , 9 , 150 –154.

5. Shannon, M., Ashworth, L.K., Mucenski, M.L., Lamerdin, J.E., Branscomb, E. and Stubbs, L. ( 1996 ) Comparative analysis of a conserved zinc finger gene cluster on human chromosome 19q and mouse chromosome 7. Genomics , 33 , 112 –120.

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