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Items: 3

1.
Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion
Michael W. Lawlor, Elizabeth T. DeChene, Emily Roumm, Amelia S. Geggel, Behzad Moghadaszadeh, Alan H Beggs
Hum Mutat. Author manuscript; available in PMC 2011 Feb 1.
Published in final edited form as: Hum Mutat. 2010 Feb; 31(2): 176–183. doi: 10.1002/humu.21157
PMCID:
PMC2815199
AbstractArticlePDF–212K
2.
A novel data mining method to identify assay-specific signatures in functional genomic studies
Derrick K Rollins, Dongmei Zhai, Alrica L Joe, Jack W Guidarelli, Abhishek Murarka, Ramon Gonzalez
BMC Bioinformatics. 2006; 7: 377. Published online 2006 Aug 14. doi: 10.1186/1471-2105-7-377
PMCID:
PMC1599756
AbstractArticlePDF–11M
3.
A nemaline myopathy mutation in α-tropomyosin causes defective regulation of striated muscle force production
Daniel E. Michele, Faris P. Albayya, Joseph M. Metzger
J Clin Invest. 1999 Dec 1; 104(11): 1575–1581. doi: 10.1172/JCI7842
PMCID:
PMC409864
AbstractArticlePDF–272K

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