Publications by authors named "Stephanie Mewborn"

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Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation.
Stephanie K Mewborn, Megan J Puckelwartz, Fida Abuisneineh, John P Fahrenbach, Yuan Zhang

PLoS One· December 2010

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Nesprin-1 mutations in human and murine cardiomyopathy.
Megan J Puckelwartz, Eric J Kessler, Gene Kim, Megan M Dewitt, Yuan Zhang, Stephanie K Mewborn

J Mol Cell Cardiol· April 2010

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Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.
Lisa M Dellefave, Peter Pytel, Stephanie Mewborn, Bassem Mora, Deborah L Guris

Circ Cardiovasc Genet· October 2009

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Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.
Megan J Puckelwartz, Eric Kessler, Yuan Zhang, Didier Hodzic, K Natalie Randles, Stephanie K Mewborn

Hum Mol Genet· February 2009

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Genetic compensation for sarcoglycan loss by integrin alpha7beta1 in muscle.
Michael J Allikian, Andrew A Hack, Stephanie Mewborn, Ulrike Mayer, Elizabeth M McNally

J Cell Sci· August 2004

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