The Missing LINC for Genetic Cardiovascular Disease?

Por Puckelwartz, Megan J.
Publicado no Circ Cardiovasc Genet (2017)

Genetic Profiling for Risk Reduction in Human Cardiovascular Disease

Por Puckelwartz, Megan J., McNally, Elizabeth M.
Publicado em 2014

Genetic variation in cardiomyopathy and cardiovascular disorders

Por McNally, Elizabeth M., Puckelwartz, Megan J.
Publicado no Circ J (2015)

Gene expression, chromosome position and lamin A/C mutations

Por Puckelwartz, Megan J, Depreux, Frederic FS, McNally, Elizabeth M
Publicado em 2011

Genetic mutations and mechanisms in dilated cardiomyopathy

Por McNally, Elizabeth M., Golbus, Jessica R., Puckelwartz, Megan J.
Publicado em 2013

The genetic landscape of cardiomyopathy and its role in heart failure

Por McNally, Elizabeth M, Barefield, David Y, Puckelwartz, Megan J
Publicado no Cell Metab (2015)

Population-Based Variation in Cardiomyopathy Genes

Por Golbus, Jessica R., Puckelwartz, Megan J., Fahrenbach, John P., Dellefave-Castillo, Lisa M., Wolfgeher, Don, McNally, Elizabeth M.
Publicado em 2012

Nesprins, but not Sun proteins, switch isoforms at the nuclear envelope during muscle development

Por Randles, K. Natalie, Lam, Le Thanh, Sewry, Caroline A., Puckelwartz, Megan, Furling, Denis, Wehnert, Manfred, McNally, Elizabeth M., Morris, Glenn E.
Publicado em 2010

Targeted Analysis of Whole Genome Sequence Data to Diagnose Genetic Cardiomyopathy

Por Golbus, Jessica R, Puckelwartz, Megan J, Dellefave-Castillo, Lisa, Fahrenbach, John P, Nelakuditi, Viswateja, Pesce, Lorenzo L, Pytel, Peter, McNally, Elizabeth M
Publicado no Circ Cardiovasc Genet (2014)

Disruption of the lamin A and matrin-3 interaction by myopathic LMNA mutations

Por Depreux, Frederic F., Puckelwartz, Megan J., Augustynowicz, Aleksandra, Wolfgeher, Don, Labno, Christine M., Pierre-Louis, Dynora, Cicka, Danielle, Kron, Stephen J., Holaska, James, McNally, Elizabeth M.
Publicado no Hum Mol Genet (2015)

Supercomputing for the parallelization of whole genome analysis

Por Puckelwartz, Megan J., Pesce, Lorenzo L., Nelakuditi, Viswateja, Dellefave-Castillo, Lisa, Golbus, Jessica R., Day, Sharlene M., Cappola, Thomas P., Dorn, Gerald W., Foster, Ian T., McNally, Elizabeth M.
Publicado em 2014

Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice

Por Puckelwartz, Megan J., Kessler, Eric, Zhang, Yuan, Hodzic, Didier, Randles, K. Natalie, Morris, Glenn, Earley, Judy U., Hadhazy, Michele, Holaska, James M., Mewborn, Stephanie K., Pytel, Peter, McNally, Elizabeth M.
Publicado em 2009

Nesprin-1 mutations in human and murine cardiomyopathy

Por Puckelwartz, Megan J., Kessler, Eric J., Kim, Gene, DeWitt, Megan M., Zhang, Yuan, Earley, Judy U., Depreux, Frederic F.S., Holaska, James, Mewborn, Stephanie K., Pytel, Peter, McNally, Elizabeth M.
Publicado em 2009

Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation

Por Mewborn, Stephanie K., Puckelwartz, Megan J., Abuisneineh, Fida, Fahrenbach, John P., Zhang, Yuan, MacLeod, Heather, Dellefave, Lisa, Pytel, Peter, Selig, Sara, Labno, Christine M., Reddy, Karen, Singh, Harinder, McNally, Elizabeth
Publicado em 2010

Experimental modeling supports a role for MyBP-HL as a novel myofilament component in arrhythmia and dilated cardiomyopathy

Por Barefield, David Y., Puckelwartz, Megan J., Kim, Ellis Y., Wilsbacher, Lisa D., Vo, Andy H., Waters, Emily A., Earley, Judy U., Hadhazy, Michele, Dellefave-Castillo, Lisa, Pesce, Lorenzo L., McNally, Elizabeth M.
Publicado no Circulation (2017)

Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis

Por Zhou, Can, Li, Chen, Zhou, Bin, Sun, Huaqin, Koullourou, Victoria, Holt, Ian, Puckelwartz, Megan J., Warren, Derek T., Hayward, Robert, Lin, Ziyuan, Zhang, Lin, Morris, Glenn E., McNally, Elizabeth M., Shackleton, Sue, Rao, Li, Shanahan, Catherine M., Zhang, Qiuping
Publicado no Hum Mol Genet (2017)