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Journal of Neuroinflammation|June 28, 2017
Evidence for an early innate immune response in the motor cortex of ALSJavier H Jara, Barış Genç, Macdonell J Stanford, et al.American Journal of Medical Genetics. Part A|May 26, 2017
Presynaptic congenital myasthenic syndrome with a homozygous sequence variant in LAMA5 combines myopia, facial tics, and failure of neuromuscular transmissionRicardo A Maselli, Juan Arredondo, Jessica Vázquez, et al.Experimental Neurology|December 3, 2014
Fluoxetine is neuroprotective in slow-channel congenital myasthenic syndromeHaipeng Zhu, Gary E Grajales-Reyes, Vivianette Alicea-Vázquez, et al.Annals of the New York Academy of Sciences|January 30, 2018
A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5Ricardo A Maselli, Juan Arredondo, Jessica Vázquez, et al.Journal of Immunology (Baltimore, Md. : 1950)|May 31, 2015
Dendritic Cell-Based Vaccines that Utilize Myeloid Rather than Plasmacytoid Cells Offer a Superior Survival Advantage in Malignant GliomaMahua Dey, Alan L Chang, Jason Miska, et al.Plos One|September 2, 2015
Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal MuscleAlexis R Demonbreun, Kaitlin E Swanson, Ann E Rossi, et al.The American Journal of Pathology|November 2, 2013
Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivityAlexis R Demonbreun, Ann E Rossi, Manuel G Alvarez, et al.Human Molecular Genetics|November 15, 2008
Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in miceMegan J Puckelwartz, Eric Kessler, Yuan Zhang, et al.Plos One|December 24, 2010
Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutationStephanie K Mewborn, Megan J Puckelwartz, Fida Abuisneineh, et al.Journal of Molecular and Cellular Cardiology|December 1, 2009
Nesprin-1 mutations in human and murine cardiomyopathyMegan J Puckelwartz, Eric J Kessler, Gene Kim, et al.Pageof 16