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Boyden, Steven, Lane Mahoney, Genri Kawahara, Jennifer Myers, Satomi Mitsuhashi, Elicia Estrella, Anna Duncan, et al. 2012. “Mutations in the Satellite Cell Gene MEGF10 Cause a Recessive Congenital Myopathy With Minicores.”. Neurogenetics 13 (2): 115-24.

Gupta, Vandana, Marie Discenza, Jeffrey Guyon, Louis Kunkel, and Alan Beggs. 2012. “α-Actinin-2 Deficiency Results in Sarcomeric Defects in Zebrafish That Cannot Be Rescued by α-Actinin-3 Revealing Functional Differences Between Sarcomeric Isoforms.”. FASEB J 26 (5): 1892-908.

Lawlor, Michael, Benjamin Read, Rachel Edelstein, Nicole Yang, Christopher Pierson, Matthew Stein, Ariana Wermer-Colan, et al. 2011. “Inhibition of Activin Receptor Type IIB Increases Strength and Lifespan in Myotubularin-Deficient Mice.”. Am J Pathol 178 (2): 784-93.

Markert, Meaney, Voelker, Grange, Dalley, Cann, Ahmed, et al. 2010. “Functional Muscle Analysis of the Tcap Knockout Mouse.”. Hum Mol Genet 19 (11): 2268-83.

Ottenheijm, Coen, Pleuni Hooijman, Elizabeth Dechene, Ger Stienen, Alan Beggs, and Henk Granzier. 2010. “Altered Myofilament Function Depresses Force Generation in Patients With Nebulin-Based Nemaline Myopathy (NEM2).”. J Struct Biol 170 (2): 334-43.

Parker, Kenneth, Sek Won Kong, Ronan Walsh, Bch, Mohammad Salajegheh, Behzad Moghadaszadeh, Anthony Amato, et al. 2009. “Fast-Twitch Sarcomeric and Glycolytic Enzyme Protein Loss in Inclusion Body Myositis.”. Muscle Nerve 39 (6): 739-53.

Murphy, Glickman, Tomczak, Wang, AH Beggs, Shannon, and Horwitz. 2008. “Acute Appendicitis Is Characterized by a Uniform and Highly Selective Pattern of Inflammatory Gene Expression.”. Mucosal Immunol 1 (4): 297-308.

Dunnen, Johan, and Alan Beggs. 2006. “Multiplex PCR for Identifying DMD Gene Deletions.”. Curr Protoc Hum Genet Chapter 9: Unit 9.3.

Pierson, Christopher, Pankaj Agrawal, Jessica Blasko, and Alan Beggs. 2007. “Myofiber Size Correlates With MTM1 Mutation Type and Outcome in X-Linked Myotubular Myopathy.”. Neuromuscul Disord 17 (7): 562-8.

Gazda, Hanna, Agnieszka Grabowska, Lilia Merida-Long, Elzbieta Latawiec, Hal Schneider, Jeffrey Lipton, Adrianna Vlachos, et al. 2006. “Ribosomal Protein S24 Gene Is Mutated in Diamond-Blackfan Anemia.”. Am J Hum Genet 79 (6): 1110-8.