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Beggs, AH, Hoffman, Snyder, Arahata, Specht, Shapiro, Angelini, Sugita, and Kunkel. 1991. “Exploring the Molecular Basis for Variability Among Patients With Becker Muscular Dystrophy: Dystrophin Gene and Protein Studies.”. Am J Hum Genet 49 (1): 54-67.

Beggs, AH, and Kunkel. 1990. “A Polymorphic CACA Repeat in the 3’ Untranslated Region of Dystrophin.”. Nucleic Acids Res 18 (7): 1931.

Beggs, AH, and Migeon. 1989. “Chromatin Loop Structure of the Human X Chromosome: Relevance to X Inactivation and CpG Clusters.”. Mol Cell Biol 9 (6): 2322-31.

Amburgey, Lawlor, Del Gaudio, Cheng, Fitzpatrick, Minor, Li, et al. 2013. “Large Duplication in MTM1 Associated With Myotubular Myopathy.”. Neuromuscul Disord 23 (3): 214-8.

Grange, Robert, Jon Doering, Erin Mitchell, Melanie Holder, Xuan Guan, Melissa Goddard, Christopher Tegeler, Alan Beggs, and Martin Childers. 2012. “Muscle Function in a Canine Model of X-Linked Myotubular Myopathy.”. Muscle Nerve 46 (4): 588-91.

Lawlor, Michael, Matthew Alexander, Marissa Viola, Hui Meng, Romain Joubert, Vandana Gupta, Norio Motohashi, et al. 2012. “Myotubularin-Deficient Myoblasts Display Increased Apoptosis, Delayed Proliferation, and Poor Cell Engraftment.”. Am J Pathol 181 (3): 961-8.

Meng, Hui, Paul Janssen, Robert Grange, Lin Yang, Alan Beggs, Lindsay Swanson, Stacy Cossette, et al. 2014. “Tissue Triage and Freezing for Models of Skeletal Muscle Disease.”. J Vis Exp, no. 89.

Lawlor, Michael, Coen Ottenheijm, Vilma-Lotta Lehtokari, Kiyomi Cho, Katarina Pelin, Carina Wallgren-Pettersson, Henk Granzier, and Alan Beggs. 2011. “Novel Mutations in NEB Cause Abnormal Nebulin Expression and Markedly Impaired Muscle Force Generation in Severe Nemaline Myopathy.”. Skelet Muscle 1 (1): 23.

Ottenheijm, Coen, Michael Lawlor, Ger Stienen, Henk Granzier, and Alan Beggs. 2011. “Changes in Cross-Bridge Cycling Underlie Muscle Weakness in Patients With Tropomyosin 3-Based Myopathy.”. Hum Mol Genet 20 (10): 2015-25.

Gupta, Vandana, Genri Kawahara, Stacey Gundry, Aye Chen, Wayne Lencer, Yi Zhou, Leonard Zon, Louis Kunkel, and Alan Beggs. 2011. “The Zebrafish Dag1 Mutant: A Novel Genetic Model for Dystroglycanopathies.”. Hum Mol Genet 20 (9): 1712-25.