Functional muscle analysis of the Tcap knockout mouse.
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.
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Altered myofilament function depresses force generation in patients with nebulin-based nemaline myopathy (NEM2).
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.
Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.
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.
Acute appendicitis is characterized by a uniform and highly selective pattern of inflammatory gene expression.
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.
Multiplex PCR for identifying DMD gene deletions.
Dunnen, Johan, and Alan Beggs. 2006. “Multiplex PCR for Identifying DMD Gene Deletions.”. Curr Protoc Hum Genet Chapter 9: Unit 9.3.
Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy.
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.
Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.
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.
Evidence by molecular profiling for a placental origin of infantile hemangioma.
Barnés, Carmen, Sui Huang, Arja Kaipainen, Despina Sanoudou, Emy Chen, Gabriel Eichler, Yuchun Guo, et al. 2005. “Evidence by Molecular Profiling for a Placental Origin of Infantile Hemangioma.”. Proc Natl Acad Sci U S A 102 (52): 19097-102.
The influence of muscle type and dystrophin deficiency on murine expression profiles.
Haslett, Judith, Peter Kang, Mei Han, Alvin Kho, Despina Sanoudou, Jay Volinski, Alan Beggs, Isaac Kohane, and Louis Kunkel. 2005. “The Influence of Muscle Type and Dystrophin Deficiency on Murine Expression Profiles.”. Mamm Genome 16 (10): 739-48.
Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1).
Sparrow, John, Kristen Nowak, Hayley Durling, Alan Beggs, Carina Wallgren-Pettersson, Norma Romero, Ikuya Nonaka, and Nigel Laing. 2003. “Muscle Disease Caused by Mutations in the Skeletal Muscle Alpha-Actin Gene (ACTA1).”. Neuromuscul Disord 13 (7-8): 519-31.