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Lawlor, Michael, Elizabeth Dechene, Emily Roumm, Amelia Geggel, Behzad Moghadaszadeh, and Alan Beggs. 2010. “Mutations of Tropomyosin 3 (TPM3) Are Common and Associated With Type 1 Myofiber Hypotrophy in Congenital Fiber Type Disproportion.”. Hum Mutat 31 (2): 176-83.

Ziane, Rahima, Hai Huang, Behzad Moghadaszadeh, Alan Beggs, Georges Levesque, and Mohamed Chahine. 2010. “Cell Membrane Expression of Cardiac Sodium Channel Na(v)1.5 Is Modulated by Alpha-Actinin-2 Interaction.”. Biochemistry 49 (1): 166-78.

Al-Qusairi, Lama, Norbert Weiss, Anne Toussaint, Céline Berbey, Nadia Messaddeq, Christine Kretz, Despina Sanoudou, et al. 2009. “T-Tubule Disorganization and Defective Excitation-Contraction Coupling in Muscle Fibers Lacking Myotubularin Lipid Phosphatase.”. Proc Natl Acad Sci U S A 106 (44): 18763-8.

Ottenheijm, Coen, Christian Witt, Ger Stienen, Siegfried Labeit, Alan Beggs, and Henk Granzier. 2009. “Thin Filament Length Dysregulation Contributes to Muscle Weakness in Nemaline Myopathy Patients With Nebulin Deficiency.”. Hum Mol Genet 18 (13): 2359-69.

Farrar, Jason, Michelle Nater, Emi Caywood, Michael McDevitt, Jeanne Kowalski, Clifford Takemoto, Conover Talbot, et al. 2008. “Abnormalities of the Large Ribosomal Subunit Protein, Rpl35a, in Diamond-Blackfan Anemia.”. Blood 112 (5): 1582-92.

Keller, Christian, Arthur Hays, Lewis Rowland, Behzad Moghadaszadeh, Alan Beggs, and Govind Bhagat. 2006. “Adult-Onset Nemaline Myopathy and Monoclonal Gammopathy.”. Arch Neurol 63 (1): 132-4.

Liadaki, Kho, Sanoudou, Schienda, Flint, AH Beggs, Kohane, and Kunkel. 2005. “Side Population Cells Isolated from Different Tissues Share Transcriptome Signatures and Express Tissue-Specific Markers.”. Exp Cell Res 303 (2): 360-74.

Sanoudou, Despina, Judith Haslett, Alvin Kho, Shaoqiang Guo, Hanna Gazda, Steven Greenberg, Hart Lidov, Isaac Kohane, Louis Kunkel, and Alan Beggs. 2003. “Expression Profiling Reveals Altered Satellite Cell Numbers and Glycolytic Enzyme Transcription in Nemaline Myopathy Muscle.”. Proc Natl Acad Sci U S A 100 (8): 4666-71.

Zervos, Hunt, Tong, Avallone, Morales, Friedman, Cohen, et al. 2002. “Clinical, Genetic and Histopathologic Findings in Two Siblings With Muscle-Eye-Brain Disease.”. Eur J Ophthalmol 12 (4): 253-61.

Splawski, Igor, Katherine Timothy, Michihiro Tateyama, Colleen Clancy, Alka Malhotra, Alan Beggs, Francesco Cappuccio, Giuseppe Sagnella, Robert Kass, and Mark Keating. 2002. “Variant of SCN5A Sodium Channel Implicated in Risk of Cardiac Arrhythmia.”. Science 297 (5585): 1333-6.