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Scientific Reports|July 26, 2017
Ryanodine receptors are part of the myospryn complex in cardiac muscleMatthew A Benson, Caroline L Tinsley, Adrian J Waite, et al.
Neurology. Genetics|August 13, 2021
Out-of-Frame Mutations in <i>ACTN2</i> Last Exon Cause a Dominant Distal Myopathy With Facial WeaknessMarco Savarese, Anna Vihola, Manu E Jokela, et al.
The Journal of Physiology|February 16, 2011
Preferential skeletal muscle myosin loss in response to mechanical silencing in a novel rat intensive care unit model: underlying mechanismsJulien Ochala, Ann-Marie Gustafson, Monica Llano Diez, et al.
Human Molecular Genetics|May 29, 2015
Epigenetic changes as a common trigger of muscle weakness in congenital myopathiesOri Rokach, Marijana Sekulic-Jablanovic, Nicol Voermans, et al.
Circulation Research|January 7, 2026
Location-Dependent Differences in Cardiac and Skeletal Muscle Dysfunction Associated With Truncating Titin (<i>ttn.2</i>) VariantsCeline F Santiago, Inken G Huttner, Ailbhe O Brien, et al.
Journal of Molecular and Cellular Cardiology|April 1, 2017
Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defectsJennifer England, Javier Granados-Riveron, Luis Polo-Parada, et al.
The Journal of Cell Biology|September 16, 2015
α5β1 integrin recycling promotes Arp2/3-independent cancer cell invasion via the formin FHOD3Nikki R Paul, Jennifer L Allen, Anna Chapman, et al.
Journal of Molecular and Cellular Cardiology|April 21, 2009
Overexpression of the transcription factor Hand1 causes predisposition towards arrhythmia in miceRoss A Breckenridge, Zia Zuberi, John Gomes, et al.
The Journal of Biological Chemistry|April 3, 2024
Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomereChen Li, Derek T Warren, Can Zhou, et al.
Annals of Neurology|April 21, 2007
C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathyVirginie Carmignac, Mustafa A M Salih, Susana Quijano-Roy, et al.
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