An Unbiased Drug Screen in a Drosophila Model of <i>LMNA</i>-Muscular Dystrophy Identifies Calcium Channel Blockers as Potential Treatments. [PDF]
Mohar NP +9 more
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Emerging roles of α/β hydrolase domain (ABHD) proteins in S-palmitoylation modification: molecular mechanisms, structural features, and pathological implications. [PDF]
Wen X, Liu M, Quan Y, Xu Y, Xu J, Shi X.
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Atrial Dilated Cardiomyopathy: From Molecular Pathogenesis to Clinical Implications. [PDF]
Carella MC +14 more
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Telomere shortening in laminopathic dilated cardiomyopathy. [PDF]
Chang ACY +11 more
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A Viewpoint on Reframing Genetic Myopathy Classification: A Unified, Semiotic, Tri-Axis Approach. [PDF]
Khadilkar SV, Halani HA.
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Understanding Brain Functional Dynamics Through Neural Koopman Operator With Control Mechanism. [PDF]
Zhou Z, Dan T, Wu G.
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A-type lamins anchor emerin at the inner nuclear membrane via two independent binding sites. [PDF]
Odell J, Nedza K, Lammerding J.
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Comparative Analysis of Splicing Alterations in Three Muscular Dystrophies. [PDF]
Todorow V +3 more
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Impaired Myogenic Differentiation Is a Shared Feature Across Genetic Myopathies. [PDF]
Soule TGB +8 more
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Emerin is necessary for microtubule-organizing center translocation to the nuclear envelope of muscle cells. [PDF]
Mattioli E +14 more
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