t/desmin

Desmin

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Desmin p.R406W mutation is associated with arrhythmias through structural and electrophysiological remodeling
Desmin
Cardiomyopathy-Associated Mutations in a Hotspot Region at the C-Terminal Part of Desmin Coil-2 Domain Impair the Intermediate Filament Assembly.
Desmin
Desmin Mutations Disrupt Filament Elongation and Drive Polymorphic Aggregation
Desmin
A Novel Variant in the Desmin Gene: Case Report
Desmin
Desmin c.322G>A variant is associated with cardiomyopathy: a case series.
Desmin
Pathogenic desmin variants impair nuclear integrity and drive atrial cardiomyopathy
Desmin
Novel in-frame variant in DES (p.Glu353dup) causes myofibrillar myopathy: clinical, in silico and functional studies.
Desmin
Desmin mutations in cardiomyocytes increase susceptibility to coxsackievirus B3 infection by impairing antiviral IFN-β response and upregulating viral receptors expression.
Desmin
Genotype-Dependent Morpho-Mechanical Profiling of Patient-Derived Human Myotubes on Nanogrooved Substrates.
Desmin
Plexiform Fibromyxoma with MALAT1–GLI1 Fusion with Limited Myxoid Stroma, Aberrant KIT Expression, and Diffuse D2-40 Expression: A Case Report
Desmin

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