Pages that link to "Q34728529"

The following pages link to A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies. (Q34728529):

Displaying 24 items.

• autosomal recessive limb-girdle muscular dystrophy type 2R (Q27677708) (← links)
• Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect (Q28115277) (← links)
• Protein alterations in women with chronic widespread pain--An explorative proteomic study of the trapezius muscle. (Q35684873) (← links)
• Molecular Signatures of Membrane Protein Complexes Underlying Muscular Dystrophy. (Q37372312) (← links)
• The Classification, Natural History and Treatment of the Limb Girdle Muscular Dystrophies (Q37610524) (← links)
• Posttranslational modifications of desmin and their implication in biological processes and pathologies (Q38148976) (← links)
• Genetic basis of limb-girdle muscular dystrophies: the 2014 update (Q38213016) (← links)
• Anesthetic considerations in myofibrillar myopathy (Q38248683) (← links)
• Desmin related disease: a matter of cell survival failure. (Q38354714) (← links)
• The Growing Family of Limb-Girdle Muscular Dystrophies: Old and Newly Identified Members (Q38528085) (← links)
• Costamere proteins and their involvement in myopathic processes. (Q38531654) (← links)
• Limb-girdle muscular dystrophies - international collaborations for translational research (Q38795106) (← links)
• Early signs of architectural and biomechanical failure in isolated myofibers and immortalized myoblasts from desmin-mutant knock-in mice (Q38806298) (← links)
• Prenatal diagnosis of congenital myopathies and muscular dystrophies. (Q38838661) (← links)
• Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue (Q39619930) (← links)
• Type III Intermediate Filaments Desmin, Glial Fibrillary Acidic Protein (GFAP), Vimentin, and Peripherin (Q47340446) (← links)
• Desmin, desminopathy and the complexity of genetics. (Q53297380) (← links)
• Molecular insights into cardiomyopathies associated with desmin (DES) mutations (Q57171610) (← links)
• Limb Girdle Muscular Dystrophy due to Digenic Inheritance of and Mutations (Q57493090) (← links)
• A novel phenotype with splicing mutation identified in a Chinese family with desminopathy (Q61804267) (← links)
• Recessive DES cardio/myopathy without myofibrillar aggregates: intronic splice variant silences one allele leaving only missense L190P-desmin (Q64039438) (← links)
• Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy. (Q64950195) (← links)
• Intermediate filaments in cardiomyopathy (Q90356556) (← links)
• AAV-mediated cardiac gene transfer of wild-type desmin in mouse models for recessive desminopathies (Q93163715) (← links)