Pages that link to "Q82973787"

The following pages link to Mutations in desmin's carboxy-terminal "tail" domain severely modify filament and network mechanics (Q82973787):

Displaying 22 items.

• Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants (Q24627911) (← links)
• Intermediate Filaments Play a Pivotal Role in Regulating Cell Architecture and Function (Q26865818) (← links)
• Intermediate filament mechanics in vitro and in the cell: from coiled coils to filaments, fibers and networks (Q27004169) (← links)
• Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect (Q28115277) (← links)
• Nebulin binding impedes mutant desmin filament assembly (Q30540621) (← links)
• Nebulette is a powerful cytolinker organizing desmin and actin in mouse hearts (Q30832463) (← links)
• αB-crystallin is a sensor for assembly intermediates and for the subunit topology of desmin intermediate filaments. (Q33779909) (← links)
• Alexander disease causing mutations in the C-terminal domain of GFAP are deleterious both to assembly and network formation with the potential to both activate caspase 3 and decrease cell viability (Q34200416) (← links)
• Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy. (Q34505071) (← links)
• Attractive interactions among intermediate filaments determine network mechanics in vitro (Q35137290) (← links)
• The desmin coil 1B mutation K190A impairs nebulin Z-disc assembly and destabilizes actin thin filaments (Q35388987) (← links)
• The tail domain is essential but the head domain dispensable for C. elegans intermediate filament IFA-2 function (Q35572357) (← links)
• Properties of intermediate filament networks assembled from keratin 8 and 18 in the presence of Mg²+ (Q36110886) (← links)
• Desminopathies: pathology and mechanisms (Q36503373) (← links)
• Clinical and myopathological characteristics of desminopathy caused by a mutation in desmin tail domain (Q36553090) (← links)
• Myofibrillar myopathies (Q37260231) (← links)
• Posttranslational modifications of desmin and their implication in biological processes and pathologies (Q38148976) (← links)
• Desmin Mutation in the C-Terminal Domain Impairs Traction Force Generation in Myoblasts (Q38801420) (← links)
• Intermediate Filaments: Structure and Assembly (Q38996176) (← links)
• The domain organization of the bacterial intermediate filament-like protein crescentin is important for assembly and function (Q41874929) (← links)
• Deconstructing the late phase of vimentin assembly by total internal reflection fluorescence microscopy (TIRFM). (Q42721112) (← links)
• Molecular insights into cardiomyopathies associated with desmin (DES) mutations (Q57171610) (← links)