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Nebulin binding impedes mutant desmin filament assembly.Myofibrillar myopathies: new developments.Multiple sites in αB-crystallin modulate its interactions with desmin filaments assembled in vitro.Genetics of mechanosensation in the heart.Selective degradation of aggregate-prone CryAB mutants by HSPB1 is mediated by ubiquitin-proteasome pathwaysA novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies.Compound heterozygosity of predicted loss-of-function DES variants in a family with recessive desminopathyAbnormal accumulation of desmin in gastrocnemius myofibers of patients with peripheral artery disease: associations with altered myofiber morphology and density, mitochondrial dysfunction and impaired limb function.Desmin-related cardiomyopathy: an unfolding storyFilamin C: a novel component of the KCNE2 interactome during hypoxia.Right ventricular protein expression profile in end-stage heart failurePregnancy in Desmin-Related CardiomyopathyVoltage-Dependent Anion Channel 1(VDAC1) Participates the Apoptosis of the Mitochondrial Dysfunction in Desminopathy.Small heat shock proteins and α-crystallins: dynamic proteins with flexible functions.Desminopathies: pathology and mechanisms.Clinical and myopathological characteristics of desminopathy caused by a mutation in desmin tail domain.Heat shock proteins in the retina: Focus on HSP70 and alpha crystallins in ganglion cell survival.The Classification, Natural History and Treatment of the Limb Girdle Muscular DystrophiesDesmin-related myopathy.Desmin in muscle and associated diseases: beyond the structural function.Muscle creatine kinase deficiency triggers both actin depolymerization and desmin disorganization by advanced glycation end products in dilated cardiomyopathy.Role of sepsis in the development of limb muscle weakness in a porcine intensive care unit model.Phenotypic characterization of adenomyosis occurring at the inner and outer myometrium.Intermediate filaments and cellular mechanics.Gene and protein expressions of vimentin and desmin during embryonic development of the mylohyoid muscle.Cullin3-RING ubiquitin ligase activity is required for striated muscle function in mice.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Intermediate filament diseases: desminopathy.
@en
Intermediate filament diseases: desminopathy.
@nl
type
label
Intermediate filament diseases: desminopathy.
@en
Intermediate filament diseases: desminopathy.
@nl
prefLabel
Intermediate filament diseases: desminopathy.
@en
Intermediate filament diseases: desminopathy.
@nl
P2093
P2860
P1476
Intermediate filament diseases: desminopathy
@en
P2093
Hans H Goebel
Lev G Goldfarb
Patrick Vicart
P2860
P304
P356
10.1007/978-0-387-84847-1_11
P407
P50
P577
2008-01-01T00:00:00Z