Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.

Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.

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http://www.wikidata.org/entity/Q37107108
In vivo cell biology in zebrafish - providing insights into vertebrate development and disease.Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegenerationAtomic-resolution structure of the CAP-Gly domain of dynactin on polymeric microtubules determined by magic angle spinning NMR spectroscopy.A novel DYNC1H1 mutation causing spinal muscular atrophy with lower extremity predominance.Dynein disruption perturbs post-synaptic components and contributes to impaired MuSK clustering at the NMJ: implication in ALS.Cytoplasmic dynein heavy chain: the servant of many mastersDYNC1H1 mutations associated with neurological diseases compromise processivity of dynein-dynactin-cargo adaptor complexes.Mitochondrial implications in bulbospinal muscular atrophy (Kennedy disease).GSK-3β Phosphorylation of Cytoplasmic Dynein Reduces Ndel1 Binding to Intermediate Chains and Alters Dynein MotilityMorphological changes and altered expression of antioxidant proteins in a heterozygous dynein mutant; a mouse model of spinal muscular atrophy.A quadratically regularized functional canonical correlation analysis for identifying the global structure of pleiotropy with NGS data.Role of Dynein Axonemal Heavy Chain 6 Gene Expression as a Possible Biomarker for Huntington's Disease: a Translational Study.Exome Sequencing Identifies De Novo DYNC1H1 Mutations Associated With Distal Spinal Muscular Atrophy and Malformations of Cortical Development.Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth Disease.Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders.
P2860

Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.

Item
http://www.wikidata.org/entity/Q37107108
description
article científic
@ca
article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
@tr
scientific article published on 04 June 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Dynein mutations associated wi ...... phology and function with age.
@en
Dynein mutations associated wi ...... phology and function with age.
@nl
type
label
Dynein mutations associated wi ...... phology and function with age.
@en
Dynein mutations associated wi ...... phology and function with age.
@nl
prefLabel
Dynein mutations associated wi ...... phology and function with age.
@en
Dynein mutations associated wi ...... phology and function with age.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P478
P50
P577
P698
P921
P932
P356
P1433
P1476
Dynein mutations associated wi ...... phology and function with age.
@en
P2093
P2860
P304
P31
P356
P478
P50
P577
P698
P921
P932