DYNC1H1 mutations associated with neurological diseases compromise processivity of dynein-dynactin-cargo adaptor complexes.
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Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features.Differential effects of the dynein-regulatory factor Lissencephaly-1 on processive dynein-dynactin motility.Cryo-EM Reveals How Human Cytoplasmic Dynein Is Auto-inhibited and ActivatedLissencephaly-1 is a context-dependent regulator of the human dynein complex.Disease-associated mutations in human BICD2 hyperactivate motility of dynein-dynactin.A novel mouse model carrying a human cytoplasmic dynein mutation shows motor behavior deficits consistent with Charcot-Marie-Tooth type 2O disease.Cryo-electron tomography reveals that dynactin recruits a team of dyneins for processive motility.A mathematical understanding of how cytoplasmic dynein walks on microtubules
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DYNC1H1 mutations associated with neurological diseases compromise processivity of dynein-dynactin-cargo adaptor complexes.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 14 February 2017
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
DYNC1H1 mutations associated w ...... actin-cargo adaptor complexes.
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DYNC1H1 mutations associated w ...... actin-cargo adaptor complexes.
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type
label
DYNC1H1 mutations associated w ...... actin-cargo adaptor complexes.
@en
DYNC1H1 mutations associated w ...... actin-cargo adaptor complexes.
@nl
prefLabel
DYNC1H1 mutations associated w ...... actin-cargo adaptor complexes.
@en
DYNC1H1 mutations associated w ...... actin-cargo adaptor complexes.
@nl
P2860
P356
P1476
DYNC1H1 mutations associated w ...... actin-cargo adaptor complexes.
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P2093
Ha Thi Hoang
Max A Schlager
P2860
P304
E1597-E1606
P356
10.1073/PNAS.1620141114
P407
P577
2017-02-14T00:00:00Z