Results 31 to 40 of about 6,058 (200)

Dynein Regulators Are Important for Ecotropic Murine Leukemia Virus Infection [PDF]

open access: yes, 2016
Indexación: Web of Science.During the early steps of infection, retroviruses must direct the movement of the viral genome into the nucleus to complete their replication cycle.
Arriagada, Gloria   +4 more
core   +1 more source

Lis1 is an initiation factor for dynein-driven organelle transport [PDF]

open access: yes, 2012
The molecular motor cytoplasmic dynein is responsible for most minus-end–directed, microtubule-based transport in eukaryotic cells. It is especially important in neurons, where defects in microtubule-based motility have been linked to neurological ...
Egan, Martin   +2 more
core   +1 more source

LIS1 regulates osteoclast formation and function through its interactions with dynein/dynactin and Plekhm1. [PDF]

open access: yesPLoS ONE, 2011
Microtubule organization and lysosomal secretion are both critical for the activation and function of osteoclasts, highly specialized polykaryons that are responsible for bone resorption and skeletal homeostasis.
Shiqiao Ye   +9 more
doaj   +1 more source

New insights into the mechanism of dynein motor regulation by lissencephaly-1

open access: yeseLife, 2020
Lissencephaly (‘smooth brain’) is a severe brain disease associated with numerous symptoms, including cognitive impairment, and shortened lifespan. The main causative gene of this disease – lissencephaly-1 (LIS1) – has been a focus of intense scrutiny ...
Steven M Markus   +2 more
doaj   +1 more source

Molecular and Genetic Determinants of Glioma Cell Invasion. [PDF]

open access: yes, 2017
A diffusely invasive nature is a major obstacle in treating a malignant brain tumor, "diffuse glioma", which prevents neurooncologists from surgically removing the tumor cells even in combination with chemotherapy and radiation.
Kato, Yoichiro   +4 more
core   +2 more sources

Lis1 controls dynamics of neuronal filopodia and spines to impact synaptogenesis and social behaviour

open access: yesEMBO Molecular Medicine, 2013
LIS1 (PAFAH1B1) mutation can impair neuronal migration, causing lissencephaly in humans. LIS1 loss is associated with dynein protein motor dysfunction, and disrupts the actin cytoskeleton through disregulated RhoGTPases.
Anamaria Sudarov   +4 more
doaj   +1 more source

A developmental and genetic classification for malformations of cortical development: update 2012. [PDF]

open access: yes, 2012
Malformations of cerebral cortical development include a wide range of developmental disorders that are common causes of neurodevelopmental delay and epilepsy. In addition, study of these disorders contributes greatly to the understanding of normal brain
Barkovich, A James   +4 more
core   +3 more sources

Regulation of Cytoplasmic Dynein ATPase by Lis1 [PDF]

open access: yesThe Journal of Neuroscience, 2006
Mutations in Lis1 cause classical lissencephaly, a developmental brain abnormality characterized by defects in neuronal positioning. Over the last decade, a clear link has been forged between Lis1 and the microtubule motor cytoplasmic dynein. Substantial evidence indicates that Lis1 functions in a highly conserved pathway with dynein to regulate ...
Mesngon, Mariano T.   +8 more
openaire   +3 more sources

Conserved roles for the dynein intermediate chain and Ndel1 in assembly and activation of dynein

open access: yesNature Communications, 2023
Processive transport by the microtubule motor cytoplasmic dynein requires the regulated assembly of a dynein-dynactin-adapter complex. Interactions between dynein and dynactin were initially ascribed to the dynein intermediate chain N-terminus and the ...
Kyoko Okada   +6 more
doaj   +1 more source

Abnormalities in Cortical GABAergic Interneurons of the Primary Motor Cortex Caused by Lis1 (Pafah1b1) Mutation Produce a Non-drastic Functional Phenotype

open access: yesFrontiers in Cell and Developmental Biology, 2022
LIS1 (PAFAH1B1) plays a major role in the developing cerebral cortex, and haploinsufficient mutations cause human lissencephaly type 1. We have studied morphological and functional properties of the cerebral cortex of mutant mice harboring a deletion in ...
E. Domínguez-Sala   +10 more
doaj   +1 more source

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