MSC p43 required for axonal development in motor neurons. - Wikidata - awgldk - TriplyDB

MSC p43 required for axonal development in motor neurons.

MSC p43 required for axonal development in motor neurons.

http://www.wikidata.org/entity/Q37354227

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Mutations in RARS cause hypomyelination Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration.Structure of the ArgRS-GlnRS-AIMP1 complex and its implications for mammalian translation.Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutation.New functions of aminoacyl-tRNA synthetases beyond translation.Misfolded human tRNA isodecoder binds and neutralizes a 3' UTR-embedded Alu element The N terminus of pro-endothelial monocyte-activating polypeptide II (EMAP II) regulates its binding with the C terminus, arginyl-tRNA synthetase, and neurofilament light protein.Large Conformational Changes of Insertion 3 in Human Glycyl-tRNA Synthetase (hGlyRS) during Catalysis.Essential nontranslational functions of tRNA synthetases.Neurofilamentopathy in neurodegenerative diseases Stepping Out of the Cytosol: AIMp1/p43 Potentiates the Link Between Innate and Adaptive Immunity.Hypomyelinating leukodystrophies - a molecular insight into the white matter pathology.Identification of a Vav2-dependent mechanism for GDNF/Ret control of mesolimbic DAT trafficking.Neurofilaments and Neurofilament Proteins in Health and Disease.AIMP1 deficiency presents as a cortical neurodegenerative disease with infantile onset.Multidirectional inhibition of cortico-hippocampal neurodegeneration by kolaviron treatment in rats.

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P2860

MSC p43 required for axonal development in motor neurons.

http://www.wikidata.org/entity/Q37354227

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 26 August 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

MSC p43 required for axonal development in motor neurons.

@en

MSC p43 required for axonal development in motor neurons.

@nl

type

label

MSC p43 required for axonal development in motor neurons.

@en

MSC p43 required for axonal development in motor neurons.

@nl

prefLabel

MSC p43 required for axonal development in motor neurons.

@en

MSC p43 required for axonal development in motor neurons.

@nl

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PNAS.0901872106

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Proceedings of the National Academy of Sciences of the United States of America

P1476

MSC p43 required for axonal development in motor neurons

@en

P2093

Aiyun Shao

http://www.w3.org/2001/XMLSchema#string

Bo Zhang

http://www.w3.org/2001/XMLSchema#string

Sunghoon Kim

http://www.w3.org/2001/XMLSchema#string

Xiaodong Zhu

http://www.w3.org/2001/XMLSchema#string

Yang Liu

http://www.w3.org/2001/XMLSchema#string

Yanqing Yin

http://www.w3.org/2001/XMLSchema#string

P2860

Association of beta-arrestin and TRAF6 negatively regulates Toll-like receptor-interleukin 1 receptor signaling

NF-M is an essential target for the myelin-directed "outside-in" signaling cascade that mediates radial axonal growth

Role of phosphorylation on the structural dynamics and function of types III and IV intermediate filaments

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene.

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy

Regulation of endothelial monocyte-activating polypeptide II release by apoptosis

Delayed maturation of regenerating myelinated axons in mice lacking neurofilaments

Heterodimeric associations between neuronal intermediate filament proteins

A NUDEL-dependent mechanism of neurofilament assembly regulates the integrity of CNS neurons

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15944-15949

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scholarly article

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10.1073/PNAS.0901872106

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106

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2009-08-26T00:00:00Z

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19717447

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2747223

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