Amyotrophic lateral sclerosis: Protein chaperone dysfunction revealed by proteomic studies of animal models
about
Redox regulation of T-cell function: from molecular mechanisms to significance in human health and diseaseAltered nucleocytoplasmic proteome and transcriptome distributions in an in vitro model of amyotrophic lateral sclerosisProteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model mice.Analysis of mutant SOD1 electrophoretic mobility by Blue Native gel electrophoresis; evidence for soluble multimeric assembliesA rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation.
P2860
Amyotrophic lateral sclerosis: Protein chaperone dysfunction revealed by proteomic studies of animal models
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on May 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Amyotrophic lateral sclerosis: ...... eomic studies of animal models
@en
Amyotrophic lateral sclerosis: ...... omic studies of animal models.
@nl
type
label
Amyotrophic lateral sclerosis: ...... eomic studies of animal models
@en
Amyotrophic lateral sclerosis: ...... omic studies of animal models.
@nl
prefLabel
Amyotrophic lateral sclerosis: ...... eomic studies of animal models
@en
Amyotrophic lateral sclerosis: ...... omic studies of animal models.
@nl
P2093
P2860
P356
P1476
Amyotrophic lateral sclerosis: ...... eomic studies of animal models
@en
P2093
Mohit Raja Jain
Stella Elkabes
Wei-Wen Ge
P2860
P304
P356
10.1002/PRCA.200780023
P577
2008-05-01T00:00:00Z