about
Exploitation of KESTREL to identify NDRG family members as physiological substrates for SGK1 and GSK3A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth diseaseDysfunctions of neuronal and glial intermediate filaments in diseaseTracing myelin protein zero (P0) in vivo by construction of P0-GFP fusion proteinsNeuropathic pain in hereditary peripheral neuropathyZebrafish as a Model to Investigate Dynamin 2-Related Diseases.The tetraspan protein EMP2 modulates the surface expression of caveolins and glycosylphosphatidyl inositol-linked proteinsNdrg1-deficient mice exhibit a progressive demyelinating disorder of peripheral nervesProteomics of bovine myelin sheath: characterization of a truncated form of P0 by MALDI-TOF/TOF mass spectrometry.A genome-wide siRNA screen reveals diverse cellular processes and pathways that mediate genome stability.Rapid genetic screening of Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies patientsUnderstanding Schwann cell-neurone interactions: the key to Charcot-Marie-Tooth disease?Locus-wide identification of Egr2/Krox20 regulatory targets in myelin genesImplications of mitochondrial dynamics on neurodegeneration and on hypothalamic dysfunction.Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease.Membrane association of myotubularin-related protein 2 is mediated by a pleckstrin homology-GRAM domain and a coiled-coil dimerization moduleHereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population.Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.Charcot-marie-tooth disease: seventeen causative genes.HoxB2 binds mutant SOD1 and is altered in transgenic model of ALS.Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A).LITAF (SIMPLE) regulates Wallerian degeneration after injury but is not essential for peripheral nerve development and maintenance: implications for Charcot-Marie-Tooth disease.Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մարտին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Molecular cell biology of Charcot-Marie-Tooth disease.
@ast
Molecular cell biology of Charcot-Marie-Tooth disease.
@en
Molecular cell biology of Charcot-Marie-Tooth disease.
@nl
type
label
Molecular cell biology of Charcot-Marie-Tooth disease.
@ast
Molecular cell biology of Charcot-Marie-Tooth disease.
@en
Molecular cell biology of Charcot-Marie-Tooth disease.
@nl
prefLabel
Molecular cell biology of Charcot-Marie-Tooth disease.
@ast
Molecular cell biology of Charcot-Marie-Tooth disease.
@en
Molecular cell biology of Charcot-Marie-Tooth disease.
@nl
P1433
P1476
Molecular cell biology of Charcot-Marie-Tooth disease
@en
P2093
Peter Young
Ueli Suter
P2888
P356
10.1007/S10048-002-0130-Z
P577
2002-03-01T00:00:00Z