A point mutation in translation initiation factor eIF2B leads to function--and time-specific changes in brain gene expression.
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Astrocytes are central in the pathomechanisms of vanishing white matterDevelopmental splicing deregulation in leukodystrophies related to EIF2B mutationsProteomics-level analysis of myelin formation and regeneration in a mouse model for Vanishing White Matter disease.Mutant eIF2B leads to impaired mitochondrial oxidative phosphorylation in vanishing white matter disease.Endoplasmic Reticulum Protein Quality Control Failure in Myelin Disorders.Drug Screening Identifies Sigma-1-Receptor as a Target for the Therapy of VWM Leukodystrophy
P2860
A point mutation in translation initiation factor eIF2B leads to function--and time-specific changes in brain gene expression.
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2011 nî lūn-bûn
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2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հոտեմբերին հրատարակված գիտական հոդված
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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name
A point mutation in translatio ...... nges in brain gene expression.
@ast
A point mutation in translatio ...... nges in brain gene expression.
@en
A point mutation in translatio ...... nges in brain gene expression.
@nl
type
label
A point mutation in translatio ...... nges in brain gene expression.
@ast
A point mutation in translatio ...... nges in brain gene expression.
@en
A point mutation in translatio ...... nges in brain gene expression.
@nl
prefLabel
A point mutation in translatio ...... nges in brain gene expression.
@ast
A point mutation in translatio ...... nges in brain gene expression.
@en
A point mutation in translatio ...... nges in brain gene expression.
@nl
P2093
P2860
P1433
P1476
A point mutation in translatio ...... nges in brain gene expression.
@en
P2093
Liraz Marom
Ron Shamir
Yuval Cabilly
P2860
P304
P356
10.1371/JOURNAL.PONE.0026992
P407
P577
2011-10-31T00:00:00Z