eIF2γ mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiation.
about
Pharmacological brake-release of mRNA translation enhances cognitive memoryeIF2B is a decameric guanine nucleotide exchange factor with a γ2ε2 tetrameric core.Translation initiation requires cell division cycle 123 (Cdc123) to facilitate biogenesis of the eukaryotic initiation factor 2 (eIF2).Prioritizing genes for X-linked diseases using population exome data.BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomalies.Pharmacological dimerization and activation of the exchange factor eIF2B antagonizes the integrated stress response.Increased high-density lipoprotein cholesterol levels in mice with XX versus XY sex chromosomes.Mechanism and Regulation of Protein Synthesis in Saccharomyces cerevisiae.De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation.ProNGF Drives Localized and Cell Selective Parvalbumin Interneuron and Perineuronal Net Depletion in the Dentate Gyrus of Transgenic MiceMolecular Determinants of the Regulation of Development and Metabolism by Neuronal eIF2α Phosphorylation in Caenorhabditis elegans.eIF2β is critical for eIF5-mediated GDP-dissociation inhibitor activity and translational control.Endoplasmic reticulum stress and eIF2α phosphorylation: The Achilles heel of pancreatic β cells.EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO.Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy.EIF2B2 mutations in Vanishing White Matter Disease hyper- suppress translation and delay recovery during the integrated stress response.Review of X-linked syndromes with arthrogryposis or early contractures-aid to diagnosis and pathway identification.Analysis of eIF2B bodies and their relationships with stress granules and P-bodies
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P2860
eIF2γ mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiation.
description
2012 nî lūn-bûn
@nan
2012 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
eIF2γ mutation that disrupts e ...... paired translation initiation.
@ast
eIF2γ mutation that disrupts e ...... paired translation initiation.
@en
eIF2γ mutation that disrupts e ...... paired translation initiation.
@nl
type
label
eIF2γ mutation that disrupts e ...... paired translation initiation.
@ast
eIF2γ mutation that disrupts e ...... paired translation initiation.
@en
eIF2γ mutation that disrupts e ...... paired translation initiation.
@nl
prefLabel
eIF2γ mutation that disrupts e ...... paired translation initiation.
@ast
eIF2γ mutation that disrupts e ...... paired translation initiation.
@en
eIF2γ mutation that disrupts e ...... paired translation initiation.
@nl
P2093
P2860
P50
P921
P3181
P1433
P1476
eIF2γ mutation that disrupts e ...... paired translation initiation.
@en
P2093
Adi Har-Zahav
Aviva Mimouni-Bloch
Barbara Stiller
Byung-Sik Shin
Charles E Schwartz
Cindy Skinner
Doron Gothelf
Guntram Borck
Holger Thiele
Joo-Ran Kim
P2860
P3181
P356
10.1016/J.MOLCEL.2012.09.005
P407
P50
P5008
P577
2012-11-30T00:00:00Z