EIF2B5

An Error has occured retrieving Wikidata item for infobox EIF2B5‏ (Eukaryotic translation initiation factor 2B subunit epsilon) هوَ بروتين يُشَفر بواسطة جين EIF2B5 في الإنسان.

قراءة متعمقة

• Leegwater PA، Pronk JC، van der Knaap MS (سبتمبر 2003). "Leukoencephalopathy with vanishing white matter: from magnetic resonance imaging pattern to five genes". Journal of Child Neurology. ج. 18 ع. 9: 639–45. DOI:10.1177/08830738030180091101. PMID:14572143.
• Chaudhri MA، Crawford AC (1991). "Carbon determination in human teeth by activation with He-3 ions". Biological Trace Element Research. 26–27: 521–7. DOI:10.1007/BF02992708. PMID:1704758.
• Welsh GI، Miyamoto S، Price NT، Safer B، Proud CG (مايو 1996). "T-cell activation leads to rapid stimulation of translation initiation factor eIF2B and inactivation of glycogen synthase kinase-3". The Journal of Biological Chemistry. ج. 271 ع. 19: 11410–3. DOI:10.1074/jbc.271.19.11410. PMID:8626696.
• Kimball SR، Heinzinger NK، Horetsky RL، Jefferson LS (يناير 1998). "Identification of interprotein interactions between the subunits of eukaryotic initiation factors eIF2 and eIF2B". The Journal of Biological Chemistry. ج. 273 ع. 5: 3039–44. DOI:10.1074/jbc.273.5.3039. PMID:9446619.
• Welsh GI، Miller CM، Loughlin AJ، Price NT، Proud CG (يناير 1998). "Regulation of eukaryotic initiation factor eIF2B: glycogen synthase kinase-3 phosphorylates a conserved serine which undergoes dephosphorylation in response to insulin". FEBS Letters. ج. 421 ع. 2: 125–30. DOI:10.1016/S0014-5793(97)01548-2. PMID:9468292.
• Leegwater PA، Könst AA، Kuyt B، Sandkuijl LA، Naidu S، Oudejans CB، Schutgens RB، Pronk JC، van der Knaap MS (سبتمبر 1999). "The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27". American Journal of Human Genetics. ج. 65 ع. 3: 728–34. DOI:10.1086/302548. PMC:1377979. PMID:10441579.
• Gomez E، Pavitt GD (يونيو 2000). "Identification of domains and residues within the epsilon subunit of eukaryotic translation initiation factor 2B (eIF2Bepsilon) required for guanine nucleotide exchange reveals a novel activation function promoted by eIF2B complex formation". Molecular and Cellular Biology. ج. 20 ع. 11: 3965–76. DOI:10.1128/MCB.20.11.3965-3976.2000. PMC:85753. PMID:10805739.
• Anthony TG، Fabian JR، Kimball SR، Jefferson LS (يونيو 2000). "Identification of domains within the epsilon-subunit of the translation initiation factor eIF2B that are necessary for guanine nucleotide exchange activity and eIF2B holoprotein formation". Biochimica et Biophysica Acta. ج. 1492 ع. 1: 56–62. DOI:10.1016/S0167-4781(00)00062-2. PMID:10858531.
• Williams DD، Price NT، Loughlin AJ، Proud CG (يوليو 2001). "Characterization of the mammalian initiation factor eIF2B complex as a GDP dissociation stimulator protein". The Journal of Biological Chemistry. ج. 276 ع. 27: 24697–703. DOI:10.1074/jbc.M011788200. PMID:11323413.
• Wang X، Paulin FE، Campbell LE، Gomez E، O'Brien K، Morrice N، Proud CG (أغسطس 2001). "Eukaryotic initiation factor 2B: identification of multiple phosphorylation sites in the epsilon-subunit and their functions in vivo". The EMBO Journal. ج. 20 ع. 16: 4349–59. DOI:10.1093/emboj/20.16.4349. PMC:125262. PMID:11500362.
• Leegwater PA، Vermeulen G، Könst AA، Naidu S، Mulders J، Visser A، Kersbergen P، Mobach D، Fonds D، van Berkel CG، Lemmers RJ، Frants RR، Oudejans CB، Schutgens RB، Pronk JC، van der Knaap MS (ديسمبر 2001). "Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter". Nature Genetics. ج. 29 ع. 4: 383–8. DOI:10.1038/ng764. PMID:11704758.
• Wang X، Janmaat M، Beugnet A، Paulin FE، Proud CG (أكتوبر 2002). "Evidence that the dephosphorylation of Ser(535) in the epsilon-subunit of eukaryotic initiation factor (eIF) 2B is insufficient for the activation of eIF2B by insulin". The Biochemical Journal. ج. 367 ع. Pt 2: 475–81. DOI:10.1042/BJ20020677. PMC:1222905. PMID:12133000.
• Fogli A، Wong K، Eymard-Pierre E، Wenger J، Bouffard JP، Goldin E، Black DN، Boespflug-Tanguy O، Schiffmann R (أكتوبر 2002). "Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus". Annals of Neurology. ج. 52 ع. 4: 506–10. DOI:10.1002/ana.10339. PMID:12325082.
• Fogli A، Dionisi-Vici C، Deodato F، Bartuli A، Boespflug-Tanguy O، Bertini E (ديسمبر 2002). "A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation". Neurology. ج. 59 ع. 12: 1966–8. DOI:10.1212/01.wnl.0000041666.76863.47. PMID:12499492.
• Fogli A، Rodriguez D، Eymard-Pierre E، Bouhour F، Labauge P، Meaney BF، Zeesman S، Kaneski CR، Schiffmann R، Boespflug-Tanguy O (يونيو 2003). "Ovarian failure related to eukaryotic initiation factor 2B mutations". American Journal of Human Genetics. ج. 72 ع. 6: 1544–50. DOI:10.1086/375404. PMC:1180314. PMID:12707859.
• van der Knaap MS، van Berkel CG، Herms J، van Coster R، Baethmann M، Naidu S، Boltshauser E، Willemsen MA، Plecko B، Hoffmann GF، Proud CG، Scheper GC، Pronk JC (نوفمبر 2003). "eIF2B-related disorders: antenatal onset and involvement of multiple organs". American Journal of Human Genetics. ج. 73 ع. 5: 1199–207. DOI:10.1086/379524. PMC:1180499. PMID:14566705.