EIF2B4
EIF2B4 (Eukaryotic translation initiation factor 2B subunit delta) هوَ بروتين يُشَفر بواسطة جين EIF2B4 في الإنسان.[1][2][3]
المراجع
- "Entrez Gene: EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa"، مؤرشف من الأصل في 7 مارس 2010.
- "The delta-subunit of murine guanine nucleotide exchange factor eIF-2B. Characterization of cDNAs predicts isoforms differing at the amino-terminal end"، J. Biol. Chem.، 269 (48): 30517–23، ديسمبر 1994، PMID 7982969.
- "eIF2B, the guanine nucleotide-exchange factor for eukaryotic initiation factor 2. Sequence conservation between the alpha, beta and delta subunits of eIF2B from mammals and yeast"، Biochem. J.، 318 (2): 637–43، نوفمبر 1996، PMC 1217679، PMID 8929216.
قراءة متعمقة
- "T-cell activation leads to rapid stimulation of translation initiation factor eIF2B and inactivation of glycogen synthase kinase-3."، J. Biol. Chem.، 271 (19): 11410–3، 1996، doi:10.1074/jbc.271.19.11410، PMID 8626696.
- "Identification of a regulatory subcomplex in the guanine nucleotide exchange factor eIF2B that mediates inhibition by phosphorylated eIF2."، Mol. Cell. Biol.، 16 (11): 6603–16، 1996، PMC 231662، PMID 8887689.
- "Identification of interprotein interactions between the subunits of eukaryotic initiation factors eIF2 and eIF2B."، J. Biol. Chem.، 273 (5): 3039–44، 1998، doi:10.1074/jbc.273.5.3039، PMID 9446619.
- "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."، Mol. Cell. Biol.، 20 (11): 3965–76، 2000، doi:10.1128/MCB.20.11.3965-3976.2000، PMC 85753، PMID 10805739.
- "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."، Biochim. Biophys. Acta، 1492 (1): 56–62، 2000، doi:10.1016/S0167-4781(00)00062-2، PMID 10858531.
- "Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning."، Proc. Natl. Acad. Sci. U.S.A.، 97 (17): 9543–8، 2000، doi:10.1073/pnas.160270997، PMC 16901، PMID 10931946.
- "Characterization of the mammalian initiation factor eIF2B complex as a GDP dissociation stimulator protein."، J. Biol. Chem.، 276 (27): 24697–703، 2001، doi:10.1074/jbc.M011788200، PMID 11323413.
- "Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter."، Ann. Neurol.، 51 (2): 264–70، 2002، doi:10.1002/ana.10112، PMID 11835386.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences."، Proc. Natl. Acad. Sci. U.S.A.، 99 (26): 16899–903، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation."، Neurology، 59 (12): 1966–8، 2003، doi:10.1212/01.wnl.0000041666.76863.47، PMID 12499492.
- "Reduced amino acid availability inhibits muscle protein synthesis and decreases activity of initiation factor eIF2B."، Am. J. Physiol. Endocrinol. Metab.، 284 (3): E488–98، 2003، doi:10.1152/ajpendo.00094.2002، PMID 12556349.
- "Ovarian failure related to eukaryotic initiation factor 2B mutations."، Am. J. Hum. Genet.، 72 (6): 1544–50، 2003، doi:10.1086/375404، PMC 1180314، PMID 12707859.
- "eIF2B-related disorders: antenatal onset and involvement of multiple organs."، Am. J. Hum. Genet.، 73 (5): 1199–207، 2004، doi:10.1086/379524، PMC 1180499، PMID 14566705.
- "Decreased guanine nucleotide exchange factor activity in eIF2B-mutated patients."، Eur. J. Hum. Genet.، 12 (7): 561–6، 2005، doi:10.1038/sj.ejhg.5201189، PMID 15054402.
- "Mutations linked to leukoencephalopathy with vanishing white matter impair the function of the eukaryotic initiation factor 2B complex in diverse ways."، Mol. Cell. Biol.، 24 (8): 3295–306، 2004، doi:10.1128/MCB.24.8.3295-3306.2004، PMC 381664، PMID 15060152.
- "The life and death of oligodendrocytes in vanishing white matter disease."، J. Neuropathol. Exp. Neurol.، 63 (6): 618–30، 2004، PMID 15217090.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."، Genome Res.، 14 (10B): 2121–7، 2004، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- "Screening for known mutations in EIF2B genes in a large panel of patients with premature ovarian failure."، BMC Women's Health، 4 (1): 8، 2004، doi:10.1186/1472-6874-4-8، PMC 529454، PMID 15507143.
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- بوابة الكيمياء الحيوية
- بوابة علم الأحياء الخلوي والجزيئي
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