These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
240 related articles for article (PubMed ID: 21560189)
1. Severity of vanishing white matter disease does not correlate with deficits in eIF2B activity or the integrity of eIF2B complexes. Liu R; van der Lei HD; Wang X; Wortham NC; Tang H; van Berkel CG; Mufunde TA; Huang W; van der Knaap MS; Scheper GC; Proud CG Hum Mutat; 2011 Sep; 32(9):1036-45. PubMed ID: 21560189 [TBL] [Abstract][Full Text] [Related]
2. Biochemical effects of mutations in the gene encoding the alpha subunit of eukaryotic initiation factor (eIF) 2B associated with Vanishing White Matter disease. Wortham NC; Proud CG BMC Med Genet; 2015 Aug; 16():64. PubMed ID: 26285592 [TBL] [Abstract][Full Text] [Related]
3. A yeast purification system for human translation initiation factors eIF2 and eIF2Bε and their use in the diagnosis of CACH/VWM disease. de Almeida RA; Fogli A; Gaillard M; Scheper GC; Boesflug-Tanguy O; Pavitt GD PLoS One; 2013; 8(1):e53958. PubMed ID: 23335982 [TBL] [Abstract][Full Text] [Related]
4. eIF2B: recent structural and functional insights into a key regulator of translation. Wortham NC; Proud CG Biochem Soc Trans; 2015 Dec; 43(6):1234-40. PubMed ID: 26614666 [TBL] [Abstract][Full Text] [Related]
5. Analysis of the subunit organization of the eIF2B complex reveals new insights into its structure and regulation. Wortham NC; Martinez M; Gordiyenko Y; Robinson CV; Proud CG FASEB J; 2014 May; 28(5):2225-37. PubMed ID: 24532666 [TBL] [Abstract][Full Text] [Related]
6. Mutations linked to leukoencephalopathy with vanishing white matter impair the function of the eukaryotic initiation factor 2B complex in diverse ways. Li W; Wang X; Van Der Knaap MS; Proud CG Mol Cell Biol; 2004 Apr; 24(8):3295-306. PubMed ID: 15060152 [TBL] [Abstract][Full Text] [Related]
7. The beta/Gcd7 subunit of eukaryotic translation initiation factor 2B (eIF2B), a guanine nucleotide exchange factor, is crucial for binding eIF2 in vivo. Dev K; Qiu H; Dong J; Zhang F; Barthlme D; Hinnebusch AG Mol Cell Biol; 2010 Nov; 30(21):5218-33. PubMed ID: 20805354 [TBL] [Abstract][Full Text] [Related]
8. Mutations causing childhood ataxia with central nervous system hypomyelination reduce eukaryotic initiation factor 2B complex formation and activity. Richardson JP; Mohammad SS; Pavitt GD Mol Cell Biol; 2004 Mar; 24(6):2352-63. PubMed ID: 14993275 [TBL] [Abstract][Full Text] [Related]
9. [Eukaryotic translation initiation factor 2B and leukoencephalopathy with vanishing white matter]. Pan YX; Wu Y; Niu ZP; Jiang YW Beijing Da Xue Xue Bao Yi Xue Ban; 2009 Oct; 41(5):608-10. PubMed ID: 19829687 [TBL] [Abstract][Full Text] [Related]
10. Vanishing white matter: Eukaryotic initiation factor 2B model and the impact of missense mutations. Slynko I; Nguyen S; Hamilton EMC; Wisse LE; de Esch IJP; de Graaf C; Bruning JB; Proud CG; Abbink TEM; van der Knaap MS Mol Genet Genomic Med; 2021 Mar; 9(3):e1593. PubMed ID: 33432707 [TBL] [Abstract][Full Text] [Related]
11. The large spectrum of eIF2B-related diseases. Fogli A; Boespflug-Tanguy O Biochem Soc Trans; 2006 Feb; 34(Pt 1):22-9. PubMed ID: 16246171 [TBL] [Abstract][Full Text] [Related]
12. Human-induced pluripotent stem cell-derived cerebral organoid of leukoencephalopathy with vanishing white matter. Deng J; Zhang J; Gao K; Zhou L; Jiang Y; Wang J; Wu Y CNS Neurosci Ther; 2023 Apr; 29(4):1049-1066. PubMed ID: 36650674 [TBL] [Abstract][Full Text] [Related]
13. The small molecule ISRIB rescues the stability and activity of Vanishing White Matter Disease eIF2B mutant complexes. Wong YL; LeBon L; Edalji R; Lim HB; Sun C; Sidrauski C Elife; 2018 Feb; 7():. PubMed ID: 29489452 [TBL] [Abstract][Full Text] [Related]
15. A new function and complexity for protein translation initiation factor eIF2B. Jennings MD; Pavitt GD Cell Cycle; 2014; 13(17):2660-5. PubMed ID: 25486352 [TBL] [Abstract][Full Text] [Related]
16. Vanishing white matter: deregulated integrated stress response as therapy target. Abbink TEM; Wisse LE; Jaku E; Thiecke MJ; Voltolini-González D; Fritsen H; Bobeldijk S; Ter Braak TJ; Polder E; Postma NL; Bugiani M; Struijs EA; Verheijen M; Straat N; van der Sluis S; Thomas AAM; Molenaar D; van der Knaap MS Ann Clin Transl Neurol; 2019 Aug; 6(8):1407-1422. PubMed ID: 31402619 [TBL] [Abstract][Full Text] [Related]
17. Paradoxical Sensitivity to an Integrated Stress Response Blocking Mutation in Vanishing White Matter Cells. Sekine Y; Zyryanova A; Crespillo-Casado A; Amin-Wetzel N; Harding HP; Ron D PLoS One; 2016; 11(11):e0166278. PubMed ID: 27812215 [TBL] [Abstract][Full Text] [Related]
18. Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease. Wu Y; Pan Y; Du L; Wang J; Gu Q; Gao Z; Li J; Leng X; Qin J; Wu X; Jiang Y J Hum Genet; 2009 Feb; 54(2):74-7. PubMed ID: 19158808 [TBL] [Abstract][Full Text] [Related]
19. Glial pathology in a novel spontaneous mutant mouse of the Eif2b5 gene: a vanishing white matter disease model. Terumitsu-Tsujita M; Kitaura H; Miura I; Kiyama Y; Goto F; Muraki Y; Ominato S; Hara N; Simankova A; Bizen N; Kashiwagi K; Ito T; Toyoshima Y; Kakita A; Manabe T; Wakana S; Takebayashi H; Igarashi H J Neurochem; 2020 Jul; 154(1):25-40. PubMed ID: 31587290 [TBL] [Abstract][Full Text] [Related]
20. [Three-dimensional Structure of eIF2B: A Clue to Understanding the Pathogenesis of CACH/VWM Disease]. Kashiwagi K; Ito T; Yokoyama S Brain Nerve; 2017 Jan; 69(1):45-50. PubMed ID: 28126977 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]