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Li, V. EIF2B5 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5322 (accessed on 21 September 2026).
Li V. EIF2B5 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5322. Accessed September 21, 2026.
Li, Vivi. "EIF2B5 Gene" Encyclopedia, https://encyclopedia.pub/entry/5322 (accessed September 21, 2026).
Li, V. (2020, December 24). EIF2B5 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5322
Li, Vivi. "EIF2B5 Gene." Encyclopedia. Web. 24 December, 2020.
EIF2B5 Gene
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/eif2b5

Eukaryotic translation initiation factor 2B subunit epsilon

genes

References

  1. Dietrich J, Lacagnina M, Gass D, Richfield E, Mayer-Pröschel M, Noble M,Torres C, Pröschel C. EIF2B5 mutations compromise GFAP+ astrocyte generation invanishing white matter leukodystrophy. Nat Med. 2005 Mar;11(3):277-83.
  2. Eurekah Bioscience: Mechanism of Translation Initiation in Eukaryotes
  3. Fogli A, Boespflug-Tanguy O. The large spectrum of eIF2B-related diseases.Biochem Soc Trans. 2006 Feb;34(Pt 1):22-9. Review.
  4. Fogli A, Schiffmann R, Hugendubler L, Combes P, Bertini E, Rodriguez D,Kimball SR, Boespflug-Tanguy O. Decreased guanine nucleotide exchange factoractivity in eIF2B-mutated patients. Eur J Hum Genet. 2004 Jul;12(7):561-6.
  5. Li W, Wang X, Van Der Knaap MS, Proud CG. Mutations linked toleukoencephalopathy with vanishing white matter impair the function of theeukaryotic initiation factor 2B complex in diverse ways. Mol Cell Biol. 2004Apr;24(8):3295-306.
  6. Molecular Biology of the Cell (fourth edition, 2002): The Phosphorylation of an Initiation Factor Globally Regulates Protein Synthesis
  7. Pavitt GD. eIF2B, a mediator of general and gene-specific translationalcontrol. Biochem Soc Trans. 2005 Dec;33(Pt 6):1487-92. Review.
  8. Pronk JC, van Kollenburg B, Scheper GC, van der Knaap MS. Vanishing whitematter disease: a review with focus on its genetics. Ment Retard Dev Disabil Res Rev. 2006;12(2):123-8. Review.
  9. Scali O, Di Perri C, Federico A. The spectrum of mutations for the diagnosisof vanishing white matter disease. Neurol Sci. 2006 Sep;27(4):271-7. Review.
  10. Scheper GC, Proud CG, van der Knaap MS. Defective translation initiationcauses vanishing of cerebral white matter. Trends Mol Med. 2006 Apr;12(4):159-66.
  11. van der Voorn JP, van Kollenburg B, Bertrand G, Van Haren K, Scheper GC,Powers JM, van der Knaap MS. The unfolded protein response in vanishing whitematter disease. J Neuropathol Exp Neurol. 2005 Sep;64(9):770-5.
  12. van Kollenburg B, van Dijk J, Garbern J, Thomas AA, Scheper GC, Powers JM, vander Knaap MS. Glia-specific activation of all pathways of the unfolded proteinresponse in vanishing white matter disease. J Neuropathol Exp Neurol. 2006Jul;65(7):707-15.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Vivi Li
View Times: 622
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 24 Dec 2020
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