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Li, V. ERCC3 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5407 (accessed on 21 September 2026).
Li V. ERCC3 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5407. Accessed September 21, 2026.
Li, Vivi. "ERCC3 Gene" Encyclopedia, https://encyclopedia.pub/entry/5407 (accessed September 21, 2026).
Li, V. (2020, December 24). ERCC3 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5407
Li, Vivi. "ERCC3 Gene." Encyclopedia. Web. 24 December, 2020.
ERCC3 Gene
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/ercc3

ERCC excision repair 3, TFIIH core complex helicase subunit

genes

References

  1. Coin F, Oksenych V, Egly JM. Distinct roles for the XPB/p52 and XPD/p44subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair.Mol Cell. 2007 Apr 27;26(2):245-56.
  2. Lambert WC, Gagna CE, Lambert MW. Xeroderma pigmentosum: its overlap withtrichothiodystrophy, Cockayne syndrome and other progeroid syndromes. Adv Exp MedBiol. 2008;637:128-37. Review.
  3. Oh KS, Imoto K, Boyle J, Khan SG, Kraemer KH. Influence of XPB helicase onrecruitment and redistribution of nucleotide excision repair proteins at sites ofUV-induced DNA damage. DNA Repair (Amst). 2007 Sep 1;6(9):1359-70.
  4. Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, EmmertS, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH. Phenotypicheterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum withoutand with Cockayne syndrome. Hum Mutat. 2006 Nov;27(11):1092-103.
  5. Oksenych V, Coin F. The long unwinding road: XPB and XPD helicases in damaged DNA opening. Cell Cycle. 2010 Jan 1;9(1):90-6.
  6. Riou L, Zeng L, Chevallier-Lagente O, Stary A, Nikaido O, Taïeb A, Weeda G,Mezzina M, Sarasin A. The relative expression of mutated XPB genes results inxeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellularphenotypes. Hum Mol Genet. 1999 Jun;8(6):1125-33.
  7. Weeda G, Eveno E, Donker I, Vermeulen W, Chevallier-Lagente O, Taïeb A, Stary A, Hoeijmakers JH, Mezzina M, Sarasin A. A mutation in the XPB/ERCC3 DNA repairtranscription gene, associated with trichothiodystrophy. Am J Hum Genet. 1997Feb;60(2):320-9.
  8. Weeda G, van Ham RC, Vermeulen W, Bootsma D, van der Eb AJ, Hoeijmakers JH. A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disordersxeroderma pigmentosum and Cockayne's syndrome. Cell. 1990 Aug 24;62(4):777-91.
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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: 651
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 24 Dec 2020
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