193 related articles for article (PubMed ID: 14993263)
1. Deficiency in the nuclease activity of xeroderma pigmentosum G in mice leads to hypersensitivity to UV irradiation.
Tian M; Jones DA; Smith M; Shinkura R; Alt FW
Mol Cell Biol; 2004 Mar; 24(6):2237-42. PubMed ID: 14993263
[TBL] [Abstract][Full Text] [Related]
2. Human XPG nuclease structure, assembly, and activities with insights for neurodegeneration and cancer from pathogenic mutations.
Tsutakawa SE; Sarker AH; Ng C; Arvai AS; Shin DS; Shih B; Jiang S; Thwin AC; Tsai MS; Willcox A; Her MZ; Trego KS; Raetz AG; Rosenberg D; Bacolla A; Hammel M; Griffith JD; Cooper PK; Tainer JA
Proc Natl Acad Sci U S A; 2020 Jun; 117(25):14127-14138. PubMed ID: 32522879
[TBL] [Abstract][Full Text] [Related]
3. Suppression of UV-induced apoptosis by the human DNA repair protein XPG.
Clément V; Dunand-Sauthier I; Clarkson SG
Cell Death Differ; 2006 Mar; 13(3):478-88. PubMed ID: 16167068
[TBL] [Abstract][Full Text] [Related]
4. Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene.
Harada YN; Shiomi N; Koike M; Ikawa M; Okabe M; Hirota S; Kitamura Y; Kitagawa M; Matsunaga T; Nikaido O; Shiomi T
Mol Cell Biol; 1999 Mar; 19(3):2366-72. PubMed ID: 10022922
[TBL] [Abstract][Full Text] [Related]
5. Growth retardation, early death, and DNA repair defects in mice deficient for the nucleotide excision repair enzyme XPF.
Tian M; Shinkura R; Shinkura N; Alt FW
Mol Cell Biol; 2004 Feb; 24(3):1200-5. PubMed ID: 14729965
[TBL] [Abstract][Full Text] [Related]
6. Severe growth retardation and short life span of double-mutant mice lacking Xpa and exon 15 of Xpg.
Shiomi N; Mori M; Kito S; Harada YN; Tanaka K; Shiomi T
DNA Repair (Amst); 2005 Mar; 4(3):351-7. PubMed ID: 15661658
[TBL] [Abstract][Full Text] [Related]
7. Conserved residues of human XPG protein important for nuclease activity and function in nucleotide excision repair.
Constantinou A; Gunz D; Evans E; Lalle P; Bates PA; Wood RD; Clarkson SG
J Biol Chem; 1999 Feb; 274(9):5637-48. PubMed ID: 10026181
[TBL] [Abstract][Full Text] [Related]
8. Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient.
Nouspikel T; Clarkson SG
Hum Mol Genet; 1994 Jun; 3(6):963-7. PubMed ID: 7951246
[TBL] [Abstract][Full Text] [Related]
9. The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity.
Lalle P; Nouspikel T; Constantinou A; Thorel F; Clarkson SG
J Invest Dermatol; 2002 Feb; 118(2):344-51. PubMed ID: 11841555
[TBL] [Abstract][Full Text] [Related]
10. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function.
Nouspikel T; Lalle P; Leadon SA; Cooper PK; Clarkson SG
Proc Natl Acad Sci U S A; 1997 Apr; 94(7):3116-21. PubMed ID: 9096355
[TBL] [Abstract][Full Text] [Related]
11. Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency.
Barnhoorn S; Uittenboogaard LM; Jaarsma D; Vermeij WP; Tresini M; Weymaere M; Menoni H; Brandt RM; de Waard MC; Botter SM; Sarker AH; Jaspers NG; van der Horst GT; Cooper PK; Hoeijmakers JH; van der Pluijm I
PLoS Genet; 2014 Oct; 10(10):e1004686. PubMed ID: 25299392
[TBL] [Abstract][Full Text] [Related]
12. Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress.
Soltys DT; Rocha CR; Lerner LK; de Souza TA; Munford V; Cabral F; Nardo T; Stefanini M; Sarasin A; Cabral-Neto JB; Menck CF
Hum Mutat; 2013 Mar; 34(3):481-9. PubMed ID: 23255472
[TBL] [Abstract][Full Text] [Related]
13. Isolation of active recombinant XPG protein, a human DNA repair endonuclease.
O'Donovan A; Scherly D; Clarkson SG; Wood RD
J Biol Chem; 1994 Jun; 269(23):15965-8. PubMed ID: 8206890
[TBL] [Abstract][Full Text] [Related]
14. Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage.
Thorel F; Constantinou A; Dunand-Sauthier I; Nouspikel T; Lalle P; Raams A; Jaspers NG; Vermeulen W; Shivji MK; Wood RD; Clarkson SG
Mol Cell Biol; 2004 Dec; 24(24):10670-80. PubMed ID: 15572672
[TBL] [Abstract][Full Text] [Related]
15. A stable XPG protein is required for proper ribosome biogenesis: Insights on the phenotype of combinate Xeroderma Pigmentosum/Cockayne Syndrome patients.
Taupelet F; Donnio LM; Magnani C; Mari PO; Giglia-Mari G
PLoS One; 2022; 17(7):e0271246. PubMed ID: 35802638
[TBL] [Abstract][Full Text] [Related]
16. Xeroderma pigmentosum and molecular cloning of DNA repair genes.
Boulikas T
Anticancer Res; 1996; 16(2):693-708. PubMed ID: 8687116
[TBL] [Abstract][Full Text] [Related]
17. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G.
Cooper PK; Nouspikel T; Clarkson SG; Leadon SA
Science; 1997 Feb; 275(5302):990-3. PubMed ID: 9020084
[TBL] [Abstract][Full Text] [Related]
18. XPG: a multitasking genome caretaker.
Muniesa-Vargas A; Theil AF; Ribeiro-Silva C; Vermeulen W; Lans H
Cell Mol Life Sci; 2022 Mar; 79(3):166. PubMed ID: 35230528
[TBL] [Abstract][Full Text] [Related]
19. UV-induced apoptosis in XPG-deficient fibroblasts involves activation of CD95 and caspases but not p53.
Clément V; Dunand-Sauthier I; Wiznerowicz M; Clarkson SG
DNA Repair (Amst); 2007 May; 6(5):602-14. PubMed ID: 17208056
[TBL] [Abstract][Full Text] [Related]
20. The crystal structure of human XPG, the xeroderma pigmentosum group G endonuclease, provides insight into nucleotide excision DNA repair.
González-Corrochano R; Ruiz FM; Taylor NMI; Huecas S; Drakulic S; Spínola-Amilibia M; Fernández-Tornero C
Nucleic Acids Res; 2020 Sep; 48(17):9943-9958. PubMed ID: 32821917
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]