333 related articles for article (PubMed ID: 25299392)
1. 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]
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. 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]
5. Cyclosporin A inhibits nucleotide excision repair via downregulation of the xeroderma pigmentosum group A and G proteins, which is mediated by calcineurin inhibition.
Kuschal C; Thoms KM; Boeckmann L; Laspe P; Apel A; Schön MP; Emmert S
Exp Dermatol; 2011 Oct; 20(10):795-9. PubMed ID: 21707758
[TBL] [Abstract][Full Text] [Related]
6. XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients.
Ito S; Kuraoka I; Chymkowitch P; Compe E; Takedachi A; Ishigami C; Coin F; Egly JM; Tanaka K
Mol Cell; 2007 Apr; 26(2):231-43. PubMed ID: 17466625
[TBL] [Abstract][Full Text] [Related]
7. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
Graham JM; Anyane-Yeboa K; Raams A; Appeldoorn E; Kleijer WJ; Garritsen VH; Busch D; Edersheim TG; Jaspers NG
Am J Hum Genet; 2001 Aug; 69(2):291-300. PubMed ID: 11443545
[TBL] [Abstract][Full Text] [Related]
8. First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure.
Jaspers NG; Raams A; Silengo MC; Wijgers N; Niedernhofer LJ; Robinson AR; Giglia-Mari G; Hoogstraten D; Kleijer WJ; Hoeijmakers JH; Vermeulen W
Am J Hum Genet; 2007 Mar; 80(3):457-66. PubMed ID: 17273966
[TBL] [Abstract][Full Text] [Related]
9. Non-catalytic Roles for XPG with BRCA1 and BRCA2 in Homologous Recombination and Genome Stability.
Trego KS; Groesser T; Davalos AR; Parplys AC; Zhao W; Nelson MR; Hlaing A; Shih B; Rydberg B; Pluth JM; Tsai MS; Hoeijmakers JHJ; Sung P; Wiese C; Campisi J; Cooper PK
Mol Cell; 2016 Feb; 61(4):535-546. PubMed ID: 26833090
[TBL] [Abstract][Full Text] [Related]
10. Restricted diet delays accelerated ageing and genomic stress in DNA-repair-deficient mice.
Vermeij WP; Dollé ME; Reiling E; Jaarsma D; Payan-Gomez C; Bombardieri CR; Wu H; Roks AJ; Botter SM; van der Eerden BC; Youssef SA; Kuiper RV; Nagarajah B; van Oostrom CT; Brandt RM; Barnhoorn S; Imholz S; Pennings JL; de Bruin A; Gyenis Á; Pothof J; Vijg J; van Steeg H; Hoeijmakers JH
Nature; 2016 Sep; 537(7620):427-431. PubMed ID: 27556946
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Hot topics in DNA repair: the molecular basis for different disease states caused by mutations in TFIIH and XPG.
Schärer OD
DNA Repair (Amst); 2008 Feb; 7(2):339-44. PubMed ID: 18077223
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome.
Trego KS; Chernikova SB; Davalos AR; Perry JJ; Finger LD; Ng C; Tsai MS; Yannone SM; Tainer JA; Campisi J; Cooper PK
Cell Cycle; 2011 Jun; 10(12):1998-2007. PubMed ID: 21558802
[TBL] [Abstract][Full Text] [Related]
15. Characterization of three XPG-defective patients identifies three missense mutations that impair repair and transcription.
Schäfer A; Schubert S; Gratchev A; Seebode C; Apel A; Laspe P; Hofmann L; Ohlenbusch A; Mori T; Kobayashi N; Schürer A; Schön MP; Emmert S
J Invest Dermatol; 2013 Jul; 133(7):1841-9. PubMed ID: 23370536
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Cerebro-oculo-facio-skeletal syndrome.
Suzumura H; Arisaka O
Adv Exp Med Biol; 2010; 685():210-4. PubMed ID: 20687508
[TBL] [Abstract][Full Text] [Related]
18. [The metabolic and molecular bases of Cockayne syndrome].
Flores-Alvarado LJ; Ramirez-Garcia SA; Núñez-Reveles NY
Rev Invest Clin; 2010; 62(5):480-90. PubMed ID: 21416736
[TBL] [Abstract][Full Text] [Related]
19. 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]
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]
