323 related articles for article (PubMed ID: 35230528)
1. 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]
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. XPG in the Nucleotide Excision Repair and Beyond: a study on the different functional aspects of XPG and its associated diseases.
Pal R; Paul N; Bhattacharya D; Rakshit S; Shanmugam G; Sarkar K
Mol Biol Rep; 2022 Aug; 49(8):7995-8006. PubMed ID: 35596054
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. ERCC5/XPG, ERCC1, and BRCA1 gene status and clinical benefit of trabectedin in patients with soft tissue sarcoma.
Italiano A; Laurand A; Laroche A; Casali P; Sanfilippo R; Le Cesne A; Judson I; Blay JY; Ray-Coquard I; Bui B; Coindre JM; Nieto A; Tercero JC; Jimeno J; Robert J; Pourquier P
Cancer; 2011 Aug; 117(15):3445-56. PubMed ID: 21287534
[TBL] [Abstract][Full Text] [Related]
7. Heterogeneity and overlaps in nucleotide excision repair disorders.
Ferri D; Orioli D; Botta E
Clin Genet; 2020 Jan; 97(1):12-24. PubMed ID: 30919937
[TBL] [Abstract][Full Text] [Related]
8. 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]
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. 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]
11. Modulation of DNA damage by XPF, XPG and ERCC1 gene polymorphisms in pesticide-exposed agricultural workers of Punjab, North-West India.
Kaur K; Kaur R
Mutat Res Genet Toxicol Environ Mutagen; 2021; 861-862():503302. PubMed ID: 33551103
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Regulation of Transcription Elongation by the XPG-TFIIH Complex Is Implicated in Cockayne Syndrome.
Narita T; Narita K; Takedachi A; Saijo M; Tanaka K
Mol Cell Biol; 2015 Sep; 35(18):3178-88. PubMed ID: 26149386
[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. 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]
18. 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]
19. Genetic polymorphisms of the XPG and XPD nucleotide excision repair genes in sarcoma patients.
Le Morvan V; Longy M; Bonaïti-Pellié C; Bui B; Houédé N; Coindre JM; Robert J; Pourquier P
Int J Cancer; 2006 Oct; 119(7):1732-5. PubMed ID: 16646069
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
