These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 14726017)

  • 1. The XPG story.
    Clarkson SG
    Biochimie; 2003 Nov; 85(11):1113-21. PubMed ID: 14726017
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein.
    Iyer N; Reagan MS; Wu KJ; Canagarajah B; Friedberg EC
    Biochemistry; 1996 Feb; 35(7):2157-67. PubMed ID: 8652557
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Base excision repair of oxidative DNA damage activated by XPG protein.
    Klungland A; Höss M; Gunz D; Constantinou A; Clarkson SG; Doetsch PW; Bolton PH; Wood RD; Lindahl T
    Mol Cell; 1999 Jan; 3(1):33-42. PubMed ID: 10024877
    [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 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome.
    Sarker AH; Tsutakawa SE; Kostek S; Ng C; Shin DS; Peris M; Campeau E; Tainer JA; Nogales E; Cooper PK
    Mol Cell; 2005 Oct; 20(2):187-98. PubMed ID: 16246722
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.