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 *

437 related articles for article (PubMed ID: 16116423)

  • 1. The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
    Levitus M; Waisfisz Q; Godthelp BC; de Vries Y; Hussain S; Wiegant WW; Elghalbzouri-Maghrani E; Steltenpool J; Rooimans MA; Pals G; Arwert F; Mathew CG; Zdzienicka MZ; Hiom K; De Winter JP; Joenje H
    Nat Genet; 2005 Sep; 37(9):934-5. PubMed ID: 16116423
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.
    Levran O; Attwooll C; Henry RT; Milton KL; Neveling K; Rio P; Batish SD; Kalb R; Velleuer E; Barral S; Ott J; Petrini J; Schindler D; Hanenberg H; Auerbach AD
    Nat Genet; 2005 Sep; 37(9):931-3. PubMed ID: 16116424
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway.
    Mosedale G; Niedzwiedz W; Alpi A; Perrina F; Pereira-Leal JB; Johnson M; Langevin F; Pace P; Patel KJ
    Nat Struct Mol Biol; 2005 Sep; 12(9):763-71. PubMed ID: 16116434
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked inheritance of Fanconi anemia complementation group B.
    Meetei AR; Levitus M; Xue Y; Medhurst AL; Zwaan M; Ling C; Rooimans MA; Bier P; Hoatlin M; Pals G; de Winter JP; Wang W; Joenje H
    Nat Genet; 2004 Nov; 36(11):1219-24. PubMed ID: 15502827
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression of the BRCA1-interacting protein Brip1/BACH1/FANCJ is driven by E2F and correlates with human breast cancer malignancy.
    Eelen G; Vanden Bempt I; Verlinden L; Drijkoningen M; Smeets A; Neven P; Christiaens MR; Marchal K; Bouillon R; Verstuyf A
    Oncogene; 2008 Jul; 27(30):4233-41. PubMed ID: 18345034
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fanconi anaemia genes and susceptibility to cancer.
    Mathew CG
    Oncogene; 2006 Sep; 25(43):5875-84. PubMed ID: 16998502
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.
    Tamary H; Dgany O; Toledano H; Shalev Z; Krasnov T; Shalmon L; Schechter T; Bercovich D; Attias D; Laor R; Koren A; Yaniv I
    Eur J Haematol; 2004 May; 72(5):330-5. PubMed ID: 15059067
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study.
    Auerbach AD; Greenbaum J; Pujara K; Batish SD; Bitencourt MA; Kokemohr I; Schneider H; Lobitzc S; Pasquini R; Giampietro PF; Hanenberg H; Levran O;
    Hum Mutat; 2003 Feb; 21(2):158-68. PubMed ID: 12552564
    [TBL] [Abstract][Full Text] [Related]  

  • 9. BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ.
    Litman R; Peng M; Jin Z; Zhang F; Zhang J; Powell S; Andreassen PR; Cantor SB
    Cancer Cell; 2005 Sep; 8(3):255-65. PubMed ID: 16153896
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FANCJ: solving problems in DNA replication.
    Hiom K
    DNA Repair (Amst); 2010 Mar; 9(3):250-6. PubMed ID: 20122882
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Helicase-inactivating
    Kamal L; Pierce SB; Canavati C; Rayyan AA; Jaraysa T; Lobel O; Lolas S; Norquist BM; Rabie G; Zahdeh F; Levy-Lahad E; King MC; Kanaan MN
    Cold Spring Harb Mol Case Stud; 2020 Oct; 6(5):. PubMed ID: 33028645
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Intermediate DNA repair activity associated with the 322delG allele of the fanconi anemia complementation group C gene.
    Donahue SL; Lundberg R; Campbell C
    J Mol Biol; 2004 Oct; 342(5):1443-55. PubMed ID: 15364573
    [TBL] [Abstract][Full Text] [Related]  

  • 13. BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study.
    Frank B; Hemminki K; Meindl A; Wappenschmidt B; Sutter C; Kiechle M; Bugert P; Schmutzler RK; Bartram CR; Burwinkel B
    BMC Cancer; 2007 May; 7():83. PubMed ID: 17504528
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
    Levran O; Diotti R; Pujara K; Batish SD; Hanenberg H; Auerbach AD
    Hum Mutat; 2005 Feb; 25(2):142-9. PubMed ID: 15643609
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair.
    Bridge WL; Vandenberg CJ; Franklin RJ; Hiom K
    Nat Genet; 2005 Sep; 37(9):953-7. PubMed ID: 16116421
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic subtyping of Fanconi anemia by comprehensive mutation screening.
    Ameziane N; Errami A; Léveillé F; Fontaine C; de Vries Y; van Spaendonk RM; de Winter JP; Pals G; Joenje H
    Hum Mutat; 2008 Jan; 29(1):159-66. PubMed ID: 17924555
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives.
    Cao AY; Huang J; Hu Z; Li WF; Ma ZL; Tang LL; Zhang B; Su FX; Zhou J; Di GH; Shen KW; Wu J; Lu JS; Luo JM; Yuan WT; Shen ZZ; Huang W; Shao ZM
    Breast Cancer Res Treat; 2009 May; 115(1):51-5. PubMed ID: 18483852
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [FANCA gene mutation analysis in Fanconi anemia patients].
    Chen F; Peng GJ; Zhang K; Hu Q; Zhang LQ; Liu AG
    Zhonghua Xue Ye Xue Za Zhi; 2005 Oct; 26(10):616-8. PubMed ID: 16532972
    [TBL] [Abstract][Full Text] [Related]  

  • 19. FANCJ/BRIP1 recruitment and regulation of FANCD2 in DNA damage responses.
    Zhang F; Fan Q; Ren K; Auerbach AD; Andreassen PR
    Chromosoma; 2010 Dec; 119(6):637-49. PubMed ID: 20676667
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
    Demuth I; Wlodarski M; Tipping AJ; Morgan NV; de Winter JP; Thiel M; Gräsl S; Schindler D; D'Andrea AD; Altay C; Kayserili H; Zatterale A; Kunze J; Ebell W; Mathew CG; Joenje H; Sperling K; Digweed M
    Eur J Hum Genet; 2000 Nov; 8(11):861-8. PubMed ID: 11093276
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.