BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 9719637)

  • 1. Abnormal rearrangements associated with V(D)J recombination in Fanconi anemia.
    Smith J; Andrau JC; Kallenbach S; Laquerbe A; Doyen N; Papadopoulo D
    J Mol Biol; 1998 Sep; 281(5):815-25. PubMed ID: 9719637
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining.
    Escarceller M; Buchwald M; Singleton BK; Jeggo PA; Jackson SP; Moustacchi E; Papadopoulo D
    J Mol Biol; 1998 Jun; 279(2):375-85. PubMed ID: 9642044
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The scid factor on human chromosome 8 restores V(D)J recombination in addition to double-strand break repair.
    Komatsu K; Kubota N; Gallo M; Okumura Y; Lieber MR
    Cancer Res; 1995 Apr; 55(8):1774-9. PubMed ID: 7712487
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular spectra of HPRT deletion mutations in circulating T-lymphocytes in Fanconi anemia patients.
    Laquerbe A; Sala-Trepat M; Vives C; Escarceller M; Papadopoulo D
    Mutat Res; 1999 Dec; 431(2):341-50. PubMed ID: 10635999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Templated nucleotide addition and immunoglobulin JH-gene utilization in t(11;14) junctions: implications for the mechanism of translocation and the origin of mantle cell lymphoma.
    Welzel N; Le T; Marculescu R; Mitterbauer G; Chott A; Pott C; Kneba M; Du MQ; Kusec R; Drach J; Raderer M; Mannhalter C; Lechner K; Nadel B; Jaeger U
    Cancer Res; 2001 Feb; 61(4):1629-36. PubMed ID: 11245476
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Involvement of illegitimate V(D)J recombination or microhomology-mediated nonhomologous end-joining in the formation of intragenic deletions of the Notch1 gene in mouse thymic lymphomas.
    Tsuji H; Ishii-Ohba H; Katsube T; Ukai H; Aizawa S; Doi M; Hioki K; Ogiu T
    Cancer Res; 2004 Dec; 64(24):8882-90. PubMed ID: 15604248
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome.
    Escarceller M; Rousset S; Moustacchi E; Papadopoulo D
    Somat Cell Mol Genet; 1997 Nov; 23(6):401-11. PubMed ID: 9661703
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Mechanism and control of V(D)J recombination versus class switch recombination: similarities and differences.
    Dudley DD; Chaudhuri J; Bassing CH; Alt FW
    Adv Immunol; 2005; 86():43-112. PubMed ID: 15705419
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New insights into the Fanconi anemia pathway from an isogenic FancG hamster CHO mutant.
    Tebbs RS; Hinz JM; Yamada NA; Wilson JB; Salazar EP; Thomas CB; Jones IM; Jones NJ; Thompson LH
    DNA Repair (Amst); 2005 Jan; 4(1):11-22. PubMed ID: 15533833
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fanconi anemia: genetic analysis of a human disease using chicken system.
    Takata M; Kitao H; Ishiai M
    Cytogenet Genome Res; 2007; 117(1-4):346-51. PubMed ID: 17675877
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hybrid joint formation in human V(D)J recombination requires nonhomologous DNA end joining.
    Raghavan SC; Tong J; Lieber MR
    DNA Repair (Amst); 2006 Feb; 5(2):278-85. PubMed ID: 16275127
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosomal aberrations induced by double strand DNA breaks.
    Varga T; Aplan PD
    DNA Repair (Amst); 2005 Aug; 4(9):1038-46. PubMed ID: 15935739
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gamma-irradiation directly affects the formation of coding joints in SCID cell lines.
    Binnie A; Olson S; Wu GE; Lewis SM
    J Immunol; 1999 Nov; 163(10):5418-26. PubMed ID: 10553067
    [TBL] [Abstract][Full Text] [Related]  

  • 15. V(D)J and immunoglobulin class switch recombinations: a paradigm to study the regulation of DNA end-joining.
    Soulas-Sprauel P; Rivera-Munoz P; Malivert L; Le Guyader G; Abramowski V; Revy P; de Villartay JP
    Oncogene; 2007 Dec; 26(56):7780-91. PubMed ID: 18066091
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p.
    Whitney M; Thayer M; Reifsteck C; Olson S; Smith L; Jakobs PM; Leach R; Naylor S; Joenje H; Grompe M
    Nat Genet; 1995 Nov; 11(3):341-3. PubMed ID: 7581463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. p53-dependent pathway of radio-induced apoptosis is altered in Fanconi anemia.
    Rosselli F; Ridet A; Soussi T; Duchaud E; Alapetite C; Moustacchi E
    Oncogene; 1995 Jan; 10(1):9-17. PubMed ID: 7824283
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Fanconi anemia/BRCA pathway: a coordinator of cross-link repair.
    Mirchandani KD; D'Andrea AD
    Exp Cell Res; 2006 Aug; 312(14):2647-53. PubMed ID: 16859679
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differential expression of TP53 associated genes in Fanconi anemia cells after mitomycin C and hydroxyurea treatment.
    Martinez A; Hinz JM; Gómez L; Molina B; Acuña H; Jones IM; Frias S; Coleman MA
    Mutat Res; 2008 Oct; 656(1-2):1-7. PubMed ID: 18647660
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.
    Hussain S; Witt E; Huber PA; Medhurst AL; Ashworth A; Mathew CG
    Hum Mol Genet; 2003 Oct; 12(19):2503-10. PubMed ID: 12915460
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.