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 *

399 related articles for article (PubMed ID: 9642044)

  • 21. Deregulated apoptosis is a hallmark of the Fanconi anemia syndrome.
    Ridet A; Guillouf C; Duchaud E; Cundari E; Fiore M; Moustacchi E; Rosselli F
    Cancer Res; 1997 May; 57(9):1722-30. PubMed ID: 9135015
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Compromised repair of radiation-induced DNA double-strand breaks in Fanconi anemia fibroblasts in G2.
    Zahnreich S; Weber B; Rösch G; Schindler D; Schmidberger H
    DNA Repair (Amst); 2020 Dec; 96():102992. PubMed ID: 33069004
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Functional activity of the fanconi anemia protein FAA requires FAC binding and nuclear localization.
    Näf D; Kupfer GM; Suliman A; Lambert K; D'Andrea AD
    Mol Cell Biol; 1998 Oct; 18(10):5952-60. PubMed ID: 9742112
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fanconi anemia group A and C double-mutant mice: functional evidence for a multi-protein Fanconi anemia complex.
    Noll M; Battaile KP; Bateman R; Lax TP; Rathbun K; Reifsteck C; Bagby G; Finegold M; Olson S; Grompe M
    Exp Hematol; 2002 Jul; 30(7):679-88. PubMed ID: 12135664
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Correction of the spontaneous and DEB-induced chromosomal aberrations in Fanconi anemia cells of the FA(C) complementation group by the FACC gene.
    Stavropoulos DJ; Sood S; Tomkins DJ; Buchwald M
    Cytogenet Cell Genet; 1996; 72(2-3):194-6. PubMed ID: 8978774
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation.
    Yamashita T; Kupfer GM; Naf D; Suliman A; Joenje H; Asano S; D'Andrea AD
    Proc Natl Acad Sci U S A; 1998 Oct; 95(22):13085-90. PubMed ID: 9789045
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells.
    Youssoufian H
    J Clin Invest; 1996 May; 97(9):2003-10. PubMed ID: 8621788
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cloning and analysis of the murine Fanconi anemia group C cDNA.
    Wevrick R; Clarke CA; Buchwald M
    Hum Mol Genet; 1993 Jun; 2(6):655-62. PubMed ID: 7689006
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.
    Yamashita T; Nakahata T
    Int J Hematol; 2001 Jul; 74(1):33-41. PubMed ID: 11530803
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Inhibition of non-homologous end joining in Fanconi Anemia cells results in rescue of survival after interstrand crosslinks but sensitization to replication associated double-strand breaks.
    Eccles LJ; Bell AC; Powell SN
    DNA Repair (Amst); 2018 Apr; 64():1-9. PubMed ID: 29459202
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity.
    Yamashita T; Wu N; Kupfer G; Corless C; Joenje H; Grompe M; D'Andrea AD
    Blood; 1996 May; 87(10):4424-32. PubMed ID: 8639804
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Deficient regulation of DNA double-strand break repair in Fanconi anemia fibroblasts.
    Donahue SL; Lundberg R; Saplis R; Campbell C
    J Biol Chem; 2003 Aug; 278(32):29487-95. PubMed ID: 12748186
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer.
    Pulsipher M; Kupfer GM; Naf D; Suliman A; Lee JS; Jakobs P; Grompe M; Joenje H; Sieff C; Guinan E; Mulligan R; D'Andrea AD
    Mol Med; 1998 Jul; 4(7):468-79. PubMed ID: 9713825
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dysfunctional mammalian telomeres join with DNA double-strand breaks.
    Bailey SM; Cornforth MN; Ullrich RL; Goodwin EH
    DNA Repair (Amst); 2004 Apr; 3(4):349-57. PubMed ID: 15010310
    [TBL] [Abstract][Full Text] [Related]  

  • 35. MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groups.
    Li Y; Youssoufian H
    J Clin Invest; 1997 Dec; 100(11):2873-80. PubMed ID: 9389754
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Repair of ionizing radiation induced DNA double strand breaks].
    Widłak P
    Postepy Hig Med Dosw; 2000; 54(2):133-48. PubMed ID: 10857377
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Involvement of the Fanconi anemia protein FA-C in repair processes of oxidative DNA damages.
    Lackinger D; Ruppitsch W; Ramirez MH; Hirsch-Kauffmann M; Schweiger M
    FEBS Lett; 1998 Nov; 440(1-2):103-6. PubMed ID: 9862435
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The Fanconi anemia polypeptide FACC is localized to the cytoplasm.
    Yamashita T; Barber DL; Zhu Y; Wu N; D'Andrea AD
    Proc Natl Acad Sci U S A; 1994 Jul; 91(14):6712-6. PubMed ID: 7517562
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fanconi anemia pathway--the way of DNA interstrand cross-link repair.
    Yao CJ; Du W; Zhang Q; Zhang F; Zeng F; Chen FP
    Pharmazie; 2013 Jan; 68(1):5-11. PubMed ID: 23444773
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Induction of Fanconi anemia cellular phenotype in human 293 cells by overexpression of a mutant FAC allele.
    Youssoufian H; Li Y; Martin ME; Buchwald M
    J Clin Invest; 1996 Feb; 97(4):957-62. PubMed ID: 8613549
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.