BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

236 related articles for article (PubMed ID: 15333589)

  • 41. siRNA targeting NBS1 or XIAP increases radiation sensitivity of human cancer cells independent of TP53 status.
    Ohnishi K; Scuric Z; Schiestl RH; Okamoto N; Takahashi A; Ohnishi T
    Radiat Res; 2006 Sep; 166(3):454-62. PubMed ID: 16972754
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Role of the Nijmegen breakage syndrome 1 gene in familial and sporadic prostate cancer.
    Hebbring SJ; Fredriksson H; White KA; Maier C; Ewing C; McDonnell SK; Jacobsen SJ; Cerhan J; Schaid DJ; Ikonen T; Autio V; Tammela TL; Herkommer K; Paiss T; Vogel W; Gielzak M; Sauvageot J; Schleutker J; Cooney KA; Isaacs W; Thibodeau SN
    Cancer Epidemiol Biomarkers Prev; 2006 May; 15(5):935-8. PubMed ID: 16702373
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Regulation of the Nijmegen breakage syndrome 1 gene NBS1 by c-myc, p53 and coactivators mediates estrogen protection from DNA damage in breast cancer cells.
    Wan R; Wu J; Baloue KK; Crowe DL
    Int J Oncol; 2013 Feb; 42(2):712-20. PubMed ID: 23291854
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Nijmegen breakage syndrome gene, NBS1, and molecular links to factors for genome stability.
    Tauchi H; Matsuura S; Kobayashi J; Sakamoto S; Komatsu K
    Oncogene; 2002 Dec; 21(58):8967-80. PubMed ID: 12483513
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Cre-loxP chromosome engineering of a targeted deletion in the mouse corresponding to the 3p21.3 region of homozygous loss in human tumours.
    Smith AJ; Xian J; Richardson M; Johnstone KA; Rabbitts PH
    Oncogene; 2002 Jul; 21(29):4521-9. PubMed ID: 12085230
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Fertility defects revealing germline biallelic nonsense NBN mutations.
    Warcoin M; Lespinasse J; Despouy G; Dubois d'Enghien C; Laugé A; Portnoï MF; Christin-Maitre S; Stoppa-Lyonnet D; Stern MH
    Hum Mutat; 2009 Mar; 30(3):424-30. PubMed ID: 19105185
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL).
    Varon R; Reis A; Henze G; von Einsiedel HG; Sperling K; Seeger K
    Cancer Res; 2001 May; 61(9):3570-2. PubMed ID: 11325820
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Fatal toxicity following radio- and chemotherapy of medulloblastoma in a child with unrecognized Nijmegen breakage syndrome.
    Distel L; Neubauer S; Varon R; Holter W; Grabenbauer G
    Med Pediatr Oncol; 2003 Jul; 41(1):44-8. PubMed ID: 12764742
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Mutation of the mouse Rad17 gene leads to embryonic lethality and reveals a role in DNA damage-dependent recombination.
    Budzowska M; Jaspers I; Essers J; de Waard H; van Drunen E; Hanada K; Beverloo B; Hendriks RW; de Klein A; Kanaar R; Hoeijmakers JH; Maas A
    EMBO J; 2004 Sep; 23(17):3548-58. PubMed ID: 15297881
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.
    Berardinelli F; di Masi A; Salvatore M; Banerjee S; Myung K; De Villartay JP; Revy P; Plebani A; Soresina A; Taruscio D; Tanzarella C; Antoccia A
    Eur J Med Genet; 2007; 50(3):176-87. PubMed ID: 17395558
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Characterization of the plant homolog of Nijmegen breakage syndrome 1: Involvement in DNA repair and recombination.
    Akutsu N; Iijima K; Hinata T; Tauchi H
    Biochem Biophys Res Commun; 2007 Feb; 353(2):394-8. PubMed ID: 17182003
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Chromosomal breakage syndromes.
    Carney JP
    Curr Opin Immunol; 1999 Aug; 11(4):443-7. PubMed ID: 10448147
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The clinical and biological overlap between Nijmegen Breakage Syndrome and Fanconi anemia.
    Gennery AR; Slatter MA; Bhattacharya A; Barge D; Haigh S; O'Driscoll M; Coleman R; Abinun M; Flood TJ; Cant AJ; Jeggo PA
    Clin Immunol; 2004 Nov; 113(2):214-9. PubMed ID: 15451479
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma.
    Cerosaletti KM; Morrison VA; Sabath DE; Willerford DM; Concannon P
    Genes Chromosomes Cancer; 2002 Nov; 35(3):282-6. PubMed ID: 12353271
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mutation analysis of the Nijmegen breakage syndrome gene (NBS1) in nineteen patients with acute myeloid leukemia with complex karyotypes.
    Varon R; Schoch C; Reis A; Hiddemann WC; Sperling K; Schnittger S
    Leuk Lymphoma; 2003 Nov; 44(11):1931-4. PubMed ID: 14738145
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer].
    Seemanová E; Hoch J; Seeman P
    Cas Lek Cesk; 2011; 150(2):97-9. PubMed ID: 21560448
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Radiosensitization of head/neck squamous cell carcinoma by adenovirus-mediated expression of the Nbs1 protein.
    Rhee JG; Li D; Suntharalingam M; Guo C; O'Malley BW; Carney JP
    Int J Radiat Oncol Biol Phys; 2007 Jan; 67(1):273-8. PubMed ID: 17189075
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Decreased immunoglobulin class switching in Nijmegen Breakage syndrome due to the DNA repair defect.
    van Engelen BG; Hiel JA; Gabreëls FJ; van den Heuvel LP; van Gent DC; Weemaes CM
    Hum Immunol; 2001 Dec; 62(12):1324-7. PubMed ID: 11756000
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A systematic proteomic study of irradiated DNA repair deficient Nbn-mice.
    Melchers A; Stöckl L; Radszewski J; Anders M; Krenzlin H; Kalischke C; Scholz R; Jordan A; Nebrich G; Klose J; Sperling K; Digweed M; Demuth I
    PLoS One; 2009; 4(5):e5423. PubMed ID: 19412544
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Identification of the interactors of human nibrin (NBN) and of its 26 kDa and 70 kDa fragments arising from the NBN 657del5 founder mutation.
    Cilli D; Mirasole C; Pennisi R; Pallotta V; D'Alessandro A; Antoccia A; Zolla L; Ascenzi P; di Masi A
    PLoS One; 2014; 9(12):e114651. PubMed ID: 25485873
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.