BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

284 related articles for article (PubMed ID: 15451479)

  • 1. 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]  

  • 2. Nijmegen breakage syndrome diagnosed as Fanconi anaemia.
    New HV; Cale CM; Tischkowitz M; Jones A; Telfer P; Veys P; D'Andrea A; Mathew CG; Hann I
    Pediatr Blood Cancer; 2005 May; 44(5):494-9. PubMed ID: 15593232
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interaction of FANCD2 and NBS1 in the DNA damage response.
    Nakanishi K; Taniguchi T; Ranganathan V; New HV; Moreau LA; Stotsky M; Mathew CG; Kastan MB; Weaver DT; D'Andrea AD
    Nat Cell Biol; 2002 Dec; 4(12):913-20. PubMed ID: 12447395
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differentiation of Nijmegen breakage syndrome from Fanconi anemia.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K
    Genet Mol Res; 2007 Sep; 6(3):622-6. PubMed ID: 18050081
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosome instability syndromes.
    Taylor AM
    Best Pract Res Clin Haematol; 2001 Sep; 14(3):631-44. PubMed ID: 11640873
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unique morphological spectrum of lymphomas in Nijmegen breakage syndrome (NBS) patients with high frequency of consecutive lymphoma formation.
    Gładkowska-Dura M; Dzierzanowska-Fangrat K; Dura WT; van Krieken JH; Chrzanowska KH; van Dongen JJ; Langerak AW
    J Pathol; 2008 Nov; 216(3):337-44. PubMed ID: 18788073
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly.
    Seeman P; Gebertová K; Paderová K; Sperling K; Seemanová E
    Pediatr Neurol; 2004 Mar; 30(3):195-200. PubMed ID: 15033202
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site.
    Meyer S; Kingston H; Taylor AM; Byrd PJ; Last JI; Brennan BM; Trueman S; Kelsey A; Taylor GM; Eden OB
    Cancer Genet Cytogenet; 2004 Oct; 154(2):169-74. PubMed ID: 15474156
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fanconi anemia: a pleotropic mutation with multiple cellular and developmental abnormalities.
    Chaganti RS; Houldsworth J
    Ann Genet; 1991; 34(3-4):206-11. PubMed ID: 1809228
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Positional cloning of the gene for Nijmegen breakage syndrome.
    Matsuura S; Tauchi H; Nakamura A; Kondo N; Sakamoto S; Endo S; Smeets D; Solder B; Belohradsky BH; Der Kaloustian VM; Oshimura M; Isomura M; Nakamura Y; Komatsu K
    Nat Genet; 1998 Jun; 19(2):179-81. PubMed ID: 9620777
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Nijmegen breakage syndrome associated with porokeratosis.
    Wolf EK; Shwayder TA
    Pediatr Dermatol; 2009; 26(1):106-8. PubMed ID: 19250427
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mild Nijmegen breakage syndrome phenotype due to alternative splicing.
    Varon R; Dutrannoy V; Weikert G; Tanzarella C; Antoccia A; Stöckl L; Spadoni E; Krüger LA; di Masi A; Sperling K; Digweed M; Maraschio P
    Hum Mol Genet; 2006 Mar; 15(5):679-89. PubMed ID: 16415040
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.
    Meyer S; Fergusson WD; Oostra AB; Medhurst AL; Waisfisz Q; de Winter JP; Chen F; Carr TF; Clayton-Smith J; Clancy T; Green M; Barber L; Eden OB; Will AM; Joenje H; Taylor GM
    Genes Chromosomes Cancer; 2005 Apr; 42(4):404-15. PubMed ID: 15645491
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosomal breakage study in children suspected with Fanconi anemia in the Indian population.
    Korgaonkar S; Ghosh K; Jijina F; Vundinti BR
    J Pediatr Hematol Oncol; 2010 Nov; 32(8):606-10. PubMed ID: 20881871
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Nijmegen breakage syndrome in Slovakia].
    Seemanová E; Pohanka V; Seeman P; Misovicová N; Behunová J; Kvasnicová M; Dlholucký S; Valachová A; Cisarik F; Veghová E; Varon R; Sperling K
    Cas Lek Cesk; 2004; 143(8):538-41; discussion 542. PubMed ID: 15446459
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recent advances in chromosome breakage syndromes and their diagnosis.
    Mathur R; Chowdhury MR; Singh G
    Indian Pediatr; 2000 Jun; 37(6):615-25. PubMed ID: 10869141
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cancer risk of heterozygotes with the NBN founder mutation.
    Seemanová E; Jarolim P; Seeman P; Varon R; Digweed M; Swift M; Sperling K
    J Natl Cancer Inst; 2007 Dec; 99(24):1875-80. PubMed ID: 18073374
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks.
    Digweed M; Sperling K
    DNA Repair (Amst); 2004; 3(8-9):1207-17. PubMed ID: 15279809
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability.
    Seemanová E; Sperling K; Neitzel H; Varon R; Hadac J; Butova O; Schröck E; Seeman P; Digweed M
    J Med Genet; 2006 Mar; 43(3):218-24. PubMed ID: 16033915
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.