BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

284 related articles for article (PubMed ID: 15451479)

  • 21. [Chromosome instability syndromes].
    Seemanová E; Seeman P; Jarolím P
    Cas Lek Cesk; 2002; 141(1):16-22. PubMed ID: 11899541
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations.
    Varon R; Seemanova E; Chrzanowska K; Hnateyko O; Piekutowska-Abramczuk D; Krajewska-Walasek M; Sykut-Cegielska J; Sperling K; Reis A
    Eur J Hum Genet; 2000 Nov; 8(11):900-2. PubMed ID: 11093281
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic heterogeneity for a Nijmegen breakage-like syndrome.
    Maraschio P; Spadoni E; Tanzarella C; Antoccia A; Di Masi A; Maghnie M; Varon R; Demuth I; Tiepolo L; Danesino C
    Clin Genet; 2003 Apr; 63(4):283-90. PubMed ID: 12702161
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [From gene to disease: Fanconi anemia].
    Zwaan CM; Joenje H
    Ned Tijdschr Geneeskd; 2003 Feb; 147(8):342-4. PubMed ID: 12661120
    [TBL] [Abstract][Full Text] [Related]  

  • 25. VACTERL with hydrocephalus: one end of the Fanconi anemia spectrum of anomalies?
    Porteous ME; Cross I; Burn J
    Am J Med Genet; 1992 Aug; 43(6):1032-4. PubMed ID: 1415330
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian families.
    Resnick IB; Kondratenko I; Togoev O; Vasserman N; Shagina I; Evgrafov O; Tverskaya S; Cerosaletti KM; Gatti RA; Concannon P
    J Pediatr; 2002 Mar; 140(3):355-61. PubMed ID: 11953735
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Role of Nijmegen breakage syndrome protein in specific T-lymphocyte activation pathways.
    García-Pérez MA; Allende LM; Corell A; Paz-Artal E; Varela P; López-Goyanes A; García-Martin F; Vázquez R; Sotoca A; Arnaiz-Villena A
    Clin Diagn Lab Immunol; 2001 Jul; 8(4):757-61. PubMed ID: 11427422
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. The clinical manifestation of a defective response to DNA double-strand breaks as exemplified by Nijmegen breakage syndrome.
    Demuth I; Digweed M
    Oncogene; 2007 Dec; 26(56):7792-8. PubMed ID: 18066092
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemia.
    Giampietro PF; Auerbach AD; Elias ER; Gutman A; Zellers NJ; Davis JG
    Am J Med Genet; 1998 Jun; 78(1):70-5. PubMed ID: 9637428
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Microcephaly with chromosomal instability and immunodeficiency--Nijmegen syndrome].
    Chrzanowska KH
    Pediatr Pol; 1996 Mar; 71(3):223-34. PubMed ID: 8966094
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 3R coordination by Fanconi anemia proteins.
    Macé G; Bogliolo M; Guervilly JH; Dugas du Villard JA; Rosselli F
    Biochimie; 2005 Jul; 87(7):647-58. PubMed ID: 15935541
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability.
    Demuth I; Frappart PO; Hildebrand G; Melchers A; Lobitz S; Stöckl L; Varon R; Herceg Z; Sperling K; Wang ZQ; Digweed M
    Hum Mol Genet; 2004 Oct; 13(20):2385-97. PubMed ID: 15333589
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Nijmegen breakage syndrome: a neuropathological study.
    Lammens M; Hiel JA; Gabreëls FJ; van Engelen BG; van den Heuvel LP; Weemaes CM
    Neuropediatrics; 2003 Aug; 34(4):189-93. PubMed ID: 12973659
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis.
    Dumon-Jones V; Frappart PO; Tong WM; Sajithlal G; Hulla W; Schmid G; Herceg Z; Digweed M; Wang ZQ
    Cancer Res; 2003 Nov; 63(21):7263-9. PubMed ID: 14612522
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Nijmegen breakage syndrome.
    Kondratenko I; Paschenko O; Polyakov A; Bologov A
    Adv Exp Med Biol; 2007; 601():61-7. PubMed ID: 17712992
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Gene therapy in the treatment of Fanconi anemia, a progressive bone marrow failure syndrome.
    Williams DA; Croop J; Kelly P
    Curr Opin Mol Ther; 2005 Oct; 7(5):461-6. PubMed ID: 16248281
    [TBL] [Abstract][Full Text] [Related]  

  • 39. No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper-methylation in sporadic childhood leukaemia.
    Meyer S; White DJ; Will AM; Eden T; Sim A; Brown R; Strathdee G
    Br J Haematol; 2006 Jul; 134(1):61-3. PubMed ID: 16803569
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutations in the Nijmegen breakage syndrome gene in medulloblastomas.
    Huang J; Grotzer MA; Watanabe T; Hewer E; Pietsch T; Rutkowski S; Ohgaki H
    Clin Cancer Res; 2008 Jul; 14(13):4053-8. PubMed ID: 18593981
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.