191 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. Chromosome instability syndromes.
Taylor AM
Best Pract Res Clin Haematol; 2001 Sep; 14(3):631-44. PubMed ID: 11640873
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. [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]
11. 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]
12. 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]
13. [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]
14. 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]
15. 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]
16. [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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]