BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 1548931)

  • 21. Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions.
    Quentin S; Cuccuini W; Ceccaldi R; Nibourel O; Pondarre C; Pagès MP; Vasquez N; Dubois d'Enghien C; Larghero J; Peffault de Latour R; Rocha V; Dalle JH; Schneider P; Michallet M; Michel G; Baruchel A; Sigaux F; Gluckman E; Leblanc T; Stoppa-Lyonnet D; Preudhomme C; Socié G; Soulier J
    Blood; 2011 Apr; 117(15):e161-70. PubMed ID: 21325596
    [TBL] [Abstract][Full Text] [Related]  

  • 22. GST genotype may modify clinical phenotype in patients with Fanconi anaemia.
    Davies SM; Radloff GA; DeFor TE; Levran O; Batish SD; Hanenberg H; Auerbach AD
    Br J Haematol; 2005 Oct; 131(1):118-22. PubMed ID: 16173971
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia.
    Meyer S; Barber LM; White DJ; Will AM; Birch JM; Kohler JA; Ersfeld K; Blom E; Joenje H; Eden TO; Malcolm Taylor G
    Br J Haematol; 2006 May; 133(3):284-92. PubMed ID: 16643430
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia.
    Wagner JE; Tolar J; Levran O; Scholl T; Deffenbaugh A; Satagopan J; Ben-Porat L; Mah K; Batish SD; Kutler DI; MacMillan ML; Hanenberg H; Auerbach AD
    Blood; 2004 Apr; 103(8):3226-9. PubMed ID: 15070707
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Acute myeloid leukemia with complex hypodiploidy and loss of heterozygosity of 17p in a boy with Fanconi anemia.
    Woo HI; Kim HJ; Lee SH; Yoo KH; Koo HH; Kim SH
    Ann Clin Lab Sci; 2011; 41(1):66-70. PubMed ID: 21325258
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Acute leukemia in Fanconi's anemia. Report of a patient and review of the literature].
    van Gils JE; Mandel C; van Weel-Sipman MH; de Koning J; van 't Veer-Korthof ET
    Tijdschr Kindergeneeskd; 1987 Apr; 55(2):68-72. PubMed ID: 3590139
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Physician Education: Myelodysplastic Syndrome.
    Yoshida Y
    Oncologist; 1996; 1(4):284-287. PubMed ID: 10388004
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Interleukin-2-induced graft-versus-leukemia for the treatment of AML in a BRCA2 Fanconi anemia patient.
    Yeo CJ; Gilman AL
    J Pediatr Hematol Oncol; 2014 Mar; 36(2):e78-80. PubMed ID: 23619121
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Creation and report of the Tunisian Fanconi Anemia Registry (TFAR)].
    Hadiji Mseddi S; Kammoun L; Bellaaj H; Ben Youssef Y; Aissaoui L; Torjemane L; Telmoudi F; Amouri A; Elghezal H; Ouederni M; Ben Abdennebi Y; Hammemi S; Ben Othmen T; Ben Abid H; Bejaoui M; Abdelhak S; Hachicha M; Dellagi K; Frikha M;
    Arch Pediatr; 2012 May; 19(5):467-75. PubMed ID: 22480464
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular and cellular biology of Fanconi anemia.
    Strathdee CA; Buchwald M
    Am J Pediatr Hematol Oncol; 1992 May; 14(2):177-85. PubMed ID: 1530124
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Fanconi's anemia. Current concepts.
    Alter BP
    Am J Pediatr Hematol Oncol; 1992 May; 14(2):170-6. PubMed ID: 1530123
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular Cytogenetic Approach to Characterize Novel and Cryptic Chromosome Abnormalities in Childhood Myeloid Malignances of Fanconi Anemia.
    Borges ML; Capela de Matos RR; Amaral BD; Soares-Ventura EM; Leite EP; Silva MO; Cornélio MT; Silva ML; Liehr T; Marques-Salles TD
    J Pediatr Hematol Oncol; 2017 Mar; 39(2):e85-e91. PubMed ID: 28212262
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry study.
    Gillio AP; Verlander PC; Batish SD; Giampietro PF; Auerbach AD
    Blood; 1997 Jul; 90(1):105-10. PubMed ID: 9207444
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Progressive preleukemia with a chromosomally abnormal clone in a kindred with the Estren-Dameshek variant of Fanconi's anemia.
    Nowell P; Bergman G; Besa E; Wilmoth D; Emanuel B
    Blood; 1984 Nov; 64(5):1135-8. PubMed ID: 6207874
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fanconi anaemia and leukaemia - clinical and molecular aspects.
    Tischkowitz M; Dokal I
    Br J Haematol; 2004 Jul; 126(2):176-91. PubMed ID: 15238138
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Unrelated donor bone marrow transplantation for Fanconi anemia.
    Davies SM; Khan S; Wagner JE; Arthur DC; Auerbach AD; Ramsay NK; Weisdorf DJ
    Bone Marrow Transplant; 1996 Jan; 17(1):43-7. PubMed ID: 8673053
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The molecular biology of Fanconi anemia.
    Tamary H; Bar-Yam R; Zemach M; Dgany O; Shalmon L; Yaniv I
    Isr Med Assoc J; 2002 Oct; 4(10):819-23. PubMed ID: 12389351
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Leukemia and preleukemia in Fanconi's anemia.
    Alter BP
    Cancer Genet Cytogenet; 1992 Feb; 58(2):206-8; discussion 209. PubMed ID: 1551092
    [No Abstract]   [Full Text] [Related]  

  • 39. Identification of Alu-mediated deletions in the Fanconi anemia gene FAA.
    Levran O; Doggett NA; Auerbach AD
    Hum Mutat; 1998; 12(3):145-52. PubMed ID: 9711872
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.