BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 9207444)

  • 1. 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]  

  • 2. Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.
    Faivre L; Guardiola P; Lewis C; Dokal I; Ebell W; Zatterale A; Altay C; Poole J; Stones D; Kwee ML; van Weel-Sipman M; Havenga C; Morgan N; de Winter J; Digweed M; Savoia A; Pronk J; de Ravel T; Jansen S; Joenje H; Gluckman E; Mathew CG
    Blood; 2000 Dec; 96(13):4064-70. PubMed ID: 11110674
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Carrier frequency of the IVS4 + 4 A-->T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population.
    Verlander PC; Kaporis A; Liu Q; Zhang Q; Seligsohn U; Auerbach AD
    Blood; 1995 Dec; 86(11):4034-8. PubMed ID: 7492758
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fanconi anemia: genetic testing in Ashkenazi Jews.
    Auerbach AD
    Genet Test; 1997; 1(1):27-33. PubMed ID: 10464622
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity.
    Yamashita T; Wu N; Kupfer G; Corless C; Joenje H; Grompe M; D'Andrea AD
    Blood; 1996 May; 87(10):4424-32. PubMed ID: 8639804
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation analysis of the Fanconi anemia gene FACC.
    Verlander PC; Lin JD; Udono MU; Zhang Q; Gibson RA; Mathew CG; Auerbach AD
    Am J Hum Genet; 1994 Apr; 54(4):595-601. PubMed ID: 8128956
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A 20-year perspective on the International Fanconi Anemia Registry (IFAR).
    Kutler DI; Singh B; Satagopan J; Batish SD; Berwick M; Giampietro PF; Hanenberg H; Auerbach AD
    Blood; 2003 Feb; 101(4):1249-56. PubMed ID: 12393516
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia.
    Yabe M; Koike T; Ohtsubo K; Imai E; Morimoto T; Takakura H; Koh K; Yoshida K; Ogawa S; Ito E; Okuno Y; Muramatsu H; Kojima S; Matsuo K; Mori M; Hira A; Takata M; Yabe H
    Ann Hematol; 2019 Feb; 98(2):271-280. PubMed ID: 30368588
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutations and polymorphisms in the Fanconi anemia group C gene.
    Gibson RA; Morgan NV; Goldstein LH; Pearson IC; Kesterton IP; Foot NJ; Jansen S; Havenga C; Pearson T; de Ravel TJ; Cohn RJ; Marques IM; Dokal I; Roberts I; Marsh J; Ball S; Milner RD; Llerena JC; Samochatova E; Mohan SP; Vasudevan P; Birjandi F; Hajianpour A; Murer-Orlando M; Mathew CG
    Hum Mutat; 1996; 8(2):140-8. PubMed ID: 8844212
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Assessment of mitomycin C sensitivity in Fanconi anemia complementation group C gene (Fac) knock-out mouse cells.
    Otsuki T; Wang J; Demuth I; Digweed M; Liu JM
    Int J Hematol; 1998 Apr; 67(3):243-8. PubMed ID: 9650445
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study.
    Auerbach AD; Greenbaum J; Pujara K; Batish SD; Bitencourt MA; Kokemohr I; Schneider H; Lobitzc S; Pasquini R; Giampietro PF; Hanenberg H; Levran O;
    Hum Mutat; 2003 Feb; 21(2):158-68. PubMed ID: 12552564
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry.
    Auerbach AD; Allen RG
    Cancer Genet Cytogenet; 1991 Jan; 51(1):1-12. PubMed ID: 1984836
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Induction of Fanconi anemia cellular phenotype in human 293 cells by overexpression of a mutant FAC allele.
    Youssoufian H; Li Y; Martin ME; Buchwald M
    J Clin Invest; 1996 Feb; 97(4):957-62. PubMed ID: 8613549
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development and characterization of immortalized fibroblastoid cell lines from an FA(C) mouse model.
    Tomkins DJ; Care M; Carreau M; Buchwald M
    Mutat Res; 1998 Jul; 408(1):27-35. PubMed ID: 9678061
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of FANCC gene mutations (IVS4+4A>T, del322G, and R548X)in patients with Fanconi anemia in Pakistan.
    Aftab I; Iram S; Khaliq S; Israr M; Ali N; Jahan S; Hussain S; Khaliq S; Mohsin S
    Turk J Med Sci; 2017 Apr; 47(2):391-398. PubMed ID: 28425259
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant.
    Lo ten Foe JR; Barel MT; Thuss P; Digweed M; Arwert F; Joenje H
    Hum Genet; 1996 Nov; 98(5):522-3. PubMed ID: 8882868
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.
    Bouchlaka C; Abdelhak S; Amouri A; Ben Abid H; Hadiji S; Frikha M; Ben Othman T; Amri F; Ayadi H; Hachicha M; Rebaï A; Saad A; Dellagi K;
    J Hum Genet; 2003; 48(7):352-61. PubMed ID: 12827451
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Bone marrow failure in the Fanconi anemia group C mouse model after DNA damage.
    Carreau M; Gan OI; Liu L; Doedens M; McKerlie C; Dick JE; Buchwald M
    Blood; 1998 Apr; 91(8):2737-44. PubMed ID: 9531583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells.
    Youssoufian H
    J Clin Invest; 1996 May; 97(9):2003-10. PubMed ID: 8621788
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.