BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

282 related articles for article (PubMed ID: 10861292)

  • 1. Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells.
    Ried K; Finnis M; Hobson L; Mangelsdorf M; Dayan S; Nancarrow JK; Woollatt E; Kremmidiotis G; Gardner A; Venter D; Baker E; Richards RI
    Hum Mol Genet; 2000 Jul; 9(11):1651-63. PubMed ID: 10861292
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A 700-kb physical map of a region of 16q23.2 homozygously deleted in multiple cancers and spanning the common fragile site FRA16D.
    Paige AJ; Taylor KJ; Stewart A; Sgouros JG; Gabra H; Sellar GC; Smyth JF; Porteous DJ; Watson JE
    Cancer Res; 2000 Mar; 60(6):1690-7. PubMed ID: 10749141
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Common chromosomal fragile site FRA16D mutation in cancer cells.
    Finnis M; Dayan S; Hobson L; Chenevix-Trench G; Friend K; Ried K; Venter D; Woollatt E; Baker E; Richards RI
    Hum Mol Genet; 2005 May; 14(10):1341-9. PubMed ID: 15814586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosomal fragile site FRA16D and DNA instability in cancer.
    Mangelsdorf M; Ried K; Woollatt E; Dayan S; Eyre H; Finnis M; Hobson L; Nancarrow J; Venter D; Baker E; Richards RI
    Cancer Res; 2000 Mar; 60(6):1683-9. PubMed ID: 10749140
    [TBL] [Abstract][Full Text] [Related]  

  • 5. WWOX, the common chromosomal fragile site, FRA16D, cancer gene.
    Ludes-Meyers JH; Bednarek AK; Popescu NC; Bedford M; Aldaz CM
    Cytogenet Genome Res; 2003; 100(1-4):101-10. PubMed ID: 14526170
    [TBL] [Abstract][Full Text] [Related]  

  • 6. WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer.
    Bednarek AK; Laflin KJ; Daniel RL; Liao Q; Hawkins KA; Aldaz CM
    Cancer Res; 2000 Apr; 60(8):2140-5. PubMed ID: 10786676
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations.
    Krummel KA; Roberts LR; Kawakami M; Glover TW; Smith DI
    Genomics; 2000 Oct; 69(1):37-46. PubMed ID: 11013073
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An AT-rich sequence in human common fragile site FRA16D causes fork stalling and chromosome breakage in S. cerevisiae.
    Zhang H; Freudenreich CH
    Mol Cell; 2007 Aug; 27(3):367-79. PubMed ID: 17679088
    [TBL] [Abstract][Full Text] [Related]  

  • 9. WWOX, the chromosomal fragile site FRA16D spanning gene: its role in metabolism and contribution to cancer.
    Richards RI; Choo A; Lee CS; Dayan S; O'Keefe L
    Exp Biol Med (Maywood); 2015 Mar; 240(3):338-44. PubMed ID: 25595186
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FRA16D common chromosomal fragile site oxido-reductase (FOR/WWOX) protects against the effects of ionizing radiation in Drosophila.
    O'Keefe LV; Liu Y; Perkins A; Dayan S; Saint R; Richards RI
    Oncogene; 2005 Sep; 24(43):6590-6. PubMed ID: 16007179
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma.
    Fang JM; Arlt MF; Burgess AC; Dagenais SL; Beer DG; Glover TW
    Genes Chromosomes Cancer; 2001 Mar; 30(3):292-8. PubMed ID: 11170287
    [TBL] [Abstract][Full Text] [Related]  

  • 12. WWOX, the FRA16D gene: A target of and a contributor to genomic instability.
    Hussain T; Liu B; Shrock MS; Williams T; Aldaz CM
    Genes Chromosomes Cancer; 2019 May; 58(5):324-338. PubMed ID: 30350478
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Common chromosomal fragile sites and cancer: focus on FRA16D.
    O'Keefe LV; Richards RI
    Cancer Lett; 2006 Jan; 232(1):37-47. PubMed ID: 16242840
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers.
    Ohta M; Inoue H; Cotticelli MG; Kastury K; Baffa R; Palazzo J; Siprashvili Z; Mori M; McCue P; Druck T; Croce CM; Huebner K
    Cell; 1996 Feb; 84(4):587-97. PubMed ID: 8598045
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) loci.
    Fratini A; Simmers RN; Callen DF; Hyland VJ; Tischfield JA; Stambrook PJ; Sutherland GR
    Cytogenet Cell Genet; 1986; 43(1-2):10-3. PubMed ID: 3780312
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.
    Morelli C; Karayianni E; Magnanini C; Mungall AJ; Thorland E; Negrini M; Smith DI; Barbanti-Brodano G
    Oncogene; 2002 Oct; 21(47):7266-76. PubMed ID: 12370818
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells.
    Arlt MF; Miller DE; Beer DG; Glover TW
    Genes Chromosomes Cancer; 2002 Jan; 33(1):82-92. PubMed ID: 11746990
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alterations of common chromosome fragile sites in hematopoietic malignancies.
    Ishii H; Furukawa Y
    Int J Hematol; 2004 Apr; 79(3):238-42. PubMed ID: 15168591
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors.
    Corbin S; Neilly ME; Espinosa R; Davis EM; McKeithan TW; Le Beau MM
    Cancer Res; 2002 Jun; 62(12):3477-84. PubMed ID: 12067991
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Human chromosome fragility.
    Lukusa T; Fryns JP
    Biochim Biophys Acta; 2008 Jan; 1779(1):3-16. PubMed ID: 18078840
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.