Author:
Mori Masaki,Mimori Koshi,Inoue Hiroshi,Tanaka Yoichi,Huebner Kay,Croce Carlo M.
Reference13 articles.
1. Ohta M, Inoue H, Cotticelli MG, Kastury K, Baffa R, Palazzo J, Siprashvili Z, Mori M, McCue P, Druck T, Croce CM, Huebner K (1996) The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3, 8) breakpoint, is abnormal in digestive tract cancers. Cell 84:587–597
2. Inoue H, Ishii H, Alder H, Snyder E, Druck T, Huebner K, Croce CM (1997) Sequence of the FRA3B common fragile region: implications for the mechanisms of FHIT deletion. Proc Natl Acad Sci USA 94:14584–14589
3. Mimori K, Druck T, Inoue H, Alder H, Berk L, Mori M, Huebner K, Croce CM (1999) Cancer-specific chromosome alterations in the constitutive fragile region FRA3B. Proc Natl Acad Sci USA 96:7456–7461
4. Michael D, Beer DG, Wilke CW, Miller DE, Glover TW (1997) Frequent deletions of FHIT and FRA3B in Barrett’s metaplasia and esophageal adenocarcinomas. Oncogene 15:1653–1659
5. Nelson HN, Wieneke JK, Gunn L, Wain JC, Christiani DC, Kelsey KT (1998) Chromosome 3p14 alterations in lung cancer: evidence that FHIT exon deletion is a target of tobacco carcinogens and asbestos, Cancer Res 58:1804–1807