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Volumn 21, Issue 2, 1998, Pages 152-159

Fish mapping of YAC clones at human chromosomal band 7q31.2: Identification of YACS spanning FRA7G within the common region of LOH in breast and prostate cancer

Author keywords

[No Author keywords available]

Indexed keywords

APHIDICOLIN; CONTIG; DNA;

EID: 0031892622     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199802)21:2<152::AID-GCC11>3.0.CO;2-T     Document Type: Article
Times cited : (69)

References (52)
  • 1
    • 0021675966 scopus 로고
    • Nonrandom distribution of methotrexate-induced aberrations on human chromosomes: Detection of further folie acid sensitive fragile sites
    • Barbi G, Steinbach P, Vogel W (1984) Nonrandom distribution of methotrexate-induced aberrations on human chromosomes: Detection of further folie acid sensitive fragile sites. Hum Genet 68:290-294.
    • (1984) Hum Genet , vol.68 , pp. 290-294
    • Barbi, G.1    Steinbach, P.2    Vogel, W.3
  • 3
    • 0022371326 scopus 로고
    • Report of the committee on chromosome rearrangements on neoplasia and on fragile sites (HGM8)
    • Berger R, Bloomfield CD, Sutherland GR (1985) Report of the committee on chromosome rearrangements on neoplasia and on fragile sites (HGM8). Cytogenet Cell Genet 40:490-535.
    • (1985) Cytogenet Cell Genet , vol.40 , pp. 490-535
    • Berger, R.1    Bloomfield, C.D.2    Sutherland, G.R.3
  • 9
    • 0030904279 scopus 로고    scopus 로고
    • Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons
    • Coquelle A, Pipiras E, Toledo F, Buttin G, Debatisse M (1997) Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons. Cell 89:215-225.
    • (1997) Cell , vol.89 , pp. 215-225
    • Coquelle, A.1    Pipiras, E.2    Toledo, F.3    Buttin, G.4    Debatisse, M.5
  • 12
    • 0021278143 scopus 로고
    • DNA polymerase inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
    • Glover TW, Berger C, Coyle-Morris J, Echo B (1984) DNA polymerase inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum Genet 67:882-890.
    • (1984) Hum Genet , vol.67 , pp. 882-890
    • Glover, T.W.1    Berger, C.2    Coyle-Morris, J.3    Echo, B.4
  • 13
    • 0023789150 scopus 로고
    • Chromosome breakage and recombination at fragile sites
    • Glover TW, Stein CK (1988) Chromosome breakage and recombination at fragile sites. Am J Hum Genet 43:265-273.
    • (1988) Am J Hum Genet , vol.43 , pp. 265-273
    • Glover, T.W.1    Stein, C.K.2
  • 14
    • 0026007187 scopus 로고
    • Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artitical chromosomes
    • Green ED, Mohr RM, Idol JR, Jones M, Buckingham JM, Deaven L, Moyzis RK, Olson MV (1991) Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artitical chromosomes. Genomics 11:548-564.
    • (1991) Genomics , vol.11 , pp. 548-564
    • Green, E.D.1    Mohr, R.M.2    Idol, J.R.3    Jones, M.4    Buckingham, J.M.5    Deaven, L.6    Moyzis, R.K.7    Olson, M.V.8
  • 15
    • 0025914050 scopus 로고
    • Sister chromid exchanges are preferentially induced at expressed and nonexpressed common fragile sites
    • Hirsch B (1991) Sister chromid exchanges are preferentially induced at expressed and nonexpressed common fragile sites. Hum Genet 87:302-306.
    • (1991) Hum Genet , vol.87 , pp. 302-306
    • Hirsch, B.1
  • 16
    • 0025319997 scopus 로고
    • Biochemical and genetic analysis of the Chinese hamster mutants irs1 and irs2 and their comparison to cultured ataxia telangiectasia cells
    • Jones NJ, Stewart SA, Thompson LH (1990) Biochemical and genetic analysis of the Chinese hamster mutants irs1 and irs2 and their comparison to cultured ataxia telangiectasia cells. Mutagenesis 5:15-23.
    • (1990) Mutagenesis , vol.5 , pp. 15-23
    • Jones, N.J.1    Stewart, S.A.2    Thompson, L.H.3
  • 21
    • 0028037032 scopus 로고
    • Frequent loss of heterozygosity of the long arm of chromosome 7 is closely associated with progression of human gastric carcinomas
    • Kuniyasu H, Yasui W, Yokozaki H, Akagi M, Kitahara K, Fujii K, Tahara E (1994) Frequent loss of heterozygosity of the long arm of chromosome 7 is closely associated with progression of human gastric carcinomas. Int J Cancer 59:597-600.
    • (1994) Int J Cancer , vol.59 , pp. 597-600
    • Kuniyasu, H.1    Yasui, W.2    Yokozaki, H.3    Akagi, M.4    Kitahara, K.5    Fujii, K.6    Tahara, E.7
  • 22
    • 0025262465 scopus 로고
    • Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts
    • Kuwano A, Murano I, Kajii T (1990) Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts. Hum Genet 84:527-531.
    • (1990) Hum Genet , vol.84 , pp. 527-531
    • Kuwano, A.1    Murano, I.2    Kajii, T.3
  • 24
    • 0025609090 scopus 로고
    • "PCR-karyotype" of human chromosomes in somatic cell hybrids
    • Ledbetter SA, Garcia-Heras J, Ledbetter DH (1990) "PCR-karyotype" of human chromosomes in somatic cell hybrids. Genomics 8:614-622.
    • (1990) Genomics , vol.8 , pp. 614-622
    • Ledbetter, S.A.1    Garcia-Heras, J.2    Ledbetter, D.H.3
  • 25
    • 0029963491 scopus 로고    scopus 로고
    • Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET
    • Lin JC, Scherer SW, Tongas L, Traverso G, Tsui L-C, Andrulis I, Jothy S, Park M (1996) Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET. Oncogene 13:2001-2008.
    • (1996) Oncogene , vol.13 , pp. 2001-2008
    • Lin, J.C.1    Scherer, S.W.2    Tongas, L.3    Traverso, G.4    Tsui, L.-C.5    Andrulis, I.6    Jothy, S.7    Park, M.8
  • 31
    • 0030201105 scopus 로고    scopus 로고
    • A 350-kb cosmid contig in 3p14.2 that cross the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints
    • Paradee W, Wilke CM, Wang L, Shridhar R, Mullins CM, Hoge A, Glover TW, Smith DI (1996) A 350-kb cosmid contig in 3p14.2 that cross the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints. Genomics 35:87-93.
    • (1996) Genomics , vol.35 , pp. 87-93
    • Paradee, W.1    Wilke, C.M.2    Wang, L.3    Shridhar, R.4    Mullins, C.M.5    Hoge, A.6    Glover, T.W.7    Smith, D.I.8
  • 37
    • 0030700907 scopus 로고    scopus 로고
    • Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas
    • In Press
    • Shridhar V, Sun QC, Miller OJ, Kalemkerian GP, Petros J, Smith DI (1997b) Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas. Oncogene, In Press.
    • (1997) Oncogene
    • Shridhar, V.1    Sun, Q.C.2    Miller, O.J.3    Kalemkerian, G.P.4    Petros, J.5    Smith, D.I.6
  • 42
    • 0030575839 scopus 로고    scopus 로고
    • Long CCG triplet repeat blocks exclude nucleosomes: A possible mechanism for the nature of fragile sites in chromosomes
    • Wang YH, Gellibolian R, Shimizu M, Wells RD, Griffith J (1996) Long CCG triplet repeat blocks exclude nucleosomes: A possible mechanism for the nature of fragile sites in chromosomes. J Mol Biol 263:511-516.
    • (1996) J Mol Biol , vol.263 , pp. 511-516
    • Wang, Y.H.1    Gellibolian, R.2    Shimizu, M.3    Wells, R.D.4    Griffith, J.5
  • 44
    • 0028004727 scopus 로고
    • Two independent amplification events on chromosome 7 in glioma: Amplification of rhe epidermal growth factor receptor gene and amplification of the oncogene MET
    • Wullich B, Sattler HP, Fisher U, Meese E (1994) Two independent amplification events on chromosome 7 in glioma: Amplification of rhe epidermal growth factor receptor gene and amplification of the oncogene MET. Anticancer Res 14:577-579.
    • (1994) Anticancer Res , vol.14 , pp. 577-579
    • Wullich, B.1    Sattler, H.P.2    Fisher, U.3    Meese, E.4
  • 47
    • 0021690129 scopus 로고
    • Constitutive fragile sites and cancer
    • Yunis JJ, Soreng AL (1984) Constitutive fragile sites and cancer. Science 226:1199-1204.
    • (1984) Science , vol.226 , pp. 1199-1204
    • Yunis, J.J.1    Soreng, A.L.2
  • 48
    • 0028091664 scopus 로고
    • n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer
    • n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer. Proc Natl Acad Sci USA 91:12155-12158.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 12155-12158
    • Zenklusen, J.1    Bieche, I.2    Lidereau, R.3    Conti, C.4
  • 49
    • 0028641304 scopus 로고
    • Loss of heterozygosity in human prostate carcinomas: A possible tumor suppressor gene at 7q31.1
    • Zenklusen JC, Thompson JC, Troncoso P, Kagan J, Conti CJ (1994b) Loss of heterozygosity in human prostate carcinomas: A possible tumor suppressor gene at 7q31.1. Cancer Res 54:6370-6373.
    • (1994) Cancer Res , vol.54 , pp. 6370-6373
    • Zenklusen, J.C.1    Thompson, J.C.2    Troncoso, P.3    Kagan, J.4    Conti, C.J.5
  • 50
    • 0028929987 scopus 로고
    • Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 1q31.1: Evidence for a broad range tumor suppressor gene
    • Zenklusen JC, Thompson JC, Klein-Szanto AJP, Conti CJ (1995a) Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 1q31.1: Evidence for a broad range tumor suppressor gene. Cancer Res 55:1347-1350.
    • (1995) Cancer Res , vol.55 , pp. 1347-1350
    • Zenklusen, J.C.1    Thompson, J.C.2    Klein-Szanto, A.J.P.3    Conti, C.J.4
  • 51
    • 0029121078 scopus 로고
    • Allelic loss at 7q31.1 in human primary ovarian carcinomas suggests the existence of a tumor suppressor gene
    • Zenklusen J, Weitzel J, Ball H, Conti C (1995b) Allelic loss at 7q31.1 in human primary ovarian carcinomas suggests the existence of a tumor suppressor gene. Oneogcne 11:359-363.
    • (1995) Oneogcne , vol.11 , pp. 359-363
    • Zenklusen, J.1    Weitzel, J.2    Ball, H.3    Conti, C.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.