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Volumn 114, Issue 2, 1999, Pages 89-95

Allelotype of uterine leiomyomas

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DNA MINISATELLITE;

EID: 0032856432     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(99)00053-9     Document Type: Article
Times cited : (27)

References (36)
  • 3
    • 0024840305 scopus 로고
    • Effect of treatment with LHRH analogue Zoladex on binding of oestradiol, progesterone and epidermal growth factor to uterine fibromyomata
    • Baird D.T., Bramley T.A., Hawkins T.A., Lumsden M.A., West C.P. Effect of treatment with LHRH analogue Zoladex on binding of oestradiol, progesterone and epidermal growth factor to uterine fibromyomata. Horm Res. 32:1989;154-156.
    • (1989) Horm Res , vol.32 , pp. 154-156
    • Baird, D.T.1    Bramley, T.A.2    Hawkins, T.A.3    Lumsden, M.A.4    West, C.P.5
  • 4
    • 0025863612 scopus 로고
    • Uterine leiomyoma cytogenetics II. Report of forty cases
    • Vanni R., Lecca U., Faa G. Uterine leiomyoma cytogenetics II. Report of forty cases. Cancer Genet Cytogenet. 53:1991;247-256.
    • (1991) Cancer Genet Cytogenet , vol.53 , pp. 247-256
    • Vanni, R.1    Lecca, U.2    Faa, G.3
  • 7
  • 9
    • 0029023454 scopus 로고
    • A new cytogenetic subgroup in uterine leiomyoma is characterized by a deletion of the long arm of chromosome 3
    • Dal Cin P., Moerman P., Deprest J., Brosens I., Van den Berghe H. A new cytogenetic subgroup in uterine leiomyoma is characterized by a deletion of the long arm of chromosome 3. Genes Chromosom Cancer. 13:1995;219-220.
    • (1995) Genes Chromosom Cancer , vol.13 , pp. 219-220
    • Dal Cin, P.1    Moerman, P.2    Deprest, J.3    Brosens, I.4    Van Den Berghe, H.5
  • 10
    • 0030752387 scopus 로고    scopus 로고
    • HMGIC expressed in a uterine leiomyoma with a deletion of the long arm of chromosome 7 along with a 12q14-15 rearrangement but not in tumors showing del(7) as the sole cytogenetic abnormality
    • Henning Y., Rogalla P., Wanschura S., Frey G., Deichert U., Bartnitzke S., Bullerdiek J. HMGIC expressed in a uterine leiomyoma with a deletion of the long arm of chromosome 7 along with a 12q14-15 rearrangement but not in tumors showing del(7) as the sole cytogenetic abnormality. Cancer Genet Cytogenet. 96:1997;129-133.
    • (1997) Cancer Genet Cytogenet , vol.96 , pp. 129-133
    • Henning, Y.1    Rogalla, P.2    Wanschura, S.3    Frey, G.4    Deichert, U.5    Bartnitzke, S.6    Bullerdiek, J.7
  • 11
    • 0006197831 scopus 로고    scopus 로고
    • Cytogenetic markers in selected gynecological malignancies
    • S.R. Wolman, & S. Sell. Totowa: Humana Press
    • Fletcher J.A. Cytogenetic markers in selected gynecological malignancies. Wolman S.R., Sell S. Human Cytogenetic Cancer Markers. 1997;169-202 Humana Press, Totowa.
    • (1997) Human Cytogenetic Cancer Markers , pp. 169-202
    • Fletcher, J.A.1
  • 15
    • 0344588830 scopus 로고    scopus 로고
    • Molecular analysis of chromosome 7q21.3 in uterine leiomyoma: Analysis using markers with linkage to insulin resistance
    • Sell S.M., Altungoz O., Prowse A.A., Meloni A.M., Surti U., Sandberg A.A. Molecular analysis of chromosome 7q21.3 in uterine leiomyoma. analysis using markers with linkage to insulin resistance Cancer Genet Cytogenet. 100:1998;165-168.
    • (1998) Cancer Genet Cytogenet , vol.100 , pp. 165-168
    • Sell, S.M.1    Altungoz, O.2    Prowse, A.A.3    Meloni, A.M.4    Surti, U.5    Sandberg, A.A.6
  • 16
    • 0028144839 scopus 로고
    • Analysis of androgen receptor DNA reveals the independent clonal origins of uterine leiomyomata and secondary nature of cytogenetic aberrations in the development of leiomyomata
    • Mashal R.D., Fejzo M.L., Friedman A.J., Mitchner N., Nowak R.A., Rein M.S., Morton C.C., Sklar J. Analysis of androgen receptor DNA reveals the independent clonal origins of uterine leiomyomata and secondary nature of cytogenetic aberrations in the development of leiomyomata. Genes Chromosom Cancer. 11:1994;1-6.
    • (1994) Genes Chromosom Cancer , vol.11 , pp. 1-6
    • Mashal, R.D.1    Fejzo, M.L.2    Friedman, A.J.3    Mitchner, N.4    Nowak, R.A.5    Rein, M.S.6    Morton, C.C.7    Sklar, J.8
  • 17
    • 0030800817 scopus 로고    scopus 로고
    • The del(7q) subgroup in uterine leiomyomata: Genetic and biologic characteristics. Further evidence for the secondary nature of cytogenetic abnormalities in the pathobiology of uterine leiomyomata
    • Xing Y.P., Powell W.L., Morton C.C. The del(7q) subgroup in uterine leiomyomata. genetic and biologic characteristics. Further evidence for the secondary nature of cytogenetic abnormalities in the pathobiology of uterine leiomyomata Cancer Genet Cytogenet. 98:1997;69-74.
    • (1997) Cancer Genet Cytogenet , vol.98 , pp. 69-74
    • Xing, Y.P.1    Powell, W.L.2    Morton, C.C.3
  • 21
    • 0027960790 scopus 로고
    • Loss of heterozygosity in familial tumors from three BRCA1-linked kindreds
    • Neuhausen S.L., Marshall C.J. Loss of heterozygosity in familial tumors from three BRCA1-linked kindreds. Cancer Res. 54:1994;6069-6072.
    • (1994) Cancer Res , vol.54 , pp. 6069-6072
    • Neuhausen, S.L.1    Marshall, C.J.2
  • 23
    • 0028788975 scopus 로고
    • Familial cylindromatosis (turban tumor syndrome) gene localised to chromosome 16q12-q13: Evidence for its role as a tumor suppressor gene
    • Biggs P.J., Wooster R., Ford D., Chapman P., Mangion J., Quirk Y., Easton D.F., Burn J., Stratton M.R. Familial cylindromatosis (turban tumor syndrome) gene localised to chromosome 16q12-q13. evidence for its role as a tumor suppressor gene Nature Genet. 11:1995;441-443.
    • (1995) Nature Genet , vol.11 , pp. 441-443
    • Biggs, P.J.1    Wooster, R.2    Ford, D.3    Chapman, P.4    Mangion, J.5    Quirk, Y.6    Easton, D.F.7    Burn, J.8    Stratton, M.R.9
  • 24
    • 0029883923 scopus 로고    scopus 로고
    • The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumor suppressor gene involved in the development of cylindromas
    • Biggs P.J., Chapman P., Lakhani S.R., Burn J., Stratton M.R. The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumor suppressor gene involved in the development of cylindromas. Oncogene. 12:1996;1375-1377.
    • (1996) Oncogene , vol.12 , pp. 1375-1377
    • Biggs, P.J.1    Chapman, P.2    Lakhani, S.R.3    Burn, J.4    Stratton, M.R.5
  • 29
    • 0029936369 scopus 로고    scopus 로고
    • Report of the third international workshop on human chromosome 12 mapping 1995
    • Marynen P., Kucherlapati R. Report of the third international workshop on human chromosome 12 mapping 1995. Cytogenet Cell Genet. 73:1996;1-24.
    • (1996) Cytogenet Cell Genet , vol.73 , pp. 1-24
    • Marynen, P.1    Kucherlapati, R.2
  • 31
    • 0028122661 scopus 로고
    • Report of the fourth international workshop on human chromosome 22 mapping 1994
    • Scambler P.J. Report of the fourth international workshop on human chromosome 22 mapping 1994. Cytogenet Cell Genet. 67:1994;278-294.
    • (1994) Cytogenet Cell Genet , vol.67 , pp. 278-294
    • Scambler, P.J.1
  • 32
    • 0028641304 scopus 로고
    • Loss of heterozygosity in human primary prostate carcinomas: A possible tumor suppressor gene at 7q31.1
    • a
    • Zenklusen J.C., Thompson J.C., Troncoso P., Kagan J., Conti C.J. Loss of heterozygosity in human primary prostate carcinomas. a possible tumor suppressor gene at 7q31.1 Cancer Res. 54:1994;6370-6373. a.
    • (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
  • 33
    • 0028091664 scopus 로고
    • C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer
    • b
    • Zenklusen J.C., Bieche I., Lidereau R., Conti C.J. C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer. Proc Natl Acad Sci USA. 91:1994;12155-12158. b.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 12155-12158
    • Zenklusen, J.C.1    Bieche, I.2    Lidereau, R.3    Conti, C.J.4
  • 34
    • 0028929987 scopus 로고
    • Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 7q31.1: Evidence for a broad range tumor suppressor gene
    • a
    • Zenklusen J.C., Thompson J.C., Klein-Szanto A.J., Conti C.J. Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 7q31.1. evidence for a broad range tumor suppressor gene Cancer Res. 55:1995;1347-1350. a.
    • (1995) Cancer Res , vol.55 , pp. 1347-1350
    • Zenklusen, J.C.1    Thompson, J.C.2    Klein-Szanto, A.J.3    Conti, C.J.4
  • 35
    • 0029121078 scopus 로고
    • Allelic loss at 7q31.1 in human primary ovarian carcinomas suggests the existence of a tumor suppressor gene
    • b
    • Zenklusen J.C., Weitzel J.N., Ball H.G., Conti C.J. Allelic loss at 7q31.1 in human primary ovarian carcinomas suggests the existence of a tumor suppressor gene. Oncogene. 11:1995;359-363. b.
    • (1995) Oncogene , vol.11 , pp. 359-363
    • Zenklusen, J.C.1    Weitzel, J.N.2    Ball, H.G.3    Conti, C.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.