메뉴 건너뛰기




Volumn 41, Issue 1, 1997, Pages 49-55

A high-density STS map based on a single contig of YAC and P1 clones in the chromosome 8p12-p21 region

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER;

EID: 0031127214     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4619     Document Type: Article
Times cited : (3)

References (38)
  • 1
    • 0025368589 scopus 로고
    • Construction and characterization of a human yeast artificial chromosome library containing seven haploid genome equivalents
    • Albertsen, H. M., Abderrahim, H., Cann, H. M., Dausset, J., Le Paslier, D., and Cohen, D. (1990). Construction and characterization of a human yeast artificial chromosome library containing seven haploid genome equivalents. Proc. Natl. Acad. Sci. USA 87: 4256-4260.
    • (1990) Proc. Natl. Acad. Sci. USA , vol.87 , pp. 4256-4260
    • Albertsen, H.M.1    Abderrahim, H.2    Cann, H.M.3    Dausset, J.4    Le Paslier, D.5    Cohen, D.6
  • 2
    • 0023349389 scopus 로고
    • Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors
    • Burke, D. T., Carle, G. F., and Olson, M. V. (1987). Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors. Science 236: 806-812.
    • (1987) Science , vol.236 , pp. 806-812
    • Burke, D.T.1    Carle, G.F.2    Olson, M.V.3
  • 5
    • 0028364668 scopus 로고
    • Deletion mapping of chromosome 8p in colorectal carcinoma and dysplasia arising in ulcerative colitis, prostatic carcinoma, and malignant fibrous histiocytomas
    • Chang, M., Tsuchiya, K., Batchelor, R. H., Rabinovitch, P. S., Kulander, B. G., Haggitt, R. C., and Burmer, G. C. (1994). Deletion mapping of chromosome 8p in colorectal carcinoma and dysplasia arising in ulcerative colitis, prostatic carcinoma, and malignant fibrous histiocytomas. Am. J. Pathol. 144: 1-6.
    • (1994) Am. J. Pathol. , vol.144 , pp. 1-6
    • Chang, M.1    Tsuchiya, K.2    Batchelor, R.H.3    Rabinovitch, P.S.4    Kulander, B.G.5    Haggitt, R.C.6    Burmer, G.C.7
  • 7
    • 0027723477 scopus 로고
    • A first-generation physical map of the human genome
    • Cohen, D., Chumakov, I., and Weissenbach, J. (1993). A first-generation physical map of the human genome. Nature 366: 698-701.
    • (1993) Nature , vol.366 , pp. 698-701
    • Cohen, D.1    Chumakov, I.2    Weissenbach, J.3
  • 8
    • 0024461309 scopus 로고
    • Happy mapping: A proposal for linkage mapping the human genome
    • Dear, P. H., and Cook, P. R. (1989). Happy mapping: A proposal for linkage mapping the human genome. Nucleic Acids Res. 17: 6795-6807.
    • (1989) Nucleic Acids Res. , vol.17 , pp. 6795-6807
    • Dear, P.H.1    Cook, P.R.2
  • 9
    • 0013907774 scopus 로고
    • Werner's syndrome: A review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process
    • Epstein, C. J., Martin, G. M., Schultz, A. L., and Motulsky, A. G. (1966). Werner's syndrome: A review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process. Medicine 45: 177-222.
    • (1966) Medicine , vol.45 , pp. 177-222
    • Epstein, C.J.1    Martin, G.M.2    Schultz, A.L.3    Motulsky, A.G.4
  • 10
    • 0029971818 scopus 로고    scopus 로고
    • Towards localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: Lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers
    • Goddard, K. A. B., Yu, C.-E., Oshima, J., Miki, T., Nakura, J., Piussan, C., Martin, G. M., Schellenberg, G. D., and Wijsman, E. M., and members of the International Werner's Syndrome Collaborative Group (1996). Towards localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: Lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers. Am. J. Hum. Genet. 58: 1286-1302.
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 1286-1302
    • Goddard, K.A.B.1    Yu, C.-E.2    Oshima, J.3    Miki, T.4    Nakura, J.5    Piussan, C.6    Martin, G.M.7    Schellenberg, G.D.8    Wijsman, E.M.9
  • 12
    • 0025163052 scopus 로고
    • Second-generation approach to the construction of yeast artificial-chromosome libraries
    • Imai, T., and Olson, M. V. (1990). Second-generation approach to the construction of yeast artificial-chromosome libraries. Genomics 8: 297-303.
    • (1990) Genomics , vol.8 , pp. 297-303
    • Imai, T.1    Olson, M.V.2
  • 14
    • 0027080011 scopus 로고
    • Practical application in molecular biology of sensitive fluorescence detection by a laser-excited fluorescence image analyzer
    • Ishino, Y., Mineno, J., Inoue, T., Fujimiya, H., Yamamoto, K., Tamura, T., Homma, M., Tanaka, K., and Kato, I. (1992). Practical application in molecular biology of sensitive fluorescence detection by a laser-excited fluorescence image analyzer. Biotechniques 13: 936-943.
    • (1992) Biotechniques , vol.13 , pp. 936-943
    • Ishino, Y.1    Mineno, J.2    Inoue, T.3    Fujimiya, H.4    Yamamoto, K.5    Tamura, T.6    Homma, M.7    Tanaka, K.8    Kato, I.9
  • 15
    • 0028589208 scopus 로고
    • Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus
    • Kihara, K., Nakura, J., Ye, L., Mitsuda, N., Kamino, K., Zhao, Y., Fujioka, Y., Miki, T., and Ogihara, T. (1995). Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus. Jpn. J. Hum. Genet. 39: 403-409.
    • (1995) Jpn. J. Hum. Genet. , vol.39 , pp. 403-409
    • Kihara, K.1    Nakura, J.2    Ye, L.3    Mitsuda, N.4    Kamino, K.5    Zhao, Y.6    Fujioka, Y.7    Miki, T.8    Ogihara, T.9
  • 26
    • 0002777386 scopus 로고
    • Report of the committee for clinical disorders and chromosome aberrations
    • A. J. Cuticchia and P. L. Pearson, Eds., Johns Hopkins Press, Baltimore/London
    • Schinzel, A., McKusick, V. A., Francomano, C., and Pearson, P. L. (1994). Report of the Committee for Clinical Disorders and Chromosome Aberrations. In "Human Gene Mapping, 1993" (A. J. Cuticchia and P. L. Pearson, Eds.), pp. 735-772, Johns Hopkins Press, Baltimore/London.
    • (1994) Human Gene Mapping, 1993 , pp. 735-772
    • Schinzel, A.1    McKusick, V.A.2    Francomano, C.3    Pearson, P.L.4
  • 31
    • 0029150405 scopus 로고
    • Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): Chromosome microdissection and homozygosity mapping
    • Ye, L., Nakura, J., Mitsuda, N., Fujioka, Y., Kamino, K., Ohta, T., Jinno, Y., Niikawa, N., Miki, T., and Ogihara, T. (1995b). Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): Chromosome microdissection and homozygosity mapping. Genomics 28: 566-569.
    • (1995) Genomics , vol.28 , pp. 566-569
    • Ye, L.1    Nakura, J.2    Mitsuda, N.3    Fujioka, Y.4    Kamino, K.5    Ohta, T.6    Jinno, Y.7    Niikawa, N.8    Miki, T.9    Ogihara, T.10
  • 34
    • 0025215315 scopus 로고
    • Rothmund-Thomson syndrome associated with trisomy 8 mosaicism
    • Ying, K. L., Oizumi, J., and Curry, C. J. R. (1990). Rothmund-Thomson syndrome associated with trisomy 8 mosaicism. J. Med. Genet. 27: 258-260.
    • (1990) J. Med. Genet. , vol.27 , pp. 258-260
    • Ying, K.L.1    Oizumi, J.2    Curry, C.J.R.3
  • 38
    • 0030218834 scopus 로고    scopus 로고
    • A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21
    • Yu, C.-E., Oshima, J., Hisama, F. M., Matthews, S., Trask, B. J., and Schellenberg, G. D. (1996b). A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21. Genomics 35: 431-440.
    • (1996) Genomics , vol.35 , pp. 431-440
    • Yu, C.-E.1    Oshima, J.2    Hisama, F.M.3    Matthews, S.4    Trask, B.J.5    Schellenberg, G.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.