-
1
-
-
0025368589
-
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
-
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
-
3
-
-
0029118377
-
Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: Demonstration of a "hot spot" for recombination at 16p12
-
Callen, D. F., Lane, S. A., Kozman, H., Kremmidiotis, G., Whitmore, S.A., Lowenstein, M., Doggett, N. A., Kenmochi, N., Page, D. C., Maglott, D. R., Nierman, W. C., Murakawa, K., Berry, R., Sikela, J. M., Houlgatte, R., Auffray, C., and Sutherland, G. R. (1995). Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: Demonstration of a "hot spot" for recombination at 16p12. Genomics 29: 503-511.
-
(1995)
Genomics
, vol.29
, pp. 503-511
-
-
Callen, D.F.1
Lane, S.A.2
Kozman, H.3
Kremmidiotis, G.4
Whitmore, S.A.5
Lowenstein, M.6
Doggett, N.A.7
Kenmochi, N.8
Page, D.C.9
Maglott, D.R.10
Nierman, W.C.11
Murakawa, K.12
Berry, R.13
Sikela, J.M.14
Houlgatte, R.15
Auffray, C.16
Sutherland, G.R.17
-
4
-
-
0030057689
-
A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8
-
Chaffanet, M., Imbert, A., Adelaide, J., Le-Paslier, D., Wagner, M. J., Wells, D. E., Birnbaum, D., and Pebusque, M. J. (1996). A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8. Cytogenet. Cell Genet. 72: 63-68.
-
(1996)
Cytogenet. Cell Genet.
, vol.72
, pp. 63-68
-
-
Chaffanet, M.1
Imbert, A.2
Adelaide, J.3
Le-Paslier, D.4
Wagner, M.J.5
Wells, D.E.6
Birnbaum, D.7
Pebusque, M.J.8
-
5
-
-
0028364668
-
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
-
6
-
-
0026878997
-
Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome library
-
Chumakov, I. M., Le Gall, I., Billault, A., Soularue, P., Guillou, S., Rigault, P., Bui, H., De Tand, M.-F., Barillot, E., Abderrahim, H., Cherif, D., Berger, R., Le Paslier, D., and Cohen, D. (1992). Isolation of chromosome 21-specific yeast artificial chromosomes from a total human genome library. Nature Genet. 1: 222-225.
-
(1992)
Nature Genet.
, vol.1
, pp. 222-225
-
-
Chumakov, I.M.1
Le Gall, I.2
Billault, A.3
Soularue, P.4
Guillou, S.5
Rigault, P.6
Bui, H.7
De Tand, M.-F.8
Barillot, E.9
Abderrahim, H.10
Cherif, D.11
Berger, R.12
Le Paslier, D.13
Cohen, D.14
-
7
-
-
0027723477
-
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
-
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
-
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
-
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
-
11
-
-
0029416826
-
An STS-based map of the human genome
-
Hudson, T. J., Stein, L. D., Gerety, S. S., Ma, J., Castle, A. B., Silva, J., Slonim, D. K., Baptista, R., Kruglyak, L., Xu, S. H., Hu, X., Colbert, A. M. E., Rosenberg, C., Reeve-Daly, M. P., Rozen, S., Hui, L., Wu, X., Vestergaard, C., Wilson, K. M., Bae, J. S., Maitra, S., Ganiatsas, S., Evans, C. A., DeAngelis, M. M., Ingalls, K. A., Nahf, R. W., Horton, L. T., Jr., Anderson, M. O., Collymore, A. J., Ye, W., Kouyoumjian, V., Zemsteva, I. S., Tam, J., Devine, R., Courtney, D. F., Renaud, M. T., Nguyen, H., O'Connor, T. J., Fizames, C., Faure, S., Gyapay, G., Dib, C., Morissette, J., Orlin, J. B., Birren, B. W., Goodman, N., Weissenbach, J., Hawkins, T. L., Foote, S., Page, D. C., and Lander, E. S. (1995). An STS-based map of the human genome. Science 270: 1945-1954.
-
(1995)
Science
, vol.270
, pp. 1945-1954
-
-
Hudson, T.J.1
Stein, L.D.2
Gerety, S.S.3
Ma, J.4
Castle, A.B.5
Silva, J.6
Slonim, D.K.7
Baptista, R.8
Kruglyak, L.9
Xu, S.H.10
Hu, X.11
Colbert, A.M.E.12
Rosenberg, C.13
Reeve-Daly, M.P.14
Rozen, S.15
Hui, L.16
Wu, X.17
Vestergaard, C.18
Wilson, K.M.19
Bae, J.S.20
Maitra, S.21
Ganiatsas, S.22
Evans, C.A.23
DeAngelis, M.M.24
Ingalls, K.A.25
Nahf, R.W.26
Horton L.T., Jr.27
Anderson, M.O.28
Collymore, A.J.29
Ye, W.30
Kouyoumjian, V.31
Zemsteva, I.S.32
Tam, J.33
Devine, R.34
Courtney, D.F.35
Renaud, M.T.36
Nguyen, H.37
O'Connor, T.J.38
Fizames, C.39
Faure, S.40
Gyapay, G.41
Dib, C.42
Morissette, J.43
Orlin, J.B.44
Birren, B.W.45
Goodman, N.46
Weissenbach, J.47
Hawkins, T.L.48
Foote, S.49
Page, D.C.50
Lander, E.S.51
more..
-
12
-
-
0025163052
-
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
-
13
-
-
18544412846
-
Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome
-
Imbert, A., Chaffanet, M., Essioux, L., Noguchi, T., Adelaide, J., Kerangueven, F., Le-Paslier, D., Bonaiti-Pellie, C., Sobol, H., Birnbaum, D., and Pebusque, M. J. (1996). Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome. Genomics 32: 29-38.
-
(1996)
Genomics
, vol.32
, pp. 29-38
-
-
Imbert, A.1
Chaffanet, M.2
Essioux, L.3
Noguchi, T.4
Adelaide, J.5
Kerangueven, F.6
Le-Paslier, D.7
Bonaiti-Pellie, C.8
Sobol, H.9
Birnbaum, D.10
Pebusque, M.J.11
-
14
-
-
0027080011
-
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
-
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
-
16
-
-
0029148888
-
Construction of 110 cosmid markers and a 4.5-Mb YAC contig on human chromosome 8p12-q11
-
Kurimasa, A., Suzuki, N., Kumano, S., Li, H., Wells, D., Wagner, M. J., Chen, F., Chen, D. J., and Oshimura, M. (1995). Construction of 110 cosmid markers and a 4.5-Mb YAC contig on human chromosome 8p12-q11. Genomics 28: 147-153.
-
(1995)
Genomics
, vol.28
, pp. 147-153
-
-
Kurimasa, A.1
Suzuki, N.2
Kumano, S.3
Li, H.4
Wells, D.5
Wagner, M.J.6
Chen, F.7
Chen, D.J.8
Oshimura, M.9
-
17
-
-
0028787670
-
Three dinucleotide repeat polymorphisms at the D8S1217, D8S1220 and D8S1221 loci
-
Mitsuda, N., Nakura, J., Ye, L., Takahashi-Fujii, A., Ishino, Y., Kato, I., Miki, T., and Ogihara, T. (1995). Three dinucleotide repeat polymorphisms at the D8S1217, D8S1220 and D8S1221 loci. Jpn. J. Hum. Genet. 40: 283-285.
-
(1995)
Jpn. J. Hum. Genet.
, vol.40
, pp. 283-285
-
-
Mitsuda, N.1
Nakura, J.2
Ye, L.3
Takahashi-Fujii, A.4
Ishino, Y.5
Kato, I.6
Miki, T.7
Ogihara, T.8
-
18
-
-
0029761189
-
A dinucleotide repeat polymorphism at the D8S1223 locus
-
Mitsuda, N., Nakura, J., Ye, L., Takahashi-Fujii, A., Ishino, Y., Kato, I., Miki, T., and Ogihara, T. (1996). A dinucleotide repeat polymorphism at the D8S1223 locus. Jpn. J. Hum. Genet. 41: 265-266.
-
(1996)
Jpn. J. Hum. Genet.
, vol.41
, pp. 265-266
-
-
Mitsuda, N.1
Nakura, J.2
Ye, L.3
Takahashi-Fujii, A.4
Ishino, Y.5
Kato, I.6
Miki, T.7
Ogihara, T.8
-
19
-
-
0027742147
-
Isolation and mapping of microsatellites from a library microdissected from the Werner's syndrome region, 8p11.2-p22
-
Nagano, K., Nakura, J., Kihara, K., Ye, L., Kamino, K., Mitsuda, M., Ohta, T., Jinno, Y., Niikawa, N., Miki, T., and Ogihara, T. (1993). Isolation and mapping of microsatellites from a library microdissected from the Werner's syndrome region, 8p11.2-p22. Jpn. J. Hum. Genet. 38: 391-397.
-
(1993)
Jpn. J. Hum. Genet.
, vol.38
, pp. 391-397
-
-
Nagano, K.1
Nakura, J.2
Kihara, K.3
Ye, L.4
Kamino, K.5
Mitsuda, M.6
Ohta, T.7
Jinno, Y.8
Niikawa, N.9
Miki, T.10
Ogihara, T.11
-
20
-
-
0028079995
-
Homozygosity mapping of the Werner syndrome locus (WRN)
-
Nakura, J., Wijsman, E. M., Miki, T., Kamino, K., Yu, C.-E., Oshima, J., Fukuchi, K., Weber, J. L., Piussan, C., Melaragno, M. I., Epstein, C. J., Scappaticci, S., Fraccaro, M., Matsumura, T., Murano, S., Yoshida, S., Fujiwara, Y., Saida, T., Ogihara, T., Martin, G. M., and Schellenberg, G. D. (1994a). Homozygosity mapping of the Werner syndrome locus (WRN). Genomics 23: 600-608.
-
(1994)
Genomics
, vol.23
, pp. 600-608
-
-
Nakura, J.1
Wijsman, E.M.2
Miki, T.3
Kamino, K.4
Yu, C.-E.5
Oshima, J.6
Fukuchi, K.7
Weber, J.L.8
Piussan, C.9
Melaragno, M.I.10
Epstein, C.J.11
Scappaticci, S.12
Fraccaro, M.13
Matsumura, T.14
Murano, S.15
Yoshida, S.16
Fujiwara, Y.17
Saida, T.18
Ogihara, T.19
Martin, G.M.20
Schellenberg, G.D.21
more..
-
21
-
-
0028580263
-
Dinucleotide repeat polymorphism at the D8S1053
-
Nakura, J., Ye, L., Mitsuda, N., Takahashi-Fujii, A., Ishino, Y., Miki, T., and Ogihara, T. (1994b). Dinucleotide repeat polymorphism at the D8S1053. Jpn. J. Hum. Genet. 39: 445-446.
-
(1994)
Jpn. J. Hum. Genet.
, vol.39
, pp. 445-446
-
-
Nakura, J.1
Ye, L.2
Mitsuda, N.3
Takahashi-Fujii, A.4
Ishino, Y.5
Miki, T.6
Ogihara, T.7
-
22
-
-
0030035928
-
Two polymorphic dinucleotide repeat polymorphisms at the D8S1444 and D8S1445 loci
-
Nakura, J., Ye, L., Mitsuda, N., Takahashi-Fujii, A., Ishino, Y., Kato, I., Miki, T., and Ogihara, T. (1996a). Two polymorphic dinucleotide repeat polymorphisms at the D8S1444 and D8S1445 loci. Jpn. J. Hum. Genet. 41: 261-263.
-
(1996)
Jpn. J. Hum. Genet.
, vol.41
, pp. 261-263
-
-
Nakura, J.1
Ye, L.2
Mitsuda, N.3
Takahashi-Fujii, A.4
Ishino, Y.5
Kato, I.6
Miki, T.7
Ogihara, T.8
-
23
-
-
0030586959
-
Narrowing the position of the Werner syndrome locus by homozygosity analysis: Extension of homozygosity analysis
-
Nakura, J., Miki, T., Ye, L., Mitsuda, M., Zhao, Y., Kihara, K., Yu, C.-E., Oshima, J., Fukuchi, K, Wijsman, E. M., Schellenberg, G. D., Martin, G. M., Murano, S., Hashimoto, K., Fujiwara, Y., and Ogihara, T. (1996b). Narrowing the position of the Werner syndrome locus by homozygosity analysis: Extension of homozygosity analysis. Genomics 36: 130-141.
-
(1996)
Genomics
, vol.36
, pp. 130-141
-
-
Nakura, J.1
Miki, T.2
Ye, L.3
Mitsuda, M.4
Zhao, Y.5
Kihara, K.6
Yu, C.-E.7
Oshima, J.8
Fukuchi, K.9
Wijsman, E.M.10
Schellenberg, G.D.11
Martin, G.M.12
Murano, S.13
Hashimoto, K.14
Fujiwara, Y.15
Ogihara, T.16
-
24
-
-
0028086578
-
Integrated mapping analysis of the Werner syndrome region of chromosome 8
-
Oshima, J., Yu, C.-E., Boehnke, M., Weber, J. L., Edelhoff, S., Wagner, M. J., Wells, D. E., Wood, S., Disteche, C. M., Martin, G. M., and Schellenberg, G. D. (1994). Integrated mapping analysis of the Werner syndrome region of chromosome 8. Genomics 23: 100-113.
-
(1994)
Genomics
, vol.23
, pp. 100-113
-
-
Oshima, J.1
Yu, C.-E.2
Boehnke, M.3
Weber, J.L.4
Edelhoff, S.5
Wagner, M.J.6
Wells, D.E.7
Wood, S.8
Disteche, C.M.9
Martin, G.M.10
Schellenberg, G.D.11
-
25
-
-
0025339588
-
A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones
-
Riley, J. H., Butler, R., Ogilvie, D. J., Finniear, R., Jenner, D., Anand, R., Smith, J. C., and Markham, A. F. (1990). A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res. 18: 2887-2890.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 2887-2890
-
-
Riley, J.H.1
Butler, R.2
Ogilvie, D.J.3
Finniear, R.4
Jenner, D.5
Anand, R.6
Smith, J.C.7
Markham, A.F.8
-
26
-
-
0002777386
-
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
-
27
-
-
0021911328
-
Location of the c-yes gene on the human chromosome and its expression in various tissues
-
Semba, K., Yamanashi, Y., Nishizawa, M., Sukegawa, J., Yoshida, M., Sasaki, M., Yamamoto, T., and Toyoshima, K. (1985). Location of the c-yes gene on the human chromosome and its expression in various tissues. Science 227: 1038-1040.
-
(1985)
Science
, vol.227
, pp. 1038-1040
-
-
Semba, K.1
Yamanashi, Y.2
Nishizawa, M.3
Sukegawa, J.4
Yoshida, M.5
Sasaki, M.6
Yamamoto, T.7
Toyoshima, K.8
-
28
-
-
0028936145
-
Report of the second international workshop on human chromosome 8 mapping 1994
-
Spurr, N. K., Blanton, S., Bookstein, R., Clarke, R., Cottingham, R., Daiger, S., Drayna, D., Faber, P., Horrigan, S., Kas, K., Kirchgessner, C., Kumar, S., Leach, R. J., Luedecke, H. J., Nakamura, Y., Pebusque, M. J., Ranta, S., Sim, E., Sullivan, L. S., Takle, L., Vance, J., Wagner, M., Wells, D., Westbrook, C., Yaremko, L., Zaletayev, D., Zuffardi, O., and Wood, S. (1995). Report of the Second International Workshop on Human Chromosome 8 Mapping 1994. Cytogenet. Cell Genet. 68: 148-164.
-
(1995)
Cytogenet. Cell Genet.
, vol.68
, pp. 148-164
-
-
Spurr, N.K.1
Blanton, S.2
Bookstein, R.3
Clarke, R.4
Cottingham, R.5
Daiger, S.6
Drayna, D.7
Faber, P.8
Horrigan, S.9
Kas, K.10
Kirchgessner, C.11
Kumar, S.12
Leach, R.J.13
Luedecke, H.J.14
Nakamura, Y.15
Pebusque, M.J.16
Ranta, S.17
Sim, E.18
Sullivan, L.S.19
Takle, L.20
Vance, J.21
Wagner, M.22
Wells, D.23
Westbrook, C.24
Yaremko, L.25
Zaletayev, D.26
Zuffardi, O.27
Wood, S.28
more..
-
29
-
-
0028567539
-
Dinucleotide repeat polymorphism at the D8S1055 locus
-
Ye, L., Kihara, K., Nakura, J., Kamino, K., Mitsuda, N., Takahashi-Fujii, A., Ishino, Y., Miki, T., and Ogihara, T. (1994). Dinucleotide repeat polymorphism at the D8S1055 locus. Jpn. J. Hum. Genet. 39: 441-443.
-
(1994)
Jpn. J. Hum. Genet.
, vol.39
, pp. 441-443
-
-
Ye, L.1
Kihara, K.2
Nakura, J.3
Kamino, K.4
Mitsuda, N.5
Takahashi-Fujii, A.6
Ishino, Y.7
Miki, T.8
Ogihara, T.9
-
30
-
-
0028859472
-
A highly polymorphic dinucleotide repeat polymorphism at the D8S1222 locus
-
Ye, L., Nakura, J., Mitsuda, N., Takahashi-Fujii, A., Ishino, Y., Kato, I., Miki, T., and Ogihara, T. (1995a). A highly polymorphic dinucleotide repeat polymorphism at the D8S1222 locus. Jpn. J. Hum. Genet. 40: 287-288.
-
(1995)
Jpn. J. Hum. Genet.
, vol.40
, pp. 287-288
-
-
Ye, L.1
Nakura, J.2
Mitsuda, N.3
Takahashi-Fujii, A.4
Ishino, Y.5
Kato, I.6
Miki, T.7
Ogihara, T.8
-
31
-
-
0029150405
-
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
-
32
-
-
0003356745
-
The molecular genetic analysis of Werner syndrome
-
in press
-
Ye, L., Nakura, J., Kihara, K., Mitsuda, N., Yi, Z., Miki, T., and Ogihara, T. (1996a). The molecular genetic analysis of Werner syndrome. Proc. 5th Asia Oceania Reg. Congr. Gerontol., in press.
-
(1996)
Proc. 5th Asia Oceania Reg. Congr. Gerontol.
-
-
Ye, L.1
Nakura, J.2
Kihara, K.3
Mitsuda, N.4
Yi, Z.5
Miki, T.6
Ogihara, T.7
-
33
-
-
0030036250
-
Two polymorphic dinucleotide repeat polymorphisms at the D8S1218 and D8S1219 loci
-
Ye, L., Nakura, J., Mitsuda, N., Takahashi-Fujii, A., Ishino, Y., Kato, I., Miki, T., and Ogihara, T. (1996b). Two polymorphic dinucleotide repeat polymorphisms at the D8S1218 and D8S1219 loci. Jpn. J. Hum. Genet. 41: 257-259.
-
(1996)
Jpn. J. Hum. Genet.
, vol.41
, pp. 257-259
-
-
Ye, L.1
Nakura, J.2
Mitsuda, N.3
Takahashi-Fujii, A.4
Ishino, Y.5
Kato, I.6
Miki, T.7
Ogihara, T.8
-
34
-
-
0025215315
-
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
-
35
-
-
0011858251
-
Dinucleotide repeat polymorphisms at the GSR gene
-
Yu, C.-E., Anderson, L., Oshima, J., and Schellenberg, G. D. (1994a). Dinucleotide repeat polymorphisms at the GSR gene. Hum. Mol. Genet. 3: 212.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 212
-
-
Yu, C.-E.1
Anderson, L.2
Oshima, J.3
Schellenberg, G.D.4
-
36
-
-
0028128738
-
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner's syndrome
-
Yu, C.-E., Oshima, J., Goddard, K. A. B., Miki, T., Nakura, J., Ogihara, T., Poot, M., Hoehn, H., Fraccaro, M., Piussan, C., Martin, G. M., Schellenberg, G. D., and Wijsman, E. M. (1994b). Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner's syndrome. Am. J. Hum. Genet. 55: 356-364.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, pp. 356-364
-
-
Yu, C.-E.1
Oshima, J.2
Goddard, K.A.B.3
Miki, T.4
Nakura, J.5
Ogihara, T.6
Poot, M.7
Hoehn, H.8
Fraccaro, M.9
Piussan, C.10
Martin, G.M.11
Schellenberg, G.D.12
Wijsman, E.M.13
-
37
-
-
15844409553
-
Positional cloning of the Werner's syndrome gene
-
Yu, C.-E., Oshima, J., Fu, Y. H., Wijsman, E. M., Hisama, F., Alisch, R., Matthews, S., Nakura, J., Miki, T., Ouais, S., Martin, G. M., Mulligan, J., and Schellenberg, G. D. (1996a). Positional cloning of the Werner's syndrome gene. Science 272: 258-262.
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Yu, C.-E.1
Oshima, J.2
Fu, Y.H.3
Wijsman, E.M.4
Hisama, F.5
Alisch, R.6
Matthews, S.7
Nakura, J.8
Miki, T.9
Ouais, S.10
Martin, G.M.11
Mulligan, J.12
Schellenberg, G.D.13
-
38
-
-
0030218834
-
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
|