-
1
-
-
0027433563
-
Breast Cancer Linkage Consortium. Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families
-
Easton, D. F., Bishop, D. T., Ford, D., and Crockford, G. P. Breast Cancer Linkage Consortium. Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families, Am. J. Hum. Genet. 52, 678-701 (1993).
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 678-701
-
-
Easton, D.F.1
Bishop, D.T.2
Ford, D.3
Crockford, G.P.4
-
2
-
-
0025613812
-
Linkage of early-onset familial breast cancer to chromosome 17q21
-
Hall, J. M., Lee, M. K., Newman, B., Morrow, J. E., Anderson, L. A., Huey, B., and King, M.-C. Linkage of early-onset familial breast cancer to chromosome 17q21, Science 250, 1684-1689 (1990).
-
(1990)
Science
, vol.250
, pp. 1684-1689
-
-
Hall, J.M.1
Lee, M.K.2
Newman, B.3
Morrow, J.E.4
Erson, L.A.5
Huey, B.6
King, M.-C.7
-
3
-
-
42449107062
-
Familial breast-ovarian cancer locus on chromosome 17ql2-23
-
Narod, S. A., Feunteun, J., Lynch, H. T., Watson, P., Conway, T., Lynch, J., and Lenoir, G. M. Familial breast-ovarian cancer locus on chromosome 17ql2-23, Lancet 338, 82-83 (1991).
-
(1991)
Lancet
, vol.338
, pp. 82-83
-
-
Narod, S.A.1
Feunteun, J.2
Lynch, H.T.3
Watson, P.4
Conway, T.5
Lynch, J.6
Lenoir, G.M.7
-
4
-
-
0025089488
-
Chromosome abnormalities in human epithelial ovarian malignancies
-
Gallion, H. H., Powell, D. E., Smith, L. W., Morrow, J. K., Martin, A. W., Nagell, J. R. v., and Donaldson, E. S. Chromosome abnormalities in human epithelial ovarian malignancies, Gynecol. Oncol. 38, 473-477 (1990).
-
(1990)
Gynecol. Oncol.
, vol.38
, pp. 473-477
-
-
Gallion, H.H.1
Powell, D.E.2
Smith, L.W.3
Morrow, J.K.4
Martin, A.W.5
Nagell, J.R.V.6
Donaldson, E.S.7
-
5
-
-
0026579241
-
Chromosome aberrations in 35 primary ovarian carcinomas
-
Pejovic, T., Heim, S., Mandahi, N., Baldetorp, B., Elmfors, B., Floderus, U.-M., Furgyik, S., Helm, G., Himmelmann, A., Willen, H., and Mitelman, F. Chromosome aberrations in 35 primary ovarian carcinomas, Genes Chromosomes Cancer 4, 58-69 (1992).
-
(1992)
Genes Chromosomes Cancer
, vol.4
, pp. 58-69
-
-
Pejovic, T.1
Heim, S.2
Mandahi, N.3
Baldetorp, B.4
Elmfors, B.5
Floderus, U.-M.6
Furgyik, S.7
Helm, G.8
Himmelmann, A.9
Willen, H.10
Mitelman, F.11
-
6
-
-
0026059515
-
Tumor suppressor genes
-
Marshall, C. J. Tumor suppressor genes, Cell 64, 313-326 (1991).
-
(1991)
Cell
, vol.64
, pp. 313-326
-
-
Marshall, C.J.1
-
7
-
-
0025321563
-
Frequent loss of heterozygosity on chromosomes 6q, 11, and 17 in human ovarian carcinomas
-
Lee, J. H., Kavanagh, J. J., Wildrick, D. M., Wharton, J. T., and Blick, M. Frequent loss of heterozygosity on chromosomes 6q, 11, and 17 in human ovarian carcinomas, Cancer Res. 50, 2724-2728 (1990).
-
(1990)
Cancer Res
, vol.50
, pp. 2724-2728
-
-
Lee, J.H.1
Kavanagh, J.J.2
Wildrick, D.M.3
Wharton, J.T.4
Blick, M.5
-
8
-
-
0027269573
-
Human epithelial ovarian cancer allelotype
-
Cliby, W., Ritland, S., Hartmann, L., Dodson, M., Hailing, K. C., Keeney, G., Podratz, K. C., and Jenkins, R. B. Human epithelial ovarian cancer allelotype, Cancer Res. 53,(10 Suppl.), 2393-2398 (1993).
-
(1993)
Cancer Res
, vol.53
, pp. 2393-2398
-
-
Cliby, W.1
Ritland, S.2
Hartmann, L.3
Dodson, M.4
Hailing, K.C.5
Keeney, G.6
Podratz, K.C.7
Jenkins, R.B.8
-
9
-
-
0027477595
-
Loss of heterozygosity and amplification on chromosome llq.In human ovarian cancer
-
Foulkes, W. D., Campbell, I. G., Stamp, G. W. H., and Trowsdale, J. Loss of heterozygosity and amplification on chromosome llq.in human ovarian cancer, Br. J. Cancer 67, 268-273 (1993).
-
(1993)
Br. J. Cancer
, vol.67
, pp. 268-273
-
-
Foulkes, W.D.1
Campbell, I.G.2
Stamp, G.W.H.3
Trowsdale, J.4
-
10
-
-
0025212711
-
Loss of heterozygosity on chromosomal segments 3p, 6q, and lip in human ovarian carcinoma
-
Ehlen, T., and Dubeau, L. Loss of heterozygosity on chromosomal segments 3p, 6q, and lip in human ovarian carcinoma, Oncogene 5, 219-223 (1990).
-
(1990)
Oncogene
, vol.5
, pp. 219-223
-
-
Ehlen, T.1
Dubeau, L.2
-
11
-
-
0026727299
-
Molecular genetic changes in human epithelial ovarian malignancies
-
Gallion, H. H., Powell, D. E., Morrow, J. K., Pieretti, M., Case, E., Turker, M. S., De Priest, P. D., Hunter, J. E., and van Nagell, J. R. Molecular genetic changes in human epithelial ovarian malignancies, Gynecol. Oncol. 47, 137-142 (1992).
-
(1992)
Gynecol. Oncol
, vol.47
, pp. 137-142
-
-
Gallion, H.H.1
Powell, D.E.2
Morrow, J.K.3
Pieretti, M.4
Case, E.5
Turker, M.S.6
Depriest, P.D.7
Hunter, J.E.8
Van Nagell, J.R.9
-
12
-
-
0027232050
-
Allelic loss on chromosome 17 in human ovarian cancer
-
Phillips, N., Ziegler, M., Saha, B., and Xynos, F. Allelic loss on chromosome 17 in human ovarian cancer, Int. J. Cancer 54, 85-91 (1993).
-
(1993)
Int. J. Cancer
, vol.54
, pp. 85-91
-
-
Phillips, N.1
Ziegler, M.2
Saha, B.3
Xynos, F.4
-
13
-
-
0003903343
-
-
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY
-
Sambrook, J., Fritsch, E. F., and Maniatis, T. Molecular cloning: A laboratory manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1989).
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
14
-
-
0016700864
-
Detection of specific sequences among DNA fragments separated by gel electrophoresis
-
Southern, E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis, J. Mol. Biol. 98, 503-517 (1975).
-
(1975)
J. Mol. Biol.
, vol.98
, pp. 503-517
-
-
Southern, E.M.1
-
15
-
-
0020793569
-
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
-
Feinberg, A., and Vogelstein, B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity, Anal. Biochem. 132, 6-13 (1984).
-
(1984)
Anal. Biochem.
, vol.132
, pp. 6-13
-
-
Feinberg, A.1
Vogelstein, B.2
-
16
-
-
0027536351
-
A PCR-based linkage map of human chromosome 1
-
Engelstein, M., Hudson, T. J., Lane, J. M., Lee, M. K., Leverone, M., Landes, G. M., Peltonen, L., Weber, J. L., and Dracopoli, N. C. A PCR-based linkage map of human chromosome 1, Genomics 15, 251-258 (1993).
-
(1993)
Genomics
, vol.15
, pp. 251-258
-
-
Engelstein, M.1
Hudson, T.J.2
Lane, J.M.3
Lee, M.K.4
Leverone, M.5
Landes, G.M.6
Peltonen, L.7
Weber, J.L.8
Dracopoli, N.C.9
-
17
-
-
0026509756
-
Tetranucleotide repeat polymorphism at the human beta- actin related pseudogene H-beta-Ac-psi-2 (ACTBP2)
-
Polymeropoulos, M. H., Rath, D. S., Xiao, H., and Merril, R. Tetranucleotide repeat polymorphism at the human beta- actin related pseudogene H-beta-Ac-psi-2 (ACTBP2), Nucleic Acids Res. 20, 1432 (1992).
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 1432
-
-
Polymeropoulos, M.H.1
Rath, D.S.2
Xiao, H.3
Merril, R.4
-
18
-
-
0026950190
-
Dinucleotide repeat polymorphism at the IFNA locus (9p22)
-
Kwiatkowski, D. J., and Diaz, M. O. Dinucleotide repeat polymorphism at the IFNA locus (9p22), Hum. Mol. Genet. 1, 658 (1992).
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 658
-
-
Kwiatkowski, D.J.1
Diaz, M.O.2
-
19
-
-
0026583458
-
Linkage map of human chromosome 9 microsatellite polymorphisms
-
Wilkie, P. J., Krizman, D. B., and Weber, J. L. Linkage map of human chromosome 9 microsatellite polymorphisms, Genomics 12, 607-609 (1992).
-
(1992)
Genomics
, vol.12
, pp. 607-609
-
-
Wilkie, P.J.1
Krizman, D.B.2
Weber, J.L.3
-
20
-
-
0026499652
-
Regional localization of the highly polymorphic locus D11S533 on the linkage map of human chromosome llq
-
Litt, M., Eubanks, J. H., Evans, G. A., and Phromchotikul, T. Regional localization of the highly polymorphic locus D11S533 on the linkage map of human chromosome llq, Genomics 14, 820 (1992).
-
(1992)
Genomics
, vol.14
, pp. 820
-
-
Litt, M.1
Eubanks, J.H.2
Evans, G.A.3
Phromchotikul, T.4
-
21
-
-
0025939939
-
DNA typing and genetic mapping with trimeric and tetrameric tandem repeats
-
Edwards, A., Civitello, A., Hammond, H. A., and Caskey, T. DNA typing and genetic mapping with trimeric and tetrameric tandem repeats, Am. J. Hum. Genet. 49, 746-756 (1991).
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 746-756
-
-
Edwards, A.1
Civitello, A.2
Hammond, H.A.3
Caskey, T.4
-
22
-
-
0026597196
-
Amplification and characterization of the retinoblastoma gene VNTR by PCR
-
Scharf, S. J., Bowcock, A. M., Mc Clure, G., Klitz, W., Yandell, W., and Erlich, H. A. Amplification and characterization of the retinoblastoma gene VNTR by PCR, Am. J. Hum. Genet. 50, 371-381 (1992).
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 371-381
-
-
Scharf, S.J.1
Bowcock, A.M.2
McClure, G.3
Klitz, W.4
Yandell, W.5
Erlich, H.A.6
-
23
-
-
0026680687
-
Closing in on a breast cancer gene on chromosome 17q
-
Hall, J. M., Friedman, L., Guenther, C., Lee, M. K., Weber, I. L., and Black, D. M. Closing in on a breast cancer gene on chromosome 17q, Am. J. Hum. Genet. 50, 1235-1242 (1992).
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 1235-1242
-
-
Hall, J.M.1
Friedman, L.2
Guenther, C.3
Lee, M.K.4
Weber, I.L.5
Black, D.M.6
-
24
-
-
0026764342
-
Somatic cell hybrids, sequence- tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p
-
Guzzetta, V., Franco, B., Trask, B. J., Zhang, H., Saucedo-Car- denas, O., de Oca-Luna, R. M., Greenberg, F., Chinault, A. C., Lupski, J. R., and Patel, P. I. Somatic cell hybrids, sequence- tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p, Genomics 13, 551-559 (1992).
-
(1992)
Genomics
, vol.13
, pp. 551-559
-
-
Guzzetta, V.1
Franco, B.2
Trask, B.J.3
Zhang, H.4
Saucedo-Car- Denas, O.5
De Oca-Luna, R.M.6
Greenberg, F.7
Chinault, A.C.8
Lupski, J.R.9
Patel, P.I.10
-
25
-
-
0026008884
-
A CA repeat polymorphism 30-70 kb downstream from the adenomatous polyposis coli (APC) gene
-
Spirio, L., Joslyn, G., Nelson, L., Leppert, M., and White, R. A CA repeat polymorphism 30-70 kb downstream from the adenomatous polyposis coli (APC) gene, Nucleic Acids Res. 19, 6348 (1991).
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 6348
-
-
Spirio, L.1
Joslyn, G.2
Nelson, L.3
Leppert, M.4
White, R.5
-
26
-
-
0026422117
-
Msp I RFLP at the D5S122 locus tightly linked to APC
-
Breukel, C., Tops, C., Ras, E., and Meera Khan, P. Msp I RFLP at the D5S122 locus tightly linked to APC, Nucleic Acids Res. 19, 685 (1991).
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 685
-
-
Breukel, C.1
Tops, C.2
Ras, E.3
Meera Khan, P.4
-
27
-
-
0023665446
-
Pvu II RFLP inside the estrogen receptor gene
-
Castagnoli, A., Maestri, I, Bemardi, F., and Del Senno, L. Pvu II RFLP inside the estrogen receptor gene, Nucleic Acids Res. 15, 866 (1987).
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 866
-
-
Castagnoli, A.1
Maestri, I.2
Bemardi, F.3
Del Senno, L.4
-
28
-
-
0024502562
-
Allele loss at the c-Ha-rasl locus in human ovarian cancer
-
Lee, J. H., Kavanagh, J. J., Wharton, J. T., Wildrick, D. M., and Blick, M. Allele loss at the c-Ha-rasl locus in human ovarian cancer, Cancer Res. 49, 1220-1222 (1989).
-
(1989)
Cancer Res
, vol.49
, pp. 1220-1222
-
-
Lee, J.H.1
Kavanagh, J.J.2
Wharton, J.T.3
Wildrick, D.M.4
Blick, M.5
-
29
-
-
0026495321
-
Allele loss on chromosome lip is associated with poor survival in ovarian cancer
-
Eccles, D. M., Gruber, L., Stewart, M., Steel, C. M., and Leonard, R. C. Allele loss on chromosome lip is associated with poor survival in ovarian cancer, Dis. Markers 10, 95-99 (1993).
-
(1993)
Dis. Markers
, vol.10
, pp. 95-99
-
-
Eccles, D.M.1
Gruber, L.2
Stewart, M.3
Steel, C.M.4
Leonard, R.C.5
-
30
-
-
0026495903
-
Deletion of chromosome 11p13-11p15.5 sequences in invasive human ovarian cancer is a subclonal progression factor
-
Vandamme, B., Lissens, W., Amfo, K., De Sutter, P., Bourgain, C., Vamos, E., and De Greve, J. Deletion of chromosome 11p13-11p15.5 sequences in invasive human ovarian cancer is a subclonal progression factor, Cancer Res. 52, 6646-6652 (1992).
-
(1992)
Cancer Res
, vol.52
, pp. 6646-6652
-
-
Vandamme, B.1
Lissens, W.2
Amfo, K.3
De Sutter, P.4
Bourgain, C.5
Vamos, E.6
De Greve, J.7
-
31
-
-
0026387886
-
Distinction of low grade from high grade human ovarian carcinomas on the basis of losses of heterozygosity on chromosomes 3, 6, and 11 and HER-2/neu gene amplification
-
Zheng, J., Robinson, W. R., Ehlen, T., Yu, M. C., and Dubeau, L. Distinction of low grade from high grade human ovarian carcinomas on the basis of losses of heterozygosity on chromosomes 3, 6, and 11 and HER-2/neu gene amplification, Cancer Res. 51, 4045-4051 (1991).
-
(1991)
Cancer Res
, vol.51
, pp. 4045-4051
-
-
Zheng, J.1
Robinson, W.R.2
Ehlen, T.3
Yu, M.C.4
Dubeau, L.5
-
32
-
-
0027859004
-
Histologically benign or low-grade malignant tumors adjacent to high-grade ovarian carcinomas contain molecular characteristics of high-grade carcinomas
-
Zheng, J., Wan, M., Zweizig, S., Velicescu, M., Yu, M. C., and Dubeau, L. Histologically benign or low-grade malignant tumors adjacent to high-grade ovarian carcinomas contain molecular characteristics of high-grade carcinomas, Cancer Res. 53, 4138-4142 (1993).
-
(1993)
Cancer Res
, vol.53
, pp. 4138-4142
-
-
Zheng, J.1
Wan, M.2
Zweizig, S.3
Velicescu, M.4
Yu, M.C.5
Dubeau, L.6
-
33
-
-
0027265916
-
Analysis of the llpl3 Wilms’ tumor suppressor gene (WT1) in ovarian tumors
-
Bruening, W., Gros, P., Sato, T., Stanimir, J., Nakamura, Y., Houseman, D., and Pelletier, J. Analysis of the llpl3 Wilms’ tumor suppressor gene (WT1) in ovarian tumors, Cancer Invest. 11, 393-399 (1993).
-
(1993)
Cancer Invest.
, vol.11
, pp. 393-399
-
-
Bruening, W.1
Gros, P.2
Sato, T.3
Stanimir, J.4
Nakamura, Y.5
Houseman, D.6
Pelletier, J.7
-
34
-
-
0026077581
-
Suppression of tu- morigenicity in Wilms tumor by the pl5.5-pl4 region of chromosome 11
-
Dowdy, S. F., Fasching, C. L., Araujo, D., Lai, K.-M., Livanos, M., Weissman, B. E., and Stanbridge, E. J. Suppression of tu- morigenicity in Wilms tumor by the pl5.5-pl4 region of chromosome 11, Science 254, 293-295 (1991).
-
(1991)
Science
, vol.254
, pp. 293-295
-
-
Dowdy, S.F.1
Fasching, C.L.2
Araujo, D.3
Lai, K.-M.4
Livanos, M.5
Weissman, B.E.6
Stanbridge, E.J.7
-
35
-
-
0027152142
-
Very frequent loss of heterozygosity throughout chromosome 17 in sporadic ovarian carcinoma
-
Foulkes, W. D., Black, D. M., Stamp, G. W. H., Solomon, E., and Trowsdale, J. Very frequent loss of heterozygosity throughout chromosome 17 in sporadic ovarian carcinoma, Int. J. Cancer 54, 220-225 (1993).
-
(1993)
Int. J. Cancer
, vol.54
, pp. 220-225
-
-
Foulkes, W.D.1
Black, D.M.2
Stamp, G.W.H.3
Solomon, E.4
Trowsdale, J.5
-
36
-
-
0025783622
-
Allele loss on chromosome 17q in sporadic ovarian cancer
-
Foulkes, W., Black, D., Solomon, E., and Trowsdale, J. Allele loss on chromosome 17q in sporadic ovarian cancer, Lancet 338, 444-445 (1991).
-
(1991)
Lancet
, vol.338
, pp. 444-445
-
-
Foulkes, W.1
Black, D.2
Solomon, E.3
Trowsdale, J.4
-
37
-
-
0027408639
-
A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus
-
Jacobs, I. J., Smith, S. A., Wiseman, R. W., Futreal, P. A., Harrington, T., Osborne, R. J., Leech, V., Molyneux, A., Berchuck, A., Ponder, B. A. J., and Bast, R. C., A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus, Cancer Res. 53, 1218-1221 (1993).
-
(1993)
Cancer Res
, vol.53
, pp. 1218-1221
-
-
Jacobs, I.J.1
Smith, S.A.2
Wiseman, R.W.3
Futreal, P.A.4
Harrington, T.5
Osborne, R.J.6
Leech, V.7
Molyneux, A.8
Berchuck, A.9
Ponder, B.A.J.10
Bast, R.C.11
-
38
-
-
0027250143
-
Spectrum of mutation and frequency of allelic deletion of the p53 gene in ovarian cancer
-
Kohler, M. F., Marks, J. R., Wiseman, R. W., Jacobs, I. J., Dav- idoff, A. M., Clarke-Pearson, D. L., Soper, J. T., Bast, R. C., and Berchuck, A. Spectrum of mutation and frequency of allelic deletion of the p53 gene in ovarian cancer, J. Natl. Cancer Inst. 85, 1513-1519 (1993).
-
(1993)
J. Natl. Cancer Inst.
, vol.85
, pp. 1513-1519
-
-
Kohler, M.F.1
Marks, J.R.2
Wiseman, R.W.3
Jacobs, I.J.4
Dav-Idoff, A.M.5
Clarke-Pearson, D.L.6
Soper, J.T.7
Bast, R.C.8
Berchuck, A.9
-
39
-
-
0025743791
-
Overexpression and mutation of p53 in epithelial ovarian cancer
-
Marks, J. R., Davidoff, A. M., Kerns, B. J., Humphrey, P. A., Pence, J. C., Dodge, R. K., Clarke-Pearson, D. L., Iglehart, J. D., Bast, R. C., and Berchuck, A. Overexpression and mutation of p53 in epithelial ovarian cancer, Cancer Res. 51, 2979-2984 (1991).
-
(1991)
Cancer Res
, vol.51
, pp. 2979-2984
-
-
Marks, J.R.1
Davidoff, A.M.2
Kerns, B.J.3
Humphrey, P.A.4
Pence, J.C.5
Dodge, R.K.6
Clarke-Pearson, D.L.7
Iglehart, J.D.8
Bast, R.C.9
Berchuck, A.10
-
40
-
-
0026005828
-
Frequent allelic losses and mutations of the p53 gene in human ovarian cancer
-
Okamoto, A., Sameshima, Y., Yokoyama, S., Terashima, Y., Sug- itnura, T., Terada, M., and Yokota, J. Frequent allelic losses and mutations of the p53 gene in human ovarian cancer, Cancer Res. 51, 5171-5176 (1991).
-
(1991)
Cancer Res
, vol.51
, pp. 5171-5176
-
-
Okamoto, A.1
Sameshima, Y.2
Yokoyama, S.3
Terashima, Y.4
Sug-Itnura, T.5
Terada, M.6
Yokota, J.7
-
41
-
-
0025826440
-
P53 mutations in ovarian cancer: A late event?
-
Mazars, R., Pujol, P., Maudelonde, T., Jeanteur, P., and Theillet, C. p53 mutations in ovarian cancer: A late event?, Oncogene 6, 1685-1690 (1991).
-
(1991)
Oncogene
, vol.6
, pp. 1685-1690
-
-
Mazars, R.1
Pujol, P.2
Maudelonde, T.3
Jeanteur, P.4
Theillet, C.5
-
42
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9pl3-p22
-
Cannon-Albright, L. A., Goldgar, D. E., Meyer, L. J., Lewis, M., Anderson, D. E., Fountain, J. W., Hegi, M. E., Wiseman, R. W., Petty, E. M., Bale, A. E., Olopade, O. I., Diaz, M. O., Kwiatkowski, D. J., Piepkorn, M. W., Zone, J. J., and Skolnick, M. H. Assignment of a locus for familial melanoma, MLM, to chromosome 9pl3-p22, Science 258, 1148-1152 (1992).
-
(1992)
Science
, vol.258
, pp. 1148-1152
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
Lewis, M.4
Erson, D.E.5
Fountain, J.W.6
Hegi, M.E.7
Wiseman, R.W.8
Petty, E.M.9
Bale, A.E.10
Olopade, O.I.11
Diaz, M.O.12
Kwiatkowski, D.J.13
Piepkorn, M.W.14
Zone, J.J.15
Skolnick, M.H.16
-
43
-
-
0026464014
-
Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia
-
Olopade, O. I., Bohlander, S. K., Pomykala, H., Maltepe, E., Van Melle, E., Le Beau, M. M., and Diaz, M. O. Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia, Genomics 14, 437-443 (1992).
-
(1992)
Genomics
, vol.14
, pp. 437-443
-
-
Olopade, O.I.1
Bohlander, S.K.2
Pomykala, H.3
Maltepe, E.4
Van Melle, E.5
Le Beau, M.M.6
Diaz, M.O.7
-
44
-
-
0027848939
-
Loss of heterozygosity in familial breast carcinomas
-
Lindblom, A., Skoog, L., Rotstein, S., Werelius, B., Larsson, C., and Nordenskjold, M. Loss of heterozygosity in familial breast carcinomas, Cancer Res. 53, 4356-4361 (1993).
-
(1993)
Cancer Res
, vol.53
, pp. 4356-4361
-
-
Lindblom, A.1
Skoog, L.2
Rotstein, S.3
Werelius, B.4
Larsson, C.5
Nordenskjold, M.6
-
45
-
-
0026683968
-
Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas
-
Olopade, O. I., Jenkins, R. B., Ransom, D. T., Malik, K., Pomykala, H., Nobori, T., Cowan, J. M., Rowley, J. D., and Diaz, M. O. Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas, Cancer Res. 52, 2523-2529 (1992).
-
(1992)
Cancer Res
, vol.52
, pp. 2523-2529
-
-
Olopade, O.I.1
Jenkins, R.B.2
Ransom, D.T.3
Malik, K.4
Pomykala, H.5
Nobori, T.6
Cowan, J.M.7
Rowley, J.D.8
Diaz, M.O.9
-
46
-
-
12044249989
-
Detailed analysis of genetic alterations in colorectal tumors from patients with and without familial adenomatous polyposis (FAP)
-
Ichii, S., Takeda, S., Horii, A., Nakatsuru, S., Miyoshi, Y., Emi, M., Fujiwara, Y., Koyama, K., Furuyama, J., Utsunomiya, J., and Nakamura, Y. Detailed analysis of genetic alterations in colorectal tumors from patients with and without familial adenomatous polyposis (FAP), Oncogene 8, 2399-2405 (1993).
-
(1993)
Oncogene
, vol.8
, pp. 2399-2405
-
-
Ichii, S.1
Takeda, S.2
Horii, A.3
Nakatsuru, S.4
Miyoshi, Y.5
Emi, M.6
Fujiwara, Y.7
Koyama, K.8
Furuyama, J.9
Utsunomiya, J.10
Nakamura, Y.11
-
47
-
-
0023748414
-
Genetic alterations during colorectal- tumor development
-
Vogelstein, B., Fearon, E. R., Hamilton, S. R., Kern, S. E., Preis- inger, A. C., Leppert, M., Nakamura, Y., White, R., Smits, M. M., and Bos, J. L. Genetic alterations during colorectal- tumor development, N. Engl. J. Med. 319, 525-532 (1988).
-
(1988)
N. Engl. J. Med.
, vol.319
, pp. 525-532
-
-
Vogelstein, B.1
Fearon, E.R.2
Hamilton, S.R.3
Kern, S.E.4
Preis-Inger, A.C.5
Leppert, M.6
Nakamura, Y.7
White, R.8
Smits, M.M.9
Bos, J.L.10
-
48
-
-
0025938038
-
Identification and characterization of the familial adenomatous polyposis coli gene
-
Groden, J., Thliveris, A., Samowitz, W., Carlson, M., Gelbert, L., Albertsen, H., Joslyn, G., Stevens, J., Spirio, L., Robertson, M., Sargeant, L., Krapcho, K., Wolff, E., Burt, R., Hughes, J. P., Warrington, J., Mc Pherson, J., Wasmuth, J., Le Paselier, D., Abderrahim, H., Cohen, D., Leppert, M., and White, R. Identification and characterization of the familial adenomatous polyposis coli gene, Cell 66, 589-600 (1991).
-
(1991)
Cell
, vol.66
, pp. 589-600
-
-
Groden, J.1
Thliveris, A.2
Samowitz, W.3
Carlson, M.4
Gelbert, L.5
Albertsen, H.6
Joslyn, G.7
Stevens, J.8
Spirio, L.9
Robertson, M.10
Sargeant, L.11
Krapcho, K.12
Wolff, E.13
Burt, R.14
Hughes, J.P.15
Warrington, J.16
McPherson, J.17
Wasmuth, J.18
Le Paselier, D.19
Abderrahim, H.20
Cohen, D.21
Leppert, M.22
White, R.23
more..
-
49
-
-
0023278941
-
Chromosome 5 allele loss in human colorectal carcinomas
-
Solomon, E., Voss, R., and Hall, V. Chromosome 5 allele loss in human colorectal carcinomas, Nature 328, 1411-1413 (1987).
-
(1987)
Nature
, vol.328
, pp. 1411-1413
-
-
Solomon, E.1
Voss, R.2
Hall, V.3
-
50
-
-
0026630266
-
APC mutations occur early during colorectal tumorigenesis
-
Powell, S. M., Zilz, N., Beazer-Barclay, Y., Bryan, T. M., Hamilton, S. R., Thibodeau, S. N., Vogelstein, B., and Kinzler, K. W. APC mutations occur early during colorectal tumorigenesis, Nature 359, 235-237 (1992).
-
(1992)
Nature
, vol.359
, pp. 235-237
-
-
Powell, S.M.1
Zilz, N.2
Beazer-Barclay, Y.3
Bryan, T.M.4
Hamilton, S.R.5
Thibodeau, S.N.6
Vogelstein, B.7
Kinzler, K.W.8
-
51
-
-
0026591034
-
Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers
-
Boynton, R. F., Blount, P. L., Yin, J., Brown, V. L., Huang, Y., Tong, Y., Mc Daniel, T., Newkirk, C., Resau, J. H., Raskind, W. H., Haggitt, R. C., Reid, B. J., and Meltzer, S. J. Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers, Proc. Natl. Acad. Sci. USA 89, 3385-3388 (1992).
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 3385-3388
-
-
Boynton, R.F.1
Blount, P.L.2
Yin, J.3
Brown, V.L.4
Huang, Y.5
Tong, Y.6
McDaniel, T.7
Newkirk, C.8
Resau, J.H.9
Raskind, W.H.10
Haggitt, R.C.11
Reid, B.J.12
Meltzer, S.J.13
-
52
-
-
0026470030
-
Frequent somatic mutations of the APC gene in human pancreatic cancer
-
Horii, A., Nakatsuru, S., Miyoshi, Y., Ichii, S., Nagase, H., Ando, M., Yanagisawa, A., Tsuchiya, E., Kato, Y., and Nakamura, Y. Frequent somatic mutations of the APC gene in human pancreatic cancer, Cancer Res. 52, 6696-6698 (1992).
-
(1992)
Cancer Res
, vol.52
, pp. 6696-6698
-
-
Horii, A.1
Nakatsuru, S.2
Miyoshi, Y.3
Ichii, S.4
Nagase, H.5
Ando, M.6
Yanagisawa, A.7
Tsuchiya, E.8
Kato, Y.9
Nakamura, Y.10
-
53
-
-
0026948827
-
Somatic mutation of the APC gene in gastric cancer: Frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma
-
Nakatsuru, S., Yanagisawa, A., Ichii, S., Tahara, E., Kato, Y., Nakamura, Y., and Horii, A. Somatic mutation of the APC gene in gastric cancer: Frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma, Hum. Mol. Genet. 1, 559-563 (1992)
-
(1992)
Hum. Mol. Genet
, vol.1
, pp. 559-563
-
-
Nakatsuru, S.1
Yanagisawa, A.2
Ichii, S.3
Tahara, E.4
Kato, Y.5
Nakamura, Y.6
Horii, A.7
-
54
-
-
0026453635
-
Clonal origin of epithelial ovarian carcinoma: Analysis by loss of heterozygosity, p53 mutation, and X-chromosome inactivation
-
Jacobs, I. J., Kohler, M. F., Wiseman, R. W., Marks, J. R., Whitaker, R., Kerns, B. A. J., Humphrey, P., Berchuck, A., Ponder, B. A. J., and Bast, R. C., Clonal origin of epithelial ovarian carcinoma: Analysis by loss of heterozygosity, p53 mutation, and X-chromosome inactivation, J. Natl. Cancer Inst. 84, 1793-1798 (1992).
-
(1992)
J. Natl. Cancer Inst.
, vol.84
, pp. 1793-1798
-
-
Jacobs, I.J.1
Kohler, M.F.2
Wiseman, R.W.3
Marks, J.R.4
Whitaker, R.5
Kerns, B.A.J.6
Humphrey, P.7
Berchuck, A.8
Ponder, B.A.J.9
Bast, R.C.10
-
55
-
-
0025941543
-
Allelotype of human ovarian cancer
-
Sato, T., Saito, H., Morita, R., Koi, S., Lee, J. H., and Nakamura, Y. Allelotype of human ovarian cancer, Cancer Res. 51, 5118-5122 (1991).
-
(1991)
Cancer Res
, vol.51
, pp. 5118-5122
-
-
Sato, T.1
Saito, H.2
Morita, R.3
Koi, S.4
Lee, J.H.5
Nakamura, Y.6
-
56
-
-
0024354721
-
Evidence that the familial adenomatous polyposis gene is involved in a subset of colon cancers with a complementable defect in c-myc regulation
-
Erisman, M. D., Scott, J. K., and Astrin, S. M. Evidence that the familial adenomatous polyposis gene is involved in a subset of colon cancers with a complementable defect in c-myc regulation, Proc. Natl. Acad. Sci. USA 86, 4264-4268 (1989).
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 4264-4268
-
-
Erisman, M.D.1
Scott, J.K.2
Astrin, S.M.3
-
57
-
-
0026543738
-
Suppression of deregulated c-MYC expression in human colon carcinoma cells by chromosome 5 transfer
-
Rodriguez-Alfageme, C., Stanbridge, E. J., and Astrin, S. M. Suppression of deregulated c-MYC expression in human colon carcinoma cells by chromosome 5 transfer, Proc. Natl. Acad. Sci. USA 89, 1482-1486 (1992).
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 1482-1486
-
-
Rodriguez-Alfageme, C.1
Stanbridge, E.J.2
Astrin, S.M.3
-
58
-
-
0023233174
-
Oncogene expression in ovarian cancer: A pilot study of c- myc oncoprotein in serous papillary ovarian cancer
-
Watson, J. V., Curling, O. M., Munn, C. F., and Hudson, N. Oncogene expression in ovarian cancer: A pilot study of c- myc oncoprotein in serous papillary ovarian cancer, Gynecol. Oncol. 28, 137-150 (1987).
-
(1987)
Gynecol. Oncol
, vol.28
, pp. 137-150
-
-
Watson, J.V.1
Curling, O.M.2
Munn, C.F.3
Hudson, N.4
-
59
-
-
0025087287
-
Allele loss from chromosome 17 in ovarian cancer
-
Russell, S. E., Hickey, G. I., Lowry, W. S., White, P., and Atkinson, R. J. Allele loss from chromosome 17 in ovarian cancer, Oncogene 5, 1581-1583 (1990).
-
(1990)
Oncogene
, vol.5
, pp. 1581-1583
-
-
Russell, S.E.1
Hickey, G.I.2
Lowry, W.S.3
White, P.4
Atkinson, R.J.5
-
60
-
-
0026335799
-
Accumulation of genetic alterations and progression of primary breast cancer
-
Sato, T., Akiyama, F., Sakamoto, G., Kasumi, F., and Nakamura, Y. Accumulation of genetic alterations and progression of primary breast cancer, Cancer Res. 51, 5794-5799 (1991).
-
(1991)
Cancer Res
, vol.51
, pp. 5794-5799
-
-
Sato Akiyama Sakamoto, T.F.G.1
Kasumi, F.2
Nakamura, Y.3
-
62
-
-
0023056465
-
Eco RI RF1P linked to the human myb gene
-
Dozier, C., Walbaum, S., Leprince, D., and Stehelin, D. Eco RI RF1P linked to the human myb gene, Nucleic Acids Res. 14, 1928 (1986).
-
(1986)
Nucleic Acids Res
, vol.14
, pp. 1928
-
-
Dozier, C.1
Walbaum, S.2
Leprince, D.3
Stehelin, D.4
-
63
-
-
0022653964
-
Human oestrogen receptor c DNA: Sequence, expression and homology to herb-A
-
Green, S., Walter, P., Kumar, V., Krust, A., Bornert, J.-M., Argos, P., and Chambon, P. Human oestrogen receptor c DNA: Sequence, expression and homology to herb-A, Nature 320, 134-139 (1986)
-
(1986)
Nature
, vol.320
, pp. 134-139
-
-
Green, S.1
Walter, P.2
Kumar, V.3
Krust, A.4
Bornert, J.-M.5
Argos, P.6
Chambon, P.7
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