-
1
-
-
0024582686
-
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
-
Weber, J. L., and May, P. E. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. Hum. Genet., 44: 388–396, 1989.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 388-396
-
-
Weber, J.L.1
May, P.E.2
-
2
-
-
0024245669
-
Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells
-
Jeffreys, A. J., Wilson, V., Neumann, R., and Keyte, J. Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells. Nucleic Acids Res., 16: 10953–10971, 1988.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 10953-10971
-
-
Jeffreys, A.J.1
Wilson, V.2
Neumann, R.3
Keyte, J.4
-
3
-
-
0027453998
-
Three discrete regions of deletion at 3p in head and neck cancers
-
Maestro, R., Gasparotto, D., Vukosavljevic, T., Barzan, L., Sulfaro, S., and Boiocchi, M. Three discrete regions of deletion at 3p in head and neck cancers. Cancer Res., 53: 5775–5779, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 5775-5779
-
-
Maestro, R.1
Gasparotto, D.2
Vukosavljevic, T.3
Barzan, L.4
Sulfaro, S.5
Boiocchi, M.6
-
4
-
-
0026864932
-
Isolation and characterization of 19 dinucleotide repeat polymorphisms on chromosome 3p
-
Jones, M. H., Yamakawa, K., and Nakamura, Y. Isolation and characterization of 19 dinucleotide repeat polymorphisms on chromosome 3p. Hum. Mol. Genet., 1: 131–133, 1992.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 131-133
-
-
Jones, M.H.1
Yamakawa, K.2
Nakamura, Y.3
-
5
-
-
0028299591
-
Patterns of allele losses suggest the existence of five distinct regions of LOH on chromosome 17 in breast cancer
-
Kirchweger, R., Zeillinger, R., Schneeberger, C., Speiser, P., Louason, G., and Theillet, C. Patterns of allele losses suggest the existence of five distinct regions of LOH on chromosome 17 in breast cancer. Int. J. Cancer, 56: 193–199, 1994.
-
(1994)
Int. J. Cancer
, vol.56
, pp. 193-199
-
-
Kirchweger, R.1
Zeillinger, R.2
Schneeberger, C.3
Speiser, P.4
Louason, G.5
Theillet, C.6
-
6
-
-
0026651275
-
Deletion mapping of chromosome 3p in female genital tract malignancies using microsatellite polymorphisms
-
Jones, M. H., and Nakamura, Y. Deletion mapping of chromosome 3p in female genital tract malignancies using microsatellite polymorphisms. Oncogene, 7: 1631–1634, 1992.
-
(1992)
Oncogene
, vol.7
, pp. 1631-1634
-
-
Jones, M.H.1
Nakamura, Y.2
-
7
-
-
0025800165
-
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
-
Kremer, E. J., Pritchard, M., Lynch, M., Yu, S., Holman, K., Baker, E., Warren, S. T., Schlessinger, D., Sutherland, G. R., and Richards, R. I. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n. Science (Washington DC), 252: 1711–1714, 1991.
-
(1991)
Science (Washington DC)
, vol.252
, pp. 1711-1714
-
-
Kremer, E.J.1
Pritchard, M.2
Lynch, M.3
Yu, S.4
Holman, K.5
Baker, E.6
Warren, S.T.7
Schlessinger, D.8
Sutherland, G.R.9
Richards, R.I.10
-
8
-
-
0026894334
-
Moderate instability of the trinucleotide repeat in spinobulbar muscular atrophy
-
Biancalana, V., Serville, F., Pommier, J., Julien, J., Hanauer, A., and Mandel, J. L. Moderate instability of the trinucleotide repeat in spinobulbar muscular atrophy. Hum. Mol. Genet., 1: 255–258, 1992.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 255-258
-
-
Biancalana, V.1
Serville, F.2
Pommier, J.3
Julien, J.4
Hanauer, A.5
Mandel, J.L.6
-
9
-
-
0026603841
-
Myotonic dystrophy mutation: an unstable CFG repeat in the 3′ untranslated region of the gene
-
Mahadevan, M., Tsilfidis, C., Sabourin, L., Shutler, G., Amemiya, C., Jansen, G., Neville, C., Narang, M., Barcelo, J., O'Hoy, K., Leblond, S., Earle-MacDonald, J., De Jong, P. J., Wieringa, B., and Korneluk, R. G. Myotonic dystrophy mutation: an unstable CFG repeat in the 3′ untranslated region of the gene. Science (Washington DC), 255: 1253–1255, 1992.
-
(1992)
Science (Washington DC)
, vol.255
, pp. 1253-1255
-
-
Mahadevan, M.1
Tsilfidis, C.2
Sabourin, L.3
Shutler, G.4
Amemiya, C.5
Jansen, G.6
Neville, C.7
Narang, M.8
Barcelo, J.9
O'Hoy, K.10
Leblond, S.11
Earle-MacDonald, J.12
De Jong, P.J.13
Wieringa, B.14
Korneluk, R.G.15
-
10
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The Huntington's disease collaborative research group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell, 72: 971–983, 1993.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
11
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
Orr, H. T., Chung, M-Y., Banfi, S., Kwiatkowski, T. J., Jr., Servadio, A., Beaudet, A. L., McCall, A. E., Duvick, L. A., Ranum, L. P. W., and Zoghbi, H. Y. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nature Genet., 4: 221–226, 1993.
-
(1993)
Nature Genet.
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M-Y.2
Banfi, S.3
Kwiatkowski, T.J.4
Servadio, A.5
Beaudet, A.L.6
McCall, A.E.7
Duvick, L.A.8
Ranum, L.P.W.9
Zoghbi, H.Y.10
-
12
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal cancer
-
Aaltonen, L. A., Peltomäki, P., Leach, F. S., Sistonen, P., Pylkkänen, L., Mecklin, J-P., Järvinen, H., Powell, S. M., Jen, J., Hamilton, S. R., Petersen, G. M., Kinzler, K. W., Vogelstein, B., and de la Chapelle, A. Clues to the pathogenesis of familial colorectal cancer. Science (Washington DC), 260: 812–816, 1993.
-
(1993)
Science (Washington DC)
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
Peltomäki, P.2
Leach, F.S.3
Sistonen, P.4
Pylkkänen, L.5
Mecklin, J-P.6
Järvinen, H.7
Powell, S.M.8
Jen, J.9
Hamilton, S.R.10
Petersen, G.M.11
Kinzler, K.W.12
Vogelstein, B.13
de la Chapelle, A.14
-
13
-
-
0027263363
-
Genetic mapping of a locus predisposing to human colorectal cancer
-
Peltomäki, P., Aaltonen, L. A., Sistonen, P., Pylkkänen, L., Mecklin, J-P., Järvinen, H., Green, J. S., Jass, J. R., Weber, J. L., Leach, F. S., Petersen, G. M., Hamilton, S. R., de la Chapelle, A., and Vogelstein, B. Genetic mapping of a locus predisposing to human colorectal cancer. Science (Washington DC), 260: 810–812, 1993.
-
(1993)
Science (Washington DC)
, vol.260
, pp. 810-812
-
-
Peltomäki, P.1
Aaltonen, L.A.2
Sistonen, P.3
Pylkkänen, L.4
Mecklin, J-P.5
Järvinen, H.6
Green, J.S.7
Jass, J.R.8
Weber, J.L.9
Leach, F.S.10
Petersen, G.M.11
Hamilton, S.R.12
de la Chapelle, A.13
Vogelstein, B.14
-
14
-
-
0027366916
-
Genetic instability of microsatellites in endometrial carcinoma
-
Risinger, J. I., Berchuck, A., Kohler, M. F., Watson, P., Lynch, H. T., and Boyd, J. Genetic instability of microsatellites in endometrial carcinoma. Cancer Res., 53: 5100–5103, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 5100-5103
-
-
Risinger, J.I.1
Berchuck, A.2
Kohler, M.F.3
Watson, P.4
Lynch, H.T.5
Boyd, J.6
-
15
-
-
0028154040
-
DNA alterations in cells from hereditary non-polyposis colorectal cancer patients
-
Wu, C., Akiyama, Y., Imai, K., Miyake, S., Nagasaki, H., Oto, M., Okabe, S., Iwama, T., Mitamura, K., Masumitsu, H., Nomizu, T., Baba, S., Maruyama, K., and Yuasa, Y. DNA alterations in cells from hereditary non-polyposis colorectal cancer patients. Oncogene, 9: 991–994, 1994.
-
(1994)
Oncogene
, vol.9
, pp. 991-994
-
-
Wu, C.1
Akiyama, Y.2
Imai, K.3
Miyake, S.4
Nagasaki, H.5
Oto, M.6
Okabe, S.7
Iwama, T.8
Mitamura, K.9
Masumitsu, H.10
Nomizu, T.11
Baba, S.12
Maruyama, K.13
Yuasa, Y.14
-
16
-
-
0027140481
-
Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome
-
Peltomäki, P., Lothe, R. A., Aaltonen, L. A., Pylkkänen, L., Nystrom-Lahti, M, Seruca, R., David, L., Holm, R., Ryberg, D., Haugen, A., Brogger, A., Borresen, A-L., and de la Chapelle, A. Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome. Cancer Res., 53: 585–5855, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 585-5855
-
-
Peltomäki, P.1
Lothe, R.A.2
Aaltonen, L.A.3
Pylkkänen, L.4
Nystrom-Lahti, M.5
Seruca, R.6
David, L.7
Holm, R.8
Ryberg, D.9
Haugen, A.10
Brogger, A.11
Borresen, A-L.12
de la Chapelle, A.13
-
17
-
-
0027136828
-
Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history
-
Lothe, R. A., Peltomäki, P., Meling, G. I., Aaltonen, L. A., Nystrom-Lahti, M, Pylkkänen, L., Heimdal, K., Andersen, T. I., Moller, P., Rognum, T. O., Fossa, S. D., Haldorsen, T., Langmark, F., Bregger, A., de la Chapelle, A., and Børresen, A-L. Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history. Cancer Res., 53: 5849–5852, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 5849-5852
-
-
Lothe, R.A.1
Peltomäki, P.2
Meling, G.I.3
Aaltonen, L.A.4
Nystrom-Lahti, M.5
Pylkkänen, L.6
Heimdal, K.7
Andersen, T.I.8
Moller, P.9
Rognum, T.O.10
Fossa, S.D.11
Haldorsen, T.12
Langmark, F.13
Bregger, A.14
de la Chapelle, A.15
Børresen, A-L.16
-
18
-
-
0027363208
-
Genetic instability in pancreatic cancer and poorly differentiated type of gastric cancer
-
Han, H-J., Yanagisawa, A., Kato, Y., Park, J-G., and Nakamura, Y. Genetic instability in pancreatic cancer and poorly differentiated type of gastric cancer. Cancer Res., 53: 5087–5089, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 5087-5089
-
-
Han, H-J.1
Yanagisawa, A.2
Kato, Y.3
Park, J-G.4
Nakamura, Y.5
-
19
-
-
0028029122
-
Microsatellite instability occurs frequently in human gastric carcinoma
-
Rhyu, M-G., Park, W-S., and Meltzer, S. J. Microsatellite instability occurs frequently in human gastric carcinoma. Oncogene, 9: 29–32, 1994.
-
(1994)
Oncogene
, vol.9
, pp. 29-32
-
-
Rhyu, M-G.1
Park, W-S.2
Meltzer, S.J.3
-
20
-
-
0026552140
-
Chromosome 3p deletions in head and neck carcinomas: statistical ascerteinment of alleic loss
-
Latif, F., Fivash, M., Glenn, G., Tory, K., Orcutt, M. L., Hampsch, K., Delisio, J., Lerman, M., Cowan, J., Beckett, M., and Weichselbaum, R. Chromosome 3p deletions in head and neck carcinomas: statistical ascerteinment of alleic loss. Cancer Res., 52: 1451–1456, 1992.
-
(1992)
Cancer Res.
, vol.52
, pp. 1451-1456
-
-
Latif, F.1
Fivash, M.2
Glenn, G.3
Tory, K.4
Orcutt, M.L.5
Hampsch, K.6
Delisio, J.7
Lerman, M.8
Cowan, J.9
Beckett, M.10
Weichselbaum, R.11
-
21
-
-
0027177767
-
Polymerase chain reaction-based restriction fragment length polymorphism analysis of the short arm of chromosome 3 in primary head and neck squamous carcinoma
-
El-Naggar, A. K., Lee, M. S., Wang, G., Luna, M. A., Goepfert, H., and Batsakis, J. G. Polymerase chain reaction-based restriction fragment length polymorphism analysis of the short arm of chromosome 3 in primary head and neck squamous carcinoma. Cancer (Phila.), 72: 881–886, 1993.
-
(1993)
Cancer (Phila.)
, vol.72
, pp. 881-886
-
-
El-Naggar, A.K.1
Lee, M.S.2
Wang, G.3
Luna, M.A.4
Goepfert, H.5
Batsakis, J.G.6
-
22
-
-
0028350523
-
Allelotype of head and neck squamous cell carcinoma
-
Nawroz, H., van der Riet, P., Hruban, R. H., Koch, W., Ruppert, J. M., and Sidransky, D. Allelotype of head and neck squamous cell carcinoma. Cancer Res., 54: 1152–1155, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 1152-1155
-
-
Nawroz, H.1
van der Riet, P.2
Hruban, R.H.3
Koch, W.4
Ruppert, J.M.5
Sidransky, D.6
-
23
-
-
0024371674
-
Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix
-
Yokota, J., Tsukada, Y., Nakajima, T., Gotoh, M., Shimosato, Y., Mori, N., Tsunokawa, Y., Sugimura, T., and Terada, M. Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix. Cancer Res., 49: 3598–3601, 1989.
-
(1989)
Cancer Res.
, vol.49
, pp. 3598-3601
-
-
Yokota, J.1
Tsukada, Y.2
Nakajima, T.3
Gotoh, M.4
Shimosato, Y.5
Mori, N.6
Tsunokawa, Y.7
Sugimura, T.8
Terada, M.9
-
24
-
-
0027473475
-
Prognostic significance of p53 mutations and 3p deletions in primary resected non-small cell lung cancer
-
Horio, Y., Takahashi, T., Kuroishi, T., Hibi, K., Suyama, M., Niimi, T., Shimokata, K., Yamakawa, K., Nakamura, Y., Ueda, R., and Takahashi, T. Prognostic significance of p53 mutations and 3p deletions in primary resected non-small cell lung cancer. Cancer Res., 53: 1–4, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 1-4
-
-
Horio, Y.1
Takahashi, T.2
Kuroishi, T.3
Hibi, K.4
Suyama, M.5
Niimi, T.6
Shimokata, K.7
Yamakawa, K.8
Nakamura, Y.9
Ueda, R.10
Takahashi, T.11
-
25
-
-
0345575500
-
Loss of heterozygosity on chromosomes 3, 13, and 17 in small-cell carcinoma and on chromosome 3 in adenocarcinoma of the lung
-
Yokota, J., Wada, M., Shimosato, Y., Terada, M., and Sugimura, T. Loss of heterozygosity on chromosomes 3, 13, and 17 in small-cell carcinoma and on chromosome 3 in adenocarcinoma of the lung. Proc. Natl. Acad. Sci. USA, 84: 9252–9256, 1987.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 9252-9256
-
-
Yokota, J.1
Wada, M.2
Shimosato, Y.3
Terada, M.4
Sugimura, T.5
-
26
-
-
0026550844
-
Three distinct regions involved in 3p deletion in human lung cancer
-
Hibi, K., Tkahashi, T., Yamakawa, K., Ueda, R., Sekido, Y., Ariyoshi, Y., Suyama, M., Takagi, H., Nakamura, Y., and Takahashi, T. Three distinct regions involved in 3p deletion in human lung cancer. Oncogene, 7: 445–449, 1992.
-
(1992)
Oncogene
, vol.7
, pp. 445-449
-
-
Hibi, K.1
Tkahashi, T.2
Yamakawa, K.3
Ueda, R.4
Sekido, Y.5
Ariyoshi, Y.6
Suyama, M.7
Takagi, H.8
Nakamura, Y.9
Takahashi, T.10
-
27
-
-
0023233027
-
Molecular analysis of the short arm of chromosome 3 in small-cell and non-small-cell carcinoma of the lung
-
Brauch, H., Johnson, B., Hovis, J., Yano, T., Gazdar, A., Pettengill, O. S., Graziano, S., Sorenson, G. D., Poiesz, B. J., Minna, J., Linehan, M., and Zbar, B. Molecular analysis of the short arm of chromosome 3 in small-cell and non-small-cell carcinoma of the lung. N. Engl. J. Med., 317: 1109–1113, 1987.
-
(1987)
N. Engl. J. Med.
, vol.317
, pp. 1109-1113
-
-
Brauch, H.1
Johnson, B.2
Hovis, J.3
Yano, T.4
Gazdar, A.5
Pettengill, O.S.6
Graziano, S.7
Sorenson, G.D.8
Poiesz, B.J.9
Minna, J.10
Linehan, M.11
Zbar, B.12
-
28
-
-
0028308161
-
Frequent replication errors at microsatellite loci in tumors of patients with multiple primary cancers
-
Horii, A., Han, H-J., Shimada, M., Yanagisawa, A., Kato, Y., Ohta, H., Yasui, W., Tahara, E., and Nakamura, Y. Frequent replication errors at microsatellite loci in tumors of patients with multiple primary cancers. Cancer Res., 54:3373–3375,1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 3373-3375
-
-
Horii, A.1
Han, H-J.2
Shimada, M.3
Yanagisawa, A.4
Kato, Y.5
Ohta, H.6
Yasui, W.7
Tahara, E.8
Nakamura, Y.9
-
29
-
-
0028241332
-
J., Microsatellite instability occurs frequently and in both diploid and aneuploid cell populations of Barrett's-associated esophageal adenocarcinomas
-
Meltzer, S. J., Yin, J., Manin, B., Rhyu, M-G., Cottrell, J., Hudson, E., Redd, J. L., Krasna, M. J., Abraham, J. M., and Reid, B. J., Microsatellite instability occurs frequently and in both diploid and aneuploid cell populations of Barrett's-associated esophageal adenocarcinomas. Cancer Res., 54: 3379–3382, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 3379-3382
-
-
Meltzer, S.J.1
Yin, J.2
Manin, B.3
Rhyu, M-G.4
Cottrell, J.5
Hudson, E.6
Redd, J.L.7
Krasna, M.J.8
Abraham, J.M.9
Reid, B.10
-
30
-
-
0003903343
-
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Sambrook, J., Fritsch, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1989.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
31
-
-
0027163568
-
Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3: D3S587; D3S1317; D3S1435
-
Li, H., Schmidt, L., Duh, F-M. C., Wei, M-H., Latif, F., Stackhouse, T., Lerman, M. I., Zbar, B., and Tory, K. Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3: D3S587; D3S1317; D3S1435. Hum. Mol. Genet, 2: 1326, 1993.
-
(1993)
Hum. Mol. Genet
, vol.2
, pp. 1326
-
-
Li, H.1
Schmidt, L.2
Duh, F-M.C.3
Wei, M-H.4
Latif, F.5
Stackhouse, T.6
Lerman, M.I.7
Zbar, B.8
Tory, K.9
-
32
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach, J., Gyapay, G., Dib, C., Vignal, A., Morissette, J., Millasseau, P., Vaysseix, G., and Lathrop, M. A second-generation linkage map of the human genome. Nature (Lond.), 359: 794–801, 1992.
-
(1992)
Nature (Lond.)
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
33
-
-
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., 7: 658, 1992.
-
(1992)
Hum. Mol. Genet.
, vol.7
, pp. 658
-
-
Kwiatkowski, D.J.1
Diaz, M.O.2
-
34
-
-
0028432501
-
Dinucleotide repeat polymorphism at the D3S1255 locus
-
Klauck, S. M., Whisenant, E., Wood, M., Drabkin, H. A., and Seizinger, B. R. Dinucleotide repeat polymorphism at the D3S1255 locus. Hum. Mol. Genet., 3: 840, 1994.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 840
-
-
Klauck, S.M.1
Whisenant, E.2
Wood, M.3
Drabkin, H.A.4
Seizinger, B.R.5
-
35
-
-
0024603229
-
Deletion mapping in human renal cell carcinoma
-
Bergerheim, U., Nordenskjdld, M., and Collins, V. P. Deletion mapping in human renal cell carcinoma. Cancer Res., 49: 1390–1396, 1989.
-
(1989)
Cancer Res.
, vol.49
, pp. 1390-1396
-
-
Bergerheim, U.1
Nordenskjdld, M.2
Collins, V.P.3
-
36
-
-
0011153988
-
Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma
-
Kovacs, G., Erlandsson, R., Boldog, F., Ingvarsson, S., Muller-Brechlin, R., Klein, G., and Siimegi, J. Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. Proc. Natl. Acad. Sci. USA, 55: 1571–1575, 1988.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.55
, pp. 1571-1575
-
-
Kovacs, G.1
Erlandsson, R.2
Boldog, F.3
Ingvarsson, S.4
Muller-Brechlin, R.5
Klein, G.6
Siimegi, J.7
-
37
-
-
0025726123
-
Deletion of 17p and amplification of int-2 gene in esophageal carcinomas
-
Wagata, T., Ishizaki, K., Imamura, M., Shimada, Y., Ikenaga, M., and Tobe, T. Deletion of 17p and amplification of int-2 gene in esophageal carcinomas. Cancer Res., 57:2113–2117, 1991.
-
(1991)
Cancer Res.
, vol.57
, pp. 2113-2117
-
-
Wagata, T.1
Ishizaki, K.2
Imamura, M.3
Shimada, Y.4
Ikenaga, M.5
Tobe, T.6
-
38
-
-
0028284682
-
Allelotype analysis of esophageal squamous cell carcinoma
-
Shibagaki, I., Shimada, Y., Wagata, T., Ikenaga, M., Imamura, M., and Ishizaki, K. Allelotype analysis of esophageal squamous cell carcinoma. Cancer Res., 54: 2996–3000, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 2996-3000
-
-
Shibagaki, I.1
Shimada, Y.2
Wagata, T.3
Ikenaga, M.4
Imamura, M.5
Ishizaki, K.6
-
39
-
-
0027408524
-
Accumulated allelic losses in the development of invasive urothelial cancer
-
Habuchi, T., Ogawa, O., Kakehi, Y., Ogura, K., Koshiba, M., Hamazaki, S., Takahashi, R., Sugiyama, T., and Yoshida, O. Accumulated allelic losses in the development of invasive urothelial cancer. Int. J. Cancer., 53: 579–584, 1993.
-
(1993)
Int. J. Cancer.
, vol.53
, pp. 579-584
-
-
Habuchi, T.1
Ogawa, O.2
Kakehi, Y.3
Ogura, K.4
Koshiba, M.5
Hamazaki, S.6
Takahashi, R.7
Sugiyama, T.8
Yoshida, O.9
-
40
-
-
0013878809
-
Hereditary factors in cancer: Study of two large midwestern kindreds
-
Lynch, H. T., Shaw, M. W., Magnuson, G. W., Larsen, A. L., and Krush, A. J. Hereditary factors in cancer: Study of two large midwestern kindreds. Arch. Intern. Med., 777: 206–212, 1966.
-
(1966)
Arch. Intern. Med.
, vol.777
, pp. 206-212
-
-
Lynch, H.T.1
Shaw, M.W.2
Magnuson, G.W.3
Larsen, A.L.4
Krush, A.J.5
-
41
-
-
0027467494
-
Extracolonic cancer in hereditary nonpolyposis colorectal cancer
-
Watson, P., and Lynch, H. T. Extracolonic cancer in hereditary nonpolyposis colorectal cancer. Cancer (Phila.), 77: 677–685, 1993.
-
(1993)
Cancer (Phila.)
, vol.77
, pp. 677-685
-
-
Watson, P.1
Lynch, H.T.2
-
42
-
-
0027248156
-
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review
-
Lynch, H. T., Smyrk, T. G., Watson, P., Lanspa, S. J., Lynch, J. F., Lynch, P. M., Cavalieri, R. J., and Boland, G. R. Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review. Gastroenterology, 104: 1535–1549, 1993.
-
(1993)
Gastroenterology
, vol.104
, pp. 1535-1549
-
-
Lynch, H.T.1
Smyrk, T.G.2
Watson, P.3
Lanspa, S.J.4
Lynch, J.F.5
Lynch, P.M.6
Cavalieri, R.J.7
Boland, G.R.8
-
43
-
-
0027306173
-
Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair
-
Strand, M., Prolla, T. A., Liskay, R. M., and Petes, T. D. Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair. Nature (Lond.), 365: 274–276, 1993.
-
(1993)
Nature (Lond.)
, vol.365
, pp. 274-276
-
-
Strand, M.1
Prolla, T.A.2
Liskay, R.M.3
Petes, T.D.4
-
44
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
Fishel, R., Lescoe, M. K., Rao, M. R. S., Copeland, N. G., Jenkins, N. A., Garber, J., Kane, M., and Kolodner, R. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell, 75: 1027–1038, 1993.
-
(1993)
Cell
, vol.75
, pp. 1027-1038
-
-
Fishel, R.1
Lescoe, M.K.2
Rao, M.R.S.3
Copeland, N.G.4
Jenkins, N.A.5
Garber, J.6
Kane, M.7
Kolodner, R.8
-
45
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
Leach, F. S., Nicolaides, N. G., Papadopoulos, N., Liu, B., Jen, J., Parsons, R., Peltomäki, P., Sistonen, P., Aaltonen, L. A., Nystrom-Lahti, M., Guan, X-Y., Zhang, J., Meltzer, P. S., Yu, J-W., Kao, F-T., Chen, D. J., Cerosaletti, K. M., Fournier, R. E. K., Todd, S., Lewis, T., Leach, R. J., Naylor, S. L., Weissenbach, J., Mecklin, J-P., Jirvinen, H., Petersen, G. M., Hamilton, S. R., Green, J., Jass, J., Watson, P., Lynch, H. T., Trent, J. M., de la Chapelle, A., Kinzler, K. W., and Vogelstein, B. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell, 75: 1215–1225, 1993.
-
(1993)
Cell
, vol.75
, pp. 1215-1225
-
-
Leach, F.S.1
Nicolaides, N.G.2
Papadopoulos, N.3
Liu, B.4
Jen, J.5
Parsons, R.6
Peltomäki, P.7
Sistonen, P.8
Aaltonen, L.A.9
Nystrom-Lahti, M.10
Guan, X-Y.11
Zhang, J.12
Meltzer, P.S.13
Yu, J-W.14
Kao, F-T.15
Chen, D.J.16
Cerosaletti, K.M.17
Fournier, R.E.K.18
Todd, S.19
Lewis, T.20
Leach, R.J.21
Naylor, S.L.22
Weissenbach, J.23
Mecklin, J-P.24
Jirvinen, H.25
Petersen, G.M.26
Hamilton, S.R.27
Green, J.28
Jass, J.29
Watson, P.30
Lynch, H.T.31
Trent, J.M.32
Kinzler, K.W.33
Vogelstein, B.34
more..
-
46
-
-
0028284887
-
Genetic instability of microsatellite sequences in many non-small cell lung carcinomas
-
Shridhar, V., Siegfried, J., Hunt, J., del Mar Alonso, M., and Smith, D. I. Genetic instability of microsatellite sequences in many non-small cell lung carcinomas. Cancer Res., 54: 2084–2087, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 2084-2087
-
-
Shridhar, V.1
Siegfried, J.2
Hunt, J.3
del Mar Alonso, M.4
Smith, D.I.5
-
47
-
-
0028230597
-
Frequent microsatellite instability in primary small cell lung cancer
-
Merlo, A., Mabry, M., Gabrielson, E., Vollmer, R., Baylin, S. B., and Sidransky, D. Frequent microsatellite instability in primary small cell lung cancer. Cancer Res., 54: 2098–2101, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 2098-2101
-
-
Merlo, A.1
Mabry, M.2
Gabrielson, E.3
Vollmer, R.4
Baylin, S.B.5
Sidransky, D.6
-
48
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Papadopoulos, N., Nicolaides, N. G., Wei, Y-F., Ruben, S. M., Carter, K. G., Rosen, G. A., Haseltine, W. A., Fleischmann, R. D., Fraser, G. M., Adams, M. D., Venter, J. G., Hamilton, S. R., Petersen, G. M., Watson, P., Lynch, H. T., Peltomäki, P., Mecklin, J-P., de la Chapelle, A., Kinzler, K. W., and Vogelstein, B. Mutation of a mutL homolog in hereditary colon cancer. Science (Washington DC), 263: 1625–1629, 1994.
-
(1994)
Science (Washington DC)
, vol.263
, pp. 1625-1629
-
-
Papadopoulos, N.1
Nicolaides, N.G.2
Wei, Y-F.3
Ruben, S.M.4
Carter, K.G.5
Rosen, G.A.6
Haseltine, W.A.7
Fleischmann, R.D.8
Fraser, G.M.9
Adams, M.D.10
Venter, J.G.11
Hamilton, S.R.12
Petersen, G.M.13
Watson, P.14
Lynch, H.T.15
Peltomäki, P.16
Mecklin, J-P.17
de la Chapelle, A.18
Kinzler, K.W.19
Vogelstein, B.20
more..
-
49
-
-
0027285475
-
Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
-
Ionov, Y., Peinado, M. A., Malkhosyan, S., Shibata, D., and Perucho, M. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature (Lond.), 363: 558–561, 1993.
-
(1993)
Nature (Lond.)
, vol.363
, pp. 558-561
-
-
Ionov, Y.1
Peinado, M.A.2
Malkhosyan, S.3
Shibata, D.4
Perucho, M.5
-
50
-
-
0027495408
-
Microsatellite instability in bladder cancer
-
Gonzalez-Zulueta, M., Ruppert, J. M., Tokino, K., Tsai, Y. G., Spruck, G. H., III, Miyao, N., Nichols, P. W., Hermann, G. G., Horn, T., Steven, K., Summerhayes, I. G., Sidransky, D., and Jones, P. A. Microsatellite instability in bladder cancer. Cancer Res., 53: 5620–5623, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 5620-5623
-
-
Gonzalez-Zulueta, M.1
Ruppert, J.M.2
Tokino, K.3
Tsai, Y.G.4
Spruck, G.H.5
Miyao, N.6
Nichols, P.W.7
Hermann, G.G.8
Horn, T.9
Steven, K.10
Summerhayes, I.G.11
Sidransky, D.12
Jones, P.A.13
-
51
-
-
0028269679
-
Microsatellite instability and loss of heterozygosity in breast cancer
-
Yee, G. J., Roodi, N., Verrier, G. S., and Pari, F. F. Microsatellite instability and loss of heterozygosity in breast cancer. Cancer Res., 54: 1641–1644, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 1641-1644
-
-
Yee, G.J.1
Roodi, N.2
Verrier, G.S.3
Pari, F.F.4
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