| 1. |
Vogelstein, B., Fearon, E. R., Hamilton, S. R., Kern, S. E., Preisinger, A. C., Leppert, M., Nakamura, Y., White, R., Smits,
A. M. M., and Bos, J. L. (1988) Genetic alterations during colorectal-tumor development. N. Engl.. J. Med.
319, 525–532.
|
| |
| 2. |
Wagata. T., Ishizaki, K., Imamura, M., Shimada, Y., Ikenaga, M., and Tobe, T. (1991) Deletion of 17p and amplification of
the int-2 gene in esophageal carcinomas. Cancer Res.
51, 2113–2117.
|
| |
| 3. |
Meltzer, S. J., Ahnen, D. J., Battifora, H., Yokota, J., and Cline, M. J, (1987) Protooncogene abnormalities in colon cancers
and adenomatous polyps. Gastroenterology
92, 1174–1180.
|
| |
| 4. |
Simon, D., Knowles, B, B., and Weith, A. (1991) Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary
hepatomas. Oncogene
6, 765–770.
|
| |
| 5. |
Khosla, S., Patel, V. M., Hay, I. D., Schaid, D. J., Grant, C. S., van Heeren, J. U. A., and Thibodeau, S. N. (1991) Loss
of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas. J. Clin. Invest.
87, 1691–1699.
|
| |
| 6. |
Fey, M. F., Hesketh, C., Wainscoat, J. S., Gendler, S., and Thein, S. L. (1989) Clonal allele loss in gastrointestinal cancers.
Br. J. Cancer
59, 750–754.
|
| |
| 7. |
Vogelstein, B., Fearon, E. R., Kern, S. E., Hamilton, S. R., Preisinger, A. C., Nakamura, Y., and White, R. (1989) Allelotype
of colorectal carcinomas. Science
244, 207–211.
|
| |
| 8. |
Kovacs, G., Erlandsson, R., Boldog, F., Ingvarsson, S., Muller-Brechlin, R., Klein, G., and Sumegi, J. (1988) Consistent chromosome
3p deletion and loss of het-erozygosity in renal cell carcinoma. Proc. Natl. Acad. Sci. USA
85, 1571–1575.
|
| |
| 9. |
Yokota, J., Tsukada, Y., Nakajima, T., Gotoh, M., Shimosato, Y., Mori, N., Tsunokawa, Y., Sugimura, T., and Terada, M. (1989)
Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix. Cancer Res.
49, 3598–3601.
|
| |
| 10. |
Lee, J. H., Kavanagh, J. J., Wildrick, D. M., Wharton, J. T., and Blick, M. (1990) Frequent loss of heterozygosity on chromosomes
6q, 11, and 17 in human ovarian carcinomas. Cancer Res.
50, 2724–2728.
|
| |
| 11. |
Fearon, E. R., Cho, K. R., Nigro, J. M., Kern, S. E., Simons, J. W., Ruppert, J. M., Hamilton, S. R., Preisinger, A. C., Thomas,
G., Kinzler, K. W., and Vogelstein, B. (1990) Identification of a chromosome 18q gene that is altered in colorectal cancers.
Science
247, 49–56.
|
| |
| 12. |
Kinzler, K. W., Nilbert, M. C., Vogelstein, B., Bryan, T. M., Levy, D. B., Smith, K. J., Preisinger, A. C., Hamilton, S. R..
Hedge. P., Markham, A., Carlson, M., Joslyn, G., Groden, J., White, R., Miki, Y., Miyoshi, Y., Nishisho, I., and Nakamura,
Y. (1991) Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers. Science
251, 1366–1370.
|
| |
| 13. |
Kinzler, K. W., Nilbert, M. C., Su, L.-K., Vogelstein, B., Bryan, T. M., Levy, D. B., Smith, K. J., Preisenger, A. C., Hedge,
P., McKechnie, D., Finniear, R., Markham, A., Groffen, J., Boguski, M. S., Altschul, S. F., Horii, A., Ando, H., Miyoshi,
Y., Miki, Y., Nishosho, I., and Nakamura, Y. (1991) Identification of FAP locus genes from chromosome 5q21. Science
253, 661–665.
|
| |
| 14. |
Baker, S. J., Fearon, E. R., Nigro, J. M., Hamilton, S. R., Preisinger, A. C., Jessup, J. M., van Tuinen, P., Ledbetter, D.
H., Barker, D. F.. Nakamura, Y., White, R., and Vogelstein, B. (1989) Chromosome 17 deletions and p53 gene mutations in colorectal
carcinomas. Science
244, 217–221.
|
| |
| 15. |
Baker, S. J., Preisinger, A. C., Jessup, J. M., Paraskeva, C., Markowitz, S., Willson, J. K. V., Hamilton, S., and Vogelstein,
B. (1990) p53 mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis. Cancer Res.
50, 7717–7722.
|
| |
| 16. |
Meltzer, S. J., Mane, S. M., Wood, P. K., Resau, J. H., Newkirk, C., Terzakis, J. A., Korelitz, B. I., Weinstein, W. M., and
Needleman, S. W. (1990) Activation of c-Ki-ras in human gastrointestinal dysplasias determined by direct sequencing of polymemse
chain reaction products. Cancer Res.
50, 3627–3630.
|
| |
| 17. |
Reid, B. J., Haggitt, R. C., Rubin, C. E., and Rabinovitch, P. S. (1987) Barrett’s esophagus: Correlation between flow cytometry
and histology in detection of patients at risk for adenocarcinoma. Gastroenterology
93, 1–11.
|
| |
| 18. |
Meltzer, S. J., Yin, J., Huang, Y., McDaniel, T. K., Newkirk, C., Iseri, O., Vogelstein, B., and Resau, J. H. (1991) Reduction
to homozygosity involving p53 in esophageal cancers demonstrated by the polymerase chain reaction. Proc. Natl. Acad. Sci. USA
88, 4976–4980.
|
| |
| 19. |
Boynton, R. F., Huang, Y., Blount, P. L., Reid, B. J., Rasking, W. H., Haggitt, R. C., Newkirk, C., Resau, J. H., Yin, J.,
McDaniel, T., and Meltzer, S. J. (1991) Frequent loss of beterozygosity at tbe retinoblastoma locus in human esophageal cancers.
Cancer Res., 51, 5766–5769.
|
| |
| 20. |
Feinberg, A. P. and Vogelstein, B. (1983) Hypomethylation distinguishes genes of some human cancers from their normal counterparts.
Nature
301, 89–92.
|
| |
| 21. |
de la Calle-Martin, O., Fabregat, V., Romero, M., Soler, J., Vives, J. and Yague, J. (1990) Acc II polymorphism of the p53
gene. Nucleic Acids Res.
18, 4963.
|
| |
| 22. |
McGee, T. L., Yandell, D. W., and Dryja, T. P. (1989) Structure and partial genomic sequence of the human retinoblastoma susceptibility
gene. Gene
80, 119–128.
|
| |