-
1
-
-
0030999555
-
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
-
Mitelman F., Mertens, F., and Johansson, B. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat. Genet., 15: 417-474, 1997.
-
(1997)
Nat. Genet.
, vol.15
, pp. 417-474
-
-
Mitelman, F.1
Mertens, F.2
Johansson, B.3
-
3
-
-
0027420768
-
The clinical applications of new DNA diagnostic technology on the management of cancer patients
-
Rowley, J. D., Aster, J. C., and Sklar, J. The clinical applications of new DNA diagnostic technology on the management of cancer patients. J. Am. Med. Assoc., 270: 2331-2337, 1993.
-
(1993)
J. Am. Med. Assoc.
, vol.270
, pp. 2331-2337
-
-
Rowley, J.D.1
Aster, J.C.2
Sklar, J.3
-
4
-
-
0028305291
-
Cancer cytogenetics for clinicians
-
Sandberg, A. A. Cancer cytogenetics for clinicians. CA Cancer J. Clin., 44: 136-159, 1994.
-
(1994)
CA Cancer J. Clin.
, vol.44
, pp. 136-159
-
-
Sandberg, A.A.1
-
6
-
-
0027970838
-
Chromosomal translocations in human cancer
-
Rabbitts, T. H. Chromosomal translocations in human cancer. Nature (Lond.), 372: 143-149, 1994.
-
(1994)
Nature (Lond.)
, vol.372
, pp. 143-149
-
-
Rabbitts, T.H.1
-
7
-
-
0024399684
-
Oncogenes, antioncogenes, and the molecular hases of multistep carcinogenesis
-
Weinberg, R. A. Oncogenes, antioncogenes, and the molecular hases of multistep carcinogenesis. Cancer Res., 49: 3713-3721, 1989.
-
(1989)
Cancer Res.
, vol.49
, pp. 3713-3721
-
-
Weinberg, R.A.1
-
8
-
-
0025312728
-
A genetic model for colorectal tumorigenesis
-
Fearon, E. R., and Vogelstein, B. A genetic model for colorectal tumorigenesis. Cell, 61: 759-767, 1990.
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
9
-
-
0027401607
-
The multistep nature of cancer
-
Vogelstein, B., and Kinzler, K. W. The multistep nature of cancer. Trends Genet., 9: 138-141, 1993.
-
(1993)
Trends Genet.
, vol.9
, pp. 138-141
-
-
Vogelstein, B.1
Kinzler, K.W.2
-
10
-
-
0003592020
-
-
Memphis, Tennessee, October 1994
-
Mitelman, F. (ed.), Basel: S. Karger AG, 1995. An International System for Human Cytogenetic Nomenclature. Recommendations of the International Standing Committee on Human Cytogenetic (1995): Nomenclature, p. 114. Memphis, Tennessee, October 1994.
-
(1995)
An International System for Human Cytogenetic Nomenclature. Recommendations of the International Standing Committee on Human Cytogenetic (1995): Nomenclature
, pp. 114
-
-
Mitelman, F.1
Basel, S.2
Karger, A.G.3
-
11
-
-
0027966172
-
Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors
-
Kallioniemi, O-P., Kallioniemi, A., Piper, J., Isola, J., Waldman, F. M., Gray, J. W., and Pinkel, D. Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors. Genes Chromosomes & Cancer, 10: 231-243, 1994.
-
(1994)
Genes Chromosomes & Cancer
, vol.10
, pp. 231-243
-
-
Kallioniemi, O.-P.1
Kallioniemi, A.2
Piper, J.3
Isola, J.4
Waldman, F.M.5
Gray, J.W.6
Pinkel, D.7
-
12
-
-
0030025518
-
Compilation of somatic mutations of the CDKN2 gene in human cancers: Non-random distribution of base substitutions
-
Pollock, P. M., Pearson, J. V., and Hayward, N. K. Compilation of somatic mutations of the CDKN2 gene in human cancers: non-random distribution of base substitutions. Genes Chromosomes & Cancer, 15: 77-88, 1996.
-
(1996)
Genes Chromosomes & Cancer
, vol.15
, pp. 77-88
-
-
Pollock, P.M.1
Pearson, J.V.2
Hayward, N.K.3
-
13
-
-
0023106062
-
Human retinoblastoma susceptibility gene: Cloning, identification, and sequence
-
Washington DC
-
Lee, W-H., Bookstein, R., Hong, F., Young, L-J., Shew, J-Y., and Lee, E. Y-H.P. Human retinoblastoma susceptibility gene: cloning, identification, and sequence. Science (Washington DC), 235: 1394-1399, 1987.
-
(1987)
Science
, vol.235
, pp. 1394-1399
-
-
Lee, W.-H.1
Bookstein, R.2
Hong, F.3
Young, L.-J.4
Shew, J.-Y.5
Lee, E.Y.-H.P.6
-
14
-
-
0028071555
-
Mutations in the p53 tumor suppressor gene: Clues to cancer etiology and molecular pathology
-
Greenblatt, M. S., Bennett, W. P., Hollstein, M., and Harris, C. C. Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathology. Cancer Res., 54: 4855-4878, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 4855-4878
-
-
Greenblatt, M.S.1
Bennett, W.P.2
Hollstein, M.3
Harris, C.C.4
-
15
-
-
0029774136
-
Genomic instability in 1p and human malignancies
-
Schwab, M., Prami, C., and Amler, L. C. Genomic instability in 1p and human malignancies. Genes Chromosomes & Cancer, 16: 211-229, 1996.
-
(1996)
Genes Chromosomes & Cancer
, vol.16
, pp. 211-229
-
-
Schwab, M.1
Prami, C.2
Amler, L.C.3
-
16
-
-
0030983281
-
Involvement of multiple loci on chromosome 3 in renal cell cancer development
-
van den Berg, A., and Buys, C. H. C. M. Involvement of multiple loci on chromosome 3 in renal cell cancer development. Genes Chromosomes & Cancer, 19: 59-76, 1997.
-
(1997)
Genes Chromosomes & Cancer
, vol.19
, pp. 59-76
-
-
Van Den Berg, A.1
Buys, C.H.C.M.2
-
17
-
-
0028075111
-
Isochromosomes in neoplasia
-
Mertens, F., Johansson, B., and Mitelman, F. Isochromosomes in neoplasia. Genes Chromosomes & Cancer, 10: 221-230, 1994.
-
(1994)
Genes Chromosomes & Cancer
, vol.10
, pp. 221-230
-
-
Mertens, F.1
Johansson, B.2
Mitelman, F.3
-
18
-
-
0026631328
-
Genetic alterations underlying colorectal tumorigenesis
-
Fearon, E. R. Genetic alterations underlying colorectal tumorigenesis. Cancer Surv., 12: 119-136, 1992.
-
(1992)
Cancer Surv.
, vol.12
, pp. 119-136
-
-
Fearon, E.R.1
-
19
-
-
0027367903
-
6q deletions define distinct clinicopathologic subsets of non-Hodgkin's lymphoma
-
Offit, K., Parsa, N. Z., Gaidano, G., Filippa, D. A., Louie, D., Pan, D., Jhanwar, S. C., Dalla-Favera, R., and Chaganti, R. S. K. 6q deletions define distinct clinicopathologic subsets of non-Hodgkin's lymphoma. Blood, 82: 2157-2162, 1993.
-
(1993)
Blood
, vol.82
, pp. 2157-2162
-
-
Offit, K.1
Parsa, N.Z.2
Gaidano, G.3
Filippa, D.A.4
Louie, D.5
Pan, D.6
Jhanwar, S.C.7
Dalla-Favera, R.8
Chaganti, R.S.K.9
-
20
-
-
0028986931
-
kip1 gene to 12p13 and its analysis in leukemias
-
kip1 gene to 12p13 and its analysis in leukemias. Cancer Res., 55: 1206-1210, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 1206-1210
-
-
Pietenpol, J.A.1
Bohlander, S.K.2
Sato, Y.3
Papadopoulos, N.4
Liu, B.5
Friedman, C.6
Trask, B.J.7
Roberts, J.M.8
Kinzler, K.W.9
Rowley, J.D.10
Vogelstein, J.D.11
-
21
-
-
0028986932
-
Kip1: Chromosomal mapping to 12p12-12p13.1 and absence of mutations in human tumors
-
Kip1: Chromosomal mapping to 12p12-12p13.1 and absence of mutations in human tumors. Cancer Res., 55: 1211-1214, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 1211-1214
-
-
Ponce-Castaneda, M.V.1
Lee, M.-H.2
Latres, E.3
Polyak, K.4
Lacombe, L.5
Montgomery, K.6
Mathew, S.7
Krauter, K.8
Sheinfeld, J.9
Massague, J.10
Cardon-Cardo, C.11
-
22
-
-
1842294695
-
Report of the committee on the genetic constitution of chromosome 17
-
A. J. Cuticchia, M. A. Chipperfield, and P. A. Foster (eds), Baltimore: The Johns Hopkins University Press
-
Lancet, D., and Solomon, E. Report of the committee on the genetic constitution of chromosome 17. In: A. J. Cuticchia, M. A. Chipperfield, and P. A. Foster (eds), Human Gene Mapping 1995: A Compendium, pp. 945-988, 1996. Baltimore: The Johns Hopkins University Press.
-
(1996)
Human Gene Mapping 1995: A Compendium
, pp. 945-988
-
-
Lancet, D.1
Solomon, E.2
|