-
1
-
-
0028835677
-
Cancer statistics
-
Wingo, P A., Tong, T., and Bolden, S Cancer statistics, CA Cancer J. Clin., 45: 8-30, 1995.
-
(1995)
CA Cancer J. Clin.
, vol.45
, pp. 8-30
-
-
Wingo, P.A.1
Tong, T.2
Bolden, S.3
-
2
-
-
0024742543
-
At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma
-
Devilee, P., van den Broek, M., Kuipers-Dijkshoorn, N., Kolluri, R., Khan, P. M., Pearson, P L., and Cornelisse, C. J. At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma. Genomics, 5: 554-560, 1989.
-
(1989)
Genomics
, vol.5
, pp. 554-560
-
-
Devilee, P.1
Van Den Broek, M.2
Kuipers-Dijkshoorn, N.3
Kolluri, R.4
Khan, P.M.5
Pearson, P.L.6
Cornelisse, C.J.7
-
3
-
-
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, T.1
Akiyama, F.2
Sakamoto, G.3
Kasumi, F.4
Nakamura, Y.5
-
4
-
-
0028360878
-
Deletion of two separate regions on chromosome 3p in breast cancers
-
Chen, L-C., Matsumura, K., Deng, G., Kurisu, W., Ljung, B-M., Lerman, M I., Waldman, F. M., and Smith, H S. Deletion of two separate regions on chromosome 3p in breast cancers Cancer Res., 54: 3021-3024, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 3021-3024
-
-
Chen, L.-C.1
Matsumura, K.2
Deng, G.3
Kurisu, W.4
Ljung, B.-M.5
Lerman, M.I.6
Waldman, F.M.7
Smith, H.S.8
-
5
-
-
0027516041
-
Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast
-
Pandis, N., Jin, Y., Limon, J., Bardi, G., Idvall, I., Mandahl, N., Mitelman, F., and Heim, S Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast. Genes Chromosomes & Cancer, 6: 151-155, 1993.
-
(1993)
Genes Chromosomes & Cancer
, vol.6
, pp. 151-155
-
-
Pandis, N.1
Jin, Y.2
Limon, J.3
Bardi, G.4
Idvall, I.5
Mandahl, N.6
Mitelman, F.7
Heim, S.8
-
6
-
-
0028948713
-
Chromosome analysis of 97 primary breast carcinomas identification of 8 karyotypic subgroups
-
Pandis, N., Jin, Y., Gorunova, L., Petersson, C., Bardi, G., Idvall, I., Johansson, B., Ingvar, C., Mandahl, N., Mitelman, F., and Heim, S. Chromosome analysis of 97 primary breast carcinomas identification of 8 karyotypic subgroups Genes Chromosomes & Cancer, 12: 173-185, 1995.
-
(1995)
Genes Chromosomes & Cancer
, vol.12
, pp. 173-185
-
-
Pandis, N.1
Jin, Y.2
Gorunova, L.3
Petersson, C.4
Bardi, G.5
Idvall, I.6
Johansson, B.7
Ingvar, C.8
Mandahl, N.9
Mitelman, F.10
Heim, S.11
-
7
-
-
0028241636
-
Homozygous deletion, rearrangement, and hypermethylation implicate chromosome region 3p14 3-3p21 3 in sporadic breast cancer development
-
Buchhagen, D L., Qiu, L., and Etkind, P. Homozygous deletion, rearrangement, and hypermethylation implicate chromosome region 3p14 3-3p21 3 in sporadic breast cancer development Int. J Cancer. 57: 473-479, 1994.
-
(1994)
Int. J Cancer
, vol.57
, pp. 473-479
-
-
Buchhagen, D.L.1
Qiu, L.2
Etkind, P.3
-
8
-
-
0030894455
-
Deletion of the short arm of chromosome 3 in breast tumors
-
in press
-
Pandis, N., Bardi, G., Mitelman, F., and Heim, S. Deletion of the short arm of chromosome 3 in breast tumors. Genes Chromosomes & Cancer, in press, 1996.
-
(1996)
Genes Chromosomes & Cancer
-
-
Pandis, N.1
Bardi, G.2
Mitelman, F.3
Heim, S.4
-
10
-
-
0028966394
-
Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue
-
Dietrich, C U., Pandis, N., Teixeira, M. R., Bardi, G., Gerdes, A. M., Andersen, J. A., and Heim, S Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue Int J Cancer, 60 49-53, 1995.
-
(1995)
Int J Cancer
, vol.60
, pp. 49-53
-
-
Dietrich, C.U.1
Pandis, N.2
Teixeira, M.R.3
Bardi, G.4
Gerdes, A.M.5
Andersen, J.A.6
Heim, S.7
-
11
-
-
0028918093
-
Rearrangement of chromosomal bands 3p13-14 in two hamartomas of the breast
-
Dietrich, C. U., Pandis, N., Bardi, G., Hagerstrand, I., Andersen, J A., Mitelman, F., and Heim, S. Rearrangement of chromosomal bands 3p13-14 in two hamartomas of the breast. Int. J. Oncol., 6: 559-461, 1995.
-
(1995)
Int. J. Oncol.
, vol.6
, pp. 559-1461
-
-
Dietrich, C.U.1
Pandis, N.2
Bardi, G.3
Hagerstrand, I.4
Andersen, J.A.5
Mitelman, F.6
Heim, S.7
-
12
-
-
8944261589
-
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families
-
Petersson, C., Pandis, N., Mertens, F., Adeyinka, A., Ingvar, C., Ringberg, A., Idvall, I., Bondeson, L., Borg, Å., Olsson, H., Kristoffersson, U., and Mitelman, F Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families. Genes Chromosomes & Cancer, 16: 185-188, 1996.
-
(1996)
Genes Chromosomes & Cancer
, vol.16
, pp. 185-188
-
-
Petersson, C.1
Pandis, N.2
Mertens, F.3
Adeyinka, A.4
Ingvar, C.5
Ringberg, A.6
Idvall, I.7
Bondeson, L.8
Borg, Å.9
Olsson, H.10
Kristoffersson, U.11
Mitelman, F.12
-
13
-
-
0029998976
-
Cytogenetic abnormalities in an in situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer
-
Teixeira, M. R., Pandis, N., Gerdes, A M., Dietrich, C U., Bardi, G., Andersen, J. A., Graversen, H P., Mitelman, F., and Heim, S Cytogenetic abnormalities in an in situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer. Breast Cancer Res. Treat., 38: 177-182, 1996.
-
(1996)
Breast Cancer Res. Treat.
, vol.38
, pp. 177-182
-
-
Teixeira, M.R.1
Pandis, N.2
Gerdes, A.M.3
Dietrich, C.U.4
Bardi, G.5
Andersen, J.A.6
Graversen, H.P.7
Mitelman, F.8
Heim, S.9
-
14
-
-
13344279424
-
The FHIT gene. spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers
-
Ohta, M., Inoue, H., Cotticelli, M. G., Kastury, K., Baffa, R., Palazzo, J., Siprashvili, Z., Mori, M., McCue, P., Druck, T., Croce, C. M., and Huebner, K The FHIT gene. spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers Cell, 84: 587-597, 1996.
-
(1996)
Cell
, vol.84
, pp. 587-597
-
-
Ohta, M.1
Inoue, H.2
Cotticelli, M.G.3
Kastury, K.4
Baffa, R.5
Palazzo, J.6
Siprashvili, Z.7
Mori, M.8
McCue, P.9
Druck, T.10
Croce, C.M.11
Huebner, K.12
-
15
-
-
15844384990
-
The FHIT gene at 3p14.2 is abnormal in lung cancer
-
Sozzi, G, Veronese, M. L., Negrini, M., Baffa, R. Cotticelli, M G., Inoue, H., Tomielli, S., Pilotti, S., De Gregono, L., Pastorino, U., Pierotti, M. A., Ohta, M., Huebner, K., and Croce, C. M. The FHIT gene at 3p14.2 is abnormal in lung cancer Cell, 85: 17-26, 1996.
-
(1996)
Cell
, vol.85
, pp. 17-26
-
-
Sozzi, G.1
Veronese, M.L.2
Negrini, M.3
Baffa, R.4
Cotticelli, M.G.5
Inoue, H.6
Tomielli, S.7
Pilotti, S.8
De Gregono, L.9
Pastorino, U.10
Pierotti, M.A.11
Ohta, M.12
Huebner, K.13
Croce, C.M.14
-
16
-
-
0029902071
-
The FHIT gene at 3p14.2 is abnormal in breast carcinomas
-
Negrini, M., Monaco, C., Vorechovsky, I., Ohta, M., Druck, T., Baffa, R., Huebner, K., and Croce, C. M. The FHIT gene at 3p14.2 is abnormal in breast carcinomas Cancer Res., 56: 3173-3179, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 3173-3179
-
-
Negrini, M.1
Monaco, C.2
Vorechovsky, I.3
Ohta, M.4
Druck, T.5
Baffa, R.6
Huebner, K.7
Croce, C.M.8
-
17
-
-
9344225158
-
Aberrant FHIT transcripts in Merkel cell carcinoma
-
Sozzi, G., Alder, H., Tornielli, S., Corletto, V., Baffa, R., Veronese, M. L., Negrini, M., Pilotti, S., Pierotti, M. A., Huebner, K., and Croce, C M. Aberrant FHIT transcripts in Merkel cell carcinoma. Cancer Res., 56: 2472-2474, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 2472-2474
-
-
Sozzi, G.1
Alder, H.2
Tornielli, S.3
Corletto, V.4
Baffa, R.5
Veronese, M.L.6
Negrini, M.7
Pilotti, S.8
Pierotti, M.A.9
Huebner, K.10
Croce, C.M.11
-
18
-
-
0026716989
-
Isolation, characterization, and chromosomal localization of the human CADD153 gene
-
Amst.
-
Park, J S., Luethy, J. D., Wang, M G., Fargnoli, J., Fornace, A. J., Jr., McBride, O. W., and Holbrook, N. J. Isolation, characterization, and chromosomal localization of the human CADD153 gene. Gene (Amst.). 116: 259-267, 1992.
-
(1992)
Gene
, vol.116
, pp. 259-267
-
-
Park, J.S.1
Luethy, J.D.2
Wang, M.G.3
Fargnoli, J.4
Fornace Jr., A.J.5
McBride, O.W.6
Holbrook, N.J.7
-
19
-
-
0026686674
-
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours
-
Delattre, O., Zucman, J., Plougastel, B., Desmaze, C., Melot, T., Peter, M., Kovar, H., Joubert, I., de Jong, P., Rouleau, G., Aurias, A., and Thomas, G Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours. Nature (Lond.), 359: 162-165, 1992.
-
(1992)
Nature (Lond.)
, vol.359
, pp. 162-165
-
-
Delattre, O.1
Zucman, J.2
Plougastel, B.3
Desmaze, C.4
Melot, T.5
Peter, M.6
Kovar, H.7
Joubert, I.8
De Jong, P.9
Rouleau, G.10
Aurias, A.11
Thomas, G.12
-
20
-
-
0028805220
-
The DNA rearrangement that generates the TRK-T3 oncogene involves a novel gene on chromosome 3 whose product has a potential coiled-coil domain
-
Greco, A., Mariani, C., Miranda, C., Lupas, A., Pagliardini, S., Pomati, M., and Pierotti, M. A. The DNA rearrangement that generates the TRK-T3 oncogene involves a novel gene on chromosome 3 whose product has a potential coiled-coil domain. Mol. Cell. Biol., 15: 6118-6127, 1995.
-
(1995)
Mol. Cell. Biol.
, vol.15
, pp. 6118-6127
-
-
Greco, A.1
Mariani, C.2
Miranda, C.3
Lupas, A.4
Pagliardini, S.5
Pomati, M.6
Pierotti, M.A.7
-
21
-
-
0027465044
-
Identification of a carbonic anhydrase-like domain in the extracellular region of RPTP γ defines a new subfamily of receptor tyrosine phosphatases
-
Barnea, G. Silvennoinen, O., Shaanan, B., Honegger, A M., Canoll, P. D., D'Eustachio, P., Morse, B., Levy, J. B., LaForgia, S., Huebner, K., Musacchio, J., Sap, J., and Schlessinger, J. Identification of a carbonic anhydrase-like domain in the extracellular region of RPTP γ defines a new subfamily of receptor tyrosine phosphatases. Mol. Cell. Biol., 13: 1497-1506, 1993.
-
(1993)
Mol. Cell. Biol.
, vol.13
, pp. 1497-1506
-
-
Barnea, G.1
Silvennoinen, O.2
Shaanan, B.3
Honegger, A.M.4
Canoll, P.D.5
D'Eustachio, P.6
Morse, B.7
Levy, J.B.8
LaForgia, S.9
Huebner, K.10
Musacchio, J.11
Sap, J.12
Schlessinger, J.13
-
22
-
-
0004136246
-
-
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
-
23
-
-
0029091503
-
Frequency of homozygous deletion at p16/CDKN2 in primary human tumours
-
Cairns, P., Polascik, T. J., Eby, Y., Tokino, K., Califano, J., Merlo, A., Mao, L., Herath, J., Jenkins, R., Westra, W., Rutter, J. L., Buckler, A., Gabrielson, E., Tockman, M., Cho, K. R., Hedrick, L., Bova, G. S., Isaacs, W., Koch, W., Schwab, D., and Sidransky, D. Frequency of homozygous deletion at p16/CDKN2 in primary human tumours. Nat Genet, 11: 210-212, 1995.
-
(1995)
Nat Genet
, vol.11
, pp. 210-212
-
-
Cairns, P.1
Polascik, T.J.2
Eby, Y.3
Tokino, K.4
Califano, J.5
Merlo, A.6
Mao, L.7
Herath, J.8
Jenkins, R.9
Westra, W.10
Rutter, J.L.11
Buckler, A.12
Gabrielson, E.13
Tockman, M.14
Cho, K.R.15
Hedrick, L.16
Bova, G.S.17
Isaacs, W.18
Koch, W.19
Schwab, D.20
Sidransky, D.21
more..
-
24
-
-
0029927916
-
Structure of the human receptor tyrosine phosphatase γ gene (PTPRG) and relation to the familial RCC t(3;8) chromosome translocation
-
Kastury, K., Ohta, M., Lasota, I., Moir, D., Dorman, T., LaForgia, S., Druck, T., and Huebner, K. Structure of the human receptor tyrosine phosphatase γ gene (PTPRG) and relation to the familial RCC t(3;8) chromosome translocation Genomics, 32: 225-235, 1996.
-
(1996)
Genomics
, vol.32
, pp. 225-235
-
-
Kastury, K.1
Ohta, M.2
Lasota, I.3
Moir, D.4
Dorman, T.5
Laforgia, S.6
Druck, T.7
Huebner, K.8
-
25
-
-
0028886532
-
Loss of heterozygosity at the familial RCC t(3;8) locus in most clear cell renal carcinomas
-
Druck, T., Kastury, K., Hadaczek, P., Podolski, J., Toloczko, A., Sikorski, A., Ohta, M., LaForgia, S., Lasota, J., McCue, P., Lubinski, J., and Huebner, K. Loss of heterozygosity at the familial RCC t(3;8) locus in most clear cell renal carcinomas. Cancer Res., 55: 5348-5353, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 5348-5353
-
-
Druck, T.1
Kastury, K.2
Hadaczek, P.3
Podolski, J.4
Toloczko, A.5
Sikorski, A.6
Ohta, M.7
LaForgia, S.8
Lasota, J.9
McCue, P.10
Lubinski, J.11
Huebner, K.12
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