-
1
-
-
0024350902
-
Presence of two members of c-erb a receptor gene family (c-erbaß and c-erbA2) in smallest region of somatic homozygosity on chromosome 3p21-p25 in human breast carcinoma
-
Ali IU, Lidereau R, Callahan R (1989) Presence of two members of c-erb A receptor gene family (c-erbaß and c-erbA2) in smallest region of somatic homozygosity on chromosome 3p21-p25 in human breast carcinoma. J Natl Cancer Inst 81:1815-1820.
-
(1989)
J Natl Cancer Inst
, vol.81
, pp. 1815-1820
-
-
Ali, I.U.1
Lidereau, R.2
Callahan, R.3
-
2
-
-
0029132139
-
Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3
-
Bergthorsson JT, Eiriksdottir G, Barkardottir RB, Egilsson Y, Arason A, Ingvarsson S (1995) Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3. Hum Genet 96:437-443.
-
(1995)
Hum Genet
, vol.96
, pp. 437-443
-
-
Bergthorsson, J.T.1
Eiriksdottir, G.2
Barkardottir, R.B.3
Egilsson, Y.4
Arason, A.5
Ingvarsson, S.6
-
4
-
-
0028241636
-
Homozygous deletion, rearrangement and hypemethylation implicate chromosome region 3p14.3-3p21.3 in sporadic breast cancer development
-
Huchhagen DL, Qiu L, Etkind P (1994) Homozygous deletion, rearrangement and hypemethylation implicate chromosome region 3p14.3-3p21.3 in sporadic breast cancer development. Int J Cancer 57:473-479.
-
(1994)
Int J Cancer
, vol.57
, pp. 473-479
-
-
Huchhagen, D.L.1
Qiu, L.2
Etkind, P.3
-
5
-
-
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 MI, Waldman FM, Smith HS (1994) Deletion of two separate regions on chromosome 3p in breast cancers. Cancer Res 54:3021-3024.
-
(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
-
6
-
-
0026590246
-
Fractional allelic imbalance in human breast cancer increases with tetraploidization and chromosome loss
-
Cornelisse CJ, Kuipers-Dijkshoorn N, van Vliet M, Herman J, Devilee P (1992) Fractional allelic imbalance in human breast cancer increases with tetraploidization and chromosome loss. Int J Cancer 50:544-548.
-
(1992)
Int J Cancer
, vol.50
, pp. 544-548
-
-
Cornelisse, C.J.1
Kuipers-Dijkshoorn, N.2
Van Vliet, M.3
Herman, J.4
Devilee, P.5
-
7
-
-
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 PM, Pearson PL, Cornelisse CJ (1989) At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma. Genomics 5:554-560.
-
(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
-
8
-
-
0028966394
-
Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue
-
Dietrich CU, Pandis N, Teixeira MR, Bardi G, Gerdes A-M, Andersen JA, Heim S (1995a) Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue. Int J Cancer 60:49-53.
-
(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
-
9
-
-
0028918093
-
Rearrangement of chromosomal hands 3p13-14 in two hamartomas of the breast
-
Dietrich CU, Pandis N, Bardi G, Hägerstrand I, Andersen JA, Mitelman F, Heim S (1995b) Rearrangement of chromosomal hands 3p13-14 in two hamartomas of the breast. Int J Oncol 6:559-561.
-
(1995)
Int J Oncol
, vol.6
, pp. 559-561
-
-
Dietrich, C.U.1
Pandis, N.2
Bardi, G.3
Hägerstrand, I.4
Andersen, J.A.5
Mitelman, F.6
Heim, S.7
-
10
-
-
0025212711
-
Loss of heterozygosity on chromosomal segments 3p, 6q and 11p in human ovarian carcinomas
-
Ehlen T, Dubeau L (1990) Loss of heterozygosity on chromosomal segments 3p, 6q and 11p in human ovarian carcinomas. Oncogene 5:219-223.
-
(1990)
Oncogene
, vol.5
, pp. 219-223
-
-
Ehlen, T.1
Dubeau, L.2
-
11
-
-
0028847685
-
Mapping of chromosome 3 alterations in human breast cancer using microsatellite PCR markers: Correlation with clinical variables
-
Eiriksdottir G, Bergthorsson JT, Sigurdsson H, Gudmundsson J, Skirnisdottir S, Egilsson V, Barkadottir RB, Ingvarsson S (1995) Mapping of chromosome 3 alterations in human breast cancer using microsatellite PCR markers: Correlation with clinical variables. Int J Oncol 6:369-375.
-
(1995)
Int J Oncol
, vol.6
, pp. 369-375
-
-
Eiriksdottir, G.1
Bergthorsson, J.T.2
Sigurdsson, H.3
Gudmundsson, J.4
Skirnisdottir, S.5
Egilsson, V.6
Barkadottir, R.B.7
Ingvarsson, S.8
-
13
-
-
0342591692
-
Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines
-
Kastury K, Baffa R, Druck T, Ohta M, Cotticelli MG, Inoue H, Negrini M, Rugge M, Huang D, Croce CM, Palazzo J, Huebner K (1996) Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines. Cancer Res 56:978-983.
-
(1996)
Cancer Res
, vol.56
, pp. 978-983
-
-
Kastury, K.1
Baffa, R.2
Druck, T.3
Ohta, M.4
Cotticelli, M.G.5
Inoue, H.6
Negrini, M.7
Rugge, M.8
Huang, D.9
Croce, C.M.10
Palazzo, J.11
Huebner, K.12
-
14
-
-
0026552140
-
Chromosome 3p deletions in head and neck carcinomas: Statistical ascertainment of allelic loss
-
Latif F, Fivash M, Glenn G, Tory K, Orcutt ML, Hampsch K, Delisio J, Lerman M, Cowan J, Beckett M, Weichselbaum R (1992) Chromosome 3p deletions in head and neck carcinomas: Statistical ascertainment of allelic loss. Cancet Res 52:1451-1456.
-
(1992)
Cancet 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
-
15
-
-
0021183587
-
Heritable fragile sites and cancer
-
Le Beau MM, Rowley JD (1984) Heritable fragile sites and cancer. Nature 308:607-608.
-
(1984)
Nature
, vol.308
, pp. 607-608
-
-
Le Beau, M.M.1
Rowley, J.D.2
-
16
-
-
0024697964
-
Loss of 3p or 11p alleles is associated with testicular cancer tumors
-
Lothe RA, Fosså SD, Stenwig AE, Nakamura Y, White R, Börresen AL, Brögger A (1989) Loss of 3p or 11p alleles is associated with testicular cancer tumors. Genomics 5:134-138.
-
(1989)
Genomics
, vol.5
, pp. 134-138
-
-
Lothe, R.A.1
Fosså, S.D.2
Stenwig, A.E.3
Nakamura, Y.4
White, R.5
Börresen, A.L.6
Brögger, A.7
-
17
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, Liu Q, Cochran C, Bennet LM, Ding W, Bell R, Rosenthal J, Hussey C, Tan T, Mclure M, Frye C, Hattier T, Phelps R, Hangen-Strano A, Katcer H, Yakumo K, Gholami Z, Shaffer D, Stone S, Bayer S, Wray C, Bogden R, Dayanath P, Ward J, Tonin P, Narod S, Bristovv PK, Norris FH, Helvering L, Morrison P, Rosteck P, Lai M, Barrett JC, Lewis C, Neuhausen S, Cannon-Albright L, Goldgar D, Wiseman R, Kamb A, Skolnick MH (1994) A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266:66-71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, S.6
Liu, Q.7
Cochran, C.8
Bennet, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tan, T.14
Mclure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Hangen-Strano, A.19
Katcer, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayanath, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristovv, P.K.32
Norris, F.H.33
Helvering, L.34
Morrison, P.35
Rosteck, P.36
Lai, M.37
Barrett, J.C.38
Lewis, C.39
Neuhausen, S.40
Cannon-Albright, L.41
Goldgar, D.42
Wiseman, R.43
Kamb, A.44
Skolnick, M.H.45
more..
-
19
-
-
0023220797
-
Loss of heterozygosity of chromosome 3p markers in small-cell king cancer
-
Naylor SL, Johnson BE, Minna JD, Sakaguchi AY (1987) Loss of heterozygosity of chromosome 3p markers in small-cell king cancer. Nature 329:451-153.
-
(1987)
Nature
, vol.329
, pp. 451-1153
-
-
Naylor, S.L.1
Johnson, B.E.2
Minna, J.D.3
Sakaguchi, A.Y.4
-
20
-
-
0029902071
-
The FHIT gene at 3p14.2 is abnormal in breast carcinomas
-
Negrini M, Monaco C, Verechovsky I, Ohta M, Druck T, Baffa R, Huebner K, Croce CM (1996) The FHIT gene at 3p14.2 is abnormal in breast carcinomas. Cancer Res 56:3173-3179.
-
(1996)
Cancer Res
, vol.56
, pp. 3173-3179
-
-
Negrini, M.1
Monaco, C.2
Verechovsky, I.3
Ohta, M.4
Druck, T.5
Baffa, R.6
Huebner, K.7
Croce, C.M.8
-
21
-
-
13344279424
-
The human FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated translocation breakpoint, is abnormal in digestive tract cancers
-
Ohta M, Inoue H, Cotticelli MG, Kastury K, Baffa R, Palazzo J, Siprashvili Z, Mori M, McCue P, Druck T, Croce CM, Huebner K (1996) The human FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated translocation breakpoint, is abnormal in digestive tract cancers. Cell 84:587-597.
-
(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
-
22
-
-
0027401144
-
Chromosome analysis of 20 breast carcinomas: Cytogenetic multi-clonality and karyotypic-pathologic correlations
-
Pandis N, Heim S, Bardi G, Idvall I, Mandahl N, Mitelman F (1993a) Chromosome analysis of 20 breast carcinomas: Cytogenetic multi-clonality and karyotypic-pathologic correlations. Genes Chromosom Cancer 6:51-57.
-
(1993)
Genes Chromosom Cancer
, vol.6
, pp. 51-57
-
-
Pandis, N.1
Heim, S.2
Bardi, G.3
Idvall, I.4
Mandahl, N.5
Mitelman, F.6
-
23
-
-
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, Heim S (1993b) Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast. Genes Chromosom Cancer 6:151-155.
-
(1993)
Genes Chromosom 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
-
24
-
-
0028948713
-
Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups
-
Pandis N, Jin Y, Gorunova L, Petersson C, Bardi G, Idvall I, Johansson B, Ingvar C, Mandahl N, Mitelman F, Heim S (1995a) Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups. Genes Chromosom Cancer 12:173-185.
-
(1995)
Genes Chromosom 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
-
25
-
-
0029042985
-
Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors
-
Pandis N, Teixeira MR, Gerdes A-M, Limon J, Bardi G, Andersen JA, Idvall I, Mandahl N, Mitelman F, Heim S (1995b) Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors. Cancer 76:250-258.
-
(1995)
Cancer
, vol.76
, pp. 250-258
-
-
Pandis, N.1
Teixeira, M.R.2
Gerdes, A.-M.3
Limon, J.4
Bardi, G.5
Andersen, J.A.6
Idvall, I.7
Mandahl, N.8
Mitelman, F.9
Heim, S.10
-
26
-
-
0030032666
-
New gene forges link between fragile site and many cancers
-
Pennisi E (1996) New gene forges link between fragile site and many cancers. Science 272:644.
-
(1996)
Science
, vol.272
, pp. 644
-
-
Pennisi, E.1
-
27
-
-
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, Mitelman F (1996) Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families. Genes Chromosom Cancer. 16:185-188.
-
(1996)
Genes Chromosom 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
-
28
-
-
0031045844
-
Karyotypic abnormalities in fibroadenomas of the breast
-
In press
-
Petersson C., Pandis N, Rizou H, Mertens F, Dietrich CU, Adeyinka A, Idvall I, Bondeson L, Georgiou G, Ingvar C, Heim S, Mitelman F (1997) Karyotypic abnormalities in fibroadenomas of the breast. Int J Cancer. In press.
-
(1997)
Int J Cancer
-
-
Petersson, C.1
Pandis, N.2
Rizou, H.3
Mertens, F.4
Dietrich, C.U.5
Adeyinka, A.6
Idvall, I.7
Bondeson, L.8
Georgiou, G.9
Ingvar, C.10
Heim, S.11
Mitelman, F.12
-
29
-
-
0003713172
-
Chromosome changes in leukemia and cancer and their molecular limning
-
I.R. Kirsch (ed): New York: CRC Press, .
-
Sandberg AA (1993) Chromosome changes in leukemia and cancer and their molecular limning. In I.R. Kirsch (ed): The Causes and Consequences of Chromosomal Aberrations. New York: CRC Press, pp. 141-163.
-
(1993)
The Causes and Consequences of Chromosomal Aberrations
, pp. 141-163
-
-
Sandberg, A.A.1
-
30
-
-
0026335799
-
Accumulation of genetics alterations and progression of primary breast cancer
-
Sato T, Akiyama F, Sakamoto G, Kasumi F, Nakamura V (1991) Accumulation of genetics alterations and progression of primary breast cancer. Cancer Res 51:5794-5799.
-
(1991)
Cancer Res
, vol.51
, pp. 5794-5799
-
-
Sato, T.1
Akiyama, F.2
Sakamoto, G.3
Kasumi, F.4
Nakamura, V.5
-
31
-
-
15844384990
-
The FHIT gene at 3p14.2 is abnormal in lung cancer
-
Sozzi G, Veronese ML, Negrini M, Baffa R, Cotticelli MG, Inoue H, Tornielli S, Pilotti S, De Gregorio L, Pastorino U, Pierotti MA, Ohta M, Huebner K, Croce CM (1996) The FHIT gene at 3p14.2 is abnormal in lung cancer. Cell 85:1-20.
-
(1996)
Cell
, vol.85
, pp. 1-20
-
-
Sozzi, G.1
Veronese, M.L.2
Negrini, M.3
Baffa, R.4
Cotticelli, M.G.5
Inoue, H.6
Tornielli, S.7
Pilotti, S.8
De Gregorio, L.9
Pastorino, U.10
Pierotti, M.A.11
Ohta, M.12
Huebner, K.13
Croce, C.M.14
-
32
-
-
44949275580
-
Chromosomal fragile sites
-
Sutherland GR (1991) Chromosomal fragile sites. Genet Anal Tech Appl 8:1616-1666.
-
(1991)
Genet Anal Tech Appl
, vol.8
, pp. 1616-1666
-
-
Sutherland, G.R.1
-
33
-
-
0030020692
-
Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer
-
Teixeira MR, Pandis N, Bardi G, Andersen JA, Heim S (1996a) Karyotypic comparisons of multiple tumorous and macroscopically normal surrounding tissue samples from patients with breast cancer. Cancer Res 56:855-859.
-
(1996)
Cancer Res
, vol.56
, pp. 855-859
-
-
Teixeira, M.R.1
Pandis, N.2
Bardi, G.3
Andersen, J.A.4
Heim, S.5
-
34
-
-
0029998976
-
Cytogenetic abnormalities in an in situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer
-
Teixeira MR, Pandis N, Gerdes A-M, Dietrich CU, Bardi G, Andersen JA, Graversen HP, Mitelman F, Heim S (1996b) 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)
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
-
35
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Jonathan M, Collins N, Gregory S, Gumbs C, Micklem G, Barfoot R, Hamoudi R, Sandeep P, Rice C, Biggs P, Hashim Y, Smith A, Connor F, Arason A, Gudmundsson J, Ficenec D, Kelsell D, Ford D, Tonin P, Bishop DT, Spurr NK, Ponder BAJ, Eeles R, Peto J, Devilee P, Cornelisse C, Lynch H, Narod S, Lenoir G, Egilsson V, Barkadottir RS, Easton DF, Bentley DR, Futreal PA, Ashworth A, Stratton MS (1995) Identification of the breast cancer susceptibility gene BRCA2. Nature 378:789-792.
-
(1995)
Nature
, vol.378
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
Swift, S.4
Seal, S.5
Jonathan, M.6
Collins, N.7
Gregory, S.8
Gumbs, C.9
Micklem, G.10
Barfoot, R.11
Hamoudi, R.12
Sandeep, P.13
Rice, C.14
Biggs, P.15
Hashim, Y.16
Smith, A.17
Connor, F.18
Arason, A.19
Gudmundsson, J.20
Ficenec, D.21
Kelsell, D.22
Ford, D.23
Tonin, P.24
Bishop, D.T.25
Spurr, N.K.26
Ponder, B.A.J.27
Eeles, R.28
Peto, J.29
Devilee, P.30
Cornelisse, C.31
Lynch, H.32
Narod, S.33
Lenoir, G.34
Egilsson, V.35
Barkadottir, R.S.36
Easton, D.F.37
Bentley, D.R.38
Futreal, P.A.39
Ashworth, A.40
Stratton, M.S.41
more..
-
36
-
-
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, Terada M (1989) Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix. Cancer Res 49:3598-3601.
-
(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
-
37
-
-
0021690129
-
Constitutive fragile sites and cancer
-
Yunis JJ, Soreng AL (1984) Constitutive fragile sites and cancer. Science 226:1199-1204.
-
(1984)
Science
, vol.226
, pp. 1199-1204
-
-
Yunis, J.J.1
Soreng, A.L.2
-
38
-
-
0023181644
-
Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma
-
Zbar B, Brauch H, Talmadge C, Linehan M (1987) Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma. Nature 327:721-724.
-
(1987)
Nature
, vol.327
, pp. 721-724
-
-
Zbar, B.1
Brauch, H.2
Talmadge, C.3
Linehan, M.4
-
39
-
-
0024557934
-
Rare clonal karyotypic variants in primary cultures of human breast carcinoma cells
-
Zhang R, Wiley J, Howard SP, Meisner LF, Gould M (1989) Rare clonal karyotypic variants in primary cultures of human breast carcinoma cells. Cancer Res 49:444-149.
-
(1989)
Cancer Res
, vol.49
, pp. 444-1149
-
-
Zhang, R.1
Wiley, J.2
Howard, S.P.3
Meisner, L.F.4
Gould, M.5
|