-
1
-
-
0032821552
-
Molecular genetics of breast cancer progression
-
Ingvarsson S. Molecular genetics of breast cancer progression. Semin Cancer Biol. 9:1999;277-288.
-
(1999)
Semin Cancer Biol
, vol.9
, pp. 277-288
-
-
Ingvarsson, S.1
-
2
-
-
0029027365
-
The Breast Cancer Linkage Consortium. High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCA1-linked families
-
Cornelis R.S., Neuhausen S.L., Johansson O., Arason A., Kelsell D., Ponder B.A., Tonin P., Hamann U., Lindblom A., Lalle P. The Breast Cancer Linkage Consortium. High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCA1-linked families. Genes Chromosomes Cancer. 13:1995;203-210.
-
(1995)
Genes Chromosomes Cancer
, vol.13
, pp. 203-210
-
-
Cornelis, R.S.1
Neuhausen, S.L.2
Johansson, O.3
Arason, A.4
Kelsell, D.5
Ponder, B.A.6
Tonin, P.7
Hamann, U.8
Lindblom, A.9
Lalle, P.10
-
3
-
-
0033937104
-
Multiple copies of mutant BRCA1 and BRCA2 alleles in breast tumors from germ-line mutation carriers
-
Staff S., Nupponen N.N., Borg A., Isola J.J., Tanner M.M. Multiple copies of mutant BRCA1 and BRCA2 alleles in breast tumors from germ-line mutation carriers. Genes Chromosomes Cancer. 28:2000;432-442.
-
(2000)
Genes Chromosomes Cancer
, vol.28
, pp. 432-442
-
-
Staff, S.1
Nupponen, N.N.2
Borg, A.3
Isola, J.J.4
Tanner, M.M.5
-
4
-
-
0035030368
-
Breast cancer genetics: What we know and what we need
-
Nathanson K.N., Wooster R., Weber B.L. Breast cancer genetics: what we know and what we need. Nat Med. 7:2001;552-556.
-
(2001)
Nat Med
, vol.7
, pp. 552-556
-
-
Nathanson, K.N.1
Wooster, R.2
Weber, B.L.3
-
5
-
-
0037052688
-
Loss of heterozygosity analysis at the BRCA loci in tumor samples from patients with familial breast cancer
-
Osorio A., de la Hoya M., Rodriguez-Lopez R., Martinez-Ramirez A., Cazorla A., Granizo J.J., Esteller M., Rivas C., Caldes T., Benitez J. Loss of heterozygosity analysis at the BRCA loci in tumor samples from patients with familial breast cancer. Int J Cancer. 99:2002;305-309.
-
(2002)
Int J Cancer
, vol.99
, pp. 305-309
-
-
Osorio, A.1
De La Hoya, M.2
Rodriguez-Lopez, R.3
Martinez-Ramirez, A.4
Cazorla, A.5
Granizo, J.J.6
Esteller, M.7
Rivas, C.8
Caldes, T.9
Benitez, J.10
-
6
-
-
0032587877
-
Conditional mutation of BRCA1 in mammary epithelial cells results in blunted ductal morphogenesis and tumour formation
-
Xu X., Wagner K.U., Larson D., Weaver Z., Li C., Ried T., Hennighausen L., Wynshaw-Boris A., Deng C.X. Conditional mutation of BRCA1 in mammary epithelial cells results in blunted ductal morphogenesis and tumour formation. Nat Genet. 22:1999;37-43.
-
(1999)
Nat Genet
, vol.22
, pp. 37-43
-
-
Xu, X.1
Wagner, K.U.2
Larson, D.3
Weaver, Z.4
Li, C.5
Ried, T.6
Hennighausen, L.7
Wynshaw-Boris, A.8
Deng, C.X.9
-
7
-
-
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., Croce C.M. The FHIT gene at 3p14.2 is abnormal in breast carcinomas. Cancer Res. 56:1996;3173-3179.
-
(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
-
8
-
-
0033566971
-
FHIT loss of function in human primary breast cancer correlates with advanced stage of the disease
-
Campiglio M., Pekarsky Y., Menard S., Tagliabue E., Pilotti S., Croce C.M. FHIT loss of function in human primary breast cancer correlates with advanced stage of the disease. Cancer Res. 59:1999;3866-3869.
-
(1999)
Cancer Res
, vol.59
, pp. 3866-3869
-
-
Campiglio, M.1
Pekarsky, Y.2
Menard, S.3
Tagliabue, E.4
Pilotti, S.5
Croce, C.M.6
-
9
-
-
0034653840
-
The expression of Fhit protein is related inversely to disease progression in patients with breast carcinoma
-
Gatalica Z., Lele S.M., Rampy B.A., Norris B.A. The expression of Fhit protein is related inversely to disease progression in patients with breast carcinoma. Cancer. 88:2000;1378-1383.
-
(2000)
Cancer
, vol.88
, pp. 1378-1383
-
-
Gatalica, Z.1
Lele, S.M.2
Rampy, B.A.3
Norris, B.A.4
-
10
-
-
0029132139
-
Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3
-
Bergthorsson J.T., Eiriksdottir G., Barkardottir R.B., Egilsson V., Arason A., Ingvarsson S. Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3. Hum Genet. 96:1995;437-443.
-
(1995)
Hum Genet
, vol.96
, pp. 437-443
-
-
Bergthorsson, J.T.1
Eiriksdottir, G.2
Barkardottir, R.B.3
Egilsson, V.4
Arason, A.5
Ingvarsson, S.6
-
11
-
-
0032190048
-
High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutation
-
Ingvarsson S., Geirsdottir E.K., Johannesdottir G., Sigbjornsdottir B.I., Eiriksdottir G., Ragnarsson G., Agnarsson B.A., Gudmundsson J., Jonasson J.G., Sigurdsson A., Egilsson V., Barkardottir R.B. High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutation. Cancer Res. 58:1998;4421-4425.
-
(1998)
Cancer Res
, vol.58
, pp. 4421-4425
-
-
Ingvarsson, S.1
Geirsdottir, E.K.2
Johannesdottir, G.3
Sigbjornsdottir, B.I.4
Eiriksdottir, G.5
Ragnarsson, G.6
Agnarsson, B.A.7
Gudmundsson, J.8
Jonasson, J.G.9
Sigurdsson, A.10
Egilsson, V.11
Barkardottir, R.B.12
-
12
-
-
0033152189
-
Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomas
-
Ingvarsson S., Agnarsson B.A., Sigbjornsdottir B.I., Kononen J., Kallioniemi O.P., Barkardottir R.B., Kovatich A.J., Schwarting R., Hauck W.W., Huebner K., McCue P.A. Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomas. Cancer Res. 59:1999;2682-2689.
-
(1999)
Cancer Res
, vol.59
, pp. 2682-2689
-
-
Ingvarsson, S.1
Agnarsson, B.A.2
Sigbjornsdottir, B.I.3
Kononen, J.4
Kallioniemi, O.P.5
Barkardottir, R.B.6
Kovatich, A.J.7
Schwarting, R.8
Hauck, W.W.9
Huebner, K.10
McCue, P.A.11
-
13
-
-
0030575911
-
Laser capture microdissection
-
Emmert-Buck M.R., Bonner R.F., Smith P.D., Chuaqui R.F., Zhuang Z., Goldstein S.R., Weiss R.A., Liotta L.A. Laser capture microdissection. Science. 274:1996;998-1001.
-
(1996)
Science
, vol.274
, pp. 998-1001
-
-
Emmert-Buck, M.R.1
Bonner, R.F.2
Smith, P.D.3
Chuaqui, R.F.4
Zhuang, Z.5
Goldstein, S.R.6
Weiss, R.A.7
Liotta, L.A.8
-
14
-
-
15144340686
-
Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas
-
Kerangueven F., Noguchi T., Coulier F., Allione F., Wargniez V., Simony-Lafontaine J., Longy M., Jacquemier J., Sobol H., Eisinger F., Birnbaum D. Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas. Cancer Res. 57:1997;5469-5474.
-
(1997)
Cancer Res
, vol.57
, pp. 5469-5474
-
-
Kerangueven, F.1
Noguchi, T.2
Coulier, F.3
Allione, F.4
Wargniez, V.5
Simony-Lafontaine, J.6
Longy, M.7
Jacquemier, J.8
Sobol, H.9
Eisinger, F.10
Birnbaum, D.11
-
15
-
-
0032032656
-
Consortium study on 1280 breast carcinomas: Allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters
-
Phelan C.M., Borg A., Cuny M., Crichton D.N., Baldersson T., Andersen T.I., Caligo M.A., Lidereau R., Lindblom A., Seitz S., Kelsell D., Hamann U., Rio P., Thorlacius S., Papp J., Olah E., Ponder B., Bignon Y.J., Scherneck S., Barkardottir R., Borresen-Dale A.L., Eyfjord J., Theillet C., Thompson A.M., Devilee P., Larsson C. Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters. Cancer Res. 58:1998;1004-1012.
-
(1998)
Cancer Res
, vol.58
, pp. 1004-1012
-
-
Phelan, C.M.1
Borg, A.2
Cuny, M.3
Crichton, D.N.4
Baldersson, T.5
Andersen, T.I.6
Caligo, M.A.7
Lidereau, R.8
Lindblom, A.9
Seitz, S.10
Kelsell, D.11
Hamann, U.12
Rio, P.13
Thorlacius, S.14
Papp, J.15
Olah, E.16
Ponder, B.17
Bignon, Y.J.18
Scherneck, S.19
Barkardottir, R.20
Borresen-Dale, A.L.21
Eyfjord, J.22
Theillet, C.23
Thompson, A.M.24
Devilee, P.25
Larsson, C.26
more..
-
16
-
-
0033134187
-
Loss of heterozygosity at 3p in benign lesions preceding invasive breast cancer
-
Euhus D.M., Maitra A., Wistuba I.I., Alberts A., Albores-Saavedra J., Gazdar A.F. Loss of heterozygosity at 3p in benign lesions preceding invasive breast cancer. J Surg Res. 83:1999;13-18.
-
(1999)
J Surg Res
, vol.83
, pp. 13-18
-
-
Euhus, D.M.1
Maitra, A.2
Wistuba, I.I.3
Alberts, A.4
Albores-Saavedra, J.5
Gazdar, A.F.6
-
17
-
-
78651056338
-
Field cancerization in oral stratified squamous epithelium
-
Slaughter D.P., Southwick H.W., Smejkal W. Field cancerization in oral stratified squamous epithelium. Cancer. 6:1953;963-968.
-
(1953)
Cancer
, vol.6
, pp. 963-968
-
-
Slaughter, D.P.1
Southwick, H.W.2
Smejkal, W.3
-
18
-
-
0025312728
-
A genetic model for colorectal tumorigenesis
-
Fearon E.R., Vogelstein B. A genetic model for colorectal tumorigenesis. Cell. 61:1990;759-767.
-
(1990)
Cell
, vol.61
, pp. 759-767
-
-
Fearon, E.R.1
Vogelstein, B.2
-
19
-
-
0030461224
-
Loss of heterozygosity in normal tissue adjacent to breast carcinomas
-
Deng G., Lu Y., Zlotnikov G., Thor A.D., Smith H.S. Loss of heterozygosity in normal tissue adjacent to breast carcinomas. Science. 274:1996;2057-2059.
-
(1996)
Science
, vol.274
, pp. 2057-2059
-
-
Deng, G.1
Lu, Y.2
Zlotnikov, G.3
Thor, A.D.4
Smith, H.S.5
-
20
-
-
0034908506
-
Persistence of genetically altered fields in head and neck cancer patients: Biological and clinical implications
-
Tabor M.P., Brakenhoff R.H., van Houten V.M., Kummer J.A., Snel M.H., Snijders P.J., Snow G.B., Leemans C.R., Braakhuis B.J. Persistence of genetically altered fields in head and neck cancer patients: biological and clinical implications. Clin Cancer Res. 7:2001;1523-1532.
-
(2001)
Clin Cancer Res
, vol.7
, pp. 1523-1532
-
-
Tabor, M.P.1
Brakenhoff, R.H.2
Van Houten, V.M.3
Kummer, J.A.4
Snel, M.H.5
Snijders, P.J.6
Snow, G.B.7
Leemans, C.R.8
Braakhuis, B.J.9
-
21
-
-
0035687513
-
Genetic instability in epithelial tissues at risk for cancer
-
Hittelman W.N. Genetic instability in epithelial tissues at risk for cancer. Ann N Y Acad Sci. 952:2001;1-12.
-
(2001)
Ann N Y Acad Sci
, vol.952
, pp. 1-12
-
-
Hittelman, W.N.1
-
22
-
-
0028814029
-
Molecular assessment of histopathological staging in squamous-cell carcinoma of the head and neck
-
Brennan J.A., Mao L., Hruban R.H., Boyle J.O., Eby Y.J., Koch W.M., Goodman S.N., Sidransky D. Molecular assessment of histopathological staging in squamous-cell carcinoma of the head and neck. N Engl J Med. 332:1995;429-435.
-
(1995)
N Engl J Med
, vol.332
, pp. 429-435
-
-
Brennan, J.A.1
Mao, L.2
Hruban, R.H.3
Boyle, J.O.4
Eby, Y.J.5
Koch, W.M.6
Goodman, S.N.7
Sidransky, D.8
-
23
-
-
0028096965
-
Molecular genetic studies of early breast cancer evolution
-
O'Connell P., Pekkel V., Fuqua S., Osborne C.K., Allred D.C. Molecular genetic studies of early breast cancer evolution. Breast Cancer Res Treat. 32:1994;5-12.
-
(1994)
Breast Cancer Res Treat
, vol.32
, pp. 5-12
-
-
O'Connell, P.1
Pekkel, V.2
Fuqua, S.3
Osborne, C.K.4
Allred, D.C.5
-
24
-
-
0032490119
-
Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci
-
O'Connell P., Pekkel V., Fuqua S.A., Osborne C.K., Clark G.M., Allred D.C. Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci. J Natl Cancer Inst. 90:1998;697-703.
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 697-703
-
-
O'Connell, P.1
Pekkel, V.2
Fuqua, S.A.3
Osborne, C.K.4
Clark, G.M.5
Allred, D.C.6
-
25
-
-
0033902640
-
Loss of heterozygosity in fibrocystic change of the breast: Genetic relationship between benign proliferative lesions and associated carcinomas
-
Washington C., Dalbegue F., Abreo F., Taubenberger J.K., Lichy J.H. Loss of heterozygosity in fibrocystic change of the breast: genetic relationship between benign proliferative lesions and associated carcinomas. Am J Pathol. 157:2000;323-329.
-
(2000)
Am J Pathol
, vol.157
, pp. 323-329
-
-
Washington, C.1
Dalbegue, F.2
Abreo, F.3
Taubenberger, J.K.4
Lichy, J.H.5
-
26
-
-
0034961277
-
Loss of heterozygosity in tumour-adjacent normal tissue of breast and bladder cancer
-
Forsti A., Louhelainen J., Soderberg M., Wijkstrom H., Hemminki K. Loss of heterozygosity in tumour-adjacent normal tissue of breast and bladder cancer. Eur J Cancer. 37:2001;1372-1380.
-
(2001)
Eur J Cancer
, vol.37
, pp. 1372-1380
-
-
Forsti, A.1
Louhelainen, J.2
Soderberg, M.3
Wijkstrom, H.4
Hemminki, K.5
-
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 A., Olsson H., Kristoffersson U., Mitelman F. Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families. Genes Chromosomes Cancer. 16:1996;185-188.
-
(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, A.9
Olsson, H.10
Kristoffersson, U.11
Mitelman, F.12
-
28
-
-
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., 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. 38:1996;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
-
29
-
-
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., Heim S. Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue. Int J Cancer. 60:1995;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
-
30
-
-
0029903698
-
The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14
-
Panagopoulos I., Pandis N., Thelin S., Petersson C., Mertens F., Borg A., Kristoffersson U., Mitelman F., Aman P. The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14. Cancer Res. 56:1996;4871-4875.
-
(1996)
Cancer Res
, vol.56
, pp. 4871-4875
-
-
Panagopoulos, I.1
Pandis, N.2
Thelin, S.3
Petersson, C.4
Mertens, F.5
Borg, A.6
Kristoffersson, U.7
Mitelman, F.8
Aman, P.9
|