-
1
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal cancel
-
Aaltonen LA, Peltomäki P, Leach FS, Sistonen P, Pylkkänen L, Mecklin J-P, Järvinen H, Powell SM, Jen J, Hamilton SR, Petersen GM, Kinzler KW, Vogelstein B, de la Chapelle A (1993) Clues to the pathogenesis of familial colorectal cancel. Science 260:812-816.
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
Peltomäki, P.2
Leach, F.S.3
Sistonen, P.4
Pylkkänen, L.5
Mecklin, J.-P.6
Järvinen, H.7
Powell, S.M.8
Jen, J.9
Hamilton, S.R.10
Petersen, G.M.11
Kinzler, K.W.12
Vogelstein, B.13
De La Chapelle, A.14
-
2
-
-
0029281279
-
BRCA1: More than a hereditary breast cancer gene?
-
Boyd J (1995) BRCA1: More than a hereditary breast cancer gene? Nature Genet 9:335-336.
-
(1995)
Nature Genet
, vol.9
, pp. 335-336
-
-
Boyd, J.1
-
3
-
-
0028783773
-
Aberrant subcellular localization of BRCA1 in breast cancer
-
Chen Y, Chen C-F, Riley DJ, Allred DC, Chen P-L, Von Hoff D, Osborne CK, Lee W-H (1995) Aberrant subcellular localization of BRCA1 in breast cancer. Science 270:789-791.
-
(1995)
Science
, vol.270
, pp. 789-791
-
-
Chen, Y.1
Chen, C.-F.2
Riley, D.J.3
Allred, D.C.4
Chen, P.-L.5
Von Hoff, D.6
Osborne, C.K.7
Lee, W.-H.8
-
4
-
-
0027416219
-
Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions
-
Cornelis RS, Devilee P, van Vliet M, Kuipers-Dijkshoorn N, Kersenmaecker A, Bardoel A, Khan PM, Cornelis CJ (1993) Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions. Oncogene 8:781-785.
-
(1993)
Oncogene
, vol.8
, pp. 781-785
-
-
Cornelis, R.S.1
Devilee, P.2
Van Vliet, M.3
Kuipers-Dijkshoorn, N.4
Kersenmaecker, A.5
Bardoel, A.6
Khan, P.M.7
Cornelis, C.J.8
-
5
-
-
0027445155
-
Identification of three regions on chromosome 17q in primary human breast carcinomas which are frequently deleted
-
Cropp CS, Champeme M-H, Lidereau R, Callahan R (1993) Identification of three regions on chromosome 17q in primary human breast carcinomas which are frequently deleted. Cancer Res 53: 5617-5619.
-
(1993)
Cancer Res
, vol.53
, pp. 5617-5619
-
-
Cropp, C.S.1
Champeme, M.-H.2
Lidereau, R.3
Callahan, R.4
-
6
-
-
0026499651
-
The gene for tissue inhibitor of metalloproteinases-2 is localized on human chromosome arm 17q25
-
DeClerck Y, Szpirer C, Aly MS, Cassiman J-J, Eeckhout Y, Rousseau G (1992) The gene for tissue inhibitor of metalloproteinases-2 is localized on human chromosome arm 17q25. Genomics 14:782-784.
-
(1992)
Genomics
, vol.14
, pp. 782-784
-
-
Declerck, Y.1
Szpirer, C.2
Aly, M.S.3
Cassiman, J.-J.4
Eeckhout, Y.5
Rousseau, G.6
-
7
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Fauré S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Fauré, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
9
-
-
0029817020
-
Comparison of methods for extracting DNA from formalin fixed paraffin sections for nonisotopic PCR
-
in press
-
Frank TS, Newman-Svoboda SM, Hsi ED (1996) Comparison of methods for extracting DNA from formalin fixed paraffin sections for nonisotopic PCR. Diag Mol Pathol (in press).
-
(1996)
Diag Mol Pathol
-
-
Frank, T.S.1
Newman-Svoboda, S.M.2
Hsi, E.D.3
-
10
-
-
0028953433
-
Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome
-
Frebourg T, Barbier N, Yan YX, Garber JE, Dreyfus M, Fraumeni J Jr, Li FP, Friend SH (1995) Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome. Am J Hum Genet 56:608-615.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 608-615
-
-
Frebourg, T.1
Barbier, N.2
Yan, Y.X.3
Garber, J.E.4
Dreyfus, M.5
Fraumeni Jr., J.6
Li, F.P.7
Friend, S.H.8
-
11
-
-
0028050103
-
A common region of deletion on chromosome 17q in both sporadic and familial epithelial ovarian tumors distal to BRCA1
-
Goodwin AK, Vanderverr L, Schultz DC, Lynch HT, Altomare DA, Buetow KH, Daly M, Getts LA, Mansy A, Rosenblum N, Hogan M, Ozols RF, Hamilton TC (1994) A common region of deletion on chromosome 17q in both sporadic and familial epithelial ovarian tumors distal to BRCA1. Am J Hum Genet 55:666-677.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 666-677
-
-
Goodwin, A.K.1
Vanderverr, L.2
Schultz, D.C.3
Lynch, H.T.4
Altomare, D.A.5
Buetow, K.H.6
Daly, M.7
Getts, L.A.8
Mansy, A.9
Rosenblum, N.10
Hogan, M.11
Ozols, R.F.12
Hamilton, T.C.13
-
12
-
-
0023584218
-
Genetics of cancer predisposition
-
Hansen MF, Cavenee WK (1987) Genetics of cancer predisposition. Cancer Res 47:5518-5527.
-
(1987)
Cancer Res
, vol.47
, pp. 5518-5527
-
-
Hansen, M.F.1
Cavenee, W.K.2
-
13
-
-
0027523066
-
A study of the origin of 'shadow bands' seen when typing dinucleotide repeat polymorphisms by the PCR
-
Hauge XY, Litt M (1993) A study of the origin of 'shadow bands' seen when typing dinucleotide repeat polymorphisms by the PCR. Hum Mol Genet 2:411-415.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 411-415
-
-
Hauge, X.Y.1
Litt, M.2
-
14
-
-
0029155863
-
Palmoplantar keratoderma in association with carcinoma of the esophagus maps to chromosome 17q distal to the keratin gene cluster
-
Hennies H-C, Hagedorn M, Reis A (1995) Palmoplantar keratoderma in association with carcinoma of the esophagus maps to chromosome 17q distal to the keratin gene cluster. Genomics 29:537-540.
-
(1995)
Genomics
, vol.29
, pp. 537-540
-
-
Hennies, H.-C.1
Hagedorn, M.2
Reis, A.3
-
15
-
-
0027408639
-
A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus
-
Jacobs IJ, Smith SA, Wiseman RW, Futreal PA, Harrington T, Osborne RJ, Leech V, Molyneux A, Berchuck A, Ponder BAJ, Bast RC (1993) A deletion unit on chromosome 17q in epithelial ovarian tumors distal to the familial breast/ovarian cancer locus. Cancer Res 53:1218-1221.
-
(1993)
Cancer Res
, vol.53
, pp. 1218-1221
-
-
Jacobs, I.J.1
Smith, S.A.2
Wiseman, R.W.3
Futreal, P.A.4
Harrington, T.5
Osborne, R.J.6
Leech, V.7
Molyneux, A.8
Berchuck, A.9
Ponder, B.A.J.10
Bast, R.C.11
-
16
-
-
0028299591
-
Patterns of allele losses suggest the existence of five distinct regions of LOH on chromosome 17 in breast cancer
-
Kirchweger R, Zeillinger R, Schneeberger C, Speiser P, Louason G, Theillet C (1994) Patterns of allele losses suggest the existence of five distinct regions of LOH on chromosome 17 in breast cancer. Int J Cancer 56:193-199.
-
(1994)
Int J Cancer
, vol.56
, pp. 193-199
-
-
Kirchweger, R.1
Zeillinger, R.2
Schneeberger, C.3
Speiser, P.4
Louason, G.5
Theillet, C.6
-
17
-
-
0028340435
-
Loss of chromosome arm 8p loci in prostate cancer: Mapping by quantitative allelic imbalance
-
MacGrogan D, Levy A, Bostwich D, Wagner M, Wells D, Bookstein R (1994) Loss of chromosome arm 8p loci in prostate cancer: Mapping by quantitative allelic imbalance. Genes Chromosom Cancer 10:151-159.
-
(1994)
Genes Chromosom Cancer
, vol.10
, pp. 151-159
-
-
MacGrogan, D.1
Levy, A.2
Bostwich, D.3
Wagner, M.4
Wells, D.5
Bookstein, R.6
-
18
-
-
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, Bennett LM, Ding W, Bell R, Rosenthal J, Hussey C, Tran T, McClure M, Frye C, Hattier T, Phelps R, Haugen-Strano A, Katcher H, Yakumo K, Gholami Z, Shaffer D, Stone S, Bayer S, Wray C, Bogden R, Dayananth P, Ward J, Tonin P, Narod S, Bristow 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 (1995) A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266:66-71.
-
(1995)
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
Bennett, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Haugen-Strano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristow, 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
-
-
0027942568
-
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)
-
Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Manion F, Quillen J, Sheffield VC, Suden S, Duyk GM (1994) A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC). Science 265:2049-2055.
-
(1994)
Science
, vol.265
, pp. 2049-2055
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Scherpbier-Heddema, T.5
Manion, F.6
Quillen, J.7
Sheffield, V.C.8
Suden, S.9
Duyk, G.M.10
-
20
-
-
0029920758
-
FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors
-
Petty EM, Miller DE, Grant AL, Collins EE, Glover TW, Law DJ (1996) FISH localization of the soluble thymidine kinase gene (TK1) to human 17q25, a region of chromosomal loss in sporadic breast tumors. Cytogenet Cell Genet 72:319-321.
-
(1996)
Cytogenet Cell Genet
, vol.72
, pp. 319-321
-
-
Petty, E.M.1
Miller, D.E.2
Grant, A.L.3
Collins, E.E.4
Glover, T.W.5
Law, D.J.6
-
21
-
-
0027217756
-
Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM Region on 17q21.3 often and commonly deleted in tumors
-
Saito H, Inazawa S, Kasmuni F, Koi S, Sagae S, Kudo R, Saito J, Noda K, Nakamura Y (1993) Detailed deletion mapping of chromosome 17q in ovarian and breast cancers: 2-cM Region on 17q21.3 often and commonly deleted in tumors. Cancer Res 53: 3382-3385.
-
(1993)
Cancer Res
, vol.53
, pp. 3382-3385
-
-
Saito, H.1
Inazawa, S.2
Kasmuni, F.3
Koi, S.4
Sagae, S.5
Kudo, R.6
Saito, J.7
Noda, K.8
Nakamura, Y.9
-
23
-
-
0029057336
-
A single ataxia telangiectasia gene with a product similar to P1-3 kinase
-
Savitsky K, Bar-Shira A, Gilad S, Rotman G, Ziv Y, Vanagaite L, Tagle DA, Smith S, Uziel T, Sfez S, Ashkenazi M, Pecker I, Frydman M, Harnik R, Patanjali SR, Simmons A, Clines GA, Sartiel A, Gatti RA, Chessa L, Sanal O, Lavin MF, Jaspers NGJ, Taylor MR, Arlett CF, Miki T, Weissman SM, Lovett M, Collins FS, Shiloh Y (1995) A single ataxia telangiectasia gene with a product similar to P1-3 kinase. Science 268:1749-1753.
-
(1995)
Science
, vol.268
, pp. 1749-1753
-
-
Savitsky, K.1
Bar-Shira, A.2
Gilad, S.3
Rotman, G.4
Ziv, Y.5
Vanagaite, L.6
Tagle, D.A.7
Smith, S.8
Uziel, T.9
Sfez, S.10
Ashkenazi, M.11
Pecker, I.12
Frydman, M.13
Harnik, R.14
Patanjali, S.R.15
Simmons, A.16
Clines, G.A.17
Sartiel, A.18
Gatti, R.A.19
Chessa, L.20
Sanal, O.21
Lavin, M.F.22
Jaspers, N.G.J.23
Taylor, M.R.24
Arlett, C.F.25
Miki, T.26
Weissman, S.M.27
Lovett, M.28
Collins, F.S.29
Shiloh, Y.30
more..
-
25
-
-
0029125296
-
Inherited breast and ovarian cancer
-
Szabo CI, King M-K (1995) Inherited breast and ovarian cancer. Hum Mol Genet 4:1811-1817.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1811-1817
-
-
Szabo, C.I.1
King, M.-K.2
-
26
-
-
0028853405
-
Suppression of tumorigenicity of breast cancer cells by transfer of human chromosome 17 does not require transferred BRCA1 and p53 genes
-
Theile M, Hartmann S, Scherthan H, Arnold W, Deppert W, Frege R, Glaab F, Haensch W, Scherneck S (1995) Suppression of tumorigenicity of breast cancer cells by transfer of human chromosome 17 does not require transferred BRCA1 and p53 genes. Oncogene 10:439-447.
-
(1995)
Oncogene
, vol.10
, pp. 439-447
-
-
Theile, M.1
Hartmann, S.2
Scherthan, H.3
Arnold, W.4
Deppert, W.5
Frege, R.6
Glaab, F.7
Haensch, W.8
Scherneck, S.9
-
27
-
-
0027168744
-
Molecular genetic changes in human breast cancer
-
van de Vijver M (1993) Molecular genetic changes in human breast cancer. Adv Cancer Res 61:25-56.
-
(1993)
Adv Cancer Res
, vol.61
, pp. 25-56
-
-
Van De Vijver, M.1
|