-
2
-
-
27944490866
-
Tumor suppressor genetics
-
Payne SR, Kemp CJ: Tumor suppressor genetics. Carcinogenesis 2005, 26:2031-2045
-
(2005)
Carcinogenesis
, vol.26
, pp. 2031-2045
-
-
Payne, S.R.1
Kemp, C.J.2
-
3
-
-
0034614637
-
The hallmarks of cancer
-
Hanahan D, Weinberg RA: The hallmarks of cancer. Cell 2000, 100:57-70
-
(2000)
Cell
, vol.100
, pp. 57-70
-
-
Hanahan, D.1
Weinberg, R.A.2
-
4
-
-
0347132559
-
Clinical implications of advanced molecular cytogenetics in cancer
-
Mundle SD, Sokolova I: Clinical implications of advanced molecular cytogenetics in cancer. Expert Rev Mol Diagn 2004, 4:71-81
-
(2004)
Expert Rev Mol Diagn
, vol.4
, pp. 71-81
-
-
Mundle, S.D.1
Sokolova, I.2
-
5
-
-
0034016185
-
Genome changes and gene expression in human solid tumors
-
Gray JW, Collins C: Genome changes and gene expression in human solid tumors. Carcinogenesis 2000, 21:443-452
-
(2000)
Carcinogenesis
, vol.21
, pp. 443-452
-
-
Gray, J.W.1
Collins, C.2
-
6
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenic analysis of solid tumors
-
Kallioniemi A, Kallionemi OP, Sudar D, Rutovitz D, Gray JW, Waldman F, Pinkel D: Comparative genomic hybridization for molecular cytogenic analysis of solid tumors. Science 1992, 258:818-821
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallionemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
Waldman, F.6
Pinkel, D.7
-
7
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
Solinas-Toldo S, Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H, Cremer T, Lichter P: Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosom Cancer 1997, 20:399-407
-
(1997)
Genes Chromosom Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Dohner, H.6
Cremer, T.7
Lichter, P.8
-
8
-
-
17344371740
-
Quantitative high resolution analysis of DNA copy number variation in breast cancer using comparative genomic hybridization to DNA microarrays
-
Pinkel D, Segraves R, Sudar D, Clark S, Poole I, Kowbel D, Collins C, Kuo WL, Chen C, Zhai Y, Dairkee SH, Ljung BM, Gray JW, Albertson DG: Quantitative high resolution analysis of DNA copy number variation in breast cancer using comparative genomic hybridization to DNA microarrays. Nat Genet 1998, 20:207-211
-
(1998)
Nat Genet
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
Kowbel, D.6
Collins, C.7
Kuo, W.L.8
Chen, C.9
Zhai, Y.10
Dairkee, S.H.11
Ljung, B.M.12
Gray, J.W.13
Albertson, D.G.14
-
9
-
-
0032823523
-
Genome-wide analysis of DNA copy-number changes using cDNA microarrays
-
Pollack JR, Perou CM, Alizadeh AA, Eisen MB, Pergamenschikov A, Williams CF, Jeffrey SS, Botstein D, Brown PO: Genome-wide analysis of DNA copy-number changes using cDNA microarrays. Nat Genet 1999, 23:41-46
-
(1999)
Nat Genet
, vol.23
, pp. 41-46
-
-
Pollack, J.R.1
Perou, C.M.2
Alizadeh, A.A.3
Eisen, M.B.4
Pergamenschikov, A.5
Williams, C.F.6
Jeffrey, S.S.7
Botstein, D.8
Brown, P.O.9
-
10
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number
-
Snijders AM, Nowak N, Segraves R, Blackwood S, Brown N, Conroy J, Hamilton G, Hindle AK, Huey B, Kimura K, Law S, Myambo K, Palmer J, Ylstra B, Yue JP, Gray JW, Jain AN, Pinkel D, Albertson DG: Assembly of microarrays for genome-wide measurement of DNA copy number. Nat Genet 2001, 29:263-264
-
(2001)
Nat Genet
, vol.29
, pp. 263-264
-
-
Snijders, A.M.1
Nowak, N.2
Segraves, R.3
Blackwood, S.4
Brown, N.5
Conroy, J.6
Hamilton, G.7
Hindle, A.K.8
Huey, B.9
Kimura, K.10
Law, S.11
Myambo, K.12
Palmer, J.13
Ylstra, B.14
Yue, J.P.15
Gray, J.W.16
Jain, A.N.17
Pinkel, D.18
Albertson, D.G.19
-
11
-
-
0037738895
-
Profiling breast cancer by array CGH
-
Albertson DG: Profiling breast cancer by array CGH. Breast Cancer Res Treat 2003, 78:289-298
-
(2003)
Breast Cancer Res Treat
, vol.78
, pp. 289-298
-
-
Albertson, D.G.1
-
12
-
-
10844222511
-
Molecular karyotyping using an SNP array for genomewide genotyping
-
Rauch A, Ruschendorf F, Huang J, Trautmann U, Becker C, Thiel C, Jones KW, Reis A, Nurnberg P: Molecular karyotyping using an SNP array for genomewide genotyping. J Med Genet 2004, 41:916-922
-
(2004)
J Med Genet
, vol.41
, pp. 916-922
-
-
Rauch, A.1
Ruschendorf, F.2
Huang, J.3
Trautmann, U.4
Becker, C.5
Thiel, C.6
Jones, K.W.7
Reis, A.8
Nurnberg, P.9
-
13
-
-
2342453338
-
An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays
-
Zhao X, Li C, Paez JG, Chin K, Janne PA, Chen TH, Girard L, Minna J, Christiani D, Leo C, Gray JW, Sellers WR, Meyerson M: An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays. Cancer Res 2004, 64:3060-3071
-
(2004)
Cancer Res
, vol.64
, pp. 3060-3071
-
-
Zhao, X.1
Li, C.2
Paez, J.G.3
Chin, K.4
Janne, P.A.5
Chen, T.H.6
Girard, L.7
Minna, J.8
Christiani, D.9
Leo, C.10
Gray, J.W.11
Sellers, W.R.12
Meyerson, M.13
-
14
-
-
2442667212
-
Highly parallel SNP genotyping
-
Fan JB, Oliphant A, Shen R, Kermani BG, Garcia F, Gunderson KL, Hansen M, Steemers F, Butler SL, Deloukas P, Galver L, Hunt S, McBride C, Bibikova M, Rubano T, Chen J, Wickham E, Doucet D, Chang W, Campbell D, Zhang B, Kruglyak S, Bentley D, Haas J, Rigault P, Zhou L, Stuelpnagel J, Chee MS: Highly parallel SNP genotyping. Cold Spring Harb Symp Quant Biol 2003, 68:69-78
-
(2003)
Cold Spring Harb Symp Quant Biol
, vol.68
, pp. 69-78
-
-
Fan, J.B.1
Oliphant, A.2
Shen, R.3
Kermani, B.G.4
Garcia, F.5
Gunderson, K.L.6
Hansen, M.7
Steemers, F.8
Butler, S.L.9
Deloukas, P.10
Galver, L.11
Hunt, S.12
McBride, C.13
Bibikova, M.14
Rubano, T.15
Chen, J.16
Wickham, E.17
Doucet, D.18
Chang, W.19
Campbell, D.20
Zhang, B.21
Kruglyak, S.22
Bentley, D.23
Haas, J.24
Rigault, P.25
Zhou, L.26
Stuelpnagel, J.27
Chee, M.S.28
more..
-
15
-
-
0141452071
-
High-throughput loss of heterozygosity mapping in 26 commonly deleted regions in breast cancer
-
Ellsworth RE, Ellsworth DL, Lubert SM, Hooke J, Somiari RI, Shriver CD: High-throughput loss of heterozygosity mapping in 26 commonly deleted regions in breast cancer. Cancer Epidemiol Biomarkers Prev 2003, 129:915-919
-
(2003)
Cancer Epidemiol Biomarkers Prev
, vol.129
, pp. 915-919
-
-
Ellsworth, R.E.1
Ellsworth, D.L.2
Lubert, S.M.3
Hooke, J.4
Somiari, R.I.5
Shriver, C.D.6
-
16
-
-
10644241225
-
Outer breast quadrants demonstrate increased levels of genomic instability
-
Ellsworth DL, Ellsworth RE, Love B, Deyarmin B, Lubert SM, Mittal V, Hooke JA, Shriver CD: Outer breast quadrants demonstrate increased levels of genomic instability. Ann Surg Oncol 2004, 11:861-868
-
(2004)
Ann Surg Oncol
, vol.11
, pp. 861-868
-
-
Ellsworth, D.L.1
Ellsworth, R.E.2
Love, B.3
Deyarmin, B.4
Lubert, S.M.5
Mittal, V.6
Hooke, J.A.7
Shriver, C.D.8
-
17
-
-
27844601106
-
Timing of critical genetic changes in human breast disease
-
Ellsworth RE, Ellsworth DL, Deyarmin B, Hoffman LR, Love B, Hooke JA, Shriver CD: Timing of critical genetic changes in human breast disease. Ann Surg Oncol 2005, 12:1054-1060
-
(2005)
Ann Surg Oncol
, vol.12
, pp. 1054-1060
-
-
Ellsworth, R.E.1
Ellsworth, D.L.2
Deyarmin, B.3
Hoffman, L.R.4
Love, B.5
Hooke, J.A.6
Shriver, C.D.7
-
18
-
-
4544354302
-
Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array
-
Zhou X, Mok SC, Chen Z, Li Y, Wong DT: Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array. Hum Genet 2004, 115:327-330
-
(2004)
Hum Genet
, vol.115
, pp. 327-330
-
-
Zhou, X.1
Mok, S.C.2
Chen, Z.3
Li, Y.4
Wong, D.T.5
-
19
-
-
33644851549
-
Genotyping pooled DNA using 100K SNP microarrays: A step towards genomewide association scans
-
Meaburn E, Butcher LM, Schalkwyk LC, Plomin R: Genotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans. Nucleic Acids Res 2006, 34:e27
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Meaburn, E.1
Butcher, L.M.2
Schalkwyk, L.C.3
Plomin, R.4
-
20
-
-
20844442281
-
A highly informative SNP linkage panel for human genetic studies
-
Murray SS, Oliphant A, Shen R, McBride C, Steeke RJ, Shannon SG, Rubano T, Kermani BG, Fan JB, Chee MS, Hansen MS: A highly informative SNP linkage panel for human genetic studies. Nat Methods 2004, 1:113-117
-
(2004)
Nat Methods
, vol.1
, pp. 113-117
-
-
Murray, S.S.1
Oliphant, A.2
Shen, R.3
McBride, C.4
Steeke, R.J.5
Shannon, S.G.6
Rubano, T.7
Kermani, B.G.8
Fan, J.B.9
Chee, M.S.10
Hansen, M.S.11
-
21
-
-
28544450977
-
Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays
-
Lips EH, Dierssen JW, van Eijk R, Costing J, Eilers PH, Tollenaar RA, de Graaf EJ, van't Slot R, Wijmenga C, Morreau H, van Wezel T: Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays. Cancer Res 2005, 65:10188-10191
-
(2005)
Cancer Res
, vol.65
, pp. 10188-10191
-
-
Lips, E.H.1
Dierssen, J.W.2
van Eijk, R.3
Costing, J.4
Eilers, P.H.5
Tollenaar, R.A.6
de Graaf, E.J.7
van't Slot, R.8
Wijmenga, C.9
Morreau, H.10
van Wezel, T.11
-
22
-
-
23444459574
-
Array CGH technologies and their applications to cancer genomes
-
Davies JJ, Wilson IM, Lam WL: Array CGH technologies and their applications to cancer genomes. Chromosome Res 2005, 13:237-248
-
(2005)
Chromosome Res
, vol.13
, pp. 237-248
-
-
Davies, J.J.1
Wilson, I.M.2
Lam, W.L.3
-
23
-
-
0033038385
-
Loss of heterozygosity analysis using whole genome amplification, cell sorting, and fluorescence-based PCR
-
Paulson TG, Galipeau PC, Reid BJ: Loss of heterozygosity analysis using whole genome amplification, cell sorting, and fluorescence-based PCR. Genome Res 1999, 9:482-491
-
(1999)
Genome Res
, vol.9
, pp. 482-491
-
-
Paulson, T.G.1
Galipeau, P.C.2
Reid, B.J.3
-
24
-
-
0033824264
-
Loss of heterozygosity assay for molecular detection of cancer using energy-transfer primers and capillary array electrophoresis
-
Medintz IL, Lee CC, Wong WW, Pirkola K, Sidransky D, Mathies RA: Loss of heterozygosity assay for molecular detection of cancer using energy-transfer primers and capillary array electrophoresis. Genome Res 2000, 10:1211-1218
-
(2000)
Genome Res
, vol.10
, pp. 1211-1218
-
-
Medintz, I.L.1
Lee, C.C.2
Wong, W.W.3
Pirkola, K.4
Sidransky, D.5
Mathies, R.A.6
-
25
-
-
0035334774
-
Evaluation of loss of heterozygosity/allelic imbalance scoring in tumor DNA
-
Skotheim RI, Diep CB, Kraggerud SM, Jakobsen KS, Lothe RA: Evaluation of loss of heterozygosity/allelic imbalance scoring in tumor DNA. Cancer Genet Cytogenet 2001, 127:64-70
-
(2001)
Cancer Genet Cytogenet
, vol.127
, pp. 64-70
-
-
Skotheim, R.I.1
Diep, C.B.2
Kraggerud, S.M.3
Jakobsen, K.S.4
Lothe, R.A.5
|