-
1
-
-
0026483716
-
Homozygous deletions within human chromosome band 9p21 in melanoma
-
1. Fountain JW, Karayiorgou M, Ernstoff MS, et al. Homozygous deletions within human chromosome band 9p21 in melanoma. Proc Natl Acad Sci USA 1992, 89, 10557-10561.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 10557-10561
-
-
Fountain, J.W.1
Karayiorgou, M.2
Ernstoff, M.S.3
-
2
-
-
0029017087
-
Chromosome 9p deletions in cutaneous malignant melanoma tumors - The minimal deleted region involves markers outside the p16 (cdkn2) gene
-
2. Puig S, Ruiz A, Lazaro C, et al. Chromosome 9p deletions in cutaneous malignant melanoma tumors - the minimal deleted region involves markers outside the p16 (cdkn2) gene. Am J Hum Genet 1995, 57, 395-402.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 395-402
-
-
Puig, S.1
Ruiz, A.2
Lazaro, C.3
-
3
-
-
0027452508
-
Chromosome 10 allelic loss in malignant melanoma
-
3. Isshiki K, Elder DE, Guerry D, Linnenbach AJ. Chromosome 10 allelic loss in malignant melanoma. Genes Chrom Cancer 1993, 8, 178-184.
-
(1993)
Genes Chrom Cancer
, vol.8
, pp. 178-184
-
-
Isshiki, K.1
Elder, D.E.2
Guerry, D.3
Linnenbach, A.J.4
-
4
-
-
0026049238
-
Loss of heterozygosity for loci on the long arm of chromosome 6 in human malignant melanoma
-
4. Millikin D, Meese E, Vogelstein B, Witkowski C, Trent J. Loss of heterozygosity for loci on the long arm of chromosome 6 in human malignant melanoma. Cancer Res 1991, 51, 5440-5453.
-
(1991)
Cancer Res
, vol.51
, pp. 5440-5453
-
-
Millikin, D.1
Meese, E.2
Vogelstein, B.3
Witkowski, C.4
Trent, J.5
-
5
-
-
0027189805
-
Loss of heterozygosity in malignant melanoma at loci on chromosomes 11 and 17 implicated in the pathogenesis of other cancers
-
5. Tomlinson IPM, Gammack AJ, Stickland JE, et al. Loss of heterozygosity in malignant melanoma at loci on chromosomes 11 and 17 implicated in the pathogenesis of other cancers. Genes Chrom Cancer 1993, 7, 169-172.
-
(1993)
Genes Chrom Cancer
, vol.7
, pp. 169-172
-
-
Tomlinson, I.P.M.1
Gammack, A.J.2
Stickland, J.E.3
-
6
-
-
0028888926
-
A genetic model of melanoma tumorigenesis based on allelic losses
-
6. Walker GJ, Palmer JM, Walters MK, Hayward NK. A genetic model of melanoma tumorigenesis based on allelic losses. Genes Chrom Cancer 1995, 12, 134-141.
-
(1995)
Genes Chrom Cancer
, vol.12
, pp. 134-141
-
-
Walker, G.J.1
Palmer, J.M.2
Walters, M.K.3
Hayward, N.K.4
-
7
-
-
0028896973
-
Loss of heterozygosity in sporadic cutaneous melanoma
-
7. Healy E, Rehman I, Angus B, Rees JL. Loss of heterozygosity in sporadic cutaneous melanoma. Genes Chrom Cancer 1995, 12, 152-156.
-
(1995)
Genes Chrom Cancer
, vol.12
, pp. 152-156
-
-
Healy, E.1
Rehman, I.2
Angus, B.3
Rees, J.L.4
-
8
-
-
0029002574
-
A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma
-
8. Herbst RA, Larson A, Weiss J, Cavanee WK, Hampton GM, Srden KC. A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma. Cancer Res 1995, 55, 2494-2496.
-
(1995)
Cancer Res
, vol.55
, pp. 2494-2496
-
-
Herbst, R.A.1
Larson, A.2
Weiss, J.3
Cavanee, W.K.4
Hampton, G.M.5
Srden, K.C.6
-
9
-
-
0025928829
-
Cytogenetic analysis in melanoma and naevi
-
9. Cowan JM, Francke U. Cytogenetic analysis in melanoma and naevi. Cancer Treat Res 1991, 54, 3-16.
-
(1991)
Cancer Treat Res
, vol.54
, pp. 3-16
-
-
Cowan, J.M.1
Francke, U.2
-
10
-
-
0026489603
-
Characterisation of four melanoma cell lines with electron microscopy, immunocytochemistry, cytogenetics, flow cytometry, and southern analysis
-
10. Kopf I, Stierner U, Islam Q, Delle U, Kindblom LG, Martinsson T. Characterisation of four melanoma cell lines with electron microscopy, immunocytochemistry, cytogenetics, flow cytometry, and southern analysis. Cancer Genet Cytogenet 1992, 62, 111-123.
-
(1992)
Cancer Genet Cytogenet
, vol.62
, pp. 111-123
-
-
Kopf, I.1
Stierner, U.2
Islam, Q.3
Delle, U.4
Kindblom, L.G.5
Martinsson, T.6
-
11
-
-
0027099958
-
Preferential chromosome 11q and/or chromosome 17q aberrations in short-term cultures of metastatic melanoma in resections from human brain
-
11. Morse HG, Gonzalez R, Moore GE, Robinson WA. Preferential chromosome 11q and/or chromosome 17q aberrations in short-term cultures of metastatic melanoma in resections from human brain. Cancer Genet Cytogenet 1992, 64, 118-126.
-
(1992)
Cancer Genet Cytogenet
, vol.64
, pp. 118-126
-
-
Morse, H.G.1
Gonzalez, R.2
Moore, G.E.3
Robinson, W.A.4
-
12
-
-
0029148164
-
Cytogenetics of 158 patients with regional or disseminated melanoma. Subset analysis of near-diploid and simple karyotypes
-
12. Thompson FH, Emerson J, Olson S, et al. Cytogenetics of 158 patients with regional or disseminated melanoma. Subset analysis of near-diploid and simple karyotypes. Cancer Genet Cytogenet 1995, 83, 93-104.
-
(1995)
Cancer Genet Cytogenet
, vol.83
, pp. 93-104
-
-
Thompson, F.H.1
Emerson, J.2
Olson, S.3
-
13
-
-
0011809855
-
Allelic loss on chromosome 11q is a frequent event in breast cancer
-
13. Stickland JE, Tomlinson IPM, Lee ASG, Evans MF, McGee JO'D. Allelic loss on chromosome 11q is a frequent event in breast cancer. Br J Cancer 1992, 66, (Suppl. xvii), 3.
-
(1992)
Br J Cancer
, vol.66
, Issue.SUPPL. XVII
, pp. 3
-
-
Stickland, J.E.1
Tomlinson, I.P.M.2
Lee, A.S.G.3
Evans, M.F.4
McGee, J.O.'D.5
-
14
-
-
0028123002
-
Loss of heterozygosity in human breast carcinoma: A common region between 11q22 and 11q23.3
-
14. Hampton GM, Winqvist R, Mannermaa A, et al. Loss of heterozygosity in human breast carcinoma: a common region between 11q22 and 11q23.3. Cancer Res 1994, 54, 4586-4589.
-
(1994)
Cancer Res
, vol.54
, pp. 4586-4589
-
-
Hampton, G.M.1
Winqvist, R.2
Mannermaa, A.3
-
15
-
-
0027945323
-
Loss of heterozygosity at 11q22-q23 in breast cancer
-
15. Carter SL, Negrini M, Baffa R, et al. Loss of heterozygosity at 11q22-q23 in breast cancer. Cancer Res 1994, 54, 6270-6274.
-
(1994)
Cancer Res
, vol.54
, pp. 6270-6274
-
-
Carter, S.L.1
Negrini, M.2
Baffa, R.3
-
16
-
-
0029025482
-
Frequent loss of heterozygosity on chromosome 11q in breast cancer
-
16. Tomlinson IPM, Stickland JE, Lee AS-G, et al. Frequent loss of heterozygosity on chromosome 11q in breast cancer. J Clin Pathol 1995, 48, 424-428.
-
(1995)
J Clin Pathol
, vol.48
, pp. 424-428
-
-
Tomlinson, I.P.M.1
Stickland, J.E.2
Lee, A.S.-G.3
-
17
-
-
0028365264
-
Loss of heterozygosity in cervical carcinoma: Sub-chromosomal location of a putative tumour suppressor gene at 11q22-q24
-
17. Hampton GM, Penny LA, Baergen RN, et al. Loss of heterozygosity in cervical carcinoma: sub-chromosomal location of a putative tumour suppressor gene at 11q22-q24. Proc Natl Acad Sci USA 1994, 91, 6953-6957.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6953-6957
-
-
Hampton, G.M.1
Penny, L.A.2
Baergen, R.N.3
-
18
-
-
0028907736
-
Loss of heterozygosity occurs at the d11s29 locus on chromosome 11q23 in invasive cervical carcinoma
-
18. Bethwaite PB, Koreth J, Herrington CS, McGee JO'D. Loss of heterozygosity occurs at the D11S29 locus on chromosome 11q23 in invasive cervical carcinoma. Br J Cancer 1995, 71, 814-818.
-
(1995)
Br J Cancer
, vol.71
, pp. 814-818
-
-
Bethwaite, P.B.1
Koreth, J.2
Herrington, C.S.3
McGee, JO'D.4
-
19
-
-
0027477595
-
Loss of heterozygosity and amplification on chromosome 11q in human ovarian cancer
-
19. Foulkes WD, Campbell IG, Stamp GWH, Trowsdale J. Loss of heterozygosity and amplification on chromosome 11q in human ovarian cancer. Br J Cancer 1993, 67, 268-273.
-
(1993)
Br J Cancer
, vol.67
, pp. 268-273
-
-
Foulkes, W.D.1
Campbell, I.G.2
Stamp, G.W.H.3
Trowsdale, J.4
-
20
-
-
0028911522
-
Microsatellite instability in human non-melanoma and melanoma skin cancer
-
20. Quinn AG, Healy E, Rehman I, Sikkink S, Rees JL. Microsatellite instability in human non-melanoma and melanoma skin cancer. J Invest Derm 1995, 104, 309-312.
-
(1995)
J Invest Derm
, vol.104
, pp. 309-312
-
-
Quinn, A.G.1
Healy, E.2
Rehman, I.3
Sikkink, S.4
Rees, J.L.5
-
21
-
-
0028231090
-
The 1993-94 Genethon human genetic-linkage map
-
21. Gyapay G, Morissette J, Vignal A, et al. The 1993-94 Genethon human genetic-linkage map. Nature Genet 1994, 7, 246-339.
-
(1994)
Nature Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
-
22
-
-
0026664114
-
Highly informative dinucleotide repeat polymorphism at the D11s29 locus on chromosome 11q23
-
22. Warnich L, Groenewald I, Theart L, Relief AE. Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23. Hum Genet 1992, 89, 357-359.
-
(1992)
Hum Genet
, vol.89
, pp. 357-359
-
-
Warnich, L.1
Groenewald, I.2
Theart, L.3
Relief, A.E.4
-
23
-
-
0027136828
-
Genomic instability in colorectal cancer: Relationship to clinicopathological variables and family history
-
23. Lothe RA, Peltomaki P, Meling GI, et al. Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history. Cancer Res 1993, 53, 5849-5852.
-
(1993)
Cancer Res
, vol.53
, pp. 5849-5852
-
-
Lothe, R.A.1
Peltomaki, P.2
Meling, G.I.3
-
24
-
-
0028085975
-
Analysis of the p16 gene (cdkn2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
24. Kamb A, Shattuckeidens D, Eeles R, et al. Analysis of the p16 gene (cdkn2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nature Genet 1994, 8, 22-26.
-
(1994)
Nature Genet
, vol.8
, pp. 22-26
-
-
Kamb, A.1
Shattuckeidens, D.2
Eeles, R.3
-
25
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
25. Hussussian CJ, Struewing JP, Goldstein AM, et al. Germline p16 mutations in familial melanoma. Nature Genet 1994, 8, 15-21.
-
(1994)
Nature Genet
, vol.8
, pp. 15-21
-
-
Hussussian, C.J.1
Struewing, J.P.2
Goldstein, A.M.3
-
26
-
-
0029009926
-
Homozygotes for cdkn2 (p 16) germline mutation in dutch familial melanoma kindreds
-
26. Gruis NA, Vandervelden PA, Sandkuijl LA, et al. Homozygotes for cdkn2 (p 16) germline mutation in Dutch familial melanoma kindreds. Nature Genet 1995, 10, 351-353.
-
(1995)
Nature Genet
, vol.10
, pp. 351-353
-
-
Gruis, N.A.1
Vandervelden, P.A.2
Sandkuijl, L.A.3
-
27
-
-
0028998866
-
Mutations associated with familial melanoma impair p16(ink4) function
-
27. Ranade K, Hussussian CJ, Sikorski RS, et al. Mutations associated with familial melanoma impair p16(ink4) function. Nature Genet 1995, 10, 114-116.
-
(1995)
Nature Genet
, vol.10
, pp. 114-116
-
-
Ranade, K.1
Hussussian, C.J.2
Sikorski, R.S.3
-
28
-
-
0028901842
-
Cdkn2 (mts1) tumor-suppressor gene-mutations in human tumor-cell lines
-
28. Liu Q, Neuhausen S, McClure M, et al. Cdkn2 (mts1) tumor-suppressor gene-mutations in human tumor-cell lines. Oncogene 1995, 10, 1061-1067.
-
(1995)
Oncogene
, vol.10
, pp. 1061-1067
-
-
Liu, Q.1
Neuhausen, S.2
McClure, M.3
-
29
-
-
0013513408
-
Loss of alleles from the distal short arm of chromosome-1 occurs late in melanoma tumor progression
-
29. Dracopoli NC, Harnett P, Bale SJ, et al. Loss of alleles from the distal short arm of chromosome-1 occurs late in melanoma tumor progression. Proc Natl Acad Sci USA 1989, 86, 4614-4618.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 4614-4618
-
-
Dracopoli, N.C.1
Harnett, P.2
Bale, S.J.3
-
30
-
-
0026744752
-
Molecular genetics of colorectal carcinoma
-
30. Hamilton SR. Molecular genetics of colorectal carcinoma. Cancer 1992, 70, 1216-1221.
-
(1992)
Cancer
, vol.70
, pp. 1216-1221
-
-
Hamilton, S.R.1
-
31
-
-
0028999629
-
Detailed deletion mapping of chromosome 6q in borderline epithelial ovarian tumors
-
31. Rodabaugh KJ, Blanchard G, Welch WR, Bell DA, Berkowitz RS, Mok SC. Detailed deletion mapping of chromosome 6q in borderline epithelial ovarian tumors. Cancer Res 1995, 55, 2169-2172.
-
(1995)
Cancer Res
, vol.55
, pp. 2169-2172
-
-
Rodabaugh, K.J.1
Blanchard, G.2
Welch, W.R.3
Bell, D.A.4
Berkowitz, R.S.5
Mok, S.C.6
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