-
1
-
-
0025820745
-
Cutaneous melanoma
-
Koh, H. K. Cutaneous melanoma. N. Engl. J. Med., 325: 171-182, 1991.
-
(1991)
N. Engl. J. Med.
, vol.325
, pp. 171-182
-
-
Koh, H.K.1
-
2
-
-
0028959985
-
Genes involved in melanoma susceptibility and progression
-
Albino, A. P. Genes involved in melanoma susceptibility and progression. Curr. Opin. Oncol., 7: 162-169, 1995.
-
(1995)
Curr. Opin. Oncol.
, vol.7
, pp. 162-169
-
-
Albino, A.P.1
-
3
-
-
0028264298
-
Loss of heterozygosity for 10q22-10qter in malignant melanoma progression
-
Herbst, R. A., Weiss, J., Ehnis, A., Cavenee, W. K., and Arden, K. C. Loss of heterozygosity for 10q22-10qter in malignant melanoma progression. Cancer Res., 54: 3111-3114, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 3111-3114
-
-
Herbst, R.A.1
Weiss, J.2
Ehnis, A.3
Cavenee, W.K.4
Arden, K.C.5
-
4
-
-
0027452508
-
Chromosome 10 allelic loss in malignant melanoma
-
Isshiki, K., Elder, D. E., Guerry, D., and Linnenbach, A. J. Chromosome 10 allelic loss in malignant melanoma. Genes Chromosomes Cancer, 8: 178-184, 1993.
-
(1993)
Genes Chromosomes Cancer
, vol.8
, pp. 178-184
-
-
Isshiki, K.1
Elder, D.E.2
Guerry, D.3
Linnenbach, A.J.4
-
5
-
-
0028896973
-
Loss of heterozygosity in sporadic primary cutaneous melanoma
-
Healy, E., Rehman, I., Angus, B., and Rees, J. L. Loss of heterozygosity in sporadic primary cutaneous melanoma. Genes Chromosomes Cancer, 12: 152-156, 1995.
-
(1995)
Genes Chromosomes Cancer
, vol.12
, pp. 152-156
-
-
Healy, E.1
Rehman, I.2
Angus, B.3
Rees, J.L.4
-
6
-
-
0028888926
-
A genetic model of melanoma tumortgenesis based on allelic losses
-
Walker, G. J., Palmer, J. M., Walters, M. K., and Hayward, N. K. A genetic model of melanoma tumortgenesis based on allelic losses. Genes Chromosomes Cancer, 12: 134-141, 1995.
-
(1995)
Genes Chromosomes Cancer
, vol.12
, pp. 134-141
-
-
Walker, G.J.1
Palmer, J.M.2
Walters, M.K.3
Hayward, N.K.4
-
7
-
-
17144436629
-
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 thai is mutated in multiple advanced cancers
-
Steck, P. A., Pershouse, M. A., Jasser, S. A., Yung, W. K. A., Lin, H., Ligon, A. H., Langford, L. A., Baumgard, M. L., Hattier, T., Davis, T., Frye, C., Hu, R., Swedlund, B., Teng, D. H. F., and Tavtigian, S. V. Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 thai is mutated in multiple advanced cancers. Nat. Genet., 15: 356-362, 1997.
-
(1997)
Nat. Genet.
, vol.15
, pp. 356-362
-
-
Steck, P.A.1
Pershouse, M.A.2
Jasser, S.A.3
Yung, W.K.A.4
Lin, H.5
Ligon, A.H.6
Langford, L.A.7
Baumgard, M.L.8
Hattier, T.9
Davis, T.10
Frye, C.11
Hu, R.12
Swedlund, B.13
Teng, D.H.F.14
Tavtigian, S.V.15
-
8
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
-
Washington DC
-
Li. J., Yen, C., Liaw, D., Podsypanina, K., Bose, S., Wang, S. I., Puc, J., Miliaresis, C., Rodgers, L., McCombie, R., Bigner, S. H., Giovanella, B. C., Ittmann, M., Tycko, B., Hibshoosh, H., Wigler, M. H., and Parsons, R. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science (Washington DC), 275: 1943-1947, 1997.
-
(1997)
Science
, vol.275
, pp. 1943-1947
-
-
Li, J.1
Yen, C.2
Liaw, D.3
Podsypanina, K.4
Bose, S.5
Wang, S.I.6
Puc, J.7
Miliaresis, C.8
Rodgers, L.9
McCombie, R.10
Bigner, S.H.11
Giovanella, B.C.12
Ittmann, M.13
Tycko, B.14
Hibshoosh, H.15
Wigler, M.H.16
Parsons, R.17
-
9
-
-
0028978590
-
Generation of human melanoma-specific T lymphocyte clones defining novel cytolytic targets with panels of newly established melanoma cell lines
-
Kirkin, A. F., Petersen, T. R., Olsen, A. C., Li, L., thor Straten, P., and Zeuthen, J. Generation of human melanoma-specific T lymphocyte clones defining novel cytolytic targets with panels of newly established melanoma cell lines. Cancer Immunol. Immunother., 41: 71-81, 1995.
-
(1995)
Cancer Immunol. Immunother.
, vol.41
, pp. 71-81
-
-
Kirkin, A.F.1
Petersen, T.R.2
Olsen, A.C.3
Li, L.4
Thor Straten, P.5
Zeuthen, J.6
-
10
-
-
0030891643
-
Expression of transporter associated with antigen processing 1 and 2 (TAP1/2) in malignant melanoma cell lines
-
thor Straten, P., Kirkin, A. F., Seremet, T., and Zeuthen, J. Expression of transporter associated with antigen processing 1 and 2 (TAP1/2) in malignant melanoma cell lines. Int. J. Cancer, 70: 582-586, 1997.
-
(1997)
Int. J. Cancer
, vol.70
, pp. 582-586
-
-
Thor Straten, P.1
Kirkin, A.F.2
Seremet, T.3
Zeuthen, J.4
-
11
-
-
0027377157
-
Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: Implications for diagnosis of hyperphenylalaninemia in southern Europe
-
Guldberg, P., Romano, V., Ceratto, N., Bosco, P., Ciuna, M., Indelicato, A., Mollica, F., Meli, C., Giovannini, M., Riva, E., Biasucci, G., Henriksen, K. F., and Güttler, F. Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southern Europe. Hum. Mol. Genet., 2: 1703-1707, 1993.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1703-1707
-
-
Guldberg, P.1
Romano, V.2
Ceratto, N.3
Bosco, P.4
Ciuna, M.5
Indelicato, A.6
Mollica, F.7
Meli, C.8
Giovannini, M.9
Riva, E.10
Biasucci, G.11
Henriksen, K.F.12
Güttler, F.13
-
12
-
-
0023476285
-
Detection and localization of single base changes by denaturing gradient gel electrophoresis
-
Myers, R. M., Maniatis, T., and Lerman, L. S. Detection and localization of single base changes by denaturing gradient gel electrophoresis. Methods Enzymol., 155: 501-527, 1987.
-
(1987)
Methods Enzymol.
, vol.155
, pp. 501-527
-
-
Myers, R.M.1
Maniatis, T.2
Lerman, L.S.3
-
13
-
-
0030903084
-
Single-step DGGE-based mutation scanning of the p5J gene: Application to genetic diagnosis of colorectal cancer
-
Guldberg, P., Nedergaard, T., Nielsen, H. J., Olsen, A. C., Ahrenkiel, V., and Zeuthen, J. Single-step DGGE-based mutation scanning of the p5J gene: application to genetic diagnosis of colorectal cancer. Hum. Mutat., 9: 348-355, 1997.
-
(1997)
Hum. Mutat.
, vol.9
, pp. 348-355
-
-
Guldberg, P.1
Nedergaard, T.2
Nielsen, H.J.3
Olsen, A.C.4
Ahrenkiel, V.5
Zeuthen, J.6
-
14
-
-
0023476284
-
Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis
-
Lerman, L. S., and Silverstein, K. Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis. Methods Enzymol., 155: 482-501, 1987.
-
(1987)
Methods Enzymol.
, vol.155
, pp. 482-501
-
-
Lerman, L.S.1
Silverstein, K.2
-
15
-
-
0000023099
-
Attachment of a 40-base-pair G+C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction in improved detection of single-base changes
-
Sheffield, V. C., Cox, D. R., Lerman, L. S., and Myers, R. M. Attachment of a 40-base-pair G+C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction in improved detection of single-base changes. Proc. Natl. Acad. Sci. USA, 86: 232-236, 1989.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 232-236
-
-
Sheffield, V.C.1
Cox, D.R.2
Lerman, L.S.3
Myers, R.M.4
-
16
-
-
0031051628
-
Double-gradient UGGE for optimized detection of DNA point mutations
-
Cremonesi, L., Firpo, S., Ferrari, M., Righetti, P. G., and Gelfi, C. Double-gradient UGGE for optimized detection of DNA point mutations. Biotechniques, 22: 326-330, 1997.
-
(1997)
Biotechniques
, vol.22
, pp. 326-330
-
-
Cremonesi, L.1
Firpo, S.2
Ferrari, M.3
Righetti, P.G.4
Gelfi, C.5
-
17
-
-
0026794668
-
The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences
-
Krawczak, M., Reiss, J., and Cooper, D. N. The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences. Hum. Genet., 90: 41-54, 1992.
-
(1992)
Hum. Genet.
, vol.90
, pp. 41-54
-
-
Krawczak, M.1
Reiss, J.2
Cooper, D.N.3
-
18
-
-
0031004088
-
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
-
Liaw, D., Marsh, D. J., Li, J., Dahia, P. L. M., Wang, S. I., Zheng, Z., Bose, S., Call, K. M., Tsou, H. C., Peacocke, M., Eng, C., and Parsons, R. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat. Genet., 16: 64-67, 1997.
-
(1997)
Nat. Genet.
, vol.16
, pp. 64-67
-
-
Liaw, D.1
Marsh, D.J.2
Li, J.3
Dahia, P.L.M.4
Wang, S.I.5
Zheng, Z.6
Bose, S.7
Call, K.M.8
Tsou, H.C.9
Peacocke, M.10
Eng, C.11
Parsons, R.12
-
19
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Washington DC
-
Kamb, A., Gruis, N. A., Weaver-Feldhaus, J., Liu, Q., Harshman, K., Tavtigian, S. V., Stockert, E., Day, R. S. I. I. I., Johnson, B. E., and Skolnick, M. H. A cell cycle regulator potentially involved in genesis of many tumor types. Science (Washington DC), 264: 436-440, 1994.
-
(1994)
Science
, vol.264
, pp. 436-440
-
-
Kamb, A.1
Gruis, N.A.2
Weaver-Feldhaus, J.3
Liu, Q.4
Harshman, K.5
Tavtigian, S.V.6
Stockert, E.7
Day, R.S.I.I.I.8
Johnson, B.E.9
Skolnick, M.H.10
-
20
-
-
0028275733
-
Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
-
Nobori, T., Miura, K., Wu, D. J., Lois, A., Takabayashi, K., and Carson, D. A. Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature (Lond.), 368: 753-756, 1994.
-
(1994)
Nature (Lond.)
, vol.368
, pp. 753-756
-
-
Nobori, T.1
Miura, K.2
Wu, D.J.3
Lois, A.4
Takabayashi, K.5
Carson, D.A.6
-
21
-
-
0029147195
-
Evidence for u.v, induction of CDKN2 mutations in melanoma cell lines
-
Pollock, P. M., Yu, F., Qiu, L., Parsons, P. G., and Hayward, N. K. Evidence for u.v, induction of CDKN2 mutations in melanoma cell lines. Oncogene, 11: 663-668, 1995.
-
(1995)
Oncogene
, vol.11
, pp. 663-668
-
-
Pollock, P.M.1
Yu, F.2
Qiu, L.3
Parsons, P.G.4
Hayward, N.K.5
-
22
-
-
0030467624
-
The p16-cyclin D/Cdk4-pRB pathway as a functional unit frequently altered in melanoma pathogenesis
-
Bartkova, J., Lukas, J., Guldberg, P., Alsner, J., Kirkin, A. F., Zeuthen, J., and Bartek, J. The p16-cyclin D/Cdk4-pRB pathway as a functional unit frequently altered in melanoma pathogenesis. Cancer Res., 56: 5475-5483, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 5475-5483
-
-
Bartkova, J.1
Lukas, J.2
Guldberg, P.3
Alsner, J.4
Kirkin, A.F.5
Zeuthen, J.6
Bartek, J.7
-
23
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian, C. J., Struewing, J. P., Goldstein, A. M., Higgins, P. A. T., Ally, D. S., Sheahan, M. D., Clark, W. H., Tucker, M. A., and Dracopoli, N. C. Germline p16 mutations in familial melanoma. Nat. Genet., 8: 15-21, 1994.
-
(1994)
Nat. Genet.
, vol.8
, pp. 15-21
-
-
Hussussian, C.J.1
Struewing, J.P.2
Goldstein, A.M.3
Higgins, P.A.T.4
Ally, D.S.5
Sheahan, M.D.6
Clark, W.H.7
Tucker, M.A.8
Dracopoli, N.C.9
-
24
-
-
0028085975
-
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb, A., Shattuck-Eidens, D., Eeles, R., Liu, Q., Gruis, N. A., Ding, W., Hussey, C., Tran, T., Miki, Y., Weaver-Feldhaus, J., McClure, M., Aitken, J. F., Anderson, D. E., Bergman, W., Frants, R., Goldgar, D. E., Green, A., MacLennan, R., Martin, N. G., Meyer, L. J., Youl, P., Zone, J. J., Skolnick, M. H., and Cannon-Albright, L. A. Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat. Genet., 8: 22-26, 1994.
-
(1994)
Nat. Genet.
, vol.8
, pp. 22-26
-
-
Kamb, A.1
Shattuck-Eidens, D.2
Eeles, R.3
Liu, Q.4
Gruis, N.A.5
Ding, W.6
Hussey, C.7
Tran, T.8
Miki, Y.9
Weaver-Feldhaus, J.10
McClure, M.11
Aitken, J.F.12
Anderson, D.E.13
Bergman, W.14
Frants, R.15
Goldgar, D.E.16
Green, A.17
MacLennan, R.18
Martin, N.G.19
Meyer, L.J.20
Youl, P.21
Zone, J.J.22
Skolnick, M.H.23
Cannon-Albright, L.A.24
more..
-
25
-
-
0030070484
-
CDKN2/p16 or RB alterations occur in the majority of glioblastomas and are inversely correlated
-
Ueki, K., Ono, Y., Henson, J. W., Efird, J. T., von Deimling, A., and Louis, D. N. CDKN2/p16 or RB alterations occur in the majority of glioblastomas and are inversely correlated. Cancer Res., 56: 150-153, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 150-153
-
-
Ueki, K.1
Ono, Y.2
Henson, J.W.3
Efird, J.T.4
Von Deimling, A.5
Louis, D.N.6
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