-
1
-
-
0017970363
-
Origin of familial malignant melanomas from heritable melanocytic lesions
-
Clark WH, Reimer RR, Greene M, Ainsworth AM, Mastrangelo MJ. Origin of familial malignant melanomas from heritable melanocytic lesions. Arch Dermatol 1978;114:732-8.
-
(1978)
Arch Dermatol
, vol.114
, pp. 732-738
-
-
Clark, W.H.1
Reimer, R.R.2
Greene, M.3
Ainsworth, A.M.4
Mastrangelo, M.J.5
-
2
-
-
0028172648
-
Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM)
-
Cannon-Albright LA, Meyer LJ, Goldgar DE, et al. Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM). Cancer Res 1994;54:6041-4.
-
(1994)
Cancer Res
, vol.54
, pp. 6041-6044
-
-
Cannon-Albright, L.A.1
Meyer, L.J.2
Goldgar, D.E.3
-
3
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-22
-
Cannon-Albright LA, Goldgar DE, Meyer LJ, et al. Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-22. Science 1992;258:1148-52.
-
(1992)
Science
, vol.258
, pp. 1148-1152
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
-
4
-
-
0026483716
-
Homozygous deletions within human chromosome band 9p21 in melanoma
-
Fountain JW, Karayiorgou M, Ernstoff MS, et al. Homozygous deletions within human chromosome band 9p21 in melanoma. Proc Natl Acad Sci USA 1992;89:10557-61.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 10557-10561
-
-
Fountain, J.W.1
Karayiorgou, M.2
Ernstoff, M.S.3
-
5
-
-
0029883639
-
Two-locus linkage analysis of cutaneous malignant melanoma/dyspiastic nevi
-
Goldstein AM, Goldin R, Dracopoii NC, Clark WH Jr, Tucker MA. Two-locus linkage analysis of cutaneous malignant melanoma/dyspiastic nevi. Am J Hum Genet 1996;58:1050-6.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1050-1056
-
-
Goldstein, A.M.1
Goldin, R.2
Dracopoii, N.C.3
Clark Jr., W.H.4
Tucker, M.A.5
-
6
-
-
0028275733
-
Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
-
Nobori T, Miura K, Wu DJ, Lois A, Takabayashi K, Carson DA. Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature 1994;368:753-6.
-
(1994)
Nature
, 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
-
7
-
-
0027769876
-
A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4
-
Serrano M, Hannon GJ, Beach D. A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4. Nature 1993;366:704-7.
-
(1993)
Nature
, vol.366
, pp. 704-707
-
-
Serrano, M.1
Hannon, G.J.2
Beach, D.3
-
8
-
-
0032549711
-
ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways
-
Zhang Y, Xiong Y, Yarbrough WG. ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways. Cell 1998;92:725-34.
-
(1998)
Cell
, vol.92
, pp. 725-734
-
-
Zhang, Y.1
Xiong, Y.2
Yarbrough, W.G.3
-
10
-
-
0028998866
-
Mutations associated with familial melanoma impair p16ink4 function
-
Ranade K, Hussussian CJ, Sikorsi RS, et al. Mutations associated with familial melanoma impair p16ink4 function. Nat Genet 1995;10:114-16.
-
(1995)
Nat Genet
, vol.10
, pp. 114-116
-
-
Ranade, K.1
Hussussian, C.J.2
Sikorsi, R.S.3
-
11
-
-
0028085975
-
Analysis of the p16 gene (CDKN2A) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb A, Shattuck-Eidens, Eeles R, et al. Analysis of the p16 gene (CDKN2A) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet 1994;8:22-6.
-
(1994)
Nat Genet
, vol.8
, pp. 22-26
-
-
Kamb, A.1
Shattuck-Eidens2
Eeles, R.3
-
12
-
-
0029664339
-
Germline mutations in the p16ink4a binding domain of CDK4 in familial melanoma
-
Zuo L, Weger J, Yang Q, et al. Germline mutations in the p16ink4a binding domain of CDK4 in familial melanoma. Nat Genet 1996;12:97-9.
-
(1996)
Nat Genet
, vol.12
, pp. 97-99
-
-
Zuo, L.1
Weger, J.2
Yang, Q.3
-
13
-
-
6844226190
-
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France
-
Soufir N, Avril MF, Chompret A, Demenais F, et al. Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. Hum Mol Genet 1998;7:209-16.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 209-216
-
-
Soufir, N.1
Avril, M.F.2
Chompret, A.3
Demenais, F.4
-
14
-
-
0032568258
-
CDKN2A mutations in multiple melanomas
-
Monzon J, Liu L, Brill H, et al. CDKN2A mutations in multiple melanomas. N Eng J Med 1998;338:879-87.
-
(1998)
N Eng J Med
, vol.338
, pp. 879-887
-
-
Monzon, J.1
Liu, L.2
Brill, H.3
-
15
-
-
0031777910
-
Retention of the CDKN2A locus and low frequency of point mutations in primary and metastatic malignant melanoma
-
Ruiz A, Puig S, Lynch M, Castel T, Estivill X. Retention of the CDKN2A locus and low frequency of point mutations in primary and metastatic malignant melanoma. Int J Cancer 1998;76:312-16.
-
(1998)
Int J Cancer
, vol.76
, pp. 312-316
-
-
Ruiz, A.1
Puig, S.2
Lynch, M.3
Castel, T.4
Estivill, X.5
-
16
-
-
0031448010
-
Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A (p16INK4A) gene
-
Puig S, Ruiz A, Castel T, et al. Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A (p16INK4A) gene. Hum Genet 1997;101:359-64.
-
(1997)
Hum Genet
, vol.101
, pp. 359-364
-
-
Puig, S.1
Ruiz, A.2
Castel, T.3
-
18
-
-
0006180750
-
Italian melanoma prone families: Analysis of CDKN2A/p16 mutations and linkage to 9p21
-
Ghiorzo P, Mantelli M, Ciotti P, et al. Italian melanoma prone families: analysis of CDKN2A/p16 mutations and linkage to 9p21. Am J Hum Genet Suppl 1996;59:A68.
-
(1996)
Am J Hum Genet Suppl
, vol.59
-
-
Ghiorzo, P.1
Mantelli, M.2
Ciotti, P.3
-
20
-
-
9444276546
-
Prevalence of germ-line mutations in p165 p19ARF, and CDK4 in familial melanoma: Analysis of a clinic-based population
-
Fitzgerald MG, Harkin DP, Silva-Arrieta S, et al. Prevalence of germ-line mutations in p165 p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population. Proc Natl Acad Sci USA 1996;93:8541-5.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 8541-8545
-
-
Fitzgerald, M.G.1
Harkin, D.P.2
Silva-Arrieta, S.3
-
21
-
-
0030964344
-
Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous melanoma
-
Platz A, Hansson J, Mansson-Brahme E, et al. Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous melanoma. J Natl Cancer Inst 1997;89:697-702.
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 697-702
-
-
Platz, A.1
Hansson, J.2
Mansson-Brahme, E.3
-
22
-
-
0031894534
-
Molecular genetics of familial cutaneous melanoma
-
Haluska FG, Hodi FS. Molecular genetics of familial cutaneous melanoma. J Clin Oncol 1998;2:670-82.
-
(1998)
J Clin Oncol
, vol.2
, pp. 670-682
-
-
Haluska, F.G.1
Hodi, F.S.2
-
23
-
-
0029587551
-
Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest
-
Quelle DE, Zindy F, Ashmun RA, Sherr CJ. Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest. Cell 1995;83:993-1000.
-
(1995)
Cell
, vol.83
, pp. 993-1000
-
-
De Quelle1
Zindy, F.2
Ashmun, R.A.3
Sherr, C.J.4
-
24
-
-
0031030325
-
Cancer-associated mutations at the INK4a locus cancel cell cycle arrest by p16INK4a but not by the alternative reading frame protein p19ARF
-
Quelle DE, Cheng M, Ashmun RA, Sherr CJ. Cancer-associated mutations at the INK4a locus cancel cell cycle arrest by p16INK4a but not by the alternative reading frame protein p19ARF. Proc Natl Acad Sci USA 1997;94:669-73.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 669-673
-
-
De Quelle1
Cheng, M.2
Ashmun, R.A.3
Sherr, C.J.4
-
25
-
-
0031000617
-
Affected members of melanoma-prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF
-
Liu L, Goldstein AM, Tucker MA, et al. Affected members of melanoma-prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF. Genes Chrom Cancer 1997;19:52-4.
-
(1997)
Genes Chrom Cancer
, vol.19
, pp. 52-54
-
-
Liu, L.1
Goldstein, A.M.2
Tucker, M.A.3
-
26
-
-
9844219745
-
Germline mutations of the CDKN2 gene in UK melanoma families
-
Harland M, Meloni R, Gruis N, et al. Germline mutations of the CDKN2 gene in UK melanoma families. Hum Mol Genet 1997;12:2061-7.
-
(1997)
Hum Mol Genet
, vol.12
, pp. 2061-2067
-
-
Harland, M.1
Meloni, R.2
Gruis, N.3
|