-
1
-
-
0029548624
-
Epidemiology of sun exposure and skin cancer
-
Armstrong BK, Kricker A: Epidemiology of sun exposure and skin cancer. Cancer Surv 26:133-153, 1996
-
(1996)
Cancer Surv
, vol.26
, pp. 133-153
-
-
Armstrong, B.K.1
Kricker, A.2
-
2
-
-
0024320151
-
Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p
-
Bale SJ, Dracopoli NC, Tucker MA, et al: Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p. N Engl J Med 320:1367-1372, 1989
-
(1989)
N Engl J Med
, vol.320
, pp. 1367-1372
-
-
Bale, S.J.1
Dracopoli, N.C.2
Tucker, M.A.3
-
3
-
-
0026584353
-
The Dutch FAMMM family material: Clinical and genetic data
-
Bergman W, Gruis NA, Frants RR: The Dutch FAMMM family material: clinical and genetic data. Cytogenet Cell Genet 59:161-164, 1992
-
(1992)
Cytogenet Cell Genet
, vol.59
, pp. 161-164
-
-
Bergman, W.1
Gruis, N.A.2
Frants, R.R.3
-
4
-
-
0028037272
-
Genetics of seven Dutch familial atypical multiple mole-melanoma syndrome families: A review of linkage results including chromosomes 1 and 9
-
Bergman W, Gruis NA, Sandkuijl LA, Frants RR: Genetics of seven Dutch familial atypical multiple mole-melanoma syndrome families: a review of linkage results including chromosomes 1 and 9. J Invest Dermatol 103:122S-125S, 1994
-
(1994)
J Invest Dermatol
, vol.103
-
-
Bergman, W.1
Gruis, N.A.2
Sandkuijl, L.A.3
Frants, R.R.4
-
5
-
-
0030782275
-
Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair
-
Box NF, Wyeth JR, O'Gorman LE, Martin NG, Sturm RA: Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair. Hum Mol Genet 6:1891-1897, 1997
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1891-1897
-
-
Box, N.F.1
Wyeth, J.R.2
O'Gorman, L.E.3
Martin, N.G.4
Sturm, R.A.5
-
6
-
-
0025338277
-
Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome 1p36
-
Cannon-Albright LA, Goldgar DE, Wright EC, et al: Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome 1p36. Am J Hum Genet 46:912-918, 1990
-
(1990)
Am J Hum Genet
, vol.46
, pp. 912-918
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Wright, E.C.3
-
7
-
-
0026471719
-
Assignment of a locus for familial melanoma. MLM, to chromosome 9p13- P22
-
Cannon-Albright LA, Goldgar DE, Meyer LJ, et al: Assignment of a locus for familial melanoma. MLM, to chromosome 9p13- P22. Science 258:1148-1152, 1992
-
(1992)
Science
, vol.258
, pp. 1148-1152
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
-
8
-
-
0017970363
-
Origin of familial malignant melanomas from heritable melanocytic lesions. "The BK mole syndrome"
-
Clark WH, Reimer RR, Greene M, Ainsworth AM, Mastrangelo MJ: Origin of familial malignant melanomas from heritable melanocytic lesions. "The BK mole syndrome". Arch Dermatol 732:732-738, 1978
-
(1978)
Arch Dermatol
, vol.732
, pp. 732-738
-
-
Clark, W.H.1
Reimer, R.R.2
Greene, M.3
Ainsworth, A.M.4
Mastrangelo, M.J.5
-
9
-
-
9444276546
-
Prevalence of germ-line mutations in p16, 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 p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population. Proc Natl Acad Sci USA 93:8541-8545, 1996
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 8541-8545
-
-
Fitzgerald, M.G.1
Harkin, D.P.2
Silva-Arrieta, S.3
-
10
-
-
0030899774
-
The CDKN2A (p16) gene and human cancer
-
Foulkes WD, Flanders TY, Pollock PM, Hayward NK: The CDKN2A (p16) gene and human cancer. Mol Med 3:5-20, 1997
-
(1997)
Mol Med
, vol.3
, pp. 5-20
-
-
Foulkes, W.D.1
Flanders, T.Y.2
Pollock, P.M.3
Hayward, N.K.4
-
11
-
-
0028091349
-
Mapping of the gene encoding the melanocortin-1 (alpha-melanocyte stimulating hormone) receptor (MC1R) to human chromosome 16q24.3 by Fluorescence in situ hybridization
-
Gantz I, Yamada T, Tashiro T, Konda Y, Shimoto V, Miwa H, Trent JM: Mapping of the gene encoding the melanocortin-1 (alpha-melanocyte stimulating hormone) receptor (MC1R) to human chromosome 16q24.3 by Fluorescence in situ hybridization. Genomics 19:394-395, 1994
-
(1994)
Genomics
, vol.19
, pp. 394-395
-
-
Gantz, I.1
Yamada, T.2
Tashiro, T.3
Konda, Y.4
Shimoto, V.5
Miwa, H.6
Trent, J.M.7
-
12
-
-
0029883639
-
Two-locus linkage analysis of cutaneous malignant melanoma/dysplastic nevi
-
Goldstein AM, Goldin LR, Dracopoli NC, Clark WH Jr, Tucker MA: Two-locus linkage analysis of cutaneous malignant melanoma/dysplastic nevi. Am J Hum Genet 58:1050-1056, 1996
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1050-1056
-
-
Goldstein, A.M.1
Goldin, L.R.2
Dracopoli, N.C.3
Clark W.H., Jr.4
Tucker, M.A.5
-
13
-
-
0030697181
-
Low frequency of p16/CDKN2A methylation in sporadic melanoma: Comparative approaches for methylation analysis of primary tumors
-
Gonzalgo ML, Bender CM, You EH, et al: Low frequency of p16/CDKN2A methylation in sporadic melanoma: comparative approaches for methylation analysis of primary tumors. Cancer Res 57:5336-5347, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 5336-5347
-
-
Gonzalgo, M.L.1
Bender, C.M.2
You, E.H.3
-
14
-
-
0002941239
-
The hereditary variant of malignant melanoma
-
Clark WH, Goldman L, Mastrangelo M (eds). New York: Grune and Stratton
-
Greene MH, Fraumeni JF: The hereditary variant of malignant melanoma. In: Clark WH, Goldman L, Mastrangelo M (eds). Human Malignant Melanoma. New York: Grune and Stratton, 1979, pp. 139-166
-
(1979)
Human Malignant Melanoma
, pp. 139-166
-
-
Greene, M.H.1
Fraumeni, J.F.2
-
15
-
-
0020514915
-
The familial occurrence of cutancous melanoma, intraocular melanoma, and the dysplastic nevus syndrome
-
Greene MH, Sanders RJ, Chu FC, Clark WH Jr, Elder DE, Cogan DG: The familial occurrence of cutancous melanoma, intraocular melanoma, and the dysplastic nevus syndrome. Am J Ophthalmol 96:238-245, 1983
-
(1983)
Am J Ophthalmol
, vol.96
, pp. 238-245
-
-
Greene, M.H.1
Sanders, R.J.2
Chu, F.C.3
Clark W.H., Jr.4
Elder, D.E.5
Cogan, D.G.6
-
16
-
-
0025348509
-
Locus for susceptibility to melanoma on chromosome Ip
-
Gruis NA, Bergman W, Frants RR: Locus for susceptibility to melanoma on chromosome Ip. N Engl J Med 322:853-854, 1990
-
(1990)
N Engl J Med
, vol.322
, pp. 853-854
-
-
Gruis, N.A.1
Bergman, W.2
Frants, R.R.3
-
17
-
-
0027495164
-
Linkage analysis in Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families. Effect of naevus count
-
Gruis NA, Sandkuijl LA, Weber JL, van der Zee A, Borgstein AM, Bergman W, Frants RR: Linkage analysis in Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families. Effect of naevus count. Melanoma Res 3:271-277, 1993
-
(1993)
Melanoma Res
, vol.3
, pp. 271-277
-
-
Gruis, N.A.1
Sandkuijl, L.A.2
Weber, J.L.3
Van Der Zee, A.4
Borgstein, A.M.5
Bergman, W.6
Frants, R.R.7
-
18
-
-
0029038538
-
CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families
-
Gruis NA, Sandkuijl LA, van der Velden PA, Bergman W, Frants RR: CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. Melanoma Res 5:169-177, 1995a
-
(1995)
Melanoma Res
, vol.5
, pp. 169-177
-
-
Gruis, N.A.1
Sandkuijl, L.A.2
Van Der Velden, P.A.3
Bergman, W.4
Frants, R.R.5
-
19
-
-
0029009926
-
Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds
-
Gruis NA, van der Velden PA, Sandkuijl LA, et al: Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds. Nat Genet 10:351-353, 1995b
-
(1995)
Nat Genet
, vol.10
, pp. 351-353
-
-
Gruis, N.A.1
Van Der Velden, P.A.2
Sandkuijl, L.A.3
-
20
-
-
0029005856
-
Genetic evidence in melanoma and bladder cancers that p16 and p53 function in separate pathways of tumor suppression
-
Gruis NA, Weaver-Feldhaus J, Liu Q, et al: Genetic evidence in melanoma and bladder cancers that p16 and p53 function in separate pathways of tumor suppression. Am J Pathol 146:1199-1206, 1995c
-
(1995)
Am J Pathol
, vol.146
, pp. 1199-1206
-
-
Gruis, N.A.1
Weaver-Feldhaus, J.2
Liu, Q.3
-
21
-
-
0024693775
-
Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families
-
van Haeringen A, Bergman W, Nelen MR, et al: Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families. Genomics 5:61-64, 1989
-
(1989)
Genomics
, vol.5
, pp. 61-64
-
-
Van Haeringen, A.1
Bergman, W.2
Nelen, M.R.3
-
22
-
-
0031776706
-
Association of CDKN2A (p16) /CDKN2B (p15) alterations and homozygous chromosome arm 9p deletions in human lung carcinoma
-
Hamada K, Kohno T, Kawanishi M, Ohwada S, Yokota J: Association of CDKN2A (p16) /CDKN2B (p15) alterations and homozygous chromosome arm 9p deletions in human lung carcinoma. Genes Chromosomes Cancer 22:232-240, 1998
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 232-240
-
-
Hamada, K.1
Kohno, T.2
Kawanishi, M.3
Ohwada, S.4
Yokota, J.5
-
23
-
-
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 6:2061-2067, 1997
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2061-2067
-
-
Harland, M.1
Meloni, R.2
Gruis, N.3
-
24
-
-
0028845142
-
Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers
-
Herman JG, Merlo A, Mao L, et al: Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers. Cancer Res 55:4525-4530, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 4525-4530
-
-
Herman, J.G.1
Merlo, A.2
Mao, L.3
-
25
-
-
0031899804
-
Excess cancer mortality in six Dutch pedigrees with the familial atypical multiple mole-melanoma syndrome from 1830 to
-
Hille ET, van Duijn F, Gruis NA, Rosendaal FR, Bergman W, Vandenbroucke JP: Excess cancer mortality in six Dutch pedigrees with the familial atypical multiple mole-melanoma syndrome from 1830 to. J Invest Dermatol 110:788-792, 1998
-
(1998)
J Invest Dermatol
, vol.110
, pp. 788-792
-
-
Hille, E.T.1
Van Duijn, F.2
Gruis, N.A.3
Rosendaal, F.R.4
Bergman, W.5
Vandenbroucke, J.P.6
-
26
-
-
0028981255
-
Nle4DPhe7 alpha-melanocyte-stimulating honnone increases the eumelanin: Phaeomelanin ratio in cultured human melanocytes
-
Hunt G, Kyne S, Wakamatsu K, Ito S, Thody AJ: Nle4DPhe7 alpha-melanocyte-stimulating honnone increases the eumelanin: phaeomelanin ratio in cultured human melanocytes. J Invest Dermatol 104:83-85, 1995
-
(1995)
J Invest Dermatol
, vol.104
, pp. 83-85
-
-
Hunt, G.1
Kyne, S.2
Wakamatsu, K.3
Ito, S.4
Thody, A.J.5
-
28
-
-
7344236227
-
Susceptibility to melanoma: Influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene
-
Ichii-Jones F, Lear JT, Heagerty AH, et al: Susceptibility to melanoma: influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene. J Invest Dermatol 111:218-221, 1998
-
(1998)
J Invest Dermatol
, vol.111
, pp. 218-221
-
-
Ichii-Jones, F.1
Lear, J.T.2
Heagerty, A.H.3
-
29
-
-
0030614550
-
Potential role for concurrent abnormalities of the cyclin D1, p16CDKN2 and p15CDKN2B genes in certain B cell non-Hodgkin's lymphomas. Functional studies in a cell line (Granta 519)
-
Jadayel DM, Lukas J, Nacheva E, et al: Potential role for concurrent abnormalities of the cyclin D1, p16CDKN2 and p15CDKN2B genes in certain B cell non-Hodgkin's lymphomas. Functional studies in a cell line (Granta 519). Leukemia 11:64-72, 1997
-
(1997)
Leukemia
, vol.11
, pp. 64-72
-
-
Jadayel, D.M.1
Lukas, J.2
Nacheva, E.3
-
30
-
-
0030120492
-
Red coat color in Holstein cattle is associated with a deletion in the MSHR gene
-
Joerg H, Fries HR, Meijerink E, Stranzinger GF: Red coat color n Holstein cattle is associated with a deletion in the MSHR gene. Mamm Genome 7:317-318, 1996
-
(1996)
Mamm Genome
, vol.7
, pp. 317-318
-
-
Joerg, H.1
Fries, H.R.2
Meijerink, E.3
Stranzinger, G.F.4
-
31
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Kamb A, Gruis NA, Weaver-Feldhaus J, et al: A cell cycle regulator potentially involved in genesis of many tumor types. Science 264:436-440, 1994a
-
(1994)
Science
, vol.264
, pp. 436-440
-
-
Kamb, A.1
Gruis, N.A.2
Weaver-Feldhaus, J.3
-
32
-
-
0028085975
-
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb A, Shattuck-Eidens D, Eeles R, et al: Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet 8:23-26, 1994b
-
(1994)
Nat Genet
, vol.8
, pp. 23-26
-
-
Kamb, A.1
Shattuck-Eidens, D.2
Eeles, R.3
-
33
-
-
0030728468
-
Tumor suppression at the mouse INK4a locus mediated by the alternative reading frame product p19ARF
-
Kamijo T, Zindy F, Roussel MF, et al: Tumor suppression at the mouse INK4a locus mediated by the alternative reading frame product p19ARF. Cell 91:649-659, 1997
-
(1997)
Cell
, vol.91
, pp. 649-659
-
-
Kamijo, T.1
Zindy, F.2
Roussel, M.F.3
-
34
-
-
0032493350
-
Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2
-
Kamijo T, Weber JD, Zambetti G, Zindy F, Roussel MF, Sherr CJ: Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2. Proc Natl Acad Sci USA 95:8292-8297, 1998
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 8292-8297
-
-
Kamijo, T.1
Weber, J.D.2
Zambetti, G.3
Zindy, F.4
Roussel, M.F.5
Sherr, C.J.6
-
35
-
-
0025977735
-
Hereditary melanoma in Australia. Variable association with dysplastic nevi and absence of genetic linkage to chromosome 1p
-
Kefford RF, Salmon J, Shaw HM, Donald JA, McCarthy WH: Hereditary melanoma in Australia. Variable association with dysplastic nevi and absence of genetic linkage to chromosome 1p. Cancer Genet Cytogenet 51:45-55, 1991
-
(1991)
Cancer Genet Cytogenet
, vol.51
, pp. 45-55
-
-
Kefford, R.F.1
Salmon, J.2
Shaw, H.M.3
Donald, J.A.4
McCarthy, W.H.5
-
36
-
-
0031012096
-
Identification of common polymorphisms in the coding sequence of the human MSH receptor (MCIR) with possible biological effects
-
Koppula SV, Robbins LS, Lu D, Baack H, White CR Jr, Swanson NA, Cone RD: Identification of common polymorphisms in the coding sequence of the human MSH receptor (MCIR) with possible biological effects. Hum Mutat 9:30-36, 1997
-
(1997)
Hum Mutat
, vol.9
, pp. 30-36
-
-
Koppula, S.V.1
Robbins, L.S.2
Lu, D.3
Baack, H.4
White C.R., Jr.5
Swanson, N.A.6
Cone, R.D.7
-
37
-
-
0028981664
-
Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma
-
Liu L, Lassam NJ, Slingerland JM, Bailey D, Cole D, Jenkins R, Hogg D: Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma. Oncogene 11:405-412, 1995
-
(1995)
Oncogene
, vol.11
, pp. 405-412
-
-
Liu, L.1
Lassam, N.J.2
Slingerland, J.M.3
Bailey, D.4
Cole, D.5
Jenkins, R.6
Hogg, D.7
-
38
-
-
0028901842
-
CDKN2 (MTS1) tumor suppressor gene mutations in human tumor cell lines
-
Liu Q, Neuhausen S, McClure M, et al: CDKN2 (MTS1) tumor suppressor gene mutations in human tumor cell lines. Oncogene 10:1061-1067, 1995
-
(1995)
Oncogene
, vol.10
, pp. 1061-1067
-
-
Liu, Q.1
Neuhausen, S.2
McClure, M.3
-
39
-
-
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, Brill H, Gruis NA, Hogg D, Lassam NJ: 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 Chromosomes Cancer 19:52-54, 1997
-
(1997)
Genes Chromosomes Cancer
, vol.19
, pp. 52-54
-
-
Liu, L.1
Goldstein, A.M.2
Tucker, M.A.3
Brill, H.4
Gruis, N.A.5
Hogg, D.6
Lassam, N.J.7
-
40
-
-
0028566386
-
Genetic heterogeneity in familial malignant melanoma
-
MacGeoch C, Bishop JA, Bataille V, et al: Genetic heterogeneity in familial malignant melanoma. Hum Mol Genet 3:2195-2200, 1994
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2195-2200
-
-
MacGeoch, C.1
Bishop, J.A.2
Bataille, V.3
-
41
-
-
0026800892
-
The cloning of a family of genes that encode the melanocortin receptors
-
Mountjoy KG, Robbins LS, Mortrud MT, Cone RD: The cloning of a family of genes that encode the melanocortin receptors. Science 257:1248-1251, 1992
-
(1992)
Science
, vol.257
, pp. 1248-1251
-
-
Mountjoy, K.G.1
Robbins, L.S.2
Mortrud, M.T.3
Cone, R.D.4
-
42
-
-
0026580909
-
Exclusion of the familial melanoma locus (MLM) from the PND/D1S47 and MYCL1 regions of chromosome arm 1p in 7 Australian pedigrees
-
Nancarrow DJ, Palmer JM, Walters MK, et al: Exclusion of the familial melanoma locus (MLM) from the PND/D1S47 and MYCL1 regions of chromosome arm 1p in 7 Australian pedigrees. Genomics 12:18-25, 1992
-
(1992)
Genomics
, vol.12
, pp. 18-25
-
-
Nancarrow, D.J.1
Palmer, J.M.2
Walters, M.K.3
-
43
-
-
0027507837
-
Confirmation of chromosome 9p linkage in familial melanoma
-
Nancarrow DJ, Mann GJ, Holland EA, et al: Confirmation of chromosome 9p linkage in familial melanoma. Am J Hum Genet 53:936-942, 1993
-
(1993)
Am J Hum Genet
, vol.53
, pp. 936-942
-
-
Nancarrow, D.J.1
Mann, G.J.2
Holland, E.A.3
-
44
-
-
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 368:753-756, 1994
-
(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
-
45
-
-
85056036856
-
A case of fungoid disease
-
Norris W: A case of fungoid disease. Edinb Med Surg J 16:562-565, 1820
-
(1820)
Edinb Med Surg J
, vol.16
, pp. 562-565
-
-
Norris, W.1
-
46
-
-
7144229363
-
Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations
-
Pollock PM, Spurr N, Bishop T, et al: Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations. Hum Mutat 11:424-431, 1998
-
(1998)
Hum Mutat
, vol.11
, pp. 424-431
-
-
Pollock, P.M.1
Spurr, N.2
Bishop, T.3
-
47
-
-
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 94:669-673, 1997
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 669-673
-
-
Quelle, D.E.1
Cheng, M.2
Ashmun, R.A.3
Sherr, C.J.4
-
48
-
-
0030612751
-
Differential expression of p16INK4a and p16beta transcripts in B- lymphoblastoid cells from members of hereditary melanoma families without CDKN2A exon mutations
-
Rizos H, Becker TM, Holland EA, Kefford RF, Mann GJ: Differential expression of p16INK4a and p16beta transcripts in B- lymphoblastoid cells from members of hereditary melanoma families without CDKN2A exon mutations. Oncogene 15:515-523, 1997
-
(1997)
Oncogene
, vol.15
, pp. 515-523
-
-
Rizos, H.1
Becker, T.M.2
Holland, E.A.3
Kefford, R.F.4
Mann, G.J.5
-
49
-
-
0027413475
-
Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function
-
Robbins LS, Nadeau JH, Johnson KR, et al: Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function. Cell 72:827-834, 1993
-
(1993)
Cell
, vol.72
, pp. 827-834
-
-
Robbins, L.S.1
Nadeau, J.H.2
Johnson, K.R.3
-
50
-
-
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 366:704-707, 1993
-
(1993)
Nature
, vol.366
, pp. 704-707
-
-
Serrano, M.1
Hannon, G.J.2
Beach, D.3
-
51
-
-
7144254441
-
Melanocortin 1 receptor variants in an Irish population
-
Smith R, Healy E, Siddiqui S, et al: Melanocortin 1 receptor variants in an Irish population. J Invest Dermatol 111:119-122, 1998
-
(1998)
J Invest Dermatol
, vol.111
, pp. 119-122
-
-
Smith, R.1
Healy, E.2
Siddiqui, S.3
-
52
-
-
6844226190
-
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French familial melanoma study group
-
Soufir N, Avril MF, Chompret A, et al: Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group. Hum Mol Genet 7:209-216, 1998
-
(1998)
Hum Mol Genet
, vol.7
, pp. 209-216
-
-
Soufir, N.1
Avril, M.F.2
Chompret, A.3
-
53
-
-
0029791633
-
The 9p21 region in bladder cancer cell lines: Large homozygous deletion inactivate the CDKN2, CDKN2B and MTAP genes
-
Stadler WM, Olopade OI: The 9p21 region in bladder cancer cell lines: large homozygous deletion inactivate the CDKN2, CDKN2B and MTAP genes. Urol Res 24:239-244, 1996
-
(1996)
Urol Res
, vol.24
, pp. 239-244
-
-
Stadler, W.M.1
Olopade, O.I.2
-
54
-
-
0029113837
-
Genomic structure, expression and mutational analysis of the P15 (MTS2) gene
-
Stone S, Dayananth P, Jiang P, Weaver-Feldhaus JM, Tavtigian SV, Cannon-Albright L, Kamb A: Genomic structure, expression and mutational analysis of the P15 (MTS2) gene. Oncogene 11:987-991, 1995
-
(1995)
Oncogene
, vol.11
, pp. 987-991
-
-
Stone, S.1
Dayananth, P.2
Jiang, P.3
Weaver-Feldhaus, J.M.4
Tavtigian, S.V.5
Cannon-Albright, L.6
Kamb, A.7
-
55
-
-
0032169516
-
The alternative product from the human CDKN2A locus, p14 (ARF), participates in a regulatory feedback loop with p53 and MDM2
-
Stott FJ, Hates S, James MC, et al: The alternative product from the human CDKN2A locus, p14 (ARF), participates in a regulatory feedback loop with p53 and MDM2. Embo J 17:5001-5014, 1998
-
(1998)
Embo J
, vol.17
, pp. 5001-5014
-
-
Stott, F.J.1
Hates, S.2
James, M.C.3
-
56
-
-
0028822526
-
Intragenic mutations of CDKN2B and CDKN2A in primary human esophageal cancers
-
Suzuki H, Zhou X, Yin J, et al: Intragenic mutations of CDKN2B and CDKN2A in primary human esophageal cancers. Hum Mol Genet 4:1883-1887, 1995
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1883-1887
-
-
Suzuki, H.1
Zhou, X.2
Yin, J.3
-
57
-
-
1842339332
-
A non-epistatic interaction of agouti and extension in the fox, Vulpes vulpes
-
Vage DI, Lu D, Klungland H, Lien S, Adalsteinsson S, Cone RD: A non-epistatic interaction of agouti and extension in the fox, Vulpes vulpes. Nat Genet 15:311-315, 1997
-
(1997)
Nat Genet
, vol.15
, pp. 311-315
-
-
Vage, D.I.1
Lu, D.2
Klungland, H.3
Lien, S.4
Adalsteinsson, S.5
Cone, R.D.6
-
58
-
-
0028786945
-
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
-
Valverde P, Healy F, Jackson J, Rees JL, Thody AJ: Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nat Genet 11:328-330, 1995
-
(1995)
Nat Genet
, vol.11
, pp. 328-330
-
-
Valverde, P.1
Healy, F.2
Jackson, J.3
Rees, J.L.4
Thody, A.J.5
-
59
-
-
0029839525
-
The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma
-
Valverde P, Healy E, Sikkink S, et al: The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma. Hum Mol Genet 5:1663-1666, 1996
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1663-1666
-
-
Valverde, P.1
Healy, E.2
Sikkink, S.3
-
60
-
-
0031980540
-
Virtually 100% of melanoma cell lines harbor alterations at the DNA level within CDKN2A, CDKN2B, or one of their downstream targets
-
Walker GJ, Flores JF, Glendening JM, Lin AH, Markl ID, Fountain JW: Virtually 100% of melanoma cell lines harbor alterations at the DNA level within CDKN2A, CDKN2B, or one of their downstream targets. Genes Chromosomes Cancer 22:157-163, 1998
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 157-163
-
-
Walker, G.J.1
Flores, J.F.2
Glendening, J.M.3
Lin, A.H.4
Markl, I.D.5
Fountain, J.W.6
-
61
-
-
0027958821
-
Localization of a putative tumor suppressor gene by using homozygous deletions in melanomas
-
Weaver-Feldhaus J, Gruis NA, Neuhausen S, Le Paslier D, Stockert E, Skolnick MH, Kamb A: Localization of a putative tumor suppressor gene by using homozygous deletions in melanomas. Proc Natl Acad Sci USA 91:7563-7567, 1994
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 7563-7567
-
-
Weaver-Feldhaus, J.1
Gruis, N.A.2
Neuhausen, S.3
Le Paslier, D.4
Stockert, E.5
Skolnick, M.H.6
Kamb, A.7
-
62
-
-
0030340912
-
Val92Met variant of the melanocyte stimulating hormone receptor gene
-
Xu X: Val92Met variant of the melanocyte stimulating hormone receptor gene. Nat Genet 14:384, 1996
-
(1996)
Nat Genet
, vol.14
, pp. 384
-
-
Xu, X.1
-
63
-
-
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 12:97-99, 1996
-
(1996)
Nat Genet
, vol.12
, pp. 97-99
-
-
Zuo, L.1
Weger, J.2
Yang, Q.3
|