-
1
-
-
0003077969
-
Cutaneous melanoma
-
DeVita VT Jr, Hellman S, Rosenberg SA (eds): Philadelphia, PA, Lippincott-Raven
-
Balch CM, Reintgen DS, Kirkwood JM, et al: Cutaneous melanoma, in DeVita VT Jr, Hellman S, Rosenberg SA (eds): Cancer: Principles and Practice of Oncology. Philadelphia, PA, Lippincott-Raven, 1997, pp 1947-1994
-
(1997)
Cancer: Principles and Practice of Oncology
, pp. 1947-1994
-
-
Balch, C.M.1
Reintgen, D.S.2
Kirkwood, J.M.3
-
2
-
-
0002950402
-
The worldwide incidence of malignant melanoma
-
Balch CM, Houghton AN, Milton GW, et al (eds): Philadelphia, PA, Lippincott
-
Grin-Jorgensen CM, Rigel DS, Friedman RJ: The worldwide incidence of malignant melanoma, in Balch CM, Houghton AN, Milton GW, et al (eds): Cutaneous Melanoma (ed 2). Philadelphia, PA, Lippincott, 1992, pp 27-39
-
(1992)
Cutaneous Melanoma (Ed 2)
, pp. 27-39
-
-
Grin-Jorgensen, C.M.1
Rigel, D.S.2
Friedman, R.J.3
-
3
-
-
0031014450
-
Cancer statistics, 1997
-
Parker SL, Tong T, Bolden S, et al: Cancer statistics, 1997. CA Cancer J Clin. 47:5-27, 1997
-
(1997)
CA Cancer J Clin.
, vol.47
, pp. 5-27
-
-
Parker, S.L.1
Tong, T.2
Bolden, S.3
-
4
-
-
0002405906
-
Epidemiologic studies
-
Balch CM, Houghton AN, Milton GW, et al (eds): Philadelphia, PA. Lippincott
-
Armstrong BK, English DR: Epidemiologic studies, in Balch CM, Houghton AN, Milton GW, et al (eds): Cutaneous Melanoma (ed 2). Philadelphia, PA. Lippincott, 1992, pp 12-26
-
(1992)
Cutaneous Melanoma (Ed 2)
, pp. 12-26
-
-
Armstrong, B.K.1
English, D.R.2
-
5
-
-
0001020051
-
Genetic aspects of malignant melanoma
-
Cawley EP: Genetic aspects of malignant melanoma. Arch Dermatol Syphilis 65:440-450, 1952
-
(1952)
Arch Dermatol Syphilis
, vol.65
, pp. 440-450
-
-
Cawley, E.P.1
-
6
-
-
0002941239
-
The hereditary variant of malignant melanoma
-
Clark WH Jr, Goldman LI, Mastrangelo MJ (eds): New York, NY, Grune Stratton
-
Greene MH, Fraumeni JF Jr: The hereditary variant of malignant melanoma, in Clark WH Jr, Goldman LI, Mastrangelo MJ (eds): Human Malignant Melanoma. New York, NY, Grune Stratton, 1979, pp 139-166
-
(1979)
Human Malignant Melanoma
, pp. 139-166
-
-
Greene, M.H.1
Fraumeni J.F., Jr.2
-
7
-
-
0015127330
-
Clinical characteristics of the genetic variety of cutaneous melanoma in man
-
Anderson DE: Clinical characteristics of the genetic variety of cutaneous melanoma in man. Cancer 28:721, 1971
-
(1971)
Cancer
, vol.28
, pp. 721
-
-
De Anderson1
-
9
-
-
0019404148
-
A genetic analysis of melanoma-polygenic inheritance as a threshold trait
-
Duggleby WF, Stoll H, Priore RL, et al: A genetic analysis of melanoma-polygenic inheritance as a threshold trait. Am J Epidemiol 114:61-72, 1981
-
(1981)
Am J Epidemiol
, vol.114
, pp. 61-72
-
-
Duggleby, W.F.1
Stoll, H.2
Priore, R.L.3
-
10
-
-
0017970363
-
Origin of familial malignant melanomas from heritable melanocytic lesions: The B-K mole syndrome
-
Clark WH Jr, Reimer RR, Greene M, et al: Origin of familial malignant melanomas from heritable melanocytic lesions: The B-K mole syndrome. Arch Dermatol 114:723-728, 1978
-
(1978)
Arch Dermatol
, vol.114
, pp. 723-728
-
-
Clark W.H., Jr.1
Reimer, R.R.2
Greene, M.3
-
11
-
-
0018123909
-
Familial atypical multiple mole-melanoma syndrome
-
Lynch HT, Frichot BC III, Lynch JF: Familial atypical multiple mole-melanoma syndrome. J Med Genet 15:352-356, 1978
-
(1978)
J Med Genet
, vol.15
, pp. 352-356
-
-
Lynch, H.T.1
Frichot B.C. III2
Lynch, J.F.3
-
12
-
-
0021774346
-
Prevalence of dysplastic nevi in a community practice
-
Crutcher WA, Sagebiel RW: Prevalence of dysplastic nevi in a community practice. Lancet 1:729, 1984
-
(1984)
Lancet
, vol.1
, pp. 729
-
-
Crutcher, W.A.1
Sagebiel, R.W.2
-
13
-
-
0024592959
-
The dysplastic melanocytic nevus: A prevalent lesion that correlates poorly with clinical phenotype
-
Piepkorn M, Meyer LJ, Goldgar D, et al: The dysplastic melanocytic nevus: A prevalent lesion that correlates poorly with clinical phenotype. J Am Acad Dermatol 20:407-415, 1989
-
(1989)
J Am Acad Dermatol
, vol.20
, pp. 407-415
-
-
Piepkorn, M.1
Meyer, L.J.2
Goldgar, D.3
-
14
-
-
0021063979
-
Familial cutaneous malignant melanoma: Autosomal dominant trait possibly linked to the Rh locus
-
Greene MH, Goldin LR, Clark WH Jr, et al: Familial cutaneous malignant melanoma: Autosomal dominant trait possibly linked to the Rh locus. Proc Natl Acad Sci USA 80:6071-6075, 1983
-
(1983)
Proc Natl Acad Sci USA
, vol.80
, pp. 6071-6075
-
-
Greene, M.H.1
Goldin, L.R.2
Clark W.H., Jr.3
-
15
-
-
0022542636
-
Cutaneous malignant melanoma and familial dysplastic nevi: Evidence for autosomal dominance and pleiotropy
-
Bale SJ, Chakravarti A, Greene MH: Cutaneous malignant melanoma and familial dysplastic nevi: Evidence for autosomal dominance and pleiotropy. Amer J Hum Genet 38:188-196, 1986
-
(1986)
Amer J Hum Genet
, vol.38
, pp. 188-196
-
-
Bale, S.J.1
Chakravarti, A.2
Greene, M.H.3
-
18
-
-
0027349349
-
Molecular genetics of malignant melanoma
-
Nathanson L (ed): Norwell, MA, Kluwer Academic
-
Albino AP, Fountain JW: Molecular genetics of malignant melanoma, in Nathanson L (ed): Current Research and Clinical Management of Melanoma. Norwell, MA, Kluwer Academic, 1993, pp 201-255
-
(1993)
Current Research and Clinical Management of Melanoma
, pp. 201-255
-
-
Albino, A.P.1
Fountain, J.W.2
-
19
-
-
0029148164
-
Cytogenetics of 158 patients with regional or disseminated melanoma
-
Thompson FH, Emerson J, Oison S, et al: Cytogenetics of 158 patients with regional or disseminated melanoma. Cancer Genet Cytogenet 83:93-104, 1995
-
(1995)
Cancer Genet Cytogenet
, vol.83
, pp. 93-104
-
-
Thompson, F.H.1
Emerson, J.2
Oison, S.3
-
20
-
-
0021916368
-
Loss of polymorphic restriction fragments in malignant melanoma: Implications for tumor heterogeneity
-
Dracopoli NC, Houghton AN, Old LJ: Loss of polymorphic restriction fragments in malignant melanoma: Implications for tumor heterogeneity. Proc Natl Acad Sci USA 82:1470-1474, 1985
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 1470-1474
-
-
Dracopoli, N.C.1
Houghton, A.N.2
Old, L.J.3
-
21
-
-
0013513408
-
Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression
-
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 86:4614-4618, 1989
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 4614-4618
-
-
Dracopoli, N.C.1
Harnett, P.2
Bale, S.J.3
-
22
-
-
0023224894
-
Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma
-
Dracopoli NC, Alhadeff B, Houghton AN, et al: Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma. Cancer Res 47:3995-4000, 1987
-
(1987)
Cancer Res
, vol.47
, pp. 3995-4000
-
-
Dracopoli, N.C.1
Alhadeff, B.2
Houghton, A.N.3
-
23
-
-
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 89:10557-10561, 1992
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 10557-10561
-
-
Fountain, J.W.1
Karayiorgou, M.2
Ernstoff, M.S.3
-
24
-
-
0344134771
-
The genetics of human cutaneous malignant melanoma
-
Balch CM, Houghton AN, Milton GW, et al (eds): Philadelphia, PA, Lippincott
-
Bale SJ, Dracopoli NC, Tucker MA: The genetics of human cutaneous malignant melanoma, in Balch CM, Houghton AN, Milton GW, et al (eds): Cutaneous Melanoma. Philadelphia, PA, Lippincott, 1992, pp 93-100
-
(1992)
Cutaneous Melanoma
, pp. 93-100
-
-
Bale, S.J.1
Dracopoli, N.C.2
Tucker, M.A.3
-
25
-
-
0023774804
-
A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome 1
-
Dracopoli NC, Stanger BZ, Ito CY, et al: A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome 1. Amer J Hum Genet 43:462-470, 1988
-
(1988)
Amer J Hum Genet
, vol.43
, pp. 462-470
-
-
Dracopoli, N.C.1
Stanger, B.Z.2
Ito, C.Y.3
-
26
-
-
0024320151
-
Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus syndrome to chromosome 1p
-
Bale SJ, Dracopoli NC, Tucker MA, et al: Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus syndrome 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
-
27
-
-
0024693775
-
Exclusion of the dysplastic naevus syndrome (DNS) 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 naevus syndrome (DNS) 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
-
28
-
-
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. Amer J Hum Genet 46:912-918, 1990
-
(1990)
Amer J Hum Genet
, vol.46
, pp. 912-918
-
-
Cannon-Albright, L.A.1
De Goldgar2
Wright, E.C.3
-
29
-
-
0025348509
-
Locus for susceptibility to melanoma on chromosome 1p
-
Gruis NA, Bergman W, Fronts RR: Locus for susceptibility to melanoma on chromosome 1p. 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
Fronts, R.R.3
-
30
-
-
0025977735
-
Hereditary melanoma in Australia: Variable association with dysplastic nevi and absence of genetic linkage to chromosome 1p
-
Kefford RF, Salmon J, Shaw HM, et al: 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
-
31
-
-
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
-
32
-
-
0027370901
-
Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity
-
Goldstein AM, Dracopoli NC, Ho EC, et al: Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity. Amer J Hum Genet 52:537-550, 1993
-
(1993)
Amer J Hum Genet
, vol.52
, pp. 537-550
-
-
Goldstein, A.M.1
Dracopoli, N.C.2
Ho, E.C.3
-
33
-
-
0028013327
-
Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity
-
Goldstein AM, Dracopoli NC, Engelstein M, et al: Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity. Amer J Hum Genet 54:489-496, 1994
-
(1994)
Amer J Hum Genet
, vol.54
, pp. 489-496
-
-
Goldstein, A.M.1
Dracopoli, N.C.2
Engelstein, M.3
-
34
-
-
0029883639
-
Two-locus linkage analysis of cutaneous malignant melanoma/dysplastic nevi
-
Goldstein AM, Goldin LR, Dracopoli NC, et al: 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
-
35
-
-
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
De Goldgar2
Meyer, L.J.3
-
36
-
-
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. Amer J Hum Genet 53:936-942, 1993
-
(1993)
Amer J Hum Genet
, vol.53
, pp. 936-942
-
-
Nancarrow, D.J.1
Mann, G.J.2
Holland, E.A.3
-
37
-
-
0027495164
-
Linkage analysis in Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families. Effect of nevus count
-
Gruis NA, Sandkuijl LA, Weber JL: Linkage analysis in Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families. Effect of nevus 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
-
38
-
-
0029614340
-
Recent advances in the molecular genetics of malignant melanoma
-
Ponder BAJ, Cavenee WK, Solomon E (eds): Cold Spring Harbor, Cold Spring Harbor Laboratory Press
-
Haluska FG, Housman DE: Recent advances in the molecular genetics of malignant melanoma, in Ponder BAJ, Cavenee WK, Solomon E (eds): Genetics and Cancer: A Second Look. Cancer Surveys. Cold Spring Harbor, Cold Spring Harbor Laboratory Press, 1995, pp 277-292
-
(1995)
Genetics and Cancer: A Second Look. Cancer Surveys
, pp. 277-292
-
-
Haluska, F.G.1
De Housman2
-
39
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Kamb A, Gruis N, Weaver-Feldhaus J, et al: A cell cycle regulator potentially involved in genesis of many tumor types. Science 264:436-440, 1994
-
(1994)
Science
, vol.264
, pp. 436-440
-
-
Kamb, A.1
Gruis, N.2
Weaver-Feldhaus, J.3
-
40
-
-
0028275733
-
Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
-
Nobori T, Miura K, Wu DJ, et al: 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
-
41
-
-
0027938209
-
Cyclins and cancer II: Cyclin D and CDK inhibitors come of age
-
Hunter T, Pines J: Cyclins and cancer II: Cyclin D and CDK inhibitors come of age. Cell 79:573-582, 1994
-
(1994)
Cell
, vol.79
, pp. 573-582
-
-
Hunter, T.1
Pines, J.2
-
42
-
-
0027301324
-
Subunit rearrangement of the cyclin-dependent kinases is associated with cellular transformation
-
Xiong Y, Zhang H, Beach D: Subunit rearrangement of the cyclin-dependent kinases is associated with cellular transformation. Genes Devel 7:1572-1583, 1993
-
(1993)
Genes Devel
, vol.7
, pp. 1572-1583
-
-
Xiong, Y.1
Zhang, H.2
Beach, D.3
-
43
-
-
0027769876
-
A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK 4
-
Serrano M, Hannon GJ, Beach D: A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK 4. Nature 366:704-707, 1993
-
(1993)
Nature
, vol.366
, pp. 704-707
-
-
Serrano, M.1
Hannon, G.J.2
Beach, D.3
-
44
-
-
0028168242
-
p15 INK4B is a potential effector of TGF-β-induced cell cycle arrest
-
Hannon GJ, Beach D: p15 INK4B is a potential effector of TGF-β-induced cell cycle arrest. Nature 371:257-261, 1994
-
(1994)
Nature
, vol.371
, pp. 257-261
-
-
Hannon, G.J.1
Beach, D.2
-
45
-
-
0028582034
-
INK4B/MTS2-related CDK6 inhibitor, correlates with wild-type pRb function
-
INK4B/MTS2-related CDK6 inhibitor, correlates with wild-type pRb function. Genes Devel 8:2939-2952, 1994
-
(1994)
Genes Devel
, vol.8
, pp. 2939-2952
-
-
Guan, K.-L.1
Jenkins, C.W.2
Li, Y.3
-
47
-
-
0029060657
-
Complex structure and regulation of the p16(MTS1) locus
-
Stone S, Jiang P, Dayananth P, et al: Complex structure and regulation of the p16(MTS1) locus. Cancer Res. 55:2988-2994, 1995
-
(1995)
Cancer Res.
, vol.55
, pp. 2988-2994
-
-
Stone, S.1
Jiang, P.2
Dayananth, P.3
-
48
-
-
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, et al: Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest. Cell 83:993-1000, 1995
-
(1995)
Cell
, vol.83
, pp. 993-1000
-
-
De Quelle1
Zindy, F.2
Ashmun, R.A.3
-
50
-
-
0028033422
-
Rates of p16(MTS1) mutations in primary tumors with 9p loss
-
Cairns P, Mao L, Merlo A, et al: Rates of p16(MTS1) mutations in primary tumors with 9p loss. Science 265:415-416, 1994
-
(1994)
Science
, vol.265
, pp. 415-416
-
-
Cairns, P.1
Mao, L.2
Merlo, A.3
-
51
-
-
0030025518
-
Compilation of somatic mutations of the CDKN2 gene in human cancers: Non-random distribution of base substitutions
-
Pollock PM, Pearson JV, Hayward NK: Compilation of somatic mutations of the CDKN2 gene in human cancers: Non-random distribution of base substitutions. Genes Chromosom Cancer 15:77-88, 1996
-
(1996)
Genes Chromosom Cancer
, vol.15
, pp. 77-88
-
-
Pollock, P.M.1
Pearson, J.V.2
Hayward, N.K.3
-
52
-
-
0029715628
-
CDKN2A (P16(INK4A)) somatic and germline mutations
-
Smith-Sorenson B, Hovig E: CDKN2A (P16(INK4A)) somatic and germline mutations. Hum Mutat 7:294-303, 1996
-
(1996)
Hum Mutat
, vol.7
, pp. 294-303
-
-
Smith-Sorenson, B.1
Hovig, E.2
-
54
-
-
0029658666
-
INK4b genes, as well as neighboring 9p21 markers, in sporadic melanoma
-
INK4b genes, as well as neighboring 9p21 markers, in sporadic melanoma. Cancer Res 56:5023-5032, 1996
-
(1996)
Cancer Res
, vol.56
, pp. 5023-5032
-
-
Flores, J.F.1
Walker, G.J.2
Glendening, J.M.3
-
55
-
-
0029011539
-
5′ CpG island methylation is associated with inactivation of the tumor suppressor CDKN2/p16 in human tumors
-
Merlo A, Herman J, Mao L, et al: 5′ CpG island methylation is associated with inactivation of the tumor suppressor CDKN2/p16 in human tumors. Nature Med 1:686-692, 1995
-
(1995)
Nature Med
, vol.1
, pp. 686-692
-
-
Merlo, A.1
Herman, J.2
Mao, L.3
-
57
-
-
0028845142
-
Inactivation of the CDKN2/p16MTS1 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/p16MTS1 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
-
58
-
-
0028875205
-
Methylation of the 5′ CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing
-
Gonzalez-Zulueta M, Bender CM, Yang AS, et al: Methylation of the 5′ CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing. Cancer Res 55:4531-4535, 1995
-
(1995)
Cancer Res
, vol.55
, pp. 4531-4535
-
-
Gonzalez-Zulueta, M.1
Bender, C.M.2
Yang, A.S.3
-
59
-
-
0029967152
-
Silencing of p16/CDKN2 expression in human gliomas by methylation and chromatin condensation
-
Costello JF, Berger MS, Huang H-JS, et al: Silencing of p16/CDKN2 expression in human gliomas by methylation and chromatin condensation. Cancer Res 56:2405-2410, 1996
-
(1996)
Cancer Res
, vol.56
, pp. 2405-2410
-
-
Costello, J.F.1
Berger, M.S.2
Huang, H.-J.S.3
-
60
-
-
9344271110
-
Hypermethylation of the p16 gene in nasopharyngeal carcinoma
-
Lo K-W, Cheung S-T, Leung S-F, et al: Hypermethylation of the p16 gene in nasopharyngeal carcinoma. Cancer Res 56:2721-2725, 1996
-
(1996)
Cancer Res
, vol.56
, pp. 2721-2725
-
-
Lo, K.-W.1
Cheung, S.-T.2
Leung, S.-F.3
-
61
-
-
0031035406
-
Frequent and selective methylation of p15 and deletion of both p15 and p16 in T-cell acute lymphoblastic leukemia
-
Batova A, Diccianni MB, Yu JC, et al: Frequent and selective methylation of p15 and deletion of both p15 and p16 in T-cell acute lymphoblastic leukemia. Cancer Res 57:832-836, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 832-836
-
-
Batova, A.1
Diccianni, M.B.2
Yu, J.C.3
-
62
-
-
0031030343
-
Deletion map of chromosome 9 and p16(CDKN2A) gene alterations in neuroblastoma
-
Takita J, Hayashi Y, Kohno T, et al: Deletion map of chromosome 9 and p16(CDKN2A) gene alterations in neuroblastoma. Cancer Res 57:907-912, 1997
-
(1997)
Cancer Res
, vol.57
, pp. 907-912
-
-
Takita, J.1
Hayashi, Y.2
Kohno, T.3
-
64
-
-
0028085975
-
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb A, Shattuck-Eidens D, Eelens R, et al: Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nature Genet 8:22-26, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 22-26
-
-
Kamb, A.1
Shattuck-Eidens, D.2
Eelens, R.3
-
65
-
-
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. Nature Genet 10:351-353, 1995
-
(1995)
Nature Genet
, vol.10
, pp. 351-353
-
-
Gruis, N.A.1
Van Der Velden, P.A.2
Sandkuijl, L.A.3
-
66
-
-
0001537730
-
Germ-line mutations in p16 and CDK4 genes in 38 melanoma families
-
Bressac-de Paillerets B, Soufir N, Chompret A, et al: Germ-line mutations in p16 and CDK4 genes in 38 melanoma families. Melanoma Res 7:S132, 1997 (supp. 1)
-
(1997)
Melanoma Res
, vol.7
, Issue.1 SUPPL.
-
-
Bressac-de Paillerets, B.1
Soufir, N.2
Chompret, A.3
-
67
-
-
0019785626
-
Tumour spectrum in the FAMMM syndrome
-
Lynch HT, Fusaro RM, Pester J, et al: Tumour spectrum in the FAMMM syndrome. Br J Cancer 44:553-560, 1981
-
(1981)
Br J Cancer
, vol.44
, pp. 553-560
-
-
Lynch, H.T.1
Fusaro, R.M.2
Pester, J.3
-
68
-
-
0025284650
-
Systemic cancer and the FAMMM syndrome
-
Bergman W, Watson P, de Jong J, et al: Systemic cancer and the FAMMM syndrome. Br J Cancer 61:932-936, 1990
-
(1990)
Br J Cancer
, vol.61
, pp. 932-936
-
-
Bergman, W.1
Watson, P.2
De Jong, J.3
-
69
-
-
84944282897
-
Familial malignant melanoma
-
Kopf AW, Hellman LJ, Rogers GS, et al: Familial malignant melanoma. JAMA 256:1915-1919, 1986
-
(1986)
JAMA
, vol.256
, pp. 1915-1919
-
-
Kopf, A.W.1
Hellman, L.J.2
Rogers, G.S.3
-
70
-
-
0029025203
-
Risks of second primary malignancy in patients with cutaneous and ocular melanoma
-
Swerdlow AJ, Storm HH, Sasieni PD: Risks of second primary malignancy in patients with cutaneous and ocular melanoma. Int J Cancer 61:773-779, 1995
-
(1995)
Int J Cancer
, vol.61
, pp. 773-779
-
-
Swerdlow, A.J.1
Storm, H.H.2
Sasieni, P.D.3
-
71
-
-
0028059330
-
Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma
-
Caldas C, Hahn S, da Costa L et al: Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma. Nature Genet 8:27-32, 1994
-
(1994)
Nature Genet
, vol.8
, pp. 27-32
-
-
Caldas, C.1
Hahn, S.2
Da Costa, L.3
-
73
-
-
0029102927
-
Brief report: A familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor suppressor gene
-
Whelan AJ, Bartsch D, Goodfellow PJ: Brief report: A familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor suppressor gene. N Engl J Med 333:975-977, 1995
-
(1995)
N Engl J Med
, vol.333
, pp. 975-977
-
-
Whelan, A.J.1
Bartsch, D.2
Goodfellow, P.J.3
-
76
-
-
0028138707
-
Higher frequency of alterations in the p16/CDKN2 gene in squamous cell carcinoma cell lines than in primary tumors of the head and neck
-
Zhang S-Y, Klein-Szanto AJP, Sauter ER, et al: Higher frequency of alterations in the p16/CDKN2 gene in squamous cell carcinoma cell lines than in primary tumors of the head and neck. Cancer Res 54:5050-5053, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 5050-5053
-
-
Zhang, S.-Y.1
Klein-Szanto, A.J.P.2
Sauter, E.R.3
-
77
-
-
0028338514
-
Frequent somatic mutations of the MTS1/CDK41 (multiple tumor suppressor/cyclin-dependent kinase 4 inhibitor) gene in esophageal squamous cell carcinoma
-
Mori T, Koh M, Aoki T, et al: Frequent somatic mutations of the MTS1/CDK41 (multiple tumor suppressor/cyclin-dependent kinase 4 inhibitor) gene in esophageal squamous cell carcinoma. Cancer Res 54:3396-3397, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 3396-3397
-
-
Mori, T.1
Koh, M.2
Aoki, T.3
-
78
-
-
0022623369
-
Second primary neoplasms in patients with retinoblastoma
-
Draper GJ, Sanders BM, Kingston JE: Second primary neoplasms in patients with retinoblastoma. Br J Cancer 53:661-671, 1986
-
(1986)
Br J Cancer
, vol.53
, pp. 661-671
-
-
Draper, G.J.1
Sanders, B.M.2
Kingston, J.E.3
-
79
-
-
0023936853
-
Non-ocular cancer in patients with hereditary retinoblastoma and their relatives
-
DerKinderen DJ, Koten JW, Nagelkerke NJD, et al: Non-ocular cancer in patients with hereditary retinoblastoma and their relatives. Int J Cancer 41:499-504, 1988
-
(1988)
Int J Cancer
, vol.41
, pp. 499-504
-
-
DerKinderen, D.J.1
Koten, J.W.2
Nagelkerke, N.J.D.3
-
80
-
-
0027172571
-
Mortality from second tumors among long-term survivors of retinoblastoma
-
Eng C, Li FP, Abramson DH, et al: Mortality from second tumors among long-term survivors of retinoblastoma. J Natl Cancer Inst 85:1121-1129, 1993
-
(1993)
J Natl Cancer Inst
, vol.85
, pp. 1121-1129
-
-
Eng, C.1
Li, F.P.2
Abramson, D.H.3
-
81
-
-
0028913458
-
Retinoblastoma, melanoma and the atypical mole syndrome
-
Bataille V, Hiles R, Bishop JAN: Retinoblastoma, melanoma and the atypical mole syndrome. Br J Dermatol 132:134-138, 1995
-
(1995)
Br J Dermatol
, vol.132
, pp. 134-138
-
-
Bataille, V.1
Hiles, R.2
Bishop, J.A.N.3
-
82
-
-
0025304297
-
Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells
-
Horowitz JM, Park S-H, Bogenmann E, et al: Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells. Proc Natl Acad Sci USA 87:2775-2779, 1990
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 2775-2779
-
-
Horowitz, J.M.1
Park, S.-H.2
Bogenmann, E.3
-
83
-
-
0029963811
-
Involvement of the pRb/p16/cdk4/cyclinD1 pathway in the tumorigenesis of sporadic malignant melanomas
-
Maelandsmo GM, Florenes VA, Hovig E, et al: Involvement of the pRb/p16/cdk4/cyclinD1 pathway in the tumorigenesis of sporadic malignant melanomas. Br J Cancer 73:909-916, 1996
-
(1996)
Br J Cancer
, vol.73
, pp. 909-916
-
-
Maelandsmo, G.M.1
Florenes, V.A.2
Hovig, E.3
-
84
-
-
0000852849
-
Identification of melanoma antigens recognized by T lymphocytes and their use in the immunotherapy of cancer
-
Kawakami Y, Robbins PF, Wang RF, et al: Identification of melanoma antigens recognized by T lymphocytes and their use in the immunotherapy of cancer. PPO Updates 10:1-20, 1996
-
(1996)
PPO Updates
, vol.10
, pp. 1-20
-
-
Kawakami, Y.1
Robbins, P.F.2
Wang, R.F.3
-
85
-
-
0028978274
-
INK4a-insensitive CDK4 mutant targeted by cytolytic T lymphocytes in a human melanoma
-
INK4a-insensitive CDK4 mutant targeted by cytolytic T lymphocytes in a human melanoma. Science 269:1281-1284, 1995
-
(1995)
Science
, vol.269
, pp. 1281-1284
-
-
Wolfel, T.1
Hauer, M.2
Schneider, J.3
-
86
-
-
0030467624
-
The p16-cyclin D/Cdk4-pRb pathway as a functional unit frequently altered in melanoma pathogenesis
-
Bartkova J, Lukas J, Guldberg P, et al: 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
-
87
-
-
0030917395
-
P16/CDKN2 and CDK4 gene mutations in sporadic melanoma development and progression
-
Piccinin S, Doglioni C, Maestro R, et al: p16/CDKN2 and CDK4 gene mutations in sporadic melanoma development and progression. Int J Cancer 74:26-30, 1997
-
(1997)
Int J Cancer
, vol.74
, pp. 26-30
-
-
Piccinin, S.1
Doglioni, C.2
Maestro, R.3
-
88
-
-
0029664339
-
INK4a binding domain of CDK4 in familial melanoma
-
INK4a binding domain of CDK4 in familial melanoma. Nature Genet 12:97-99, 1996
-
(1996)
Nature Genet
, vol.12
, pp. 97-99
-
-
Zuo, L.1
Weger, J.2
Yang, Q.3
-
89
-
-
9444276546
-
Prevalence of germ-line mutations in p16, p19ARF, and CDK4: 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: 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
-
90
-
-
0343527658
-
Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds
-
Hayward N, Flores J, Pollock P, et al: Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds. Melanoma Res 7 S37, 1997 (supp 1)
-
(1997)
Melanoma Res
, vol.7
, Issue.1 SUPPL.
-
-
Hayward, N.1
Flores, J.2
Pollock, P.3
-
91
-
-
0007965954
-
Mutation analysis of CDKN2A and CDK4 in familial melanoma
-
Holland EA, Becker TM, Kefford RF, et al: Mutation analysis of CDKN2A and CDK4 in familial melanoma. Melanoma Res 7 S133, 1997 (supp 1)
-
(1997)
Melanoma Res
, vol.7
, Issue.1 SUPPL.
-
-
Holland, E.A.1
Becker, T.M.2
Kefford, R.F.3
-
92
-
-
0344134758
-
Population based screening of germline mutations in the CDKN2A, CDKN2B, CDK4 and p53 genes in Swedish families with hereditary cutaneous melanoma
-
Platz A, Hansson J, Mansson-Brahme E, et al: Population based screening of germline mutations in the CDKN2A, CDKN2B, CDK4 and p53 genes in Swedish families with hereditary cutaneous melanoma. Melanoma Res 7 S37, 1997 (supp. 1)
-
(1997)
Melanoma Res
, vol.7
, Issue.1 SUPPL.
-
-
Platz, A.1
Hansson, J.2
Mansson-Brahme, E.3
-
93
-
-
0030912777
-
Clinically recognized dysplastic nevi: A central risk factor for cutaneous melanoma
-
Tucker MA, Halpern A, Holly EA, et al: Clinically recognized dysplastic nevi: A central risk factor for cutaneous melanoma. JAMA 277:1439-1444, 1997
-
(1997)
JAMA
, vol.277
, pp. 1439-1444
-
-
Tucker, M.A.1
Halpern, A.2
Holly, E.A.3
-
94
-
-
0030993087
-
Screening strategies for cancer: Implications and results
-
Chabner BA, Haluska FG, Talcott JA: Screening strategies for cancer: Implications and results. JAMA 277:1475-1476, 1997
-
(1997)
JAMA
, vol.277
, pp. 1475-1476
-
-
Chabner, B.A.1
Haluska, F.G.2
Talcott, J.A.3
-
95
-
-
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 89:697-702, 1997
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 697-702
-
-
Platz, A.1
Hansson, J.2
Mansson-Brahme, E.3
-
96
-
-
0028172648
-
Penetrance and expressivity of the chromosome 9p susceptibility locus
-
Cannon-Albright L, Meyer LJ, Goldgar DE, et al: Penetrance and expressivity of the chromosome 9p susceptibility locus. Cancer Res 54:6041-6044, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 6041-6044
-
-
Cannon-Albright, L.1
Meyer, L.J.2
Goldgar, D.E.3
-
97
-
-
0028971713
-
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds
-
Walker GJ, Hussussian CJ, Flores JF, et al: Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds. Hum Molec Genet 4:1845-1852, 1995
-
(1995)
Hum Molec Genet
, vol.4
, pp. 1845-1852
-
-
Walker, G.J.1
Hussussian, C.J.2
Flores, J.F.3
-
98
-
-
0029864134
-
Statement of the American Society of Clinical Oncology: Genetic testing for cancer susceptibility
-
American SoCO: Statement of the American Society of Clinical Oncology: Genetic testing for cancer susceptibility. J Clin Oncol 14:1730-1736, 1996
-
(1996)
J Clin Oncol
, vol.14
, pp. 1730-1736
-
-
-
99
-
-
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. Amer J Pathol 146:1199-1207, 1995
-
(1995)
Amer J Pathol
, vol.146
, pp. 1199-1207
-
-
Gruis, N.A.1
Weaver-Feldhaus, J.2
Liu, Q.3
-
100
-
-
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
-
101
-
-
0027946010
-
Rarity of somatic and germline mutations of the cyclin-dependent kinase 4 inhibitor gene. CDK4I, in melanoma
-
Ohta M, Nagai H, Shimizu M, et al: Rarity of somatic and germline mutations of the cyclin-dependent kinase 4 inhibitor gene. CDK4I, in melanoma. Cancer Res 54:5269-5272, 1994
-
(1994)
Cancer Res
, vol.54
, pp. 5269-5272
-
-
Ohta, M.1
Nagai, H.2
Shimizu, M.3
-
102
-
-
0029147195
-
Evidence for u.v. induction of CDKN2 mutations in melanoma cell lines
-
Pollock PM, Yu F, Qiu L, et al: 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
-
103
-
-
0028972730
-
INK4/MTS-1) gene in human melanoma cells: Relevance to tumor growth and metastasis
-
INK4/MTS-1) gene in human melanoma cells: Relevance to tumor growth and metastasis. Oncogene 11:1399-1402, 1995
-
(1995)
Oncogene
, vol.11
, pp. 1399-1402
-
-
Luca, M.1
Xie, S.2
Gutman, M.3
-
104
-
-
0030067374
-
Mutational analysis of the CDKN2 gene in metastasis from patients with cutaneous malignant melanoma
-
Platz A, Ringborg U, Lagerlof B, et al: Mutational analysis of the CDKN2 gene in metastasis from patients with cutaneous malignant melanoma. Br J Cancer 73:344-348, 1996
-
(1996)
Br J Cancer
, vol.73
, pp. 344-348
-
-
Platz, A.1
Ringborg, U.2
Lagerlof, B.3
-
106
-
-
0028981664
-
Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma
-
Liu L, Lassam NJ, Slingerland JM, et al: 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
-
107
-
-
0029562169
-
Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds
-
Holland EA, Beaton SC, Becker TM, et al: Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds. Oncogene 11:2289-2294, 1995
-
(1995)
Oncogene
, vol.11
, pp. 2289-2294
-
-
Holland, E.A.1
Beaton, S.C.2
Becker, T.M.3
-
108
-
-
0029891364
-
Novel germline p16 mutation in familial malignant melanoma in southern Sweden
-
Borg A, Johansson U, Johannsson O, et al: Novel germline p16 mutation in familial malignant melanoma in southern Sweden. Cancer Res 56:2497-2500, 1996
-
(1996)
Cancer Res
, vol.56
, pp. 2497-2500
-
-
Borg, A.1
Johansson, U.2
Johannsson, O.3
|