-
1
-
-
0028971713
-
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds
-
Walker GJ, Hussussian CJ, Flores JF, Glendening JM, Haluska FG, Dracopoli NC, et al. Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds. Hum Mol Genet 1995;4:1845-52.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1845-1852
-
-
Walker, G.J.1
Hussussian, C.J.2
Flores, J.F.3
Glendening, J.M.4
Haluska, F.G.5
Dracopoli, N.C.6
-
2
-
-
0029562169
-
Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds
-
Holland EA, Beaton SC, Becker TM, Grulet OM, Peters BA, Rizos H, et al. Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds. Oncogene 1995;11:.2289-94.
-
(1995)
Oncogene
, vol.11
, pp. 2289-2294
-
-
Holland, E.A.1
Beaton, S.C.2
Becker, T.M.3
Grulet, O.M.4
Peters, B.A.5
Rizos, H.6
-
3
-
-
0031441652
-
Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds
-
Flores JF, Pollock PM, Walker GJ, Glendening JM, Lin AH, Palmer JM, et al. Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds. Oncogene 1997;15:2999-3005.
-
(1997)
Oncogene
, vol.15
, pp. 2999-3005
-
-
Flores, J.F.1
Pollock, P.M.2
Walker, G.J.3
Glendening, J.M.4
Lin, A.H.5
Palmer, J.M.6
-
4
-
-
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 1995;5:169-77.
-
(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
-
5
-
-
9844219745
-
Germline mutations of the CDKN2 gene in UK melanoma families
-
Harland M, Meloni R, Gruis N, Pinney E, Brookes S, Spurr NK, et al. Germline mutations of the CDKN2 gene in UK melanoma families. Hum Mol Genet 1997;6:2061-7.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2061-2067
-
-
Harland, M.1
Meloni, R.2
Gruis, N.3
Pinney, E.4
Brookes, S.5
Spurr, N.K.6
-
6
-
-
6844226190
-
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France
-
Soufir N, Avril MF, Chompret A, Demenais F, Bombled J, Spatz A, 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
Bombled, J.5
Spatz, A.6
-
7
-
-
0030056309
-
Familial melanoma and pancreatic cancer. Ligurian Skin Tumor Study Group
-
Ciotti P, Strigini P, Bianchi-Scarra G. Familial melanoma and pancreatic cancer. Ligurian Skin Tumor Study Group [letter]. N Engl J Med 1996; 334:469-70.
-
(1996)
N Engl J Med
, vol.334
, pp. 469-470
-
-
Ciotti, P.1
Strigini, P.2
Bianchi-Scarra, G.3
-
8
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian CJ, Struewing JP, Goldstein AM, Higgins PA, Ally DS, Sheahan MD, et al. Germline p16 mutations in familial melanoma. Nat Genet 1994;8:15-21.
-
(1994)
Nat Genet
, vol.8
, pp. 15-21
-
-
Hussussian, C.J.1
Struewing, J.P.2
Goldstein, A.M.3
Higgins, P.A.4
Ally, D.S.5
Sheahan, M.D.6
-
9
-
-
0028085975
-
Analysis of the p16 gene (CDKN2A) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis NA, Ding W, et al. Analysis of the p16 gene (CDKN2A) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet 1994;8:23-6.
-
(1994)
Nat Genet
, vol.8
, pp. 23-26
-
-
Kamb, A.1
Shattuck-Eidens, D.2
Eeles, R.3
Liu, Q.4
Gruis, N.A.5
Ding, W.6
-
10
-
-
0027946010
-
Rarity of somatic and germline mutations of the cyclin-dependent kinase 4 inhibitor gene, CDK4I, in melanoma
-
Ohta M, Nagai H, Shimizu M, Rasio D, Berd D, Mastrangelo M, et al. Rarity of somatic and germline mutations of the cyclin-dependent kinase 4 inhibitor gene, CDK4I, in melanoma. Cancer Res 1994;54:5269-72.
-
(1994)
Cancer Res
, vol.54
, pp. 5269-5272
-
-
Ohta, M.1
Nagai, H.2
Shimizu, M.3
Rasio, D.4
Berd, D.5
Mastrangelo, M.6
-
12
-
-
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, MacDonald DJ, Lucchina LC, Unsal H, 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 U S A 1996;93:8541-5.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 8541-8545
-
-
Fitzgerald, M.G.1
Harkin, D.P.2
Silva-Arrieta, S.3
MacDonald, D.J.4
Lucchina, L.C.5
Unsal, H.6
-
13
-
-
0029891364
-
Novel germline p16 mutation in familial malignant melanoma in southern Sweden
-
Borg A, Johannsson U, Johannsson O, Hakansson S, Westerdahl J, Masback A, et al. Novel germline p16 mutation in familial malignant melanoma in southern Sweden. Cancer Res 1996;56:2497-500.
-
(1996)
Cancer Res
, vol.56
, pp. 2497-2500
-
-
Borg, A.1
Johannsson, U.2
Johannsson, O.3
Hakansson, S.4
Westerdahl, J.5
Masback, A.6
-
14
-
-
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, Lagerlof B, Linder S, Lundqvist 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
Lagerlof, B.4
Linder, S.5
Lundqvist, E.6
-
16
-
-
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 Chromosomes Cancer 1996;15:77-88.
-
(1996)
Genes Chromosomes Cancer
, vol.15
, pp. 77-88
-
-
Pollock, P.M.1
Pearson, J.V.2
Hayward, N.K.3
-
17
-
-
0028998866
-
Mutations associated with familial melanoma impair p16INK4 function
-
Ranade K, Hussussian CJ, Sikorski RS, Varmus HE, Goldstein AM, Tucker MA, et al. Mutations associated with familial melanoma impair p16INK4 function [letter]. Nat Genet 1995;10:114-6.
-
(1995)
Nat Genet
, vol.10
, pp. 114-116
-
-
Ranade, K.1
Hussussian, C.J.2
Sikorski, R.S.3
Varmus, H.E.4
Goldstein, A.M.5
Tucker, M.A.6
-
18
-
-
0028971677
-
P16 proteins from melanoma-prone families are deficient in binding to Cdk4
-
Reymond A, Brent R. p16 proteins from melanoma-prone families are deficient in binding to Cdk4. Oncogene 1995;11:1173-8.
-
(1995)
Oncogene
, vol.11
, pp. 1173-1178
-
-
Reymond, A.1
Brent, R.2
-
19
-
-
0029052951
-
Tumour-derived p16 alleles encoding proteins defective in cell-cycle inhibition
-
Koh J, Enders GH, Dynlacht BD, Harlow E. Tumour-derived p16 alleles encoding proteins defective in cell-cycle inhibition. Nature 1995;375: 506-10.
-
(1995)
Nature
, vol.375
, pp. 506-510
-
-
Koh, J.1
Enders, G.H.2
Dynlacht, B.D.3
Harlow, E.4
-
20
-
-
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, et al. Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma. Oncogene 1995;11:405-12.
-
(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
-
22
-
-
17744405579
-
CDKN2A mutation in a non-FAMMM kindred with cancers at multiple sites results in a functionally abnormal protein
-
Sun S, Pollock PM, Liu L, Karimi S, Jothy S, Milner BJ, et al. CDKN2A mutation in a non-FAMMM kindred with cancers at multiple sites results in a functionally abnormal protein. Int J Cancer 1997;73:531-6.
-
(1997)
Int J Cancer
, vol.73
, pp. 531-536
-
-
Sun, S.1
Pollock, P.M.2
Liu, L.3
Karimi, S.4
Jothy, S.5
Milner, B.J.6
-
23
-
-
0028073074
-
Heterogeneity of melanoma risk in families of melanoma patients
-
Aitken JF, Duffy DL, Green A, Youl P, MacLennan R, Martin NG. Heterogeneity of melanoma risk in families of melanoma patients. Am J Epidemiol 1994;140:961-73.
-
(1994)
Am J Epidemiol
, vol.140
, pp. 961-973
-
-
Aitken, J.F.1
Duffy, D.L.2
Green, A.3
Youl, P.4
MacLennan, R.5
Martin, N.G.6
-
24
-
-
0029739140
-
The Queensland familial melanoma project: Study design and characteristics of participants
-
Aitken JF, Green AC, MacLennan R, Youl P, Martin NG. The Queensland Familial Melanoma Project: study design and characteristics of participants. Melanoma Res 1996;6:155-65.
-
(1996)
Melanoma Res
, vol.6
, pp. 155-165
-
-
Aitken, J.F.1
Green, A.C.2
MacLennan, R.3
Youl, P.4
Martin, N.G.5
-
25
-
-
0029787393
-
Accuracy of case-reported family history of melanoma in Queensland, Australia
-
Aitken JF, Youl P, Green A, MacLennan R, Martin NG. Accuracy of case-reported family history of melanoma in Queensland, Australia. Melanoma Res 1996;6:313-7.
-
(1996)
Melanoma Res
, vol.6
, pp. 313-317
-
-
Aitken, J.F.1
Youl, P.2
Green, A.3
MacLennan, R.4
Martin, N.G.5
-
26
-
-
0017714879
-
Ascertainment in the sequential sampling of pedigrees
-
Cannings C, Thompson EA. Ascertainment in the sequential sampling of pedigrees. Clin Genet 1977;12:208-12.
-
(1977)
Clin Genet
, vol.12
, pp. 208-212
-
-
Cannings, C.1
Thompson, E.A.2
-
27
-
-
0027316177
-
Comparability of surrogate and self-reported information on melanoma risk factors
-
Aitken JF, Green A, MacLennan R, Jackman L, Martin NG. Comparability of surrogate and self-reported information on melanoma risk factors. Br J Cancer 1993;67:1036-41.
-
(1993)
Br J Cancer
, vol.67
, pp. 1036-1041
-
-
Aitken, J.F.1
Green, A.2
MacLennan, R.3
Jackman, L.4
Martin, N.G.5
-
28
-
-
0030734275
-
Genetic and environmental contributions to alcohol dependence risk in a national twin sample: Consistency of findings in women and men
-
Heath AC, Bucholz KK, Madden PA, Dinwiddie SH, Slutske WS, Bierut LJ, et al. Genetic and environmental contributions to alcohol dependence risk in a national twin sample: consistency of findings in women and men. Psychol Med 1997;27:1381-96.
-
(1997)
Psychol Med
, vol.27
, pp. 1381-1396
-
-
Heath, A.C.1
Bucholz, K.K.2
Madden, P.A.3
Dinwiddie, S.H.4
Slutske, W.S.5
Bierut, L.J.6
-
29
-
-
0022498988
-
The causes of malignant melanoma: Results from the West Australian lions melanoma research project
-
Holman CD, Armstrong BK, Heenan PJ, Blackwell JB, Cumming FJ, English DR, et al. The causes of malignant melanoma: results from the West Australian Lions Melanoma Research Project. Recent Results Cancer Res 1986;102:18-37.
-
(1986)
Recent Results Cancer Res
, vol.102
, pp. 18-37
-
-
Holman, C.D.1
Armstrong, B.K.2
Heenan, P.J.3
Blackwell, J.B.4
Cumming, F.J.5
English, D.R.6
-
30
-
-
0029122011
-
Risk of cutaneous melanoma associated with a family history of the disease. The International Melanoma Analysis Group (IMAGE)
-
Ford D, Bliss JM, Swerdlow AJ, Armstrong BK, Franceschi S, Green A, et al. Risk of cutaneous melanoma associated with a family history of the disease. The International Melanoma Analysis Group (IMAGE). Int J Cancer 1995;62:377-81.
-
(1995)
Int J Cancer
, vol.62
, pp. 377-381
-
-
Ford, D.1
Bliss, J.M.2
Swerdlow, A.J.3
Armstrong, B.K.4
Franceschi, S.5
Green, A.6
-
31
-
-
0029153708
-
Risk of cutaneous melanoma associated with pigmentation characteristics and freckling: Systematic overview of 10 case-control studies. The International Melanoma Analysis Group (IMAGE)
-
Bliss JM, Ford D, Swerdlow AJ, Armstrong BK, Cristofolini M, Elwood JM, et al. Risk of cutaneous melanoma associated with pigmentation characteristics and freckling: systematic overview of 10 case-control studies. The International Melanoma Analysis Group (IMAGE). Int J Cancer 1995; 62:367-76.
-
(1995)
Int J Cancer
, vol.62
, pp. 367-376
-
-
Bliss, J.M.1
Ford, D.2
Swerdlow, A.J.3
Armstrong, B.K.4
Cristofolini, M.5
Elwood, J.M.6
-
32
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16: 1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
33
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Kamb A, Gruis NA, Weaver-Feldhaus J, Liu Q, Harshman K, Tavtigian SV, et al. A cell cycle regulator potentially involved in genesis of many tumor types. Science 1994;264:436-40.
-
(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
-
36
-
-
0023894935
-
The affected-pedigree-member method of linkage analysis
-
Weeks DE, Lange K. The affected-pedigree-member method of linkage analysis. Am J Hum Genet 1988;42:315-26.
-
(1988)
Am J Hum Genet
, vol.42
, pp. 315-326
-
-
Weeks, D.E.1
Lange, K.2
-
37
-
-
0024190141
-
Programs for pedigree analysis: MENDEL, FISHER and dGENE
-
Lange K, Weeks D, Boenhke M. Programs for pedigree analysis: MENDEL, FISHER and dGENE. Genet Epidemiol 1998;5:471-2.
-
(1998)
Genet Epidemiol
, vol.5
, pp. 471-472
-
-
Lange, K.1
Weeks, D.2
Boenhke, M.3
-
38
-
-
0025964920
-
Allele frequency estimation from data on relatives
-
Boehnke M. Allele frequency estimation from data on relatives. Am J Hum Genet 1991;48:22-5.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 22-25
-
-
Boehnke, M.1
-
39
-
-
0031253976
-
Germline CDKN2A mutations in childhood melanoma
-
Whiteman DC, Milligan A, Welch J, Green AC, Hayward NK. Germline CDKN2A mutations in childhood melanoma [letter]. J Natl Cancer Inst 1997;89:1460.
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 1460
-
-
Whiteman, D.C.1
Milligan, A.2
Welch, J.3
Green, A.C.4
Hayward, N.K.5
-
40
-
-
0032568258
-
CDKN2A mutations in multiple primary melanomas
-
Monzon J, Liu L, Brill H, Goldstein AM, Tucker MA, From L, et al. CDKN2A mutations in multiple primary melanomas. N Engl J Med 1998; 338:879-87.
-
(1998)
N Engl J Med
, vol.338
, pp. 879-887
-
-
Monzon, J.1
Liu, L.2
Brill, H.3
Goldstein, A.M.4
Tucker, M.A.5
From, L.6
-
41
-
-
15444350658
-
Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors
-
Bahuau M, Vidaud D, Jenkins R, Bieche I, Kimmel DW, Assouline B, et al. Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors. Cancer Res 1998;58:2298-303.
-
(1998)
Cancer Res
, vol.58
, pp. 2298-2303
-
-
Bahuau, M.1
Vidaud, D.2
Jenkins, R.3
Bieche, I.4
Kimmel, D.W.5
Assouline, B.6
-
42
-
-
0030728259
-
CDKN2A/p16 is inactivated in most melanoma cell lines
-
Castellano M, Pollock PM, Walters MK, Sparrow LE, Down LM, Gabrielli BG, et al. CDKN2A/p16 is inactivated in most melanoma cell lines. Cancer Res 1997;57:4868-75.
-
(1997)
Cancer Res
, vol.57
, pp. 4868-4875
-
-
Castellano, M.1
Pollock, P.M.2
Walters, M.K.3
Sparrow, L.E.4
Down, L.M.5
Gabrielli, B.G.6
-
43
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and Insulin-dependent Diabetes Mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993;52:506-16.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
44
-
-
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 1997;6:1891-7.
-
(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
-
45
-
-
0029839525
-
The Asp84Glu variant of the Melanocortin 1 Receptor (MC1R) is associated with melanoma
-
Valverde P, Healy E, Sikkink S, Haldane F, Thody AJ, Carothers A, et al. The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma. Hum Mol Genet 1996;5:1663-6.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1663-1666
-
-
Valverde, P.1
Healy, E.2
Sikkink, S.3
Haldane, F.4
Thody, A.J.5
Carothers, A.6
|