-
1
-
-
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, N.A., Sandkuijl, L.A. & Frants, R.R. 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
-
2
-
-
0028013327
-
Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity
-
Goldstein, A.M. et al. Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity. Am. J. Hum. Genet. 54, 489-496 (1994).
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 489-496
-
-
Goldstein, A.M.1
-
3
-
-
0022542636
-
Cutaneous malignant melanoma and familial dysplastic nevi: Evidence for autosomal dominance and pleiotropy
-
Bale, S.J., Chakravarti, A. & Greene, M.H. Cutaneous malignant melanoma and familial dysplastic nevi: evidence for autosomal dominance and pleiotropy. Am. J. Hum. Genet. 38, 188-196 (1986).
-
(1986)
Am. J. Hum. Genet.
, vol.38
, pp. 188-196
-
-
Bale, S.J.1
Chakravarti, A.2
Greene, M.H.3
-
4
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22
-
Cannon-Albright, L.A. 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
-
5
-
-
0028172648
-
Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM)
-
Cannon-Albright, L.A. et al. Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM). Cancer Res. 54, 6041-6044 (1994).
-
(1994)
Cancer Res.
, vol.54
, pp. 6041-6044
-
-
Cannon-Albright, L.A.1
-
6
-
-
0027989888
-
Age at diagnosis and transmission of invasive melanoma in 23 families with cutaneous malignant melanoma/dysplastic nevi
-
Goldstein, A.M., Fraser, M.C., Clark, W.H. Jr & Tucker, M.A. Age at diagnosis and transmission of invasive melanoma in 23 families with cutaneous malignant melanoma/dysplastic nevi. J. Natl Cancer. Inst. 86, 1385-1390 (1994).
-
(1994)
J. Natl Cancer. Inst.
, vol.86
, pp. 1385-1390
-
-
Goldstein, A.M.1
Fraser, M.C.2
Clark W.H., Jr.3
Tucker, M.A.4
-
7
-
-
0029119849
-
Genetic epidemiology of familial melanoma
-
Goldstein, A.M. & Tucker, M.A. Genetic epidemiology of familial melanoma. Dermatol. Clin. 13, 605-612 (1995).
-
(1995)
Dermatol. Clin.
, vol.13
, pp. 605-612
-
-
Goldstein, A.M.1
Tucker, M.A.2
-
8
-
-
0031749061
-
Role of the cyclin-dependent kinase inhibitor CDKN2A in familial melanoma
-
Hogg, D. et al. Role of the cyclin-dependent kinase inhibitor CDKN2A in familial melanoma. J. Cutan. Med. Surg. 2, 172-179 (1998).
-
(1998)
J. Cutan. Med. Surg.
, vol.2
, pp. 172-179
-
-
Hogg, D.1
-
9
-
-
0029947139
-
The current situation with regard to human melanoma and genetic inferences
-
Hayward, N.K. The current situation with regard to human melanoma and genetic inferences. Curr. Opin. Oncol. B, 136-142 (1996).
-
(1996)
Curr. Opin. Oncol.
, vol.8
, pp. 136-142
-
-
Hayward, N.K.1
-
10
-
-
0028940722
-
Cell-cycle regulators and cancer
-
Kamb, A. Cell-cycle regulators and cancer. Trends Genet. 11, 136-140 (1995).
-
(1995)
Trends Genet.
, vol.11
, pp. 136-140
-
-
Kamb, A.1
-
11
-
-
0028988585
-
Inhibitors of mammalian G1 cyclin-dependent kinases
-
Sherr, C.J. & Roberts, J.M. Inhibitors of mammalian G1 cyclin-dependent kinases. Genes Dev. 9, 1149-1163 (1995).
-
(1995)
Genes Dev.
, vol.9
, pp. 1149-1163
-
-
Sherr, C.J.1
Roberts, J.M.2
-
12
-
-
0029849620
-
Cancer cell cycles
-
Sherr, C.J. Cancer cell cycles. Science 274, 1672-1677 (1996).
-
(1996)
Science
, vol.274
, pp. 1672-1677
-
-
Sherr, C.J.1
-
13
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian, C.J. et al. Germline p16 mutations in familial melanoma. Nature Genet. 8, 15-21 (1994).
-
(1994)
Nature Genet.
, vol.8
, pp. 15-21
-
-
Hussussian, C.J.1
-
14
-
-
0028085975
-
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb, A. et al. Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nature Genet. 8, 23-26 (1994).
-
(1994)
Nature Genet.
, vol.8
, pp. 23-26
-
-
Kamb, A.1
-
15
-
-
0029038538
-
CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families
-
Gruis, N.A., Sandkuijl, L.A., van der Velden, P.A., Bergman, W. & Frants, R.R. CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. Melanoma Res. 5, 169-177 (1995).
-
(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
-
16
-
-
0029562169
-
Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds
-
Holland, E.A. 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
-
17
-
-
0028971713
-
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds
-
Walker, G.J. et al. Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds. Hum. Mol. Genet. 4, 1845-1852 (1995).
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1845-1852
-
-
Walker, G.J.1
-
18
-
-
0028981664
-
Germline p16INK4A mutation and protein dysfunction in a family with inherited melanoma
-
Liu, L. 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
-
19
-
-
9444276546
-
Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: Analysis of a clinic-based population
-
FitzGerald, M.G. 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
-
20
-
-
0032568258
-
CDKN2A mutations in multiple primary melanomas
-
Monzon, J. et al. CDKN2A mutations in multiple primary melanomas. N. Engl. J. Med. 338, 879-887 (1998).
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 879-887
-
-
Monzon, J.1
-
21
-
-
0026649524
-
Mutation creates an open reading frame within the 5′ untranslated region of macaque erythrocyte carbonic anhydrase (CA) I mRNA that suppresses CA I expression and supports the scanning model for translation
-
Bergenhem, N.C., Venta, P.J., Hopkins, P.J., Kim, H.J. & Tashian, R.E. Mutation creates an open reading frame within the 5′ untranslated region of macaque erythrocyte carbonic anhydrase (CA) I mRNA that suppresses CA I expression and supports the scanning model for translation. Proc. Natl Acad. Sci. USA 89, 8798-8802 (1992).
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.89
, pp. 8798-8802
-
-
Bergenhem, N.C.1
Venta, P.J.2
Hopkins, P.J.3
Kim, H.J.4
Tashian, R.E.5
-
22
-
-
0031838353
-
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
-
Krude, H. et al. Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. Nature Genet. 19, 155-157 (1998).
-
(1998)
Nature Genet.
, vol.19
, pp. 155-157
-
-
Krude, H.1
-
23
-
-
7144229363
-
Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations
-
Pollock, P.M. 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
-
24
-
-
0028566386
-
Genetic heterogeneity in familial malignant melanoma
-
MacGeoch, C. 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
-
25
-
-
0029891364
-
Novel germline p16 mutation in familial malignant melanoma in southern Sweden
-
Borg, A. 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
|