-
1
-
-
0031014450
-
Cancer statistics, 1997
-
Parker,S.L., Tong,T., Bolden,S. and Wingo,P.A. (1997) Cancer statistics, 1997. CA Cancer J. Clin., 47, 5-27.
-
(1997)
CA Cancer J. Clin.
, vol.47
, pp. 5-27
-
-
Parker, S.L.1
Tong, T.2
Bolden, S.3
Wingo, P.A.4
-
2
-
-
0003627457
-
-
Editions INSERM, Paris, France
-
de Vathaire,F., Koscielny,S., Rezvani,A., Laplanche,A., Estève,J. and Ferlay,J. (1996) Estimation de l'Incidence des Cancers en France, 1983-1987. Editions INSERM, Paris, France.
-
(1996)
Estimation de l'Incidence des Cancers en France, 1983-1987
-
-
De Vathaire, F.1
Koscielny, S.2
Rezvani, A.3
Laplanche, A.4
Estève, J.5
Ferlay, J.6
-
3
-
-
0001020051
-
Genetic aspects of malignant melanoma
-
Cawley,E.P. (1952) Genetic aspects of malignant melanoma. Arch. Dermatol., 65, 440-450.
-
(1952)
Arch. Dermatol.
, vol.65
, pp. 440-450
-
-
Cawley, E.P.1
-
4
-
-
0002941239
-
The hereditary variant of familial melanoma
-
Clark,W.H.,Jr, Goldman,L.I. and Mastrangelo,M.J. (eds), Grune and Stratton, New York, NY
-
Greene,M.H. and Fraumeni,J.F. (1979) The hereditary variant of familial melanoma. In Clark,W.H.,Jr, Goldman,L.I. and Mastrangelo,M.J. (eds), Human Malignant Melanoma. Grune and Stratton, New York, NY, pp. 139-166.
-
(1979)
Human Malignant Melanoma
, pp. 139-166
-
-
Greene, M.H.1
Fraumeni, J.F.2
-
5
-
-
0029130598
-
Comparison between familial and non familial melanoma in France
-
Grange,F., Chompret,A., Guilloud-Bataille,M., Guillaume,J.-C., Margulis,A., Prade,M., Demenais,F. and Avril,M.F. (1995) Comparison between familial and non familial melanoma in France. Arch. Dermatol., 131, 1154-1159.
-
(1995)
Arch. Dermatol.
, vol.131
, pp. 1154-1159
-
-
Grange, F.1
Chompret, A.2
Guilloud-Bataille, M.3
Guillaume, J.-C.4
Margulis, A.5
Prade, M.6
Demenais, F.7
Avril, M.F.8
-
6
-
-
0029739140
-
The Queensland familial melanoma project: Study design and characteristics of participants
-
Aitken,J.F., Green,A.C., MacLennan,R., Youl,P. and Martin,N.G. (1996) The Queensland familial melanoma project: study design and characteristics of participants. Melanoma Res., 6, 155-165.
-
(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
-
7
-
-
0026483716
-
Homozygous deletions within human chromosome band 9p21 in melanoma
-
Fountain,J.W., Karayiorgou,M., Ernstoff,M.S., Kirkwood,J.M., Vlock,D.R., Titus-Ernstoff,L., Bouchard,B., Vijayasaradhi,S., Houghton,A.N., Lahti,J., Kidd,V.J., Housman,D.E. and Dracopoli,N.C. (1992) Homozygous deletions within human chromosome band 9p21 in melanoma. Proc. Natl Acad. Sci. USA, 89, 10557-10561.
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.89
, pp. 10557-10561
-
-
Fountain, J.W.1
Karayiorgou, M.2
Ernstoff, M.S.3
Kirkwood, J.M.4
Vlock, D.R.5
Titus-Ernstoff, L.6
Bouchard, B.7
Vijayasaradhi, S.8
Houghton, A.N.9
Lahti, J.10
Kidd, V.J.11
Housman, D.E.12
Dracopoli, N.C.13
-
8
-
-
0027420429
-
Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: Implications for 9p tumor-suppressor gene(s)
-
Petty,E.M., Gibson,L.H., Fountain,J.W., Bolognia,J.L., Yang-Feng,T.L., Housman,D.E. and Bale,A.E. (1993) Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s). Am. J. Hum. Genet., 53, 96-104.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 96-104
-
-
Petty, E.M.1
Gibson, L.H.2
Fountain, J.W.3
Bolognia, J.L.4
Yang-Feng, T.L.5
Housman, D.E.6
Bale, A.E.7
-
9
-
-
0027507837
-
Confirmation of chromosome 9p linkage in familial melanoma
-
Nancarrow,D.J., Mann,G.J., Holland,E., Walker,G.J., Beaton,S.C., Walters,M.K., Luxford,C., Palmer,J.M., Donald,J.A., Weber,J.L., Fountain,J.W., Kefford,R.F. and Hayward,N.K. (1993) Confirmation of chromosome 9p linkage in familial melanoma. Am. J. Hum. Genet., 53, 936-942.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 936-942
-
-
Nancarrow, D.J.1
Mann, G.J.2
Holland, E.3
Walker, G.J.4
Beaton, S.C.5
Walters, M.K.6
Luxford, C.7
Palmer, J.M.8
Donald, J.A.9
Weber, J.L.10
Fountain, J.W.11
Kefford, R.F.12
Hayward, N.K.13
-
10
-
-
0028013327
-
Linkage of cutaneous malignant melanoma/ dysplastic nevi to chromosome 9p and evidence for genetic heterogeneity
-
Goldstein,A.M., Dracopoli,N.C., Engelstein,M., Fraser,M.C., Clark,W.H.,Jr and Tucker,M.A. (1994) Linkage of cutaneous malignant melanoma/ dysplastic nevi to chromosome 9p and evidence for genetic heterogeneity. Am. J. Hum. Genet., 54, 489-496.
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 489-496
-
-
Goldstein, A.M.1
Dracopoli, N.C.2
Engelstein, M.3
Fraser, M.C.4
Clark Jr., W.H.5
Tucker, M.A.6
-
11
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22
-
Cannon-Albright,L.A., Goldgar,D.E., Meyer,L.J., Lewis,C.M., Anderson,D.E., Fountain,J.W., Hegi,M.E., Wiseman,R.W., Petty,E.M., Bale,A.E., Olopade,O.I., Diaz,M.O., Kwiatkowski,D.J., Piepkorn,M.W., Zone,J.J. and Skolnick,M.H. (1992) Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22. Science, 258, 1148-1152.
-
(1992)
Science
, vol.258
, pp. 1148-1152
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
Lewis, C.M.4
Anderson, D.E.5
Fountain, J.W.6
Hegi, M.E.7
Wiseman, R.W.8
Petty, E.M.9
Bale, A.E.10
Olopade, O.I.11
Diaz, M.O.12
Kwiatkowski, D.J.13
Piepkorn, M.W.14
Zone, J.J.15
Skolnick, M.H.16
-
12
-
-
0027769876
-
A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4
-
Serrano,M., Hannon,G.J. and Beach,D. (1993) A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4. Nature, 366, 704-707.
-
(1993)
Nature
, vol.366
, pp. 704-707
-
-
Serrano, M.1
Hannon, G.J.2
Beach, D.3
-
13
-
-
0028121279
-
A cell cycle regulator potentially involved in genesis of many tumor types
-
Kamb,A., Gruis,N.A., Weaver-Feldhaus,J., Liu,Q., Harshman,K., Tavtigian,S.V., Stockert,E., Day,R.S., Johnson,B.E. and Skolnick,M.H. (1994) A cell cycle regulator potentially involved in genesis of many tumor types. Science, 264, 436-440.
-
(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
Stockert, E.7
Day, R.S.8
Johnson, B.E.9
Skolnick, M.H.10
-
14
-
-
0028275733
-
Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers
-
Nobori,T., Miura,K., Wu,D.J., Lois,A., Takabayashi,K. and Carson,D.A. (1994) Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers. Nature, 368, 753-756.
-
(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
-
15
-
-
0029921317
-
Genetic alterations of cyclins, cyclin-dependant kinases, and CDK inhibitors in human cancers
-
Hall,M. and Peters,G. (1996) Genetic alterations of cyclins, cyclin-dependant kinases, and CDK inhibitors in human cancers. Adv. Cancer Res., 68, 67-108.
-
(1996)
Adv. Cancer Res.
, vol.68
, pp. 67-108
-
-
Hall, M.1
Peters, G.2
-
17
-
-
0029054399
-
Retinoblastoma-protem-dependant cell-cycle inhibition by the tumour suppressor p16
-
Lukas,J., Parry,D., Aagaard,L., Mann,D.J., Bartkova,J., Strauss,M., Peters,G. and Bartek,J. (1995) Retinoblastoma-protem-dependant cell-cycle inhibition by the tumour suppressor p16. Nature, 375, 503-506.
-
(1995)
Nature
, vol.375
, pp. 503-506
-
-
Lukas, J.1
Parry, D.2
Aagaard, L.3
Mann, D.J.4
Bartkova, J.5
Strauss, M.6
Peters, G.7
Bartek, J.8
-
18
-
-
0029052951
-
Tumour-derived p16 alleles encoding proteins defective in cell-cycle inhibition
-
Koh,J., Enders,G.H., Dynlacht,B.D. and Harlow,E. (1995) Tumour-derived p16 alleles encoding proteins defective in cell-cycle inhibition. Nature, 375, 506-510.
-
(1995)
Nature
, vol.375
, pp. 506-510
-
-
Koh, J.1
Enders, G.H.2
Dynlacht, B.D.3
Harlow, E.4
-
20
-
-
0028085975
-
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb,A., Shattuck-Eidens,D., Eeles,R., Liu,Q., Gruis,N.A., Ding,W., Hussey,C., Tran,T., Miki,Y., Weaver-Feldhaus,J., McClure,M., Aitken,J.F., Anderson,D.E., Bergman,W., Frants,R., Goldar,D.E., Green,A., MacLennan,R., Martin,N.G., Meyer,L.J., Youl,P., Zone,J.J., Skolnick,M.H. and Cannon-Albright,L.A. (1994) Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nature Genet., 8, 22-26.
-
(1994)
Nature Genet.
, vol.8
, pp. 22-26
-
-
Kamb, A.1
Shattuck-Eidens, D.2
Eeles, R.3
Liu, Q.4
Gruis, N.A.5
Ding, W.6
Hussey, C.7
Tran, T.8
Miki, Y.9
Weaver-Feldhaus, J.10
McClure, M.11
Aitken, J.F.12
Anderson, D.E.13
Bergman, W.14
Frants, R.15
Goldar, D.E.16
Green, A.17
MacLennan, R.18
Martin, N.G.19
Meyer, L.J.20
Youl, P.21
Zone, J.J.22
Skolnick, M.H.23
Cannon-Albright, L.A.24
more..
-
21
-
-
0029664339
-
INK4a binding domain of CDK4 in familial melanoma
-
INK4a binding domain of CDK4 in familial melanoma. Nature Genet., 12, 97-99.
-
(1996)
Nature Genet.
, vol.12
, pp. 97-99
-
-
Zuo, L.1
Weger, J.2
Yang, Q.3
Goldstein, A.M.4
Tucker, M.A.5
Walker, G.J.6
Hayward, N.7
Dracopoli, N.C.8
-
22
-
-
0028566386
-
Genetic heterogeneity in familial malignant melanoma
-
MacGeoch,C., Bishop,J.A., Bataille,V., Bishop,D.T., Frischauf,A.M., Meloni,R., Cuzik,J., Pinney,E. and Spurr,N.K. (1994) Genetic heterogeneity in familial malignant melanoma. Hum. Mol. Genet., 3, 2195-2200.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 2195-2200
-
-
MacGeoch, C.1
Bishop, J.A.2
Bataille, V.3
Bishop, D.T.4
Frischauf, A.M.5
Meloni, R.6
Cuzik, J.7
Pinney, E.8
Spurr, N.K.9
-
23
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian,C.J., Struewing,J.P., Goldstein,A.M., Higgins,P.A.T., Ally,D.S., Steahan,M.D., Clark,W.H.,Jr, Tucker,M.A. and Dracopoli,N.C. (1994) Germline p16 mutations in familial melanoma. Nature Genet., 8, 15-21.
-
(1994)
Nature Genet.
, vol.8
, pp. 15-21
-
-
Hussussian, C.J.1
Struewing, J.P.2
Goldstein, A.M.3
Higgins, P.A.T.4
Ally, D.S.5
Steahan, M.D.6
Clark Jr., W.H.7
Tucker, M.A.8
Dracopoli, N.C.9
-
24
-
-
0029102927
-
Brief report: A familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene
-
Whelan,A.J., Bartsch,D. and Goodfellow,P.J. (1995) 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)
N. Engl. J. Med.
, vol.333
, pp. 975-977
-
-
Whelan, A.J.1
Bartsch, D.2
Goodfellow, P.J.3
-
25
-
-
0029129816
-
INK4 mutations
-
INK4 mutations. N. Engl. J. Med., 333, 970-971.
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 970-971
-
-
Goldstein, A.-M.1
Fraser, M.C.2
Struewing, J.P.3
Hussussian, C.J.4
Ranade, K.5
Zametkin, D.P.6
Fontaine, L.S.7
Organic, S.M.8
Dracopoli, N.C.9
Clark, W.H.10
Tucker, M.A.11
-
27
-
-
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)
Science
, vol.269
, pp. 1281-1284
-
-
Wölfel, T.1
Hauer, M.2
Schneider, J.3
Serrano, M.4
Wölfel, C.5
Klehmann-Hieb, E.6
De Plaen, E.7
Hankeln, T.8
Meyer Zum Büschenfelde, K.-H.9
Beach, D.10
-
28
-
-
9444276546
-
Prevalence of germline mutations in p16, p19ARF, and CDK4 in familial melanoma: Analysis of a clinic-based population
-
Fitzgerald,M.G., Harkin,D.P., Silva-Arrieta,S., MacDonald,D.J., Lucchina,L.C., Unsal,H., O'Neill,E., Koh,J., Finkelstein,D.M., Isselbacher,K.J., Sober,A.J. and Haber,D.A. (1996) Prevalence of germline mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population. Proc. Natl Acad. Sci. USA, 93, 8541-8545.
-
(1996)
Proc. Natl Acad. Sci. USA
, 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
O'Neill, E.7
Koh, J.8
Finkelstein, D.M.9
Isselbacher, K.J.10
Sober, A.J.11
Haber, D.A.12
-
30
-
-
0029119852
-
INK4b genes
-
INK4b genes. Oncogenc, 11, 635-645.
-
(1995)
Oncogenc
, vol.11
, pp. 635-645
-
-
Quelle, D.E.1
Ashmun, R.A.2
Hannon, G.J.3
Rehberger, P.A.4
Trono, D.5
Richter, K.H.6
Walker, C.7
Beach, D.8
Sherr, C.J.9
Serrano, M.10
-
32
-
-
0029664738
-
Analysis of p16INK4A and its interaction with CDK4
-
Yang,R., Serrano,M., Slater,J., Leung,E. and Koeffler,H.P. (1996) Analysis of p16INK4A and its interaction with CDK4. Biochem. Biophys. Res. Commun., 218, 254-259.
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.218
, pp. 254-259
-
-
Yang, R.1
Serrano, M.2
Slater, J.3
Leung, E.4
Koeffler, H.P.5
-
34
-
-
0028862489
-
Biochemical and mutagenic analysis of the melanoma tumor suppressor gene product/p16
-
Wick,S.T., Dubay,M.M., Imanil,I. and Brizuela,L. (1995) Biochemical and mutagenic analysis of the melanoma tumor suppressor gene product/p16. Oncogene, 11, 2013-2019.
-
(1995)
Oncogene
, vol.11
, pp. 2013-2019
-
-
Wick, S.T.1
Dubay, M.M.2
Imanil, I.3
Brizuela, L.4
-
35
-
-
0029980941
-
CDKN2 associated with familial melanoma
-
CDKN2 associated with familial melanoma. Mol. Cell Biol., 16, 3844-3852.
-
(1996)
Mol. Cell Biol.
, vol.16
, pp. 3844-3852
-
-
Parry, D.1
Gordon, P.2
-
36
-
-
0029562169
-
Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds
-
Holland,E.A., Beaton,S.C., Becker,T.M., Grulet,O.M.C., Peters,B.A., Rizos,H., Kefford,R.F. and Mann,G.J. (1995) Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds. Oncogene, 11, 2289-2294.
-
(1995)
Oncogene
, vol.11
, pp. 2289-2294
-
-
Holland, E.A.1
Beaton, S.C.2
Becker, T.M.3
Grulet, O.M.C.4
Peters, B.A.5
Rizos, H.6
Kefford, R.F.7
Mann, G.J.8
-
37
-
-
0028971713
-
INKA gene in Australian melanoma kindreds
-
INKA gene in Australian melanoma kindreds. Hum. Mol. Genet., 4, 1845-1852.
-
(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
Hayward, N.K.7
Fountain, J.W.8
-
38
-
-
0028981089
-
INK4B/MTS2 genes in biliary tract cancers
-
INK4B/MTS2 genes in biliary tract cancers. Cancer Res., 55, 2756-2760.
-
(1995)
Cancer Res.
, vol.55
, pp. 2756-2760
-
-
Yoshida, S.1
Todoroki, T.2
Ichikawa, Y.3
Hanai, S.4
Suzuki, H.5
Hori, M.6
Fukao, K.7
Miwa, M.8
Uchida, K.9
-
39
-
-
0028059330
-
Frequent somatic mutations and homozygous deletions of the p16 (MTSI) gene in pancreatic adenocarcinoma
-
Caldas,C., Hahn,S.A., da Costa,L.T., Redston,M.S., Schutte,M., Seymour,A.B., Weinstein,C.L., Hruban,R.H., Yeo,C.J. and Kern,S.E. (1994) Frequent somatic mutations and homozygous deletions of the p16 (MTSI) gene in pancreatic adenocarcinoma. Nature Genet., 8, 27-32.
-
(1994)
Nature Genet.
, vol.8
, pp. 27-32
-
-
Caldas, C.1
Hahn, S.A.2
Da Costa, L.T.3
Redston, M.S.4
Schutte, M.5
Seymour, A.B.6
Weinstein, C.L.7
Hruban, R.H.8
Yeo, C.J.9
Kern, S.E.10
-
40
-
-
0029880379
-
Frequent codeletion of p16/MTSI and p15/MTS2 and genetic alterations in p 16/MTSI in pancreatic tumors
-
Naumann,M., Savitskaia,N., Eilert,C., Schramm,A., Kalthoff,H. and Schmiegel,W. (1996) Frequent codeletion of p16/MTSI and p15/MTS2 and genetic alterations in p 16/MTSI in pancreatic tumors. Gastroenterology, 110, 1215-1224.
-
(1996)
Gastroenterology
, vol.110
, pp. 1215-1224
-
-
Naumann, M.1
Savitskaia, N.2
Eilert, C.3
Schramm, A.4
Kalthoff, H.5
Schmiegel, W.6
-
41
-
-
0028985436
-
p16 gene homozygous deletions in acute lymphoblastic leukemia
-
Quesnel,B., Preudhomme,C., Philippe,N., Vanrumbeke,M., Dervite,I., Lai,J.-L., Bauters,F., Wattel,E. and Fenaux,P. (1995) p16 gene homozygous deletions in acute lymphoblastic leukemia. Blood, 85, 657-663.
-
(1995)
Blood
, vol.85
, pp. 657-663
-
-
Quesnel, B.1
Preudhomme, C.2
Philippe, N.3
Vanrumbeke, M.4
Dervite, I.5
Lai, J.-L.6
Bauters, F.7
Wattel, E.8
Fenaux, P.9
-
42
-
-
0030917395
-
p16/CDKN2 and CDK4 gene mutations in sporadic melanoma development and progression
-
Piccinin,S., Doglioni,C., Maestro,R., Vukosavljevic,T., Gasparotto,D., D'Orazi,C. and Boiocchi,M. (1997) p16/CDKN2 and CDK4 gene mutations in sporadic melanoma development and progression. Int. J. Cancer (Pred. Oncol.), 74, 26-30.
-
(1997)
Int. J. Cancer (Pred. Oncol.)
, vol.74
, pp. 26-30
-
-
Piccinin, S.1
Doglioni, C.2
Maestro, R.3
Vukosavljevic, T.4
Gasparotto, D.5
D'Orazi, C.6
Boiocchi, M.7
-
43
-
-
0030025518
-
Compilation of somatic mutations of the CDKN2 gene in human cancers: Non-random distribution of base substitutions
-
Pollock,P.M., Pearson,J.V and Hayward,N.K. (1996) Compilation of somatic mutations of the CDKN2 gene in human cancers: non-random distribution of base substitutions. Genes Chromosomes Cancer, 15, 77-88.
-
(1996)
Genes Chromosomes Cancer
, vol.15
, pp. 77-88
-
-
Pollock, P.M.1
Pearson, J.V.2
Hayward, N.K.3
-
44
-
-
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., Lagerlöf,B., Linder,S., Lundqvist,E., Sevigny,P., Inganäs,M. and Ringborg,U. (1997) 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)
J. Natl Cancer Inst.
, vol.89
, pp. 697-702
-
-
Platz, A.1
Hansson, J.2
Mansson-Brahme, E.3
Lagerlöf, B.4
Linder, S.5
Lundqvist, E.6
Sevigny, P.7
Inganäs, M.8
Ringborg, U.9
-
45
-
-
0029891364
-
Novel germline p16 mutation in familial melanoma in Southern Sweden
-
Borg,A., Johansson,U., Johansson,O., Håkansson,S., Westerdahl,J., Måsbäck,A., Olsson,H. and Ingvar,C. (1996) Novel germline p16 mutation in familial melanoma in Southern Sweden. Cancer Res., 56, 2497-2500.
-
(1996)
Cancer Res.
, vol.56
, pp. 2497-2500
-
-
Borg, A.1
Johansson, U.2
Johansson, O.3
Håkansson, S.4
Westerdahl, J.5
Måsbäck, A.6
Olsson, H.7
Ingvar, C.8
-
46
-
-
0029009926
-
Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds
-
Gruis,N.A., van der Velden,P.A., Sandkuijl,L.A., Prins,D.E., Weaver-Feldhaus,J., Kamb,A., Bergman,W. and Frants,R.R. (1995) Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds. Nature Genet., 10, 351-353.
-
(1995)
Nature Genet.
, vol.10
, pp. 351-353
-
-
Gruis, N.A.1
Van Der Velden, P.A.2
Sandkuijl, L.A.3
Prins, D.E.4
Weaver-Feldhaus, J.5
Kamb, A.6
Bergman, W.7
Frants, R.R.8
-
47
-
-
0028998866
-
INK4 function
-
INK4 function. Nature Genet., 10, 114-116.
-
(1995)
Nature 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
Serrano, M.7
Hannon, G.J.8
Beach, D.9
Dracopoli, N.C.10
-
48
-
-
0027370901
-
Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity
-
Goldstein,A.M., Dracopoli,N.C., Ho,E.C., Fraser,M.C., Kearns,K.S., Bale,S.J., McBride,O.W., Clark,W.H.,Jr and Tucker,M.A. (1993) Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity. Am. J. Hum. Genet., 52, 537-550.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 537-550
-
-
Goldstein, A.M.1
Dracopoli, N.C.2
Ho, E.C.3
Fraser, M.C.4
Kearns, K.S.5
Bale, S.J.6
McBride, O.W.7
Clark Jr., W.H.8
Tucker, M.A.9
-
49
-
-
0029883639
-
Two-locus linkage analysis of cutaneous malignant melanoma/ dysplastic nevi
-
Goldstein,A., Goldin,L.R., Dracopoli,N.C., Clark,W.H. and Tucker,M.A. (1996) Two-locus linkage analysis of cutaneous malignant melanoma/ dysplastic nevi. Am. J. Hum. Genet., 58, 1050-1056.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1050-1056
-
-
Goldstein, A.1
Goldin, L.R.2
Dracopoli, N.C.3
Clark, W.H.4
Tucker, M.A.5
-
50
-
-
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. and Frants,R.R. (1995) CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. Melanoma Res., 5, 169-177.
-
(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
-
51
-
-
0031000617
-
ARF
-
ARF. Genes Chromosomes Cancer, 19, 52-54.
-
(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
-
52
-
-
0029113837
-
Genomic structure, expression and mutational analysis of the p15 (MTS2) gene
-
Stone,S., Dayananth,P., Jiang,P., Weaver-Feldhaus,J.M., Tavtigian,S.V., Cannon-Albright,L. and Kamb,A. (1995) Genomic structure, expression and mutational analysis of the p15 (MTS2) gene. Oncogene, 11, 987-991.
-
(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
-
53
-
-
0029587551
-
Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest
-
Quelle,D.E., Zindy,F., Ashmun,R.A. and Sherr,C.J. (1995) Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest. Cell, 83, 993-1000.
-
(1995)
Cell
, vol.83
, pp. 993-1000
-
-
Quelle, D.E.1
Zindy, F.2
Ashmun, R.A.3
Sherr, C.J.4
-
54
-
-
0029658666
-
Loss of the p16INK4a and p15INK4b genes, as well as neighboring 9p21 markers in sporadic melanoma
-
Flores,J.F., Walker,G.J., Glendening,J.M., Haluska,F.G., Castresana,J.S., Rubio,M.P., Pastorfide,G.C., Boyer,L.A., Kao,W.H., Bulyk,M.L., Bamhill,R.L., Hayward,N.K., Housman,D.E. and Fountain,J.W. (1996) Loss of the p16INK4a and p15INK4b genes, as well as neighboring 9p21 markers in sporadic melanoma. Cancer Res., 56, 5023-5032.
-
(1996)
Cancer Res.
, vol.56
, pp. 5023-5032
-
-
Flores, J.F.1
Walker, G.J.2
Glendening, J.M.3
Haluska, F.G.4
Castresana, J.S.5
Rubio, M.P.6
Pastorfide, G.C.7
Boyer, L.A.8
Kao, W.H.9
Bulyk, M.L.10
Bamhill, R.L.11
Hayward, N.K.12
Housman, D.E.13
Fountain, J.W.14
-
55
-
-
0029011539
-
5′ CpG island melhylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTSI in human cancers
-
Merlo,A., Herman,J.G., Mao,L., Lee,D.J., Gabrielson,E., Burger,P.C., Baylin,S.B. and Sidransky,D. (1995) 5′ CpG island melhylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTSI in human cancers. Nature Med., 1, 686-692.
-
(1995)
Nature Med.
, vol.1
, pp. 686-692
-
-
Merlo, A.1
Herman, J.G.2
Mao, L.3
Lee, D.J.4
Gabrielson, E.5
Burger, P.C.6
Baylin, S.B.7
Sidransky, D.8
-
56
-
-
0029067841
-
Methylation and p16: Suppressing the suppressor
-
Little,M. and Wainwright,B. (1995) Methylation and p16: suppressing the suppressor. Nature Med., 1, 633-634.
-
(1995)
Nature Med.
, vol.1
, pp. 633-634
-
-
Little, M.1
Wainwright, B.2
-
57
-
-
0025284650
-
Systemic cancer and the FAMMM syndrome
-
Bergman,W., Watson,P., de Jong,J., Lynch,H.T. and Fusaro,R.M. (1990) Systemic cancer and the FAMMM syndrome. Br. J. Cancer, 61, 932-936.
-
(1990)
Br. J. Cancer
, vol.61
, pp. 932-936
-
-
Bergman, W.1
Watson, P.2
De Jong, J.3
Lynch, H.T.4
Fusaro, R.M.5
-
58
-
-
0028572431
-
Accumulation of multiple mutations in tumour suppressor genes during colorectal tumorigenesis in HNPCC patients
-
Lazar,V., Grandjouan,S., Bognel,C., Couturier,D., Rougier,P., Bellet,D. and Bressac-de Paillerets,B. (1994) Accumulation of multiple mutations in tumour suppressor genes during colorectal tumorigenesis in HNPCC patients. Ham. Mol. Genet., 3, 2257-2260.
-
(1994)
Ham. Mol. Genet.
, vol.3
, pp. 2257-2260
-
-
Lazar, V.1
Grandjouan, S.2
Bognel, C.3
Couturier, D.4
Rougier, P.5
Bellet, D.6
Bressac-de Paillerets, B.7
-
59
-
-
0027253408
-
Simple sequence repeat polymorphism within the p53 gene
-
Lazar,V., Hazard,F., Bertin,F., Janin,N., Bellet,D. and Bressac,B. (1993) Simple sequence repeat polymorphism within the p53 gene. Oncogene, 8, 1703-1705.
-
(1993)
Oncogene
, vol.8
, pp. 1703-1705
-
-
Lazar, V.1
Hazard, F.2
Bertin, F.3
Janin, N.4
Bellet, D.5
Bressac, B.6
-
60
-
-
0028168242
-
ink4b is a potential effector of TGF-b-induced cell cycle arrest
-
INK4B is a potential effector of TGF-b-induced cell cycle arrest. Nature, 371, 257-261.
-
(1994)
Nature
, vol.371
, pp. 257-261
-
-
Hannon, G.H.1
Beach, D.2
|