-
1
-
-
0035989912
-
Molecular regulation of melanocyte senescence
-
Bennett DC, Medrano EE. 2002. Molecular regulation of melanocyte senescence. Pigment Cell Res 15:242-250.
-
(2002)
Pigment Cell Res
, vol.15
, pp. 242-250
-
-
Bennett, D.C.1
Medrano, E.E.2
-
2
-
-
18444380541
-
INK4a-deficient human diploid fibroblasts are resistant to RAS-induced senescence
-
Brookes S, Rowe J, Ruas M, Llanos S, Clark PA, Lomax M, James MC, Vatcheva R, Bates S, Vousden KH, Parry D, Gruis N, Smit N, Bergman W, Peters G. 2002. INK4a-deficient human diploid fibroblasts are resistant to RAS-induced senescence. Embo J 21:2936-2945.
-
(2002)
Embo J
, vol.21
, pp. 2936-2945
-
-
Brookes, S.1
Rowe, J.2
Ruas, M.3
Llanos, S.4
Clark, P.A.5
Lomax, M.6
James, M.C.7
Vatcheva, R.8
Bates, S.9
Vousden, K.H.10
Parry, D.11
Gruis, N.12
Smit, N.13
Bergman, W.14
Peters, G.15
-
3
-
-
0032231919
-
A point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British families
-
Burrows NP, Nicholls AC, Richards AJ, Luccarini C, Harrison JB, Yates JR, Pope FM. 1998. A point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British families. Am J Hum Genet 63:390-398.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 390-398
-
-
Burrows, N.P.1
Nicholls, A.C.2
Richards, A.J.3
Luccarini, C.4
Harrison, J.B.5
Yates, J.R.6
Pope, F.M.7
-
4
-
-
0033865120
-
A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families
-
Ciotti P, Struewing JP, Mantelli M, Chompret A, Avril MF, Santi PL, Tucker MA, Bianchi-Scarra G, Bressac-de Paillerets B, Goldstein AM. 2000. A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families. Am J Hum Genet 67:311-319.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 311-319
-
-
Ciotti, P.1
Struewing, J.P.2
Mantelli, M.3
Chompret, A.4
Avril, M.F.5
Santi, P.L.6
Tucker, M.A.7
Bianchi-Scarra, G.8
Bressac-de Paillerets, B.9
Goldstein, A.M.10
-
6
-
-
0037047644
-
Predictive identification of exonic splicing enhancers in human genes
-
Fairbrother WG, Yeh RF, Sharp PA, Burge CB. 2002. Predictive identification of exonic splicing enhancers in human genes. Science 297:1007-1013.
-
(2002)
Science
, vol.297
, pp. 1007-1013
-
-
Fairbrother, W.G.1
Yeh, R.F.2
Sharp, P.A.3
Burge, C.B.4
-
7
-
-
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, Walters MK, Hayward NK, Fountain JW. 1997. Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds. Oncogene 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
Walters, M.K.7
Hayward, N.K.8
Fountain, J.W.9
-
9
-
-
0031582331
-
Screening for CDKN2A mutations in hereditary melanoma
-
Goldstein AM, Tucker MA. 1997. Screening for CDKN2A mutations in hereditary melanoma. J Natl Cancer Inst 89:676-678.
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 676-678
-
-
Goldstein, A.M.1
Tucker, M.A.2
-
10
-
-
0035902848
-
A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families
-
Goldstein AM, Liu L, Shennan MG, Hogg D, Tucker MA, Struewing JP. 2001. A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families. Br J Cancer 85:527-530.
-
(2001)
Br J Cancer
, vol.85
, pp. 527-530
-
-
Goldstein, A.M.1
Liu, L.2
Shennan, M.G.3
Hogg, D.4
Tucker, M.A.5
Struewing, J.P.6
-
11
-
-
0029009926
-
Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds
-
Gruis NA, van der Velden PA, Sandkuijl LA, Prins DE, Weaver-Feldhaus J, Kamb A, Bergman W, Frants RR. 1995. Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds. Nat Genet 10:351-353.
-
(1995)
Nat 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
-
12
-
-
9844219745
-
Germline mutations of the CDKN2 gene in UK melanoma families
-
Harland M, Meloni R, Gruis N, Pinney E, Brookes S, Spurr NK, Frischauf AM, Bataille V, Peters G, Cuzick J, Selby P, Bishop DT, Newton Bishop J. 1997. Germline mutations of the CDKN2 gene in UK melanoma families. Hum Mol Genet 6:2061-2067.
-
(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
Frischauf, A.M.7
Bataille, V.8
Peters, G.9
Cuzick, J.10
Selby, R.11
Bishop, D.T.12
Newton Bishop, J.13
-
13
-
-
6744226360
-
Mutation screening of the CDKN2A promoter in melanoma families
-
Harland M, Holland EA, Ghiorzo P, Mantelli M, Bianchi-Scarra G, Goldstein AM, Tucker MA, Ponder BA, Mann GJ, Bishop DT, Newton Bishop J. 2000. Mutation screening of the CDKN2A promoter in melanoma families. Genes Chromosomes Cancer 28:45-57.
-
(2000)
Genes Chromosomes Cancer
, vol.28
, pp. 45-57
-
-
Harland, M.1
Holland, E.A.2
Ghiorzo, P.3
Mantelli, M.4
Bianchi-Scarra, G.5
Goldstein, A.M.6
Tucker, M.A.7
Ponder, B.A.8
Mann, G.J.9
Bishop, D.T.10
Newton Bishop, J.11
-
14
-
-
0035510173
-
A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees
-
Harland M, Mistry S, Bishop DT, Newton Bishop JA. 2001. A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees. Hum Mol Genet 10:2679-2686.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2679-2686
-
-
Harland, M.1
Mistry, S.2
Bishop, D.T.3
Newton Bishop, J.A.4
-
15
-
-
0035020632
-
Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families
-
Hashemi J, Bendahl PO, Sandberg T, Platz A, Linder S, Stierner U, Olsson H, Ingvar C, Hansson J, Borg A. 2001. Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families. Genes Chromosomes Cancer 31:107-116.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 107-116
-
-
Hashemi, J.1
Bendahl, P.O.2
Sandberg, T.3
Platz, A.4
Linder, S.5
Stierner, U.6
Olsson, H.7
Ingvar, C.8
Hansson, J.9
Borg, A.10
-
16
-
-
0029947139
-
The current situation with regard to human melanoma and genetic inferences
-
Hayward NK. 1996. The current situation with regard to human melanoma and genetic inferences. Curr Opin Oncol 8:136-142.
-
(1996)
Curr Opin Oncol
, vol.8
, pp. 136-142
-
-
Hayward, N.K.1
-
17
-
-
0037093319
-
Germline mutation of ARF in a melanoma kindred
-
Hewitt C, Lee Wu C, Evans G, Howell A, Elles RG, Jordan R, Sloan P, Read AP, Thakker N. 2002. Germline mutation of ARF in a melanoma kindred. Hum Mol Genet 11:1273-1279.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1273-1279
-
-
Hewitt, C.1
Lee Wu, C.2
Evans, G.3
Howell, A.4
Elles, R.G.5
Jordan, R.6
Sloan, P.7
Read, A.P.8
Thakker, N.9
-
18
-
-
0346786528
-
Cytoplasmic degradation of splicedefective pre-mRNAs and intermediates
-
Hilleren PJ, Parker R. 2003. Cytoplasmic degradation of splicedefective pre-mRNAs and intermediates. Mol Cell 12:1453-1465.
-
(2003)
Mol Cell
, vol.12
, pp. 1453-1465
-
-
Hilleren, P.J.1
Parker, R.2
-
19
-
-
0029562169
-
Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds
-
Holland EA, Beaton SC, Becker TM, Grulet OM, Peters BA, Rizos H, Kefford RF, Mann GJ. 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.4
Peters, B.A.5
Rizos, H.6
Kefford, R.F.7
Mann, G.J.8
-
20
-
-
0032784037
-
CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: Effect of family history and multiple primary melanomas
-
Holland EA, Schmid H, Kefford RF, Mann GJ. 1999. CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: effect of family history and multiple primary melanomas. Genes Chromosomes Cancer 25:339-348.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 339-348
-
-
Holland, E.A.1
Schmid, H.2
Kefford, R.F.3
Mann, G.J.4
-
21
-
-
18644365331
-
Biallelic mutations in p16(INK4a) confer resistance to Rasand Ets-induced senescence in human diploid fibroblasts
-
Huot TJ, Rowe J, Harland M, Drayton S, Brookes S, Gooptu C, Purkis P, Fried M, Bataille V, Hara E, Newton Bishop J, Peters G. 2002. Biallelic mutations in p16(INK4a) confer resistance to Rasand Ets-induced senescence in human diploid fibroblasts. Mol Cell Biol 22:8135-8143.
-
(2002)
Mol Cell Biol
, vol.22
, pp. 8135-8143
-
-
Huot, T.J.1
Rowe, J.2
Harland, M.3
Drayton, S.4
Brookes, S.5
Gooptu, C.6
Purkis, P.7
Fried, M.8
Bataille, V.9
Hara, E.10
Newton Bishop, J.11
Peters, G.12
-
22
-
-
0034533698
-
A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder
-
Janssen RJ, Wevers RA, Haussler M, Luyten JA, SteenbergenSpanjers GC, Hoffmann GF, Nagatsu T, Van den Heuvel LP. 2000. A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder. Ann Hum Genet 64:375-382.
-
(2000)
Ann Hum Genet
, vol.64
, pp. 375-382
-
-
Janssen, R.J.1
Wevers, R.A.2
Haussler, M.3
Luyten, J.A.4
Steenbergenspanjers, G.C.5
Hoffmann, G.F.6
Nagatsu, T.7
Van Den Heuvel, L.P.8
-
23
-
-
0032878113
-
Optimal temperature selection for mutation detection hy denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis
-
Jones AC, Austin J, Hansen N, Hoogendoorn B, Oefner PJ, Cheadle JP, O'Donovan MC. 1999. Optimal temperature selection for mutation detection hy denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis. Clin Chem 45:1133-1140.
-
(1999)
Clin Chem
, vol.45
, pp. 1133-1140
-
-
Jones, A.C.1
Austin, J.2
Hansen, N.3
Hoogendoorn, B.4
Oefner, P.J.5
Cheadle, J.P.6
O'Donovan, M.C.7
-
24
-
-
0036934214
-
Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome
-
King K, Flinter FA, Nihalani V, Green PM. 2002. Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome. Hum Genet 111:548-554.
-
(2002)
Hum Genet
, vol.111
, pp. 548-554
-
-
King, K.1
Flinter, F.A.2
Nihalani, V.3
Green, P.M.4
-
25
-
-
0026794668
-
The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences
-
Krawczak M, Reiss J, Cooper DN. 1992. The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences. Hum Genet 90:41-54.
-
(1992)
Hum Genet
, vol.90
, pp. 41-54
-
-
Krawczak, M.1
Reiss, J.2
Cooper, D.N.3
-
26
-
-
0027291689
-
Allelic discrimination by nicktranslation PCR with fluorogenic probes
-
Lee LG, Connell CR, Bloch W. 1993. Allelic discrimination by nicktranslation PCR with fluorogenic probes. Nucleic Acids Res 21:3761-3766.
-
(1993)
Nucleic Acids Res
, vol.21
, pp. 3761-3766
-
-
Lee, L.G.1
Connell, C.R.2
Bloch, W.3
-
27
-
-
0034674541
-
Characterization of the effects of mutations in the putative branchpoint sequence of intron 4 on the splicing within the human lecithin:cholesterol acyltransferase gene
-
Li M, Pritchard PH. 2000. Characterization of the effects of mutations in the putative branchpoint sequence of intron 4 on the splicing within the human lecithin:cholesterol acyltransferase gene. J Biol Chem 275:18079-18084.
-
(2000)
J Biol Chem
, vol.275
, pp. 18079-18084
-
-
Li, M.1
Pritchard, P.H.2
-
28
-
-
0344301900
-
Role of the p16 tumor suppressor gene in cancer
-
Liggett WH Jr., Sidransky D. 1998. Role of the p16 tumor suppressor gene in cancer. J Clin Oncol 16:1197-1206.
-
(1998)
J Clin Oncol
, vol.16
, pp. 1197-1206
-
-
Liggett Jr., W.H.1
Sidransky, D.2
-
29
-
-
0031000617
-
Affected members of melanoma-prone families with linkage to 9p21 hut 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. 1997. Affected members of melanoma-prone families with linkage to 9p21 hut lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19ARF. 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
-
30
-
-
0032900535
-
Mutation of the CDKN2A 5′ UTR creates an aberrant initiation codon and predisposes to melanoma
-
Liu L, Dilworth D, Gao L, Monzon J, Summers A, Lassam N, Hogg D. 1999. Mutation of the CDKN2A 5′ UTR creates an aberrant initiation codon and predisposes to melanoma. Nat Genet 21:128-132.
-
(1999)
Nat Genet
, vol.21
, pp. 128-132
-
-
Liu, L.1
Dilworth, D.2
Gao, L.3
Monzon, J.4
Summers, A.5
Lassam, N.6
Hogg, D.7
-
31
-
-
0142072167
-
Germline splicing mutations of CDKN2A predispose to melanoma
-
Loo JC, Liu L, Hao A, Gao L, Agatep R, Shennan M, Summers A, Goldstein AM, Tucker MA, Deters C, Fusaro R, Blazer K, Weitzel J, Lassam N, Lynch H, Hogg D. 2003. Germline splicing mutations of CDKN2A predispose to melanoma. Oncogene 22:6387-6394.
-
(2003)
Oncogene
, vol.22
, pp. 6387-6394
-
-
Loo, J.C.1
Liu, L.2
Hao, A.3
Gao, L.4
Agatep, R.5
Shennan, M.6
Summers, A.7
Goldstein, A.M.8
Tucker, M.A.9
Deters, C.10
Fusaro, R.11
Blazer, K.12
Weitzel, J.13
Lassam, N.14
Lynch, H.15
Hogg, D.16
-
32
-
-
0034670066
-
Three novel types of splicing aberrations in the tuberous sclerosis TSC2 gene caused by mutations apart from splice consensus sequences
-
Mayer K, Ballhausen W, Leistner W, Rott H. 2000. Three novel types of splicing aberrations in the tuberous sclerosis TSC2 gene caused by mutations apart from splice consensus sequences. Biochim Biophys Acta 1502:495-507.
-
(2000)
Biochim Biophys Acta
, vol.1502
, pp. 495-507
-
-
Mayer, K.1
Ballhausen, W.2
Leistner, W.3
Rott, H.4
-
33
-
-
0029819493
-
Mutations associated with variant phenotypes in ataxia-telangiectasia
-
McConville CM, Stankovic T, Byrd PJ, McGuire GM, Yao QY, Lennox GG, Taylor MR. 1996. Mutations associated with variant phenotypes in ataxia-telangiectasia. Am J Hum Genet 59:320-330.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 320-330
-
-
McConville, C.M.1
Stankovic, T.2
Byrd, P.J.3
McGuire, G.M.4
Yao, Q.Y.5
Lennox, G.G.6
Taylor, M.R.7
-
34
-
-
0032950332
-
Mutation testing in melanoma families: INK4A, CDK4 and INK4D
-
Newton Bishop JA, Harland M, Bennett DC, Bataille V, Goldstein AM, Tucker MA, Ponder BA, Cuzick J, Selby P, Bishop DT 1999. Mutation testing in melanoma families: INK4A, CDK4 and INK4D. Br J Cancer 80:295-300.
-
(1999)
Br J Cancer
, vol.80
, pp. 295-300
-
-
Newton Bishop, J.A.1
Harland, M.2
Bennett, D.C.3
Bataille, V.4
Goldstein, A.M.5
Tucker, M.A.6
Ponder, B.A.7
Cuzick, J.8
Selby, P.9
Bishop, D.T.10
-
35
-
-
1942467065
-
Genomic variants in exons and intron: Identifying the splicing spoilers
-
Pagani F, Baralle FE. 2004. Genomic variants in exons and intron: identifying the splicing spoilers. Nat Rev Genet 5:389-396.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 389-396
-
-
Pagani, F.1
Baralle, F.E.2
-
36
-
-
0034945349
-
CDKN2A germline splicing mutation affecting both p16(ink4) and p14(arf) RNA processing in a melanoma/neurofibroma kindred
-
Petronzelli F, Sollima D, Coppola G, Martini-Neri ME, Neri G, Genuardi M. 2001. CDKN2A germline splicing mutation affecting both p16(ink4) and p14(arf) RNA processing in a melanoma/neurofibroma kindred. Genes Chromosomes Cancer 31:398-401.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 398-401
-
-
Petronzelli, F.1
Sollima, D.2
Coppola, G.3
Martini-Neri, M.E.4
Neri, G.5
Genuardi, M.6
-
37
-
-
0031818039
-
Screening of germline mutations in the CDK4, CDKN2C and TP53 genes in familial melanoma: A clinic-based population study
-
Platz A, Hansson J, Ringborg U. 1998. Screening of germline mutations in the CDK4, CDKN2C and TP53 genes in familial melanoma: a clinic-based population study. Int J Cancer 78:13-15.
-
(1998)
Int J Cancer
, vol.78
, pp. 13-15
-
-
Platz, A.1
Hansson, J.2
Ringborg, U.3
-
38
-
-
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, Newton-Bishop J, Gruis N, van der Velden PA, Goldstein AM, Tucker MA, Foulkes WD, Barnhill R, Haber D, Fountain J, Hayward NK. 1998. Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations. Hum Mutat 11:424-431.
-
(1998)
Hum Mutat
, vol.11
, pp. 424-431
-
-
Pollock, P.M.1
Spurr, N.2
Bishop, T.3
Newton-Bishop, J.4
Gruis, N.5
Van Der Velden, P.A.6
Goldstein, A.M.7
Tucker, M.A.8
Foulkes, W.D.9
Barnhill, R.10
Haber, D.11
Fountain, J.12
Hayward, N.K.13
-
39
-
-
0034910561
-
Mutation analysis of the CDKN2A promoter in Australian melanoma families
-
Pollock PM, Stark MS, Palmer JM, Walters MK, Aitken JF, Martin NG, Hayward NK. 2001. Mutation analysis of the CDKN2A promoter in Australian melanoma families. Genes Chromosomes Cancer 32:89-94.
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 89-94
-
-
Pollock, P.M.1
Stark, M.S.2
Palmer, J.M.3
Walters, M.K.4
Aitken, J.F.5
Martin, N.G.6
Hayward, N.K.7
-
40
-
-
0035170850
-
A germline deletion of p14(ARF) but not CDKN2A in a melanoma-neural system tumour syndrome family
-
Randerson-Moor JA, Harland M, Williams S, Cuthbert-Heavens D, Sheridan E, Aveyard J, Sibley K, Whitaker L, Knowles M, Newton Bishop J, Bishop DT. 2001. A germline deletion of p14(ARF) but not CDKN2A in a melanoma-neural system tumour syndrome family. Hum Mol Genet 10:55-62.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 55-62
-
-
Randerson-Moor, J.A.1
Harland, M.2
Williams, S.3
Cuthbert-Heavens, D.4
Sheridan, E.5
Aveyard, J.6
Sibley, K.7
Whitaker, L.8
Knowles, M.9
Newton Bishop, J.10
Bishop, D.T.11
-
41
-
-
0035817722
-
A melanoma-associated germline mutation in exon 1beta inactivates p14ARF
-
Rizos H, Puig S, Badenas C, Malvehy J, Darmanian AP, Jimenez L, Mila M, Kefford RF. 2001a. A melanoma-associated germline mutation in exon 1beta inactivates p14ARF. Oncogene 20:5543-5547.
-
(2001)
Oncogene
, vol.20
, pp. 5543-5547
-
-
Rizos, H.1
Puig, S.2
Badenas, C.3
Malvehy, J.4
Darmanian, A.P.5
Jimenez, L.6
Mila, M.7
Kefford, R.F.8
-
42
-
-
0035798659
-
Mutations in the INK4a/ARF melanoma susceptibility locus functionally impair p14ARF
-
Rizos H, Darmanian AP, Holland EA, Mann GJ, Kefford RF. 2001b. Mutations in the INK4a/ARF melanoma susceptibility locus functionally impair p14ARF. J Biol Chem 276:41424-41434.
-
(2001)
J Biol Chem
, vol.276
, pp. 41424-41434
-
-
Rizos, H.1
Darmanian, A.P.2
Holland, E.A.3
Mann, G.J.4
Kefford, R.F.5
-
43
-
-
0033588882
-
The INK4 family of cell cycle inhibitors in cancer
-
Roussel MF. 1999. The INK4 family of cell cycle inhibitors in cancer. Oncogene 18:5311-17.
-
(1999)
Oncogene
, vol.18
, pp. 5311-5317
-
-
Roussel, M.F.1
-
44
-
-
0041302145
-
CDKN2A point mutations D153spl(c.457G > T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF
-
Rutter JL, Goldstein AM, Davila MR, Tucker MA, Struewing JP. 2003. CDKN2A point mutations D153spl(c.457G > T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF. Oncogene 22:4444-4448.
-
(2003)
Oncogene
, vol.22
, pp. 4444-4448
-
-
Rutter, J.L.1
Goldstein, A.M.2
Davila, M.R.3
Tucker, M.A.4
Struewing, J.P.5
-
45
-
-
6844226190
-
Prevalence of p16 and CDK4 germline mutations in 48 melanomaprone families in France
-
The French Familial Melanoma Study Group
-
Soufir N, Avril MF, Chompret A, Demenais F, Bombled J, Spatz A, Stoppa-Lyonnet D, Benard J, Bressac-de Paillerets B. 1998. Prevalence of p16 and CDK4 germline mutations in 48 melanomaprone families in France. The French Familial Melanoma Study Group. Hum Mol Genet 7:209-216.
-
(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
Stoppa-Lyonnet, D.7
Benard, J.8
Bressac-de Paillerets, B.9
-
46
-
-
0029060657
-
Complex structure and regulation of the P16 (MTS1) locus
-
Stone S, Jiang P, Dayananth P, Tavtigian SV, Katcher H, Parry D, Peters G, Kamb A. 1995. Complex structure and regulation of the P16 (MTS1) locus. Cancer Res 55:2988-2994.
-
(1995)
Cancer Res
, vol.55
, pp. 2988-2994
-
-
Stone, S.1
Jiang, P.2
Dayananth, P.3
Tavtigian, S.V.4
Katcher, H.5
Parry, D.6
Peters, G.7
Kamb, A.8
-
47
-
-
0037139615
-
p16(Ink4a) in melanocyte senescence and differentiation
-
Sviderskaya EV, Hill SP, Evans-Whipp TJ, Chin L, Orlow SJ, Easty DJ, Cheong SC, Beach D, DePinho RA, Bennett DC. 2002. p16(Ink4a) in melanocyte senescence and differentiation. J Natl Cancer Inst 94:446-454.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 446-454
-
-
Sviderskaya, E.V.1
Hill, S.P.2
Evans-Whipp, T.J.3
Chin, L.4
Orlow, S.J.5
Easty, D.J.6
Cheong, S.C.7
Beach, D.8
DePinho, R.A.9
Bennett, D.C.10
|