-
1
-
-
84875235432
-
MEK162 for patients with advanced melanoma harbouring NRAS or Val600 BRAF mutations: A non-randomised, open-label phase 2 study
-
Ascierto PA, Schadendorf D, Berking C et al. (2013) MEK162 for patients with advanced melanoma harbouring NRAS or Val600 BRAF mutations: a non-randomised, open-label phase 2 study. Lancet Oncol 14:249-56
-
(2013)
Lancet Oncol
, vol.14
, pp. 249-256
-
-
Ascierto, P.A.1
Schadendorf, D.2
Berking, C.3
-
2
-
-
0038456527
-
Understanding the progression of melanocytic neoplasia using genomic analysis: From fields to cancer
-
Bastian BC (2003) Understanding the progression of melanocytic neoplasia using genomic analysis: from fields to cancer. Oncogene 22:3081-6
-
(2003)
Oncogene
, vol.22
, pp. 3081-3086
-
-
Bastian, B.C.1
-
3
-
-
0033396288
-
Molecular cytogenetic analysis of Spitz nevi shows clear differences to melanoma
-
Bastian BC, Wesselmann U, Pinkel D et al. (1999) Molecular cytogenetic analysis of Spitz nevi shows clear differences to melanoma. J Invest Dermatol 113:1065-9
-
(1999)
J Invest Dermatol
, vol.113
, pp. 1065-1069
-
-
Bastian, B.C.1
Wesselmann, U.2
Pinkel, D.3
-
4
-
-
33845726945
-
Congenital melanocytic nevi frequently harbor NRAS mutations but no BRAF mutations
-
Bauer J, Curtin JA, Pinkel D et al. (2007) Congenital melanocytic nevi frequently harbor NRAS mutations but no BRAF mutations. J Invest Dermatol 127:179-82
-
(2007)
J Invest Dermatol
, vol.127
, pp. 179-182
-
-
Bauer, J.1
Curtin, J.A.2
Pinkel, D.3
-
5
-
-
79951497419
-
The genomic complexity of primary human prostate cancer
-
Berger MF, Lawrence MS, Demichelis F et al. (2011) The genomic complexity of primary human prostate cancer. Nature 470:214-20
-
(2011)
Nature
, vol.470
, pp. 214-220
-
-
Berger, M.F.1
Lawrence, M.S.2
Demichelis, F.3
-
6
-
-
33646078949
-
Large or multiple congenital melanocytic nevi: Occurrence of neurocutaneous melanocytosis in 1008 persons
-
Bett BJ (2006) Large or multiple congenital melanocytic nevi: occurrence of neurocutaneous melanocytosis in 1008 persons. J Am Acad Dermatol 54:767-77
-
(2006)
J Am Acad Dermatol
, vol.54
, pp. 767-777
-
-
Bett, B.J.1
-
7
-
-
0028086086
-
Point mutations in the N-ras oncogene in malignant melanoma and congenital naevi
-
Carr J, Mackie RM (1994) Point mutations in the N-ras oncogene in malignant melanoma and congenital naevi. Br J Dermatol 131:72-7
-
(1994)
Br J Dermatol
, vol.131
, pp. 72-77
-
-
Carr, J.1
Mackie, R.M.2
-
8
-
-
79951494668
-
Initial genome sequencing and analysis of multiple myeloma
-
Chapman MA, Lawrence MS, Keats JJ et al. (2011) Initial genome sequencing and analysis of multiple myeloma. Nature 471:467-72
-
(2011)
Nature
, vol.471
, pp. 467-472
-
-
Chapman, M.A.1
Lawrence, M.S.2
Keats, J.J.3
-
10
-
-
0030470941
-
Neurocutaneous melanosis: Clinical features of large congenital melanocytic nevi in patients with manifest central nervous system melanosis
-
DeDavid M, Orlow SJ, Provost N et al. (1996) Neurocutaneous melanosis: clinical features of large congenital melanocytic nevi in patients with manifest central nervous system melanosis. J Am Acad Dermatol 35: 529-38
-
(1996)
J Am Acad Dermatol
, vol.35
, pp. 529-538
-
-
Dedavid, M.1
Orlow, S.J.2
Provost, N.3
-
11
-
-
58149342088
-
Genotypic and gene expression studies in congenital melanocytic nevi: Insight into initial steps of melanotumorigenesis
-
Dessars B, De Raeve LE, Morandini R et al. (2009) Genotypic and gene expression studies in congenital melanocytic nevi: insight into initial steps of melanotumorigenesis. J Invest Dermatol 129:139-47
-
(2009)
J Invest Dermatol
, vol.129
, pp. 139-147
-
-
Dessars, B.1
De Raeve, L.E.2
Morandini, R.3
-
12
-
-
80051873884
-
Clinical outcome and pathological features associated, with NRAS mutation in cutaneous melanoma
-
Devitt B, Liu W, Salemi R et al. (2011) Clinical outcome and pathological features associated, with NRAS mutation in cutaneous melanoma. Pigment Cell Melanoma Res 24:666-72
-
(2011)
Pigment Cell Melanoma Res
, vol.24
, pp. 666-672
-
-
Devitt, B.1
Liu, W.2
Salemi, R.3
-
13
-
-
0027981723
-
Familial site-specific congenital melanocytic nevus: Report of two families
-
Frieden IJ, Williams ML (1994) Familial site-specific congenital melanocytic nevus: report of two families. Arch Dermatol 130:1075-6
-
(1994)
Arch Dermatol
, vol.130
, pp. 1075-1076
-
-
Frieden, I.J.1
Williams, M.L.2
-
14
-
-
17444366529
-
Association of melanoma and neurocutaneous melanocytosis with large congenital melano-cytic naevi-results from the NYU-LCMN registry
-
Hale EK, Stein J, Ben-Porat L et al. (2005) Association of melanoma and neurocutaneous melanocytosis with large congenital melano-cytic naevi-results from the NYU-LCMN registry. Br J Dermatol 152: 512-7
-
(2005)
Br J Dermatol
, vol.152
, pp. 512-517
-
-
Hale, E.K.1
Stein, J.2
Ben-Porat, L.3
-
15
-
-
79952284127
-
Hallmarks of cancer: The next generation
-
Hanahan D, Weinberg RA (2011) Hallmarks of cancer: the next generation. Cell 144:646-74
-
(2011)
Cell
, vol.144
, pp. 646-674
-
-
Hanahan, D.1
Weinberg, R.A.2
-
16
-
-
84885428325
-
Sensitive detection of KRAS mutations using E-ice-COLD-PCR mutation enrichment and direct sequence identification
-
How Kit A, Mazaleyrat N, Daunay A et al. (2013) Sensitive detection of KRAS mutations using E-ice-COLD-PCR mutation enrichment and direct sequence identification. Hum Mutat 34:1568-80
-
(2013)
Hum Mutat
, vol.34
, pp. 1568-1580
-
-
How Kit, A.1
Mazaleyrat, N.2
Daunay, A.3
-
17
-
-
33746819361
-
High frequency of BRAFV600E mutation in acquired nevi and small congenital nevi, but low frequency of mutation in medium-sized congenital nevi
-
Ichii-Nakato N, Takata M, Takayanagi S et al. (2006) High frequency of BRAFV600E mutation in acquired nevi and small congenital nevi, but low frequency of mutation in medium-sized congenital nevi. J Invest Dermatol 126:2111-8
-
(2006)
J Invest Dermatol
, vol.126
, pp. 2111-2118
-
-
Ichii-Nakato, N.1
Takata, M.2
Takayanagi, S.3
-
18
-
-
84884412000
-
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS
-
Kinsler VA, Thomas AC, Ishida M et al. (2013) Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS. J Invest Dermatol 133: 2229-36
-
(2013)
J Invest Dermatol
, vol.133
, pp. 2229-2236
-
-
Kinsler, V.A.1
Thomas, A.C.2
Ishida, M.3
-
19
-
-
84863942861
-
Germline melanocortin-1-receptor genotype, is associated with severity of cutaneous phenotype in congenital melanocytic nevi: A role for, MC1R in human fetal development
-
Kinsler VA, Abu-Amero S, Budd P et al. (2012) Germline melanocortin-1-receptor genotype, is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for, MC1R in human fetal development. J Invest Dermatol 132:2026-32
-
(2012)
J Invest Dermatol
, vol.132
, pp. 2026-2032
-
-
Kinsler, V.A.1
Abu-Amero, S.2
Budd, P.3
-
20
-
-
33745027181
-
Melanoma risk in congenital melanocytic naevi: A systematic review
-
Krengel S, Hauschild A, Schafer T (2006) Melanoma risk in congenital melanocytic naevi: a systematic review. Br J Dermatol 155:1-8
-
(2006)
Br J Dermatol
, vol.155
, pp. 1-8
-
-
Krengel, S.1
Hauschild, A.2
Schafer, T.3
-
21
-
-
84864746573
-
A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers
-
Lee RS, Stewart C, Carter SL et al. (2012) A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers. J Clin Invest 122:2983-8
-
(2012)
J Clin Invest
, vol.122
, pp. 2983-2988
-
-
Lee, R.S.1
Stewart, C.2
Carter, S.L.3
-
22
-
-
0030024543
-
Large congenital melanocytic nevi and the risk for the development of malignant melanoma
-
Marghoob AA, Schoenbach SP, Kopf AW et al. (1996) Large congenital melanocytic nevi and the risk for the development of malignant melanoma. A prospective study. Arch Dermatol 132:170-5
-
(1996)
A Prospective Study. Arch Dermatol
, vol.132
, pp. 170-175
-
-
Marghoob, A.A.1
Schoenbach, S.P.2
Kopf, A.W.3
-
23
-
-
0032706623
-
A general approach to single-nucleotide polymorphism discovery
-
Marth GT, Korf I, Yandell MD et al. (1999) A general approach to single-nucleotide polymorphism discovery. Nat Genet 23:452-6
-
(1999)
Nat Genet
, vol.23
, pp. 452-456
-
-
Marth, G.T.1
Korf, I.2
Yandell, M.D.3
-
24
-
-
0032767677
-
Mutational analysis of the N-ras, p53, p16INK4a, CDK4, and MC1R genes in human congenital melanocytic naevi
-
Papp T, Pemsel H, Zimmermann R et al. (1999) Mutational analysis of the N-ras, p53, p16INK4a, CDK4, and MC1R genes in human congenital melanocytic naevi. J Med Genet 36:610-4
-
(1999)
J Med Genet
, vol.36
, pp. 610-614
-
-
Papp, T.1
Pemsel, H.2
Zimmermann, R.3
-
25
-
-
27644559365
-
Mutational analysis of the BRAF gene in human congenital and dysplastic melanocytic naevi
-
Papp T, Schipper H, Kumar K et al. (2005) Mutational analysis of the BRAF gene in human congenital and dysplastic melanocytic naevi. Melanoma Res 15:401-7
-
(2005)
Melanoma Res
, vol.15
, pp. 401-407
-
-
Papp, T.1
Schipper, H.2
Kumar, K.3
-
27
-
-
33746263912
-
BRAF and NRAS mutations in melanoma and melanocytic nevi
-
Poynter JN, Elder JT, Fullen DR et al. (2006) BRAF and NRAS mutations in melanoma and melanocytic nevi. Melanoma Res 16:267-73
-
(2006)
Melanoma Res
, vol.16
, pp. 267-273
-
-
Poynter, J.N.1
Elder, J.T.2
Fullen, D.R.3
-
28
-
-
79954703723
-
BRAF exon 15 T1799A mutation is common in melanocytic nevi, but less prevalent in cutaneous malignant melanoma, in Chinese Han
-
Qi RQ, He L, Zheng S et al. (2011) BRAF exon 15 T1799A mutation is common in melanocytic nevi, but less prevalent in cutaneous malignant melanoma, in Chinese Han. J Invest Dermatol 131:1129-38
-
(2011)
J Invest Dermatol
, vol.131
, pp. 1129-1138
-
-
Qi, R.Q.1
He, L.2
Zheng, S.3
-
30
-
-
1942485286
-
Measuring congenital melanocytic nevi
-
Ruiz-Maldonado R (2004) Measuring congenital melanocytic nevi. Pediatr. Dermatol. 21:178-9
-
(2004)
Pediatr. Dermatol.
, vol.21
, pp. 178-179
-
-
Ruiz-Maldonado, R.1
-
31
-
-
84874865318
-
Next generation sequencing in cancer research and clinical application
-
Shyr D, Liu Q (2013) Next generation sequencing in cancer research and clinical application. Biol Proced Online 15:4
-
(2013)
Biol Proced Online
, vol.15
, pp. 4
-
-
Shyr, D.1
Liu, Q.2
-
32
-
-
80052158097
-
The mutational landscape of head and neck squamous cell carcinoma
-
Stransky N, Egloff AM, Tward AD et al. (2011) The mutational landscape of head and neck squamous cell carcinoma. Science 333:1157-60
-
(2011)
Science
, vol.333
, pp. 1157-1160
-
-
Stransky, N.1
Egloff, A.M.2
Tward, A.D.3
-
33
-
-
33744535687
-
Genetic alterations in melanocytic tumors
-
Takata M, Saida T (2006) Genetic alterations in melanocytic tumors. J Dermatol Sci 43:1-10
-
(2006)
J Dermatol Sci
, vol.43
, pp. 1-10
-
-
Takata, M.1
Saida, T.2
-
34
-
-
38449113853
-
DNA methylation analysis by pyrosequencing
-
Tost J, Gut IG (2007) DNA methylation analysis by pyrosequencing. Nat Protoc 2:2265-75
-
(2007)
Nat Protoc
, vol.2
, pp. 2265-2275
-
-
Tost, J.1
Gut, I.G.2
-
35
-
-
79958267573
-
Lack of BRAF(V600E) mutations in giant congenital melanocytic nevi in a Chinese population
-
Wu D, Wang M, Wang X et al. (2011) Lack of BRAF(V600E) mutations in giant congenital melanocytic nevi in a Chinese population. Am J Dermato-pathol 33:341-4
-
(2011)
Am J Dermato-pathol
, vol.33
, pp. 341-344
-
-
Wu, D.1
Wang, M.2
Wang, X.3
-
36
-
-
36348936129
-
Distribution of BRAF T1799A(V600E) mutations across various types of benign nevi: Implications for melanocytic tumorigenesis
-
Wu J, Rosenbaum E, Begum S et al. (2007) Distribution of BRAF T1799A(V600E) mutations across various types of benign nevi: implications for melanocytic tumorigenesis. Am J Dermatopathol 29:534-7
-
(2007)
Am J Dermatopathol
, vol.29
, pp. 534-537
-
-
Wu, J.1
Rosenbaum, E.2
Begum, S.3
|