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Volumn 133, Issue 9, 2013, Pages 2127-2130

Making a mountain out of a Molehill: NRAS, mosaicism, and large congenital nevi

Author keywords

[No Author keywords available]

Indexed keywords

MELANOCORTIN 1 RECEPTOR; MITOGEN ACTIVATED PROTEIN KINASE; PHOSPHATIDYLINOSITOL 3 KINASE; SMALL INTERFERING RNA;

EID: 84884365535     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2013.146     Document Type: Note
Times cited : (24)

References (10)
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  • 2
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    • Genetic changes in neoplasms arising in congenital melanocytic nevi: Differences between nodular proliferations and melanomas
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  • 3
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    • 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
  • 4
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    • Phosphorylation by Cdk2 is required for Myc to repress Ras-induced senescence in cotransformation
    • Hydbring P, Bahram F, Su Y et al. (2010) Phosphorylation by Cdk2 is required for Myc to repress Ras-induced senescence in cotransformation. Proc Natl Acad Sci USA 107: 58-63
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  • 5
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    • 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
  • 6
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    • Targeting NRAS in melanoma
    • Kelleher FC, McArthur GA (2012) Targeting NRAS in melanoma. Cancer J 18:132-6
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  • 7
    • 84863942861 scopus 로고    scopus 로고
    • 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
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  • 8
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    • Kinsler VA, Thomas AC, Ishida M et al. (2013) Multiple congenital melanocytic naevi and neurocutaneous melanosis are caused by post-zygotic mutations in codon 61 of NRAS. J Invest Dermatol 133:2229-36
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.