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Volumn 129, Issue 6, 2015, Pages 921-923

Primary leptomeningeal melanoma is part of the BAP1-related cancer syndrome

Author keywords

[No Author keywords available]

Indexed keywords

B RAF KINASE; BRCA1 ASSOCIATED PROTEIN 1; HYDROLASE; RAS PROTEIN; UNCLASSIFIED DRUG; BAP1 PROTEIN, HUMAN; TUMOR SUPPRESSOR PROTEIN; UBIQUITIN THIOLESTERASE;

EID: 84929706460     PISSN: 00016322     EISSN: 14320533     Source Type: Journal    
DOI: 10.1007/s00401-015-1423-2     Document Type: Letter
Times cited : (23)

References (11)
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    • Battaglia, A.1
  • 2
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    • COI: 1:STN:280:DyaK1MzjtVSqsg%3D%3D, PID: 10403296
    • Brat DJ, Giannini C, Scheithauer BW, Burger PC (1999) Primary melanocytic neoplasms of the central nervous systems. Am J Surg Pathol 23:745–754
    • (1999) Am J Surg Pathol , vol.23 , pp. 745-754
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  • 5
    • 84930352872 scopus 로고    scopus 로고
    • Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma
    • COI: 1:CAS:528:DC%2BC2cXktlGltL4%3D, PID: 24633195
    • Koopmans AE, Verdijk RM, Brouwer RW, van den Bosch TP, van den Berg MM, Vaarwater J, Kockx CE et al (2014) Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma. Mod Pathol 27:1321–1330. doi:10.1038/modpathol.2014.43
    • (2014) Mod Pathol , vol.27 , pp. 1321-1330
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  • 9
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    • PID: 22307269
    • Murali R, Wiesner T, Rosenblum MK, Bastian BC (2012) GNAQ and GNA11 mutations in melanocytomas of the central nervous system. Acta Neuropathol 123:457–459. doi:10.1007/s00401-012-0948-x
    • (2012) Acta Neuropathol , vol.123 , pp. 457-459
    • Murali, R.1    Wiesner, T.2    Rosenblum, M.K.3    Bastian, B.C.4
  • 10
    • 84873827063 scopus 로고    scopus 로고
    • Tumours associated with BAP1 mutations
    • COI: 1:CAS:528:DC%2BC3sXhtVahtA%3D%3D, PID: 23277170
    • Murali R, Wiesner T, Scolyer RA (2013) Tumours associated with BAP1 mutations. Pathology 45:116–126. doi:10.1097/PAT.0b013e32835d0efb
    • (2013) Pathology , vol.45 , pp. 116-126
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  • 11
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    • Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ
    • COI: 1:CAS:528:DC%2BC3sXhtVOgsL7O, PID: 23656586
    • Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE et al (2013) Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ. N Engl J Med 368:1971–1979. doi:10.1056/NEJMoa1213507
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.