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Volumn 58, Issue 1, 2017, Pages 233-236

Detection of activating MAP2K1 mutations in atypical hairy cell leukemia and hairy cell leukemia variant

Author keywords

[No Author keywords available]

Indexed keywords

B RAF KINASE; GLYCOPROTEIN P 15095; IMMUNOGLOBULIN LAMBDA CHAIN; MAP2K1 PROTEIN, HUMAN; MITOGEN ACTIVATED PROTEIN KINASE KINASE 1;

EID: 84973092326     PISSN: 10428194     EISSN: 10292403     Source Type: Journal    
DOI: 10.1080/10428194.2016.1185786     Document Type: Letter
Times cited : (43)

References (15)
  • 1
    • 79959293462 scopus 로고    scopus 로고
    • BRAF mutations in hairy-cell leukemia
    • E.Tiacci, V.Trifonov, G.Schiavoni,. BRAF mutations in hairy-cell leukemia. N Engl J Med. 2011;364:2305–2315.
    • (2011) N Engl J Med , vol.364 , pp. 2305-2315
    • Tiacci, E.1    Trifonov, V.2    Schiavoni, G.3
  • 2
    • 84883873669 scopus 로고    scopus 로고
    • Hairy cell leukemia-new genes, new targets
    • R.J.Kreitman Hairy cell leukemia-new genes, new targets. Curr Hematol Malig Rep. 2013;8:184–195.
    • (2013) Curr Hematol Malig Rep , vol.8 , pp. 184-195
    • Kreitman, R.J.1
  • 3
    • 84891371044 scopus 로고    scopus 로고
    • High prevalence of MAP2K1 mutations in variant and IGHV4-34-expressing hairy-cell leukemias
    • J.J.Waterfall, E.Arons, R.L.Walker,. High prevalence of MAP2K1 mutations in variant and IGHV4-34-expressing hairy-cell leukemias. Nat Genet. 2014;46:8–10.
    • (2014) Nat Genet , vol.46 , pp. 8-10
    • Waterfall, J.J.1    Arons, E.2    Walker, R.L.3
  • 4
    • 84907009615 scopus 로고    scopus 로고
    • High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative langerhans cell histiocytosis
    • N.A.Brown, L.V.Furtado, B.L.Betz,. High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative langerhans cell histiocytosis. Blood. 2014;124:1655–1658.
    • (2014) Blood , vol.124 , pp. 1655-1658
    • Brown, N.A.1    Furtado, L.V.2    Betz, B.L.3
  • 5
    • 84866429139 scopus 로고    scopus 로고
    • The coding genome of splenic marginal zone lymphoma: Activation of NOTCH2 and other pathways regulating marginal zone development
    • D.Rossi, V.Trifonov, M.Fangazio,. The coding genome of splenic marginal zone lymphoma:Activation of NOTCH2 and other pathways regulating marginal zone development. J Exp Med. 2012;209:1537–1551.
    • (2012) J Exp Med , vol.209 , pp. 1537-1551
    • Rossi, D.1    Trifonov, V.2    Fangazio, M.3
  • 6
    • 84958036005 scopus 로고    scopus 로고
    • NOTCH1, TP53, and MAP2K1 mutations in splenic diffuse red pulp small B-cell lymphoma are associated with progressive disease
    • D.Martinez, A.Navarro, A.Martinez-Trillos,. NOTCH1, TP53, and MAP2K1 mutations in splenic diffuse red pulp small B-cell lymphoma are associated with progressive disease. Am J Surg Pathol. 2016;40:192–201.
    • (2016) Am J Surg Pathol , vol.40 , pp. 192-201
    • Martinez, D.1    Navarro, A.2    Martinez-Trillos, A.3
  • 7
    • 84922793976 scopus 로고    scopus 로고
    • Ewing sarcoma mimicking atypical carcinoid tumor: detection of unexpected genomic alterations demonstrates the use of next generation sequencing as a diagnostic tool
    • L.A.Doyle, K.K.Wong, R.Bueno,. Ewing sarcoma mimicking atypical carcinoid tumor:detection of unexpected genomic alterations demonstrates the use of next generation sequencing as a diagnostic tool. Cancer Genet. 2014;207:335–339.
    • (2014) Cancer Genet , vol.207 , pp. 335-339
    • Doyle, L.A.1    Wong, K.K.2    Bueno, R.3
  • 8
    • 48649107410 scopus 로고    scopus 로고
    • Novel MEK1 mutation identified by mutational analysis of epidermal growth factor receptor signaling pathway genes in lung adenocarcinoma
    • J.L.Marks, Y.Gong, D.Chitale,. Novel MEK1 mutation identified by mutational analysis of epidermal growth factor receptor signaling pathway genes in lung adenocarcinoma. Cancer Res. 2008;68:5524–5528.
    • (2008) Cancer Res , vol.68 , pp. 5524-5528
    • Marks, J.L.1    Gong, Y.2    Chitale, D.3
  • 9
    • 84859576293 scopus 로고    scopus 로고
    • Both variant and IGHV4-34-expressing hairy cell leukemia lack the BRAF V600E mutation
    • L.Xi, E.Arons, W.Navarro,. Both variant and IGHV4-34-expressing hairy cell leukemia lack the BRAF V600E mutation. Blood. 2012;119:3330–3332.
    • (2012) Blood , vol.119 , pp. 3330-3332
    • Xi, L.1    Arons, E.2    Navarro, W.3
  • 10
    • 84920053873 scopus 로고    scopus 로고
    • Age-related clonal hematopoiesis associated with adverse outcomes
    • S.Jaiswal, P.Fontanillas, J.Flannick,. Age-related clonal hematopoiesis associated with adverse outcomes. N Engl J Med. 2014;371:2488–2498.
    • (2014) N Engl J Med , vol.371 , pp. 2488-2498
    • Jaiswal, S.1    Fontanillas, P.2    Flannick, J.3
  • 11
    • 80051625929 scopus 로고    scopus 로고
    • Dissecting therapeutic resistance to RAF inhibition in melanoma by tumor genomic profiling
    • N.Wagle, C.Emery, M.F.Berger,. Dissecting therapeutic resistance to RAF inhibition in melanoma by tumor genomic profiling. J Clin Oncol. 2011;29:3085–3096.
    • (2011) J Clin Oncol , vol.29 , pp. 3085-3096
    • Wagle, N.1    Emery, C.2    Berger, M.F.3
  • 12
    • 84867163670 scopus 로고    scopus 로고
    • Molecular pathogenesis of mantle cell lymphoma
    • P.Jares, D.Colomer, E.Campo Molecular pathogenesis of mantle cell lymphoma. J Clin Invest. 2012;122:3416–3423.
    • (2012) J Clin Invest , vol.122 , pp. 3416-3423
    • Jares, P.1    Colomer, D.2    Campo, E.3
  • 13
    • 84857763426 scopus 로고    scopus 로고
    • Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma
    • R.Kridel, B.Meissner, S.Rogic,. Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma. Blood. 2012;119:1963–1971.
    • (2012) Blood , vol.119 , pp. 1963-1971
    • Kridel, R.1    Meissner, B.2    Rogic, S.3
  • 14
    • 84887285547 scopus 로고    scopus 로고
    • Landscape of somatic mutations and clonal evolution in mantle cell lymphoma
    • S.Bea, R.Valdes-Mas, A.Navarro,. Landscape of somatic mutations and clonal evolution in mantle cell lymphoma. Proc Natl Acad Sci USA. 2013;110:18250–18255.
    • (2013) . Proc Natl Acad Sci USA , vol.110 , pp. 18250-18255
    • Bea, S.1    Valdes-Mas, R.2    Navarro, A.3
  • 15
    • 37249006234 scopus 로고    scopus 로고
    • Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and costello syndrome
    • A.L.Schulz, B.Albrecht, C.Arici,. Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and costello syndrome. Clin Genet. 2008;73:62–70.
    • (2008) Clin Genet , vol.73 , pp. 62-70
    • Schulz, A.L.1    Albrecht, B.2    Arici, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.