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Volumn 123, Issue 17, 2014, Pages 2744-2745

Somatic mutations in calreticulin can be found in pedigrees with familial predisposition to myeloproliferative neoplasms

Author keywords

[No Author keywords available]

Indexed keywords

CALRETICULIN; JANUS KINASE 2;

EID: 84902097145     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2014-01-550863     Document Type: Letter
Times cited : (18)

References (10)
  • 1
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    • Myeloproliferative disorders
    • Levine RL, Gilliland DG. Myeloproliferative disorders. Blood. 2008;112(6):2190-2198.
    • (2008) Blood , vol.112 , Issue.6 , pp. 2190-2198
    • Levine, R.L.1    Gilliland, D.G.2
  • 2
    • 80051931772 scopus 로고    scopus 로고
    • New mutations and pathogenesis of myeloproliferative neoplasms
    • Vainchenker W, Delhommeau F, Constantinescu SN, Bernard OA. New mutations and pathogenesis of myeloproliferative neoplasms. Blood. 2011;118(7):1723-1735.
    • (2011) Blood , vol.118 , Issue.7 , pp. 1723-1735
    • Vainchenker, W.1    Delhommeau, F.2    Constantinescu, S.N.3    Bernard, O.A.4
  • 3
    • 84890372480 scopus 로고    scopus 로고
    • Somatic mutations of calreticulin in myeloproliferative neoplasms
    • Klampfl T, Gisslinger H, Harutyunyan AS, et al. Somatic mutations of calreticulin in myeloproliferative neoplasms. N Engl J Med. 2013;369(25):2379- 2390.
    • (2013) N Engl J Med , vol.369 , Issue.25 , pp. 2379-2390
    • Klampfl, T.1    Gisslinger, H.2    Harutyunyan, A.S.3
  • 4
    • 84890328032 scopus 로고    scopus 로고
    • Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2
    • Nangalia J, Massie CE, Baxter EJ, et al. Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2. N Engl J Med. 2013; 369(25):2391-2405.
    • (2013) N Engl J Med , vol.369 , Issue.25 , pp. 2391-2405
    • Nangalia, J.1    Massie, C.E.2    Baxter, E.J.3
  • 6
    • 33747199312 scopus 로고    scopus 로고
    • Acquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders
    • DOI 10.1182/blood-2005-11-009605
    • Kralovics R, Teo SS, Li S, et al. Acquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders. Blood. 2006;108(4):1377-1380. (Pubitemid 44232040)
    • (2006) Blood , vol.108 , Issue.4 , pp. 1377-1380
    • Kralovics, R.1    Teo, S.-S.2    Li, S.3    Theocharides, A.4    Buser, A.S.5    Tichelli, A.6    Skoda, R.C.7
  • 8
    • 39149117989 scopus 로고    scopus 로고
    • The JAK2(V617F) mutation may be present several years before the occurrence of overt myeloproliferative disorders
    • French group on myeloproliferative disorders
    • Bellanné-Chantelot C, Jego P, Lionne-Huyghe P, Tulliez M, Najman A; French group on myeloproliferative disorders. The JAK2(V617F) mutation may be present several years before the occurrence of overt myeloproliferative disorders. Leukemia. 2008;22(2):450-451.
    • (2008) Leukemia , vol.22 , Issue.2 , pp. 450-451
    • Bellanné-Chantelot, C.1    Jego, P.2    Lionne-Huyghe, P.3    Tulliez, M.4    Najman, A.5
  • 9
    • 73949134350 scopus 로고    scopus 로고
    • Hereditary myeloproliferative disorders
    • Skoda RC. Hereditary myeloproliferative disorders. Haematologica. 2010;95(1):6-8.
    • (2010) Haematologica , vol.95 , Issue.1 , pp. 6-8
    • Skoda, R.C.1
  • 10
    • 84993813872 scopus 로고    scopus 로고
    • Inherited predisposition to myeloproliferative neoplasms
    • Jones AV, Cross NC. Inherited predisposition to myeloproliferative neoplasms. Ther Adv Hematol. 2013;4(4):237-253.
    • (2013) Ther Adv Hematol , vol.4 , Issue.4 , pp. 237-253
    • Jones, A.V.1    Cross, N.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.