메뉴 건너뛰기




Volumn 83, Issue 3, 2009, Pages 215-219

Fast and reliable mutation detection of the complete exon 11-15 JAK2 coding region using non-isotopic RNase cleavage assay (NIRCA)

Author keywords

JAK2; Myeloproliferative disorders; NIRCA

Indexed keywords

JANUS KINASE 2; PHENYLALANINE; RIBONUCLEASE; VALINE;

EID: 68849105965     PISSN: 09024441     EISSN: 16000609     Source Type: Journal    
DOI: 10.1111/j.1600-0609.2009.01279.x     Document Type: Article
Times cited : (2)

References (19)
  • 2
    • 2442677685 scopus 로고    scopus 로고
    • The chronic myeloproliferative disorders: Clonality and clinical heterogeneity
    • Spivak JL. The chronic myeloproliferative disorders: clonality and clinical heterogeneity. Semin Hematol 2004 41 (Suppl. 3 1 5.
    • (2004) Semin Hematol , vol.41 , Issue.3 , pp. 1-5
    • Spivak, J.L.1
  • 3
    • 0019818299 scopus 로고
    • Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell
    • Fialkow PJ, Faguet GB, Jacobson RJ, Vaidya K, Murphy S. Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell. Blood 1981 58 : 916 9.
    • (1981) Blood , vol.58 , pp. 916-919
    • Fialkow, P.J.1    Faguet, G.B.2    Jacobson, R.J.3    Vaidya, K.4    Murphy, S.5
  • 4
    • 17844383458 scopus 로고    scopus 로고
    • A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
    • James C, Ugo V, Le Couedic JP, et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature 2005 434 : 1144 8.
    • (2005) Nature , vol.434 , pp. 1144-1148
    • James, C.1    Ugo, V.2    Le Couedic, J.P.3
  • 5
    • 20144363192 scopus 로고    scopus 로고
    • Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
    • Baxter EJ, Scott LM, Campbell PJ, et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 2005 365 : 1054 61.
    • (2005) Lancet , vol.365 , pp. 1054-1061
    • Baxter, E.J.1    Scott, L.M.2    Campbell, P.J.3
  • 7
    • 38349101871 scopus 로고    scopus 로고
    • Classification and diagnosis of myeloproliferative neoplasms: The 2008 World Health Organization criteria and point-of-care diagnostic algorithms
    • Tefferi A, Vardiman JW. Classification and diagnosis of myeloproliferative neoplasms: The 2008 World Health Organization criteria and point-of-care diagnostic algorithms. Leukemia 2008 22 : 14 22.
    • (2008) Leukemia , vol.22 , pp. 14-22
    • Tefferi, A.1    Vardiman, J.W.2
  • 8
    • 33751234537 scopus 로고    scopus 로고
    • Report on two novel nucleotide exchanges in the JAK2 pseudokinase domain: D620E and E627E
    • Schnittger S, Bacher U, Kern W, Schröder M, Haferlach T, Schoch C. Report on two novel nucleotide exchanges in the JAK2 pseudokinase domain: D620E and E627E. Leukemia 2006 20 : 2195 7.
    • (2006) Leukemia , vol.20 , pp. 2195-2197
    • Schnittger, S.1    Bacher, U.2    Kern, W.3    Schröder, M.4    Haferlach, T.5    Schoch, C.6
  • 9
    • 33751246214 scopus 로고    scopus 로고
    • Detection of a new JAK2 D620E mutation in addition to V617F in a patient with polycythemia vera
    • Grunebach F, Bross-Bach U, Kanz L, Brossart P. Detection of a new JAK2 D620E mutation in addition to V617F in a patient with polycythemia vera. Leukemia 2006 20 : 2210 1.
    • (2006) Leukemia , vol.20 , pp. 2210-2211
    • Grunebach, F.1    Bross-Bach, U.2    Kanz, L.3    Brossart, P.4
  • 11
    • 38949160429 scopus 로고    scopus 로고
    • Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders
    • Pietra D, Li S, Brisci A, et al. Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders. Blood 2008 111 : 1686 9.
    • (2008) Blood , vol.111 , pp. 1686-1689
    • Pietra, D.1    Li, S.2    Brisci, A.3
  • 12
    • 33846660947 scopus 로고    scopus 로고
    • JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
    • Scott LM, Tong W, Levine RL, et al. JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. N Engl J Med 2007 356 : 459 68.
    • (2007) N Engl J Med , vol.356 , pp. 459-468
    • Scott, L.M.1    Tong, W.2    Levine, R.L.3
  • 13
    • 62949227518 scopus 로고    scopus 로고
    • Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera
    • Schnittger S, Bacher U, Haferlach C, et al. Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera. Haematologica 2009 94 : 414 8.
    • (2009) Haematologica , vol.94 , pp. 414-418
    • Schnittger, S.1    Bacher, U.2    Haferlach, C.3
  • 15
    • 34249876924 scopus 로고    scopus 로고
    • Correlations of JAK2-V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders
    • Speletas M, Katodritou E, Daiou C, Mandala E, Papadakis E, Kioumi A, Ritis K, Korantzis I. Correlations of JAK2-V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders. Leuk Res 2007 31 : 1053 62.
    • (2007) Leuk Res , vol.31 , pp. 1053-1062
    • Speletas, M.1    Katodritou, E.2    Daiou, C.3    Mandala, E.4    Papadakis, E.5    Kioumi, A.6    Ritis, K.7    Korantzis, I.8
  • 16
    • 0034871732 scopus 로고    scopus 로고
    • RNase cleavage-based methods for mutationSNP detection, past and present
    • Goldrick MM. RNase cleavage-based methods for mutationSNP detection, past and present. Hum Mutat 2001 18 : 190 204.
    • (2001) Hum Mutat , vol.18 , pp. 190-204
    • Goldrick, M.M.1
  • 18
    • 11144354882 scopus 로고    scopus 로고
    • Non-isotopic RNase cleavage assay for mutation detection in MEFV, the gene responsible for familial Mediterranean fever, in a cohort of Greek patients
    • Ritis K, Giaglis S, Spathari N, et al. Non-isotopic RNase cleavage assay for mutation detection in MEFV, the gene responsible for familial Mediterranean fever, in a cohort of Greek patients. Ann Rheum Dis 2004 63 : 438 43.
    • (2004) Ann Rheum Dis , vol.63 , pp. 438-443
    • Ritis, K.1    Giaglis, S.2    Spathari, N.3
  • 19
    • 7344262556 scopus 로고    scopus 로고
    • Absence of Bruton's tyrosine kinase (Btk) mutations in patients with acute myeloid leukaemia
    • Ritis K, Speletas M, Tsironidou V, et al. Absence of Bruton's tyrosine kinase (Btk) mutations in patients with acute myeloid leukaemia. Br J Haematol 1998 102 : 1241 8.
    • (1998) Br J Haematol , vol.102 , pp. 1241-1248
    • Ritis, K.1    Speletas, M.2    Tsironidou, V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.