메뉴 건너뛰기




Volumn 92, Issue 1, 2010, Pages 194-197

T cell acute lymphoblastic leukemia arising from familial platelet disorder

Author keywords

Familial platelet disorder; RUNX1; t(1; 7); T acute lymphoblastic leukemia

Indexed keywords

TRANSCRIPTION FACTOR RUNX1;

EID: 77955175742     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12185-010-0612-y     Document Type: Article
Times cited : (37)

References (10)
  • 1
    • 0021998315 scopus 로고
    • Studies of a familial platelet disorder
    • 1:STN:280:DyaL2M7itlajsA%3D%3D 3855665
    • SB Dowton D Beardsley D Jamison S Blattner FP Li 1985 Studies of a familial platelet disorder Blood 65 557 563 1:STN:280:DyaL2M7itlajsA%3D%3D 3855665
    • (1985) Blood , vol.65 , pp. 557-563
    • Dowton, S.B.1    Beardsley, D.2    Jamison, D.3    Blattner, S.4    Li, F.P.5
  • 2
    • 8944224533 scopus 로고    scopus 로고
    • Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2
    • 1:CAS:528:DyaK28XjsFGit7g%3D 8652836
    • CY Ho B Otterud RD Legare T Varvil R Saxena DB DeHart, et al. 1996 Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2 Blood 87 5218 5224 1:CAS:528:DyaK28XjsFGit7g%3D 8652836
    • (1996) Blood , vol.87 , pp. 5218-5224
    • Ho, C.Y.1    Otterud, B.2    Legare, R.D.3    Varvil, T.4    Saxena, R.5    Dehart, D.B.6
  • 3
    • 0032830638 scopus 로고    scopus 로고
    • Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
    • 10.1038/13793 1:CAS:528:DyaK1MXmtlOhtbw%3D 10508512
    • WJ Song MG Sullivan RD Legare S Hutchings X Tan D Kufrin, et al. 1999 Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia Nat Genet 23 166 175 10.1038/13793 1:CAS:528:DyaK1MXmtlOhtbw%3D 10508512
    • (1999) Nat Genet , vol.23 , pp. 166-175
    • Song, W.J.1    Sullivan, M.G.2    Legare, R.D.3    Hutchings, S.4    Tan, X.5    Kufrin, D.6
  • 4
    • 67049162141 scopus 로고    scopus 로고
    • High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder
    • 10.1182/blood-2008-07-168260 1:CAS:528:DC%2BD1MXntVerurY%3D 19357396
    • C Preudhomme A Renneville V Bourdon N Philippe C Roche-Lestienne N Boissel, et al. 2009 High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder Blood 113 5583 5587 10.1182/blood-2008-07-168260 1:CAS:528:DC%2BD1MXntVerurY%3D 19357396
    • (2009) Blood , vol.113 , pp. 5583-5587
    • Preudhomme, C.1    Renneville, A.2    Bourdon, V.3    Philippe, N.4    Roche-Lestienne, C.5    Boissel, N.6
  • 5
    • 9444264705 scopus 로고    scopus 로고
    • Haploinsufficiency of AML1 results in a decrease in the number of LTR-HSCs while simultaneously inducing an increase in more mature progenitors
    • 10.1182/blood-2003-12-4349 1:CAS:528:DC%2BD2cXhtVGltb7L 15297309
    • W Sun JR Downing 2004 Haploinsufficiency of AML1 results in a decrease in the number of LTR-HSCs while simultaneously inducing an increase in more mature progenitors Blood 104 3565 3572 10.1182/blood-2003-12-4349 1:CAS:528: DC%2BD2cXhtVGltb7L 15297309
    • (2004) Blood , vol.104 , pp. 3565-3572
    • Sun, W.1    Downing, J.R.2
  • 6
    • 2342451948 scopus 로고    scopus 로고
    • AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis
    • 10.1038/nm997 1:CAS:528:DC%2BD2cXhs1Wnurk%3D 14966519
    • M Ichikawa T Asai T Saito S Seo I Yamazaki T Yamagata, et al. 2004 AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis Nat Med 10 299 304 10.1038/nm997 1:CAS:528:DC%2BD2cXhs1Wnurk%3D 14966519
    • (2004) Nat Med , vol.10 , pp. 299-304
    • Ichikawa, M.1    Asai, T.2    Saito, T.3    Seo, S.4    Yamazaki, I.5    Yamagata, T.6
  • 7
    • 0036463950 scopus 로고    scopus 로고
    • Expression of a conditional AML1-ETO oncogene bypasses embryonic lethality and establishes a murine model of human t(8;21) acute myeloid leukemia
    • 10.1016/S1535-6108(02)00016-8 1:CAS:528:DC%2BD38XitlCmsbs%3D 12086889
    • M Higuchi D O'Brien P Kumaravelu N Lenny EJ Yeoh JR Downing 2002 Expression of a conditional AML1-ETO oncogene bypasses embryonic lethality and establishes a murine model of human t(8;21) acute myeloid leukemia Cancer Cell 1 63 74 10.1016/S1535-6108(02)00016-8 1:CAS:528:DC%2BD38XitlCmsbs%3D 12086889
    • (2002) Cancer Cell , vol.1 , pp. 63-74
    • Higuchi, M.1    O'Brien, D.2    Kumaravelu, P.3    Lenny, N.4    Yeoh, E.J.5    Downing, J.R.6
  • 8
    • 2542554191 scopus 로고    scopus 로고
    • Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies
    • 10.1002/gcc.20030 1:CAS:528:DC%2BD2cXlsFWht7o%3D 15138996
    • A Minelli E Maserati G Rossi ME Bernardo P De Stefano MP Cecchini, et al. 2004 Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies Genes Chromosom Cancer 40 165 171 10.1002/gcc.20030 1:CAS:528:DC%2BD2cXlsFWht7o%3D 15138996
    • (2004) Genes Chromosom Cancer , vol.40 , pp. 165-171
    • Minelli, A.1    Maserati, E.2    Rossi, G.3    Bernardo, M.E.4    De Stefano, P.5    Cecchini, M.P.6
  • 9
    • 58149378467 scopus 로고    scopus 로고
    • Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy
    • 10.1182/blood-2008-05-156745 1:CAS:528:DC%2BD1cXhsVCltbvP 18723428
    • CJ Owen CL Toze A Koochin DL Forrest CA Smith JM Stevens, et al. 2008 Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy Blood 112 4639 4645 10.1182/blood-2008-05-156745 1:CAS:528:DC%2BD1cXhsVCltbvP 18723428
    • (2008) Blood , vol.112 , pp. 4639-4645
    • Owen, C.J.1    Toze, C.L.2    Koochin, A.3    Forrest, D.L.4    Smith, C.A.5    Stevens, J.M.6
  • 10
    • 27744505649 scopus 로고    scopus 로고
    • Runx1 deficiency predisposes mice to T-lymphoblastic lymphoma
    • 10.1182/blood-2005-04-1447 1:CAS:528:DC%2BD2MXht1ehsbrO 16051740
    • M Kundu S Compton L Garrett-Beal T Stacy MF Starost M Eckhaus, et al. 2005 Runx1 deficiency predisposes mice to T-lymphoblastic lymphoma Blood 106 3621 3624 10.1182/blood-2005-04-1447 1:CAS:528:DC%2BD2MXht1ehsbrO 16051740
    • (2005) Blood , vol.106 , pp. 3621-3624
    • Kundu, M.1    Compton, S.2    Garrett-Beal, L.3    Stacy, T.4    Starost, M.F.5    Eckhaus, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.