메뉴 건너뛰기




Volumn 8, Issue 4, 2009, Pages 581-584

Molecular study of CEPBA in familial hematological malignancies

Author keywords

CEBPA; Germline mutation; Haematological familial malignancies

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOCYTIC LEUKEMIA; ARTICLE; CEPBA GENE; CHRONIC LYMPHATIC LEUKEMIA; CONTROLLED STUDY; FAMILIAL CANCER; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GERM CELL; HEMATOLOGIC MALIGNANCY; HODGKIN DISEASE; HUMAN; MAJOR CLINICAL STUDY; MYELODYSPLASTIC SYNDROME; MYELOPROLIFERATIVE DISORDER; NONHODGKIN LYMPHOMA; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RUNX1 GENE; SEQUENCE ANALYSIS; ADULT; AMINO ACID SEQUENCE; BLOOD DISEASE; GENETICS; MIDDLE AGED; MOLECULAR GENETICS; MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE ALIGNMENT;

EID: 70449427713     PISSN: 13899600     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10689-009-9289-x     Document Type: Article
Times cited : (6)

References (16)
  • 1
    • 34250878481 scopus 로고    scopus 로고
    • Growth-inhibiting activity of transcription factor C/EBPalpha, its role in haematopoiesis and its tumour suppressor or oncogenic properties in leukaemias
    • 1:STN:280:DC%2BD2szmsFGntQ%3D%3D
    • O Fuchs 2007 Growth-inhibiting activity of transcription factor C/EBPalpha, its role in haematopoiesis and its tumour suppressor or oncogenic properties in leukaemias Folia Biol (Praha) 53 3 97 108 1:STN:280: DC%2BD2szmsFGntQ%3D%3D
    • (2007) Folia Biol (Praha) , vol.53 , Issue.3 , pp. 97-108
    • Fuchs, O.1
  • 4
    • 63849241865 scopus 로고    scopus 로고
    • Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome
    • 10.1182/blood-2008-09-179895 1:CAS:528:DC%2BD1MXktFWnt74%3D 19171880
    • BJ Wouters B Lowenberg CA Erpelinck-Verschueren WL van Putten PJ Valk R Delwel 2009 Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome Blood 113 13 3088 3091 10.1182/blood-2008-09-179895 1:CAS:528:DC%2BD1MXktFWnt74%3D 19171880
    • (2009) Blood , vol.113 , Issue.13 , pp. 3088-3091
    • Wouters, B.J.1    Lowenberg, B.2    Erpelinck-Verschueren, C.A.3    Van Putten, W.L.4    Valk, P.J.5    Delwel, R.6
  • 5
    • 41949109794 scopus 로고    scopus 로고
    • CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin's lymphoma
    • 10.1016/j.bcmd.2007.11.005 1:CAS:528:DC%2BD1cXkvFaht70%3D 18182175
    • O Fuchs D Provaznikova M Kocova, et al. 2008 CEBPA polymorphisms and mutations in patients with acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin's lymphoma Blood Cells Mol Dis 40 3 401 405 10.1016/j.bcmd.2007.11.005 1:CAS:528:DC%2BD1cXkvFaht70%3D 18182175
    • (2008) Blood Cells Mol Dis , vol.40 , Issue.3 , pp. 401-405
    • Fuchs, O.1    Provaznikova, D.2    Kocova, M.3
  • 6
    • 16544391755 scopus 로고    scopus 로고
    • Mutation of CEBPA in familial acute myeloid leukemia
    • 10.1056/NEJMoa041331 1:CAS:528:DC%2BD2cXhtVCrtrjN 15575056
    • ML Smith JD Cavenagh TA Lister J Fitzgibbon 2004 Mutation of CEBPA in familial acute myeloid leukemia N Engl J Med 351 23 2403 2407 10.1056/NEJMoa041331 1:CAS:528:DC%2BD2cXhtVCrtrjN 15575056
    • (2004) N Engl J Med , vol.351 , Issue.23 , pp. 2403-2407
    • Smith, M.L.1    Cavenagh, J.D.2    Lister, T.A.3    Fitzgibbon, J.4
  • 7
    • 35348838187 scopus 로고    scopus 로고
    • A pedigree harboring a germ-line N-terminal C/EBP{alpha} mutation and development of acute myeloblastic leukemia with a somatic C-terminal C/EBP{alpha} mutation
    • T Nanri N Uike T Kawakita, et al. 2006 A pedigree harboring a germ-line N-terminal C/EBP{alpha} mutation and development of acute myeloblastic leukemia with a somatic C-terminal C/EBP{alpha} mutation Blood 108 11 1916
    • (2006) Blood , vol.108 , Issue.11 , pp. 1916
    • Nanri, T.1    Uike, N.2    Kawakita, T.3
  • 8
    • 55549133272 scopus 로고    scopus 로고
    • Somatic CEBPA mutations are a frequent second event in families with germline CEBPA mutations and familial acute myeloid leukemia
    • 10.1200/JCO.2008.16.5563 1:CAS:528:DC%2BD1cXhsVGhsrvP 18768433
    • T Pabst M Eyholzer S Haefliger J Schardt BU Mueller 2008 Somatic CEBPA mutations are a frequent second event in families with germline CEBPA mutations and familial acute myeloid leukemia J Clin Oncol 26 31 5088 5093 10.1200/JCO.2008.16.5563 1:CAS:528:DC%2BD1cXhsVGhsrvP 18768433
    • (2008) J Clin Oncol , vol.26 , Issue.31 , pp. 5088-5093
    • Pabst, T.1    Eyholzer, M.2    Haefliger, S.3    Schardt, J.4    Mueller, B.U.5
  • 9
    • 21744438305 scopus 로고    scopus 로고
    • Further evidence that germline CEBPA mutations cause dominant inheritance of acute myeloid leukaemia [6]
    • DOI 10.1038/sj.leu.2403788
    • GS Sellick HE Spendlove D Catovsky K Pritchard-Jones RS Houlston 2005 Further evidence that germline CEBPA mutations cause dominant inheritance of acute myeloid leukaemia Leukemia 19 7 1276 1278 10.1038/sj.leu.2403788 1:CAS:528:DC%2BD2MXmvVOis7g%3D 15902292 (Pubitemid 40946018)
    • (2005) Leukemia , vol.19 , Issue.7 , pp. 1276-1278
    • Sellick, G.S.1    Spendlove, H.E.2    Catovsky, D.3    Pritchard-Jones, K.4    Houlston, R.S.5
  • 10
    • 64849093213 scopus 로고    scopus 로고
    • Another pedigree with familial acute myeloid leukemia and germline CEBPA mutation
    • 10.1038/leu.2008.294 1:CAS:528:DC%2BD1MXks1Siurg%3D 18946494
    • A Renneville V Mialou N Philippe, et al. 2009 Another pedigree with familial acute myeloid leukemia and germline CEBPA mutation Leukemia 23 4 804 806 10.1038/leu.2008.294 1:CAS:528:DC%2BD1MXks1Siurg%3D 18946494
    • (2009) Leukemia , vol.23 , Issue.4 , pp. 804-806
    • Renneville, A.1    Mialou, V.2    Philippe, N.3
  • 11
    • 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, et al. 2009 High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder Blood 113 22 5583 5587 10.1182/blood-2008-07-168260 1:CAS:528:DC%2BD1MXntVerurY%3D 19357396
    • (2009) Blood , vol.113 , Issue.22 , pp. 5583-5587
    • Preudhomme, C.1    Renneville, A.2    Bourdon, V.3
  • 12
    • 20044388101 scopus 로고    scopus 로고
    • Characterization of CEBPA mutations in acute myeloid leukemia: Most patients with CEBPA mutations have biallelic mutations and show a distinct immunophenotype of the leukemic cells
    • DOI 10.1158/1078-0432.CCR-04-1816
    • LI Lin CY Chen DT Lin, et al. 2005 Characterization of CEBPA mutations in acute myeloid leukemia: most patients with CEBPA mutations have biallelic mutations and show a distinct immunophenotype of the leukemic cells Clin Cancer Res 11 4 1372 1379 10.1158/1078-0432.CCR-04-1816 1:CAS:528:DC%2BD2MXhvVSrs7Y%3D 15746035 (Pubitemid 40326229)
    • (2005) Clinical Cancer Research , vol.11 , Issue.4 , pp. 1372-1379
    • Lin, L.-I.1    Chen, C.-Y.2    Lin, D.-T.3    Tsay, W.4    Tang, J.-L.5    Yeh, Y.-C.6    Shen, H.-L.7    Su, F.-H.8    Yao, M.9    Huang, S.-Y.10    Tien, H.-F.11
  • 13
    • 40749106150 scopus 로고    scopus 로고
    • Recurrent in-frame insertion in C/EBPalpha TAD2 region is a polymorphism without prognostic value in AML
    • 10.1038/sj.leu.2404926 1:CAS:528:DC%2BD1cXjt1Gnsrs%3D 17851556
    • V Biggio A Renneville O Nibourel, et al. 2008 Recurrent in-frame insertion in C/EBPalpha TAD2 region is a polymorphism without prognostic value in AML Leukemia 22 3 655 657 10.1038/sj.leu.2404926 1:CAS:528: DC%2BD1cXjt1Gnsrs%3D 17851556
    • (2008) Leukemia , vol.22 , Issue.3 , pp. 655-657
    • Biggio, V.1    Renneville, A.2    Nibourel, O.3
  • 14
    • 34347253936 scopus 로고    scopus 로고
    • Genetic changes of CEBPA in cancer: Mutations or polymorphisms? [6]
    • DOI 10.1200/JCO.2007.10.7227
    • C Resende G Regalo C Duraes F Carneiro JC Machado 2007 Genetic changes of CEBPA in cancer: mutations or polymorphisms? J Clin Oncol 25 17 2493 2494 10.1200/JCO.2007.10.7227 1:CAS:528:DC%2BD2sXns1Kmtbo%3D 17557966 (author reply 4-5) (Pubitemid 46999227)
    • (2007) Journal of Clinical Oncology , vol.25 , Issue.17 , pp. 2493-2494
    • Resende, C.1    Regalo, G.2    Duraes, C.3    Carneiro, F.4    Machado, J.C.5
  • 15
    • 33846030429 scopus 로고    scopus 로고
    • A recurrent in-frame insertion in a CEBPA transactivation domain is a polymorphism rather than a mutation that does not affect gene expression profiling-based clustering of AML [5]
    • DOI 10.1182/blood-2006-08-042325
    • BJ Wouters I Louwers PJ Valk B Lowenberg R Delwel 2007 A recurrent in-frame insertion in a CEBPA transactivation domain is a polymorphism rather than a mutation that does not affect gene expression profiling-based clustering of AML Blood 109 1 389 390 10.1182/blood-2006-08-042325 1:CAS:528: DC%2BD2sXivVyqsrY%3D 17190859 (Pubitemid 46053086)
    • (2007) Blood , vol.109 , Issue.1 , pp. 389-390
    • Wouters, B.J.1    Louwers, I.2    Valk, P.J.M.3    Lowenberg, B.4    Delwel, R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.