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Volumn 123, Issue 6, 2014, Pages 799-800

GATA2 deficiency: Flesh and blood

Author keywords

[No Author keywords available]

Indexed keywords

CCAAT ENHANCER BINDING PROTEIN ALPHA; TRANSCRIPTION FACTOR GATA 2; TRANSCRIPTION FACTOR PAX5; TRANSCRIPTION FACTOR RUNX1;

EID: 84894034716     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2013-12-539858     Document Type: Review
Times cited : (8)

References (10)
  • 1
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    • GATA2 deficiency: A protean disorder of hematopoiesis, lymphatics, and immunity
    • Spinner MA, Sanchez LA, Hsu AP, et al. GATA2 deficiency: A protean disorder of hematopoiesis, lymphatics, and immunity. Blood. 2014;123(6):809-821.
    • (2014) Blood. , vol.123 , Issue.6 , pp. 809-821
    • Spinner, M.A.1    Sanchez, L.A.2    Hsu, A.P.3
  • 2
    • 84894078016 scopus 로고    scopus 로고
    • The evolution of cellular deficiency in GATA2 mutation
    • Dickinson RE, Milne P, Jardine L, et al. The evolution of cellular deficiency in GATA2 mutation. Blood. 2014;123(6):863-874.
    • (2014) Blood. , vol.123 , Issue.6 , pp. 863-874
    • Dickinson, R.E.1    Milne, P.2    Jardine, L.3
  • 3
    • 80053383273 scopus 로고    scopus 로고
    • Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
    • Hahn CN, Chong CE, Carmichael CL, et al. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia. Nat Genet. 2011;43(10):1012-1017.
    • (2011) Nat Genet. , vol.43 , Issue.10 , pp. 1012-1017
    • Hahn, C.N.1    Chong, C.E.2    Carmichael, C.L.3
  • 4
    • 80053385569 scopus 로고    scopus 로고
    • Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome
    • Ostergaard P, Simpson MA, Connell FC, et al. Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Nat Genet. 2011; 43(10):929-931.
    • (2011) Nat Genet. , vol.43 , Issue.10 , pp. 929-931
    • Ostergaard, P.1    Simpson, M.A.2    Connell, F.C.3
  • 5
    • 79961074298 scopus 로고    scopus 로고
    • Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
    • Hsu AP, Sampaio EP, Khan J, et al. Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome. Blood. 2011;118(10): 2653-2655.
    • (2011) Blood. , vol.118 , Issue.10 , pp. 2653-2655
    • Hsu, A.P.1    Sampaio, E.P.2    Khan, J.3
  • 6
    • 80052089944 scopus 로고    scopus 로고
    • Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
    • Dickinson RE, Griffin H, Bigley V, et al. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency. Blood. 2011;118(10):2656-2658.
    • (2011) Blood. , vol.118 , Issue.10 , pp. 2656-2658
    • Dickinson, R.E.1    Griffin, H.2    Bigley, V.3
  • 7
    • 84873530537 scopus 로고    scopus 로고
    • High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia
    • Pasquet M, Bellanné-Chantelot C, Tavitian S, et al. High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia. Blood. 2013;121(5):822-829.
    • (2013) Blood. , vol.121 , Issue.5 , pp. 822-829
    • Pasquet, M.1    Bellanné-Chantelot, C.2    Tavitian, S.3
  • 8
    • 84894104009 scopus 로고    scopus 로고
    • Unexpected high frequency of GATA2 mutations in children with non-familial MDS and monosomy 7
    • Hirabayashi S, Strahm B, Urbaniak S, et al. Unexpected high frequency of GATA2 mutations in children with non-familial MDS and monosomy 7. Blood. 2012;120(21):1699.
    • (2012) Blood. , vol.120 , Issue.21 , pp. 1699
    • Hirabayashi, S.1    Strahm, B.2    Urbaniak, S.3
  • 10
    • 84884999671 scopus 로고    scopus 로고
    • A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia
    • Shah S, Schrader KA, Waanders E, et al. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia. Nat Genet. 2013; 45(10):1226-1231.
    • (2013) Nat Genet. , vol.45 , Issue.10 , pp. 1226-1231
    • Shah, S.1    Schrader, K.A.2    Waanders, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.