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Volumn 118, Issue 16, 2011, Pages 4301-4302

HbA2: At the borderline of the KLF

Author keywords

[No Author keywords available]

Indexed keywords

ERYTHROID KRUPPEL LIKE FACTOR; HEMOGLOBIN A2;

EID: 80054872216     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2011-08-373324     Document Type: Note
Times cited : (3)

References (10)
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    • KLF1 gene mutations cause borderline HbA2
    • Perseu L, Satta S, Moi P, et al. KLF1 gene mutations cause borderline HbA2. Blood. 2011;118(16):4454-4458.
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    • Perseu, L.1    Satta, S.2    Moi, P.3
  • 2
  • 3
    • 80052153840 scopus 로고    scopus 로고
    • The multifunctional role of EKLF/KLF1 during erythropoiesis
    • Siatecka M, Bieker JJ. The multifunctional role of EKLF/KLF1 during erythropoiesis. Blood. 2011;118(8): 2044-2054.
    • (2011) Blood , vol.118 , Issue.8 , pp. 2044-2054
    • Siatecka, M.1    Bieker, J.J.2
  • 4
    • 52649088204 scopus 로고    scopus 로고
    • Mutations in EKLF/KLF1 form the molecular basis of the rare blood group in(Lu) phenotype
    • Singleton BK, Burton NM, Green C, Brady RL, Anstee DJ. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype. Blood. 2008;112(5): 2081-2088.
    • (2008) Blood , vol.112 , Issue.5 , pp. 2081-2088
    • Singleton, B.K.1    Burton, N.M.2    Green, C.3    Brady, R.L.4    Anstee, D.J.5
  • 5
    • 78249264453 scopus 로고    scopus 로고
    • A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia
    • Arnaud L, Saison C, Helias V, et al. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia. Am J Hum Genet. 2010;87(5):721-727.
    • (2010) Am J Hum Genet , vol.87 , Issue.5 , pp. 721-727
    • Arnaud, L.1    Saison, C.2    Helias, V.3
  • 6
    • 77956622584 scopus 로고    scopus 로고
    • Haploin-sufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
    • Borg J, Papadopoulos P, Georgitsi M, et al. Haploin-sufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin. Nat Genet. 2010; 42(9):801-805.
    • (2010) Nat Genet , vol.42 , Issue.9 , pp. 801-805
    • Borg, J.1    Papadopoulos, P.2    Georgitsi, M.3
  • 7
    • 77950930726 scopus 로고    scopus 로고
    • Transcriptional silencing of {gamma}-globin by BCL11A involves long-range interactions and cooperation with SOX6
    • Xu J, Sankaran VG, Ni M, et al. Transcriptional silencing of {gamma}-globin by BCL11A involves long-range interactions and cooperation with SOX6. Genes Dev. 2010;24(8):783-798.
    • (2010) Genes Dev , vol.24 , Issue.8 , pp. 783-798
    • Xu, J.1    Sankaran, V.G.2    Ni, M.3
  • 8
    • 77956630402 scopus 로고    scopus 로고
    • KLF1 regulates BCL11A expression and gamma- To beta-globin gene switching
    • Zhou D, Liu K, Sun CW, Pawlik KM, Townes TM. KLF1 regulates BCL11A expression and gamma- to beta-globin gene switching. Nat Genet. 2010;42(9):742-744.
    • (2010) Nat Genet , vol.42 , Issue.9 , pp. 742-744
    • Zhou, D.1    Liu, K.2    Sun, C.W.3    Pawlik, K.M.4    Townes, T.M.5
  • 9
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    • Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin
    • Satta S, Perseu L, Moi P, et al. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin. Haematologica. 2011;96(5):767-770.
    • (2011) Haematologica , vol.96 , Issue.5 , pp. 767-770
    • Satta, S.1    Perseu, L.2    Moi, P.3
  • 10
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    • Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes
    • published online ahead of print July 21
    • Singleton BK, Lau W, Fairweather VS, et al. Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes [published online ahead of print July 21, 2011]. Blood.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.