Accès gratuit
Numéro
Med Sci (Paris)
Volume 28, Numéro 11, Novembre 2012
Page(s) 923 - 925
Section Nouvelles
DOI https://doi.org/10.1051/medsci/20122811007
Publié en ligne 12 novembre 2012
  1. Lettre G, Sankaran VG, Bezerra MAC, et al. DNA polymorphisms at the BCL11A, HBS1L-MYB and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proc Nat Acad Sci USA 2008 ; 105 : 11869–11874. [CrossRef]
  2. Labie D, Dunda-Belkhodja O, Rouabhi F, et al. The -158 site 5’ to the Gγ gene and Gγ expression. Blood 1985 ; 66 : 1463–1465. [PubMed]
  3. Neishabury M, Zamani S, Azarkeivan A, et al. The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5’HS4. Blood Cells Mol Dis 2012 ; 48 : 1–5. [CrossRef] [PubMed]
  4. Sankaran VG, Menne TF, Xu J, et al. Human fetal hemoglobin expression is regulated by the developmental stage-specific repressor BCL11A. Science 2008 ; 322 : 1839–1842. [CrossRef] [PubMed]
  5. Sankaran VG, Xu J, Ragoczy T, et al. Developmental and species-divergent globin switching are driven by BCL11A. Nature 2009 ; 460 : 1093–1097. [CrossRef] [PubMed]
  6. Thein SL, Menzel S, Peng X, et al. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults. Proc Nat Acad Sci USA 2007 ; 104 : 11346–11351. [CrossRef]
  7. Wahlberg K, Jiang J, Rooks H, et al. The HSB1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells. Blood 2009 ; 114 : 1254–1262. [CrossRef] [PubMed]
  8. Borg J, Papadopoulos P, Georgitsi M, et al. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin. Nat Genet 2010 ; 42 : 501–505. [CrossRef]
  9. Zhou D, Liu K, Sun CW, et al. KLF1 regulates BCL11A expression and γ- to β-globin gene switching. Nat Genet 2010 ; 42 : 742–744. [CrossRef] [PubMed]
  10. Galarneau G, Palmer CD, Sankaran VG, et al. Fine-mapping at three loci known to affect fetal hemoglobin levels explain additional genetic variation. Nat Genet 2010 ; 42 : 1049–1051. [CrossRef] [PubMed]
  11. Xu J, Sankaran VG, Ni M, et al. Transcriptional silencing of γ-globin by BCL11A involves long-range interactions and cooperation with SOX. Genes Dev 2010 ; 24 : 783–798. [CrossRef] [PubMed]
  12. Xu J, Peng C, Sankaran VG, et al. Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencing. Science 2011 ; 334 : 993–996. [CrossRef] [PubMed]

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