Seung Jae Noh

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. pmc Let-7 microRNAs are developmentally regulated in circulating human erythroid cells
    Seung Jae Noh
    Molecular Medicine Branch, National Institute of Diabetes, Digestive, and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA
    J Transl Med 7:98. 2009
  2. pmc LIN28B-mediated expression of fetal hemoglobin and production of fetal-like erythrocytes from adult human erythroblasts ex vivo
    Y Terry Lee
    Molecular Genomics and Therapeutics Section, Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases NIH, 10 Center Drive, Bethesda, MD 20892, USA
    Blood 122:1034-41. 2013
  3. pmc Identification of TWSG1 as a second novel erythroid regulator of hepcidin expression in murine and human cells
    Toshihiko Tanno
    Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases NIDDK, National Institutes of Health NIH, Bethesda, MD 20892, USA
    Blood 114:181-6. 2009
  4. pmc A synthetic model of human beta-thalassemia erythropoiesis using CD34+ cells from healthy adult donors
    Y Terry Lee
    Molecular Genomics and Therapeutics Section, Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA
    PLoS ONE 8:e68307. 2013
  5. pmc Cytokine-mediated increases in fetal hemoglobin are associated with globin gene histone modification and transcription factor reprogramming
    Orapan Sripichai
    Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA
    Blood 114:2299-306. 2009

Collaborators

Detail Information

Publications5

  1. pmc Let-7 microRNAs are developmentally regulated in circulating human erythroid cells
    Seung Jae Noh
    Molecular Medicine Branch, National Institute of Diabetes, Digestive, and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA
    J Transl Med 7:98. 2009
    ....
  2. pmc LIN28B-mediated expression of fetal hemoglobin and production of fetal-like erythrocytes from adult human erythroblasts ex vivo
    Y Terry Lee
    Molecular Genomics and Therapeutics Section, Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases NIH, 10 Center Drive, Bethesda, MD 20892, USA
    Blood 122:1034-41. 2013
    ..LIN28B expression regulates HbF levels and causes adult human erythroblasts to differentiate with a more fetal-like phenotype. ..
  3. pmc Identification of TWSG1 as a second novel erythroid regulator of hepcidin expression in murine and human cells
    Toshihiko Tanno
    Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases NIDDK, National Institutes of Health NIH, Bethesda, MD 20892, USA
    Blood 114:181-6. 2009
    ..These data demonstrate that twisted gastrulation protein interferes with BMP-mediated hepcidin expression and may act with GDF15 to dysregulate iron homeostasis in thalassemia syndromes...
  4. pmc A synthetic model of human beta-thalassemia erythropoiesis using CD34+ cells from healthy adult donors
    Y Terry Lee
    Molecular Genomics and Therapeutics Section, Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA
    PLoS ONE 8:e68307. 2013
    ..Knockdown of beta-globin expression in cultured primary human erythroblasts provides a robust ex vivo model for beta-thalassemia. ..
  5. pmc Cytokine-mediated increases in fetal hemoglobin are associated with globin gene histone modification and transcription factor reprogramming
    Orapan Sripichai
    Molecular Medicine Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA
    Blood 114:2299-306. 2009
    ....