Jun Seita

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. pmc Gene Expression Commons: an open platform for absolute gene expression profiling
    Jun Seita
    Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, United States of America
    PLoS ONE 7:e40321. 2012
  2. pmc Hematopoietic stem cell: self-renewal versus differentiation
    Jun Seita
    Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
    Wiley Interdiscip Rev Syst Biol Med 2:640-53. 2010
  3. pmc MiDReG: a method of mining developmentally regulated genes using Boolean implications
    Debashis Sahoo
    Department of Electrical Engineering, Stanford University, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 107:5732-7. 2010
  4. ncbi request reprint Hematopoietic stem cell quiescence attenuates DNA damage response and permits DNA damage accumulation during aging
    Derrick J Rossi
    Department of Pathology, Stanford Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA
    Cell Cycle 6:2371-6. 2007
  5. pmc Ly6d marks the earliest stage of B-cell specification and identifies the branchpoint between B-cell and T-cell development
    Matthew A Inlay
    Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA
    Genes Dev 23:2376-81. 2009
  6. pmc Identification of the earliest natural killer cell-committed progenitor in murine bone marrow
    John W Fathman
    Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
    Blood 118:5439-47. 2011
  7. pmc Isolation of primitive endoderm, mesoderm, vascular endothelial and trophoblast progenitors from human pluripotent stem cells
    Micha Drukker
    Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA
    Nat Biotechnol 30:531-42. 2012
  8. pmc Anti-CD47 antibody-mediated phagocytosis of cancer by macrophages primes an effective antitumor T-cell response
    Diane Tseng
    Institute for Stem Cell Biology and Regenerative Medicine, Stanford University Medical Center, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 110:11103-8. 2013
  9. ncbi request reprint Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age
    Derrick J Rossi
    Department of Pathology, and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA
    Nature 447:725-9. 2007
  10. pmc Clonal precursor of bone, cartilage, and hematopoietic niche stromal cells
    Charles K F Chan
    Department of Surgery, H3680, Stanford University School of Medicine, Stanford, CA 94305
    Proc Natl Acad Sci U S A 110:12643-8. 2013

Collaborators

Detail Information

Publications10

  1. pmc Gene Expression Commons: an open platform for absolute gene expression profiling
    Jun Seita
    Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, United States of America
    PLoS ONE 7:e40321. 2012
    ....
  2. pmc Hematopoietic stem cell: self-renewal versus differentiation
    Jun Seita
    Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
    Wiley Interdiscip Rev Syst Biol Med 2:640-53. 2010
    ....
  3. pmc MiDReG: a method of mining developmentally regulated genes using Boolean implications
    Debashis Sahoo
    Department of Electrical Engineering, Stanford University, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 107:5732-7. 2010
    ..These data demonstrate the power of MiDReG in predicting functionally important intermediate genes in a given developmental pathway that is defined by a mutually exclusive gene expression pattern...
  4. ncbi request reprint Hematopoietic stem cell quiescence attenuates DNA damage response and permits DNA damage accumulation during aging
    Derrick J Rossi
    Department of Pathology, Stanford Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA
    Cell Cycle 6:2371-6. 2007
    ..Moreover, the cytoprotection afforded by stem cell quiescence in stress-free, steady-state conditions suggests a mechanism through which potentially dangerous lesions can accumulate in the stem cell pool with age...
  5. pmc Ly6d marks the earliest stage of B-cell specification and identifies the branchpoint between B-cell and T-cell development
    Matthew A Inlay
    Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA
    Genes Dev 23:2376-81. 2009
    ....
  6. pmc Identification of the earliest natural killer cell-committed progenitor in murine bone marrow
    John W Fathman
    Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
    Blood 118:5439-47. 2011
    ..Taken together, our data provide a high-resolution in vivo analysis of the earliest steps of NK cell commitment and maturation...
  7. pmc Isolation of primitive endoderm, mesoderm, vascular endothelial and trophoblast progenitors from human pluripotent stem cells
    Micha Drukker
    Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA
    Nat Biotechnol 30:531-42. 2012
    ..These markers and progenitors provide tools for purifying human tissue-regenerating progenitors and for studying the commitment of pluripotent stem cells to lineage progenitors...
  8. pmc Anti-CD47 antibody-mediated phagocytosis of cancer by macrophages primes an effective antitumor T-cell response
    Diane Tseng
    Institute for Stem Cell Biology and Regenerative Medicine, Stanford University Medical Center, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 110:11103-8. 2013
    ..This response protected animals from tumor challenge. We conclude that anti-CD47 antibody treatment not only enables macrophage phagocytosis of cancer but also can initiate an antitumor cytotoxic T-cell immune response. ..
  9. ncbi request reprint Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age
    Derrick J Rossi
    Department of Pathology, and Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California 94305, USA
    Nature 447:725-9. 2007
    ..These data are consistent with DNA damage accrual being a physiological mechanism of stem cell ageing that may contribute to the diminished capacity of aged tissues to return to homeostasis after exposure to acute stress or injury...
  10. pmc Clonal precursor of bone, cartilage, and hematopoietic niche stromal cells
    Charles K F Chan
    Department of Surgery, H3680, Stanford University School of Medicine, Stanford, CA 94305
    Proc Natl Acad Sci U S A 110:12643-8. 2013
    ....