John W Fathman

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. 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
  2. pmc Identification of multipotent progenitors that emerge prior to hematopoietic stem cells in embryonic development
    Matthew A Inlay
    Institute for Stem Cell Biology and Regenerative Medicine ISCBRM, Stanford University, Stanford, CA 94305, USA
    Stem Cell Reports 2:457-72. 2014
  3. pmc Upregulation of CD11A on hematopoietic stem cells denotes the loss of long-term reconstitution potential
    John W Fathman
    Stanford Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA 94305, USA Electronic address
    Stem Cell Reports 3:707-15. 2014
  4. 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
  5. 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

Detail Information

Publications5

  1. 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...
  2. pmc Identification of multipotent progenitors that emerge prior to hematopoietic stem cells in embryonic development
    Matthew A Inlay
    Institute for Stem Cell Biology and Regenerative Medicine ISCBRM, Stanford University, Stanford, CA 94305, USA
    Stem Cell Reports 2:457-72. 2014
    ..These experiments indicate that multipotent cells appear in concert within both the YS and AGM and strongly implicate YS-derived progenitors as contributors to definitive hematopoiesis. ..
  3. pmc Upregulation of CD11A on hematopoietic stem cells denotes the loss of long-term reconstitution potential
    John W Fathman
    Stanford Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA 94305, USA Electronic address
    Stem Cell Reports 3:707-15. 2014
    ..We propose that CD11A(+)Lin-KIT(+)SCA-1(+)CD150(+)CD34- cells are multipotent progenitors and CD11A-Lin-KIT(+)SCA-1(+)CD150(+)CD34- cells are true HSCs...
  4. 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
    ....
  5. 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. ..