Toshiyuki Yamane

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. pmc Enforced Bcl-2 expression overrides serum and feeder cell requirements for mouse embryonic stem cell self-renewal
    Toshiyuki Yamane
    Institute of Cancer and Stem Cell Biology and Medicine and Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 102:3312-7. 2005
  2. ncbi request reprint Stimulation of paracrine pathways with growth factors enhances embryonic stem cell engraftment and host-specific differentiation in the heart after ischemic myocardial injury
    Theo Kofidis
    Department of Cardiothoracic Surgery, Falk Research Center, Stanford University Medical School, Stanford, Calif 94305, USA
    Circulation 111:2486-93. 2005
  3. ncbi request reprint Myocardial restoration with embryonic stem cell bioartificial tissue transplantation
    Theo Kofidis
    Department of Cardiothoracic Surgery, Falk Research Center, Stanford University Medical School, Stanford, California, USA
    J Heart Lung Transplant 24:737-44. 2005
  4. ncbi request reprint Bmi-1-green fluorescent protein-knock-in mice reveal the dynamic regulation of bmi-1 expression in normal and leukemic hematopoietic cells
    Naoki Hosen
    Department of Pathology, Stanford University School of Medicine, Stanford, California, USA
    Stem Cells 25:1635-44. 2007
  5. pmc Expression of AA4.1 marks lymphohematopoietic progenitors in early mouse development
    Toshiyuki Yamane
    Department of Pathology, Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 106:8953-8. 2009
  6. ncbi request reprint Injectable bioartificial myocardial tissue for large-scale intramural cell transfer and functional recovery of injured heart muscle
    Theo Kofidis
    Cardiothoracic Surgery Falk Research Center, Stanford University Medical School, CA 94305, USA
    J Thorac Cardiovasc Surg 128:571-8. 2004
  7. ncbi request reprint Insulin-like growth factor promotes engraftment, differentiation, and functional improvement after transfer of embryonic stem cells for myocardial restoration
    Theo Kofidis
    Cardiothoracic Surgery, Falk Research Center, Stanford University Medical School, Stanford, CA 94305, USA
    Stem Cells 22:1239-45. 2004
  8. ncbi request reprint Development of melanocytes from ES cells
    Takahiro Kunisada
    Department of Tissue and Organ Development, Regeneration and Advanced Medical Science, Gifu University Graduate School of Medicine, Gifu 500 8705, Japan
    Methods Enzymol 365:341-9. 2003
  9. ncbi request reprint Presence and distribution of neural crest-derived cells in the murine developing thymus and their potential for differentiation
    Hidetoshi Yamazaki
    Department of Genetic Medicine and Regenerative Therapeutics, Institute of Regenerative Medicine and Biofunction, Tottori University Graduate School of Medical Science, Yonago 683 8503, Japan
    Int Immunol 17:549-58. 2005
  10. ncbi request reprint In vitro differentiation of mouse ES cells into hematopoietic, endothelial, and osteoblastic cell lineages: the possibility of in vitro organogenesis
    Motokazu Tsuneto
    Division of Immunology, Department of Molecular and Cellular Biology, School of Life Science, Faculty of Medicine, Tottori University, 86 Nishi Machi, Yonago, Tottori 683 8503, Japan
    Methods Enzymol 365:98-114. 2003

Detail Information

Publications14

  1. pmc Enforced Bcl-2 expression overrides serum and feeder cell requirements for mouse embryonic stem cell self-renewal
    Toshiyuki Yamane
    Institute of Cancer and Stem Cell Biology and Medicine and Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 102:3312-7. 2005
    ..These results suggest that LIF and Bcl-2 overexpression are sufficient to expand these mouse pluripotent stem cells in vitro...
  2. ncbi request reprint Stimulation of paracrine pathways with growth factors enhances embryonic stem cell engraftment and host-specific differentiation in the heart after ischemic myocardial injury
    Theo Kofidis
    Department of Cardiothoracic Surgery, Falk Research Center, Stanford University Medical School, Stanford, Calif 94305, USA
    Circulation 111:2486-93. 2005
    ..We examine the potential of growth factors to enhance cell engraftment and differentiation and to promote functional improvement after transfer of undifferentiated embryonic stem cells into the injured heart...
  3. ncbi request reprint Myocardial restoration with embryonic stem cell bioartificial tissue transplantation
    Theo Kofidis
    Department of Cardiothoracic Surgery, Falk Research Center, Stanford University Medical School, Stanford, California, USA
    J Heart Lung Transplant 24:737-44. 2005
    ..The present study utilizes embryonic stem cells as the substrate of bioartificial myocardial tissue and evaluates engraftment in, and functional recovery of, the recipient heart...
  4. ncbi request reprint Bmi-1-green fluorescent protein-knock-in mice reveal the dynamic regulation of bmi-1 expression in normal and leukemic hematopoietic cells
    Naoki Hosen
    Department of Pathology, Stanford University School of Medicine, Stanford, California, USA
    Stem Cells 25:1635-44. 2007
    ..Disclosure of potential conflicts of interest is found at the end of this article...
  5. pmc Expression of AA4.1 marks lymphohematopoietic progenitors in early mouse development
    Toshiyuki Yamane
    Department of Pathology, Institute of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 106:8953-8. 2009
    ..These data suggest that AA4.1 is a cell surface marker that can identify the earliest lymphohematopoietic progenitors in mouse development...
  6. ncbi request reprint Injectable bioartificial myocardial tissue for large-scale intramural cell transfer and functional recovery of injured heart muscle
    Theo Kofidis
    Cardiothoracic Surgery Falk Research Center, Stanford University Medical School, CA 94305, USA
    J Thorac Cardiovasc Surg 128:571-8. 2004
    ..Most tissue-engineering approaches to restore injured heart muscle result in distortion of left ventricular geometry. In the present study we suggest seeding embryonic stem cells in a liquid matrix for myocardial restoration...
  7. ncbi request reprint Insulin-like growth factor promotes engraftment, differentiation, and functional improvement after transfer of embryonic stem cells for myocardial restoration
    Theo Kofidis
    Cardiothoracic Surgery, Falk Research Center, Stanford University Medical School, Stanford, CA 94305, USA
    Stem Cells 22:1239-45. 2004
    ..01). IGF did not affect the cellular response to the donor cells or tumorigenicity. IGF-1 promotes expression of cardiomyocyte phenotype in ESCs in vivo. It should be considered as an adjuvant to cell transfer for myocardial restoration...
  8. ncbi request reprint Development of melanocytes from ES cells
    Takahiro Kunisada
    Department of Tissue and Organ Development, Regeneration and Advanced Medical Science, Gifu University Graduate School of Medicine, Gifu 500 8705, Japan
    Methods Enzymol 365:341-9. 2003
  9. ncbi request reprint Presence and distribution of neural crest-derived cells in the murine developing thymus and their potential for differentiation
    Hidetoshi Yamazaki
    Department of Genetic Medicine and Regenerative Therapeutics, Institute of Regenerative Medicine and Biofunction, Tottori University Graduate School of Medical Science, Yonago 683 8503, Japan
    Int Immunol 17:549-58. 2005
    ....
  10. ncbi request reprint In vitro differentiation of mouse ES cells into hematopoietic, endothelial, and osteoblastic cell lineages: the possibility of in vitro organogenesis
    Motokazu Tsuneto
    Division of Immunology, Department of Molecular and Cellular Biology, School of Life Science, Faculty of Medicine, Tottori University, 86 Nishi Machi, Yonago, Tottori 683 8503, Japan
    Methods Enzymol 365:98-114. 2003
  11. ncbi request reprint Distinct osteoclast precursors in the bone marrow and extramedullary organs characterized by responsiveness to Toll-like receptor ligands and TNF-alpha
    Shin ichi Hayashi
    Department of Molecular and Cellular Biology, School of Life Science, Faculty of Medicine, Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Science, Tottori University, Tottori, Japan
    J Immunol 171:5130-9. 2003
    ....
  12. ncbi request reprint Discrete types of osteoclast precursors can be generated from embryonic stem cells
    Hiromi Okuyama
    Division of Immunology, Department of Molecular and Cellular Biology, School of Life Science, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan
    Stem Cells 21:670-80. 2003
    ..We thus showed that OCPs expanded in phase II, but the majority of OCPs arose from ES cells in a manner dependent on VEGFR-1 binding factor(s) in phase I...
  13. ncbi request reprint Regulation of osteoclast development by Notch signaling directed to osteoclast precursors and through stromal cells
    Takayuki Yamada
    Division of Immunology, Department of Molecular and Cellular Biology, School of Life Science, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan
    Blood 101:2227-34. 2003
    ..Taken together, these findings indicate that Notch signaling affects both osteoclast precursors and stromal cells and thereby negatively regulates osteoclastogenesis...
  14. ncbi request reprint Cooperative and indispensable roles of endothelin 3 and KIT signalings in melanocyte development
    Hitomi Aoki
    Department of Tissue and Organ Development, Regeneration and Advanced Medical Science, Gifu University Graduate School of Medicine, Gifu, Japan
    Dev Dyn 233:407-17. 2005
    ..Simultaneous blockade of EDNRB and KIT signalings eliminated melanocyte precursors completely, suggesting that the maintenance or survival of early melanocyte precursors at least required the existence of either EDNRB or KIT signalings...