Cell Stem Cell

Journal

Publication Venue For

  • Erratum: MAP4K4 Inhibition Promotes Survival of Human Stem Cell-Derived Cardiomyocytes and Reduces Infarct Size In Vivo (Cell Stem Cell (2019) 24(4) (579–591.e12), (S193459091930013X), (10.1016/j.stem.2019.01.013)).  26:458. 2020
  • Erratum: Mesenchymal Niche-Specific Expression of Cxcl12 Controls Quiescence of Treatment-Resistant Leukemia Stem Cells (Cell Stem Cell (2019) 24(5) (769–784.e6), (S1934590919300700), (10.1016/j.stem.2019.02.018)).  26:123. 2020
  • Single-Cell Transcriptomic Analyses of Cell Fate Transitions during Human Cardiac Reprogramming.  25:149-164.e9. 2019
  • Mesenchymal Niche-Specific Expression of Cxcl12 Controls Quiescence of Treatment-Resistant Leukemia Stem Cells.  24:769-784.e6. 2019
  • MAP4K4 Inhibition Promotes Survival of Human Stem Cell-Derived Cardiomyocytes and Reduces Infarct Size In Vivo.  24:579-591.e12. 2019
  • SIRT1 Activation Disrupts Maintenance of Myelodysplastic Syndrome Stem and Progenitor Cells by Restoring TET2 Function.  23:355-369.e9. 2018
  • CD82 Is a Marker for Prospective Isolation of Human Muscle Satellite Cells and Is Linked to Muscular Dystrophies.  19:800-807. 2016
  • Advanced Technologies Lead iNto New Reprogramming Routes.  19:286-288. 2016
  • Dual SMAD Signaling Inhibition Enables Long-Term Expansion of Diverse Epithelial Basal Cells.  19:217-231. 2016
  • Retinas in a Dish Peek into Inherited Retinal Degeneration.  18:688-689. 2016
  • Bmi1 Is a Key Epigenetic Barrier to Direct Cardiac Reprogramming.  18:382-395. 2016
  • HDAC8 Inhibition Specifically Targets Inv(16) Acute Myeloid Leukemic Stem Cells by Restoring p53 Acetylation.  17:597-610. 2015
  • Hematopoietic Differentiation Is Required for Initiation of Acute Myeloid Leukemia.  17:611-623. 2015
  • Erratum: Cardiac repair in a porcine model of acute myocardial infarction with human induced pluripotent stem cell-derived cardiovascular cells (Cell Stem Cell (2014) 15 (750-761)).  16:102. 2015
  • Cardiac repair in a porcine model of acute myocardial infarction with human induced pluripotent stem cell-derived cardiovascular cells.  15:750-761. 2014
  • Pushing the limits: Defeating leukemia stem cells by depleting telomerase.  15:673-675. 2014
  • Notch-dependent repression of miR-155 in the bone marrow niche regulates hematopoiesis in an NF-κB-dependent manner.  15:51-65. 2014
  • Targeted gene correction minimally impacts whole-genome mutational load in human-disease-specific induced pluripotent stem cell clones.  15:31-36. 2014
  • Trrap-dependent histone acetylation specifically regulates cell-cycle gene transcription to control neural progenitor fate decisions.  14:632-643. 2014
  • 9-1-1: HSCs respond to emergency calls.  14:415-416. 2014
  • SIRT1 activation by a c-MYC oncogenic network promotes the maintenance and drug resistance of human FLT3-ITD acute myeloid leukemia stem cells.  15:431-446. 2014
  • Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells.  10:570-582. 2012
  • Self-renewing endodermal progenitor lines generated from human pluripotent stem cells.  10:371-384. 2012
  • Signaling network crosstalk in human pluripotent cells: A Smad2/3-regulated switch that controls the balance between self-renewal and differentiation.  10:312-326. 2012
  • Stem-cell-like qualities of immune memory; CD4 + T cells join the party.  10:107-108. 2012
  • Erratum: In vivo fate mapping and expression analysis reveals molecular hallmarks of prospectively isolated adult neural stem cells (Cell Stem Cell (2010) 7 (744-758)).  8:119. 2011
  • In vivo fate mapping and expression analysis reveals molecular hallmarks of prospectively isolated adult neural stem cells.  7:744-758. 2010
  • Microglia shape adult hippocampal neurogenesis through apoptosis-coupled phagocytosis.  7:483-495. 2010
  • Integrin Alpha 6 regulates glioblastoma stem cells.  6:421-432. 2010

    • International Standard Serial Number (issn)

  • 1934-5909

    • Electronic International Standard Serial Number (eissn)

  • 1875-9777