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1. Full Text Human CD34+ AC133+ VEGFR-2+ cells are not endothelial progenitor cells but distinct, primitive hematopoietic progenitors
by Case, Jamie and Mead, Laura E and Bessler, Waylan K and Prater, Daniel and White, Hilary A and Saadatzadeh, M. Reza and Bhavsar, Janak R and Yoder, Mervin C and Haneline, Laura S and Ingram, David A
Experimental Hematology, ISSN 0301-472X, 2007, Volume 35, Issue 7, pp. 1109 - 1118
Objective Endothelial progenitor cells (EPCs) are used for angiogenic therapies or as biomarkers to assess cardiovascular disease risk. However, there is no... 
Hematology, Oncology and Palliative Medicine | Advanced Basic Science | MEDICINE, RESEARCH & EXPERIMENTAL | STEM-CELLS | ORIGIN | ANGIOGENESIS | VASCULOGENESIS | REGENERATION | BONE-MARROW | UMBILICAL-CORD BLOOD | HEMATOLOGY | CORONARY-ARTERY-DISEASE | MOLECULAR-MECHANISMS | TRANSPLANTATION | Antigens, CD34 - analysis | Vascular Endothelial Growth Factor Receptor-2 - analysis | Cell Separation | Humans | Middle Aged | Cells, Cultured | Male | Stem Cells - cytology | AC133 Antigen | Antigens, CD - analysis | Leukocyte Common Antigens - analysis | Endothelial Cells - cytology | Hematopoietic Stem Cells - cytology | Adult | Female | Glycoproteins - analysis | Peptides - analysis | Index Medicus
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2. Bone marrow-derived progenitors
by Kauser, Katalin and Zeiher, Andreas-Michael
2007, 1. Aufl., Handbook of experimental pharmacology, ISBN 9783540689751, Volume 180, viii, 289
There is excitement generated almost daily about the possible uses of stem cells to treat human disease. The ability of stem cells to acquire different desired... 
Stem cells | B cells | Toxicology | Cancer Research | Neurosciences | Biomedicine | Immunology | Pharmacology/Toxicology
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3. Full Text Cell circuits between B cell progenitors and IL-7+ mesenchymal progenitor cells control B cell development
by Fistonich, Chris and Zehentmeier, Sandra and Bednarski, Jeffrey J and Miao, Runfeng and Schjerven, Hilde and Sleckman, Barry P and Pereira, João P
The Journal of experimental medicine, ISSN 0022-1007, 10/2018, Volume 215, Issue 10, pp. 2586 - 2599
B cell progenitors require paracrine signals such as interleukin-7 (IL-7) provided by bone marrow stromal cells for proliferation and survival. Yet, how B... 
MEDICINE, RESEARCH & EXPERIMENTAL | COMBINED IMMUNODEFICIENCY | LYMPHOPOIESIS | PRE-B | HEMATOPOIETIC STEM-CELLS | WHIM-SYNDROME | IMMUNOLOGY | MOUSE BONE-MARROW | STROMAL CELLS | EXPRESSION | CXCR4 DESENSITIZATION | STRAND BREAKS ACTIVATE | Index Medicus | 315 | 304
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4. Full Text Identification of cDC1- and cDC2-committed DC progenitors reveals early lineage priming at the common DC progenitor stage in the bone marrow
by Schlitzer, Andreas and Sivakamasundari, V and Chen, Jinmiao and Sumatoh, Hermi Rizal Bin and Schreuder, Jaring and Lum, Josephine and Malleret, Benoit and Zhang, Sanqian and Larbi, Anis and Zolezzi, Francesca and Renia, Laurent and Poidinger, Michael and Naik, Shalin and Newell, Evan W and Robson, Paul and Ginhoux, Florent
Nature Immunology, ISSN 1529-2908, 07/2015, Volume 16, Issue 7, pp. 718 - 728
Mouse conventional dendritic cells (cDCs) can be classified into two functionally distinct lineages: the CD8 alpha(+) (CD103(+)) cDC1 lineage, and the CD11b(+)... 
CLASSICAL DENDRITIC CELLS | HOMEOSTASIS | LYMPHOID-TISSUE | HEMATOPOIETIC STEM-CELLS | MOUSE | DYNAMICS | RECEPTOR | TRANSCRIPTION-FACTOR | IMMUNOLOGY | COMMITTED PROGENITORS | EXPRESSION | Antigens, CD - immunology | Stem Cells - immunology | Oligonucleotide Array Sequence Analysis | Dendritic Cells - immunology | Antigens, Ly - genetics | Transcriptome - immunology | Stem Cells - metabolism | Antigens, CD - metabolism | Lectins - metabolism | Flow Cytometry | Single-Cell Analysis - methods | Bone Marrow Cells - immunology | Integrin alpha Chains - immunology | Antigens, Ly - metabolism | Cell Lineage - genetics | Dendritic Cells - metabolism | Microscopy, Electron, Scanning | CD11b Antigen - immunology | Lectins - immunology | Mice, Inbred C57BL | Cells, Cultured | Receptors, Cell Surface - metabolism | Mice, Transgenic | Integrin alpha Chains - metabolism | Transcriptome - genetics | Receptors, Cell Surface - immunology | CD8 Antigens - immunology | CD8 Antigens - metabolism | Animals | Antigens, Ly - immunology | Dendritic Cells - ultrastructure | Lectins - genetics | CD11b Antigen - metabolism | Bone Marrow Cells - metabolism | Cell Lineage - immunology | Cluster Analysis | Receptors, Cell Surface - genetics | Medical research | Immune response | Dendritic cells | Cell development (Biology) | Bone marrow | Medicine, Experimental | Genetic aspects | Research | Properties | Index Medicus
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5. Stem cells
Stem cells, ISSN 1066-5099, 1993
Clone cells | Cloning | Stem cells
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6. Full Text CXCL12 in early mesenchymal progenitors is required for haematopoietic stem-cell maintenance
by Greenbaum, Adam and Hsu, Yen-Michael S and Day, Ryan B and Schuettpelz, Laura G and Christopher, Matthew J and Borgerding, Joshua N and Nagasawa, Takashi and Link, Daniel C
Nature, ISSN 0028-0836, 03/2013, Volume 495, Issue 7440, pp. 227 - 230
Haematopoietic stem cells (HSCs) primarily reside in the bone marrow where signals generated by stromal cells regulate their self-renewal, proliferation and... 
ENGRAFTMENT | REGENERATION | MULTIDISCIPLINARY SCIENCES | BONE-MARROW NICHE | IN-VIVO | QUIESCENCE | CXCR4 | MICE | RECONSTITUTION | EXPRESSION | REVEALS | B-Lymphocytes - cytology | Nestin | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Lymphoid Progenitor Cells - metabolism | Homeodomain Proteins - metabolism | Nerve Tissue Proteins - deficiency | Chemokine CXCL2 - deficiency | Mesenchymal Stromal Cells - metabolism | Hematopoietic Stem Cells - metabolism | Lymphoid Progenitor Cells - cytology | Homeodomain Proteins - genetics | Mesenchymal Stromal Cells - cytology | Animals | Intermediate Filament Proteins - deficiency | Receptor, Platelet-Derived Growth Factor alpha - genetics | Bone Marrow - metabolism | Hematopoietic Stem Cells - cytology | Chemokine CXCL2 - genetics | Stem Cell Niche - physiology | Mice | Chemokine CXCL2 - metabolism | Cell Movement | Genetic code | Medical research | Ligand binding (Biochemistry) | Ligands (Biochemistry) | Physiological aspects | Medicine, Experimental | Research | Hematopoietic stem cells | Chemokines | Bone marrow | Population | Rodents | Index Medicus
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7. Full Text Isolation and characterization of human myeloid progenitor populations—TpoR as discriminator between common myeloid and megakaryocyte/erythroid progenitors
by Edvardsson, Louise and Dykes, Josefina and Olofsson, Tor and Division of Hematology and Transfusion Medicine and Lund University and Lunds universitet and Avdelningen för hematologi och transfusionsmedicin
Experimental Hematology, ISSN 0301-472X, 2006, Volume 34, Issue 5, pp. 599 - 609
The common myeloid progenitor (CMP) and its progeny, the granulocyte/monocyte progenitor (GMP) and megakaryocyte/erythrocyte progenitor (MEP), have been... 
LINEAGE COMMITMENT | MEDICINE, RESEARCH & EXPERIMENTAL | IN-VITRO | CORD-BLOOD | HEMATOPOIETIC STEM-CELLS | BONE-MARROW | RECEPTOR EXPRESSION | C-MPL | LYMPHOID PROGENITORS | HEMATOLOGY | TRANSCRIPTIONAL REGULATION | ERYTHROID-DIFFERENTIATION | Erythroid Precursor Cells - cytology | Cell Separation | Humans | Receptors, Thrombopoietin | Immunophenotyping | Gene Expression Profiling | Reverse Transcriptase Polymerase Chain Reaction | Receptors, Cytokine - physiology | fms-Like Tyrosine Kinase 3 - genetics | Flow Cytometry | Proto-Oncogene Proteins - physiology | Myeloid Progenitor Cells - cytology | Adult | Megakaryocytes - cytology | Index Medicus | Clinical Medicine | Hematologi | Medical and Health Sciences | Hematology | Klinisk medicin | Medicin och hälsovetenskap
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8. Full Text Human RORγt+CD34+ Cells Are Lineage-Specified Progenitors of Group 3 RORγt+ Innate Lymphoid Cells
by Montaldo, Elisa and Teixeira-Alves, Luiz Gustavo and Glatzer, Timor and Durek, Pawel and Stervbo, Ulrik and Hamann, Wiebke and Babic, Marina and Paclik, Daniela and Stölzel, Katharina and Gröne, Jörn and Lozza, Laura and Juelke, Kerstin and Matzmohr, Nadine and Loiacono, Fabrizio and Petronelli, Francesca and Huntington, Nicholas David and Moretta, Lorenzo and Mingari, Maria Cristina and Romagnani, Chiara
Immunity, ISSN 1074-7613, 12/2014, Volume 41, Issue 6, pp. 988 - 1000
Group 3 innate lymphoid cells (ILC3s) are defined by the expression of the transcription factor RORγt, which is selectively required for their development. The... 
TISSUE-INDUCER CELLS | NATURAL-KILLER-CELLS | HELPER 17 CELLS | ROR-GAMMA-T | ARYL-HYDROCARBON RECEPTOR | MURINE BONE-MARROW | SURFACE-MOLECULE | NKP46(+) CELLS | SELECTIVELY EXPRESS | IMMUNOLOGY | ACTIVATING RECEPTOR | Antigens, CD34 - metabolism | Signal Transduction | Humans | Cells, Cultured | Immunity, Innate | Interleukins - metabolism | Intestines - immunology | Killer Cells, Natural - physiology | Palatine Tonsil - immunology | Cell Lineage | Lymphocytes - physiology | Microarray Analysis | Nuclear Receptor Subfamily 1, Group F, Member 3 - metabolism | Hematopoietic Stem Cells - physiology | Adult | Cell Differentiation | Nuclear Receptor Subfamily 1, Group F, Member 3 - genetics | Index Medicus
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9. Full Text Tissue-resident macrophages originate from yolk-sac-derived erythro-myeloid progenitors
by Gomez Perdiguero, Elisa and Klapproth, Kay and Schulz, Christian and Busch, Katrin and Azzoni, Emanuele and Crozet, Lucile and Garner, Hannah and Trouillet, Celine and De Bruijn, Marella F and Geissmann, Frederic and Rodewald, Hans-Reimer
Nature, ISSN 0028-0836, 02/2015, Volume 518, Issue 7540, pp. 547 - 551
Most haematopoietic cells renew from adult haematopoietic stem cells (HSCs)(1-3), however, macrophages in adult tissues can self-maintain independently of... 
CIRCULATING MONOCYTES | MICROGLIA DERIVE | MULTIDISCIPLINARY SCIENCES | HEMATOPOIETIC STEM-CELLS | IN-VIVO | ONTOGENY | DIFFERENTIATION | ADULT LIFE | MATURATION | FETAL LIVER | MOUSE EMBRYO | Microglia - cytology | Granulocytes - cytology | Cell Proliferation | Kupffer Cells - cytology | Monocytes - cytology | Male | Stem Cells - cytology | Macrophages - cytology | Liver - embryology | Receptor, Macrophage Colony-Stimulating Factor - metabolism | Yolk Sac - cytology | fms-Like Tyrosine Kinase 3 - metabolism | Cell Tracking | Fetus - cytology | Cell Lineage | Animals | Hematopoiesis | Erythrocytes - cytology | Female | Macrophages, Alveolar - cytology | Receptor, TIE-2 - metabolism | Liver - cytology | Mice | Langerhans Cells - cytology | Physiological aspects | Genetic aspects | Research | Macrophages | Hematopoietic stem cells | Studies | Tissue | Rodents | Stem cells | Bone marrow | Embryos | Blood | Index Medicus
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10. Full Text Transcriptional Heterogeneity and Lineage Commitment in Myeloid Progenitors
by Paul, Franziska and Arkin, Ya’ara and Giladi, Amir and Jaitin, Diego Adhemar and Kenigsberg, Ephraim and Keren-Shaul, Hadas and Winter, Deborah and Lara-Astiaso, David and Gury, Meital and Weiner, Assaf and David, Eyal and Cohen, Nadav and Lauridsen, Felicia Kathrine Bratt and Haas, Simon and Schlitzer, Andreas and Mildner, Alexander and Ginhoux, Florent and Jung, Steffen and Trumpp, Andreas and Porse, Bo Torben and Tanay, Amos and Amit, Ido
Cell, ISSN 0092-8674, 12/2015, Volume 163, Issue 7, pp. 1663 - 1677
Within the bone marrow, stem cells differentiate and give rise to diverse blood cell types and functions. Currently, hematopoietic progenitors are defined... 
C/EBP-ALPHA | COLONY-STIMULATING FACTOR | RNA-SEQ | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEMATOPOIETIC STEM-CELLS | BONE-MARROW | GATA-1 | SELF-RENEWAL | EPSILON-DEFICIENT MICE | DIFFERENTIATION | EXPRESSION | CELL BIOLOGY | Myeloid Progenitor Cells - metabolism | Mice, Inbred C57BL | Transcriptome | Gene Knockout Techniques | Transcription Factors - metabolism | Animals | Sequence Analysis, RNA | Hematopoiesis | Bone Marrow Transplantation | Myeloid Progenitor Cells - cytology | High-Throughput Nucleotide Sequencing | Mice | CCAAT-Enhancer-Binding Proteins - genetics | Single-Cell Analysis | Computer science | Genetic research | Genetic aspects | Genetic transcription | Analysis | Stem cells | Epigenetic inheritance | DNA binding proteins | Index Medicus
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11. Full Text IDH1(R132H) mutation increases murine haematopoietic progenitors and alters epigenetics
by Sasaki, Masato and Knobbe, Christiane B and Munger, Joshua C and Lind, Evan F and Brenner, Dirk and Brüstle, Anne and Harris, Isaac S and Holmes, Roxanne and Wakeham, Andrew and Haight, Jillian and You-Ten, Annick and Li, Wanda Y and Schalm, Stefanie and Su, Shinsan M and Virtanen, Carl and Reifenberger, Guido and Ohashi, Pamela S and Barber, Dwayne L and Figueroa, Maria E and Melnick, Ari and Zúñiga-Pflücker, Juan-Carlos and Mak, Tak W
Nature, ISSN 0028-0836, 08/2012, Volume 488, Issue 7413, pp. 656 - 659
Mutations in the IDH1 and IDH2 genes encoding isocitrate dehydrogenases are frequently found in human glioblastomas(1) and cytogenetically normal acute myeloid... 
FALSE DISCOVERY RATE | STEM-CELLS | IDH2 MUTATIONS | MULTIDISCIPLINARY SCIENCES | NOTCH | MICE | ACUTE MYELOID-LEUKEMIA | DIFFERENTIATION | ONCOMETABOLITE 2-HYDROXYGLUTARATE | GENOME | Myeloid Cells - cytology | Humans | Male | DNA Methylation | Hematopoiesis | Glioma - pathology | Aging | Female | Spleen - pathology | Disease Models, Animal | Mutant Proteins - genetics | Isocitrate Dehydrogenase - genetics | Mutant Proteins - metabolism | Hematopoietic Stem Cells - metabolism | Mutation - genetics | Gene Knock-In Techniques | Cell Lineage | Animals | Epigenesis, Genetic - genetics | Bone Marrow - pathology | Hematopoietic Stem Cells - cytology | CpG Islands - genetics | Myeloid Cells - metabolism | Isocitrate Dehydrogenase - metabolism | Mice | Histones - metabolism | Leukemia, Myeloid, Acute - genetics | Histones | Genetic aspects | Research | Methylation | Bone marrow | DNA methylation | Mutation | Stem cells | Index Medicus
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12. Full Text Human T‐Lymphoid Progenitors Generated in a Feeder‐Cell‐Free Delta‐Like‐4 Culture System Promote T‐Cell Reconstitution in NOD/SCID/γc−/− Mice
by Reimann, Christian and Six, Emmanuelle and Dal‐Cortivo, Liliane and Schiavo, Andrea and Appourchaux, Kevin and Lagresle‐Peyrou, Chantal and de Chappedelaine, Corinne and Ternaux, Brigitte and Coulombel, Laure and Beldjord, Kheira and Cavazzana‐Calvo, Marina and Andre‐Schmutz, Isabelle
STEM CELLS, ISSN 1066-5099, 08/2012, Volume 30, Issue 8, pp. 1771 - 1780
Slow T‐cell reconstitution is a major clinical concern after transplantation of cord blood (CB)‐derived hematopoietic stem cells. Adoptive transfer of in... 
DLL4 protein | T‐lymphoid precursor cells | Notch1 | Immunotherapy | Hematopoietic stem cell transplantation | T-lymphoid precursor cells | NATURAL-KILLER | BONE-MARROW-TRANSPLANTATION | IMMUNE RECONSTITUTION | CELL & TISSUE ENGINEERING | CELL BIOLOGY | LINEAGE COMMITMENT | CORD BLOOD TRANSPLANTATION | IN-VITRO | DELTA-LIKE 4 | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HEMATOPOIETIC STEM-CELLS | GENE-EXPRESSION | HEMATOLOGY | THYMIC PROGENITORS | Recombinant Fusion Proteins - immunology | Humans | Intercellular Signaling Peptides and Proteins - genetics | Mice, SCID | Hematopoietic Stem Cells - immunology | Animals | Lymphopoiesis - physiology | T-Lymphocytes - cytology | Hematopoietic Stem Cells - cytology | Recombinant Fusion Proteins - genetics | Mice, Inbred NOD | T-Lymphocytes - immunology | Mice | Hematopoietic Stem Cell Transplantation - methods | Cell Differentiation - physiology | Intercellular Signaling Peptides and Proteins - immunology | Index Medicus | Translational and Clinical Research
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