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1. Full Text Head neck squamous cell carcinoma c‐Met+ cells display cancer stem cell properties and are responsible for cisplatin‐resistance and metastasis
by Sun, Shuyang and Wang, Zuolin
International Journal of Cancer, ISSN 0020-7136, 11/2011, Volume 129, Issue 10, pp. 2337 - 2348
c‐Met, the tyrosine kinase receptor for hepatocyte growth factor, is overexpressed in a variety of tumors in which it plays a central role in malignant... 
c‐Met | head neck squamous cell carcinoma | chemoresistance | cancer stem cell marker | metastasis | c-Met | BMI-1 | ALDEHYDE DEHYDROGENASE | TYROSINE KINASE | PANCREATIC-CANCER | IDENTIFICATION | BREAST-CANCER | INVASIVE GROWTH | ONCOLOGY | THERAPEUTIC TARGET | STEM/PROGENITOR CELLS | Proto-Oncogene Proteins c-met - metabolism | Neoplasm Transplantation | Biomarkers, Tumor - analysis | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Humans | Drug Resistance, Neoplasm | Mice, SCID | Head and Neck Neoplasms - metabolism | Head and Neck Neoplasms - pathology | Neoplasm Metastasis | Animals | Cisplatin - therapeutic use | Cell Division | Cell Line, Tumor | Neoplastic Stem Cells - pathology | Mice, Inbred NOD | Mice
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2. Full Text Functional Characterization of TPO‐Expanded CD34+ Cord Blood Cells Identifies CD34−CD61− Cells as Platelet‐Producing Cells Early After Transplantation in NOD/SCID Mice and rCD34+ Cells as CAFC Colony‐Forming Cells
by Schipper, Laurus F and Brand, Anneke and Fibbe, Willem E and Van Hensbergen, Yvette
STEM CELLS, ISSN 1066-5099, 05/2012, Volume 30, Issue 5, pp. 988 - 996
Transplantation of thrombopoietin (TPO)‐expanded cord blood CD34+ cells accelerates human platelet recovery in NOD/SCID mice. It is unknown which... 
Megakaryocyte | Cord blood | Expansion | CD34 | Thrombopoietin | PROGENITOR CELLS | IMMUNODEFICIENT MICE | MOBILIZED PERIPHERAL-BLOOD | CELL & TISSUE ENGINEERING | CELL BIOLOGY | EX-VIVO EXPANSION | TERM ENGRAFTMENT | RECOVERY | IN-VITRO | ONCOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HEMATOPOIETIC STEM-CELLS | STEM/PROGENITOR CELLS | HEMATOLOGY | Antigens, CD34 | Humans | Cells, Cultured | Male | Transplantation, Heterologous | Integrin beta3 | Thrombopoietin - pharmacology | Fetal Blood - cytology | Fetal Blood - metabolism | Mice, SCID | Cord Blood Stem Cell Transplantation | Megakaryocyte Progenitor Cells - metabolism | Animals | Blood Platelets - cytology | Blood Platelets - metabolism | Female | Mice, Inbred NOD | Mice | Cell Culture Techniques | Megakaryocytes - cytology | Megakaryocytes - metabolism | Megakaryocyte Progenitor Cells - cytology | Stem cell research | Analysis | Stem cells | Bone marrow | Transplantation | Universities and colleges | Chemical properties | Transplants & implants | Blood platelets
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3. Full Text Human placenta-derived mesenchymal stem cells suppress T cell proliferation and support the culture expansion of cord blood CD34+ cells: A comparison with human bone marrow-derived mesenchymal stem cells
by Luan, Xiying and Li, Guangyun and Wang, Guoyan and Wang, Feifei and Lin, Yanhua
Tissue and Cell, ISSN 0040-8166, 2012, Volume 45, Issue 1, pp. 32 - 38
Abstract Human placenta-derived mesenchymal stem cells (hPMSCs) have been shown to possess immunosuppressive effects against T cells and support the expansion... 
Advanced Basic Science | Bone marrow | Hematopoietic stem/progenitor cells (HSPCs) | Mesenchymal stem cells (MSCs) | Placenta | T cells | Immunoregulation | MULTIPOTENT CELLS | ANATOMY & MORPHOLOGY | UNRELATED DONORS | TISSUE REGENERATION | LYMPHOCYTE-PROLIFERATION | TRANSPLANTATION | CELL BIOLOGY | FACTOR-1 | UMBILICAL-CORD | Antigens, CD34 - metabolism | Cell Proliferation | Bone Marrow Cells - cytology | Lymphocyte Activation | Humans | Mesenchymal Stromal Cells - metabolism | Hematopoietic Stem Cells - metabolism | Fetal Blood - cytology | Pregnancy | Mesenchymal Stromal Cells - cytology | Antigens, CD34 - immunology | T-Lymphocytes - cytology | Placenta - cytology | Hematopoietic Stem Cells - cytology | Female | Bone Marrow Cells - metabolism
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4. Full Text CD44 CD24 prostate cells are early cancer progenitor stem cells that provide a model for patients with poor prognosis
by Hurt, E.M and Kawasaki, B.T and Klarmann, G.J and Thomas, S.B and Farrar, W.L
British Journal of Cancer, ISSN 0007-0920, 02/2008, Volume 98, Issue 4, pp. 756 - 765
Recent evidence supports the hypothesis that cancer stem cells are responsible for tumour initiation and formation. Using flow cytometry, we isolated a... 
CD24 | Prostate cancer | Genomics | CD44 | Tumour stem cells | prostate cancer | tumour stem cells | ONCOLOGY | TUMOR STEM-CELLS | PROSPECTIVE IDENTIFICATION | genomics | STEM/PROGENITOR CELLS | IN-VITRO PROPAGATION | Prostatic Neoplasms - metabolism | Prognosis | Oligonucleotide Array Sequence Analysis | CD24 Antigen - metabolism | Humans | Male | Transplantation, Heterologous | Gene Expression Profiling | RNA, Messenger - metabolism | Prostate - metabolism | Prostate - pathology | Flow Cytometry | Neoplastic Stem Cells - metabolism | Hyaluronan Receptors - metabolism | Biomarkers, Tumor - metabolism | Prostatic Neoplasms - pathology | Tumor Stem Cell Assay | Neoplasm Invasiveness | RNA, Messenger - genetics | Mice, SCID | Reverse Transcriptase Polymerase Chain Reaction | Phenotype | Animals | Models, Biological | Mice, Inbred NOD | Biomarkers, Tumor - genetics | Mice | Translational Therapeutics
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5. Full Text A novel view of the adult bone marrow stem cell hierarchy and stem cell trafficking
by Ratajczak, M.Z
Leukemia, ISSN 0887-6924, 04/2015, Volume 29, Issue 4, pp. 776 - 782
This review presents a novel view and working hypothesis about the hierarchy within the adult bone marrow stem cell compartment and the still-intriguing... 
PROGENITOR CELLS | SDF-1 GRADIENT | HEMATOPOIETIC STEM/PROGENITOR CELLS | IN-VITRO | COMPLEMENT | ONCOLOGY | MOBILIZATION | GERM-CELLS | CORD BLOOD | REGENERATIVE MEDICINE | HEMATOLOGY | INNATE IMMUNITY | Gene Expression | Bone Marrow - immunology | Bone Marrow Cells - cytology | Humans | Hematopoietic Stem Cell Transplantation | Hematopoietic Stem Cells - metabolism | Bone Marrow Cells - classification | Hematopoietic Stem Cells - immunology | Chemokine CXCL12 - genetics | Bone Marrow - metabolism | Bone Marrow Cells - immunology | Hematopoietic Stem Cells - cytology | Adult | Complement System Proteins - genetics | Germ Cells - cytology | Germ Cells - metabolism | Hematopoietic Stem Cell Mobilization | Bone Marrow Cells - metabolism | Cell Lineage - genetics | Chemokine CXCL12 - immunology | Germ Cells - immunology | Cell Lineage - immunology | Cell Movement | Physiological aspects | Care and treatment | Genetic aspects | Research | Leukemia | Hematopoietic stem cells | Review
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6. Full Text Pre-Evaluated Safe Human iPSC-Derived Neural Stem Cells Promote Functional Recovery after Spinal Cord Injury in Common Marmoset without Tumorigenicity
by Kobayashi, Yoshiomi and Okada, Yohei and Itakura, Go and Iwai, Hiroki and Nishimura, Soraya and Yasuda, Akimasa and Nori, Satoshi and Hikishima, Keigo and Konomi, Tsunehiko and Fujiyoshi, Kanehiro and Tsuji, Osahiko and Toyama, Yoshiaki and Yamanaka, Shinya and Nakamura, Masaya and Okano, Hideyuki
PLoS ONE, ISSN 1932-6203, 12/2012, Volume 7, Issue 12, p. e52787
Murine and human iPSC-NS/PCs (induced pluripotent stem cell-derived neural stem/progenitor cells) promote functional recovery following transplantation into... 
FIBERS | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | EXPRESSION PROFILE | GENE-EXPRESSION | FETAL-BRAIN | STEM/PROGENITOR CELLS | PLURIPOTENCY | GENERATION | GROWTH-FACTOR | TRANSPLANTATION | Humans | Induced Pluripotent Stem Cells - secretion | Motor Neurons - pathology | Recovery of Function | Spinal Cord Injuries - pathology | Microglia - physiology | Spinal Cord - pathology | Neural Stem Cells - transplantation | Female | Cell Differentiation | Calcitonin Gene-Related Peptide - metabolism | Spinal Cord Injuries - therapy | Hand Strength | Induced Pluripotent Stem Cells - physiology | Nerve Growth Factors - secretion | Callithrix | Cell Survival | Induced Pluripotent Stem Cells - transplantation | Cells, Cultured | Neural Stem Cells - physiology | Nerve Regeneration | Spinal Cord - blood supply | Demyelinating Diseases - prevention & control | Motor Neurons - metabolism | Locomotion | Animals | Neural Stem Cells - secretion | Cicatrix - pathology | Spinal Cord - physiopathology | Cell Transformation, Neoplastic - pathology | Neovascularization, Physiologic | Stem Cell Transplantation - adverse effects | Transplantation | Spinal cord injuries | RNA | Stem cells | Cell culture | Spinal cord | Recovery of function | Stem cell transplantation | Spinal cord injury | Bone surgery | Recovery | Proteins | Angiogenesis | Allografts | Demyelination | Rodents | Fibroblasts | Primates | Physiology | Injuries | Injury analysis | Cloning | Regrowth | Attorneys | Tumorigenicity | Neurotrophic factors | Gene expression | Polymerase chain reaction | Medicine | Orthopedics | Cells (biology) | Neural stem cells | Skin | Laboratory animals | Human behavior | Pluripotency
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7. Full Text Aggregation of human mesenchymal stromal cells (MSCs) into 3D spheroids enhances their antiinflammatory properties
by Thomas J. Bartosh and Joni H. Ylöstalo and Arezoo Mohammadipoor and Nikolay Bazhanov and Katie Coble and Kent Claypool and Ryang Hwa Lee and Hosoon Choi and Darwin J. Prockop
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2010, Volume 107, Issue 31, pp. 13724 - 13729
Previous reports suggested that culture as 3D aggregates or as spheroids can increase the therapeutic potential of the adult stem/progenitor cells referred to... 
Antiinflammatories | Lungs | Stromal cells | Medical treatment | Multipotent stem cells | Cultured cells | Inflammation | Spheroids | Endothelial cells | Mesenchymal stem cells | Spheroid | Stanniocalcin-1 | MSC | TNFα stimulated gene/protein 6 | STEM-CELLS | MULTIDISCIPLINARY SCIENCES | BONE-MARROW | spheroid | TNF alpha stimulated gene/protein 6 | IN-VITRO | inflammation | ENDOTHELIAL-CELLS | STEM/PROGENITOR CELLS | DIFFERENTIATION | EXPRESSION | MODULATION | stanniocalcin-1 | Kangai-1 Protein - immunology | Myocardial Infarction - genetics | Oligonucleotide Array Sequence Analysis | Cell Survival | Humans | Mice, Inbred C57BL | Cells, Cultured | Glycoproteins - metabolism | Pneumonia - pathology | Mesenchymal Stromal Cells - metabolism | Male | Myocardial Infarction - metabolism | Cell Adhesion | Cell Adhesion Molecules - metabolism | Mesenchymal Stromal Cells - cytology | Animals | Myocardial Infarction - pathology | Cell Aggregation | Pneumonia - immunology | Ligands | Mice | Pneumonia - metabolism | Macrophages - immunology | Pneumonia - genetics | Genetic aspects | Anti-inflammatory drugs | Health aspects | Stem cells | Spleen | Cell culture | Animal models | Mesenchyme | stromal cells | Lung | spheroids | Biological Sciences | protein 6 | TNFα stimulated gene
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8. Full Text Single‐cell analysis reveals cancer stem cell heterogeneity in hepatocellular carcinoma
by Zheng, Hongping and Pomyen, Yotsawat and Hernandez, Maria Olga and Li, Caiyi and Livak, Ferenc and Tang, Wei and Dang, Hien and Greten, Tim F and Davis, Jeremy L and Zhao, Yongmei and Mehta, Monika and Levin, Yelena and Shetty, Jyoti and Tran, Bao and Budhu, Anuradha and Wang, Xin Wei
Hepatology, ISSN 0270-9139, 07/2018, Volume 68, Issue 1, pp. 127 - 140
Intratumor molecular heterogeneity of hepatocellular carcinoma is partly attributed to the presence of hepatic cancer stem cells (CSCs). Different CSC... 
LIVER-CANCER | EVOLUTION | RNA-SEQ | MARKER | THERAPEUTIC TARGET | STEM/PROGENITOR CELLS | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | CHALLENGES | TUMOR-INITIATING CELLS | Subpopulations | Liver cancer | Phenotypes | Prognosis | Stem cells | Hepatocellular carcinoma | Gene expression | Biodiversity | Surface markers | Cell surface | Index Medicus | intratumor heterogeneity | single cell genome | cancer stem cells | tumor cell community | cancer stem cell heterogeneity
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9. Full Text Characterization of CD133 + hepatocellular carcinoma cells as cancer stem/progenitor cells
by Suetsugu, Atsushi and Nagaki, Masahito and Aoki, Hitomi and Motohashi, Tsutomu and Kunisada, Takahiro and Moriwaki, Hisataka
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 2006, Volume 351, Issue 4, pp. 820 - 824
The CD133 antigen, identified as a hematopoietic stem cell marker, appears in various human embryonic epithelia including the neural tube, gut, and kidney. We... 
Hepatocellular carcinoma | Stem/progenitor cells | CD133 | SYSTEM | SIDE POPULATION | MARKER | BIOCHEMISTRY & MOLECULAR BIOLOGY | TUMOR | ACUTE MYELOID-LEUKEMIA | IDENTIFICATION | BREAST-CANCER | HETEROGENEITY | BIOPHYSICS | stem/progenitor cells | HEMATOPOIETIC STEM-CELLS | AC133 | hepatocellular carcinoma | Glycoproteins - genetics | Liver Neoplasms - genetics | Peptides - physiology | Humans | Peptides - genetics | Liver Neoplasms - chemistry | Mice, SCID | AC133 Antigen | Antigens, CD - genetics | Glycoproteins - physiology | Stem Cells - chemistry | Antigens, CD - analysis | Animals | Carcinoma, Hepatocellular - genetics | Carcinoma, Hepatocellular - pathology | Stem Cells - pathology | Antigens, CD - physiology | Liver Neoplasms - pathology | Carcinoma, Hepatocellular - chemistry | Mice | Neoplasm Transplantation - pathology | Glycoproteins - analysis | Peptides - analysis | KIDNEYS | THERAPY | GLUTAMINE | HEPATOMAS | IN VITRO | LIGASES | ANTIGENS | MICE | STEM CELLS | 60 APPLIED LIFE SCIENCES
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10. Full Text Ceramide‐1‐Phosphate Regulates Migration of Multipotent Stromal Cells and Endothelial Progenitor Cells—Implications for Tissue Regeneration
by Kim, Chihwa and Schneider, Gabriela and Abdel‐Latif, Ahmed and Mierzejewska, Kasia and Sunkara, Manjula and Borkowska, Sylwia and Ratajczak, Janina and Morris, Andrew J and Kucia, Magda and Ratajczak, Mariusz Z
STEM CELLS, ISSN 1066-5099, 03/2013, Volume 31, Issue 3, pp. 500 - 510
Ceramide‐1‐phosphate (C1P) is a bioactive lipid that, in contrast to ceramide, is an antiapoptotic molecule released from cells that are damaged and “leaky.”... 
Angiogenesis | Ceramide‐1‐phosphate | Human umbilical vein endothelial cell | Chemotaxis | Multipotent stromal cell | Ceramide-1-phosphate | COLONY-STIMULATING FACTOR | BONE-MARROW | MESENCHYMAL STEM-CELLS | SPHINGOSINE 1-PHOSPHATE | CELL & TISSUE ENGINEERING | CELL BIOLOGY | CERAMIDE 1-PHOSPHATE | ONCOLOGY | PLASMA SPHINGOSINE-1-PHOSPHATE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ACUTE MYOCARDIAL-INFARCTION | STEM/PROGENITOR CELLS | BIOACTIVE LIPIDS | HEMATOLOGY | HEMATOPOIETIC STEM | Myocardial Ischemia - metabolism | Up-Regulation | Ceramides - metabolism | Human Umbilical Vein Endothelial Cells - metabolism | Humans | Mice, Inbred C57BL | Mesenchymal Stromal Cells - metabolism | Cell Growth Processes - physiology | Stem Cells - cytology | Regeneration - physiology | Stem Cells - metabolism | Regenerative Medicine - methods | Cell Movement - physiology | Ceramides - biosynthesis | Myocardial Ischemia - pathology | Chemotactic Factors - biosynthesis | Mesenchymal Stromal Cells - cytology | Animals | Chemotactic Factors - metabolism | Human Umbilical Vein Endothelial Cells - cytology | Mice | Phosphates | Physiological aspects | Lipids | Universities and colleges | Stem cells | Endothelium | Bone marrow | HUVEC | C1P | MSC | angiogenesis | chemoataxis
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11. Airway progenitor clone formation is enhanced by Y-27632-dependent changes in the transcriptome
by Reynolds, Susan D and Rios, Cydney and Wesolowska-Andersen, Agata and Zhuang, Yongbin and Pinter, Mary and Happoldt, Carrie and Hill, Cynthia L and Lallier, Scott W and Cosgrove, Gregory P and Solomon, George M and Nichols, David P and Seibold, Max A
American Journal of Respiratory Cell and Molecular Biology, ISSN 1044-1549, 09/2016, Volume 55, Issue 3, pp. 323 - 336
The application of conditional reprogramming culture (CRC) methods to nasal airway epithelial cells would allow more widespread incorporation of primary airway... 
Conditionally reprogrammed cells | Y-27632 | Airway stem progenitor | Clone-forming cell frequency | airway stem progenitor | STEM-CELLS | NASAL | REGENERATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | conditionally reprogrammed cells | PROLIFERATION | BASAL-CELLS | CELL BIOLOGY | IN-VITRO | ROCK INHIBITOR | EPITHELIAL-CELLS | RESPIRATORY SYSTEM | clone-forming cell frequency | GENE-EXPRESSION | ASTHMA | NIH 3T3 Cells | Epithelial Cells - metabolism | Epithelial Cells - drug effects | Humans | Extracellular Matrix - metabolism | Stem Cells - cytology | Lung - cytology | Cell Differentiation - genetics | Cell-Matrix Junctions - metabolism | Clone Cells | Cell Culture Techniques | Epithelial Cells - cytology | Bronchi - cytology | Cellular Reprogramming - genetics | Amides - pharmacology | Extracellular Matrix - drug effects | Transcriptome - drug effects | Transcriptome - genetics | Nose - cytology | Cell-Matrix Junctions - drug effects | Cellular Reprogramming - drug effects | Gene Expression Regulation - drug effects | Animals | Cell Differentiation - drug effects | Fibroblasts - drug effects | Cell Communication - drug effects | Culture Media - pharmacology | Fibroblasts - cytology | Mice | Pyridines - pharmacology | Flow cytometry | Transcription factors | Lung diseases | Cloning | Cystic fibrosis | Gene expression | Asthma | Studies | Cell growth | Pulmonary fibrosis | Cell cycle | Chronic obstructive pulmonary disease | Growth factors | Methods
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