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1. Full Text CD24 + Liver Tumor-Initiating Cells Drive Self-Renewal and Tumor Initiation through STAT3-Mediated NANOG Regulation
by Lee, Terence Kin Wah and Castilho, Antonia and Cheung, Vincent Chi Ho and Tang, Kwan Ho and Ma, Stephanie and Ng, Irene Oi Lin
Cell stem cell, ISSN 1934-5909, 2011, Volume 9, Issue 1, pp. 50 - 63
Cell & Tissue Engineering | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Cell differentiation, maturation, development, hematopoiesis | Liver. Biliary tract. Portal circulation. Exocrine pancreas | Biological and medical sciences | Cell physiology | Molecular and cellular biology | Medical sciences | Tumors | Phosphorylation | Cell Proliferation | CD24 Antigen - metabolism | Homeodomain Proteins - metabolism | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Gene Knockdown Techniques | Neoplasm Metastasis | Carcinoma, Hepatocellular - drug therapy | Neoplastic Stem Cells - metabolism | Carcinoma, Hepatocellular - genetics | Aged, 80 and over | Neoplastic Stem Cells - pathology | Adult | Liver Neoplasms - pathology | Cell Differentiation | STAT3 Transcription Factor - metabolism | Nanog Homeobox Protein | Liver Neoplasms - genetics | Liver Neoplasms - drug therapy | Up-Regulation - genetics | Homeodomain Proteins - genetics | Xenograft Model Antitumor Assays | Animals | Carcinoma, Hepatocellular - pathology | Cell Line, Tumor | Aged | Mice | Index Medicus
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2. Full Text N 6-methyladenosine RNA modification regulates embryonic neural stem cell self-renewal through histone modifications
by Wang, Yang and Li, Yue and Yue, Minghui and Wang, Jun and Kumar, Sandeep and Wechsler-Reya, Robert J and Zhang, Zhaolei and Ogawa, Yuya and Kellis, Manolis and Duester, Gregg and Zhao, Jing Crystal
Nature neuroscience, ISSN 1097-6256, 02/2018, Volume 21, Issue 2, pp. 195 - 206
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Embryo, Mammalian | Cell Self Renewal - physiology | Methyltransferases - metabolism | Methyltransferases - genetics | Gene Expression Regulation, Developmental - genetics | Male | RNA, Messenger - metabolism | Cerebral Cortex - cytology | PAX6 Transcription Factor - genetics | Cell Self Renewal - genetics | Neurogenesis - genetics | Cell Differentiation - genetics | Deoxyadenosines - genetics | Female | Neurogenesis - drug effects | Protein Synthesis Inhibitors - pharmacology | Gene Expression Regulation, Developmental - physiology | Animals, Newborn | PAX6 Transcription Factor - metabolism | Mice, Inbred C57BL | Gene Expression Regulation, Developmental - drug effects | Neural Stem Cells - physiology | Mice, Transgenic | Deoxyadenosines - metabolism | Fibronectins - metabolism | Animals | Cerebral Cortex - embryology | Cell Differentiation - drug effects | Neurogenesis - physiology | Mice | Histones - metabolism | Dactinomycin - pharmacology | RNA modification | Chromatin | Gene regulation | Embryo cells | Cortex | Methyltransferase | Stem cell transplantation | Genomes | Gene expression | Ribonucleic acid--RNA | Neurogenesis | Mammalian cells | Embryogenesis | Stem cells | Neural stem cells
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3. Full Text miR-130b Promotes CD133 + Liver Tumor-Initiating Cell Growth and Self-Renewal via Tumor Protein 53-Induced Nuclear Protein 1
by Ma, Stephanie and Tang, Kwan Ho and Chan, Yuen Piu and Lee, Terence K and Kwan, Pak Shing and Castilho, Antonia and Ng, Irene and Man, Kwan and Wong, Nathalie and To, Ka-Fai and Zheng, Bo-Jian and Lai, Paul B.S and Lo, Chung Mau and Chan, Kwok Wah and Guan, Xin-Yuan
Cell stem cell, ISSN 1934-5909, 12/2010, Volume 7, Issue 6, pp. 694 - 707
Cell & Tissue Engineering | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Cell differentiation, maturation, development, hematopoiesis | Liver. Biliary tract. Portal circulation. Exocrine pancreas | Biological and medical sciences | Cell physiology | Molecular and cellular biology | Medical sciences | Tumors | Liver - pathology | Cell Proliferation | Humans | Middle Aged | Glycoproteins - metabolism | Peptides - genetics | Male | MicroRNAs - metabolism | Antigens, CD - genetics | Antigens, CD - metabolism | Peptides - metabolism | Neoplastic Stem Cells - metabolism | Carcinoma, Hepatocellular - genetics | Aged, 80 and over | Adult | Female | Glycoproteins - genetics | Liver Neoplasms - genetics | Heat-Shock Proteins - metabolism | Liver - metabolism | Nuclear Proteins - metabolism | Mice, SCID | AC133 Antigen | Animals | Carrier Proteins - metabolism | Liver Neoplasms - metabolism | Cell Line, Tumor | Aged | Mice | Carcinoma, Hepatocellular - metabolism | Index Medicus
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4. Full Text Genome-Wide Analysis of Self-Renewal in Drosophila Neural Stem Cells by Transgenic RNAi
by Neumüller, Ralph A and Richter, Constance and Fischer, Anja and Novatchkova, Maria and Neumüller, Klaus G and Knoblich, Juergen A
Cell stem cell, ISSN 1934-5909, 05/2011, Volume 8, Issue 5, pp. 580 - 593
Cell & Tissue Engineering | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Cell physiology | Molecular and cellular biology | Cell differentiation, maturation, development, hematopoiesis | Spliceosomes - genetics | Cell Survival - genetics | RNA, Messenger - analysis | Chromatin Assembly and Disassembly - genetics | Drosophila Proteins - metabolism | Neural Stem Cells - cytology | DNA-Binding Proteins - metabolism | Cell Differentiation - genetics | Chaperonin Containing TCP-1 - genetics | Trans-Activators - genetics | Cell Cycle Proteins - genetics | Larva - genetics | Transcriptional Elongation Factors - genetics | Chaperonin Containing TCP-1 - metabolism | Drosophila - genetics | Multigene Family - genetics | Genome-Wide Association Study | High Mobility Group Proteins - metabolism | Alternative Splicing - genetics | Cell Cycle Proteins - metabolism | Cells, Cultured | Computational Biology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Transcription Factors - metabolism | Transcriptional Elongation Factors - metabolism | Animals | Trans-Activators - metabolism | Drosophila Proteins - genetics | Neural Stem Cells - metabolism | High Mobility Group Proteins - genetics | Index Medicus | Resource
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5. Full Text The Long Noncoding RNA lncTCF7 Promotes Self-Renewal of Human Liver Cancer Stem Cells through Activation of Wnt Signaling
by Wang, Yanying and He, Lei and Du, Ying and Zhu, Pingping and Huang, Guanling and Luo, Jianjun and Yan, Xinlong and Ye, Buqing and Li, Chong and Xia, Pengyan and Zhang, Geng and Tian, Yong and Chen, Runsheng and Fan, Zusen
Cell stem cell, ISSN 1934-5909, 04/2015, Volume 16, Issue 4, pp. 413 - 425
RNA, Small Interfering - genetics | Up-Regulation | Humans | Gene Expression Regulation, Neoplastic | Transcriptome | Promoter Regions, Genetic - genetics | Cell Self Renewal - genetics | Microarray Analysis | Carcinoma, Hepatocellular - genetics | Tumor Burden - genetics | T Cell Transcription Factor 1 - metabolism | Neoplastic Stem Cells - physiology | Wnt Signaling Pathway | Chromosomal Proteins, Non-Histone - metabolism | Liver Neoplasms - genetics | Carcinogenesis - genetics | RNA, Long Noncoding - genetics | T Cell Transcription Factor 1 - genetics | Transcription Factors - metabolism | Xenograft Model Antitumor Assays | Animals | Mice, Nude | Liver Neoplasms - metabolism | Cell Line, Tumor | Mice | RNA, Long Noncoding - metabolism | Carcinoma, Hepatocellular - metabolism | Index Medicus
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6. Full Text TGF-β Increases Glioma-Initiating Cell Self-Renewal through the Induction of LIF in Human Glioblastoma
by Peñuelas, Silvia and Anido, Judit and Prieto-Sánchez, Rosa M and Folch, Gerard and Barba, Ignasi and Cuartas, Isabel and García-Dorado, David and Poca, M. Antonia and Sahuquillo, Juan and Baselga, Jose and Seoane, Joan
Cancer cell, ISSN 1535-6108, 2009, Volume 15, Issue 4, pp. 315 - 327
STEMCELL | CELLCYCLE | Oncology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Transforming Growth Factor beta2 - metabolism | Humans | Brain Neoplasms - pathology | STAT Transcription Factors - metabolism | Neurons - cytology | Leukemia Inhibitory Factor - genetics | Smad3 Protein - metabolism | Stem Cells - metabolism | Brain Neoplasms - metabolism | Leukemia Inhibitory Factor - metabolism | Janus Kinase 1 - metabolism | Smad3 Protein - genetics | Glioblastoma - genetics | Janus Kinase 1 - genetics | Glioblastoma - metabolism | Cell Differentiation | Neurons - metabolism | Promoter Regions, Genetic | Signal Transduction | Cells, Cultured | Brain Neoplasms - genetics | Mice, SCID | STAT Transcription Factors - genetics | Animals | Transforming Growth Factor beta - genetics | Glioblastoma - pathology | Mice, Inbred NOD | Mice | Transforming Growth Factor beta2 - genetics | Transforming Growth Factor beta - metabolism | Index Medicus
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7. Full Text Opposing microRNA families regulate self-renewal in mouse embryonic stem cells
by Blelloch, Robert and Melton, Collin and Judson, Robert L
Nature (London), ISSN 0028-0836, 02/2010, Volume 463, Issue 7281, pp. 621 - 626
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Molecular and cellular biology | Embryonic Stem Cells - metabolism | RNA-Binding Proteins - genetics | Cell Proliferation | Embryonic Stem Cells - cytology | MicroRNAs - antagonists & inhibitors | Computational Biology | Gene Silencing | 3' Untranslated Regions - genetics | MicroRNAs - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Open Reading Frames - genetics | Proteins - genetics | Transcription Factors - metabolism | Animals | Genes, myc - genetics | Transcription, Genetic | Mice | MicroRNAs - genetics | Induced Pluripotent Stem Cells - cytology | Cell Dedifferentiation - genetics | Cellular Reprogramming - genetics | Cell Lineage - genetics | Induced Pluripotent Stem Cells - metabolism | Stem cell research | MicroRNA | Research | Embryonic stem cells | Genomics | Analysis | Evacuations & rescues | Cell cycle | Cancer | Index Medicus
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8. Full Text Sox2 maintains self renewal of tumor-initiating cells in osteosarcomas
by Basu-Roy, U and Seo, E and Ramanathapuram, L and Rapp, T.B and Perry, J.A and Orkin, S.H and Mansukhani, A and Basilico, C
Oncogene, ISSN 0950-9232, 05/2012, Volume 31, Issue 18, pp. 2270 - 2282
mesenchymal tumors | wnt signaling | differentiation | cancer stem cell | osteosarcoma | sarcosphere | Biochemistry & Molecular Biology | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Cell Proliferation | Signal Transduction | Membrane Proteins - genetics | Humans | Antigens, Ly - genetics | Antigens, Surface - genetics | Bone Neoplasms - pathology | Cell Differentiation - genetics | Animals | Neoplastic Stem Cells - metabolism | SOXB1 Transcription Factors - genetics | Cell Transformation, Neoplastic - genetics | Antigens, Surface - metabolism | Cell Line, Tumor | Neoplastic Stem Cells - pathology | Antigens, Ly - metabolism | Bone Neoplasms - genetics | Membrane Proteins - metabolism | Mice | Osteosarcoma - genetics | Osteosarcoma - pathology | Wnt Signaling Pathway | Transcription factors | Osteosarcoma | Stem cells | Physiological aspects | Genetic aspects | Research | Risk factors | Signal transduction | Gene expression | Tumors | Index Medicus | Osteoprogenitor cells | Pediatrics | Mesenchyme | Sarcoma | Wnt protein | biomarkers | Data processing | survival factor | Malignancy | Tumorigenicity | Self | Osteosarcoma cells | Osteoblasts | Mutation | Cancer | Sox2 | Wnt signaling | tumor initiating cell
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