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PLoS Pathogens, ISSN 1553-7366, 12/2011, Volume 7, Issue 12, pp. e1002439 - e1002439
Journal Article
2005, Molecular biology intelligence unit (Unnumbered), ISBN 030648241X, 229
"Nuclear Import and Export in Plants and Animals" provides insight into the remarkable mechanisms of nuclear import and export. This book covers a range of... 
Proteins | Nucleocytoplasmic Transport Proteins | genetics | Biological transport | Nuclear membranes | physiology | Active Transport, Cell Nucleus | Physiological transport | Biology, life sciences | Life Sciences | Cell Biology
Book
Journal of Biological Chemistry, ISSN 0021-9258, 07/2007, Volume 282, Issue 28, pp. 20621 - 20633
Journal Article
Journal Article
Nature Cell Biology, ISSN 1465-7392, 02/2009, Volume 11, Issue 2, pp. 162 - 171
EpCAM was found to be overexpressed on epithelial progenitors, carcinomas and cancer-initiating cells. The role of EpCAM in proliferation, and its association... 
BREAST-CANCER | TARGET | STEM-CELLS | ADHESION MOLECULE | DEPENDENT GAMMA-SECRETASE | EP-CAM | COLORECTAL-CANCER | C-MYC | CELL-PROLIFERATION | BETA-CATENIN | CELL BIOLOGY | ADAM17 Protein | NIH 3T3 Cells | Cell Adhesion Molecules - genetics | Colonic Neoplasms - genetics | Cell Proliferation | Active Transport, Cell Nucleus - physiology | Homeodomain Proteins - metabolism | Humans | Lymphoid Enhancer-Binding Factor 1 - genetics | Male | Presenilin-2 - metabolism | Cell Membrane - genetics | Colonic Neoplasms - metabolism | Epithelial Cell Adhesion Molecule | Cell Nucleus - metabolism | Cell Transformation, Neoplastic - genetics | Muscle Proteins - metabolism | Antigens, Neoplasm - metabolism | Cell Membrane - metabolism | Protein Structure, Tertiary | Antigens, Neoplasm - genetics | Transcription Factors - genetics | Cell Adhesion Molecules - metabolism | Cell Transformation, Neoplastic - metabolism | Lymphoid Enhancer-Binding Factor 1 - metabolism | beta Catenin - metabolism | Homeodomain Proteins - genetics | beta Catenin - genetics | Muscle Proteins - genetics | Transcription Factors - metabolism | ADAM Proteins - metabolism | Animals | Cell Nucleus - genetics | Mitosis - physiology | Carcinoma - genetics | LIM-Homeodomain Proteins | Signal Transduction - physiology | Mice | Carcinoma - metabolism | Tumor antigens | Physiological aspects | Genetic aspects | Research | Health aspects | Cell adhesion molecules | Membrane proteins | Index Medicus
Journal Article
Cell, ISSN 0092-8674, 2007, Volume 129, Issue 4, pp. 723 - 733
Transcriptional activation of the nuclear receptor RAR by retinoic acid (RA) often leads to inhibition of cell growth. However, in some tissues, RA promotes... 
ACUTE-PROMYELOCYTIC-LEUKEMIA | PPAR-BETA | BREAST-CANCER CELLS | TERATOCARCINOMA STEM-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MAMMARY-CARCINOMA | SYMPATHETIC NEURONS | E-FABP | FATTY-ACIDS | TARGET GENE | BINDING PROTEIN-II | CELL BIOLOGY | Active Transport, Cell Nucleus - physiology | Apoptosis - drug effects | Humans | Transcriptional Activation - drug effects | Cell Survival - genetics | Apoptosis - genetics | Mammary Neoplasms, Experimental - physiopathology | Fatty Acid-Binding Proteins - metabolism | Mammary Neoplasms, Experimental - metabolism | Mammary Neoplasms, Experimental - genetics | Receptors, Retinoic Acid - genetics | Cell Nucleus - metabolism | Mammary Neoplasms, Animal - physiopathology | Female | Gene Expression Regulation, Neoplastic - physiology | Mammary Neoplasms, Animal - genetics | Tretinoin - pharmacology | Receptors, Retinoic Acid - drug effects | Cell Survival - drug effects | PPAR-beta - metabolism | Keratinocytes | Receptors, Retinoic Acid - metabolism | Cell Transformation, Neoplastic - metabolism | Fatty Acid-Binding Proteins - genetics | Animals | PPAR-beta - drug effects | Active Transport, Cell Nucleus - drug effects | Mammary Neoplasms, Animal - metabolism | Cell Line, Tumor | Cell Proliferation - drug effects | Mice | Transcriptional Activation - physiology | Cell Transformation, Neoplastic - drug effects | Cell Nucleus - drug effects | Growth | Tretinoin | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2014, Volume 111, Issue 8, pp. 3068 - 3073
Extracellular high-mobility group box (HMGB)1 mediates inflammation during sterile and infectious injury and contributes importantly to disease pathogenesis.... 
Cytokines | Secretion | Cell nucleus | Disulfides | Inflammation | Pharmacology | Gene expression regulation | Acetylation | Macrophages | Cytoplasm | Pathogen-associated molecular pattern | Therapy | Innate immunity | Cytokine | Damage-associated molecular pattern | cytokine | CELLS | STERILE INFLAMMATION | therapy | INFLAMMASOME ACTIVATION | MULTIDISCIPLINARY SCIENCES | NLRP3 INFLAMMASOME | RECEPTOR 4 | innate immunity | IMMUNE-RESPONSES | damage-associated molecular pattern | GENE-EXPRESSION | MOBILITY GROUP BOX-1 | CYTOKINE RELEASE | PROTEIN HMGB1 | pathogen-associated molecular pattern | Immunohistochemistry | Enzyme-Linked Immunosorbent Assay | Active Transport, Cell Nucleus - physiology | Escherichia coli | Blotting, Western | Lipopolysaccharides | Janus Kinase 1 - metabolism | Tandem Mass Spectrometry | STAT1 Transcription Factor - metabolism | Animals | Cell Nucleus - metabolism | Analysis of Variance | Signal Transduction - drug effects | Interferon Type I - pharmacology | Active Transport, Cell Nucleus - drug effects | HMGB1 Protein - metabolism | Chromatography, Liquid | Benzimidazoles - pharmacology | Signal Transduction - physiology | Mice | Pyridones - pharmacology | Translocation (Genetics) | Interferon | Research | Properties | Protein kinases | Immunological research | Cellular biology | Pathogenesis | Mass spectrometry | Cells | Index Medicus | Biological Sciences
Journal Article