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The Journal of experimental medicine, ISSN 1540-9538, 01/2009, Volume 206, Issue 1, pp. 249 - 258
Psoriasis is a type I interferon-driven T cell–mediated disease characterized by the recruitment of plasmacytoid dendritic cells (pDC) into the skin. The... 
Immunology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | CD8-Positive T-Lymphocytes - cytology | Neutrophils - cytology | Membrane Glycoproteins - metabolism | Skin - metabolism | Humans - metabolism | Antigens, CD - metabolism | Chemotaxis, Leukocyte - physiology | Lectins, C-Type - metabolism | Chemotaxis, Leukocyte - drug effects | Psoriasis - pathology | Psoriasis - metabolism | CD8-Positive T-Lymphocytes - metabolism | Receptors, Chemokine - genetics | Neutrophils - metabolism | Antibodies, Monoclonal - immunology | Fibroblasts - metabolism | Tretinoin - pharmacology | Antibodies, Monoclonal - pharmacology | Neutrophils - drug effects | Reverse Transcriptase Polymerase Chain Reaction | Chemokines - genetics | Blotting, Western | Intercellular Adhesion Molecule-1 - metabolism | Calcitriol - pharmacology | Fibroblasts - drug effects | Chemokines - metabolism | Fibroblasts - cytology | Receptors, Immunologic - genetics | Chemokine CXCL10 - metabolism | Dermatitis, Atopic - genetics | Gene Expression - drug effects | Culture Media, Conditioned - pharmacology | Extracellular Signal-Regulated MAP Kinases - metabolism | Lectins, C-Type - genetics | Psoriasis - genetics | Adult | Dendritic Cells - metabolism | Skin - pathology | Intercellular Signaling Peptides and Proteins | Receptors, Chemokine - metabolism | Cells, Cultured | Dermatitis, Atopic - pathology | Receptors, Chemokine - immunology | Membrane Glycoproteins - genetics | Chemokine CXCL10 - genetics | CD8-Positive T-Lymphocytes - drug effects | Dendritic Cells - cytology | Dermatitis, Atopic - metabolism | Receptors, Immunologic - metabolism | Index Medicus
Journal Article
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 05/2014, Volume 146, Issue 5, pp. 1278 - 1288.e2
Background & Aims Reduced generation of all-trans retinoic acid (RA) by CD103+ intestinal dendritic cells (DCs) is linked to intestinal inflammation in mice.... 
Gastroenterology and Hepatology | Regulation | Inflammatory Bowel Disease | Immune Response | Cytokine | Keywords | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Crohn Disease - genetics | Up-Regulation | Ileum - pathology | Intestinal Mucosa - metabolism | Dendritic Cells - immunology | Humans | Retinal Dehydrogenase - metabolism | Crohn Disease - metabolism | Ileum - metabolism | Colon - immunology | Ileum - immunology | Case-Control Studies | Antigens, CD - metabolism | Lipopolysaccharide Receptors - metabolism | Tretinoin - metabolism | Intestinal Mucosa - immunology | Receptors, Retinoic Acid - immunology | Aldehyde Dehydrogenase - metabolism | Dendritic Cells - metabolism | Macrophages - immunology | Macrophages - pathology | Signal Transduction | Colon - pathology | Cells, Cultured | Aldehyde Dehydrogenase - genetics | Receptors, Retinoic Acid - metabolism | Integrin alpha Chains - metabolism | Retinal Dehydrogenase - genetics | Crohn Disease - immunology | Colon - metabolism | Gene Expression Regulation, Enzymologic | Macrophages - metabolism | Phenotype | Crohn Disease - pathology | Retinoic Acid Receptor alpha | Intestinal Mucosa - pathology | Medical colleges | Genetic aspects | Dendritic cells | Macrophages | Gastrointestinal diseases | Tretinoin | Index Medicus | Abridged Index Medicus
Journal Article
Molecular cell, ISSN 1097-2765, 10/2009, Volume 36, Issue 1, pp. 61 - 74
Polycomb group (PcG) proteins exert essential functions in the most disparate biological processes. The contribution of PcG proteins to cell commitment and... 
RNA | STEMCELL | DEVBIO | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Embryonic Stem Cells - metabolism | Embryonic Stem Cells - cytology | Gene Expression - genetics | MyoD Protein - genetics | 3' Untranslated Regions - genetics | MicroRNAs - metabolism | Muscle, Skeletal - metabolism | Myogenin - genetics | Muscle Fibers, Skeletal - metabolism | Muscle, Skeletal - cytology | Embryo, Mammalian - metabolism | Myoblasts, Skeletal - cytology | Muscle, Skeletal - embryology | Cell Differentiation - physiology | Gene Expression Regulation, Developmental - physiology | Myoblasts, Skeletal - metabolism | Tretinoin - pharmacology | Cell Line | Histone-Lysine N-Methyltransferase - genetics | Muscle, Skeletal - growth & development | Liver - metabolism | Mice, Inbred C57BL | Muscle Development - physiology | MyoD Protein - metabolism | Enhancer of Zeste Homolog 2 Protein | Transcription Factors - metabolism | Polycomb Repressive Complex 2 | Animals | Embryonic Stem Cells - drug effects | Histone-Lysine N-Methyltransferase - metabolism | Cell Differentiation - drug effects | Epigenesis, Genetic - genetics | Models, Biological | Muscle Fibers, Skeletal - cytology | Mice | MicroRNAs - genetics | Feedback, Physiological - physiology | MicroRNAs - physiology | Myogenin - metabolism | Proteins | Skin diseases | Embryonic stem cells | Gene expression | Index Medicus
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 10/2010, Volume 107, Issue 44, pp. 18886 - 18891
The proper function of the bone morphogenic protein (BMP) pathway during embryonic development and organ maintenance requires its communication with other... 
Receptors | Phosphorylation | Plasmids | Neurons | Ubiquitins | Antibodies | Gene expression regulation | Embryos | Progenitor cells | Cells | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Phosphorylation - physiology | Mitogen-Activated Protein Kinase Kinases - genetics | Cell Proliferation | Stem Cells - metabolism | Wnt Proteins - metabolism | Embryo, Mammalian - metabolism | Receptors, Retinoic Acid - genetics | Mitogen-Activated Protein Kinase Kinases - metabolism | Bone Morphogenetic Proteins - metabolism | Wnt Proteins - genetics | Tretinoin - metabolism | Smad1 Protein - genetics | Cell Cycle Proteins - genetics | Ubiquitination - physiology | Nuclear Proteins - genetics | Bone Morphogenetic Proteins - genetics | Cell Differentiation - physiology | Epidermal Growth Factor - genetics | Cell Cycle Proteins - metabolism | Ubiquitin-Protein Ligases - metabolism | Embryonic Development - physiology | Epidermal Growth Factor - metabolism | Nuclear Proteins - metabolism | Receptors, Retinoic Acid - metabolism | Glycogen Synthase Kinase 3 - metabolism | Chick Embryo | Proteasome Endopeptidase Complex - genetics | Animals | Glycogen Synthase Kinase 3 - genetics | Embryo, Mammalian - cytology | Cell Line, Tumor | Smad1 Protein - metabolism | Signal Transduction - physiology | Mice | Proteasome Endopeptidase Complex - metabolism | Neural Tube - embryology | Ubiquitin-Protein Ligases - genetics | Physiological aspects | Bone morphogenetic proteins | Research | Properties | Proteolysis | Tretinoin | Index Medicus | Cell proliferation | Fibroblast growth factor | Pattern formation | Smad protein | Transcription | Wnt protein | Retinoic acid receptors | proteasomes | MAP kinase | Signal transduction | Embryogenesis | Neural tube | ubiquitination | GADD45 protein | Neural stem cells | Differentiation | Retinoic acid | Ubiquitin-protein ligase | Communication | Biological Sciences
Journal Article
Pathology international, ISSN 1320-5463, 04/2012, Volume 62, Issue 4, pp. 246 - 253
Journal Article
The Journal of biological chemistry, ISSN 1083-351X, 12/2012, Volume 287, Issue 50, pp. 42195 - 42205
Journal Article