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PloS one, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, p. e0177516
Myogenic stem cells are a promising avenue for the treatment of muscular disorders. Freshly isolated muscle stem cells have a remarkable engraftment ability in... 
PROGENITOR CELLS | SATELLITE CELL NICHE | MESENCHYMAL PROGENITORS | GENE | MYOD | MULTIDISCIPLINARY SCIENCES | EXPANSION | SELF-RENEWAL | DUCHENNE MUSCULAR-DYSTROPHY | HUMAN SKELETAL-MUSCLE | TRANSPLANTATION | Immunohistochemistry | Jagged-1 Protein - metabolism | MyoD Protein - genetics | Receptors, Notch - metabolism | PAX7 Transcription Factor - genetics | Receptors, Notch - genetics | Intracellular Signaling Peptides and Proteins - metabolism | PAX7 Transcription Factor - metabolism | Stem Cells - cytology | Stem Cells - metabolism | Cell Differentiation - genetics | Intercellular Signaling Peptides and Proteins - metabolism | Myoblasts - metabolism | Regeneration - genetics | Myoblasts - cytology | Membrane Proteins - metabolism | Cell Differentiation - physiology | Intracellular Signaling Peptides and Proteins - genetics | Real-Time Polymerase Chain Reaction | Membrane Proteins - genetics | Muscle Development - physiology | Cells, Cultured | Intercellular Signaling Peptides and Proteins - genetics | MyoD Protein - metabolism | Signal Transduction - genetics | Regeneration - physiology | Jagged-1 Protein - genetics | Muscle Cells - cytology | Animals | Muscle Development - genetics | Signal Transduction - physiology | Mice | Transplantation | Research | Health aspects | Ligands (Biochemistry) | Analysis | Stem cells | Musculoskeletal diseases | Musculoskeletal system | Cell culture | MyoD protein | Allografts | Cell number | Stem cell transplantation | Ligands | Notch protein | Gene expression | Myoblasts | Signal Transduction | Intercellular Signaling Peptides and Proteins | PAX7 Transcription Factor | Intracellular Signaling Peptides and Proteins | Cellular Biology | Stem Cells | Membrane Proteins | Life Sciences | Regeneration | Muscle Development | Receptors, Notch | Cell Differentiation | Muscle Cells | MyoD Protein | Jagged-1 Protein
Journal Article
The EMBO journal, ISSN 0261-4189, 2011, Volume 30, Issue 4, pp. 770 - 782
Notch signalling is important for development and tissue homeostasis and activated in many human cancers. Nevertheless, mutations in Notch pathway components... 
miR‐200 | ZEB1 | EMT | Notch | stemness | miR-200 | STEM-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DOWN-REGULATION | PHENOTYPE | E-CADHERIN | MIR-200 FAMILY | REPRESSORS ZEB1 | CELL BIOLOGY | EPITHELIAL-MESENCHYMAL TRANSITION | BREAST-CANCER | COLORECTAL-CANCER | Receptors, Notch - metabolism | Humans | Receptors, Notch - genetics | Gene Knockdown Techniques | Intercellular Signaling Peptides and Proteins - physiology | DNA-Binding Proteins - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Neoplasms - genetics | Membrane Proteins - physiology | Serrate-Jagged Proteins | Base Sequence | Membrane Proteins - metabolism | Nuclear Proteins - genetics | Jagged-1 Protein | Calcium-Binding Proteins - metabolism | Transcription Factors - physiology | DNA-Binding Proteins - antagonists & inhibitors | Membrane Proteins - genetics | Cells, Cultured | Intercellular Signaling Peptides and Proteins - genetics | Nuclear Proteins - metabolism | Transcription Factors - antagonists & inhibitors | Signal Transduction - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Models, Biological | Calcium-Binding Proteins - physiology | Homeodomain Proteins - antagonists & inhibitors | Nuclear Proteins - antagonists & inhibitors | Signal Transduction - physiology | MicroRNAs - genetics | Feedback, Physiological - physiology | MicroRNAs - physiology | Homeodomain Proteins - physiology | Calcium-Binding Proteins - genetics | Zinc Finger E-box-Binding Homeobox 1 | Proteins | Signal transduction | Cellular biology | Molecular biology | Gene expression | Cancer
Journal Article
Journal of Virology, ISSN 0022-538X, 02/2010, Volume 84, Issue 4, pp. 2047 - 2062
Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
AMINO-TERMINAL ENHANCER | BINDING PROTEIN-ALPHA | DNA-SEQUENCES | VIROLOGY | RBP-J-KAPPA | NUCLEAR ANTIGEN | TRANSDUCIN-LIKE ENHANCER | PRIMARY EFFUSION LYMPHOMA | GENE-EXPRESSION | NOTCH SIGNALING PATHWAY | MULTICENTRIC CASTLEMANS-DISEASE | RNA, Small Interfering - genetics | Humans | Transcriptional Activation | DNA Primers - genetics | Trans-Activators - chemistry | Recombinant Fusion Proteins - metabolism | Repressor Proteins - antagonists & inhibitors | Trans-Activators - physiology | Repressor Proteins - physiology | Base Sequence | Immediate-Early Proteins - chemistry | Trans-Activators - genetics | Protein Interaction Domains and Motifs | Nuclear Proteins - genetics | Virus Activation | Herpesvirus 8, Human - physiology | Cell Line | Repressor Proteins - chemistry | Immediate-Early Proteins - physiology | Repressor Proteins - genetics | Herpesvirus 8, Human - genetics | Recombinant Fusion Proteins - chemistry | Nuclear Proteins - chemistry | Protein Interaction Mapping | Host-Pathogen Interactions | Two-Hybrid System Techniques | Immediate-Early Proteins - genetics | Virus Replication | Nuclear Proteins - antagonists & inhibitors | Recombinant Fusion Proteins - genetics | Nuclear Proteins - physiology | Repressor Proteins | Trans-Activators | Herpesvirus 8, Human | DNA Primers | Recombinant Fusion Proteins | Nuclear Proteins | Immediate-Early Proteins | Life Sciences | Microbiology and Parasitology | RNA, Small Interfering | Virus-Cell Interactions
Journal Article
Nature cell biology, ISSN 1465-7392, 03/2010, Volume 12, Issue 3, pp. 278 - 285
The Notch signalling pathway has a crucial function in determining cell fates in multiple tissues within metazoan organisms(1). On binding to ligands, the... 
COACTIVATOR | PROTEIN | DROSOPHILA MASTERMIND | PHOSPHORYLATION | PATHWAY | HOMOLOG | DIFFERENTIATION | NLK | RECEPTORS | EXPRESSION | CELL BIOLOGY | Phosphorylation - physiology | Xenopus | RNA, Small Interfering - genetics | ELAV-Like Protein 3 | Transcription Factor HES-1 | Protein Interaction Domains and Motifs - physiology | Receptors, Notch - metabolism | Homeodomain Proteins - metabolism | Humans | Embryo, Nonmammalian - metabolism | Receptors, Notch - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Transfection | Basic Helix-Loop-Helix Transcription Factors - metabolism | Nuclear Proteins - genetics | Immunoglobulin J Recombination Signal Sequence-Binding Protein - genetics | Intracellular Signaling Peptides and Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | Immunoglobulin J Recombination Signal Sequence-Binding Protein - metabolism | Basic Helix-Loop-Helix Transcription Factors - genetics | Zebrafish Proteins - metabolism | ELAV Proteins - metabolism | Protein-Serine-Threonine Kinases - genetics | Gene Expression Regulation - physiology | Nuclear Proteins - metabolism | Zebrafish | DNA - metabolism | Receptor, Notch1 - metabolism | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Animals | Oligonucleotides, Antisense - genetics | Amino Acid Substitution - physiology | Models, Biological | Neurogenesis - physiology | Cell Line, Tumor | Mitogen-Activated Protein Kinases - genetics | Signal Transduction - physiology | Mice | Zebrafish Proteins - genetics | Receptor, Notch1 - genetics | Mitogen-Activated Protein Kinases - metabolism | Protein Binding - physiology | Physiological aspects | Cellular signal transduction | Genetic aspects | Research | Genetic transcription | Protein kinases
Journal Article
PloS one, ISSN 1932-6203, 2012, Volume 7, Issue 7, p. e41116
.... The E3 ubiquitin ligase Fbxw7 is part of the SCF protein complex responsible for the polyubiquitination and thereby proteasomal degradation of substrates such as Notch, c-Myc and c-Jun... 
TIP CELL-FORMATION | ACTIVATION | ZEBRAFISH | PATHWAY | VEGF | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | KINASE | TUMOR-SUPPRESSOR | EXPRESSION | NEGATIVE REGULATOR | F-Box-WD Repeat-Containing Protein 7 | Retina - metabolism | Human Umbilical Vein Endothelial Cells - metabolism | Receptors, Notch - metabolism | Humans | Receptors, Notch - genetics | Zebrafish - embryology | Ubiquitin-Protein Ligase Complexes | Retina - cytology | Human Umbilical Vein Endothelial Cells - cytology | Cell Cycle Proteins - genetics | F-Box Proteins - metabolism | Proto-Oncogene Proteins c-jun - genetics | Zebrafish Proteins - metabolism | Cell Cycle Proteins - metabolism | Ubiquitin-Protein Ligases - metabolism | Mice, Transgenic | Proto-Oncogene Proteins c-myc - metabolism | Zebrafish - genetics | Neovascularization, Physiologic - physiology | Animals | Proto-Oncogene Proteins c-jun - metabolism | Morpholinos - pharmacology | Cell Proliferation - drug effects | Mice | Proto-Oncogene Proteins c-myc - genetics | Zebrafish Proteins - genetics | Ubiquitin-Protein Ligases - genetics | F-Box Proteins - genetics | Ubiquitin | Embryonic development | Neovascularization | Ligases | Endothelium | Cell proliferation | Transcription factors | Laboratories | Genes | c-Myc protein | Retina | Myc protein | Kinases | Inactivation | Blood | Cdc4 protein | Degradation | Morphogenesis | Proteins | Angiogenesis | SCF protein | Rodents | Ubiquitin-protein ligase | Deactivation | c-Jun protein | Blood vessels | Zebrafish | siRNA | Embryos | Substrates | Endothelial cells | Studies | Signaling | Microscopy | Proteasomes | Ligands | Notch protein
Journal Article
BMC evolutionary biology, ISSN 1471-2148, 2009, Volume 9, Issue 1, pp. 249 - 249
Journal Article
PloS one, ISSN 1932-6203, 03/2016, Volume 11, Issue 3, p. e0151954
Background Neurobeachin (NBEA) is an autism spectrum disorders (ASD) candidate gene. NBEA deficiency affects regulated secretion, receptor trafficking, synaptic architecture and protein kinase... 
RUGOSE | KINASE ANCHOR PROTEIN | MULTIDISCIPLINARY SCIENCES | INVOLVEMENT | AGGREGATED PROTEINS | TRAFFICKING | HOMOLOG | MUTATIONS | COPY NUMBER VARIANTS | BEACH-DOMAIN | EXPRESSION | Autistic Disorder - genetics | Protein Structure, Tertiary | Cell Line | Genetic Association Studies | Humans | Receptor, Notch1 - chemistry | Nuclear Localization Signals - metabolism | Receptor, Notch1 - metabolism | Gene Knockdown Techniques | Protein Transport | Membrane Proteins | Nerve Tissue Proteins - metabolism | Two-Hybrid System Techniques | Animals | Carrier Proteins - metabolism | Cell Nucleus - metabolism | Protein Binding | Transcription, Genetic | Mice | Autism | Physiological aspects | Genetic aspects | Research | Genetic transcription | Protein kinases | Mitogens | Protein-protein interactions | Risk factors | Protein kinase A | Enrichment | Regulators | Phosphorylation | Yeast | Transcription | Pathogenesis | Modules | Confocal microscopy | Homology | Nervous system | Confocal | Kinases | Proteins | Consortia | Rodents | Pleckstrin | Genetics | Localization | Fusion protein | Protein transport | Anchoring | Secretion | Cloning | C-Terminus | Concanavalin A | Screens | Substrates | Signaling | Brain research | Microscopy | Scaffolding | Lectins | Nuclei (cytology) | Notch protein | Intracellular | Protein interaction | Cytoplasm | A kinase-anchoring protein
Journal Article
PloS one, ISSN 1932-6203, 11/2013, Volume 8, Issue 11, p. e78439
Neuroinflammation mediated by the activated microglia is suggested to play a pivotal role in the pathogenesis of hypoxic brain injury; however, the underlying... 
MURINE BV-2 CELLS | MULTIDISCIPLINARY SCIENCES | NITRIC-OXIDE | RECEPTOR | NEURAL PROGENITOR CELLS | RAT-BRAIN | DIFFERENTIATION | INFLAMMATORY RESPONSE | EXPRESSION | AMEBOID MICROGLIA | INNATE IMMUNITY | Amyloid Precursor Protein Secretases - genetics | Microglia - metabolism | Transcription Factor HES-1 | Homeodomain Proteins - metabolism | NF-kappa B - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Hypoxia - metabolism | Basic Helix-Loop-Helix Transcription Factors - metabolism | Gene Expression Regulation, Developmental | Microglia - pathology | Membrane Proteins - metabolism | TNF Receptor-Associated Factor 6 - genetics | Immunoglobulin J Recombination Signal Sequence-Binding Protein - genetics | Intracellular Signaling Peptides and Proteins - genetics | Animals, Newborn | Immunoglobulin J Recombination Signal Sequence-Binding Protein - metabolism | Basic Helix-Loop-Helix Transcription Factors - genetics | Signal Transduction | Membrane Proteins - genetics | Dipeptides - pharmacology | Enzyme Inhibitors - pharmacology | Myeloid Differentiation Factor 88 - genetics | Rats | Toll-Like Receptor 4 - genetics | Receptor, Notch1 - metabolism | Toll-Like Receptor 4 - metabolism | Homeodomain Proteins - genetics | Amyloid Precursor Protein Secretases - metabolism | Hypoxia - genetics | Animals | NF-kappa B - genetics | Hypoxia - pathology | TNF Receptor-Associated Factor 6 - metabolism | Cell Line, Tumor | Mice | Amyloid Precursor Protein Secretases - antagonists & inhibitors | Receptor, Notch1 - antagonists & inhibitors | Cell Hypoxia - genetics | Receptor, Notch1 - genetics | Myeloid Differentiation Factor 88 - metabolism | Brain | Mental disorders | Laboratories | Pathogenesis | Crosstalk | Activation | Neurogenesis | Signal transduction | Embryology | Head injuries | Pathways | Rodents | Cerebrum | Toll-like receptors | Microglial cells | Inhibition | Pretreatment | Casualties | Translocation | NF-κB protein | Adenosine | TRAF6 protein | Cytokines | Histology | Exposure | Inflammation | TLR4 protein | Gene expression | Microglia | Medicine | Studies | Signaling | Brain research | DELTA protein | Stem cells | MyD88 protein | Hypoxia | Ligands | Brain damage | Notch protein | Brain injury | Secretase
Journal Article
Structure (London), ISSN 0969-2126, 01/2014, Volume 22, Issue 1, pp. 70 - 81
... or corepressor proteins, respectively. Although the structures of CSL-coactivator complexes have been determined, the structures of CSL-corepressor complexes are unknown... 
LIM PROTEIN | DOMAIN | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | FACTOR RBP-J | TRANSCRIPTION | EBNA2 | CELL BIOLOGY | EFFECTOR | BIOPHYSICS | CSL | BINDING | INSIGHTS | Receptors, Notch - metabolism | Molecular Sequence Data | Crystallography, X-Ray | Receptors, Notch - genetics | Intracellular Signaling Peptides and Proteins - metabolism | LIM Domain Proteins - metabolism | Thermodynamics | Escherichia coli - metabolism | Muscle Proteins - metabolism | Transcription, Genetic | Binding Sites | Immunoglobulin J Recombination Signal Sequence-Binding Protein - genetics | Intracellular Signaling Peptides and Proteins - genetics | Genes, Reporter | LIM Domain Proteins - chemistry | Immunoglobulin J Recombination Signal Sequence-Binding Protein - chemistry | Recombinant Proteins - metabolism | Amino Acid Sequence | Immunoglobulin J Recombination Signal Sequence-Binding Protein - metabolism | Signal Transduction | Gene Expression Regulation | Cell Communication | Models, Molecular | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Muscle Proteins - genetics | Animals | Receptors, Notch - chemistry | Escherichia coli - genetics | Intracellular Signaling Peptides and Proteins - chemistry | Protein Binding | LIM Domain Proteins - genetics | Mice | Muscle Proteins - chemistry | Mutation | Proteins | Embryonic development | Genetic transcription
Journal Article
The EMBO Journal, ISSN 0261-4189, 09/2004, Volume 23, Issue 17, pp. 3441 - 3451
... orthologs, respectively). Both DSL and Notch are modular type I transmembrane proteins, which engage one another to effect intracellular signaling. CSL is a DNA‐binding... 
Rel homology region | transcription factor | RAM domain | Lag‐1 | beta‐trefoil domain | Beta-trefoil domain | Lag-1 | Transcription factor | COMPLEX | DOMAIN | RECOGNITION | beta-trefoil domain | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | BINDING-PROTEIN | RECEPTOR | CELL BIOLOGY | REPLACEMENT | KAPPA | SEQUENCE | BARR-VIRUS EBNA2 | Caenorhabditis elegans Proteins - chemistry | Humans | Caenorhabditis elegans Proteins - metabolism | Molecular Sequence Data | Crystallography, X-Ray | Drosophila Proteins - metabolism | DNA-Binding Proteins - metabolism | DNA, Recombinant - chemistry | Receptors, Notch | Base Sequence | Membrane Proteins - metabolism | Nuclear Proteins - genetics | Binding Sites | Repressor Proteins - metabolism | Protein Structure, Tertiary | Recombinant Proteins - metabolism | Amino Acid Sequence | DNA, Recombinant - genetics | Repressor Proteins - chemistry | Models, Molecular | Recombinant Proteins - chemistry | Repressor Proteins - genetics | Nuclear Proteins - metabolism | Recombinant Proteins - genetics | Drosophila Proteins - chemistry | DNA-Binding Proteins - genetics | Nuclear Proteins - chemistry | Static Electricity | DNA-Binding Proteins - chemistry | Protein Folding | Macromolecular Substances | Sequence Homology, Amino Acid | Animals | Immunoglobulin J Recombination Signal Sequence-Binding Protein | DNA, Recombinant - metabolism | Drosophila Proteins - genetics | In Vitro Techniques | Caenorhabditis elegans Proteins - genetics
Journal Article