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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
Developmental cell, ISSN 1534-5807, 2012, Volume 22, Issue 3, pp. 501 - 514
... (Hes1, Hey1, Jagged1, VEGFR1, and Id1-3). Moreover, Id proteins act as competence factors for stalk cells and form complexes with Hes1, which augment Hes1 levels in the endothelium... 
DEFECTS | TIP CELLS | ANGIOGENESIS | VEGF | ENDOTHELIAL-CELLS | ID PROTEINS | HES1 | DEVELOPMENTAL BIOLOGY | DIFFERENTIATION | EXPRESSION | INHIBITS TUMOR-GROWTH | CELL BIOLOGY | Transcription Factor HES-1 | Humans | Intercellular Signaling Peptides and Proteins - biosynthesis | Intracellular Signaling Peptides and Proteins - metabolism | Inhibitor of Differentiation Proteins - biosynthesis | Inhibitor of Differentiation Protein 1 - biosynthesis | Serrate-Jagged Proteins | Smad5 Protein - metabolism | Basic Helix-Loop-Helix Transcription Factors - biosynthesis | Smad1 Protein - genetics | Membrane Proteins - metabolism | Smad5 Protein - genetics | Intracellular Signaling Peptides and Proteins - genetics | Jagged-1 Protein | Calcium-Binding Proteins - biosynthesis | Homeodomain Proteins - biosynthesis | Signal Transduction | Inhibitor of Differentiation Protein 2 - biosynthesis | Membrane Proteins - genetics | Down-Regulation | Cells, Cultured | Mice, Transgenic | Cell Cycle Proteins - biosynthesis | Vascular Endothelial Growth Factor Receptor-1 - biosynthesis | Mice, Knockout | Membrane Proteins - biosynthesis | Phenotype | Animals | Smad1 Protein - metabolism | Mice | Neovascularization, Physiologic | Proteins | Endothelial growth factors | Genes | Genetic aspects | Transforming growth factors | Vascular endothelial growth factor | Endothelium | Dll4 | tip cell | lateral inhibition | sprouting angiogenesis | BMP | directed migration | Notch | stalk cell | mouse embryo | Smad | polarity
Journal Article
Molecular cell, ISSN 1097-2765, 2015, Volume 57, Issue 5, pp. 912 - 924
Mind bomb (Mib) proteins are large, multi-domain E3 ligases that promote ubiquitination of the cytoplasmic tails of Notch ligands... 
SYSTEM | MORPHOGENESIS | ACTIVATION | PROTEIN | UBIQUITIN LIGASE | DELTA | BIOCHEMISTRY & MOLECULAR BIOLOGY | DIFFERENTIATION | SERRATE | INTRACELLULAR MOTIFS | DROSOPHILA | CELL BIOLOGY | Wnt1 Protein | Epitopes - metabolism | Receptors, Notch - metabolism | Humans | Intercellular Signaling Peptides and Proteins - chemistry | Molecular Sequence Data | Crystallography, X-Ray | Receptors, Notch - genetics | Drosophila Proteins - metabolism | Drosophila melanogaster - genetics | Drosophila melanogaster - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Serrate-Jagged Proteins | HEK293 Cells | Membrane Proteins - metabolism | Jagged-1 Protein | Calcium-Binding Proteins - chemistry | Calcium-Binding Proteins - metabolism | Protein Structure, Tertiary | Amino Acid Sequence | Protein Structure, Secondary | Membrane Proteins - genetics | Intercellular Signaling Peptides and Proteins - genetics | Ubiquitin-Protein Ligases - metabolism | Models, Molecular | Drosophila Proteins - chemistry | Epitopes - genetics | Ubiquitin-Protein Ligases - chemistry | Blotting, Western | Sequence Homology, Amino Acid | Animals | Membrane Proteins - chemistry | Receptors, Notch - chemistry | Cell Line, Tumor | Protein Binding | Ligands | Epitopes - chemistry | Drosophila Proteins - genetics | Mutation | Ubiquitin-Protein Ligases - genetics | Calcium-Binding Proteins - genetics | Ubiquitin | Cellular signal transduction | Ligases | Antigenic determinants | Structure | Crystals | BASIC BIOLOGICAL SCIENCES
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 1/2013, Volume 110, Issue 5, pp. 1714 - 1719
Expression of the Notch ligand Jagged 1 (JAG1) and Notch activation promote poor-prognosis in breast cancer. We used high throughput screens to identify... 
Tumor cell line | Cell lines | Small interfering RNA | Breast cancer | Cells | Regulator genes | Genetic screening | Tumors | Mesenchymal stem cells | Cancer | EPITHELIAL-MESENCHYMAL TRANSITION | STEM-CELLS | IN-VITRO | ACTIVATED PROTEIN-KINASE | SIGNALING PATHWAY | TRIBBLES HOMOLOG | MULTIDISCIPLINARY SCIENCES | HYPOXIA | EXPRESSION | ESTROGEN-RECEPTOR | MAMMARY-GLAND | Humans | Breast Neoplasms - metabolism | MAP Kinase Signaling System | Intercellular Signaling Peptides and Proteins - metabolism | RNA Interference | Serrate-Jagged Proteins | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Cell Cycle Proteins - genetics | Female | Membrane Proteins - metabolism | Protein-Serine-Threonine Kinases - metabolism | Repressor Proteins - metabolism | Jagged-1 Protein | Calcium-Binding Proteins - metabolism | Cell Line | Membrane Proteins - genetics | Cell Cycle Proteins - metabolism | Intercellular Signaling Peptides and Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Repressor Proteins - genetics | Protein Kinase Inhibitors - isolation & purification | Receptor, Notch1 - metabolism | Mice, SCID | Reverse Transcriptase Polymerase Chain Reaction | Interleukin Receptor Common gamma Subunit - genetics | Blotting, Western | Hep G2 Cells | Mice, Knockout | Interleukin Receptor Common gamma Subunit - deficiency | Xenograft Model Antitumor Assays | Animals | Breast Neoplasms - genetics | Transforming Growth Factor beta - genetics | Signal Transduction - drug effects | Breast Neoplasms - pathology | Cell Line, Tumor | Mice, Inbred NOD | Mice | Protein Kinase Inhibitors - pharmacology | Receptor, Notch1 - genetics | Transforming Growth Factor beta - metabolism | Calcium-Binding Proteins - genetics | Biological Sciences
Journal Article
Journal Article
Cancer cell, ISSN 1535-6108, 2013, Volume 23, Issue 2, pp. 171 - 185
We report a paracrine effect whereby endothelial cells (ECs) promote the cancer stem cell (CSC) phenotype of human colorectal cancer (CRC) cells. We showed... 
COLON-CANCER | METASTASIS | ONCOLOGY | NOTCH | NICHE | SELF-RENEWAL | RECEPTOR | GROWTH-FACTOR | TUMOR ANGIOGENESIS | DIFFERENTIATION | ANGIOCRINE FACTORS | CELL BIOLOGY | ADAM17 Protein | RNA, Small Interfering - genetics | Immunoprecipitation | Receptors, Notch - metabolism | Colorectal Neoplasms - genetics | Humans | Calcium-Binding Proteins - antagonists & inhibitors | Culture Media, Conditioned - pharmacology | Drug Resistance, Neoplasm | Immunoblotting | Peptide Fragments - pharmacology | Intercellular Signaling Peptides and Proteins - metabolism | Neoplastic Stem Cells - metabolism | Serrate-Jagged Proteins | Neoplastic Stem Cells - pathology | Antineoplastic Agents - pharmacology | Membrane Proteins - metabolism | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Tumor Cells, Cultured | Liver Neoplasms - secondary | Colorectal Neoplasms - metabolism | Jagged-1 Protein | Biomarkers - metabolism | Calcium-Binding Proteins - metabolism | ADAM Proteins - antagonists & inhibitors | Liver Neoplasms - genetics | Signal Transduction | Endothelial Cells - metabolism | Membrane Proteins - genetics | Intercellular Signaling Peptides and Proteins - genetics | Cell Communication | Xenograft Model Antitumor Assays | ADAM Proteins - metabolism | Phenotype | Animals | Membrane Proteins - antagonists & inhibitors | Mice, Nude | Liver Neoplasms - metabolism | Mice | ADAM Proteins - genetics | Colorectal Neoplasms - pathology | Endothelial Cells - pathology | Calcium-Binding Proteins - genetics | Genetic aspects | Colorectal cancer | Stem cells | Endothelium
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2016, Volume 11, Issue 11, p. e0166984
.... Defects in Bone Morphogenetic Protein (BMP) signaling are associated with cleft lip/palate... 
BRANCHIAL ARCH | DLX GENES | HEAD SKELETON | ALAGILLE-SYNDROME | DOWNS-SYNDROME | MULTIDISCIPLINARY SCIENCES | AURICULOCONDYLAR SYNDROME | LEFT-RIGHT ASYMMETRY | REPEAT PROTEIN | HUMAN JAGGED1 | NEURAL CREST CELLS | Jagged-1 Protein - metabolism | Zebrafish - embryology | Intercellular Signaling Peptides and Proteins - metabolism | Somites - embryology | Basic Helix-Loop-Helix Transcription Factors - metabolism | Nuclear Proteins - biosynthesis | Smad5 Protein - metabolism | Smad1 Protein - genetics | Smad5 Protein - genetics | Nuclear Proteins - genetics | Repressor Proteins - metabolism | Gene Expression Regulation, Developmental - physiology | Zebrafish Proteins - biosynthesis | Basic Helix-Loop-Helix Transcription Factors - genetics | Endothelin-1 - genetics | Endothelin-1 - metabolism | Zebrafish Proteins - metabolism | Intercellular Signaling Peptides and Proteins - genetics | Repressor Proteins - genetics | Jagged-1 Protein - genetics | Zebrafish - genetics | Body Patterning - physiology | Animals | Transforming Growth Factor beta - genetics | Facial Bones - enzymology | Smad1 Protein - metabolism | Signal Transduction - physiology | Zebrafish Proteins - genetics | Transforming Growth Factor beta - metabolism | Bone morphogenetic proteins | Genetic aspects | Research | Craniofacial abnormalities | Neural crest | Pattern formation | Jaw | Transcription factors | Endothelin | Arches | Congenital defects | Alagille syndrome | Genomics | Transforming growth factor-b | Genomes | Somites | Kinases | Defects | Proteins | Cartilage | Signal transduction | Pathways | Growth factors | Territory | Patterning | Mandible | Interference | Craniofacial syndromes | Zebrafish | Infant mortality | Birth defects | Endothelin 1 | Gene expression | Embryos | Mutants | Cleft lip/palate | Craniofacial growth | Signaling | Scaffolding | In vivo methods and tests | Notch protein
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 4, p. e60244
Endocardial to mesenchymal transformation (EMT) is a fundamental cellular process required for heart valve formation. Notch, Wnt and Bmp pathways are known to... 
EPITHELIAL-MESENCHYMAL TRANSITION | TRANSFORMATION | DEVELOPING CHICKEN HEART | MORPHOGENESIS | CUSHION | CELLS | NF-ATC | MULTIDISCIPLINARY SCIENCES | GROWTH-FACTOR | TRANSCRIPTION FACTOR | CARDIAC DEVELOPMENT | Wnt4 Protein - metabolism | Embryo, Mammalian | Heart Valves - metabolism | Epithelial-Mesenchymal Transition - genetics | Endocardium - metabolism | Wnt4 Protein - genetics | Intercellular Signaling Peptides and Proteins - metabolism | Gene Expression Regulation, Developmental | Serrate-Jagged Proteins | Bone Morphogenetic Protein 2 - metabolism | Myocardium - metabolism | Membrane Proteins - metabolism | Heart Valves - embryology | Extracellular Matrix Proteins - metabolism | Jagged-1 Protein | Calcium-Binding Proteins - metabolism | Bone Morphogenetic Protein 2 - genetics | Signal Transduction | Endocardium - embryology | Membrane Proteins - genetics | Extracellular Matrix Proteins - genetics | Intercellular Signaling Peptides and Proteins - genetics | Mice, Transgenic | Receptor, Notch1 - metabolism | Animals | Organogenesis - genetics | Mice | Receptor, Notch1 - genetics | Calcium-Binding Proteins - genetics | Cellular signal transduction | Research | Wnt proteins | Heart valves | Heart | Transformation | Immunoglobulins | Bone morphogenetic protein 2 | Wnt protein | Mesenchyme | Laboratories | Paracrine signalling | Histology | Ribonucleic acid--RNA | Embryos | Defects | Morphogenesis | Medicine | Signal transduction | Cell growth | Hospitals | Pathways | Rodents | Myocardium | Notch protein | Jagged1 protein | Cardiology | RNA | Ribonucleic acid
Journal Article
PloS one, ISSN 1932-6203, 2014, Volume 9, Issue 5, pp. e96365 - e96365
Epithelial-mesenchymal transition (EMT) of retinal pigment epithelium (RPE) cells is a major pathologic change in the development of proliferative... 
FIBROSIS | PROLIFERATIVE VITREORETINAL DISEASES | ACTIVATION | TISSUE GROWTH-FACTOR | FACTOR-BETA | MULTIDISCIPLINARY SCIENCES | INVOLVEMENT | KINASE | SMAD | INHIBITOR | EXPRESSION | Epithelial Cells - metabolism | Gene Expression - drug effects | Nitriles - pharmacology | Receptors, Notch - metabolism | Epithelial Cells - drug effects | Humans | Mitogen-Activated Protein Kinase 3 - antagonists & inhibitors | Epithelial-Mesenchymal Transition - drug effects | Receptors, Notch - genetics | Smad3 Protein - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Multiprotein Complexes - metabolism | Serrate-Jagged Proteins | Dioxoles - pharmacology | Benzamides - pharmacology | Membrane Proteins - metabolism | Jagged-1 Protein | Calcium-Binding Proteins - metabolism | Cell Line | Butadienes - pharmacology | Membrane Proteins - genetics | Mitogen-Activated Protein Kinase 1 - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Intercellular Signaling Peptides and Proteins - genetics | Smad2 Protein - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Transforming Growth Factor beta2 - pharmacology | MAP Kinase Signaling System - drug effects | Mitogen-Activated Protein Kinase 3 - metabolism | Signal Transduction - drug effects | Receptor, Notch3 | Smad Proteins - metabolism | Retinal Pigment Epithelium - cytology | Calcium-Binding Proteins - genetics | Mitogen-Activated Protein Kinase 1 - metabolism | Disabled people | Smad protein | Mesenchyme | Laboratories | Transforming growth factor | Retina | Activation | Kinases | Carcinogenesis | Fibronectin | Retinal pigment epithelium | Metastases | Signal transduction | Carcinogens | N-Cadherin | Pathways | Breakdowns | Smad2 protein | Collagen (type IV) | Growth factors | Immunoglobulins | Cytokines | Medical treatment | Extracellular signal-regulated kinase | Epithelium | Cadherin | Trauma | Signaling | Inhibitors | Fibrosis | Notch protein | Cancer | Index Medicus
Journal Article
Cancer research (Chicago, Ill.), ISSN 1538-7445, 2009, Volume 69, Issue 6, pp. 2400 - 2407
Despite rapid advances in many fronts, pancreatic cancer (PC) remains one of the most difficult human malignancies to treat due, in part, to de novo and... 
TARGET | STEM-CELLS | GROWTH INHIBITION | INVASION | TUMOR PROGRESSION | ONCOLOGY | PROSTATE-CANCER | TAMOXIFEN RESISTANCE | DOWN-REGULATION | E-CADHERIN | NF-KAPPA-B | RNA, Small Interfering - genetics | Pancreatic Neoplasms - metabolism | Receptors, Notch - metabolism | Humans | Deoxycytidine - pharmacology | Drug Resistance, Neoplasm | Intercellular Signaling Peptides and Proteins - biosynthesis | NF-kappa B - metabolism | Receptor, Notch2 - genetics | Receptors, Notch - genetics | Proto-Oncogene Proteins - biosynthesis | Cell Movement - physiology | Pancreatic Neoplasms - drug therapy | Intercellular Signaling Peptides and Proteins - metabolism | Transfection | Receptors, Notch - biosynthesis | Serrate-Jagged Proteins | Antimetabolites, Antineoplastic - pharmacology | Membrane Proteins - metabolism | Jagged-1 Protein | Calcium-Binding Proteins - metabolism | Proto-Oncogene Proteins - metabolism | Calcium-Binding Proteins - biosynthesis | Signal Transduction | Membrane Proteins - genetics | Down-Regulation | Pancreatic Neoplasms - pathology | Intercellular Signaling Peptides and Proteins - genetics | Receptor, Notch2 - metabolism | Epithelial Cells - pathology | Pancreatic Neoplasms - genetics | Proto-Oncogene Proteins - genetics | Membrane Proteins - biosynthesis | Phenotype | Receptor, Notch2 - biosynthesis | Mesoderm - pathology | RNA, Messenger | Deoxycytidine - analogs & derivatives | Receptor, Notch4 | Calcium-Binding Proteins - genetics | Index Medicus
Journal Article
Cell reports (Cambridge), ISSN 2211-1247, 2015, Volume 12, Issue 12, pp. 1968 - 1977
Breast cancers (BCs) typically express estrogen receptors (ERs) but frequently exhibit de novo or acquired resistance to hormonal therapies. Here, we show that... 
NOTCH | ESTROGEN | ADJUVANT TAMOXIFEN | RECEPTOR | CELL BIOLOGY