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PLoS ONE, ISSN 1932-6203, 01/2014, Volume 9, Issue 1, pp. e85469 - e85469
Tendinopathy is characterized histopathologically by lipid accumulation and tissue calcification. Adipogenic and osteogenic differentiation of tendon stem... 
RESPONSES | RECEPTOR-GAMMA | REPETITIVE MOTION | MULTIDISCIPLINARY SCIENCES | OSTEOBLASTS | GENE-EXPRESSION | INCREASES | OSTEOGENIC DIFFERENTIATION | ADIPOCYTE DIFFERENTIATION | FIBROBLASTS | DEGENERATION | RNA, Small Interfering - genetics | Tendons - drug effects | Adipogenesis - drug effects | Adipocytes - cytology | Insulin-Like Growth Factor I - genetics | Stem Cells - cytology | Adipocytes - drug effects | PPAR gamma - metabolism | RNA, Messenger - metabolism | Stem Cells - metabolism | Tendons - cytology | Cyclic AMP-Dependent Protein Kinases - genetics | Bone Morphogenetic Protein 2 - metabolism | CCAAT-Enhancer-Binding Protein-delta - metabolism | Cell Differentiation | Cyclic AMP-Dependent Protein Kinases - antagonists & inhibitors | Adipogenesis - genetics | Cyclic AMP - metabolism | PPAR gamma - genetics | Cyclic AMP-Dependent Protein Kinases - metabolism | Bone Morphogenetic Protein 2 - genetics | Dinoprostone - pharmacology | Signal Transduction | RNA, Messenger - genetics | Tendons - metabolism | Bone Morphogenetic Protein 2 - antagonists & inhibitors | Cells, Cultured | Gene Expression Regulation | Rats | Smad Proteins - genetics | Rats, Sprague-Dawley | Animals | CCAAT-Enhancer-Binding Protein-delta - antagonists & inhibitors | CCAAT-Enhancer-Binding Protein-delta - genetics | Adipocytes - metabolism | Stem Cells - drug effects | Protein Kinase Inhibitors - pharmacology | Smad Proteins - metabolism | Insulin-Like Growth Factor I - antagonists & inhibitors | Insulin-Like Growth Factor I - metabolism | RNA, Small Interfering - metabolism | Enzymes | RNA | Prostaglandins E | Stem cells | Bone morphogenetic proteins | Cyclic adenylic acid | Protein kinases | Enzyme-linked immunosorbent assay | Protein binding | Protein kinase A | Phosphorylation | Smad protein | Insulin-like growth factor I | Prostaglandin E2 | Reverse transcription | Stem cell transplantation | Insulin-like growth factors | Adipocytes | CCAAT/enhancer-binding protein | Kinases | Proteins | Biomedical materials | Bone growth | Allografts | Bioaccumulation | Rodents | Bone marrow | Biocompatibility | Injuries | Adipogenesis | Incubation | Bone morphogenetic protein 2 | Cyclic AMP | Inflammation | Cyclic AMP response element-binding protein | Gene expression | Insulin | Tendons | Polymerase chain reaction | Calcification | Bone | Differentiation | Index Medicus
Journal Article
Molecular Endocrinology, ISSN 0888-8809, 03/2004, Volume 18, Issue 3, pp. 653 - 665
Growth differentiation factor-9 (GDF-9) is an oocyte-derived growth factor and a member of the TGF-β superfamily that includes TGF-β, activin, and bone... 
ALK7 SIGNALS | BONE MORPHOGENETIC PROTEIN | MAD-RELATED PROTEIN | ENDOCRINOLOGY & METABOLISM | OSTEOGENIC PROTEIN-1 | FOLLICULAR-GROWTH | TGF-BETA RECEPTOR | OVARIAN GRANULOSA-CELLS | IDENTIFICATION | HOMOLOG GDF-9B | LUTEAL CELLS | Phosphorylation | Receptors, Transforming Growth Factor beta - genetics | Trans-Activators - drug effects | Protein-Serine-Threonine Kinases | Activin Receptors - drug effects | Activins - metabolism | COS Cells - drug effects | Activin Receptors - genetics | Granulosa Cells - drug effects | Granulosa Cells - metabolism | COS Cells - metabolism | DNA-Binding Proteins - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Bone Morphogenetic Proteins - metabolism | Growth Differentiation Factor 9 | Trans-Activators - genetics | Female | Smad7 Protein | Promoter Regions, Genetic | Signal Transduction | Smad6 Protein | Cells, Cultured | DNA-Binding Proteins - drug effects | Rats | Activin Receptors, Type I - metabolism | DNA-Binding Proteins - genetics | Activin Receptors, Type I - genetics | Rats, Sprague-Dawley | Activin Receptors, Type I - drug effects | Transforming Growth Factor beta - pharmacology | Bone Morphogenetic Protein 15 | Smad3 Protein | Activin Receptors - metabolism | Animals | Activins - pharmacology | Receptors, Transforming Growth Factor beta - drug effects | Receptors, Transforming Growth Factor beta - metabolism | Intercellular Signaling Peptides and Proteins - pharmacology | Smad Proteins | Trans-Activators - metabolism | RNA, Small Interfering | Transforming Growth Factor beta - metabolism | Smad2 Protein | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2014, Volume 9, Issue 10, pp. e109523 - e109523
The Protein Kinase A (PKA) and Wnt signaling cascades are fundamental pathways involved in cellular development and maintenance. In the osteoblast lineage,... 
CYCLIC-AMP | MCCUNE-ALBRIGHT SYNDROME | PATHWAY | PHOSPHORYLATION | MULTIDISCIPLINARY SCIENCES | CARNEY COMPLEX | PROLIFERATION | WNT | INHIBITS OSTEOGENIC DIFFERENTIATION | MESENCHYMAL STEM-CELLS | OSTEOBLASTIC CELLS | Wnt3A Protein - metabolism | Bone and Bones - pathology | Phosphorylation | Cytosol - drug effects | Gene Expression Regulation, Neoplastic | Bone Neoplasms - pathology | Bone Neoplasms - metabolism | Wnt3A Protein - pharmacology | Cell Nucleus - metabolism | Bone and Bones - metabolism | Transcription, Genetic | Bone Neoplasms - genetics | Cyclic AMP-Dependent Protein Kinase RIalpha Subunit - metabolism | Wnt3A Protein - genetics | Signal Transduction | Receptor Tyrosine Kinase-like Orphan Receptors - metabolism | Osteoblasts - drug effects | beta Catenin - metabolism | beta Catenin - genetics | Protein Transport | Cyclic AMP Response Element-Binding Protein - genetics | Osteoblasts - pathology | Animals | Cyclic AMP-Dependent Protein Kinase RIalpha Subunit - genetics | Cyclic AMP Response Element-Binding Protein - metabolism | Cell Line, Tumor | Protein Binding | Cytosol - metabolism | Receptor Tyrosine Kinase-like Orphan Receptors - genetics | Mice | Cell Nucleus - drug effects | Osteoblasts - metabolism | Protein kinase A | Wnt protein | Crosstalk | Colorectal cancer | Activation | Bone tumors | Kinases | Osteoblasts | Proteins | β-catenin | Signal transduction | Biomedical materials | Immunology | Pathways | Cascades | Transcription activation | Gastroenterology | Biocompatibility | Tumorigenesis | Localization | Pharmacology | Cyclic AMP response element-binding protein | Mammals | Organogenesis | Virology | Signaling | Mutation | Bone | Position (location) | Protein interaction | Cellular structure | Tumors | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 04/2010, Volume 285, Issue 16, pp. 12169 - 12180
Bone morphogenetic proteins (BMPs) are used clinically to induce new bone formation in spinal fusions and long bone nonunion fractures. However, large amounts... 
I RECEPTORS | CELLS | ACTIVATION | DEFECTS | INDUCE | BIOCHEMISTRY & MOLECULAR BIOLOGY | COMPONENTS | OSTEOGENIC PROTEIN-1 | DIFFERENTIATION | EXPRESSION | BINDING | Bone Regeneration - physiology | RNA, Small Interfering - genetics | Recombinant Fusion Proteins - pharmacology | Bone Morphogenetic Protein 7 - genetics | Humans | Cercopithecus aethiops | Molecular Sequence Data | Male | Bone Morphogenetic Protein 6 - pharmacology | RNA, Messenger - metabolism | Recombinant Fusion Proteins - metabolism | Bone Morphogenetic Protein 6 - genetics | Protein Engineering | Cell Differentiation | Protein Interaction Domains and Motifs | Osteoblasts - cytology | Carrier Proteins - physiology | Amino Acid Sequence | Cell Line | Rabbits | Gene Expression | Osteogenesis - drug effects | RNA, Messenger - genetics | Carrier Proteins - antagonists & inhibitors | Mesenchymal Stromal Cells - metabolism | Models, Molecular | Sequence Homology, Amino Acid | Carrier Proteins - genetics | Feedback, Physiological | Animals | Recombinant Fusion Proteins - genetics | Lysine - chemistry | COS Cells | Bone Morphogenetic Protein 6 - physiology | Bone Morphogenetic Protein 7 - pharmacology | Index Medicus | Noggin | Protein Structure and Folding | Bone Morphogenetic Protein (BMP) | Transforming Growth Factor Beta (TGFbeta) | Regeneration | Receptor Serine Threonine Kinase | Bone | Differentiation
Journal Article
STEM CELLS, ISSN 1066-5099, 07/2017, Volume 35, Issue 7, pp. 1760 - 1772
Bre is a conserved cellular protein expressed in various tissues. Its major function includes DNA damage repair and anti‐apoptosis. Recent studies indicate... 
Mdm2 | Ubiquitination | Bre | Osteogenesis | Mesenchymal stem cells | p53 | ANTI-APOPTOTIC PROTEIN | Ubiqu nation | OSTEOGENIC DIFFERENTIATION | MESENCHYMAL STEM-CELLS | NEGATIVE REGULATOR | CELL & TISSUE ENGINEERING | CELL BIOLOGY | ONCOLOGY | BONE-FORMATION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | TRANSCRIPTION FACTOR OSTERIX | IN-VIVO | HUMAN HEPATOCELLULAR-CARCINOMA | HEMATOLOGY | SKELETAL DEVELOPMENT | ORPHAN RECEPTOR NUR77 | Bone and Bones - pathology | RNA, Small Interfering - genetics | Proto-Oncogene Proteins c-mdm2 - genetics | Osteoporosis - therapy | Tumor Suppressor Protein p53 - antagonists & inhibitors | Tumor Suppressor Protein p53 - genetics | Tissue Scaffolds | Toluene - analogs & derivatives | Mesenchymal Stromal Cells - cytology | Cyclin-Dependent Kinase Inhibitor p21 - genetics | Osteoporosis - metabolism | Bone and Bones - metabolism | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Bone Marrow Cells - drug effects | Female | Osteoporosis - genetics | Cell Differentiation | Nuclear Proteins - genetics | Toluene - pharmacology | Proto-Oncogene Proteins c-mdm2 - metabolism | Osteogenesis - genetics | Disease Models, Animal | Tissue Engineering | Mesenchymal Stromal Cells - drug effects | Nerve Tissue Proteins - antagonists & inhibitors | Signal Transduction | Benzothiazoles - pharmacology | Bone Marrow Cells - cytology | Gene Expression Regulation | Tumor Suppressor Protein p53 - metabolism | Mesenchymal Stromal Cells - metabolism | Nuclear Proteins - metabolism | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Animals | Osteoporosis - pathology | Mice, Nude | Nuclear Proteins - antagonists & inhibitors | Protein Stability - drug effects | Mice | Mice, Inbred BALB C | Primary Cell Culture | Bone Marrow Cells - metabolism | RNA, Small Interfering - metabolism | Proteins | Osteoporosis | Phosphatases | Analysis | Stem cells | Cell differentiation | Gene expression | GTP-binding protein | Alkaline phosphatase | Transcription | Mesenchyme | p53 Protein | DNA damage | Differentiation (biology) | Stem cell transplantation | Activation | Tissues | Osteoblasts | DNA repair | Degradation | Biomedical materials | Pathways | Mineralization | Bone marrow | Bones | Biocompatibility | Inhibition | Damage | Deoxyribonucleic acid--DNA | MDM2 protein | siRNA | Molecular modelling | Osteoblastogenesis | In vivo methods and tests | In vitro methods and tests | Apoptosis | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 12/2002, Volume 420, Issue 6916, pp. 636 - 642
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 6, pp. e11167 - e11167
Background: Bone Morphogenetic Protein (BMP) signaling pathways are involved in differentiation of stem cells into diverse cell types, and thus BMPs can be... 
SIGNALING PATHWAYS | FGF | MULTIDISCIPLINARY SCIENCES | BONE MORPHOGENETIC PROTEINS | DEFINITIVE ENDODERM | OSTEOGENIC DIFFERENTIATION | SELF-RENEWAL | RECEPTOR | ACTIVITY IN-VITRO | MESODERM INDUCTION | BETA | Biomarkers - metabolism | Bone Morphogenetic Protein 2 - genetics | Bone Morphogenetic Protein 6 - chemistry | Cell Line | Embryonic Stem Cells - cytology | Humans | Transforming Growth Factor beta1 - metabolism | Bone Morphogenetic Protein 2 - chemistry | Gene Expression Profiling | DNA Primers | Bone Morphogenetic Protein 2 - physiology | Receptors, CXCR4 - metabolism | Bone Morphogenetic Protein 6 - genetics | Culture Media | Base Sequence | Polymerase Chain Reaction | Fibroblast Growth Factor 2 - metabolism | Cell Differentiation - physiology | Dimerization | Bone Morphogenetic Protein 6 - physiology | Circuit components | Fibroblast growth factors | Comparative analysis | Cell differentiation | Embryonic stem cells | Mitogens | Protein kinases | Flow cytometry | Smad protein | Phosphorylation | Laboratories | Differentiation (biology) | Embryo cells | Biology | CDX2 protein | Kinases | Proteins | Signal transduction | Pathways | Bone morphogenetic proteins | Growth factors | Recombinant | Fibroblast growth factor 2 | Bone morphogenetic protein 6 | Bone morphogenetic protein 2 | Bone morphogenetic protein receptor type II | Markers | Extracellular signal-regulated kinase | Gene expression | Embryos | CXCR4 protein | Biological activity | Cytometry | Signaling | Insects | Morphology | Stem cells | Ligands | Index Medicus
Journal Article
Acta Biomaterialia, ISSN 1742-7061, 04/2018, Volume 71, pp. 184 - 199
Localization of recombinant human bone morphogenetic protein-2 (rhBMP-2) with continuous and effective osteogenic stimulation is still a great challenge in the... 
rhBMP-2 bioactivity | Chondroitin sulfate | Bone regeneration | Bioinspired interactions | MATERIALS SCIENCE, BIOMATERIALS | BMP-2 DELIVERY | ENGINEERING, BIOMEDICAL | REGENERATION | CONTROLLED-RELEASE | OSTEOGENIC DIFFERENTIATION | IMMOBILIZATION | STEM-CELL DIFFERENTIATION | RHBMP-2 | GROWTH-FACTORS | IN-VIVO | SURFACE | Humans | Rats | Recombinant Proteins - chemistry | Bone Morphogenetic Protein 2 - chemistry | Calcium Phosphates - chemistry | Delayed-Action Preparations - chemistry | Male | Recombinant Proteins - pharmacokinetics | Chondroitin Sulfates - chemistry | Rats, Sprague-Dawley | Extracellular Matrix - chemistry | Animals | Bone Morphogenetic Protein 2 - pharmacokinetics | Delayed-Action Preparations - pharmacokinetics | Bone Cements - chemistry | Yuan (China) | Tissue engineering | Bone morphogenetic proteins | Calcium phosphate | Sulfates | Protein kinases | Chondroitin | Protein binding | Glycosaminoglycans | Calcium | Stimulation | Kinases | Calcium sulfate | Mimicry | Proteins | Receptors | Biomedical materials | Bone growth | Biomimetics | Biocompatibility | Cements | Extracellular matrix | Protein transport | Localization | Bone matrix | Growth factors | Controlled release | Recombinant | Translocation | Bone morphogenetic protein 2 | Drosophila | Extracellular signal-regulated kinase | Biological activity | Bone morphogenetic protein receptor type I | Calcium phosphates | Regeneration | Decapentaplegic protein | Cement | Sustained release | In vivo methods and tests | Bone | Kinetics | Bone morphogenetic protein receptors | Position (location) | Ossification (ectopic) | Scaffolds | Osteogenesis | Index Medicus
Journal Article
Journal Article