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Journal Article
Journal of cellular and molecular medicine, ISSN 1582-1838, 11/2017, Volume 21, Issue 11, pp. 2773 - 2781
It is assumed that the activity of osteoblasts and osteoclasts is decreased in bone tissue of aged individuals. However, detailed investigation of the... 
RANKL | osteoblasts | bone ageing | RUNX‐2 | osteoclasts | RUNX-2 | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Cell Biology | Research & Experimental Medicine | Osteopontin - genetics | RANK Ligand - metabolism | Cancellous Bone - metabolism | Wnt-5a Protein - genetics | Humans | Osteocalcin - genetics | Bone Density - genetics | Osteopontin - metabolism | Osteoclasts - cytology | Core Binding Factor Alpha 1 Subunit - metabolism | Radius - anatomy & histology | Matrix Metalloproteinase 9 - metabolism | Wnt-5a Protein - metabolism | Aging - genetics | Gene Expression Regulation, Developmental | Matrix Metalloproteinase 9 - genetics | Aged, 80 and over | Adult | Osteoblasts - cytology | Radius - metabolism | Osteogenesis - genetics | Signal Transduction | Osteocalcin - metabolism | Cancellous Bone - growth & development | NFATC Transcription Factors - metabolism | Osteoclasts - metabolism | RANK Ligand - genetics | Cancellous Bone - anatomy & histology | Radius - growth & development | Sp7 Transcription Factor - genetics | Tartrate-Resistant Acid Phosphatase - metabolism | Adolescent | Sp7 Transcription Factor - metabolism | Aged | Osteoblasts - metabolism | Tartrate-Resistant Acid Phosphatase - genetics | Core Binding Factor Alpha 1 Subunit - genetics | Aging - metabolism | NFATC Transcription Factors - genetics | Radius | Matrix metalloproteinases | Genes | Osteoblasts | Osteoprotegerin | Bone growth | Acid resistance | Biocompatibility | Bone density | TRANCE protein | Bone matrix | Age | Fibroblast growth factor 2 | Osteocalcin | Bone morphogenetic protein 2 | Markers | Osteopontin | Bone healing | Group dynamics | Gene expression | Collagenase 3 | Osteoid | Gelatinase B | Polymerase chain reaction | Osteoclastogenesis | Regeneration | Osteoclasts | Acid phosphatase (tartrate-resistant) | Acid phosphatase | Osteogenesis | Bone (cancellous) | Index Medicus | Original
Journal Article
Acta biomaterialia, ISSN 1742-7061, 04/2019, Volume 88, pp. 325 - 331
[Display omitted] Cholesterol esterase-like (CE) activity from saliva and esterase from cariogenic bacteria hydrolyze ester linkages of dental methacrylate... 
Biodegradation | Dental restoration failure | Dental caries | Matrix metalloproteinases | Esterase | Engineering | Materials Science | Technology | Engineering, Biomedical | Materials Science, Biomaterials | Science & Technology | Leukocyte Elastase - metabolism | Neutrophils - enzymology | Cell Survival | Collagen - ultrastructure | Dentin - metabolism | Humans | Hydroxyproline - metabolism | Sterol Esterase - metabolism | Methacrylates - metabolism | Tooth - chemistry | Composite Resins - metabolism | Collagen - metabolism | Propane - metabolism | Acrylic Resins - metabolism | Polyurethanes - metabolism | Proteolysis | Matrix Metalloproteinases - metabolism | Neutrophils - metabolism | Biological products | Collagen | Esters | Bacteria | Liquid chromatography | Dentin | Hydroxyproline | Collagens | Matrix metalloproteinase | Bisphenol A glycidyl methacrylate | Degradation | Dental restorative materials | Dental materials | Restoration | Acrylic resins | Metalloproteinase | Resins | Polymers | Buffers | Interstitial collagenase | Demineralizing | Polymer matrix composites | Incubation | Neutrophils | Teeth | Byproducts | Mass spectroscopy | Leukocytes (neutrophilic) | Collagenase | Gelatinase | Cholesterol | Substrates | Gelatinase B | Gelatinase A | Interfaces | Oral cavity | Composite materials | Human performance | Neutrophil collagenase | Mass spectrometry | Saliva | Propane | Index Medicus | dental caries | biodegradation | esterase | dental restoration failure
Journal Article
The Journal of cell biology, ISSN 0021-9525, 11/1999, Volume 147, Issue 3, pp. 619 - 629
Active matrix metalloproteinases and degraded collagen are observed in disease states, such as atherosclerosis. To examine whether degraded collagen fragments... 
Calpain | Extracellular matrix | Focal adhesion kinase | Matrix metalloproteinase | Pp125(FAK) | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Cell Adhesion Molecules - chemistry | Crk-Associated Substrate Protein | Calpain - metabolism | Molecular Weight | Muscle, Smooth, Vascular - metabolism | Protein-Tyrosine Kinases - metabolism | Humans | Actins - metabolism | Vinculin - metabolism | Collagen - chemistry | Cytoplasm - metabolism | Peptide Fragments - pharmacology | Phosphoproteins - metabolism | Focal Adhesion Kinase 1 | Integrins - metabolism | Arteries | Proteins | Protein Processing, Post-Translational - drug effects | Protein-Tyrosine Kinases - chemistry | Cytoskeletal Proteins - metabolism | Collagen - pharmacology | Infant, Newborn | Actinin - metabolism | Muscle, Smooth, Vascular - drug effects | Peptide Fragments - metabolism | Cell Size - drug effects | Cells, Cultured | Collagen - antagonists & inhibitors | Focal Adhesion Protein-Tyrosine Kinases | Cell Adhesion - drug effects | Muscle, Smooth, Vascular - cytology | Talin - metabolism | Cell Adhesion Molecules - metabolism | Collagen - metabolism | Peptide Fragments - chemistry | Peptide Fragments - antagonists & inhibitors | Retinoblastoma-Like Protein p130 | Cytoskeleton - metabolism | Matrix Metalloproteinase Inhibitors | Receptors, Collagen | Matrix Metalloproteinases - metabolism | Collagenases - metabolism | Cytoplasm - drug effects | Muscle, Smooth, Vascular - enzymology | Paxillin | Calpain - antagonists & inhibitors | Cytoskeleton - drug effects | Physiological aspects | Research | Collagen | Cell adhesion | Index Medicus
Journal Article
PloS one, ISSN 1932-6203, 02/2014, Volume 9, Issue 2, pp. e88021 - e88021
Journal Article
Developmental cell, ISSN 1534-5807, 05/2012, Volume 22, Issue 5, pp. 927 - 939
During endochondral ossification, small, immature chondrocytes enlarge to form hypertrophic chondrocytes, which express collagen X. In this work, we... 
Life Sciences & Biomedicine | Developmental Biology | Science & Technology | Cell Biology | Chondrocytes - cytology | Hepatocyte Nuclear Factor 3-beta - genetics | Chondrogenesis - genetics | Alkaline Phosphatase - metabolism | Hepatocyte Nuclear Factor 3-gamma - genetics | Core Binding Factor Alpha 1 Subunit - metabolism | Embryo, Mammalian - metabolism | Cell Differentiation - genetics | Collagen Type X - metabolism | Hepatocyte Nuclear Factor 3-gamma - metabolism | Mice, Mutant Strains | Hepatocyte Nuclear Factor 3-gamma - deficiency | Binding Sites | Chondrocytes - metabolism | Genes, Reporter | Fibroblasts - metabolism | Hepatocyte Nuclear Factor 3-beta - metabolism | Dwarfism - embryology | Matrix Metalloproteinase 13 - genetics | Cells, Cultured | Metatarsal Bones - cytology | Myogenic Regulatory Factors - metabolism | Collagen Type X - genetics | Metatarsal Bones - metabolism | Cell Enlargement | Growth Plate - metabolism | Chick Embryo | Matrix Metalloproteinase 13 - metabolism | Dwarfism - genetics | Animals | Embryo, Mammalian - cytology | Smad1 Protein - metabolism | Fibroblasts - cytology | Mice | Hepatocyte Nuclear Factor 3-beta - deficiency | Physiological aspects | Phosphatases | Collagen | Genes | Index Medicus | Alkaline phosphatase | Collagenase 3 | Ossification | Dwarfism | Growth plate | Enhancers | Collagen (type X) | Mineralization | Chondrocytes | Fibroblasts | Chondrogenesis | Bone (endochondral) | Hypertrophy
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, pp. e42714 - e42714
The hormone, relaxin, inhibits aberrant myofibroblast differentiation and collagen deposition by disrupting the TGF-beta 1/Smad2 axis, via its cognate... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Relaxin - metabolism | Matrix Metalloproteinases - genetics | Receptors, G-Protein-Coupled - metabolism | Humans | Male | Receptors, Peptide - genetics | Matrix Metalloproteinase 9 - metabolism | Relaxin - genetics | Matrix Metalloproteinase 9 - genetics | Fibroblasts - metabolism | Cell Line | Matrix Metalloproteinase 2 - metabolism | Matrix Metalloproteinase 13 - genetics | Cells, Cultured | Rats | Kidney - cytology | Signal Transduction - genetics | Extracellular Signal-Regulated MAP Kinases | Rats, Sprague-Dawley | Matrix Metalloproteinase 13 - metabolism | Mice, Knockout | Matrix Metalloproteinase 2 - genetics | Animals | Cyclic GMP - metabolism | Nitric Oxide Synthase Type I - metabolism | Signal Transduction - physiology | Fibroblasts - cytology | Mice | Nitric Oxide Synthase Type I - genetics | Receptors, G-Protein-Coupled - genetics | Matrix Metalloproteinases - metabolism | Nitric Oxide - metabolism | Receptors, Peptide - metabolism | Physiological aspects | Genetic aspects | Research | Transforming growth factors | Metalloenzymes | Nitric oxide | Neurosciences | Phosphorylation | Matrix metalloproteinases | Guanosine | Smooth muscle | Genomes | Arthritis | Biochemistry | Matrix metalloproteinase | Guanylate cyclase | Western blotting | Signal transduction | Arginine | Gelatin | Rodents | Cyclic GMP | Fibroblasts | Metalloproteinase | Interstitial collagenase | Kidneys | Extracellular signal-regulated kinase | Collagenase 3 | Nitric-oxide synthase | Gelatinase B | NG-Nitroarginine methyl ester | Gelatinase A | Signaling | Inhibitors | Human performance | Collagen | Isoforms | Fibrosis | Skin | Aberration | Molecular biology | Ornithine | Index Medicus
Journal Article
International journal of molecular sciences, ISSN 1422-0067, 01/2019, Volume 20, Issue 3, p. 619
Systemic sclerosis (SSc) is a connective tissue disease of autoimmune origin characterized by vascular dysfunction and extensive fibrosis of the skin and... 
Fibrinolytic regulators | SSc | Vascular dysfunction | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Multidisciplinary | Science & Technology | Endothelium - pathology | Signal Transduction | Tissue Plasminogen Activator - metabolism | Humans | Scleroderma, Systemic - metabolism | Scleroderma, Systemic - pathology | Fibrinolytic Agents - metabolism | Plasminogen - metabolism | Endothelium - cytology | Receptors, Urokinase Plasminogen Activator - metabolism | Endothelium - metabolism | Plasminogen Activator Inhibitor 1 - metabolism | Urokinase-Type Plasminogen Activator - metabolism | Angiostatins - metabolism | Fibrinolysin - metabolism | alpha-2-Antiplasmin - metabolism | Apoptosis | Cerebellum | Brain | Regulators | Adipose tissue | Pathogenesis | Coagulation | Smooth muscle | Leukocytes | Fibronectin | Recruitment | Degradation | Proteins | Angiogenesis | Bone growth | Cell growth | Cell adhesion | Fibroblasts | Bone (cortical) | Vascular endothelial growth factor | Growth factors | Spleen | Wound healing | Autoantibodies | Abnormalities | Bone healing | Bone turnover | Metabolism | Gene expression | Insulin | Thrombosis | Membrane proteins | Beta cells | Domains | Placenta | Rheumatoid arthritis | Fibrosis | Cerebral cortex | Antibodies | Homeostasis | Amino acids | mRNA | Activation | Arthritis | Cell surface | Cell adhesion & migration | Epidermal growth factor | Blood platelets | Lymphocytes | Intestine | Hypertension | Immune response | Kidneys | Bone remodelling | Muscles | Inflammation | Endothelial cells | Differentiation | Cancer | Index Medicus | vascular dysfunction
Journal Article