BioFactors, ISSN 0951-6433, 01/2010, Volume 36, Issue 1, pp. 25 - 32
In recent years, much progress has been made in understanding the factors that regulate the gene expression program that underlies the induction,...
Lef1 | NFATc | Osterix | SMAD | Atf4 | miRs | Runx2 | HDAC | CLEIDOCRANIAL DYSPLASIA | BONE MORPHOGENETIC PROTEIN-2 | C-FOS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ACTIVATING TRANSCRIPTION FACTOR-4 | SAETHRE-CHOTZEN-SYNDROME | BETA-CATENIN | COLLAGENASE-3 PROMOTER | OSTEOCALCIN GENE | ENDOCRINOLOGY & METABOLISM | PARATHYROID-HORMONE | HISTONE DEACETYLASE INHIBITORS | Transcription Factors - physiology | Histone Deacetylases - genetics | Epigenesis, Genetic | Humans | Core Binding Factor Alpha 1 Subunit - physiology | NFATC Transcription Factors - physiology | Smad Proteins - physiology | Calcineurin - physiology | T Cell Transcription Factor 1 - physiology | Animals | Gene Expression Regulation, Developmental | Transcription Factor AP-1 - physiology | Twist-Related Protein 1 - physiology | Lymphoid Enhancer-Binding Factor 1 - physiology | Sp7 Transcription Factor | Mice | Zinc Fingers - physiology | MicroRNAs - physiology | Osteoblasts - metabolism | Activating Transcription Factor 4 - physiology
Lef1 | NFATc | Osterix | SMAD | Atf4 | miRs | Runx2 | HDAC | CLEIDOCRANIAL DYSPLASIA | BONE MORPHOGENETIC PROTEIN-2 | C-FOS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ACTIVATING TRANSCRIPTION FACTOR-4 | SAETHRE-CHOTZEN-SYNDROME | BETA-CATENIN | COLLAGENASE-3 PROMOTER | OSTEOCALCIN GENE | ENDOCRINOLOGY & METABOLISM | PARATHYROID-HORMONE | HISTONE DEACETYLASE INHIBITORS | Transcription Factors - physiology | Histone Deacetylases - genetics | Epigenesis, Genetic | Humans | Core Binding Factor Alpha 1 Subunit - physiology | NFATC Transcription Factors - physiology | Smad Proteins - physiology | Calcineurin - physiology | T Cell Transcription Factor 1 - physiology | Animals | Gene Expression Regulation, Developmental | Transcription Factor AP-1 - physiology | Twist-Related Protein 1 - physiology | Lymphoid Enhancer-Binding Factor 1 - physiology | Sp7 Transcription Factor | Mice | Zinc Fingers - physiology | MicroRNAs - physiology | Osteoblasts - metabolism | Activating Transcription Factor 4 - physiology
Journal Article
Gene, ISSN 0378-1119, 09/2013, Volume 527, Issue 1, pp. 321 - 331
Osteogenesis is the result of a complex sequence of events that involve the differentiation of mesenchymal stem cells (MSC) into osteoblasts. MSCs are...
miRNA | Sp7 | MSC | Transcription factor | Osteogenesis | Antigens, Differentiation | Oligonucleotide Array Sequence Analysis | Humans | Transcriptome | Gene Expression Profiling | Journal Article | Bone Marrow Cells | MCF-7 Cells | Mesenchymal Stromal Cells | RNA Interference | Research Support, Non-U.S. Gov't | MicroRNAs | Sp7 Transcription Factor | Cell Differentiation | Transcription Factors | 3' Untranslated Regions | RNA, Messenger | TRANSCRIPTION FACTORS | OSTEOBLAST DIFFERENTIATION | INTERNATIONAL-SOCIETY | RNA | THERAPY POSITION STATEMENT | REPRESSION | GENETICS & HEREDITY | GENE-EXPRESSION | STROMAL CELLS | PROGRESSION | PROGRAM | RNA, Messenger - genetics | Bone Marrow Cells - physiology | Transcription Factors - genetics | RNA, Messenger - metabolism | Transcription Factors - metabolism | Antigens, Differentiation - metabolism | MicroRNAs - genetics | Mesenchymal Stromal Cells - physiology | Analysis | MicroRNA | Stem cells
miRNA | Sp7 | MSC | Transcription factor | Osteogenesis | Antigens, Differentiation | Oligonucleotide Array Sequence Analysis | Humans | Transcriptome | Gene Expression Profiling | Journal Article | Bone Marrow Cells | MCF-7 Cells | Mesenchymal Stromal Cells | RNA Interference | Research Support, Non-U.S. Gov't | MicroRNAs | Sp7 Transcription Factor | Cell Differentiation | Transcription Factors | 3' Untranslated Regions | RNA, Messenger | TRANSCRIPTION FACTORS | OSTEOBLAST DIFFERENTIATION | INTERNATIONAL-SOCIETY | RNA | THERAPY POSITION STATEMENT | REPRESSION | GENETICS & HEREDITY | GENE-EXPRESSION | STROMAL CELLS | PROGRESSION | PROGRAM | RNA, Messenger - genetics | Bone Marrow Cells - physiology | Transcription Factors - genetics | RNA, Messenger - metabolism | Transcription Factors - metabolism | Antigens, Differentiation - metabolism | MicroRNAs - genetics | Mesenchymal Stromal Cells - physiology | Analysis | MicroRNA | Stem cells
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2013, Volume 8, Issue 6, p. e65940
The nature of the cellular and molecular mechanisms for the transition of avascular cartilage replacement with bone during endochondral ossification remains...
RECEPTOR-MEDIATED TRANSCRIPTION | SCLEROSTIN | PROTEIN | GROWTH-FACTOR VEGF | BONE-FORMATION | OSX | TRANSCRIPTION FACTOR OSTERIX | MULTIDISCIPLINARY SCIENCES | MASS | HYPOXIA | SKELETAL DEVELOPMENT | Glycoproteins - genetics | Cell Line | Cell Hypoxia - physiology | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Humans | Glycoproteins - metabolism | Wnt Signaling Pathway - physiology | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Animals | Wnt Signaling Pathway - genetics | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Mice | RNA, Small Interfering | Cell Hypoxia - genetics | Osteoblasts - metabolism | Hypoxia-inducible factor 1 | Wnt protein | Transcription | Gene regulation | Activation | SOST protein | Gene deletion | Kinases | Osteoblasts | Deferoxamine | Ossification | Cartilage | Angiogenesis | Signal transduction | Transfection | Vitamin D | Clonal deletion | Rodents | Deletion | Biocompatibility | Inhibition | Vascular endothelial growth factor | Bone (endochondral) | Hypoxia-inducible factors | siRNA | Gene expression | Mutants | Polymerase chain reaction | Signaling | Molecular modelling | Hypoxia | Osteogenesis
RECEPTOR-MEDIATED TRANSCRIPTION | SCLEROSTIN | PROTEIN | GROWTH-FACTOR VEGF | BONE-FORMATION | OSX | TRANSCRIPTION FACTOR OSTERIX | MULTIDISCIPLINARY SCIENCES | MASS | HYPOXIA | SKELETAL DEVELOPMENT | Glycoproteins - genetics | Cell Line | Cell Hypoxia - physiology | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Humans | Glycoproteins - metabolism | Wnt Signaling Pathway - physiology | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Animals | Wnt Signaling Pathway - genetics | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Mice | RNA, Small Interfering | Cell Hypoxia - genetics | Osteoblasts - metabolism | Hypoxia-inducible factor 1 | Wnt protein | Transcription | Gene regulation | Activation | SOST protein | Gene deletion | Kinases | Osteoblasts | Deferoxamine | Ossification | Cartilage | Angiogenesis | Signal transduction | Transfection | Vitamin D | Clonal deletion | Rodents | Deletion | Biocompatibility | Inhibition | Vascular endothelial growth factor | Bone (endochondral) | Hypoxia-inducible factors | siRNA | Gene expression | Mutants | Polymerase chain reaction | Signaling | Molecular modelling | Hypoxia | Osteogenesis
Journal Article
11/2011
Osterix (Osx) is a transcription factor required for osteoblast differentiation and bone formation. We previously demonstrated that continuous parathyroid...
parathyroid hormone | gene regulation | Osterix | 0419 | osteoblast
parathyroid hormone | gene regulation | Osterix | 0419 | osteoblast
Dissertation
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 08/2016, Volume 476, Issue 4, pp. 574 - 579
Osteoporosis is the most common metabolic bone disease characterized by decreased bone mass, decreased bone strength, and increased risk of fracture. It is due...
Osteoblast | Bone sialoprotein | Transcription | Osx | Bsp | Osterix | RECEPTOR-MEDIATED TRANSCRIPTION | OSTEOBLAST DIFFERENTIATION | PROTEIN | RNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | HYDROXYAPATITE | BIOPHYSICS | GROWTH | NUCLEATION | FACTOR OSTERIX OSX | Cell Line | Promoter Regions, Genetic | RNA, Small Interfering - genetics | Sequence Deletion | Mutagenesis, Site-Directed | Gene Expression Regulation | Transcription Factors - antagonists & inhibitors | Binding Sites - genetics | Transcription Factors - genetics | GC Rich Sequence | Mice, Knockout | Transcription Factors - metabolism | Cell Differentiation - genetics | Animals | Sp7 Transcription Factor | Integrin-Binding Sialoprotein - genetics | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Osteogenesis - genetics | Osteoporosis | Stem cells | Physiological aspects | Bones | Genetic aspects | Genetic transcription | Density | Index Medicus
Osteoblast | Bone sialoprotein | Transcription | Osx | Bsp | Osterix | RECEPTOR-MEDIATED TRANSCRIPTION | OSTEOBLAST DIFFERENTIATION | PROTEIN | RNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | HYDROXYAPATITE | BIOPHYSICS | GROWTH | NUCLEATION | FACTOR OSTERIX OSX | Cell Line | Promoter Regions, Genetic | RNA, Small Interfering - genetics | Sequence Deletion | Mutagenesis, Site-Directed | Gene Expression Regulation | Transcription Factors - antagonists & inhibitors | Binding Sites - genetics | Transcription Factors - genetics | GC Rich Sequence | Mice, Knockout | Transcription Factors - metabolism | Cell Differentiation - genetics | Animals | Sp7 Transcription Factor | Integrin-Binding Sialoprotein - genetics | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Osteogenesis - genetics | Osteoporosis | Stem cells | Physiological aspects | Bones | Genetic aspects | Genetic transcription | Density | Index Medicus
Journal Article
PLOS ONE, ISSN 1932-6203, 08/2019, Volume 14, Issue 8, p. e0220653
Vitamin C (ascorbic acid, AA) is a well-known regulator of bone and cartilage metabolism. However, the mechanisms of AA's action in these tissues are only...
OSTERIX EXPRESSION | IN-VITRO | ACTIVATION | COLLAGEN | BONE-MINERAL DENSITY | PROTEASOMAL DEGRADATION | ALKALINE-PHOSPHATASE | MULTIDISCIPLINARY SCIENCES | DIFFERENTIATION | ASCORBIC-ACID | PROLYL HYDROXYLASE | Growth | Nutrient interactions | Vitamin C | Physiological aspects | Bones | Genetic aspects | Cartilage cells | Gene expression | Health aspects | Osteoblasts | Ascorbic acid | Genes | Systematic review | Arthritis | Biochemistry | Bone (trabecular) | Proteins | Antioxidants | Cartilage | Osteoporosis | Demethylation | Biomedical materials | Cell cycle | DNA methylation | Biocompatibility | Prolyl hydroxylase | Bone density | Chondrogenesis | Deoxyribonucleic acid--DNA | Enzymes | Hydroxylase | Cartilage (articular) | Metabolism | Medicine | Studies | Osteoblastogenesis | Fractures | Womens health | Chondrocytes | Stem cells | Hypoxia | Nuclei (cytology) | Bone | Differentiation | Osteoarthritis | Cytoplasm | Health disparities | Cartilage diseases | Deoxyribonucleic acid | DNA
OSTERIX EXPRESSION | IN-VITRO | ACTIVATION | COLLAGEN | BONE-MINERAL DENSITY | PROTEASOMAL DEGRADATION | ALKALINE-PHOSPHATASE | MULTIDISCIPLINARY SCIENCES | DIFFERENTIATION | ASCORBIC-ACID | PROLYL HYDROXYLASE | Growth | Nutrient interactions | Vitamin C | Physiological aspects | Bones | Genetic aspects | Cartilage cells | Gene expression | Health aspects | Osteoblasts | Ascorbic acid | Genes | Systematic review | Arthritis | Biochemistry | Bone (trabecular) | Proteins | Antioxidants | Cartilage | Osteoporosis | Demethylation | Biomedical materials | Cell cycle | DNA methylation | Biocompatibility | Prolyl hydroxylase | Bone density | Chondrogenesis | Deoxyribonucleic acid--DNA | Enzymes | Hydroxylase | Cartilage (articular) | Metabolism | Medicine | Studies | Osteoblastogenesis | Fractures | Womens health | Chondrocytes | Stem cells | Hypoxia | Nuclei (cytology) | Bone | Differentiation | Osteoarthritis | Cytoplasm | Health disparities | Cartilage diseases | Deoxyribonucleic acid | DNA
Journal Article
Developmental Dynamics, ISSN 1058-8388, 02/2009, Volume 238, Issue 2, pp. 459 - 466
The transcription factors RUNX2 and OSX have been shown to act sequentially to direct mammalian osteoblast differentiation. RUNX2 is required during the early...
runx2/cbfa1/osf1/pebp2αA | crossveinless2 | osteonectin | mesenchymal stem cell | cranial | collagen10a1 | neural crest | bone | osteoblast | osterix | osteoprogenetor | osteoblastogenesis | tcf7 | collagenIa2 | dermal bone | Mesenchymal stem cell | Osteoprogenetor | Cranial | Neural crest | Osteoblastogenesis | Dermal bone | Osteoblast | Bone | DANIO-RERIO | DEVELOPMENTAL BIOLOGY | FAMILY | ELEMENTS | runx2/cbfa1/osf1/pebp2 alpha A | BONE-FORMATION | CBFA1 | SKELETAL DEVELOPMENT | CELLS | ANATOMY & MORPHOLOGY | ISOFORM | IDENTIFICATION | Biomarkers - metabolism | Bone Matrix - metabolism | Transcription Factors - metabolism | Animals | Zebrafish Proteins - metabolism | Zebrafish - metabolism | Body Patterning | Sp7 Transcription Factor | Osteoblasts - cytology | Osteoblasts - metabolism | Zebrafish - embryology | Cell Differentiation - physiology
runx2/cbfa1/osf1/pebp2αA | crossveinless2 | osteonectin | mesenchymal stem cell | cranial | collagen10a1 | neural crest | bone | osteoblast | osterix | osteoprogenetor | osteoblastogenesis | tcf7 | collagenIa2 | dermal bone | Mesenchymal stem cell | Osteoprogenetor | Cranial | Neural crest | Osteoblastogenesis | Dermal bone | Osteoblast | Bone | DANIO-RERIO | DEVELOPMENTAL BIOLOGY | FAMILY | ELEMENTS | runx2/cbfa1/osf1/pebp2 alpha A | BONE-FORMATION | CBFA1 | SKELETAL DEVELOPMENT | CELLS | ANATOMY & MORPHOLOGY | ISOFORM | IDENTIFICATION | Biomarkers - metabolism | Bone Matrix - metabolism | Transcription Factors - metabolism | Animals | Zebrafish Proteins - metabolism | Zebrafish - metabolism | Body Patterning | Sp7 Transcription Factor | Osteoblasts - cytology | Osteoblasts - metabolism | Zebrafish - embryology | Cell Differentiation - physiology
Journal Article
BIOMED RESEARCH INTERNATIONAL, ISSN 2314-6133, 2018, Volume 2018, pp. 4901591 - 8
Rheumatoid arthritis (RA) is an autoimmune inflammatory disease characterized by bone loss. Degree of inflammation has been identified as an important...
MEDICINE, RESEARCH & EXPERIMENTAL | CONTROLLED-TRIAL | IN-VITRO | OSTERIX | IGURATIMOD THERAPY | BONE-FORMATION | PHOSPHORYLATION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ACTIVE RHEUMATOID-ARTHRITIS | DOUBLE-BLIND | CLINICAL-USE | MESENCHYMAL STEM-CELLS | Cell culture | Alkaline phosphatase | Phosphorylation | Transcription factors | Collagen (type I) | Calcium | Mesenchyme | Differentiation (biology) | Activation | Arthritis | Research | Kinases | Phosphatase | Osteoblasts | Proteins | Bone growth | Bone marrow | Biocompatibility | Bone loss | NF-κB protein | Osteocalcin | Manufacturers | Inflammation | Cell differentiation | Gene expression | Osteoblastogenesis | Damage detection | Rheumatoid arthritis | Stem cells | Bone | Osteogenesis
MEDICINE, RESEARCH & EXPERIMENTAL | CONTROLLED-TRIAL | IN-VITRO | OSTERIX | IGURATIMOD THERAPY | BONE-FORMATION | PHOSPHORYLATION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ACTIVE RHEUMATOID-ARTHRITIS | DOUBLE-BLIND | CLINICAL-USE | MESENCHYMAL STEM-CELLS | Cell culture | Alkaline phosphatase | Phosphorylation | Transcription factors | Collagen (type I) | Calcium | Mesenchyme | Differentiation (biology) | Activation | Arthritis | Research | Kinases | Phosphatase | Osteoblasts | Proteins | Bone growth | Bone marrow | Biocompatibility | Bone loss | NF-κB protein | Osteocalcin | Manufacturers | Inflammation | Cell differentiation | Gene expression | Osteoblastogenesis | Damage detection | Rheumatoid arthritis | Stem cells | Bone | Osteogenesis
Journal Article
Scientific Reports, ISSN 2045-2322, 06/2015, Volume 5, Issue 1, p. 10020
Bone regeneration involves a series of events in a coordinated manner, including recruitment of mesenchymal stem cells, induction of immune response,...
ANGIOGENESIS | BONE-FORMATION | VEGF | MULTIDISCIPLINARY SCIENCES | DISEASE | OSTEOGENESIS | TRANSCRIPTIONAL REGULATION | SKELETAL DEVELOPMENT | FACTOR OSTERIX OSX | Cell Line | Cell Hypoxia - drug effects | Animals | Cyclooxygenase 2 Inhibitors - pharmacology | Cyclooxygenase 2 - metabolism | Gene Expression Regulation | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Tumor Necrosis Factor-alpha - biosynthesis
ANGIOGENESIS | BONE-FORMATION | VEGF | MULTIDISCIPLINARY SCIENCES | DISEASE | OSTEOGENESIS | TRANSCRIPTIONAL REGULATION | SKELETAL DEVELOPMENT | FACTOR OSTERIX OSX | Cell Line | Cell Hypoxia - drug effects | Animals | Cyclooxygenase 2 Inhibitors - pharmacology | Cyclooxygenase 2 - metabolism | Gene Expression Regulation | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Tumor Necrosis Factor-alpha - biosynthesis
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2015, Volume 10, Issue 12, p. e0144982
Osteoblast differentiation from mesenchymal cells is regulated by multiple signalling pathways. Here we have analysed the roles of Fibroblast Growth Factor...
RETINOIC ACID | BONE-FORMATION | TRANSCRIPTION FACTOR OSTERIX | MAP-KINASE | ALKALINE-PHOSPHATASE | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | FIBROBLAST-GROWTH-FACTOR | MESENCHYMAL STEM-CELLS | ZEBRAFISH DEVELOPMENT | MESODERM INDUCTION | Osteogenesis - physiology | Zebrafish Proteins - biosynthesis | Fibroblast Growth Factors - genetics | Wnt Signaling Pathway - physiology | Transcription Factors - biosynthesis | Transcription Factors - genetics | beta Catenin - metabolism | Zebrafish - genetics | beta Catenin - genetics | Fibroblast Growth Factors - metabolism | Animals | Zebrafish - metabolism | Sp7 Transcription Factor | Osteoblasts - cytology | Zebrafish Proteins - genetics | Osteoblasts - metabolism | Cell Differentiation - physiology | Fibroblast growth factor | Transcription factors | Wnt protein | Mesenchyme | Transgenic | Kinases | β-catenin | Signal transduction | Bone growth | Biomedical materials | Pathways | Transcription activation | Bone marrow | Biocompatibility | Zebrafish | Gene expression | Embryos | Chemical interference | Studies | Signaling | Osteoblastogenesis | Mutation | Kinetics | Bone | Differentiation | Osteogenesis
RETINOIC ACID | BONE-FORMATION | TRANSCRIPTION FACTOR OSTERIX | MAP-KINASE | ALKALINE-PHOSPHATASE | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | FIBROBLAST-GROWTH-FACTOR | MESENCHYMAL STEM-CELLS | ZEBRAFISH DEVELOPMENT | MESODERM INDUCTION | Osteogenesis - physiology | Zebrafish Proteins - biosynthesis | Fibroblast Growth Factors - genetics | Wnt Signaling Pathway - physiology | Transcription Factors - biosynthesis | Transcription Factors - genetics | beta Catenin - metabolism | Zebrafish - genetics | beta Catenin - genetics | Fibroblast Growth Factors - metabolism | Animals | Zebrafish - metabolism | Sp7 Transcription Factor | Osteoblasts - cytology | Zebrafish Proteins - genetics | Osteoblasts - metabolism | Cell Differentiation - physiology | Fibroblast growth factor | Transcription factors | Wnt protein | Mesenchyme | Transgenic | Kinases | β-catenin | Signal transduction | Bone growth | Biomedical materials | Pathways | Transcription activation | Bone marrow | Biocompatibility | Zebrafish | Gene expression | Embryos | Chemical interference | Studies | Signaling | Osteoblastogenesis | Mutation | Kinetics | Bone | Differentiation | Osteogenesis
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 10/2017, Volume 37, Issue 20
Here we assess histone modification, chromatin remodeling, and DNA methylation processes that coordinately control the expression of the bone master...
Tet enzymes | Epigenetics | DNA demethylation | Sp7 | Osteoblast differentiation | METHYLATION | MAMMALIAN DNA | BONE MORPHOGENETIC PROTEIN-2 | BIOCHEMISTRY & MOLECULAR BIOLOGY | epigenetics | CELL BIOLOGY | HUMAN GENOME | osteoblast differentiation | TRANSCRIPTION FACTOR OSTERIX | EMBRYONIC STEM-CELLS | COMPASS FAMILY | RIC-8B GENE | DIFFERENTIATION | UP-REGULATION | Chromatin - metabolism | Transcriptional Activation - genetics | Chromosomal Proteins, Non-Histone - metabolism | Gene Expression Regulation - genetics | Epigenesis, Genetic | Humans | Chromatin Assembly and Disassembly - genetics | DNA - metabolism | Transcription Factors - metabolism | Cell Differentiation - genetics | Cell Lineage | DNA Methylation | Sp7 Transcription Factor | Histones - metabolism | Osteoblasts - metabolism
Tet enzymes | Epigenetics | DNA demethylation | Sp7 | Osteoblast differentiation | METHYLATION | MAMMALIAN DNA | BONE MORPHOGENETIC PROTEIN-2 | BIOCHEMISTRY & MOLECULAR BIOLOGY | epigenetics | CELL BIOLOGY | HUMAN GENOME | osteoblast differentiation | TRANSCRIPTION FACTOR OSTERIX | EMBRYONIC STEM-CELLS | COMPASS FAMILY | RIC-8B GENE | DIFFERENTIATION | UP-REGULATION | Chromatin - metabolism | Transcriptional Activation - genetics | Chromosomal Proteins, Non-Histone - metabolism | Gene Expression Regulation - genetics | Epigenesis, Genetic | Humans | Chromatin Assembly and Disassembly - genetics | DNA - metabolism | Transcription Factors - metabolism | Cell Differentiation - genetics | Cell Lineage | DNA Methylation | Sp7 Transcription Factor | Histones - metabolism | Osteoblasts - metabolism
Journal Article
Bone, ISSN 8756-3282, 2014, Volume 65, pp. 25 - 32
Abstract Micro- and nanoscale surface modifications have been the focus of multiple studies in the pursuit of accelerating bone apposition or osseointegration...
Orthopedics | Nanotopography | Osseointegration | Gene expression | Nanomechanics | OSTERIX | OSTEOBLAST DIFFERENTIATION | DEPOSITION | KNOWLEDGE | HYDROXYAPATITE-COATED IMPLANTS | ROUGHNESS | CALCIUM-PHOSPHATE | MINERALIZATION | ENDOCRINOLOGY & METABOLISM | ROOT FORM IMPLANTS | Gene Expression | Microscopy, Electron, Scanning | Bone and Bones - physiology | Rats | Male | DNA Primers | Reverse Transcriptase Polymerase Chain Reaction | Rats, Sprague-Dawley | Biomechanical Phenomena | Animals | Base Sequence | Bone and Bones - metabolism | Surface Properties | Bone and Bones - ultrastructure | Genetic research | Hardness | Collagen | Analysis | Genes | MEDICINE | MEDICIN
Orthopedics | Nanotopography | Osseointegration | Gene expression | Nanomechanics | OSTERIX | OSTEOBLAST DIFFERENTIATION | DEPOSITION | KNOWLEDGE | HYDROXYAPATITE-COATED IMPLANTS | ROUGHNESS | CALCIUM-PHOSPHATE | MINERALIZATION | ENDOCRINOLOGY & METABOLISM | ROOT FORM IMPLANTS | Gene Expression | Microscopy, Electron, Scanning | Bone and Bones - physiology | Rats | Male | DNA Primers | Reverse Transcriptase Polymerase Chain Reaction | Rats, Sprague-Dawley | Biomechanical Phenomena | Animals | Base Sequence | Bone and Bones - metabolism | Surface Properties | Bone and Bones - ultrastructure | Genetic research | Hardness | Collagen | Analysis | Genes | MEDICINE | MEDICIN
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 02/2008, Volume 283, Issue 7, pp. 3816 - 3826
Osterix, a zinc-finger transcription factor, is specifically expressed in osteoblasts and osteocytes of all developing bones. Because no bone formation occurs...
PRX1 HOMEOBOX GENE | SIGNALING PATHWAYS | ACTIVATED PROTEIN-KINASE | OSTEOBLAST DIFFERENTIATION |
PRX1 HOMEOBOX GENE | SIGNALING PATHWAYS | ACTIVATED PROTEIN-KINASE | OSTEOBLAST DIFFERENTIATION |