Journal of Bone and Mineral Research, ISSN 0884-0431, 02/2015, Volume 30, Issue 2, pp. 318 - 329
ABSTRACT Transforming growth factor (TGF)‐β signaling plays critical roles during skeletal development and its excessive signaling causes genetic diseases of...
ENDOCHONDRAL OSSIFICATION | DULLARD/CTDNEP1 | TGF‐β | CHONDROCYTES | PRX1‐CRE | TGF-β | Dullard/Ctdnep1 | PRX1-CRE | Endochondral ossification | Chondrocytes | OSTEOBLAST DIFFERENTIATION | DULLARD | AORTIC-ANEURYSM | WEILL-MARCHESANI-SYNDROME | CHONDROCYTE DIFFERENTIATION | CARTILAGE | CTDNEP1 | TGF | GROWTH-FACTOR-BETA | IN-VITRO | BONE-FORMATION | ENDOCRINOLOGY & METABOLISM | MUTATIONS | SKELETAL DEVELOPMENT | Signal Transduction | Cartilage - pathology | Homeodomain Proteins - metabolism | Phosphoprotein Phosphatases - metabolism | Male | Mesoderm - cytology | Cartilage - metabolism | Mice, Knockout | Animals | Limb Buds - metabolism | Calcification, Physiologic | Sternum - pathology | Integrases - metabolism | Cell Differentiation | Mesoderm - metabolism | Chondrogenesis | Transforming Growth Factor beta - metabolism | Osteogenesis
ENDOCHONDRAL OSSIFICATION | DULLARD/CTDNEP1 | TGF‐β | CHONDROCYTES | PRX1‐CRE | TGF-β | Dullard/Ctdnep1 | PRX1-CRE | Endochondral ossification | Chondrocytes | OSTEOBLAST DIFFERENTIATION | DULLARD | AORTIC-ANEURYSM | WEILL-MARCHESANI-SYNDROME | CHONDROCYTE DIFFERENTIATION | CARTILAGE | CTDNEP1 | TGF | GROWTH-FACTOR-BETA | IN-VITRO | BONE-FORMATION | ENDOCRINOLOGY & METABOLISM | MUTATIONS | SKELETAL DEVELOPMENT | Signal Transduction | Cartilage - pathology | Homeodomain Proteins - metabolism | Phosphoprotein Phosphatases - metabolism | Male | Mesoderm - cytology | Cartilage - metabolism | Mice, Knockout | Animals | Limb Buds - metabolism | Calcification, Physiologic | Sternum - pathology | Integrases - metabolism | Cell Differentiation | Mesoderm - metabolism | Chondrogenesis | Transforming Growth Factor beta - metabolism | Osteogenesis
Journal Article
Calcified Tissue International, ISSN 0171-967X, 08/2016, Volume 99, Issue 2, p. 199
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s00223-016-0139-1
Phosphates | Anopheles | Interleukins | Genes | Stem cells | Genetic research | Nucleosides | Gene expression | Mineralization | Cells
Phosphates | Anopheles | Interleukins | Genes | Stem cells | Genetic research | Nucleosides | Gene expression | Mineralization | Cells
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 05/2015, Volume 30, Issue 5, p. 947
Journal Article
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Full Text
Collagens VI and XII form complexes mediating osteoblast interactions during osteogenesis
Cell and Tissue Research, ISSN 0302-766X, 6/2016, Volume 364, Issue 3, pp. 623 - 635
Bone formation is precisely regulated by cell-cell communication in osteoblasts. We have previously demonstrated that genetic deletion of Col6a1 or Col12a1...
Human Genetics | Primary osteoblasts | Biomedicine | Proteomics | Collagen VI | Molecular Medicine | Communicating cell network | Collagen XII | Osteogenesis | APOPTOSIS | BETHLEM MYOPATHY | SPLICE VARIANTS | DEFICIENCY | CELL BIOLOGY | MUSCULAR-DYSTROPHIES | MICE | MUTATIONS | DYSFUNCTION | EXPRESSION | COMMUNICATION | Collagen Type I - metabolism | Cells, Cultured | Collagen Type VI - metabolism | Cell Communication | Extracellular Matrix - metabolism | Animals | Culture Media - pharmacology | Protein Binding | Collagen Type XII - metabolism | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Bones | Density | Collagen | Analysis | Studies | Genes | Mutation | Cells | Muscular dystrophy | Regular
Human Genetics | Primary osteoblasts | Biomedicine | Proteomics | Collagen VI | Molecular Medicine | Communicating cell network | Collagen XII | Osteogenesis | APOPTOSIS | BETHLEM MYOPATHY | SPLICE VARIANTS | DEFICIENCY | CELL BIOLOGY | MUSCULAR-DYSTROPHIES | MICE | MUTATIONS | DYSFUNCTION | EXPRESSION | COMMUNICATION | Collagen Type I - metabolism | Cells, Cultured | Collagen Type VI - metabolism | Cell Communication | Extracellular Matrix - metabolism | Animals | Culture Media - pharmacology | Protein Binding | Collagen Type XII - metabolism | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Bones | Density | Collagen | Analysis | Studies | Genes | Mutation | Cells | Muscular dystrophy | Regular
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 02/2016, Volume 231, Issue 2, pp. 496 - 504
Osteoporosis affects over 20 million patients in the United States. Among those, disuse osteoporosis is serious as it is induced by bed‐ridden conditions in...
Recombinant Proteins - metabolism | Osteoblasts - drug effects | Cells, Cultured | Adrenergic beta-Agonists - pharmacology | Mice, Transgenic | Parathyroid Hormone - pharmacology | Recombinant Proteins - genetics | Cell Movement - drug effects | Cell Cycle Checkpoints | Animals | Isoproterenol - pharmacology | Luminescent Proteins - genetics | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Receptors, Adrenergic, beta - metabolism | Single-Cell Analysis | Luminescent Proteins - metabolism | Ubiquitin | Osteoporosis | Image processing | Parathyroid hormone | Cell cycle | Imaging systems | Equipment and supplies | Genetic engineering
Recombinant Proteins - metabolism | Osteoblasts - drug effects | Cells, Cultured | Adrenergic beta-Agonists - pharmacology | Mice, Transgenic | Parathyroid Hormone - pharmacology | Recombinant Proteins - genetics | Cell Movement - drug effects | Cell Cycle Checkpoints | Animals | Isoproterenol - pharmacology | Luminescent Proteins - genetics | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Receptors, Adrenergic, beta - metabolism | Single-Cell Analysis | Luminescent Proteins - metabolism | Ubiquitin | Osteoporosis | Image processing | Parathyroid hormone | Cell cycle | Imaging systems | Equipment and supplies | Genetic engineering
Journal Article
Calcified Tissue International, ISSN 0171-967X, 3/2016, Volume 98, Issue 3, pp. 306 - 315
Osteoporosis is a common disease that increases individual’s fragility fracture risk. PTH is the only therapeutic agent for severe osteoporosis that requires...
Life Sciences | Biochemistry, general | PTH | Orthopedics | Osteoblast | Usp2 | Proliferation | Endocrinology | Cell Biology | IGF-I | RECEPTOR | INTERLEUKIN-11 | OSTEOPOROSIS | MECHANICAL-STRESS | ENDOCRINOLOGY & METABOLISM | CELL-CYCLE | GROWTH-FACTOR | DIFFERENTIATION | BONE | PROTEASE | Cyclin D1 - metabolism | Up-Regulation | Cell Proliferation | Alternative Splicing | Signal Transduction | Gene Expression Regulation | Mice, Transgenic | Animals | Parathyroid Hormone - metabolism | Bone and Bones - metabolism | Mice | Osteoblasts - cytology | Ubiquitin-Specific Proteases - metabolism | 3T3 Cells | RNA, Small Interfering - metabolism | Ubiquitin | Enzymes | Osteoporosis | Parathyroid hormone | Genetic research | Genetic engineering | Gene expression | Health aspects | Therapy | Fractures | Peptides
Life Sciences | Biochemistry, general | PTH | Orthopedics | Osteoblast | Usp2 | Proliferation | Endocrinology | Cell Biology | IGF-I | RECEPTOR | INTERLEUKIN-11 | OSTEOPOROSIS | MECHANICAL-STRESS | ENDOCRINOLOGY & METABOLISM | CELL-CYCLE | GROWTH-FACTOR | DIFFERENTIATION | BONE | PROTEASE | Cyclin D1 - metabolism | Up-Regulation | Cell Proliferation | Alternative Splicing | Signal Transduction | Gene Expression Regulation | Mice, Transgenic | Animals | Parathyroid Hormone - metabolism | Bone and Bones - metabolism | Mice | Osteoblasts - cytology | Ubiquitin-Specific Proteases - metabolism | 3T3 Cells | RNA, Small Interfering - metabolism | Ubiquitin | Enzymes | Osteoporosis | Parathyroid hormone | Genetic research | Genetic engineering | Gene expression | Health aspects | Therapy | Fractures | Peptides
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 07/2017, Volume 232, Issue 7, pp. 1761 - 1766
LGR4 is expressed in bone and has been shown to be involved in bone metabolism. Oxidative stress is one of the key issues in pathophysiology of osteoporosis....
OXIDATIVE STRESS | PHYSIOLOGY | TGF-BETA | INHIBITION | PROTEIN | GENE | INVOLVEMENT | CATENIN | RECEPTOR | CELL BIOLOGY | Hydrogen Peroxide - toxicity | Cell Line | Transcription, Genetic - drug effects | Receptors, G-Protein-Coupled - metabolism | Osteoblasts - drug effects | RNA, Messenger - genetics | Alkaline Phosphatase - metabolism | Down-Regulation - drug effects | RNA, Messenger - metabolism | Animals | Time Factors | Mice | Receptors, G-Protein-Coupled - genetics | Protein Synthesis Inhibitors - pharmacology | Osteoblasts - metabolism | Cytokines - pharmacology | RNA, Small Interfering - metabolism | Bone morphogenetic proteins | Protein biosynthesis | Hydrogen peroxide | Index Medicus
OXIDATIVE STRESS | PHYSIOLOGY | TGF-BETA | INHIBITION | PROTEIN | GENE | INVOLVEMENT | CATENIN | RECEPTOR | CELL BIOLOGY | Hydrogen Peroxide - toxicity | Cell Line | Transcription, Genetic - drug effects | Receptors, G-Protein-Coupled - metabolism | Osteoblasts - drug effects | RNA, Messenger - genetics | Alkaline Phosphatase - metabolism | Down-Regulation - drug effects | RNA, Messenger - metabolism | Animals | Time Factors | Mice | Receptors, G-Protein-Coupled - genetics | Protein Synthesis Inhibitors - pharmacology | Osteoblasts - metabolism | Cytokines - pharmacology | RNA, Small Interfering - metabolism | Bone morphogenetic proteins | Protein biosynthesis | Hydrogen peroxide | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 02/2009, Volume 284, Issue 8, pp. 4857 - 4864
Renin angiotensin system (RAS) regulates circulating blood volume and blood pressure systemically, whereas RAS also plays a role in the local milieu. Previous...
CELLS | OSTEOPONTIN | RESORPTION | MARROW | SYMPATHETIC-NERVOUS-SYSTEM | BIOCHEMISTRY & MOLECULAR BIOLOGY | OSTEOBLASTS | PARATHYROID-HORMONE | DIFFERENTIATION | EXPRESSION | OSTEOPOROSIS | Vasoconstrictor Agents - pharmacology | Bone Development - drug effects | Bone Development - physiology | Humans | Male | Organ Size - physiology | Renin-Angiotensin System - physiology | Imidazoles - pharmacology | Osteoclasts - cytology | Osteoclasts - metabolism | Mice, Knockout | Organ Size - drug effects | Animals | Receptor, Angiotensin, Type 2 - metabolism | Bone and Bones - metabolism | Angiotensin II Type 2 Receptor Blockers | Renin-Angiotensin System - drug effects | Blood Pressure - drug effects | Blood Pressure - physiology | Mice | Pyridines - pharmacology | Osteoblasts - cytology | Osteoblasts - metabolism | Bone and Bones - cytology
CELLS | OSTEOPONTIN | RESORPTION | MARROW | SYMPATHETIC-NERVOUS-SYSTEM | BIOCHEMISTRY & MOLECULAR BIOLOGY | OSTEOBLASTS | PARATHYROID-HORMONE | DIFFERENTIATION | EXPRESSION | OSTEOPOROSIS | Vasoconstrictor Agents - pharmacology | Bone Development - drug effects | Bone Development - physiology | Humans | Male | Organ Size - physiology | Renin-Angiotensin System - physiology | Imidazoles - pharmacology | Osteoclasts - cytology | Osteoclasts - metabolism | Mice, Knockout | Organ Size - drug effects | Animals | Receptor, Angiotensin, Type 2 - metabolism | Bone and Bones - metabolism | Angiotensin II Type 2 Receptor Blockers | Renin-Angiotensin System - drug effects | Blood Pressure - drug effects | Blood Pressure - physiology | Mice | Pyridines - pharmacology | Osteoblasts - cytology | Osteoblasts - metabolism | Bone and Bones - cytology
Journal Article
Cell and Tissue Research, ISSN 0302-766X, 6/2016, Volume 364, Issue 3, pp. 677 - 679
Journal Article
JOURNAL OF CELLULAR PHYSIOLOGY, ISSN 0021-9541, 11/2015, Volume 230, Issue 11, pp. 2788 - 2795
Ift88 is an intraflagella transport protein, critical for the cilium, and has been shown to be required for the maintenance of chondrocytes and cartilage....
PHYSIOLOGY | ARTICULAR-CARTILAGE | SIGNALS | DIFFERENTIATION | INTRAFLAGELLAR TRANSPORT | PRIMARY CILIUM | CHONDROGENESIS | CELL BIOLOGY
PHYSIOLOGY | ARTICULAR-CARTILAGE | SIGNALS | DIFFERENTIATION | INTRAFLAGELLAR TRANSPORT | PRIMARY CILIUM | CHONDROGENESIS | CELL BIOLOGY
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 02/2015, Volume 30, Issue 2, p. 318
Transforming growth factor (TGF)-[beta] signaling plays critical roles during skeletal development and its excessive signaling causes genetic diseases of...
Bone morphogenetic proteins | Dysplasia | RNA | Transforming growth factors
Bone morphogenetic proteins | Dysplasia | RNA | Transforming growth factors
Journal Article
Journal of Cellular Biochemistry, ISSN 0730-2312, 07/2017, Volume 118, Issue 7, pp. 1670 - 1677
ABSTRACT Osteoporosis is one of the most prevalent ageing‐associated diseases that are soaring in the modern world. Although various aspects of the disease...
POLDIP2 | FGF | OSTEOBLAST | PATHWAYS | MIGRATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL-CYCLE | NADPH OXIDASES | OSTEOPOROSIS | CELL BIOLOGY | Cell Line | Mice, Inbred C57BL | Osteoblasts - drug effects | RNA, Messenger - genetics | Nuclear Proteins - metabolism | Fibroblast Growth Factors - pharmacology | Mitochondrial Proteins - genetics | Cell Movement - genetics | Cell Movement - drug effects | Animals | Mitochondrial Proteins - metabolism | Mice | Nuclear Proteins - genetics | Osteoblasts - metabolism | Real-Time Polymerase Chain Reaction | Fibroblast growth factor | Femur | Dexamethasone | Transcription | Leukocyte migration | Cultures | Protein biosynthesis | siRNA | Hormones | Gene expression | Osteoblasts | Cell adhesion & migration | Osteoporosis | Angiogenesis | Protein synthesis | Rodents | Bone | Bone loss | Cell migration
POLDIP2 | FGF | OSTEOBLAST | PATHWAYS | MIGRATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL-CYCLE | NADPH OXIDASES | OSTEOPOROSIS | CELL BIOLOGY | Cell Line | Mice, Inbred C57BL | Osteoblasts - drug effects | RNA, Messenger - genetics | Nuclear Proteins - metabolism | Fibroblast Growth Factors - pharmacology | Mitochondrial Proteins - genetics | Cell Movement - genetics | Cell Movement - drug effects | Animals | Mitochondrial Proteins - metabolism | Mice | Nuclear Proteins - genetics | Osteoblasts - metabolism | Real-Time Polymerase Chain Reaction | Fibroblast growth factor | Femur | Dexamethasone | Transcription | Leukocyte migration | Cultures | Protein biosynthesis | siRNA | Hormones | Gene expression | Osteoblasts | Cell adhesion & migration | Osteoporosis | Angiogenesis | Protein synthesis | Rodents | Bone | Bone loss | Cell migration
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 08/2005, Volume 280, Issue 34, pp. 30192 - 30200
Osteoporosis is one of the major health problems in our modern world. Especially, disuse (unloading) osteoporosis occurs commonly in bedridden patients, a...
RESPONSES | OSTEOPONTIN | POSTMENOPAUSAL OSTEOPOROSIS | THERAPY | BIOCHEMISTRY & MOLECULAR BIOLOGY | Biomarkers - metabolism | Body Weight | Bone Marrow Cells - cytology | Mice, Inbred C57BL | Male | Tomography, X-Ray Computed | Osteoclasts - metabolism | Sympathetic Nervous System - metabolism | Amino Acids - pharmacology | Propranolol - pharmacology | Animals | Osteoporosis - pathology | Time Factors | Bone and Bones - metabolism | Isoproterenol - pharmacology | Dopamine beta-Hydroxylase - metabolism | Sympatholytics - pharmacology | Mice | Osteoblasts - metabolism | Guanethidine - pharmacology
RESPONSES | OSTEOPONTIN | POSTMENOPAUSAL OSTEOPOROSIS | THERAPY | BIOCHEMISTRY & MOLECULAR BIOLOGY | Biomarkers - metabolism | Body Weight | Bone Marrow Cells - cytology | Mice, Inbred C57BL | Male | Tomography, X-Ray Computed | Osteoclasts - metabolism | Sympathetic Nervous System - metabolism | Amino Acids - pharmacology | Propranolol - pharmacology | Animals | Osteoporosis - pathology | Time Factors | Bone and Bones - metabolism | Isoproterenol - pharmacology | Dopamine beta-Hydroxylase - metabolism | Sympatholytics - pharmacology | Mice | Osteoblasts - metabolism | Guanethidine - pharmacology
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2015, Volume 112, Issue 50, pp. 15432 - 15437
Migration of the cells in osteoblastic lineage, including preosteoblasts and osteoblasts, has been postulated to influence bone formation. However, the...
MULTIDISCIPLINARY SCIENCES | Nck | migration | bone remodeling | osteoblast | MESENCHYMAL STEM-CELLS | bone repair | Insulin-Like Growth Factor I - pharmacology | Insulin Receptor Substrate Proteins - metabolism | Bone and Bones - drug effects | Gene Knockdown Techniques | Bone and Bones - diagnostic imaging | Protein Binding - drug effects | Bone Resorption - metabolism | Osteoblasts - cytology | Skull - drug effects | Wound Healing - drug effects | Bone and Bones - cytology | Skull - metabolism | Osteoblasts - drug effects | Osteogenesis - drug effects | Cells, Cultured | Oncogene Proteins - metabolism | Organ Size | Mice, Knockout | Cell Shape - drug effects | Radiography | Cell Movement - drug effects | Animals | Adaptor Proteins, Signal Transducing - deficiency | Bone Resorption - pathology | Oncogene Proteins - deficiency | Adaptor Proteins, Signal Transducing - metabolism | Osteoblasts - metabolism | Cell research | Physiological aspects | Bones | Research | Osteoblasts | Protein kinases | Density | Cell migration | Biological Sciences
MULTIDISCIPLINARY SCIENCES | Nck | migration | bone remodeling | osteoblast | MESENCHYMAL STEM-CELLS | bone repair | Insulin-Like Growth Factor I - pharmacology | Insulin Receptor Substrate Proteins - metabolism | Bone and Bones - drug effects | Gene Knockdown Techniques | Bone and Bones - diagnostic imaging | Protein Binding - drug effects | Bone Resorption - metabolism | Osteoblasts - cytology | Skull - drug effects | Wound Healing - drug effects | Bone and Bones - cytology | Skull - metabolism | Osteoblasts - drug effects | Osteogenesis - drug effects | Cells, Cultured | Oncogene Proteins - metabolism | Organ Size | Mice, Knockout | Cell Shape - drug effects | Radiography | Cell Movement - drug effects | Animals | Adaptor Proteins, Signal Transducing - deficiency | Bone Resorption - pathology | Oncogene Proteins - deficiency | Adaptor Proteins, Signal Transducing - metabolism | Osteoblasts - metabolism | Cell research | Physiological aspects | Bones | Research | Osteoblasts | Protein kinases | Density | Cell migration | Biological Sciences
Journal Article
Genes to Cells, ISSN 1356-9597, 05/2018, Volume 23, Issue 5, pp. 345 - 356
In mammals, the ovarian follicles are regulated at least in part by bone morphogenetic protein (BMP) family members. Dullard (also known as Ctdnep1) gene...
Dullard | ovary | BMP | hemorrhagic cysts | CELLS | FEMALE FERTILITY | MOUSE | NEURAL INDUCTION | MORPHOGENETIC PROTEIN SYSTEM | CELL BIOLOGY | DISRUPTION | GENE | GENETICS & HEREDITY | MICE | OSSIFICATION | EXPRESSION | Bone Morphogenetic Proteins - antagonists & inhibitors | Bone and Bones - pathology | Phosphorylation | Testis - metabolism | Male | Collagen Type I - genetics | Bone and Bones - metabolism | Ovarian Cysts - pathology | Female | Ovarian Follicle - metabolism | Pyrazoles - pharmacology | Collagen Type I - metabolism | Signal Transduction | Hemorrhage - metabolism | Pyrimidines - pharmacology | Phosphoprotein Phosphatases - physiology | Infertility, Female - metabolism | Mice, Knockout | Gene Expression Regulation - drug effects | Infertility, Female - pathology | Animals | Testis - pathology | Ovarian Cysts - metabolism | Phosphoprotein Phosphatases - deficiency | Mice | Ovarian Follicle - pathology | Hemorrhage - pathology | Smad Proteins - metabolism | Bone morphogenetic proteins | Hemorrhage | Steroid hormones | Cytochrome P-450 | Collagen (type I) | Blood cells | Erythrocytes | Homeostasis | Ovaries | Tamoxifen | Follicles | Kinases | Sertoli cells | Cysts | Clonal deletion | Infertility | Granulosa cells | Smad7 protein | Health risk assessment
Dullard | ovary | BMP | hemorrhagic cysts | CELLS | FEMALE FERTILITY | MOUSE | NEURAL INDUCTION | MORPHOGENETIC PROTEIN SYSTEM | CELL BIOLOGY | DISRUPTION | GENE | GENETICS & HEREDITY | MICE | OSSIFICATION | EXPRESSION | Bone Morphogenetic Proteins - antagonists & inhibitors | Bone and Bones - pathology | Phosphorylation | Testis - metabolism | Male | Collagen Type I - genetics | Bone and Bones - metabolism | Ovarian Cysts - pathology | Female | Ovarian Follicle - metabolism | Pyrazoles - pharmacology | Collagen Type I - metabolism | Signal Transduction | Hemorrhage - metabolism | Pyrimidines - pharmacology | Phosphoprotein Phosphatases - physiology | Infertility, Female - metabolism | Mice, Knockout | Gene Expression Regulation - drug effects | Infertility, Female - pathology | Animals | Testis - pathology | Ovarian Cysts - metabolism | Phosphoprotein Phosphatases - deficiency | Mice | Ovarian Follicle - pathology | Hemorrhage - pathology | Smad Proteins - metabolism | Bone morphogenetic proteins | Hemorrhage | Steroid hormones | Cytochrome P-450 | Collagen (type I) | Blood cells | Erythrocytes | Homeostasis | Ovaries | Tamoxifen | Follicles | Kinases | Sertoli cells | Cysts | Clonal deletion | Infertility | Granulosa cells | Smad7 protein | Health risk assessment
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 04/2016, Volume 231, Issue 4, pp. 887 - 895
Osteoporosis is one of the most prevalent diseases and the number of patients suffering from this disease is soaring due to the increase in the aged population...
SIGNALING PATHWAYS | PHYSIOLOGY | PROTEIN | GPR48 | GLUCOCORTICOIDS | MANAGEMENT | BONE-FORMATION | MINERALIZATION | DIFFERENTIATION | WNT | OSTEOPOROSIS | CELL BIOLOGY | Bone Morphogenetic Protein 2 - pharmacology | Cell Line | Transcription, Genetic - drug effects | Alkaline Phosphatase - genetics | Osteoblasts - enzymology | Receptors, G-Protein-Coupled - metabolism | Osteoblasts - drug effects | RNA, Messenger - genetics | Alkaline Phosphatase - metabolism | RNA, Messenger - metabolism | Bone and Bones - drug effects | Gene Knockdown Techniques | Gene Expression Regulation - drug effects | Phenotype | Animals | Time Factors | Bone and Bones - metabolism | Mice | Receptors, G-Protein-Coupled - genetics | Osteoblasts - cytology | Osteoblasts - metabolism | Bones | Bone morphogenetic proteins | Gene expression | Density | Genes
SIGNALING PATHWAYS | PHYSIOLOGY | PROTEIN | GPR48 | GLUCOCORTICOIDS | MANAGEMENT | BONE-FORMATION | MINERALIZATION | DIFFERENTIATION | WNT | OSTEOPOROSIS | CELL BIOLOGY | Bone Morphogenetic Protein 2 - pharmacology | Cell Line | Transcription, Genetic - drug effects | Alkaline Phosphatase - genetics | Osteoblasts - enzymology | Receptors, G-Protein-Coupled - metabolism | Osteoblasts - drug effects | RNA, Messenger - genetics | Alkaline Phosphatase - metabolism | RNA, Messenger - metabolism | Bone and Bones - drug effects | Gene Knockdown Techniques | Gene Expression Regulation - drug effects | Phenotype | Animals | Time Factors | Bone and Bones - metabolism | Mice | Receptors, G-Protein-Coupled - genetics | Osteoblasts - cytology | Osteoblasts - metabolism | Bones | Bone morphogenetic proteins | Gene expression | Density | Genes
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 08/2018, Volume 33, Issue 8, pp. 1532 - 1543
ABSTRACT Little is known about the molecular mechanisms of enthesis formation in mature animals. Here, we report that annexin A5 (Anxa5) plays a critical role...
ENTHESIS | TENDON/LIGAMENT | BONE MORPHOGENESIS | LACZ KNOCK‐IN MOUSE | ANNEXIN A5 | LACZ KNOCK-IN MOUSE | FIBROCARTILAGE CELLS | PROGENITORS | INSERTION | COLLAGEN | OSTEOBLASTIC DIFFERENTIATION | JUNCTION | FUNCTIONAL TENDON ENTHESIS | MINERALIZATION | ENDOCRINOLOGY & METABOLISM | GROWTH-PLATE CARTILAGE | EXPRESSION | Annexins | Femur | Molecular modelling | Clonal deletion | Mineralization | Mechanical unloading | Rodents | Contractility | Chondrocytes | Unloading | Calcein | Muscle contraction | Osteoblasts
ENTHESIS | TENDON/LIGAMENT | BONE MORPHOGENESIS | LACZ KNOCK‐IN MOUSE | ANNEXIN A5 | LACZ KNOCK-IN MOUSE | FIBROCARTILAGE CELLS | PROGENITORS | INSERTION | COLLAGEN | OSTEOBLASTIC DIFFERENTIATION | JUNCTION | FUNCTIONAL TENDON ENTHESIS | MINERALIZATION | ENDOCRINOLOGY & METABOLISM | GROWTH-PLATE CARTILAGE | EXPRESSION | Annexins | Femur | Molecular modelling | Clonal deletion | Mineralization | Mechanical unloading | Rodents | Contractility | Chondrocytes | Unloading | Calcein | Muscle contraction | Osteoblasts
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 05/2015, Volume 30, Issue 5, p. 947
Journal Article