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Cell and Tissue Research, ISSN 0302-766X, 10/2012, Volume 350, Issue 1, pp. 95 - 107
Epiprofin/Specificity Protein 6 (Epfn) is a Krüppel-like family (KLF) transcription factor that is critically involved in tooth morphogenesis and dental cell... 
Human Genetics | Mouse Epfn (+/−) | Biomedicine | Tooth development | Epiprofin/Sp6 | Wnt/β-catenin | Proteomics | Cell junction | Molecular Medicine | MDPC-23 | Epfn (−/−) | Mouse Epfn(+/-); Epfn(-/-) | TEETH | PROLIFERATION | BETA-CATENIN | CELL BIOLOGY | MORPHOGENESIS | EPITHELIUM | DENTIN | Wnt/beta-catenin | GROWTH | TRANSCRIPTION FACTOR | EXPRESSION | MOUSE INCISORS | Dental Pulp - embryology | Dental Pulp - metabolism | Wnt Proteins - metabolism | Incisor - cytology | Bone Morphogenetic Proteins - metabolism | Incisor - metabolism | Tooth - embryology | Tight Junctions - drug effects | Biomarkers - metabolism | Tight Junctions - metabolism | Dental Enamel - metabolism | Glycogen Synthase Kinase 3 - antagonists & inhibitors | Dental Pulp - cytology | Dental Pulp - drug effects | Dental Papilla - embryology | beta Catenin - metabolism | Molar - embryology | Signal Transduction - drug effects | Adherens Junctions - drug effects | Mice | Dental Enamel - cytology | Dental Papilla - drug effects | Adherens Junctions - metabolism | Ameloblasts - metabolism | Kruppel-Like Transcription Factors - metabolism | Molar - cytology | Ameloblasts - drug effects | Tooth - cytology | Membrane Proteins - metabolism | Molar - drug effects | Kruppel-Like Transcription Factors - deficiency | Molar - metabolism | Odontoblasts - cytology | Recombinant Proteins - metabolism | Odontoblasts - metabolism | Incisor - drug effects | Ameloblasts - cytology | Intercellular Junctions - metabolism | Dental Papilla - metabolism | Glycogen Synthase Kinase 3 - metabolism | Dental Enamel - embryology | Dental Papilla - cytology | Animals | Intercellular Junctions - drug effects | Odontoblasts - drug effects | Morphogenesis - drug effects | Oximes - pharmacology | Cell Proliferation - drug effects | Incisor - embryology | Tooth - metabolism | Dental Enamel - drug effects | Developmental biology | Rodents | Teeth | Index Medicus | Cell proliferation | Bone morphogenetic protein 4 | Nestin | Transcription factors | Mesenchyme | Tight junctions | Wnt protein | catenin | Cell junctions | Morphogenesis | Signal transduction | Dental enamel | Ameloblasts | Developmental stages | Incisors | Bone morphogenetic proteins | Differentiation | Dental pulp
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, pp. e0177557 - e0177557
Highly coordinated regulation of cell proliferation and differentiation contributes to the formation of functionally shaped and sized teeth; however, the... 
DENTINOGENESIS IMPERFECTA | METABOLIC CHECKPOINT | MUTATIONS CAUSE | OSTEOBLAST DIFFERENTIATION | MULTIDISCIPLINARY SCIENCES | TEETH | PULP CELLS | AMPK | CELL-PROLIFERATION | GAP-JUNCTION PROTEINS | EXPRESSION | AMP-Activated Protein Kinases - metabolism | Sialoglycoproteins - metabolism | Phosphoproteins - metabolism | RNA, Messenger - metabolism | Aminoimidazole Carboxamide - pharmacology | Ribonucleotides - pharmacology | Cell Differentiation - genetics | Bone Morphogenetic Proteins - metabolism | Transfection | Adenosine Triphosphate - metabolism | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Phosphorylation - drug effects | Odontoblasts - cytology | Extracellular Matrix Proteins - metabolism | Odontoblasts - metabolism | Tooth Germ - metabolism | RNA, Messenger - genetics | Connexins - genetics | Enzyme Activation - drug effects | Mice, Inbred ICR | Connexins - metabolism | Gene Expression Regulation - drug effects | Dental Papilla - cytology | Animals | Aminoimidazole Carboxamide - analogs & derivatives | Signal Transduction - drug effects | Cell Differentiation - drug effects | Models, Biological | Intracellular Space - metabolism | Odontoblasts - drug effects | Cell Proliferation - drug effects | Smad Proteins - metabolism | RNA, Small Interfering - metabolism | Cellular signal transduction | Genetic aspects | Gene expression | Health aspects | Heart | Pediatrics | Regulations | Transcription factors | Migration | Differentiation (biology) | Central nervous system | Nervous system | AKT protein | Lethality | Glucose | Proteins | Cartilage | Bone growth | Cell growth | Cellular communication | Mineralization | Neurodegeneration | Biocompatibility | Tension | Hair | Deafness | AMP | Developmental biology | Teeth | Cell division | Ions | Anatomy | Metabolism | Epithelium | Root development | Embryonic growth stage | Osteoblastogenesis | Stem cells | Mice | Mutation | Endoplasmic reticulum | Hippocampus | Tracers | Dentin | Phosphorylation | Laboratories | Homology | Biology | Kinases | AMP-activated protein kinase | Tissues | Autophagy | Defects | Morphogenesis | Biomedical materials | Metabolites | Rodents | Cell cycle | Heart diseases | Communication | University graduates | Bone morphogenetic protein 2 | Dentistry | Cell differentiation | Ribonucleic acid--RNA | Dental enamel | Skull | Bone | ATP | Apoptosis | Index Medicus | RNA | Ribonucleic acid
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 04/2012, Volume 287, Issue 15, pp. 12230 - 12240
During development, Dlx3 is expressed in ectodermal appendages such as hair and teeth. Thus far, the evidence that Dlx3 plays a crucial role in tooth... 
SIALOPHOSPHOPROTEIN EXPRESSION | CHIP-SEQ DATA | TOOTH DEVELOPMENT | ENAMEL DEFECTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MURINE DENTITION | MUTATION | GENE-EXPRESSION | TRICHODENTOOSSEOUS SYNDROME | DIFFERENTIATION | HOMEOBOX GENES | Sialoglycoproteins - genetics | Luciferases, Renilla - genetics | Dentin Dysplasia - genetics | Homeodomain Proteins - metabolism | Sialoglycoproteins - metabolism | Molecular Sequence Data | Tooth - growth & development | Phosphoproteins - metabolism | Dentin - pathology | Luciferases, Renilla - biosynthesis | Ameloblasts - physiology | Neural Crest - metabolism | Ameloblasts - metabolism | Gene Expression Regulation, Developmental | Base Sequence | Gene Deletion | Cell Differentiation | Extracellular Matrix Proteins - metabolism | Genes, Reporter | Dentin Dysplasia - pathology | Cell Line | Promoter Regions, Genetic | Odontoblasts - metabolism | Dental Enamel - metabolism | Dentin - metabolism | Down-Regulation | Extracellular Matrix Proteins - genetics | Dental Enamel - growth & development | Mice, Transgenic | Phosphoproteins - genetics | Transcription Factors - genetics | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Animals | Odontoblasts - physiology | Dentin - growth & development | Protein Binding | Mesoderm - metabolism | Mice | Tooth - metabolism | Mandible - metabolism | Tooth - pathology | Index Medicus | Dentin | Molecular Bases of Disease | Tooth Development | Genetic Diseases | Dlx3 | Transcription Factors | Odontoblast | Animal Models | TDO | Dspp
Journal Article
Bone, ISSN 8756-3282, 2008, Volume 42, Issue 5, pp. 848 - 860
Abstract Bisphosphonates (BPs) target bone due to their high affinity for calcium ions. During osteoclastic resorption, these drugs are released from the... 
Orthopedics | Bone resorption | Bisphosphonate | Osteoclast | Transcytosis | Bone mineral | APOPTOSIS | LOCALIZATION | bone resorption | ALENDRONATE | BONE-RESORPTION | RAB GERANYLGERANYL TRANSFERASE | ZOLEDRONIC ACID | IN-VITRO | transcyrosis | PRENYLATION | OSTEOBLASTS | ENDOCRINOLOGY & METABOLISM | bisphosphonate | osteoclast | bone mineral | MOLECULAR-MECHANISMS | Coculture Techniques | Osteoclasts - cytology | Etidronic Acid - pharmacokinetics | Bone Resorption - metabolism | Osteoblasts - cytology | Risedronate Sodium | Bone Density Conservation Agents - metabolism | Etidronic Acid - analogs & derivatives | Extracellular Matrix Proteins - metabolism | Bone Density Conservation Agents - pharmacokinetics | Cell Survival - drug effects | Protein Prenylation - drug effects | Rabbits | rap1 GTP-Binding Proteins - metabolism | Dentin - metabolism | Diphosphonates - pharmacokinetics | Diphosphonates - metabolism | Macrophages - cytology | Osteoclasts - metabolism | Bone Density Conservation Agents - pharmacology | Endocytosis - physiology | Alendronate - metabolism | Macrophages - metabolism | Animals | Etidronic Acid - pharmacology | Skull - cytology | Cell Line, Tumor | Mice | Etidronic Acid - metabolism | Osteoblasts - metabolism | Diphosphonates - pharmacology | Microscopy, Fluorescence | Aluminum compounds | Fluorescence | Chemical properties | G proteins | Analysis | Index Medicus
Journal Article
Bone, ISSN 8756-3282, 2015, Volume 78, pp. 150 - 164
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, pp. e38393 - e38393
Background: Inorganic pyrophosphate (PPi) is a physiologic inhibitor of hydroxyapatite mineral precipitation involved in regulating mineralized tissue... 
DENTIN MATRIX PROTEIN-1 | IN-VITRO | HYDROXYAPATITE FORMATION | INFANTILE HYPOPHOSPHATASIA | INORGANIC PYROPHOSPHATE | MULTIDISCIPLINARY SCIENCES | CELL MEMBRANE GLYCOPROTEIN-1 | ATTACHMENT APPARATUS | HUMAN PERIODONTAL-LIGAMENT | MECHANICAL-PROPERTIES | ALKALINE-PHOSPHATASE ACTIVITY | Diphosphates - metabolism | Cell Proliferation | Humans | Mandible - pathology | Pyrophosphatases - deficiency | Alkaline Phosphatase - metabolism | Phosphate Transport Proteins - metabolism | Homeostasis | Phosphate Transport Proteins - deficiency | Tooth Root - metabolism | Extracellular Space - metabolism | Time Factors | Gene Expression Regulation, Developmental | Dental Cementum - metabolism | Collagen - biosynthesis | Phosphoric Diester Hydrolases - deficiency | Molar - pathology | Molar - metabolism | Phosphoric Diester Hydrolases - metabolism | Mice, Inbred C57BL | Cells, Cultured | Dental Cementum - pathology | Mice, Knockout | Molar - ultrastructure | Pyrophosphatases - metabolism | Animals | Calcification, Physiologic | Models, Biological | Tooth Root - ultrastructure | Dental Cementum - ultrastructure | Mice | Alkaline Phosphatase - deficiency | Mandible - ultrastructure | Cementogenesis | Phosphatases | Precipitation (Meteorology) | Dentin | Alkaline phosphatase | Surgical implants | Regulators | Animal models | Laboratories | Childrens health | Hydroxyapatite | Biology | Arthritis | mRNA | Phosphatase | Apposition | Proteins | Biomedical materials | Control | Periodontal ligament | Transgenic animals | Mineralization | Bones | Skin diseases | Cements | ANK protein | Inhibition | Growth factors | Pyrophosphatase | Phosphodiesterase | Medical research | Ankylosis | Tissue engineering | Teeth | Histology | Dentistry | Metabolism | Hypophosphatasia | Root development | Children & youth | Studies | Regeneration | Detachment | Calcification | Regulation | Mutation | Cementum | Index Medicus
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 04/2017, Volume 32, Issue 4, pp. 757 - 769
In 1985, we briefly characterized “congenital sclerosing osteomalacia with cerebral calcification” (CSOCC) in infant sisters. Later, Raine syndrome (RNS)... 
CRANIOFACIAL DYSOSTOSIS | OSTEOMALACIA | RICKETS | DENTIN MATRIX PROTEIN | KINASE | PHOSPHOPROTEOME | CROUZON SYNDROME | CRANIOSYNOSTOSIS | HYPOPHOSPHATEMIA | SIBLING PROTEINS | OSTEOPONTIN | METOPIC SUTURE | MINERALIZATION | OSTEOSCLEROSIS | OSTEOPETROSIS | TRIGONOCEPHALY | AUTOSOMAL RECESSIVE SYNDROME | INTRACRANIAL CALCIFICATION | HYPOPLASTIC NOSE | SECRETED PROTEINS | ENDOCRINOLOGY & METABOLISM | OSTEOSCLEROTIC BONE DYSPLASIA | ANHYDRASE-II DEFICIENCY | CASEIN KINASE | RENAL TUBULAR-ACIDOSIS | Abnormalities, Multiple - metabolism | Calcinosis - genetics | Microcephaly - genetics | Cerebrum - diagnostic imaging | Casein Kinase I - genetics | Osteomalacia - diagnostic imaging | Humans | Calcinosis - diagnostic imaging | Male | Cleft Palate - genetics | Exophthalmos - genetics | Osteosclerosis - metabolism | Adult | Cerebrum - metabolism | Female | Osteomalacia - metabolism | Osteosclerosis - genetics | Calcinosis - metabolism | Cleft Palate - diagnostic imaging | Cerebrum - pathology | Osteosclerosis - diagnostic imaging | Abnormalities, Multiple - genetics | Extracellular Matrix Proteins - metabolism | Infant, Newborn | Extracellular Matrix Proteins - genetics | Microcephaly - metabolism | Abnormalities, Multiple - diagnostic imaging | Exophthalmos - diagnostic imaging | Microcephaly - diagnostic imaging | Osteomalacia - genetics | Exophthalmos - metabolism | Casein Kinase I - metabolism | Cleft Palate - metabolism | Medical research | Dysplasia | Genetic disorders | Calcification | Medicine, Experimental | Genetics | Genetic aspects | Histochemistry | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 5, pp. e19595 - e19595
Background: Vascular calcification is an indicator of elevated cardiovascular risk. Vascular smooth muscle cells (VSMCs), the predominant cell type involved in... 
INFANTILE ARTERIAL CALCIFICATION | DENTIN MATRIX PROTEIN-1 | IN-VITRO | ALKALINE-PHOSPHATASE | OSTEOBLASTS | BIOLOGY | BONE MINERALIZATION | REGULATORS | MICE | UP-REGULATION | CHONDROCYTE DIFFERENTIATION | Calcinosis - genetics | Pyrophosphatases - deficiency | Myocytes, Smooth Muscle - pathology | Skull - pathology | Cell Differentiation | Phosphoric Diester Hydrolases - deficiency | Tibia - metabolism | Calcinosis - metabolism | Myocytes, Smooth Muscle - metabolism | Biomarkers - metabolism | Reproducibility of Results | Phosphoric Diester Hydrolases - metabolism | Osteocytes - metabolism | Mice, Inbred C57BL | Cells, Cultured | Up-Regulation - genetics | Aorta - pathology | Pyrophosphatases - metabolism | Osteoblasts - pathology | Muscle, Smooth, Vascular - pathology | Phenotype | Animals | Mice | Calcinosis - pathology | Osteoblasts - metabolism | Calcification | Smooth muscle | Phosphatases | Cardiovascular diseases | Analysis | Organic acids | Calcification (ectopic) | Cell culture | Alkaline phosphatase | Ascorbic acid | Media (culture) | Homeostasis | Osteocytes | SOST protein | Glycerophosphate | Phosphatase | Osteoblasts | Proteins | Pit1 protein | Biomedical materials | Mineralization | Rodents | Aorta | Biocompatibility | Markers | Health risks | Glycoproteins | Osteoblastogenesis | Coronary vessels | Proteomics | Mutation | Laboratory animals | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 04/2012, Volume 287, Issue 15, pp. 12217 - 12229
Cell surface heparan sulfate (HS) is an essential regulator of cell signaling and development. HS traps signaling molecules, like Wnt in the glycosaminoglycan... 
PROTEOGLYCANS | 6-O-ENDOSULFATASES SULF1 | TOOTH DEVELOPMENT | GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | IN-VIVO | MUTATION | CELL-SURFACE | ONYCHO-DERMAL DYSPLASIA | EXPRESSION | DSPP | Sialoglycoproteins - genetics | Sulfatases - genetics | Sialoglycoproteins - metabolism | Heparitin Sulfate - physiology | Phosphoproteins - metabolism | Wnt Proteins - metabolism | Dentin - pathology | Heparitin Sulfate - metabolism | Molar - growth & development | Wnt Proteins - genetics | Gene Expression Regulation, Developmental | Dentinogenesis | Sulfatases - metabolism | Sulfotransferases - metabolism | Transcription, Genetic | Molar - pathology | Molar - metabolism | Extracellular Matrix Proteins - metabolism | Wnt Signaling Pathway | Sulfotransferases - genetics | Nerve Tissue Proteins - physiology | Odontoblasts - metabolism | Tooth Abnormalities - genetics | Dentin - metabolism | Extracellular Matrix Proteins - genetics | Cells, Cultured | Phosphoproteins - genetics | Nerve Tissue Proteins - genetics | Mice, Knockout | Nerve Tissue Proteins - metabolism | Phenotype | Tooth Abnormalities - enzymology | Animals | Heparan Sulfate Proteoglycans - metabolism | Dentin - growth & development | Protein Binding | Mice | Wnt Proteins - physiology | Index Medicus | Dentin | Proteoglycan | Wnt Signaling | Tooth Development | Extracellular Matrix Proteins | Development | Heparan Sulfate | Developmental Biology | Differentiation
Journal Article