Tooth root dentin mineralization defects in a mouse model of hypophosphatasia. - Wikidata - awgldk - TriplyDB

Tooth root dentin mineralization defects in a mouse model of hypophosphatasia.

Tooth root dentin mineralization defects in a mouse model of hypophosphatasia.

http://www.wikidata.org/entity/Q30531828

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The role of phosphatases in the initiation of skeletal mineralization Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.Rare bone diseases and their dental, oral, and craniofacial manifestations.Tissue-nonspecific alkaline phosphatase deficiency causes abnormal craniofacial bone development in the Alpl(-/-) mouse model of infantile hypophosphatasia Dual role of the Trps1 transcription factor in dentin mineralization.Improvement of the skeletal and dental hypophosphatasia phenotype in Alpl-/- mice by administration of soluble (non-targeted) chimeric alkaline phosphatase.Catalytic signature of a heat-stable, chimeric human alkaline phosphatase with therapeutic potential.Counter-regulatory phosphatases TNAP and NPP1 temporally regulate tooth root cementogenesis Mineralization defects in cementum and craniofacial bone from loss of bone sialoprotein Enzyme replacement for craniofacial skeletal defects and craniosynostosis in murine hypophosphatasia.Periodontal Defects in the A116T Knock-in Murine Model of Odontohypophosphatasia.Multiple essential MT1-MMP functions in tooth root formation, dentinogenesis, and tooth eruption.Wnt signaling regulates pulp volume and dentin thickness Current concepts in odontohypophosphatasia form of hypophosphatasia and report of two cases.Crystallographic texture and elemental composition mapped in bovine root dentin at the 200 nm level.Alkaline Phosphatase and Hypophosphatasia.Skeletal Mineralization Deficits and Impaired Biogenesis and Function of Chondrocyte-Derived Matrix Vesicles in Phospho1(-/-) and Phospho1/Pi t1 Double-Knockout Mice.Compounded PHOSPHO1/ALPL deficiencies reduce dentin mineralization The rachitic tooth.Tissue Nonspecific Alkaline Phosphatase (TNAP) Regulates Cranial Base Growth and Synchondrosis Maturation.Hypophosphatasia: an overview of the disease and its treatment.Overlapping functions of bone sialoprotein and pyrophosphate regulators in directing cementogenesis.Rsk2, the Kinase Mutated in Coffin-Lowry Syndrome, Controls Cementum Formation.Hypophosphatasia: diagnosis and clinical signs - a dental surgeon perspective.Cellular and molecular mechanisms of tooth root development.Hypophosphatasia - pathophysiology and treatment.Gene therapy improves dental manifestations in hypophosphatasia model mice.Conditional Alpl Ablation Phenocopies Dental Defects of Hypophosphatasia.Establishment of Singleton-Merten syndrome pulp cells: evidence of mineralization dysregulation.Osteopontin regulates dentin and alveolar bone development and mineralization.Matrix vesicles from chondrocytes and osteoblasts: Their biogenesis, properties, functions and biomimetic models.Postnatal Pancraniosynostosis in a Patient With Infantile Hypophosphatasia Profile of asfotase alfa in the treatment of hypophosphatasia: design, development, and place in therapy Bone-Targeted Alkaline Phosphatase Treatment of Mandibular Bone and Teeth in Lethal Hypophosphatasia via an scAAV8 Vector Nano Hydroxyapatite & Mineral Trioxide Aggregate Efficiently Promote Odontogenic Differentiation of Dental Pulp Stem Cells

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P2860

Tooth root dentin mineralization defects in a mouse model of hypophosphatasia.

http://www.wikidata.org/entity/Q30531828

description

2013 nî lūn-bûn

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2013 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2013 թվականի փետրվարին հրատարակված գիտական հոդված

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2013年の論文

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2013年论文

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Tooth root dentin mineralization defects in a mouse model of hypophosphatasia.

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Tooth root dentin mineralization defects in a mouse model of hypophosphatasia.

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Tooth root dentin mineralization defects in a mouse model of hypophosphatasia.

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Journal of Bone and Mineral Research

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Tooth root dentin mineralization defects in a mouse model of hypophosphatasia.

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P2093

A B Tran

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B L Foster

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F H Nociti

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H W Tso

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S Narisawa

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P2860

Orodental phenotype and genotype findings in all subtypes of hypophosphatasia

Six genes expressed in bones and teeth encode the current members of the SIBLING family of proteins

Postembedding colloidal-gold immunocytochemistry of noncollagenous extracellular matrix proteins in mineralized tissues

Loss of skeletal mineralization by the simultaneous ablation of PHOSPHO1 and alkaline phosphatase function: a unified model of the mechanisms of initiation of skeletal calcification

Enzyme replacement therapy for murine hypophosphatasia

Central role of pyrophosphate in acellular cementum formation.

The nature and functional significance of dentin extracellular matrix proteins.

Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasia

Impaired calcification around matrix vesicles of growth plate and bone in alkaline phosphatase-deficient mice.

Concerted regulation of inorganic pyrophosphate and osteopontin by akp2, enpp1, and ank: an integrated model of the pathogenesis of mineralization disorders.

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10.1002/JBMR.1767

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2

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hypophosphatasia

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3541444

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