Unique coexpression in osteoblasts of broadly expressed genes accounts for the spatial restriction of ECM mineralization to bone. - Wikidata - wikimedia - TriplyDB

Unique coexpression in osteoblasts of broadly expressed genes accounts for the spatial restriction of ECM mineralization to bone.

Unique coexpression in osteoblasts of broadly expressed genes accounts for the spatial restriction of ECM mineralization to bone.

http://www.wikidata.org/entity/Q42732135

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Fibrillin-1 and -2 differentially modulate endogenous TGF-β and BMP bioavailability during bone formation Kinetic analysis of substrate utilization by native and TNAP-, NPP1-, or PHOSPHO1-deficient matrix vesicles Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy Multiple Functions of MSCA-1/TNAP in Adult Mesenchymal Progenitor/Stromal Cells Role of β-hydroxybutyrate, its polymer poly-β-hydroxybutyrate and inorganic polyphosphate in mammalian health and disease Phosphate/pyrophosphate and MV-related proteins in mineralisation: discoveries from mouse models Extracellular matrix mineralization in periodontal tissues: Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemia The role of phosphatases in the initiation of skeletal mineralization Molecular and cellular aspects of calcific aortic valve disease Genetics and mechanisms of crystal deposition in calcium pyrophosphate deposition disease Inorganic polyphosphate induces osteoblastic differentiation Phospholipases of mineralization competent cells and matrix vesicles: roles in physiological and pathological mineralizations MSM enhances GH signaling via the Jak2/STAT5b pathway in osteoblast-like cells and osteoblast differentiation through the activation of STAT5b in MSCs PHOSPHO1 is essential for mechanically competent mineralization and the avoidance of spontaneous fractures 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 Upregulation of alkaline phosphatase and pyrophosphate hydrolysis: potential mechanism for uremic vascular calcification CREB-AP1 protein complexes regulate transcription of the collagen XXIV gene (Col24a1) in osteoblasts Wnt signaling in heart valve development and osteogenic gene induction Altered TNSALP expression and phosphate regulation contribute to reduced mineralization in mice lacking androgen receptor.Plasma membrane factor XIIIA transglutaminase activity regulates osteoblast matrix secretion and deposition by affecting microtubule dynamics.Global gene expression in endometrium of high and low fertility heifers during the mid-luteal phase of the estrous cycle.Association of specific proteolytic processing of bone sialoprotein and bone acidic glycoprotein-75 with mineralization within biomineralization foci.Genetics in arterial calcification: pieces of a puzzle and cogs in a wheel.Confocal laser Raman microspectroscopy of biomineralization foci in UMR 106 osteoblastic cultures reveals temporally synchronized protein changes preceding and accompanying mineral crystal deposition.Control of vertebrate skeletal mineralization by polyphosphates Discovery and validation of a series of aryl sulfonamides as selective inhibitors of tissue-nonspecific alkaline phosphatase (TNAP).Nanoanalytical Electron Microscopy Reveals a Sequential Mineralization Process Involving Carbonate-Containing Amorphous Precursors.Ultrastructural and biochemical aspects of matrix vesicle-mediated mineralization Design and synthesis of selective inhibitors of placental alkaline phosphatase.Assay format as a critical success factor for identification of novel inhibitor chemotypes of tissue-nonspecific alkaline phosphatase from high-throughput screening Phenotypic analysis of Dlx5 overexpression in post-natal bone.Proteoliposomes harboring alkaline phosphatase and nucleotide pyrophosphatase as matrix vesicle biomimetics.The role of inorganic pyrophosphate in aortic valve calcification.Zebrafish enpp1 mutants exhibit pathological mineralization, mimicking features of generalized arterial calcification of infancy (GACI) and pseudoxanthoma elasticum (PXE)Matrix recruitment and calcium sequestration for spatial specific otoconia development Enzyme replacement therapy for murine hypophosphatasia Increased risk of temporomandibular joint closed lock: a case-control study of ANKH polymorphisms Cellular and molecular mechanisms of bone remodeling.Serotonergic 5-HT(2B) receptor controls tissue-nonspecific alkaline phosphatase activity in osteoblasts via eicosanoids and phosphatidylinositol-specific phospholipase C Cranio-lenticulo-sutural dysplasia associated with defects in collagen secretion.

P2860

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P2860

Unique coexpression in osteoblasts of broadly expressed genes accounts for the spatial restriction of ECM mineralization to bone.

http://www.wikidata.org/entity/Q42732135

description

2005 nî lūn-bûn

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2005年の論文

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2005年論文

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2005年論文

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name

Unique coexpression in osteobl ...... of ECM mineralization to bone.

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Unique coexpression in osteobl ...... of ECM mineralization to bone.

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Unique coexpression in osteobl ...... of ECM mineralization to bone.

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Unique coexpression in osteobl ...... of ECM mineralization to bone.

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prefLabel

Unique coexpression in osteobl ...... of ECM mineralization to bone.

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Unique coexpression in osteobl ...... of ECM mineralization to bone.

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Unique coexpression in osteobl ...... of ECM mineralization to bone.

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Dympna Harmey

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Gerard Karsenty

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José Luis Millán

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Marc D McKee

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Monzur Murshed

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P2860

Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome

Role of the mouse ank gene in control of tissue calcification and arthritis

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

Cloning of human PEX cDNA. Expression, subcellular localization, and endopeptidase activity

Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia

osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification

Mutations in ANKH cause chondrocalcinosis

X-linked hypophosphataemia: a homologous disorder in humans and mice

Association of the human NPPS gene with ossification of the posterior longitudinal ligament of the spine (OPLL)

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9

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19

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