MEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemia - Test2 - elhamkhani - TriplyDB

MEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemia

MEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemia

http://www.wikidata.org/entity/Q34602567

about

Extracellular matrix mineralization in periodontal tissues: Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemia A unified model for bone-renal mineral and energy metabolism Priming Dental Pulp Stem Cells With Fibroblast Growth Factor-2 Increases Angiogenesis of Implanted Tissue-Engineered Constructs Through Hepatocyte Growth Factor and Vascular Endothelial Growth Factor Secretion.PHEX mimetic (SPR4-peptide) corrects and improves HYP and wild type mice energy-metabolism Dual role of the Trps1 transcription factor in dentin mineralization.Abnormal osteopontin and matrix extracellular phosphoglycoprotein localization, and odontoblast differentiation, in X-linked hypophosphatemic teeth.SPR4-peptide alters bone metabolism of normal and HYP mice.Age dependent regulation of bone-mass and renal function by the MEPE ASARM-motif Odontogenic Differentiation of Human Dental Pulp Stem Cells on Hydrogel Scaffolds Derived from Decellularized Bone Extracellular Matrix and Collagen Type I.Do ASARM peptides play a role in nephrogenic systemic fibrosis?The rachitic tooth.Review of the dental implications of X-linked hypophosphataemic rickets (XLHR).Matrix metalloproteinase 20-dentin sialophosphoprotein interaction in oral cancer.Sclerostin Deficiency Promotes Reparative Dentinogenesis.MEPE Localization in the Craniofacial Complex and Function in Tooth Dentin Formation.Wnt Acts as a Prosurvival Signal to Enhance Dentin Regeneration.Extracellular matrix of dental pulp stem cells: applications in pulp tissue engineering using somatic MSCs.Hey1 functions as a positive regulator of odontogenic differentiation in odontoblast‑lineage cells.Reduced Dentin Matrix Protein Expression in Camurati-Engelmann Disease Transgenic Mouse Model.Mineralization of dense collagen hydrogel scaffolds by human pulp cells.Defective Mineralization in X-Linked Hypophosphatemia Dental Pulp Cell Cultures.Thermoresponsive hydrogels based on a phosphorylated star-shaped copolymer: mimicking the extracellular matrix for in situ bone repair

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P2860

MEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemia

http://www.wikidata.org/entity/Q34602567

description

2013 nî lūn-bûn

@nan

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年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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MEPE-derived ASARM peptide inh ...... s of X-linked hypophosphatemia

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Anne Poliard

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Brigitte Baroukh

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Claire Bardet

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Dominique Le Denmat

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Franck Decup

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Franck Letourneur

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Jiar Naji

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Marc D McKee

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Mayssam Khaddam

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Peter S Rowe

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P2860

MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia

ASARM peptides: PHEX-dependent and -independent regulation of serum phosphate

Degradation of MEPE, DMP1, and release of SIBLING ASARM-peptides (minhibins): ASARM-peptide(s) are directly responsible for defective mineralization in HYP

Regulation and function of the FGF23/klotho endocrine pathways

Regulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathway

A new mathematical model for relative quantification in real-time RT-PCR

FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization

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

Phosphorylation-dependent inhibition of mineralization by osteopontin ASARM peptides is regulated by PHEX cleavage

Proteolytic processing of osteopontin by PHEX and accumulation of osteopontin fragments in Hyp mouse bone, the murine model of X-linked hypophosphatemia

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10.1371/JOURNAL.PONE.0056749

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2

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8

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Antonino Nicoletti

Catherine Chaussain

Agnès Linglart

Benjamin Salmon

Benjamin R Coyac

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2013-02-22T00:00:00Z

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