MEPE-ASARM peptides control extracellular matrix mineralization by binding to hydroxyapatite: an inhibition regulated by PHEX cleavage of ASARM
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ASARM peptides: PHEX-dependent and -independent regulation of serum phosphateRegulation and function of the FGF23/klotho endocrine pathwaysFibroblast Growth Factor 23: A New Dimension to Diseases of Calcium-Phosphorus MetabolismExtracellular matrix mineralization in periodontal tissues: Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemiaOsteocytes: master orchestrators of boneRegulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathwayExcessive Osteocytic Fgf23 Secretion Contributes to Pyrophosphate Accumulation and Mineralization Defect in Hyp MiceA unified model for bone-renal mineral and energy metabolismProteolytic processing of osteopontin by PHEX and accumulation of osteopontin fragments in Hyp mouse bone, the murine model of X-linked hypophosphatemiaRecent advances in the renal-skeletal-gut axis that controls phosphate homeostasisPTHrP(1-34)-mediated repression of the PHEX gene in osteoblastic cells involves the transcriptional repressor E4BP4Asporin and the mineralization process in fluoride-treated ratsMEPE is a novel regulator of growth plate cartilage mineralizationPHEX mimetic (SPR4-peptide) corrects and improves HYP and wild type mice energy-metabolismAbnormal presence of the matrix extracellular phosphoglycoprotein-derived acidic serine- and aspartate-rich motif peptide in human hypophosphatemic dentin.Identification of two novel mutations in the PHEX gene in Chinese patients with hypophosphatemic rickets/osteomalacia.Matrix extracellular phosphoglycoprotein (MEPE) is a new bone renal hormone and vascularization modulator.FGF-23 in bone biology.Different forms of DMP1 play distinct roles in mineralization.Genetic diagnosis of X-linked dominant Hypophosphatemic Rickets in a cohort study: tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type.Adaptive evolution of the matrix extracellular phosphoglycoprotein in mammalsSurface immobilization of MEPE peptide onto HA/β-TCP ceramic particles enhances bone regeneration and remodeling.Cooperative role of NF-{kappa}B and poly(ADP-ribose) polymerase 1 (PARP-1) in the TNF-induced inhibition of PHEX expression in osteoblastsSurvey of the enthesopathy of X-linked hypophosphatemia and its characterization in Hyp miceMEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemiaCollagen osteoid-like model allows kinetic gene expression studies of non-collagenous proteins in relation with mineral development to understand bone biomineralizationThe impairment of osteogenesis in bone sialoprotein (BSP) knockout calvaria cell cultures is cell density dependent.SPR4-peptide alters bone metabolism of normal and HYP mice.ASARM mineralization hypothesis: a bridge too far?Kbus/Idr, a mutant mouse strain with skeletal abnormalities and hypophosphatemia: identification as an allele of 'Hyp'.Biomineralization of bone: a fresh view of the roles of non-collagenous proteins.Age dependent regulation of bone-mass and renal function by the MEPE ASARM-motifPhosphate: known and potential roles during development and regeneration of teeth and supporting structures.Sclerostin is a locally acting regulator of late-osteoblast/preosteocyte differentiation and regulates mineralization through a MEPE-ASARM-dependent mechanism.Downregulation of PHEX in multibacillary leprosy patients: observational cross-sectional study.The chicken or the egg: PHEX, FGF23 and SIBLINGs unscrambled.Do ASARM peptides play a role in nephrogenic systemic fibrosis?Overexpression of the DMP1 C-terminal fragment stimulates FGF23 and exacerbates the hypophosphatemic rickets phenotype in Hyp mice.FGF23 production by osteocytes.Endochondral Growth Defect and Deployment of Transient Chondrocyte Behaviors Underlie Osteoarthritis Onset in a Natural Murine Model
P2860
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P2860
MEPE-ASARM peptides control extracellular matrix mineralization by binding to hydroxyapatite: an inhibition regulated by PHEX cleavage of ASARM
description
2008 nî lūn-bûn
@nan
2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@ast
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@en
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@nl
type
label
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@ast
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@en
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@nl
prefLabel
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@ast
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@en
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@nl
P2093
P2860
P3181
P356
P1476
MEPE-ASARM peptides control ex ...... ated by PHEX cleavage of ASARM
@en
P2093
Marc D McKee
Phillippe Crine
Thomas Loisel
William N Addison
Yukiko Nakano
P2860
P304
P3181
P356
10.1359/JBMR.080601
P407
P577
2008-10-01T00:00:00Z