MEPE's diverse effects on mineralization. - Test2 - elhamkhani - TriplyDB

MEPE's diverse effects on mineralization.

MEPE's diverse effects on mineralization.

http://www.wikidata.org/entity/Q41763685

about

ASARM peptides: PHEX-dependent and -independent regulation of serum phosphate Regulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathway MEPE is a novel regulator of growth plate cartilage mineralization A review of the biology of calcium phosphate sequestration with special reference to milk PHEX mimetic (SPR4-peptide) corrects and improves HYP and wild type mice energy-metabolism Intrinsically disordered proteins and biomineralization.MEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemia The 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?Separation of newly formed bone from older compact bone reveals clear compositional differences in bone matrix Post-translational modification of osteopontin: effects on in vitro hydroxyapatite formation and growth.Age dependent regulation of bone-mass and renal function by the MEPE ASARM-motif The chicken or the egg: PHEX, FGF23 and SIBLINGs unscrambled.The osteocyte: an endocrine cell ... and more.Biomimetic remineralization of dentin.The rachitic tooth.Dentin: structure, composition and mineralization Is interaction between age-dependent decline in mechanical stimulation and osteocyte-estrogen receptor levels the culprit for postmenopausal-impaired bone formation?MEPE Localization in the Craniofacial Complex and Function in Tooth Dentin Formation.Phosphatonins: physiological role and pathological changes.Pigment epithelium derived factor suppresses expression of Sost/Sclerostin by osteocytes: implication for its role in bone matrix mineralization.Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and backscattered electron imaging.Elevated solute transport at sites of diffuse matrix damage in cortical bone: Implications on bone repair.Matrix extracellular phosphoglycoprotein is expressed in causative tumors of oncogenic osteomalacia.Effects of lactic acid and glycolic acid on human osteoblasts: A way to understand PLGA involvement in PLGA/calcium phosphate composite failure

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P2860

MEPE's diverse effects on mineralization.

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2009 nî lūn-bûn

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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Calcified Tissue International

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MEPE's diverse effects on mineralization.

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Adele L Boskey

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Alexis Fermanis

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Hayat Taleb

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Jared Brown

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Peter S N Rowe

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Phyllis Chiang

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Valentin David

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P2860

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

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

MEPE-ASARM peptides control extracellular matrix mineralization by binding to hydroxyapatite: an inhibition regulated by PHEX cleavage of ASARM

Mepe, the gene encoding a tumor-secreted protein in oncogenic hypophosphatemic osteomalacia, is expressed in bone

Targeted disruption of the osteoblast/osteocyte factor 45 gene (OF45) results in increased bone formation and bone mass

A review of protein structure and gene organisation for proteins associated with mineralised tissue and calcium phosphate stabilisation encoded on human chromosome 4.

Matrix extracellular phosphoglycoprotein (MEPE) is highly expressed in osteocytes in human bone.

Matrix extracellular phosphoglycoprotein (MEPE) is a new bone renal hormone and vascularization modulator.

Post-translational modifications of sibling proteins and their roles in osteogenesis and dentinogenesis.

Surface plasmon resonance (SPR) confirms that MEPE binds to PHEX via the MEPE-ASARM motif: a model for impaired mineralization in X-linked rickets (HYP)

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