Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
about
Extracellular matrix mineralization in periodontal tissues: Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemiaRegulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathwayAbnormal presence of the matrix extracellular phosphoglycoprotein-derived acidic serine- and aspartate-rich motif peptide in human hypophosphatemic dentin.Cooperative effects in differentiation and proliferation between PDGF-BB and matrix derived synthetic peptides in human osteoblastsMEPE-derived ASARM peptide inhibits odontogenic differentiation of dental pulp stem cells and impairs mineralization in tooth models of X-linked hypophosphatemiaMMP2-cleavage of DMP1 generates a bioactive peptide promoting differentiation of dental pulp stem/progenitor cell.The chicken or the egg: PHEX, FGF23 and SIBLINGs unscrambled.Matricellular molecules and odontoblast progenitors as tools for dentin repair and regeneration.Inflammatory and immunological aspects of dental pulp repair.Phosphorylated proteins and control over apatite nucleation, crystal growth, and inhibition.Juvenile dermatomyositis calcifications selectively displayed markers of bone formation.Molecular regulation of matrix extracellular phosphoglycoprotein expression by bone morphogenetic protein-2Biological approaches toward dental pulp regeneration by tissue engineering.Pulp healing and regeneration: more questions than answers.Dentin-pulp complex regeneration: from lab to clinic.Advances in regeneration of dental pulp--a literature review.Insulin-like growth factor 1 receptor and p38 mitogen-activated protein kinase signals inversely regulate signal transducer and activator of transcription 3 activity to control human dental pulp stem cell quiescence, propagation, and differentiationInduction of reparative dentin formation on exposed dental pulp by dentin phosphophoryn/collagen composite.Minimal intervention dentistry: part 8. Biotherapies for the dental pulp.Dentin extracellular matrix molecules implanted into exposed pulps generate reparative dentin: a novel strategy in regenerative dentistry.MEPE activated by furin promotes pulpal cell adhesion.MEPE's diverse effects on mineralization.Changes in matrix extracellular phosphoglycoprotein expression before and during in vitro osteogenic differentiation of human dental papilla mesenchymal cells.Self-Assembly of a Dentinogenic Peptide Hydrogel.
P2860
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P2860
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
description
2007 nî lūn-bûn
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2007年の論文
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2007年学术文章
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2007年学术文章
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2007年学术文章
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2007年学术文章
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name
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
@en
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
@nl
type
label
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
@en
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
@nl
prefLabel
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
@en
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
@nl
P2093
P2860
P1476
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.
@en
P2093
C Chaussain-Miller
M Goldberg
P DenBesten
P2860
P304
P356
10.1177/154405910708600818
P407
P577
2007-08-01T00:00:00Z