DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.
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Inactivation of a novel FGF23 regulator, FAM20C, leads to hypophosphatemic rickets in miceThe FGF23-Klotho axis: endocrine regulation of phosphate homeostasisASARM peptides: PHEX-dependent and -independent regulation of serum phosphateDegradation of MEPE, DMP1, and release of SIBLING ASARM-peptides (minhibins): ASARM-peptide(s) are directly responsible for defective mineralization in HYPFGF23-mediated regulation of systemic phosphate homeostasis: is Klotho an essential player?Miscellaneous non-inflammatory musculoskeletal conditions. Hyperphosphatemic familial tumoral calcinosis (FGF23, GALNT3 and αKlotho)FGF23 and Phosphate Wasting DisordersNuclear receptors in bone physiology and diseasesRegulation 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 hypophosphatemiaRegulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathwayProtective roles of DMP1 in high phosphate homeostasisDysregulated gene expression in the primary osteoblasts and osteocytes isolated from hypophosphatemic Hyp miceFibroblast growth factor 23 impairs phosphorus and vitamin D metabolism in vivo and suppresses 25-hydroxyvitamin D-1alpha-hydroxylase expression in vitroRecent advances in the renal-skeletal-gut axis that controls phosphate homeostasisGenetic evidence of serum phosphate-independent functions of FGF-23 on boneRegulation of serum 1,25(OH)2 vitamin D3 levels by fibroblast growth factor 23 is mediated by FGF receptors 3 and 4Regulation of renal phosphate transport by FGF23 is mediated by FGFR1 and FGFR4Amelogenesis imperfecta and other biomineralization defects in Fam20a and Fam20c null miceA 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.PHEX mimetic (SPR4-peptide) corrects and improves HYP and wild type mice energy-metabolismPhosphate feeding induces arterial medial calcification in uremic mice: role of serum phosphorus, fibroblast growth factor-23, and osteopontin.Nuclear isoforms of fibroblast growth factor 2 are novel inducers of hypophosphatemia via modulation of FGF23 and KLOTHOKlf5 Mediates Odontoblastic Differentiation through Regulating Dentin-Specific Extracellular Matrix Gene Expression during Mouse Tooth DevelopmentIdentification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia.Loss-of-function ENPP1 mutations cause both generalized arterial calcification of infancy and autosomal-recessive hypophosphatemic ricketsAutosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene.FGF-23 in bone biology.Circulating fibroblast growth factor 23 in patients with end-stage renal disease treated by peritoneal dialysis is intact and biologically activeA Novel PHEX Gene Mutation in a Patient with Sporadic Hypophosphatemic Rickets.A novel nonsense mutation in the DMP1 gene identified by a genome-wide association study is responsible for inherited rickets in Corriedale sheep.Mineral metabolism and aging: the fibroblast growth factor 23 enigma.The calcemic response to continuous parathyroid hormone (PTH)(1-34) infusion in end-stage kidney disease varies according to bone turnover: a potential role for PTH(7-84)Constitutive nuclear expression of dentin matrix protein 1 fails to rescue the Dmp1-null phenotype.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.FGF23 decreases renal NaPi-2a and NaPi-2c expression and induces hypophosphatemia in vivo predominantly via FGF receptor 1.Hypophosphatemic rickets: revealing novel control points for phosphate homeostasis.Circling behavior developed in Dmp1 null mice is due to bone defects in the vestibular apparatus.Tumor-induced osteomalacia.
P2860
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P2860
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
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2006年學術文章
@zh-hant
name
DMP1 mutations in autosomal re ...... tion of phosphate homeostasis.
@en
DMP1 mutations in autosomal re ...... tion of phosphate homeostasis.
@nl
type
label
DMP1 mutations in autosomal re ...... tion of phosphate homeostasis.
@en
DMP1 mutations in autosomal re ...... tion of phosphate homeostasis.
@nl
prefLabel
DMP1 mutations in autosomal re ...... tion of phosphate homeostasis.
@en
DMP1 mutations in autosomal re ...... tion of phosphate homeostasis.
@nl
P2093
P2860
P356
P1433
P1476
DMP1 mutations in autosomal re ...... tion of phosphate homeostasis.
@en
P2093
Alan H Shlossberg
Anna Benet-Pagès
Bettina Lorenz-Depiereux
César Loris
Francis Glorieux
Harald Jüppner
Janine Wagenstaller
José L Olivares
Klaus Badenhoop
Murat Bastepe
P2860
P2888
P304
P356
10.1038/NG1868
P407
P577
2006-10-08T00:00:00Z