Latest papers

A novel Phex mutation with defective glycosylation causes hypophosphatemia and rickets in mice.

Distinct roles for intrinsic osteocyte abnormalities and systemic factors in regulation of FGF23 and bone mineralization in Hyp mice.

Three novel mutations of the PHEX gene in three Chinese families with X-linked dominant hypophosphatemic rickets.

PHEX gene mutations and genotype-phenotype analysis of Korean patients with hypophosphatemic rickets.

[Hypophosphatemic rickets/osteomalacia. - Mainly on patients with PHEX mutations -]

Regulation of phosphate homeostasis in infants, children, and adolescents, and the role of phosphatonins in this process.

High level expression and purification of recombinant PEX protein in cultured skeletal muscle cell expression system.

[alpha Klotho and inorganic phosphate metabolism].

[X-linked hypophosphatemic rickets].

[Calcium-phosphorus metabolic disorders and the primary care (discussion)].

Phex mutation causes the reduction of npt2b mRNA in teeth.

Novel PHEX mutation associated with hypophosphatemic rickets.

Phosphorylated acidic serine-aspartate-rich MEPE-associated motif peptide from matrix extracellular phosphoglycoprotein inhibits phosphate regulating gene with homologies to endopeptidases on the X-chromosome enzyme activity.

DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.

[Endocrine diseases accompanied by hypophosphatemia or hyperphosphatemia]

The role of tumor necrosis factor alpha in down-regulation of osteoblast Phex gene expression in experimental murine colitis.

Pathogenic role of Fgf23 in Hyp mice.

[X-linked hypophosphatemic rickets].

[From gene to disease; hypophosphataemic rickets and the PHEX gene]

[X-linked hypophosphatemic vitamin D resistant rickets: Pathogenesis, pathophysiology, and therapy]