(Q28177435)

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Partial rescue of the Hyp phenotype by osteoblast-targeted PHEX (phosphate-regulating gene with homologies to endopeptidases on the X chromosome) expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

High bone density due to a mutation in LDL-receptor-related protein 5

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

VITAMIN D-RESISTANT RICKETS. ANALYSIS OF TWENTY-FOUR PEDIGREES WITH HEREDITARY AND SPORADIC CASES.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Renal phosphate wasting in fibrous dysplasia of bone is part of a generalized renal tubular dysfunction similar to that seen in tumor-induced osteomalacia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Tumors associated with oncogenic osteomalacia express genes important in bone and mineral metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Fibroblast growth factor receptor 3 is a negative regulator of bone growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Role of abnormal neutral endopeptidase-like activities in Hyp mouse bone cells in renal phosphate transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Defective bone formation by hyp mouse bone cells transplanted into normal mice: Evidence in favor of an intrinsic osteoblast defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Defective bone formation by transplanted Hyp mouse bone cells into normal mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Endothelin-converting enzyme-2 is a membrane-bound, phosphoramidon-sensitive metalloprotease with acidic pH optimum

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Expression and cloning of the human X-linked hypophosphatemia gene cDNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

A novel in vitro culture system for analysis of functional role of phosphate transport in endochondral ossification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Analysis of recombinant Phex: an endopeptidase in search of a substrate

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Cloning and sequencing of human PEX from a bone cDNA library: evidence for its developmental stage-specific regulation in osteoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Inhibition of MEPE cleavage by Phex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Role of the mouse ank gene in control of tissue calcification and arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

WNT signals control FGF-dependent limb initiation and AER induction in the chick embryo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Loss of renal phosphate wasting in a child with autosomal dominant hypophosphatemic rickets caused by a FGF23 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

New insights into phosphate homeostasis: fibroblast growth factor 23 and frizzled-related protein-4 are phosphaturic factors derived from tumors associated with osteomalacia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Molecular defects underlying the Kell null phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Molecular cloning and primary structure of Kell blood group protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Cloning of human PEX cDNA. Expression, subcellular localization, and endopeptidase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

MEPE/OF45, a new dentin/bone matrix protein and candidate gene for dentin diseases mapping to chromosome 4q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Partial deletion of both the spermine synthase gene and the Pex gene in the X-linked hypophosphatemic, gyro (Gy) mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Interaction of FGF, Ihh/Pthlh, and BMP signaling integrates chondrocyte proliferation and hypertrophic differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

The effects of bone marrow transplantation on X-linked hypophosphatemic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Furin: a mammalian subtilisin/Kex2p-like endoprotease involved in processing of a wide variety of precursor proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Crosstransplantation of kidneys in normal and Hyp mice. Evidence that the Hyp mouse phenotype is unrelated to an intrinsic renal defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Coordinated maturational regulation of PHEX and renal phosphate transport inhibitory activity: evidence for the pathophysiological role of PHEX in X-linked hypophosphatemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Expression of type III sodium-dependent phosphate transporters/retroviral receptors mRNAs during osteoblast differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Structure of human neutral endopeptidase (Neprilysin) complexed with phosphoramidon

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Identification of osteoblast/osteocyte factor 45 (OF45), a bone-specific cDNA encoding an RGD-containing protein that is highly expressed in osteoblasts and osteocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Fibroblast growth factors, their receptors and signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Developmental expression and tissue distribution of Phex protein: effect of the Hyp mutation and relationship to bone markers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Human fibroblast growth factor-23 mutants suppress Na+-dependent phosphate co-transport activity and 1alpha,25-dihydroxyvitamin D3 production

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Neprilysin degrades both amyloid beta peptides 1-40 and 1-42 most rapidly and efficiently among thiorphan- and phosphoramidon-sensitive endopeptidases

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Ontogeny of Phex/PHEX protein expression in mouse embryo and subcellular localization in osteoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

The neprilysin family in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

XCE, a new member of the endothelin-converting enzyme and neutral endopeptidase family, is preferentially expressed in the CNS

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Hypophosphatemic rickets accompanying McCune-Albright syndrome: evidence that a humoral factor causes hypophosphatemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Fibroblast growth factor (FGF)-23 inhibits renal phosphate reabsorption by activation of the mitogen-activated protein kinase pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003

Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPENDO.00016.2003