Editorial: Pathophysiology of X-linked hypophosphatemia, tumor-induced osteomalacia, and autosomal dominant hypophosphatemia: A perPHEXing problem

Journal of Clinical Endocrinology and Metabolism

Volumn 86, Issue 2, 2001, Pages 494-496

  Quarles, L Darryl ^a   Drezner, Marc K ^b  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PARATHYROID HORMONE; VASOPRESSIN;

EDITORIAL; GENE MUTATION; HOMEOSTASIS; HUMAN; OSTEOBLAST; OSTEOMALACIA; PATHOGENESIS; PATHOPHYSIOLOGY; PHENOTYPE; PHOSPHATE TRANSPORT; PRIORITY JOURNAL; VITAMIN D RESISTANT RICKETS; ANIMAL; GENETICS; HYPOPHOSPHATEMIA; NEOPLASM; NOTE; X CHROMOSOME;

ANIMALS; HUMANS; HYPOPHOSPHATEMIA, FAMILIAL; NEOPLASMS; OSTEOMALACIA; X CHROMOSOME;

EID: 85047685774     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.86.2.7302     Document Type: Editorial

References (16)

1. Proximal tubular phosphate reabsorption: Molecular mechanisms
2. PTH-induced down-regulation of the type IIa Na/P(i)-cotransporter is independent of known endocytic motifs
3. Effect of parathyroid hormone-related protein on sodium-dependent phosphate transport in renal brush border membrane vesicles in rats. Comparison with parathyroid hormone
4. A gene (Pex) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets
5. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
6. MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia
7. Intrinsic mineralization defect in Hyp mouse osteoblasts
8. Crosstransplantation of kidneys in normal and Hyp mice. Evidence that the Hyp mouse phenotype is unrelated to an intrinsic renal defect
9. Phosphate transport in immortalized cell cultures from the renal proximal tubule of normal and Hyp mice: Evidence that the Hyp gene locus product is an extrarenal factor
10. Cloning and sequencing of human PEX from a bone cDNA library: Evidence for its developmental stage-specific regulation in osteoblasts
11. The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting
12. Phex cDNA cloning from rat bone and studies of Phex mRNA express: Tissue-specificity, age-dependency, and regulation by insulin-like growth factor (IGF) I in vivo
13. The effects of bone marrow transplantation on X-linked hypophosphatemic mice
14. Comparative analysis of mammalian stanniocalcin genes
15. Stanniocalcin 1 and 2 are secreted as phosphoproteins from human fibrosarcoma cells
16. The distribution of stanniocalcin 1 protein in fetal mouse tissues suggests a role in bone and muscle development