PHEX gene and hypophosphatemia
- 1 January 2000
- journal article
- review article
- Published by Elsevier in Kidney International
- Vol. 57 (1) , 9-18
- https://doi.org/10.1046/j.1523-1755.2000.00807.x
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Cloning and Sequencing of Human PEX from a Bone cDNA Library: Evidence for Its Developmental Stage-Specific Regulation in OsteoblastsJournal of Bone and Mineral Research, 1997
- Expression and Cloning of the Human X-Linked Hypophosphatemia Gene cDNABiochemical and Biophysical Research Communications, 1997
- Hypophosphatemia Induced in Mice by Transplantation of a Tumor-Derived Cell Line from a Patient with Oncogenic RicketsJournal of Pediatric Endocrinology and Metabolism, 1996
- Dinucleotide repeat polymorphism at the DXS1683 locusHuman Molecular Genetics, 1994
- Renal Na(+)-phosphate cotransport in murine X-linked hypophosphatemic rickets. Molecular characterization.Journal of Clinical Investigation, 1994
- Localization of a Renal Sodium-Phosphate Cotransporter Gene to Human Chromosome 5q35Genomics, 1994
- Bridging markers defining the map position of X linked hypophosphataemic rickets.Journal of Medical Genetics, 1987
- Calcitonin stimulation of renal 25-hydroxyvitamin D-1 alpha-hydroxylase activity in hypophosphatemic mice. Evidence that the regulation of calcitriol production is not universally abnormal in X-linked hypophosphatemia.Journal of Clinical Investigation, 1987
- Osteomalacia Due to 1α,25-Dihydroxycholecalciferol DeficiencyJournal of Clinical Investigation, 1977
- Vitamin D-resistant rickets associated withepidermal nevus syndrome: Demonstration of a phosphaturic substance in the dermal lesionsThe Journal of Pediatrics, 1977