The gene for X-linked hypophosphataemic rickets maps to a 200–300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)

[1]  F. Francis,et al.  Rapid isolation of DNA sequences flanking microsatellite repeats. , 1994, Nucleic acids research.

[2]  P. Rowe Molecular biology of hypophosphataemic rickets and oncogenic osteomalacia , 1994, Human Genetics.

[3]  J. Weissenbach,et al.  Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus. , 1994, The Journal of clinical endocrinology and metabolism.

[4]  P. Goodfellow,et al.  Breakpoint break for consortium studying adult polycystic kidney disease , 1994, Cell.

[5]  C. G. See,et al.  A YAC contig spanning the hypophosphatemic rickets disease gene (HYP) candidate region. , 1994, Genomics.

[6]  S. Roy,et al.  Increased renal 25-hydroxyvitamin D3-24-hydroxylase messenger ribonucleic acid and immunoreactive protein in phosphate-deprived Hyp mice: a mechanism for accelerated 1,25-dihydroxyvitamin D3 catabolism in X-linked hypophosphatemic rickets. , 1994, Endocrinology.

[7]  H. Lehrach,et al.  Dinucleotide repeat polymorphism at the DXS1683 locus. , 1994, Human Molecular Genetics.

[8]  N. Sternberg,et al.  Preparation and screening of an arrayed human genomic library generated with the P1 cloning system. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[9]  H. Lehrach,et al.  Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1–22.2) , 1994, Human Genetics.

[10]  A. Werner,et al.  Renal Na(+)-phosphate cotransport in murine X-linked hypophosphatemic rickets. Molecular characterization. , 1994, The Journal of clinical investigation.

[11]  O. Gotoh,et al.  Structural characterization of the gene encoding rat 25-hydroxyvitamin D3 24-hydroxylase. , 1993, Biochemistry.

[12]  F. Glorieux,et al.  Abnormal response of osteoblasts from Hyp mice to 1,25-dihydroxyvitamin D3. , 1992, Bone.

[13]  R. Griffiths,et al.  Crosstransplantation of kidneys in normal and Hyp mice. Evidence that the Hyp mouse phenotype is unrelated to an intrinsic renal defect. , 1992, The Journal of clinical investigation.

[14]  F. Collins,et al.  Positional cloning: Let's not call it reverse anymore , 1992, Nature Genetics.

[15]  F. Glorieux,et al.  Defective bone formation by hyp mouse bone cells transplanted into normal mice: Evidence in favor of an intrinsic osteoblast defect , 1992, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[16]  G. Semenza,et al.  Cloning and expression of cDNA for a Na/Pi cotransport system of kidney cortex. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[17]  A. Monaco,et al.  Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[18]  M. Hewison,et al.  Binding of the receptor for 1,25-dihydroxyvitamin D3 to the 5'-flanking region of the bovine parathyroid hormone gene. , 1990, The Journal of endocrinology.

[19]  R. Gray,et al.  Parabiosis suggests a humoral factor is involved in X‐linked hypophosphatemia in mice , 1989, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[20]  H. Tenenhouse,et al.  The renal phosphate transport defect in normal mice parabiosed to X‐linked hypophosphatemic mice persists after parathyroidectomy , 1989, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[21]  H. Tenenhouse,et al.  Increased renal catabolism of 1,25-dihydroxyvitamin D3 in murine X-linked hypophosphatemic rickets. , 1988, The Journal of clinical investigation.

[22]  R. Weksberg,et al.  Bridging markers defining the map position of X linked hypophosphataemic rickets. , 1987, Journal of medical genetics.

[23]  V. Palda,et al.  Side-chain hydroxylation of vitamin D3 and its physiological implications , 1987, Steroids.

[24]  T. Wienker,et al.  X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22 , 1986, Human Genetics.

[25]  K. Davies,et al.  Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis , 1986, Human Genetics.

[26]  J. Ott,et al.  Strategies for multilocus linkage analysis in humans. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[27]  A. Feinberg,et al.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.

[28]  Brian Bowen,et al.  The detection of DNA-binding proteins by protein blotting , 1980, Nucleic Acids Res..

[29]  S. Goldfarb,et al.  Evidence for an intrinsic renal tubular defect in mice with genetic hypophosphatemic rickets. , 1979, The Journal of clinical investigation.

[30]  R. Mcinnes,et al.  Renal handling of phosphate in vivo and in vitro by the X-linked hypophosphatemic male mouse: evidence for a defect in the brush border membrane. , 1978, Kidney international.

[31]  M. Haussler,et al.  1,25-Dihydroxyvitamin D3 receptors in parathyroid glands. Preliminary characterization of cytoplasmic and nuclear binding components. , 1978, The Journal of biological chemistry.

[32]  G. Danan,et al.  Micropuncture study of renal phosphorus transport in hypophosphatemic vitamin D resistant rickets mice , 1977, Pflügers Archiv.

[33]  C. Dent,et al.  VITAMIN D-RESISTANT RICKETS. ANALYSIS OF TWENTY-FOUR PEDIGREES WITH HEREDITARY AND SPORADIC CASES. , 1964, The American journal of medicine.

[34]  M. Econs,et al.  Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35. , 1994, Genomics.

[35]  H. Lehrach,et al.  Construction and preliminary analysis of the ICRF human P1 library. , 1994, Genetic analysis, techniques and applications.

[36]  G. Sutherland,et al.  Localization of the human vitamin D 24-hydroxylase gene (CYP24) to chromosome 20q13.2-->q13.3. , 1993, Cytogenetics and cell genetics.