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346 related items for PubMed ID: 25861491

  • 1. A Novel PHEX Mutation in Japanese Patients with X-Linked Hypophosphatemic Rickets.
    Kawahara T, Watanabe H, Omae R, Yamamoto T, Inazu T.
    Case Rep Genet; 2015; 2015():301264. PubMed ID: 25861491
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  • 2. A novel Phex mutation in a new mouse model of hypophosphatemic rickets.
    Owen C, Chen F, Flenniken AM, Osborne LR, Ichikawa S, Adamson SL, Rossant J, Aubin JE.
    J Cell Biochem; 2012 Jul; 113(7):2432-41. PubMed ID: 22573557
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  • 13. Mutational analysis of patients with FGF23-related hypophosphatemic rickets.
    Kinoshita Y, Saito T, Shimizu Y, Hori M, Taguchi M, Igarashi T, Fukumoto S, Fujita T.
    Eur J Endocrinol; 2012 Aug; 167(2):165-72. PubMed ID: 22577109
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  • 15. Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets.
    Ma SL, Vega-Warner V, Gillies C, Sampson MG, Kher V, Sethi SK, Otto EA.
    PLoS One; 2015 Aug; 10(6):e0130729. PubMed ID: 26107949
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  • 20. A Phex mutation in a murine model of X-linked hypophosphatemia alters phosphate responsiveness of bone cells.
    Ichikawa S, Austin AM, Gray AK, Econs MJ.
    J Bone Miner Res; 2012 Feb; 27(2):453-60. PubMed ID: 22006791
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