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141 related items for PubMed ID: 9545633

  • 1. Partial deletion of both the spermine synthase gene and the Pex gene in the X-linked hypophosphatemic, gyro (Gy) mouse.
    Meyer RA, Henley CM, Meyer MH, Morgan PL, McDonald AG, Mills C, Price DK.
    Genomics; 1998 Mar 15; 48(3):289-95. PubMed ID: 9545633
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  • 2. Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice.
    Beck L, Soumounou Y, Martel J, Krishnamurthy G, Gauthier C, Goodyer CG, Tenenhouse HS.
    J Clin Invest; 1997 Mar 15; 99(6):1200-9. PubMed ID: 9077527
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  • 3. Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEX.
    Grieff M, Whyte MP, Thakker RV, Mazzarella R.
    Genomics; 1997 Sep 01; 44(2):227-31. PubMed ID: 9299240
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  • 9. A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium.
    Nat Genet; 1995 Oct 01; 11(2):130-6. PubMed ID: 7550339
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  • 11. Developmental expression and tissue distribution of Phex protein: effect of the Hyp mutation and relationship to bone markers.
    Ruchon AF, Tenenhouse HS, Marcinkiewicz M, Siegfried G, Aubin JE, DesGroseillers L, Crine P, Boileau G.
    J Bone Miner Res; 2000 Aug 01; 15(8):1440-50. PubMed ID: 10934642
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  • 13. Cloning and sequencing of human PEX from a bone cDNA library: evidence for its developmental stage-specific regulation in osteoblasts.
    Guo R, Quarles LD.
    J Bone Miner Res; 1997 Jul 01; 12(7):1009-17. PubMed ID: 9199999
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  • 15. Use of (Gyro) Gy and spermine synthase transgenic mice to study functions of spermine.
    Wang X, Pegg AE.
    Methods Mol Biol; 2011 Jul 01; 720():159-70. PubMed ID: 21318872
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  • 16. Increased cathepsin D release by Hyp mouse osteoblast cells.
    Matsumoto N, Jo OD, Shih RN, Brochmann EJ, Murray SS, Hong V, Yanagawa J, Yanagawa N.
    Am J Physiol Endocrinol Metab; 2005 Jul 01; 289(1):E123-32. PubMed ID: 15958652
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  • 18. Three novel mutations of the PHEX gene in three Chinese families with X-linked dominant hypophosphatemic rickets.
    Xia W, Meng X, Jiang Y, Li M, Xing X, Pang L, Wang O, Pei Y, Yu LY, Sun Y, Hu Y, Zhou X.
    Calcif Tissue Int; 2007 Dec 01; 81(6):415-20. PubMed ID: 18046499
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  • 20. Cartilage abnormalities are associated with abnormal Phex expression and with altered matrix protein and MMP-9 localization in Hyp mice.
    Miao D, Bai X, Panda DK, Karaplis AC, Goltzman D, McKee MD.
    Bone; 2004 Apr 01; 34(4):638-47. PubMed ID: 15050894
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