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Journal Abstract Search

411 related items for PubMed ID: 17976082

  • 41.
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  • 42. Tumoral calcinosis presenting with eyelid calcifications due to novel missense mutations in the glycosyl transferase domain of the GALNT3 gene.
    Ichikawa S, Imel EA, Sorenson AH, Severe R, Knudson P, Harris GJ, Shaker JL, Econs MJ.
    J Clin Endocrinol Metab; 2006 Nov; 91(11):4472-5. PubMed ID: 16940445
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  • 43. Transgenic mice expressing fibroblast growth factor 23 under the control of the alpha1(I) collagen promoter exhibit growth retardation, osteomalacia, and disturbed phosphate homeostasis.
    Larsson T, Marsell R, Schipani E, Ohlsson C, Ljunggren O, Tenenhouse HS, Jüppner H, Jonsson KB.
    Endocrinology; 2004 Jul; 145(7):3087-94. PubMed ID: 14988389
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  • 46. Fibroblast growth factor 23 and its receptors.
    Yu X, White KE.
    Ther Apher Dial; 2005 Aug; 9(4):308-12. PubMed ID: 16076372
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  • 47. Vitamin D and phosphate regulate fibroblast growth factor-23 in K-562 cells.
    Ito M, Sakai Y, Furumoto M, Segawa H, Haito S, Yamanaka S, Nakamura R, Kuwahata M, Miyamoto K.
    Am J Physiol Endocrinol Metab; 2005 Jun; 288(6):E1101-9. PubMed ID: 15671080
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  • 48. Novel aspects in regulated expression of the renal type IIa Na/Pi-cotransporter.
    Bacic D, Wagner CA, Hernando N, Kaissling B, Biber J, Murer H.
    Kidney Int Suppl; 2004 Oct; (91):S5-S12. PubMed ID: 15461703
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  • 49. Skeletal secretion of FGF-23 regulates phosphate and vitamin D metabolism.
    Quarles LD.
    Nat Rev Endocrinol; 2012 Jan 17; 8(5):276-86. PubMed ID: 22249518
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  • 52. X-linked hypophosphatemic rickets and craniosynostosis.
    Murthy AS.
    J Craniofac Surg; 2009 Mar 17; 20(2):439-42. PubMed ID: 19242361
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  • 54. Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulation.
    Bastepe M, Jüppner H.
    Rev Endocr Metab Disord; 2008 Jun 17; 9(2):171-80. PubMed ID: 18365315
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  • 55. PHEXdb, a locus-specific database for mutations causing X-linked hypophosphatemia.
    Sabbagh Y, Jones AO, Tenenhouse HS.
    Hum Mutat; 2000 Jun 17; 16(1):1-6. PubMed ID: 10874297
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  • 56. Novel GALNT3 mutations causing hyperostosis-hyperphosphatemia syndrome result in low intact fibroblast growth factor 23 concentrations.
    Ichikawa S, Guigonis V, Imel EA, Courouble M, Heissat S, Henley JD, Sorenson AH, Petit B, Lienhardt A, Econs MJ.
    J Clin Endocrinol Metab; 2007 May 17; 92(5):1943-7. PubMed ID: 17311862
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  • 58. Regulation of phosphate homeostasis by the phosphatonins and other novel mediators.
    Shaikh A, Berndt T, Kumar R.
    Pediatr Nephrol; 2008 Aug 17; 23(8):1203-10. PubMed ID: 18288501
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