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Journal Abstract Search

129 related items for PubMed ID: 16789627

  • 21. Identification of two novel deletion mutations within the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophy.
    Yu D, Yu S, Schuster V, Kruse K, Clericuzio CL, Weinstein LS.
    J Clin Endocrinol Metab; 1999 Sep; 84(9):3254-9. PubMed ID: 10487696
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  • 22. Selective deficiency of Gsalpha and the possible role of alternative gene products of GNAS in Albright hereditary osteodystrophy and pseudohypoparathyroidism type Ia.
    Thiele S, Werner R, Ahrens W, Hübner A, Hinkel KG, Höppner W, Igl B, Hiort O.
    Exp Clin Endocrinol Diabetes; 2010 Feb; 118(2):127-32. PubMed ID: 19658058
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  • 26. Determination of Gs alpha protein activity in Albright's hereditary osteodystrophy.
    Ahrens W, Hiort O.
    J Pediatr Endocrinol Metab; 2006 May; 19 Suppl 2():647-51. PubMed ID: 16789630
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  • 27. [Pseudohypoparathyroidism type I b and genomic imprinting].
    Fukumoto S.
    Clin Calcium; 2007 Aug; 17(8):1222-7. PubMed ID: 17660619
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  • 28. Ovarian dysfunction by activating mutation of GS alpha: McCune-Albright syndrome as a model.
    Chanson P, Salenave S, Young J.
    Ann Endocrinol (Paris); 2010 May; 71(3):210-3. PubMed ID: 20362972
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  • 29. Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib.
    Bastepe M, Fröhlich LF, Linglart A, Abu-Zahra HS, Tojo K, Ward LM, Jüppner H.
    Nat Genet; 2005 Jan; 37(1):25-7. PubMed ID: 15592469
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  • 31. A GNAS1 imprinting defect in pseudohypoparathyroidism type IB.
    Liu J, Litman D, Rosenberg MJ, Yu S, Biesecker LG, Weinstein LS.
    J Clin Invest; 2000 Nov; 106(9):1167-74. PubMed ID: 11067869
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  • 35. [Pseudohypoparathyroidism].
    Yasuda T.
    Nihon Rinsho; 2006 Jun 28; Suppl 2():56-60. PubMed ID: 16817350
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  • 38. Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophy.
    Aldred MA, Aftimos S, Hall C, Waters KS, Thakker RV, Trembath RC, Brueton L.
    Am J Med Genet; 2002 Nov 22; 113(2):167-72. PubMed ID: 12407707
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  • 39. A maternal epimutation of GNAS leads to Albright osteodystrophy and parathyroid hormone resistance.
    Mariot V, Maupetit-Méhouas S, Sinding C, Kottler ML, Linglart A.
    J Clin Endocrinol Metab; 2008 Mar 22; 93(3):661-5. PubMed ID: 18182455
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  • 40. [Albright hereditary osteodystrophy: identification of a novel mutation in a family].
    Bastida Eizaguirre M, Iturbe Ortiz De Urbina R, Arto Urzainqui M, Ezquerra Larreina R, Escalada San Martín J.
    An Esp Pediatr; 2001 Jun 22; 54(6):598-600. PubMed ID: 11412411
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