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Journal Abstract Search

167 related items for PubMed ID: 9723884

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  • 2. Absence of mutations in parathyroid hormone (PTH)/PTH-related protein receptor complementary deoxyribonucleic acid in patients with pseudohypoparathyroidism type Ib.
    Fukumoto S, Suzawa M, Takeuchi Y, Kodama Y, Nakayama K, Ogata E, Matsumoto T, Fujita T.
    J Clin Endocrinol Metab; 1996 Jul; 81(7):2554-8. PubMed ID: 8675577
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  • 6. Tissue-specific transcription start sites and alternative splicing of the parathyroid hormone (PTH)/PTH-related peptide (PTHrP) receptor gene: a new PTH/PTHrP receptor splice variant that lacks the signal peptide.
    Joun H, Lanske B, Karperien M, Qian F, Defize L, Abou-Samra A.
    Endocrinology; 1997 Apr; 138(4):1742-9. PubMed ID: 9075739
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  • 9. Expression and modulation of the parathyroid hormone (PTH)/PTH-related peptide receptor messenger ribonucleic acid in skin fibroblasts from patients with type Ib pseudohypoparathyroidism.
    Suarez F, Lebrun JJ, Lecossier D, Escoubet B, Coureau C, Silve C.
    J Clin Endocrinol Metab; 1995 Mar; 80(3):965-70. PubMed ID: 7883858
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  • 11. Characterization of an element within the rat parathyroid hormone/parathyroid hormone-related peptide receptor gene promoter that enhances expression in osteoblastic osteosarcoma 17/2.8 cells.
    Giannoukos G, Williams LJ, Chilco PJ, Abou-Samra AB.
    Biochem Biophys Res Commun; 1999 May 10; 258(2):336-40. PubMed ID: 10329388
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  • 12. Selective resistance to parathyroid hormone caused by a novel uncoupling mutation in the carboxyl terminus of G alpha(s). A cause of pseudohypoparathyroidism type Ib.
    Wu WI, Schwindinger WF, Aparicio LF, Levine MA.
    J Biol Chem; 2001 Jan 05; 276(1):165-71. PubMed ID: 11029463
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  • 14. Sequence and activity of parathyroid hormone/parathyroid hormone-related protein receptor promoter region in human osteoblast-like cells.
    Manen D, Palmer G, Bonjour JP, Rizzoli R.
    Gene; 1998 Sep 18; 218(1-2):49-56. PubMed ID: 9751801
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  • 19. Autosomal-dominant pseudohypoparathyroidism type Ib is caused by different microdeletions within or upstream of the GNAS locus.
    Jüppner H, Linglart A, Fröhlich LF, Bastepe M.
    Ann N Y Acad Sci; 2006 Apr 18; 1068():250-5. PubMed ID: 16831926
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