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Journal Abstract Search

335 related items for PubMed ID: 3003142

  • 1. Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds.
    Levine MA, Jap TS, Mauseth RS, Downs RW, Spiegel AM.
    J Clin Endocrinol Metab; 1986 Mar; 62(3):497-502. PubMed ID: 3003142
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  • 5. An inherited mutation associated with functional deficiency of the alpha-subunit of the guanine nucleotide-binding protein Gs in pseudo- and pseudopseudohypoparathyroidism.
    Fischer JA, Egert F, Werder E, Born W.
    J Clin Endocrinol Metab; 1998 Mar; 83(3):935-8. PubMed ID: 9506752
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  • 6. The inhibitory adenylate cyclase coupling protein in pseudohypoparathyroidism.
    Downs RW, Sekura RD, Levine MA, Spiegel AM.
    J Clin Endocrinol Metab; 1985 Aug; 61(2):351-4. PubMed ID: 2989320
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  • 7. GNAS1 lesions in pseudohypoparathyroidism Ia and Ic: genotype phenotype relationship and evidence of the maternal transmission of the hormonal resistance.
    Linglart A, Carel JC, Garabédian M, Lé T, Mallet E, Kottler ML.
    J Clin Endocrinol Metab; 2002 Jan; 87(1):189-97. PubMed ID: 11788646
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  • 8. Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS.
    Turan S, Thiele S, Tafaj O, Brix B, Atay Z, Abali S, Haliloglu B, Bereket A, Bastepe M.
    Bone; 2015 Feb; 71():53-7. PubMed ID: 25464124
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  • 9. Cutaneous ossification in Albright's hereditary osteodystrophy.
    Trüeb RM, Panizzon RG, Burg G.
    Dermatology; 1993 Feb; 186(3):205-9. PubMed ID: 8453149
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  • 11. Gsα activity is reduced in erythrocyte membranes of patients with psedohypoparathyroidism due to epigenetic alterations at the GNAS locus.
    Zazo C, Thiele S, Martín C, Fernandez-Rebollo E, Martinez-Indart L, Werner R, Garin I, Spanish PHP Group, Hiort O, Perez de Nanclares G.
    J Bone Miner Res; 2011 Aug; 26(8):1864-70. PubMed ID: 21351142
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  • 12. 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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  • 13. Olfactory dysfunction in type I pseudohypoparathyroidism: dissociation from Gs alpha protein deficiency.
    Doty RL, Fernandez AD, Levine MA, Moses A, McKeown DA.
    J Clin Endocrinol Metab; 1997 Jan; 82(1):247-50. PubMed ID: 8989268
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  • 14. Analysis of the GNAS1 gene in Albright's hereditary osteodystrophy.
    Ahrens W, Hiort O, Staedt P, Kirschner T, Marschke C, Kruse K.
    J Clin Endocrinol Metab; 2001 Oct; 86(10):4630-4. PubMed ID: 11600516
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  • 15. Endocrine and molecular biological studies in a German family with Albright hereditary osteodystrophy.
    Schuster V, Eschenhagen T, Kruse K, Gierschik P, Kreth HW.
    Eur J Pediatr; 1993 Mar; 152(3):185-9. PubMed ID: 8444241
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  • 16. Stimulatory guanine nucleotide binding protein activity in the erythrocyte membrane of patients with pseudohypoparathyroidism type I and related disorders.
    Saito T, Akita Y, Fujita H, Furukawa Y, Tsuchiya Y, Yasuda T, Yamamoto M, Kitagawa T, Nakagawa Y, Takehiro A.
    Acta Endocrinol (Copenh); 1986 Apr; 111(4):507-15. PubMed ID: 3010621
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  • 17. Characterization of Albright hereditary osteodystrophy and related disorders.
    Koo BB, Schwindinger WF, Levine MA.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1995 Apr; 36(1):3-13. PubMed ID: 7778442
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  • 18. GNAS locus and pseudohypoparathyroidism.
    Bastepe M, Jüppner H.
    Horm Res; 2005 Apr; 63(2):65-74. PubMed ID: 15711092
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  • 19. Father to son transmission of decreased Ns activity in pseudohypoparathyroidism type Ia.
    Van Dop C, Bourne HR, Neer RM.
    J Clin Endocrinol Metab; 1984 Nov; 59(5):825-8. PubMed ID: 6090498
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  • 20. Mutational analysis of GNAS1 in patients with pseudohypoparathyroidism: identification of two novel mutations.
    Mantovani G, Romoli R, Weber G, Brunelli V, De Menis E, Beccio S, Beck-Peccoz P, Spada A.
    J Clin Endocrinol Metab; 2000 Nov; 85(11):4243-8. PubMed ID: 11095461
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