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Journal Abstract Search

229 related items for PubMed ID: 22205709

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  • 7. Large deletions of the PRKAR1A gene in Carney complex.
    Horvath A, Bossis I, Giatzakis C, Levine E, Weinberg F, Meoli E, Robinson-White A, Siegel J, Soni P, Groussin L, Matyakhina L, Verma S, Remmers E, Nesterova M, Carney JA, Bertherat J, Stratakis CA.
    Clin Cancer Res; 2008 Jan 15; 14(2):388-95. PubMed ID: 18223213
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  • 10. In vitro functional studies of naturally occurring pathogenic PRKAR1A mutations that are not subject to nonsense mRNA decay.
    Greene EL, Horvath AD, Nesterova M, Giatzakis C, Bossis I, Stratakis CA.
    Hum Mutat; 2008 May 15; 29(5):633-9. PubMed ID: 18241045
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  • 13. A novel splice site mutation of the PRKAR1A gene, C.440+5 G>C, in a Chinese family with Carney complex.
    Fu J, Lai F, Chen Y, Wan X, Wei G, Li Y, Xiao H, Cao X.
    J Endocrinol Invest; 2018 Aug 15; 41(8):909-917. PubMed ID: 29318463
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  • 16. Identification of a novel mutation of the PRKAR1A gene in a patient with Carney complex with significant osteoporosis and recurrent fractures.
    Papanastasiou L, Fountoulakis S, Voulgaris N, Kounadi T, Choreftaki T, Kostopoulou A, Zografos G, Lyssikatos C, Stratakis CA, Piaditis G.
    Hormones (Athens); 2016 Aug 15; 15(1):129-35. PubMed ID: 27377598
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  • 17. Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the carney complex.
    Kirschner LS, Sandrini F, Monbo J, Lin JP, Carney JA, Stratakis CA.
    Hum Mol Genet; 2000 Dec 12; 9(20):3037-46. PubMed ID: 11115848
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  • 19. PRKAR1A mutations in primary pigmented nodular adrenocortical disease.
    Cazabat L, Ragazzon B, Groussin L, Bertherat J.
    Pituitary; 2006 Dec 12; 9(3):211-9. PubMed ID: 17036196
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