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Journal Abstract Search

143 related items for PubMed ID: 16021918

  • 21. Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?
    Pérez M, Martin MA, Cañete S, Rubio JC, Fernández-Moreira D, San Juan AF, Gómez-Gallego F, Santiago C, Arenas J, Lucia A.
    Int J Sports Med; 2006 Jun; 27(6):429-35. PubMed ID: 16767606
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  • 22. Associations between cardiorespiratory responses to exercise and the C34T AMPD1 gene polymorphism in the HERITAGE Family Study.
    Rico-Sanz J, Rankinen T, Joanisse DR, Leon AS, Skinner JS, Wilmore JH, Rao DC, Bouchard C, HERITAGE Family study.
    Physiol Genomics; 2003 Jul 07; 14(2):161-6. PubMed ID: 12783984
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  • 23. Subunit composition of AMPD varies in response to changes in AMPD1 and AMPD3 gene expression in skeletal muscle.
    Fortuin FD, Morisaki T, Holmes EW.
    Proc Assoc Am Physicians; 1996 Jul 07; 108(4):329-33. PubMed ID: 8863347
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  • 24. Effects of AMPD1 common mutation on the metabolic-chronotropic relationship: Insights from patients with myoadenylate deaminase deficiency.
    Rannou F, Scotet V, Marcorelles P, Monnoyer R, Le Maréchal C.
    PLoS One; 2017 Jul 07; 12(11):e0187266. PubMed ID: 29095874
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  • 25. [Effect of neurohormone "C" on adenine nucleotide and adenosine metabolism in rat heart and brain].
    Galoian AA, Guvrits BIa, Galstian RG.
    Vopr Biokhim Mozga; 1976 Jul 07; 11():197-207. PubMed ID: 1032220
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  • 26. AMPD1 gene mutation in congestive heart failure: new insights into the pathobiology of disease progression.
    Feldman AM, Wagner DR, McNamara DM.
    Circulation; 1999 Mar 23; 99(11):1397-9. PubMed ID: 10086958
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  • 32. First missense mutations (R388W and R425H) of AMPD1 accompanied with myopathy found in a Japanese patient.
    Morisaki H, Higuchi I, Abe M, Osame M, Morisaki T.
    Hum Mutat; 2000 Dec 23; 16(6):467-72. PubMed ID: 11102975
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  • 34. [Molecular cloning and mutation site analysis of AMPD1 gene in swine].
    Liu H, Xu Y, Zhao LL, Yang XQ, Liu D.
    Yi Chuan; 2008 Feb 23; 30(2):175-8. PubMed ID: 18244922
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  • 35. C34T mutation of the AMPD1 gene in an elite white runner.
    Lucia A, Martin MA, Esteve-Lanao J, San Juan AF, Rubio JC, Oliván J, Arenas J.
    Br J Sports Med; 2006 Mar 23; 40(3):e7. PubMed ID: 16505069
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  • 36. Effect of AMP-deaminase 3 knock-out in mice on enzyme activity in heart and other organs.
    Rybakowska I, Romaszko P, Zabielska M, Turyn J, Kaletha K, Barton PJ, Slominska EM, Smolenski RT.
    Nucleosides Nucleotides Nucleic Acids; 2014 Mar 23; 33(4-6):319-22. PubMed ID: 24940686
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  • 40. Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene.
    Isackson PJ, Bujnicki H, Harding CO, Vladutiu GD.
    Mol Genet Metab; 2005 Mar 23; 86(1-2):250-6. PubMed ID: 16040263
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