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Journal Abstract Search

562 related items for PubMed ID: 30236982

  • 21. Nanoscale remodeling of ryanodine receptor cluster size underlies cerebral microvascular dysfunction in Duchenne muscular dystrophy.
    Pritchard HAT, Pires PW, Yamasaki E, Thakore P, Earley S.
    Proc Natl Acad Sci U S A; 2018 Oct 09; 115(41):E9745-E9752. PubMed ID: 30181262
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  • 22. Exacerbation of dystrophic cardiomyopathy by phospholamban deficiency mediated chronically increased cardiac Ca2+ cycling in vivo.
    Law ML, Prins KW, Olander ME, Metzger JM.
    Am J Physiol Heart Circ Physiol; 2018 Dec 01; 315(6):H1544-H1552. PubMed ID: 30118340
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  • 24. Dual AAV therapy ameliorates exercise-induced muscle injury and functional ischemia in murine models of Duchenne muscular dystrophy.
    Zhang Y, Yue Y, Li L, Hakim CH, Zhang K, Thomas GD, Duan D.
    Hum Mol Genet; 2013 Sep 15; 22(18):3720-9. PubMed ID: 23681067
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  • 25. Reducing sarcolipin expression improves muscle metabolism in mdx mice.
    Balakrishnan R, Mareedu S, Babu GJ.
    Am J Physiol Cell Physiol; 2022 Feb 01; 322(2):C260-C274. PubMed ID: 34986021
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  • 26. Hsp72 preserves muscle function and slows progression of severe muscular dystrophy.
    Gehrig SM, van der Poel C, Sayer TA, Schertzer JD, Henstridge DC, Church JE, Lamon S, Russell AP, Davies KE, Febbraio MA, Lynch GS.
    Nature; 2012 Apr 04; 484(7394):394-8. PubMed ID: 22495301
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  • 28. Proteomic profiling of x-linked muscular dystrophy.
    Lewis C, Carberry S, Ohlendieck K.
    J Muscle Res Cell Motil; 2009 Dec 04; 30(7-8):267-9. PubMed ID: 20082121
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  • 29. Long-term effect of human mini-dystrophin in transgenic mdx mice improves muscle physiological function.
    Chu X, Li J, Qiao C, Wang J, Wang Y, Jiang XC, You H, Xiao X, Wang B.
    FASEB J; 2021 Jun 04; 35(6):e21628. PubMed ID: 33982338
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  • 30. Single SERCA2a Therapy Ameliorated Dilated Cardiomyopathy for 18 Months in a Mouse Model of Duchenne Muscular Dystrophy.
    Wasala NB, Yue Y, Lostal W, Wasala LP, Niranjan N, Hajjar RJ, Babu GJ, Duan D.
    Mol Ther; 2020 Mar 04; 28(3):845-854. PubMed ID: 31981493
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  • 32. The N Terminus of Sarcolipin Plays an Important Role in Uncoupling Sarco-endoplasmic Reticulum Ca2+-ATPase (SERCA) ATP Hydrolysis from Ca2+ Transport.
    Sahoo SK, Shaikh SA, Sopariwala DH, Bal NC, Bruhn DS, Kopec W, Khandelia H, Periasamy M.
    J Biol Chem; 2015 May 29; 290(22):14057-67. PubMed ID: 25882845
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  • 35. Sarcolipin: A Key Thermogenic and Metabolic Regulator in Skeletal Muscle.
    Pant M, Bal NC, Periasamy M.
    Trends Endocrinol Metab; 2016 Dec 29; 27(12):881-892. PubMed ID: 27637585
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  • 36. Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice.
    Burkin DJ, Wallace GQ, Nicol KJ, Kaufman DJ, Kaufman SJ.
    J Cell Biol; 2001 Mar 19; 152(6):1207-18. PubMed ID: 11257121
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  • 37. Expression of a NOS transgene in dystrophin-deficient muscle reduces muscle membrane damage without increasing the expression of membrane-associated cytoskeletal proteins.
    Tidball JG, Wehling-Henricks M.
    Mol Genet Metab; 2004 Aug 19; 82(4):312-20. PubMed ID: 15308129
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  • 38. Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice.
    Ito K, Kimura S, Ozasa S, Matsukura M, Ikezawa M, Yoshioka K, Ueno H, Suzuki M, Araki K, Yamamura K, Miwa T, Dickson G, Thomas GD, Miike T.
    Hum Mol Genet; 2006 Jul 15; 15(14):2266-75. PubMed ID: 16777842
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  • 39. Effect of cyclopiazonic acid, an inhibitor of the sarcoplasmic reticulum Ca-ATPase, on skeletal muscles from normal and mdx mice.
    Divet A, Lompré AM, Huchet-Cadiou C.
    Acta Physiol Scand; 2005 Jul 15; 184(3):173-86. PubMed ID: 15954985
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  • 40. Intracellular calcium handling in ventricular myocytes from mdx mice.
    Williams IA, Allen DG.
    Am J Physiol Heart Circ Physiol; 2007 Feb 15; 292(2):H846-55. PubMed ID: 17012353
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