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Journal Abstract Search

208 related items for PubMed ID: 23784376

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  • 3. Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations.
    Agrawal PB, Strickland CD, Midgett C, Morales A, Newburger DE, Poulos MA, Tomczak KK, Ryan MM, Iannaccone ST, Crawford TO, Laing NG, Beggs AH.
    Ann Neurol; 2004 Jul; 56(1):86-96. PubMed ID: 15236405
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  • 4. Rescue of skeletal muscle alpha-actin-null mice by cardiac (fetal) alpha-actin.
    Nowak KJ, Ravenscroft G, Jackaman C, Filipovska A, Davies SM, Lim EM, Squire SE, Potter AC, Baker E, Clément S, Sewry CA, Fabian V, Crawford K, Lessard JL, Griffiths LM, Papadimitriou JM, Shen Y, Morahan G, Bakker AJ, Davies KE, Laing NG.
    J Cell Biol; 2009 Jun 01; 185(5):903-15. PubMed ID: 19468071
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  • 7. Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms.
    Nowak KJ, Ravenscroft G, Laing NG.
    Acta Neuropathol; 2013 Jan 01; 125(1):19-32. PubMed ID: 22825594
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  • 8. Sexually dimorphic myofilament function in a mouse model of nemaline myopathy.
    Lindqvist J, Hardeman EC, Ochala J.
    Arch Biochem Biophys; 2014 Dec 15; 564():37-42. PubMed ID: 25261348
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  • 9. A myopathy-related actin mutation increases contractile function.
    Lindqvist J, Pénisson-Besnier I, Iwamoto H, Li M, Yagi N, Ochala J.
    Acta Neuropathol; 2012 May 15; 123(5):739-46. PubMed ID: 22358459
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  • 11. Nemaline myopathy caused by absence of alpha-skeletal muscle actin.
    Nowak KJ, Sewry CA, Navarro C, Squier W, Reina C, Ricoy JR, Jayawant SS, Childs AM, Dobbie JA, Appleton RE, Mountford RC, Walker KR, Clement S, Barois A, Muntoni F, Romero NB, Laing NG.
    Ann Neurol; 2007 Feb 15; 61(2):175-84. PubMed ID: 17187373
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  • 13. Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene.
    Ilkovski B, Cooper ST, Nowak K, Ryan MM, Yang N, Schnell C, Durling HJ, Roddick LG, Wilkinson I, Kornberg AJ, Collins KJ, Wallace G, Gunning P, Hardeman EC, Laing NG, North KN.
    Am J Hum Genet; 2001 Jun 15; 68(6):1333-43. PubMed ID: 11333380
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