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Items: 8


Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function.

Sztal TE, Zhao M, Williams C, Oorschot V, Parslow AC, Giousoh A, Yuen M, Hall TE, Costin A, Ramm G, Bird PI, Busch-Nentwich EM, Stemple DL, Currie PD, Cooper ST, Laing NG, Nowak KJ, Bryson-Richardson RJ.

Acta Neuropathol. 2015 Sep;130(3):389-406. doi: 10.1007/s00401-015-1430-3. Epub 2015 May 1.


Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression.

Ravenscroft G, Jackaman C, Sewry CA, McNamara E, Squire SE, Potter AC, Papadimitriou J, Griffiths LM, Bakker AJ, Davies KE, Laing NG, Nowak KJ.

PLoS One. 2011;6(12):e28699. doi: 10.1371/journal.pone.0028699. Epub 2011 Dec 9.


Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.

Moraczewska J, Greenfield NJ, Liu Y, Hitchcock-DeGregori SE.

Biophys J. 2000 Dec;79(6):3217-25.


Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.

North KN, Laing NG, Wallgren-Pettersson C.

J Med Genet. 1997 Sep;34(9):705-13. Review. No abstract available. Erratum in: J Med Genet 1997 Oct;34(10):879.


Exclusion of two candidate loci for autosomal recessive nemaline myopathy.

Tahvanainen E, Beggs AH, Wallgren-Pettersson C.

J Med Genet. 1994 Jan;31(1):79-80.


Evidence for actin involvement in cardiac Z-lines and Z-line analogues.

Yamaguchi M, Robson RM, Stromer MH.

J Cell Biol. 1983 Feb;96(2):435-42.


The role of cytoskeletal and cytocontractile elements in pathologic processes.

Rungger-Brändle E, Gabbiani G.

Am J Pathol. 1983 Mar;110(3):361-92. Review. No abstract available.

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