Mutant actins that cause congenital myopathy affect sarcomeric protein expression in patient muscle and produce intranuclear and cytoplasmic aggregates in cultured myoblasts
Main Authors: | Ilkovski, B, Nowak, K, Domazetovska, A, Maxwell, A, Clement, S, Davies, K, Laing, N, North, K, Cooper, S |
---|---|
Format: | Conference item |
Published: |
2004
|
Similar Items
-
Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms.
by: Ilkovski, B, et al.
Published: (2004) -
Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression
by: Ravenscroft, G, et al.
Published: (2011) -
Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression.
by: Ravenscroft, G, et al.
Published: (2011) -
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease
by: Ishiura, Hiroyuki, et al.
Published: (2019) -
Actin dynamics in the cell cytoplasm and the role of actin associated proteins
by: McGrath, James L. (James Lionel)
Published: (2010)