Mutant actins that cause congenital myopathy affect sarcomeric protein expression in patient muscle and produce intranuclear and cytoplasmic aggregates in cultured myoblasts

Slični predmeti

• Evidence for a dominant-negative effect in ACTA1 nemaline myopathy caused by abnormal folding, aggregation and altered polymerization of mutant actin isoforms.
  od: Ilkovski, B, i dr.
  Izdano: (2004)
• Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression
  od: Ravenscroft, G, i dr.
  Izdano: (2011)
• Actin nemaline myopathy mouse reproduces disease, suggests other actin disease phenotypes and provides cautionary note on muscle transgene expression.
  od: Ravenscroft, G, i dr.
  Izdano: (2011)
• Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease
  od: Ishiura, Hiroyuki, i dr.
  Izdano: (2019)
• Actin dynamics in the cell cytoplasm and the role of actin associated proteins
  od: McGrath, James L. (James Lionel)
  Izdano: (2010)