The nemaline myopathy-causing E117K mutation in β-tropomyosin reduces thin filament activation.

Míreanna comhchosúla

• The E117K mutation in β-tropomyosin disturbs concerted conformational changes of actomyosin in muscle fibers.
  de réir: Karpicheva, O, et al.
  Foilsithe / Cruthaithe: (2014)
• Alteration of beta-tropomyosin function by nernaline myopathy-causing mutations E117K and Q147P
  de réir: Pronina, O, et al.
  Foilsithe / Cruthaithe: (2007)
• Functional investigation of beta-tropomyosin mutations that cause congenital skeletal myopathies
  de réir: Piers, A, et al.
  Foilsithe / Cruthaithe: (2011)
• α‐tropomyosin gene (TPM3) mutation in an infant with nemaline myopathy
  de réir: Sulaiman Almobarak, et al.
  Foilsithe / Cruthaithe: (2021-03-01)
• The effect of the dilated cardiomyopathy-causing mutation Glu54Lys of alpha-tropomyosin on actin-myosin interactions during the ATPase cycle.
  de réir: Borovikov, Y, et al.
  Foilsithe / Cruthaithe: (2009)