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Aiddostahtton
  • Investigation of troponin I mu...
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  • Bissovaš liŋka
Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy

Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy

Bibliográfalaš dieđut
Váldodahkkit: Abdulrazzak, H, Knott, A, Redwood, C, Esposito, G, Watkins, H, Marston, S
Materiálatiipa: Journal article
Almmustuhtton: 2001
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Geahča maid

  • Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
    Dahkki: Robinson, P, et al.
    Almmustuhtton: (2002)
  • Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.
    Dahkki: Burton, D, et al.
    Almmustuhtton: (2002)
  • Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy.
    Dahkki: Robinson, P, et al.
    Almmustuhtton: (2002)
  • Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein.
    Dahkki: Redwood, C, et al.
    Almmustuhtton: (2000)
  • Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
    Dahkki: Robinson, P, et al.
    Almmustuhtton: (2003)

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