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Functional investigation of troponin with the homozygous HCM mutation, TNNT2 K280N, obtained from an explanted heart

Functional investigation of troponin with the homozygous HCM mutation, TNNT2 K280N, obtained from an explanted heart

Detalhes bibliográficos
Main Authors: Bayliss, C, Messer, A, Leung, M, Ward, D, Van Der Velden, J, Poggesi, C, Redwood, C, Marston, S
Formato: Conference item
Publicado em: 2012
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Registos relacionados

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    Por: Ferrara, C, et al.
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  • The effect of HCM mutations in troponin T and troponin I on the calcium binding of human cardiac troponin
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  • Low expression of the K280N TNNT2 mutation is sufficient to increase basal myofilament activation in human hypertrophy cardiomyopathy
    Por: Vasco Sequeira, et al.
    Publicado em: (2022-09-01)
  • Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylation
    Por: Messer, A, et al.
    Publicado em: (2016)

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