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Functional investigation of tr...
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Functional investigation of troponin with the homozygous HCM mutation, TNNT2 K280N, obtained from an explanted heart
Manylion Llyfryddiaeth
Prif Awduron:
Bayliss, C
,
Messer, A
,
Leung, M
,
Ward, D
,
Van Der Velden, J
,
Poggesi, C
,
Redwood, C
,
Marston, S
Fformat:
Conference item
Cyhoeddwyd:
2012
Daliadau
Disgrifiad
Eitemau Tebyg
Dangos Staff
Eitemau Tebyg
The HCM-associated cardiac Troponin T mutation K280N causes reduced responsiveness to protein kinase A
gan: Van Der Velden, J, et al.
Cyhoeddwyd: (2012)
The HCM-Associated Cardiac Troponin T Mutation K280N Increases the Energetic Cost of Tension Generation in Human Cardiac Myofibrils
gan: Ferrara, C, et al.
Cyhoeddwyd: (2013)
The effect of HCM mutations in troponin T and troponin I on the calcium binding of human cardiac troponin
gan: Redwood, C, et al.
Cyhoeddwyd: (2001)
Low expression of the K280N TNNT2 mutation is sufficient to increase basal myofilament activation in human hypertrophy cardiomyopathy
gan: Vasco Sequeira, et al.
Cyhoeddwyd: (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
gan: Messer, A, et al.
Cyhoeddwyd: (2016)