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Two mutations in human cardiac...
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Two mutations in human cardiac troponin I known to cause hypertrophic cardiomyopathy have different effects on cardiac muscle contraction
Manylion Llyfryddiaeth
Prif Awduron:
Burton, D
,
Elliot, K
,
Redwood, C
,
Watkins, H
,
Ashley, C
Fformat:
Journal article
Cyhoeddwyd:
2000
Daliadau
Disgrifiad
Eitemau Tebyg
Dangos Staff
Eitemau Tebyg
Effects of hypertrophic cardiomyopathy mutations in troponin I on contractility of skinned cardiac muscle fibres
gan: Burton, D, et al.
Cyhoeddwyd: (2002)
Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.
gan: Burton, D, et al.
Cyhoeddwyd: (2002)
Altered inhibitory and troponin C-binding activities in cardiac troponin I mutants known to cause hypertrophic cardiomyopathy
gan: Elliott, K, et al.
Cyhoeddwyd: (2000)
A troponin I mutant known to cause hypertrophic cardiomyopathy shows reduced inhibition of Ca2+ independent tension
gan: Burton, D, et al.
Cyhoeddwyd: (2000)
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
gan: Robinson, P, et al.
Cyhoeddwyd: (2007)