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Investigation of troponin I mu...
Čujuhandieđut
Deakstadieđáhus
Sádde šleađgaboasttain
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Doalvvo čujuhusa
Doalvun: RefWorks
Doalvun: EndNoteWeb
Doalvun: EndNote
Bissovaš liŋka
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
Oažžasuvvandieđut
Govvádus
Geahča maid
Bargiidšearbma
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)