Skip to content
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文(繁體)
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
語言
全文檢索
題名
作者
主題
索引號
ISBN/ISSN
標簽
檢索
高級檢索
Investigation of troponin I mu...
引用
發送短信
推薦此
打印
導出紀錄
導出到 RefWorks
導出到 EndNoteWeb
導出到 EndNote
Permanent link
Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy
書目詳細資料
Main Authors:
Abdulrazzak, H
,
Knott, A
,
Redwood, C
,
Esposito, G
,
Watkins, H
,
Marston, S
格式:
Journal article
出版:
2001
持有資料
實物特徵
相似書籍
職員瀏覽
實物特徵
總結:
相似書籍
Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
由: Robinson, P, et al.
出版: (2002)
Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.
由: Burton, D, et al.
出版: (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.
由: Robinson, P, et al.
出版: (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.
由: Redwood, C, et al.
出版: (2000)
Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
由: Robinson, P, et al.
出版: (2003)