A mouse model of familial hypertrophic cardiomyopathy caused by a alpha-tropomyosin mutation.
about
Mitral valve disease--morphology and mechanisms.Understanding cardiomyopathy phenotypes based on the functional impact of mutations in the myosin motorTropomyosin de-phosphorylation in the heart: what are the consequences?Aetiology-specific patterns in end-stage heart failure patients identified by functional annotation and classification of microarray data.Investigations into tropomyosin function using mouse modelsNeonatal gene transfer of Serca2a delays onset of hypertrophic remodeling and improves function in familial hypertrophic cardiomyopathy.Cardiac-specific over-expression of epidermal growth factor receptor 2 (ErbB2) induces pro-survival pathways and hypertrophic cardiomyopathy in mice.Functional effects of a tropomyosin mutation linked to FHC contribute to maladaptation during acidosisTropomyosin-based regulation of the actin cytoskeleton in time and space.Long-term rescue of a familial hypertrophic cardiomyopathy caused by a mutation in the thin filament protein, tropomyosin, via modulation of a calcium cycling protein.Facilitated cross-bridge interactions with thin filaments by familial hypertrophic cardiomyopathy mutations in α-tropomyosin.Developmental basis of adult cardiovascular diseases: valvular heart diseases.Cell-intrinsic functional effects of the α-cardiac myosin Arg-403-Gln mutation in familial hypertrophic cardiomyopathy.Microarray analysis of active cardiac remodeling genes in a familial hypertrophic cardiomyopathy mouse model rescued by a phospholamban knockout.Decreasing tropomyosin phosphorylation rescues tropomyosin-induced familial hypertrophic cardiomyopathyAn internal domain of beta-tropomyosin increases myofilament Ca(2+) sensitivityDesigning heart performance by gene transfer.The mitral valve in hypertrophic cardiomyopathy: old versus new concepts.A study of tropomyosin's role in cardiac function and disease using thin-filament reconstituted myocardium.Nuclear tropomyosin and troponin in striated muscle: new roles in a new locale?Long-range effects of familial hypertrophic cardiomyopathy mutations E180G and D175N on the properties of tropomyosinHuman muscle-specific A-kinase anchoring protein (mAKAP) polymorphisms modulate the susceptibility to cardiovascular diseases by altering cAMP/ PKA signaling.
P2860
Q26781699-A6AD46A2-9A64-4338-9B68-7A58596E7FF9Q26996693-41793F4E-E39B-4EC6-9D22-EBEF67D56E14Q28293301-AABEF7E9-3807-46CF-B6F6-AC3C154397DAQ31043414-74AD5D7D-CF54-4916-89DD-AE65E709D138Q33854803-B7A1E003-9A21-4823-9FB8-FD9C9FE09380Q34313853-29660C71-85D3-4328-8613-B6DC5045D1C1Q34388932-B0E26B3D-1200-451F-AC29-62E5FD654119Q34561038-ED8A107F-80D1-4212-A6C6-437D4F38E6C0Q34736000-92010790-32EA-4FC4-A6F1-023696B0141FQ35565337-65BEC27E-8AF1-4E46-AAFE-1ACE8EA3F4AEQ35610475-9109ADFE-DFEF-438E-9277-4A3E32692131Q36021395-6759F4F2-11A2-455C-B930-377CA000CDC2Q36045425-A7E702DD-A5FF-420B-8451-0A0DE1F588DBQ37147195-92E1BFA0-DAA3-4884-9A6F-BA63511EDB06Q37213860-4EE092A2-D05D-4BA0-91F5-AF3C0B51BCE6Q37264422-6854F42D-C9A5-4F48-9A7F-B361739216AFQ37299072-E30B53B0-4A7E-4623-A79C-B879ED933A1DQ37930477-0D95C47A-1D17-44DA-A735-A7F963A32A5DQ38108764-413BC17D-5E98-414B-8CDF-64DF3EC2A52EQ38125907-012B5E3C-377B-4803-B90C-43D55AD99DB5Q42173536-72D0D942-6A40-4FE4-B82E-AB505B16E8CCQ54981509-D1DC7C9D-0B54-48E2-A76C-AE784CEF07CC
P2860
A mouse model of familial hypertrophic cardiomyopathy caused by a alpha-tropomyosin mutation.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
A mouse model of familial hype ...... a alpha-tropomyosin mutation.
@en
A mouse model of familial hype ...... a alpha-tropomyosin mutation.
@nl
type
label
A mouse model of familial hype ...... a alpha-tropomyosin mutation.
@en
A mouse model of familial hype ...... a alpha-tropomyosin mutation.
@nl
prefLabel
A mouse model of familial hype ...... a alpha-tropomyosin mutation.
@en
A mouse model of familial hype ...... a alpha-tropomyosin mutation.
@nl
P2093
P356
P1476
A mouse model of familial hype ...... a alpha-tropomyosin mutation.
@en
P2093
Arnold Schwartz
David F Wieczorek
Greg P Boivin
Natalia Petrashevskaya
Rethinasamy Prabhakar
P2888
P356
10.1023/A:1025409227350
P577
2003-09-01T00:00:00Z
P6179
1029493969