-
1
-
-
0032076955
-
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
-
Olson T.M., Michels V.V., Thibodeau S.N., Tai Y.S., Keating M.T. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 1998, 280:750-752.
-
(1998)
Science
, vol.280
, pp. 750-752
-
-
Olson, T.M.1
Michels, V.V.2
Thibodeau, S.N.3
Tai, Y.S.4
Keating, M.T.5
-
2
-
-
8144224216
-
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy
-
Mogensen J., Murphy R.T., Shaw T., Bahl A., Redwood C., Watkins H., et al. Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy. J Am Coll Cardiol 2004, 44:2033-2040.
-
(2004)
J Am Coll Cardiol
, vol.44
, pp. 2033-2040
-
-
Mogensen, J.1
Murphy, R.T.2
Shaw, T.3
Bahl, A.4
Redwood, C.5
Watkins, H.6
-
3
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
Kamisago M., Sharma S.D., DePalma S.R., Solomon S., Sharma P., Smoot L., et al. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. N Engl J Med 2000, 343:1688-1696.
-
(2000)
N Engl J Med
, vol.343
, pp. 1688-1696
-
-
Kamisago, M.1
Sharma, S.D.2
DePalma, S.R.3
Solomon, S.4
Sharma, P.5
Smoot, L.6
-
4
-
-
30944435503
-
Sarcomeric protein mutations in dilated cardiomyopathy
-
Chang A.N., Potter J.D. Sarcomeric protein mutations in dilated cardiomyopathy. Heart Fail Rev 2005, 10:225-235.
-
(2005)
Heart Fail Rev
, vol.10
, pp. 225-235
-
-
Chang, A.N.1
Potter, J.D.2
-
5
-
-
0037174918
-
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
-
Robinson P., Mirza M., Knott A., Abdulrazzak H., Willott R., Marston S., et al. 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. J Biol Chem 2002, 277:40710-40716.
-
(2002)
J Biol Chem
, vol.277
, pp. 40710-40716
-
-
Robinson, P.1
Mirza, M.2
Knott, A.3
Abdulrazzak, H.4
Willott, R.5
Marston, S.6
-
6
-
-
23344452467
-
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype
-
Mirza M., Marston S., Willott R., Ashley C., Mogensen J., McKenna W., et al. Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype. J Biol Chem 2005, 280:28498-28506.
-
(2005)
J Biol Chem
, vol.280
, pp. 28498-28506
-
-
Mirza, M.1
Marston, S.2
Willott, R.3
Ashley, C.4
Mogensen, J.5
McKenna, W.6
-
7
-
-
34250322240
-
The effect of mutations in alpha tropomyosin (E40K and E54K), that cause familial dilated cardiomyopathy, on the regulatory mechanism of cardiac muscle thin filaments
-
Mirza M., Robinson P., Kremneva E., Copeland O., Nikolaeva O., Watkins H., et al. The effect of mutations in alpha tropomyosin (E40K and E54K), that cause familial dilated cardiomyopathy, on the regulatory mechanism of cardiac muscle thin filaments. J Biol Chem 2007, 282:13487-13497.
-
(2007)
J Biol Chem
, vol.282
, pp. 13487-13497
-
-
Mirza, M.1
Robinson, P.2
Kremneva, E.3
Copeland, O.4
Nikolaeva, O.5
Watkins, H.6
-
8
-
-
37349042936
-
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments
-
Robinson P., Griffiths P.J., Watkins H., Redwood C.S. Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments. Circ Res 2007, 101:1266-1273.
-
(2007)
Circ Res
, vol.101
, pp. 1266-1273
-
-
Robinson, P.1
Griffiths, P.J.2
Watkins, H.3
Redwood, C.S.4
-
9
-
-
70349250125
-
Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy
-
Carballo S., Robinson P., Otway R., Fatkin D., Jongbloed J.D., de Jonge N., et al. Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy. Circ Res 2009, 105:375-382.
-
(2009)
Circ Res
, vol.105
, pp. 375-382
-
-
Carballo, S.1
Robinson, P.2
Otway, R.3
Fatkin, D.4
Jongbloed, J.D.5
de Jonge, N.6
-
10
-
-
0142180165
-
Different functional properties of Troponin T mutants that cause dilated cardiomyopathy
-
Venkatraman G., Harada K., Gomes A.V., Kerrick G.W., Potter J.D. Different functional properties of Troponin T mutants that cause dilated cardiomyopathy. J Biol Chem 2003, 278:41670-41676.
-
(2003)
J Biol Chem
, vol.278
, pp. 41670-41676
-
-
Venkatraman, G.1
Harada, K.2
Gomes, A.V.3
Kerrick, G.W.4
Potter, J.D.5
-
11
-
-
26644464382
-
Functional consequences of hypertrophic and dilated cardiomyopathy-causing mutations in alpha-tropomyosin
-
Chang A.N., Harada K., Ackerman M.J., Potter J.D. Functional consequences of hypertrophic and dilated cardiomyopathy-causing mutations in alpha-tropomyosin. J Biol Chem 2005, 280:34343-34349.
-
(2005)
J Biol Chem
, vol.280
, pp. 34343-34349
-
-
Chang, A.N.1
Harada, K.2
Ackerman, M.J.3
Potter, J.D.4
-
12
-
-
0037154179
-
Ca2+-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy
-
Morimoto S., Lu Qw., Harada K., Takahashi-Yanaga F., Minakami R., Ohta M., et al. Ca2+-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy. Proc Natl Acad Sci 2002, 99:913-918.
-
(2002)
Proc Natl Acad Sci
, vol.99
, pp. 913-918
-
-
Morimoto, S.1
Lu, Q.2
Harada, K.3
Takahashi-Yanaga, F.4
Minakami, R.5
Ohta, M.6
-
13
-
-
0344924880
-
Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca(2+) desensitization
-
Lu Q.W., Morimoto S., Harada K., Du C.K., Takahashi-Yanaga F., Miwa Y., et al. Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca(2+) desensitization. J Mol Cell Cardiol 2003, 35:1421-1427.
-
(2003)
J Mol Cell Cardiol
, vol.35
, pp. 1421-1427
-
-
Lu, Q.W.1
Morimoto, S.2
Harada, K.3
Du, C.K.4
Takahashi-Yanaga, F.5
Miwa, Y.6
-
14
-
-
0034971165
-
Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy
-
Olson T.M., Kishimoto N.Y., Whitby F.G., Michels V.V. Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy. J Mol Cell Cardiol 2001, 33:723-732.
-
(2001)
J Mol Cell Cardiol
, vol.33
, pp. 723-732
-
-
Olson, T.M.1
Kishimoto, N.Y.2
Whitby, F.G.3
Michels, V.V.4
-
15
-
-
0037373133
-
Alpha-actin isoform distribution in normal and failing human heart: a morphological, morphometric, and biochemical study
-
Suurmeijer A.J., Clement S., Francesconi A., Bocchi L., Angelini A., Van Veldhuisen D.J., et al. Alpha-actin isoform distribution in normal and failing human heart: a morphological, morphometric, and biochemical study. J Pathol 2003, 199:387-397.
-
(2003)
J Pathol
, vol.199
, pp. 387-397
-
-
Suurmeijer, A.J.1
Clement, S.2
Francesconi, A.3
Bocchi, L.4
Angelini, A.5
Van Veldhuisen, D.J.6
-
16
-
-
77955303601
-
Quantitative assay of skeletal α-actin expression in normal and pathological human and mouse hearts
-
Copeland O., Nowak K.J., Laing N.G., Ravenscroft G., Marston S. Quantitative assay of skeletal α-actin expression in normal and pathological human and mouse hearts. Biophys J 2009, 96:499a.
-
(2009)
Biophys J
, vol.96
-
-
Copeland, O.1
Nowak, K.J.2
Laing, N.G.3
Ravenscroft, G.4
Marston, S.5
-
17
-
-
18244383309
-
Transgenic overexpression of cardiac actin in the mouse heart suggests coregulation of cardiac, skeletal and vascular actin expression
-
Kumar A., Crawford K., Flick R., Klevitsky R., Lorenz J.N., Bove K.E., et al. Transgenic overexpression of cardiac actin in the mouse heart suggests coregulation of cardiac, skeletal and vascular actin expression. Transgenic Res 2004, 13:531-540.
-
(2004)
Transgenic Res
, vol.13
, pp. 531-540
-
-
Kumar, A.1
Crawford, K.2
Flick, R.3
Klevitsky, R.4
Lorenz, J.N.5
Bove, K.E.6
-
18
-
-
58149288067
-
Are transgenic mice the 'Älkahest' to understanding myocardial hypertrophy and failure?
-
Cook S., Clerk A., Sugden P. Are transgenic mice the 'Älkahest' to understanding myocardial hypertrophy and failure?. J Mol Cell Cardiol 2008, 46:118-129.
-
(2008)
J Mol Cell Cardiol
, vol.46
, pp. 118-129
-
-
Cook, S.1
Clerk, A.2
Sugden, P.3
-
19
-
-
58149305990
-
With great power comes great responsibility: using mouse genetics to study cardiac hypertrophy and failure
-
Molkentin J.D., Robbins J. With great power comes great responsibility: using mouse genetics to study cardiac hypertrophy and failure. J Mol Cell Cardiol 2008, 46:130-136.
-
(2008)
J Mol Cell Cardiol
, vol.46
, pp. 130-136
-
-
Molkentin, J.D.1
Robbins, J.2
-
20
-
-
34547610522
-
Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation
-
Du C.K., Morimoto S., Nishii K., Minakami R., Ohta M., Tadano N., et al. Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation. Circ Res 2007, 101:185-194.
-
(2007)
Circ Res
, vol.101
, pp. 185-194
-
-
Du, C.K.1
Morimoto, S.2
Nishii, K.3
Minakami, R.4
Ohta, M.5
Tadano, N.6
-
21
-
-
0034625768
-
Investigation of a truncated troponin T that causes familial hypertrophic cardiomyopathy: Ca2+ regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type peptide
-
Redwood C., Lohmann K., Bing W., Esoposito G., Elliott K., Abdulrazzak H., et al. Investigation of a truncated troponin T that causes familial hypertrophic cardiomyopathy: Ca2+ regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type peptide. Circ Res 2000, 86:1146-1152.
-
(2000)
Circ Res
, vol.86
, pp. 1146-1152
-
-
Redwood, C.1
Lohmann, K.2
Bing, W.3
Esoposito, G.4
Elliott, K.5
Abdulrazzak, H.6
-
22
-
-
34547605959
-
Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity
-
Rajan S., Ahmed R.P., Jagatheesan G., Petrashevskaya N., Boivin G.P., Urboniene D., et al. Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity. Circ Res 2007, 101:205-214.
-
(2007)
Circ Res
, vol.101
, pp. 205-214
-
-
Rajan, S.1
Ahmed, R.P.2
Jagatheesan, G.3
Petrashevskaya, N.4
Boivin, G.P.5
Urboniene, D.6
-
23
-
-
33646397564
-
Characterization of the role of gamma2 R531G mutation in AMP-activated protein kinase in cardiac hypertrophy and Wolff-Parkinson-White syndrome
-
Davies J.K., Wells D.J., Liu K., Whitrow H.R., Daniel T.D., Grignani R., et al. Characterization of the role of gamma2 R531G mutation in AMP-activated protein kinase in cardiac hypertrophy and Wolff-Parkinson-White syndrome. Am J Physiol Heart Circ Physiol 2006, 290:H1942-H1951.
-
(2006)
Am J Physiol Heart Circ Physiol
, vol.290
-
-
Davies, J.K.1
Wells, D.J.2
Liu, K.3
Whitrow, H.R.4
Daniel, T.D.5
Grignani, R.6
-
24
-
-
51449091614
-
Novel MRI method to detect altered left ventricular ejection and filling patterns in rodent models of disease
-
Stuckey D., Carr C., Tyler D.J., Aasum E., Clarke K. Novel MRI method to detect altered left ventricular ejection and filling patterns in rodent models of disease. Magn Reson Med 2008, 60:582-587.
-
(2008)
Magn Reson Med
, vol.60
, pp. 582-587
-
-
Stuckey, D.1
Carr, C.2
Tyler, D.J.3
Aasum, E.4
Clarke, K.5
-
25
-
-
0037120941
-
Left ventricular pressure-volume relationship in a murine model of congestive heart failure due to acute viral myocarditis
-
Nishio R., Sasayama S., Matsumori A. Left ventricular pressure-volume relationship in a murine model of congestive heart failure due to acute viral myocarditis. J Am Coll Cardiol 2002, 40:1506-1514.
-
(2002)
J Am Coll Cardiol
, vol.40
, pp. 1506-1514
-
-
Nishio, R.1
Sasayama, S.2
Matsumori, A.3
-
26
-
-
0028860791
-
Reduced contraction and altered frequency response of isolated ventricular myocytes from patients with heart failure
-
Davies C.H., Davia K., Bennett J.G., Pepper J.R., Poole-Wilson P.A., Harding S.E. Reduced contraction and altered frequency response of isolated ventricular myocytes from patients with heart failure. Circulation 1995, 92:2540-2549.
-
(1995)
Circulation
, vol.92
, pp. 2540-2549
-
-
Davies, C.H.1
Davia, K.2
Bennett, J.G.3
Pepper, J.R.4
Poole-Wilson, P.A.5
Harding, S.E.6
-
27
-
-
3042621438
-
Differential cross-bridge kinetics of FHC myosin mutations R403Q and R453C in heterozygous mouse myocardium
-
Palmer B.M., Fishbaugher D.E., Schmitt J.P., Wang Y., Alpert N.R., Seidman C.E., et al. Differential cross-bridge kinetics of FHC myosin mutations R403Q and R453C in heterozygous mouse myocardium. Am J Physiol Heart Circ Physiol 2004, 287:H91-H99.
-
(2004)
Am J Physiol Heart Circ Physiol
, vol.287
-
-
Palmer, B.M.1
Fishbaugher, D.E.2
Schmitt, J.P.3
Wang, Y.4
Alpert, N.R.5
Seidman, C.E.6
-
28
-
-
77951074751
-
The use of phosphate-affinity SDS-PAGE to measure the troponin I phosphorylation site distribution in human heart muscle
-
Messer A., Gallon C., McKenna W., Elliott P., Dos Remedios C., Marston S. The use of phosphate-affinity SDS-PAGE to measure the troponin I phosphorylation site distribution in human heart muscle. Proteomics Clin Appl 2009, 3:1371-1382.
-
(2009)
Proteomics Clin Appl
, vol.3
, pp. 1371-1382
-
-
Messer, A.1
Gallon, C.2
McKenna, W.3
Elliott, P.4
Dos Remedios, C.5
Marston, S.6
-
29
-
-
33845778948
-
Troponin phosphorylation and regulatory function in human heart muscle: dephosphorylation of Ser23/24 on troponin I could account for the contractile defect in end-stage heart failure
-
Messer A.E., Jacques A.M., Marston S.B. Troponin phosphorylation and regulatory function in human heart muscle: dephosphorylation of Ser23/24 on troponin I could account for the contractile defect in end-stage heart failure. J Mol Cell Cardiol 2007, 42:247-259.
-
(2007)
J Mol Cell Cardiol
, vol.42
, pp. 247-259
-
-
Messer, A.E.1
Jacques, A.M.2
Marston, S.B.3
-
30
-
-
70350448975
-
Functional analysis of a unique troponin c mutation, Gly159Asp that causes familial dilated cardiomyopathy, studied in explanted heart muscle
-
Dyer E., Jacques A., Hoskins A., Ward D., Gallon C., Messer A., et al. Functional analysis of a unique troponin c mutation, Gly159Asp that causes familial dilated cardiomyopathy, studied in explanted heart muscle. Circulation: Heart Failure 2009, 2:456-464.
-
(2009)
Circulation: Heart Failure
, vol.2
, pp. 456-464
-
-
Dyer, E.1
Jacques, A.2
Hoskins, A.3
Ward, D.4
Gallon, C.5
Messer, A.6
-
31
-
-
33644651640
-
Direct comparison of magnetic resonance imaging and conductance microcatheter in the evaluation of left ventricular function in mice
-
Jacoby C., Molojavyi A., Flögel U., Merx M.W., Ding Z., Schrader J. Direct comparison of magnetic resonance imaging and conductance microcatheter in the evaluation of left ventricular function in mice. Basic Res Cardiol 2006, 101:87-95.
-
(2006)
Basic Res Cardiol
, vol.101
, pp. 87-95
-
-
Jacoby, C.1
Molojavyi, A.2
Flögel, U.3
Merx, M.W.4
Ding, Z.5
Schrader, J.6
-
32
-
-
0022974690
-
Simultaneous expression of skeletal muscle and heart actin proteins in various striated muscle tissues and cells. A quantitative determination of the two actin isoforms
-
Vandekerckhove J., Bugaisky G., Buckingham M. Simultaneous expression of skeletal muscle and heart actin proteins in various striated muscle tissues and cells. A quantitative determination of the two actin isoforms. J Biol Chem 1986, 261:1838-1843.
-
(1986)
J Biol Chem
, vol.261
, pp. 1838-1843
-
-
Vandekerckhove, J.1
Bugaisky, G.2
Buckingham, M.3
-
33
-
-
0025276543
-
Genetic analysis of the interaction between cardiac and skeletal actin gene expression in striated muscle of the mouse
-
Alonso S., Garner I., Vandekerckhove J., Buckingham M. Genetic analysis of the interaction between cardiac and skeletal actin gene expression in striated muscle of the mouse. J Mol Biol 1990, 211:727-738.
-
(1990)
J Mol Biol
, vol.211
, pp. 727-738
-
-
Alonso, S.1
Garner, I.2
Vandekerckhove, J.3
Buckingham, M.4
-
34
-
-
0032716168
-
Variability in the ratio of mutant to wildtype myosin heavy chain present in the soleus muscle of patients with familial hypertrophic cardiomyopathy. A new approach for the quantification of mutant to wildtype protein
-
Nier V., Schultz I., Brenner B., Forssmann W., Raida M. Variability in the ratio of mutant to wildtype myosin heavy chain present in the soleus muscle of patients with familial hypertrophic cardiomyopathy. A new approach for the quantification of mutant to wildtype protein. FEBS Lett 1999, 461:246-252.
-
(1999)
FEBS Lett
, vol.461
, pp. 246-252
-
-
Nier, V.1
Schultz, I.2
Brenner, B.3
Forssmann, W.4
Raida, M.5
-
35
-
-
0031883848
-
A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity
-
Bottinelli R., Coviello D.A., Redwood C.S., Pellegrino M.A., Maron B.J., Spirito P., et al. A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity. Circ Res 1998, 82:106-115.
-
(1998)
Circ Res
, vol.82
, pp. 106-115
-
-
Bottinelli, R.1
Coviello, D.A.2
Redwood, C.S.3
Pellegrino, M.A.4
Maron, B.J.5
Spirito, P.6
-
36
-
-
34447502553
-
The pathogenesis of ACTA1-related congenital fiber type disproportion
-
Clarke N.F., Ilkovski B., Cooper S., Valova V.A., Robinson P.J., Nonaka I., et al. The pathogenesis of ACTA1-related congenital fiber type disproportion. Ann Neurol 2007, 61:552-561.
-
(2007)
Ann Neurol
, vol.61
, pp. 552-561
-
-
Clarke, N.F.1
Ilkovski, B.2
Cooper, S.3
Valova, V.A.4
Robinson, P.J.5
Nonaka, I.6
-
37
-
-
33748529918
-
Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation
-
D'Amico A., Graziano C., Pacileo G., Petrini S., Nowak K.J., Boldrini R., et al. Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation. Neuromuscul Disord 2006, 16:548-552.
-
(2006)
Neuromuscul Disord
, vol.16
, pp. 548-552
-
-
D'Amico, A.1
Graziano, C.2
Pacileo, G.3
Petrini, S.4
Nowak, K.J.5
Boldrini, R.6
-
38
-
-
0034698086
-
Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy
-
Elliott K., Watkins H., Redwood C.S. Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy. J Biol Chem 2000, 275:22069-22074.
-
(2000)
J Biol Chem
, vol.275
, pp. 22069-22074
-
-
Elliott, K.1
Watkins, H.2
Redwood, C.S.3
-
39
-
-
0025174179
-
Calcium binds cooperatively to the regulatory sites of the cardiac thin filament
-
Tobacman L., Sawyer D. Calcium binds cooperatively to the regulatory sites of the cardiac thin filament. J Biol Chem 1990, 265:931-939.
-
(1990)
J Biol Chem
, vol.265
, pp. 931-939
-
-
Tobacman, L.1
Sawyer, D.2
-
40
-
-
0035746804
-
Functional studies of yeast actin mutants corresponding to human cardiomyopathy mutations
-
Wong W.W., Doyle T.C., Cheung P., Olson T.M., Reisler E. Functional studies of yeast actin mutants corresponding to human cardiomyopathy mutations. J Musc Res Cell Motil. 2002, 22:665-674.
-
(2002)
J Musc Res Cell Motil.
, vol.22
, pp. 665-674
-
-
Wong, W.W.1
Doyle, T.C.2
Cheung, P.3
Olson, T.M.4
Reisler, E.5
-
41
-
-
0037216694
-
Increased Ca2+-sensitivity of the contractile apparatus in end-stage human heart failure results from altered phosphorylation of contractile proteins
-
van der Velden J., Papp Z., Zaremba R., Boontje N.M., de Jong J.W., Owen V.J., et al. Increased Ca2+-sensitivity of the contractile apparatus in end-stage human heart failure results from altered phosphorylation of contractile proteins. Cardiovasc Res 2003, 57:37-47.
-
(2003)
Cardiovasc Res
, vol.57
, pp. 37-47
-
-
van der Velden, J.1
Papp, Z.2
Zaremba, R.3
Boontje, N.M.4
de Jong, J.W.5
Owen, V.J.6
-
42
-
-
62449234647
-
Myofilament dysfunction in cardiac disease from mice to men
-
Hamdani N., de Waard M., Messer A.E., Boontje N.M., Kooij V., van Dijk S., et al. Myofilament dysfunction in cardiac disease from mice to men. J Musc Res Cell Motil. 2009, 29:189-201.
-
(2009)
J Musc Res Cell Motil.
, vol.29
, pp. 189-201
-
-
Hamdani, N.1
de Waard, M.2
Messer, A.E.3
Boontje, N.M.4
Kooij, V.5
van Dijk, S.6
-
43
-
-
0037423881
-
Is depressed myocyte contractility centrally involved in heart failure?
-
Houser S.R., Margulies K.B. Is depressed myocyte contractility centrally involved in heart failure?. Circ Res 2003, 92:350-358.
-
(2003)
Circ Res
, vol.92
, pp. 350-358
-
-
Houser, S.R.1
Margulies, K.B.2
-
44
-
-
77955307476
-
Structural and functional polymorphisms of troponin in failing heart
-
A. Messer. Structural and functional polymorphisms of troponin in failing heart. PhD Thesis. London: London; 2007.
-
(2007)
PhD Thesis. London: London
-
-
Messer, A.1
-
45
-
-
48849095991
-
Myosin binding protein C phosphorylation in normal, hypertrophic and failing human heart muscle
-
Jacques A., Copeland O., Messer A., Gallon C., King C., McKenna W., et al. Myosin binding protein C phosphorylation in normal, hypertrophic and failing human heart muscle. J Mol Cell Cardiol 2008, 45:209-216.
-
(2008)
J Mol Cell Cardiol
, vol.45
, pp. 209-216
-
-
Jacques, A.1
Copeland, O.2
Messer, A.3
Gallon, C.4
King, C.5
McKenna, W.6
-
46
-
-
39749142663
-
Sarcomeric dysfunction in heart failure
-
Hamdani N., Kooij V., van Dijk S., Merkus D., Paulus W.J., Remedios C.D., et al. Sarcomeric dysfunction in heart failure. Cardiovasc Res 2008, 77:649-658.
-
(2008)
Cardiovasc Res
, vol.77
, pp. 649-658
-
-
Hamdani, N.1
Kooij, V.2
van Dijk, S.3
Merkus, D.4
Paulus, W.J.5
Remedios, C.D.6
-
47
-
-
0030067394
-
A mouse model of familial hypertrophic cardiomyopathy
-
Geisterfer-Lowrance A.A., Christe M., Conner D.A., Ingwall J.S., Schoen F.J., Seidman C.E., et al. A mouse model of familial hypertrophic cardiomyopathy. Science 1996, 272:731-734.
-
(1996)
Science
, vol.272
, pp. 731-734
-
-
Geisterfer-Lowrance, A.A.1
Christe, M.2
Conner, D.A.3
Ingwall, J.S.4
Schoen, F.J.5
Seidman, C.E.6
-
48
-
-
70349359488
-
Adrenergic stress unmasks exaggerated septal hypertrophy and proteasome impairment in heterozygous cMyBP-C mutant mice
-
Schuermann F., Schlossarek S., Mearini G., Geetz B., Eschenhagen T., Carrier L. Adrenergic stress unmasks exaggerated septal hypertrophy and proteasome impairment in heterozygous cMyBP-C mutant mice. Circulation 2008, 118(Suppl 2):S521.
-
(2008)
Circulation
, vol.118
, Issue.SUPPL. 2
-
-
Schuermann, F.1
Schlossarek, S.2
Mearini, G.3
Geetz, B.4
Eschenhagen, T.5
Carrier, L.6
|