-
1
-
-
0033979552
-
Pathogenesis of diverse clinical and pathological phenotypes in hypertrophic cardiomyopathies
-
A.J. Marian Pathogenesis of diverse clinical and pathological phenotypes in hypertrophic cardiomyopathies Lancet 355 2000 58 60
-
(2000)
Lancet
, vol.355
, pp. 58-60
-
-
Marian, A.J.1
-
2
-
-
0036787237
-
Molecular mechanisms of inherited cardiomyopathies
-
D. Fatkin, and R.M. Graham Molecular mechanisms of inherited cardiomyopathies Physiol. Rev. 82 2002 945 980
-
(2002)
Physiol. Rev.
, vol.82
, pp. 945-980
-
-
Fatkin, D.1
Graham, R.M.2
-
3
-
-
0036300982
-
Risk stratification and prevention of sudden death in hypertrophic cardiomyopathy
-
B.J. Maron Risk stratification and prevention of sudden death in hypertrophic cardiomyopathy Cardiol. Rev. 10 2002 173 181
-
(2002)
Cardiol. Rev.
, vol.10
, pp. 173-181
-
-
Maron, B.J.1
-
4
-
-
0028178083
-
α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
L. Thierfelder, H. Watkins, C. MacRae, R. Lamas, W. McKenna, and H.P. Vosberg α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere Cell 77 1994 701 712
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
MacRae, C.3
Lamas, R.4
McKenna, W.5
Vosberg, H.P.6
-
5
-
-
0347320747
-
Calcineurin/NFAT coupling participates in pathological, but not physiological cardiac hypertrophy
-
B.J. Wilkins, Y.S. Dai, O.F. Bueno, S.A. Parsons, J. Xu, and D.M. Plank Calcineurin/NFAT coupling participates in pathological, but not physiological cardiac hypertrophy Circ. Res. 94 2004 110 118
-
(2004)
Circ. Res.
, vol.94
, pp. 110-118
-
-
Wilkins, B.J.1
Dai, Y.S.2
Bueno, O.F.3
Parsons, S.A.4
Xu, J.5
Plank, D.M.6
-
7
-
-
14844338880
-
Impairment of the ubiquitin-proteasome system by truncated cardiac myosin binding protein C mutants
-
A. Sarikas, L. Carrier, C. Schenke, D. Doll, J. Flavigny, and K.S. Lindenberg Impairment of the ubiquitin-proteasome system by truncated cardiac myosin binding protein C mutants Cardiovasc. Res. 66 2005 33 44
-
(2005)
Cardiovasc. Res.
, vol.66
, pp. 33-44
-
-
Sarikas, A.1
Carrier, L.2
Schenke, C.3
Doll, D.4
Flavigny, J.5
Lindenberg, K.S.6
-
8
-
-
0037630018
-
Hypertrophic cardiomyopathy-distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
-
P. Richard, P. Charron, L. Carrier, C. Ledeuil, T. Cheav, and C. Pichereau Hypertrophic cardiomyopathy-distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy Circulation 107 2003 2227 2232
-
(2003)
Circulation
, vol.107
, pp. 2227-2232
-
-
Richard, P.1
Charron, P.2
Carrier, L.3
Ledeuil, C.4
Cheav, T.5
Pichereau, C.6
-
9
-
-
0033972217
-
Myosin binding protein C, a phosphorylation-dependent force regulator that controls the attachment of myosin heads by its interaction with myosin S2
-
G. Kunst, K.R. Kress, M. Gruen, D. Uttenweiler, M. Gautel, and R.H. Fink Myosin binding protein C, a phosphorylation-dependent force regulator that controls the attachment of myosin heads by its interaction with myosin S2 Circ. Res. 86 2000 51 58
-
(2000)
Circ. Res.
, vol.86
, pp. 51-58
-
-
Kunst, G.1
Kress, K.R.2
Gruen, M.3
Uttenweiler, D.4
Gautel, M.5
Fink, R.H.6
-
10
-
-
7244245537
-
Binding of myosin binding protein-C to myosin subfragment S2 affects contractility independent of a tether mechanism
-
S.P. Harris, E. Rostkova, M. Gautel, and R.L. Moss Binding of myosin binding protein-C to myosin subfragment S2 affects contractility independent of a tether mechanism Circ. Res. 95 2004 930 936
-
(2004)
Circ. Res.
, vol.95
, pp. 930-936
-
-
Harris, S.P.1
Rostkova, E.2
Gautel, M.3
Moss, R.L.4
-
11
-
-
0032189352
-
A mouse model of myosin binding protein C human familial hypertrophic cardiomyopathy
-
Q. Yang, A. Sanbe, H. Osinska, T.E. Hewett, R. Klevitsky, and J. Robbins A mouse model of myosin binding protein C human familial hypertrophic cardiomyopathy J. Clin. Invest. 102 1998 1292 1300
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 1292-1300
-
-
Yang, Q.1
Sanbe, A.2
Osinska, H.3
Hewett, T.E.4
Klevitsky, R.5
Robbins, J.6
-
12
-
-
0032749319
-
In vivo modelling of myosin binding protein C familial hypertrophic cardiomyopathy
-
Q. Yang, A. Sanbe, H. Osinska, T.E. Hewett, R. Klevitsky, and J. Robbins In vivo modelling of myosin binding protein C familial hypertrophic cardiomyopathy Circ. Res. 85 1999 841 847
-
(1999)
Circ. Res.
, vol.85
, pp. 841-847
-
-
Yang, Q.1
Sanbe, A.2
Osinska, H.3
Hewett, T.E.4
Klevitsky, R.5
Robbins, J.6
-
13
-
-
0034724252
-
A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance
-
J.A. Moolman, S. Reith, K. Uhl, S. Bailey, M. Gautel, and B. Jeschke A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance Circulation 101 2000 1396 1400
-
(2000)
Circulation
, vol.101
, pp. 1396-1400
-
-
Moolman, J.A.1
Reith, S.2
Uhl, K.3
Bailey, S.4
Gautel, M.5
Jeschke, B.6
-
14
-
-
0347987907
-
The ubiquitin-proteasome system in cardiovascular diseases-a hypothesis extended
-
J. Herrmann, A. Ciechanover, L.O. Lerman, and A. Lerman The ubiquitin-proteasome system in cardiovascular diseases-a hypothesis extended Cardiovasc. Res. 61 2004 11 21
-
(2004)
Cardiovasc. Res.
, vol.61
, pp. 11-21
-
-
Herrmann, J.1
Ciechanover, A.2
Lerman, L.O.3
Lerman, A.4
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