-
1
-
-
0035001849
-
Molecular medicine in the 21st century
-
DOI 10.1046/j.1445-5994.2001.00001.x
-
C Semsarian CE Seidman 2001 Molecular medicine in the 21st century Internal Medicine Journal 31 53 59 10.1046/j.1445-5994.2001.00001.x 1:STN:280:DC%2BD38%2FisValtg%3D%3D 11478359 (Pubitemid 32411166)
-
(2001)
Internal Medicine Journal
, vol.31
, Issue.1
, pp. 53-59
-
-
Semsarian, C.1
Seidman, C.E.2
-
2
-
-
0035936792
-
The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms
-
DOI 10.1016/S0092-8674(01)00242-2
-
JG Seidman C Seidman 2001 The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms Cell 104 557 567 10.1016/S0092-8674(01)00242-2 1:CAS:528:DC%2BD3MXis1Kks70%3D 11239412 (Pubitemid 32201950)
-
(2001)
Cell
, vol.104
, Issue.4
, pp. 557-567
-
-
Seidman, J.G.1
Seidman, C.2
-
3
-
-
0031052480
-
The management of hypertrophic cardiomyopathy
-
DOI 10.1056/NEJM199703133361107
-
P Spirito CE Seidman WJ McKenna BJ Maron 1997 The management of hypertrophic cardiomyopathy New England Journal of Medicine 336 775 785 10.1056/NEJM199703133361107 1:STN:280:DyaK2s3gtFeksA%3D%3D 9052657 (Pubitemid 27113973)
-
(1997)
New England Journal of Medicine
, vol.336
, Issue.11
, pp. 775-785
-
-
Spirito, P.1
Seidman, C.E.2
McKenna, W.J.3
Maron, B.J.4
-
4
-
-
0037070514
-
Hypertrophic cardiomyopathy: A systematic review
-
10.1001/jama.287.10.1308 11886323
-
BJ Maron 2002 Hypertrophic cardiomyopathy: A systematic review JAMA 287 1308 1320 10.1001/jama.287.10.1308 11886323
-
(2002)
JAMA
, vol.287
, pp. 1308-1320
-
-
Maron, B.J.1
-
5
-
-
33845913222
-
Genetic basis of hypertrophic cardiomyopathy
-
DOI 10.1586/14779072.4.6.927
-
JM Lind C Chiu C Semsarian 2006 Genetic basis of hypertrophic cardiomyopathy Expert Review of Cardiovascular Therapy 4 929 934 10.1586/14779072.4.6.927 (Pubitemid 46017528)
-
(2006)
Expert Review of Cardiovascular Therapy
, vol.4
, Issue.6
, pp. 927-934
-
-
Lind, J.M.1
Chiu, C.2
Semsarian, C.3
-
6
-
-
34547188258
-
Implantable cardioverter-defibrillators and prevention of sudden cardiac death in hypertrophic cardiomyopathy
-
BJ Maron P Spirito WK Shen TS Haas F Formisano MS Link, et al. 2007 Implantable cardioverter-defibrillators and prevention of sudden cardiac death in hypertrophic cardiomyopathy JAMA 298 4 405 412 10.1001/jama.298.4.405 1:CAS:528:DC%2BD2sXot1eks7k%3D 17652294 (Pubitemid 47124061)
-
(2007)
Journal of the American Medical Association
, vol.298
, Issue.4
, pp. 405-412
-
-
Maron, B.J.1
Spirito, P.2
Shen, W.-K.3
Haas, T.S.4
Formisano, F.5
Link, M.S.6
Epstein, A.E.7
Almquist, A.K.8
Daubert, J.P.9
Lawrenz, T.10
Boriani, G.11
Estes III, N.A.M.12
Favale, S.13
Piccininno, M.14
Winters, S.L.15
Santini, M.16
Betocchi, S.17
Arribas, F.18
Sherrid, M.V.19
Buja, G.20
Semsarian, C.21
Bruzzi, P.22
more..
-
7
-
-
1942436120
-
Long-term follow-up of implantable cardioverter defibrillator therapy for hypertrophic cardiomyopathy
-
DOI 10.1016/j.amjcard.2004.01.057, PII S0002914904001493
-
I Jayatilleke A Doolan J Ingles M McGuire V Booth DR Richmond, et al. 2004 Long-term follow-up of implantable cardioverter defibrillator therapy for hypertrophic cardiomyopathy American Journal of Cardiology 93 9 1192 1194 10.1016/j.amjcard.2004.01.057 15110224 (Pubitemid 38521061)
-
(2004)
American Journal of Cardiology
, vol.93
, Issue.9
, pp. 1192-1194
-
-
Jayatilleke, I.1
Doolan, A.2
Ingles, J.3
McGuire, M.4
Booth, V.5
Richmond, D.R.6
Semsarian, C.7
-
8
-
-
0037630018
-
Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
-
DOI 10.1161/01.CIR.0000066323.15244.54
-
P Richard P Charron L Carrier C Ledeuil T Cheav C Pichereau, et al. 2003 Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy Circulation 107 2227 2232 10.1161/01.CIR.0000066323.15244.54 12707239 (Pubitemid 36547217)
-
(2003)
Circulation
, vol.107
, Issue.17
, pp. 2227-2232
-
-
Richard, P.1
Charron, P.2
Carrier, L.3
Ledeuil, C.4
Cheav, T.5
Pichereau, C.6
Benaiche, A.7
Isnard, R.8
Dubourg, O.9
Burban, M.10
Gueffet, J.-P.11
Millaire, A.12
Desnos, M.13
Schwartz, K.14
Hainque, B.15
Komajda, M.16
-
9
-
-
0026573969
-
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
-
1:STN:280:DyaK383gsVWqsQ%3D%3D 1552912
-
H Watkins A Rosenzweig DS Hwang T Levi W McKenna CE Seidman, et al. 1992 Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy New England Journal of Medicine 326 1108 1114 1:STN:280:DyaK383gsVWqsQ%3D%3D 1552912
-
(1992)
New England Journal of Medicine
, vol.326
, pp. 1108-1114
-
-
Watkins, H.1
Rosenzweig, A.2
Hwang, D.S.3
Levi, T.4
McKenna, W.5
Seidman, C.E.6
-
10
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
-
DOI 10.1016/0092-8674(90)90274-I
-
AAT Geisterfer-Lowrance S Kass G Tanigawa H-P Vosberg W McKenna CE Seidman, et al. 1990 A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation Cell 62 999 1006 10.1016/0092-8674(90)90274-I 1:CAS:528:DyaK3cXmtVGqs7w%3D 1975517 (Pubitemid 20269146)
-
(1990)
Cell
, vol.62
, Issue.5
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.T.1
Kass, S.2
Tanigawa, G.3
Vosberg, H.-P.4
McKenna, W.5
Seidman, C.E.6
Seidman, J.G.7
-
11
-
-
0003062898
-
Gene mutations that cause familial hypertrophic cardiomyopathy
-
E. Haber (eds). Scientific American New York
-
Seidman, C., & Seidman, J. G. (1995). Gene mutations that cause familial hypertrophic cardiomyopathy. In E. Haber (Ed.), Molecular cardiovascular medicine (pp. 193-210). New York: Scientific American.
-
(1995)
Molecular Cardiovascular Medicine
, pp. 193-210
-
-
Seidman, C.1
Seidman, J.G.2
-
13
-
-
0033017175
-
The pathogenesis of familial hypertrophic cardiomyopathy: Early and evolving effects from an α-cardiac myosin heavy chain missense mutation
-
DOI 10.1038/6549
-
D Georgakopoulos ME Christe M Giewat CM Seidman J Seidman DA Kass 1999 The pathogenesis of familial hypertrophic cardiomyopathy: Early and evolving effects from an α-cardiac myosin heavy chain missense mutation Nature Medicine 5 327 330 10.1038/6549 1:CAS:528:DyaK1MXhsVSktrc%3D 10086390 (Pubitemid 29124370)
-
(1999)
Nature Medicine
, vol.5
, Issue.3
, pp. 327-330
-
-
Georgakopoulos, D.1
Christe, M.E.2
Giewat, M.3
Seidman, C.M.4
Seidman, J.G.5
Kass, D.A.6
-
16
-
-
0032943836
-
Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene
-
10.1172/JCI4631 1:CAS:528:DyaK1MXjsl2ltg%3D%3D 9884344
-
D Fatkin ME Christe O Aristizabal BK McConnell S Srinivasan FJ Schoen, et al. 1999 Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene Journal of Clinical Investigation 103 147 153 10.1172/JCI4631 1:CAS:528:DyaK1MXjsl2ltg%3D%3D 9884344
-
(1999)
Journal of Clinical Investigation
, vol.103
, pp. 147-153
-
-
Fatkin, D.1
Christe, M.E.2
Aristizabal, O.3
McConnell, B.K.4
Srinivasan, S.5
Schoen, F.J.6
-
17
-
-
0033386313
-
A transgenic rabbit model for human hypertrophic cardiomyopathy
-
10.1172/JCI7956 1:CAS:528:DC%2BD3cXhtFGlsQ%3D%3D 10606622
-
AJ Marian Y Wu D-S Lim M McCluggage K Youker Q-T Yu, et al. 1999 A transgenic rabbit model for human hypertrophic cardiomyopathy Journal of Clinical Investigation 104 1683 1692 10.1172/JCI7956 1:CAS:528: DC%2BD3cXhtFGlsQ%3D%3D 10606622
-
(1999)
Journal of Clinical Investigation
, vol.104
, pp. 1683-1692
-
-
Marian, A.J.1
Wu, Y.2
Lim, D.-S.3
McCluggage, M.4
Youker, K.5
Yu, Q.-T.6
-
18
-
-
2342521939
-
Evolution of expression of cardiac phenotypes over a 4-year period in the β-myosin heavy chain-Q403 transgenic rabbit model of human hypertrophic cardiomyopathy
-
DOI 10.1016/j.yjmcc.2004.02.010, PII S0022282804000513
-
SF Nagueh S Chen R Patel N Tsybouleva S Lutucuta HA Kopelen, et al. 2004 Evolution of expression of cardiac phenotypes over a 4-year period in the β-myosin heavy chain-Q403 transgenic rabbit model of human hypertrophic cardiomyopathy Journal of Molecular and Cellular Cardiology 36 663 673 10.1016/j.yjmcc.2004.02.010 1:CAS:528:DC%2BD2cXjsl2nsbw%3D 15135661 (Pubitemid 38591599)
-
(2004)
Journal of Molecular and Cellular Cardiology
, vol.36
, Issue.5
, pp. 663-673
-
-
Nagueh, S.F.1
Chen, S.2
Patel, R.3
Tsybouleva, N.4
Lutucuta, S.5
Kopelen, H.A.6
Zoghbi, W.A.7
Quinones, M.A.8
Roberts, R.9
Marian, A.J.10
-
19
-
-
64549096033
-
Resolution of established cardiac hypertrophy and fibrosis and prevention of systolic dysfunction in a transgenic rabbit model of human cardiomyopathy through thiol-sensitive mechanisms
-
10.1161/CIRCULATIONAHA.108.790501 1:CAS:528:DC%2BD1MXivVentb0%3D 19255346
-
R Lombardi G Rodriguez SN Chen CM Ripplinger W Li J Chen, et al. 2009 Resolution of established cardiac hypertrophy and fibrosis and prevention of systolic dysfunction in a transgenic rabbit model of human cardiomyopathy through thiol-sensitive mechanisms Circulation 119 1398 1407 10.1161/CIRCULATIONAHA.108.790501 1:CAS:528:DC%2BD1MXivVentb0%3D 19255346
-
(2009)
Circulation
, vol.119
, pp. 1398-1407
-
-
Lombardi, R.1
Rodriguez, G.2
Chen, S.N.3
Ripplinger, C.M.4
Li, W.5
Chen, J.6
-
20
-
-
10244221064
-
Ablation of the murine α myosin heavy chain gene leads to dosage effects and functional deficits in the heart
-
10.1172/JCI118992 1:CAS:528:DyaK28XmtlOrsLc%3D 8878443
-
WK Jones IL Grupp T Doetschman G Grupp H Osinska TE Hewett, et al. 1996 Ablation of the murine α myosin heavy chain gene leads to dosage effects and functional deficits in the heart Journal of Clinical Investigation 98 1906 1917 10.1172/JCI118992 1:CAS:528:DyaK28XmtlOrsLc%3D 8878443
-
(1996)
Journal of Clinical Investigation
, vol.98
, pp. 1906-1917
-
-
Jones, W.K.1
Grupp, I.L.2
Doetschman, T.3
Grupp, G.4
Osinska, H.5
Hewett, T.E.6
-
21
-
-
0028824803
-
Assembly of cardiac C-protein during myofibrillogenesis in myogenic cells in culture
-
10.1247/csf.20.253 1:CAS:528:DyaK2MXovFegsLs%3D 8521525
-
S Koshida M Kurasawa M Yasuda N Sato T Obinata 1995 Assembly of cardiac C-protein during myofibrillogenesis in myogenic cells in culture Cell Structure and Function 20 253 261 10.1247/csf.20.253 1:CAS:528:DyaK2MXovFegsLs%3D 8521525
-
(1995)
Cell Structure and Function
, vol.20
, pp. 253-261
-
-
Koshida, S.1
Kurasawa, M.2
Yasuda, M.3
Sato, N.4
Obinata, T.5
-
22
-
-
0030030825
-
The carboxyl terminus of myosin binding protein C (MyBP-C, C-protein) specifies incorporation into the A-band of striated muscle
-
1:CAS:528:DyaK28XosVahuw%3D%3D 8834795
-
R Gilbert MG Kelly T Mikawa DA Fischman 1996 The carboxyl terminus of myosin binding protein C (MyBP-C, C-protein) specifies incorporation into the A-band of striated muscle Journal of Cell Science 109 101 111 1:CAS:528:DyaK28XosVahuw%3D%3D 8834795
-
(1996)
Journal of Cell Science
, vol.109
, pp. 101-111
-
-
Gilbert, R.1
Kelly, M.G.2
Mikawa, T.3
Fischman, D.A.4
-
23
-
-
0032580520
-
Mutations in the gene for cardiac myosin-binding protein C and late- onset familial hypertrophic cardiomyopathy
-
DOI 10.1056/NEJM199804303381802
-
H Niimura LL Bachinski S Sangwatanaroj H Watkins AE Chudley W McKenna, et al. 1998 Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy New England Journal of Medicine 338 1248 1257 10.1056/NEJM199804303381802 1:CAS:528:DyaK1cXivF2qtrY%3D 9562578 (Pubitemid 28216578)
-
(1998)
New England Journal of Medicine
, vol.338
, Issue.18
, pp. 1248-1257
-
-
Niimura, H.1
Bachinski, L.L.2
Sangwatanaroj, S.3
Watkins, H.4
Chudley, A.E.5
Mckenna, W.6
Kristinsson, A.7
Roberts, R.8
Sole, M.9
Maron, B.J.10
Seidman, J.G.11
Seidman, C.E.12
Thierfelder, L.13
Jarcho, J.A.14
Anastasakis, A.15
Toutouzas, P.16
Elstein, E.17
Liew, C.-C.18
Liew, J.19
Mably, J.20
Rakowski, H.21
Wigle, D.22
Zhao, M.23
Salerni, R.24
Bjornsdottir, H.25
more..
-
24
-
-
0032555955
-
Familial hypertrophic cardiomyopathy: From mutations to functional defects
-
G Bonne L Carrier P Richard B Hainque K Schwartz 1998 Familial hypertrophic cardiomyopathy: From mutations to functional defects Circulation Research 83 580 593 1:CAS:528:DyaK1cXmt1Knt7w%3D 9742053 (Pubitemid 28427741)
-
(1998)
Circulation Research
, vol.83
, Issue.6
, pp. 580-593
-
-
Bonne, G.1
Carrier, L.2
Richard, P.3
Hainque, B.4
Schwartz, K.5
-
25
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
10.1038/ng1295-434 1:CAS:528:DyaK2MXpvVCksb4%3D 7493025
-
H Watkins D Conner L Thierfelder JA Jarcho C MacRae WJ McKenna, et al. 1995 Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy Nature Genetics 11 434 437 10.1038/ng1295-434 1:CAS:528:DyaK2MXpvVCksb4%3D 7493025
-
(1995)
Nature Genetics
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
Jarcho, J.A.4
MacRae, C.5
McKenna, W.J.6
-
27
-
-
75949086359
-
Multiple mutations in genetic cardiovascular disease: A marker of disease severity?
-
10.1161/CIRCGENETICS.108.836478 1:CAS:528:DC%2BD1MXmvVyhtrc%3D
-
M Kelly C Semsarian 2009 Multiple mutations in genetic cardiovascular disease: A marker of disease severity? Circulation: Cardiovascular Genetics 2 182 190 10.1161/CIRCGENETICS.108.836478 1:CAS:528:DC%2BD1MXmvVyhtrc%3D
-
(2009)
Circulation: Cardiovascular Genetics
, vol.2
, pp. 182-190
-
-
Kelly, M.1
Semsarian, C.2
-
28
-
-
0037155775
-
Hypertrophic cardiomyopathy in cardiac myosin binding protein-C knockout mice
-
DOI 10.1161/01.RES.0000012222.70819.64
-
SP Harris CR Bartley TA Hacker KS McDonald PS Douglas ML Greaser, et al. 2002 Hypertrophic cardiomyopathy in cardiac myosin binding protein-C knockout mice Circulation Research 90 594 601 10.1161/01.RES.0000012222.70819.64 1:CAS:528:DC%2BD38XisFWlsLo%3D 11909824 (Pubitemid 34640910)
-
(2002)
Circulation Research
, vol.90
, Issue.5
, pp. 594-601
-
-
Harris, S.P.1
Bartley, C.R.2
Hacker, T.A.3
McDonald, K.S.4
Douglas, P.S.5
Greaser, M.L.6
Powers, P.A.7
Moss, R.L.8
-
29
-
-
3142570567
-
Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice
-
DOI 10.1016/j.cardiores.2004.04.009, PII S0008636304001683
-
L Carrier R Knöll N Vignier DI Keller P Bausero B Prudhon, et al. 2004 Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice Cardiovascular Research 63 293 304 10.1016/j.cardiores.2004.04.009 1:CAS:528:DC%2BD2cXlsFymu78%3D 15249187 (Pubitemid 38900843)
-
(2004)
Cardiovascular Research
, vol.63
, Issue.2
, pp. 293-304
-
-
Carrier, L.1
Knoll, R.2
Vignier, N.3
Keller, D.I.4
Bausero, P.5
Prudhon, B.6
Isnard, R.7
Ambroisine, M.-L.8
Fiszman, M.9
Ross Jr., J.10
Schwartz, K.11
Chien, K.R.12
-
30
-
-
0028178083
-
α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
10.1016/0092-8674(94)90054-X 8205619
-
L Thierfelder H Watkins C MacRae R Lamas W McKenna H-P Vosberg, et al. 1994 α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere Cell 77 701 712 10.1016/0092-8674(94)90054-X 8205619
-
(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
-
31
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy
-
10.1056/NEJM199504203321603 1:CAS:528:DyaK2MXlslCnsrw%3D 7898523
-
H Watkins WJ McKenna L Thierfelder HJ Suk R Anan A O'Donoghue, et al. 1995 Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy New England Journal of Medicine 332 1058 1064 10.1056/NEJM199504203321603 1:CAS:528:DyaK2MXlslCnsrw%3D 7898523
-
(1995)
New England Journal of Medicine
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.J.2
Thierfelder, L.3
Suk, H.J.4
Anan, R.5
O'Donoghue, A.6
-
32
-
-
0031052924
-
Sudden death due to troponin T mutations
-
DOI 10.1016/S0735-1097(96)00530-X, PII S073510979600530X
-
JC Moolman VA Corfield B Posen K Ngumbela C Seidman PA Brink, et al. 1997 Sudden death due to troponin T mutations Journal of the American College of Cardiology 29 549 555 10.1016/S0735-1097(96)00530-X 1:STN:280: DyaK2s3hsVGisA%3D%3D 9060892 (Pubitemid 27116096)
-
(1997)
Journal of the American College of Cardiology
, vol.29
, Issue.3
, pp. 549-555
-
-
Moolman, J.C.1
Corfield, V.A.2
Posen, B.3
Ngumbela, K.4
Seidman, C.5
Brink, P.A.6
Watkins, H.7
-
33
-
-
0032526155
-
A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy
-
10.1172/JCI2389 1:CAS:528:DyaK1cXktVSiu78%3D 9637714
-
JC Tardiff SM Factor BD Tompkins TE Hewett BM Palmer RL Moore, et al. 1998 A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy Journal of Clinical Investigation 101 2800 2811 10.1172/JCI2389 1:CAS:528: DyaK1cXktVSiu78%3D 9637714
-
(1998)
Journal of Clinical Investigation
, vol.101
, pp. 2800-2811
-
-
Tardiff, J.C.1
Factor, S.M.2
Tompkins, B.D.3
Hewett, T.E.4
Palmer, B.M.5
Moore, R.L.6
-
34
-
-
0033886318
-
Transgenic rat hearts expressing a human cardiac troponin T deletion reveal diastolic dysfunction and ventricular arrhythmias
-
DOI 10.1016/S0008-6363(00)00114-0, PII S0008636300001140
-
N Frey WM Franz K Gloeckner M Degenhardt M Müller O Müller, et al. 2000 Transgenic rat hearts expressing a human cardiac troponin T deletion reveal diastolic dysfunction and ventricular arrhythmias Cardiovascular Research 47 254 264 10.1016/S0008-6363(00)00114-0 1:CAS:528:DC%2BD3cXlsFChsbg%3D 10946062 (Pubitemid 30625288)
-
(2000)
Cardiovascular Research
, vol.47
, Issue.2
, pp. 254-264
-
-
Frey, N.1
Franz, W.M.2
Gloeckner, K.3
Degenhardt, M.4
Muller, M.5
Muller, O.6
Merz, H.7
Katus, H.A.8
-
35
-
-
64149087448
-
Decreased contractility due to energy deprivation in a transgenic rat model of hypertrophic cardiomyopathy
-
10.1007/s00109-008-0436-x 1:CAS:528:DC%2BD1MXktFCitbs%3D 19189074
-
M Luedde U Flögel M Knorr C Grundt H-J Hippe B Brors, et al. 2009 Decreased contractility due to energy deprivation in a transgenic rat model of hypertrophic cardiomyopathy Journal of Molecular Medicine 87 411 422 10.1007/s00109-008-0436-x 1:CAS:528:DC%2BD1MXktFCitbs%3D 19189074
-
(2009)
Journal of Molecular Medicine
, vol.87
, pp. 411-422
-
-
Luedde, M.1
Flögel, U.2
Knorr, M.3
Grundt, C.4
Hippe, H.-J.5
Brors, B.6
-
36
-
-
64149087448
-
Decreased contractility due to energy deprivation in a transgenic rat model of hypertrophic cardiomyopathy
-
10.1007/s00109-008-0436-x 1:CAS:528:DC%2BD1MXktFCitbs%3D 19189074
-
M Luedde U Flogel M Knorr C Grundt HJ Hippe B Brors, et al. 2009 Decreased contractility due to energy deprivation in a transgenic rat model of hypertrophic cardiomyopathy Journal of Molecular Medicine 87 4 411 422 10.1007/s00109-008-0436-x 1:CAS:528:DC%2BD1MXktFCitbs%3D 19189074
-
(2009)
Journal of Molecular Medicine
, vol.87
, Issue.4
, pp. 411-422
-
-
Luedde, M.1
Flogel, U.2
Knorr, M.3
Grundt, C.4
Hippe, H.J.5
Brors, B.6
-
37
-
-
85047691343
-
Decreased energetics in murine hearts bearing the R92Q mutation in cardiac troponin T
-
1:CAS:528:DC%2BD3sXntlSiu70%3D 12952925
-
MM Javadpour JC Tardiff I Pinz JS Ingwall 2003 Decreased energetics in murine hearts bearing the R92Q mutation in cardiac troponin T Journal of Clinical Investigation 112 768 775 1:CAS:528:DC%2BD3sXntlSiu70%3D 12952925
-
(2003)
Journal of Clinical Investigation
, vol.112
, pp. 768-775
-
-
Javadpour, M.M.1
Tardiff, J.C.2
Pinz, I.3
Ingwall, J.S.4
-
38
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
DOI 10.1038/ng0897-379
-
A Kimura PJ-E Haruhito H Nishi M Satoh M Takahashi, et al. 1997 Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy Nature Genetics 16 379 382 10.1038/ng0897-379 1:CAS:528:DyaK2sXkvFChtrk%3D 9241277 (Pubitemid 27323305)
-
(1997)
Nature Genetics
, vol.16
, Issue.4
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park, J.-E.3
Nishi, H.4
Satoh, M.5
Takahashi, M.6
Hiroi, S.7
Sasaoka, T.8
Ohbuchi, N.9
Nakamura, T.10
Koyanagi, T.11
Hwang, T.-H.12
Choo, J.-A.13
Chung, K.-S.14
Hasegawa, A.15
Nagai, R.16
Okazaki, O.17
Nakamura, H.18
Matsuzaki, M.19
Sakamoto, T.20
Toshima, H.21
Koga, Y.22
Imaizumi, T.23
Sasazuki, T.24
more..
-
39
-
-
20844448376
-
Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: Clinical, genetic and functional consequences
-
DOI 10.1016/j.yjmcc.2004.12.006
-
A Doolan M Tebo J Ingles L Nguyen T Tsoutsman L Lam, et al. 2005 Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: Clinical, genetic and functional consequences Journal of Molecular and Cellular Cardiology 38 2 387 393 10.1016/j.yjmcc.2004.12.006 1:CAS:528: DC%2BD2MXhtFGrs7o%3D 15698845 (Pubitemid 40215208)
-
(2005)
Journal of Molecular and Cellular Cardiology
, vol.38
, Issue.2
, pp. 387-393
-
-
Doolan, A.1
Tebo, M.2
Ingles, J.3
Nguyen, L.4
Tsoutsman, T.5
Lam, L.6
Chiu, C.7
Chung, J.8
Weintraub, R.G.9
Semsarian, C.10
-
40
-
-
0034721807
-
Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy
-
J James Y Zhang H Osinska A Sanbe R Klevitsky TE Hewett, et al. 2000 Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy Circulation Research 87 805 811 1:CAS:528: DC%2BD3cXnvVOlu7Y%3D 11055985 (Pubitemid 30813011)
-
(2000)
Circulation Research
, vol.87
, Issue.9
, pp. 805-811
-
-
James, J.1
Zhang, Y.2
Osinska, H.3
Sanbe, A.4
Klevitsky, R.5
Hewett, T.E.6
Robbins, J.7
-
41
-
-
20844459661
-
Transgenic rabbit model for human troponin I-based hypertrophic cardiomyopathy
-
DOI 10.1161/01.CIR.0000164234.24957.75
-
A Sanbe J James V Tuzcu S Nas L Martin J Gulick, et al. 2005 Transgenic rabbit model for human troponin I-based hypertrophic cardiomyopathy Circulation 111 2330 2338 10.1161/01.CIR.0000164234.24957.75 1:CAS:528:DC%2BD2MXjsl2itr8%3D 15867176 (Pubitemid 40647069)
-
(2005)
Circulation
, vol.111
, Issue.18
, pp. 2330-2338
-
-
Sanbe, A.1
James, J.2
Tuzcu, V.3
Nas, S.4
Martin, L.5
Gulick, J.6
Osinska, H.7
Sakthivel, S.8
Klevitsky, R.9
Ginsburg, K.S.10
Bers, D.M.11
Zinman, B.12
Lakatta, E.G.13
Robbins, J.14
-
42
-
-
33748537975
-
Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathy
-
DOI 10.1016/j.yjmcc.2006.07.016, PII S0022282806007267
-
T Tsoutsman J Chung A Doolan L Nguyen IA Williams E Tu, et al. 2006 Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathy Journal of Molecular and Cellular Cardiology 41 623 632 10.1016/j.yjmcc.2006.07.016 1:CAS:528:DC%2BD28Xps1OksL0%3D 16950368 (Pubitemid 44374544)
-
(2006)
Journal of Molecular and Cellular Cardiology
, vol.41
, Issue.4
, pp. 623-632
-
-
Tsoutsman, T.1
Chung, J.2
Doolan, A.3
Nguyen, L.4
Williams, I.A.5
Tu, E.6
Lam, L.7
Bailey, C.G.8
Rasko, J.E.J.9
Allen, D.G.10
Semsarian, C.11
-
43
-
-
0031933491
-
Molecular genetic basis of hypertrophic cardiomyopathy: Genetic markers for sudden cardiac death
-
10.1111/j.1540-8167.1998.tb00871.x 1:STN:280:DyaK1c7jtlOhuw%3D%3D 9475582
-
AJ Marian R Roberts 1998 Molecular genetic basis of hypertrophic cardiomyopathy: Genetic markers for sudden cardiac death Journal of Cardiovascular Electrophysiology 9 88 99 10.1111/j.1540-8167.1998.tb00871.x 1:STN:280:DyaK1c7jtlOhuw%3D%3D 9475582
-
(1998)
Journal of Cardiovascular Electrophysiology
, vol.9
, pp. 88-99
-
-
Marian, A.J.1
Roberts, R.2
-
44
-
-
0031042881
-
Clinical features of hypertrophic cardiomyopathy caused by mutation of a 'hot spot' in the alpha-tropomyosin gene
-
DOI 10.1016/S0735-1097(96)00538-4, PII S0735109796005384
-
DA Coviello BJ Maron P Spirito H Watkins H-P Vosberg L Thierfelder, et al. 1997 Clinical features of hypertrophic cardiomyopathy caused by mutation of a "hot spot" in the alpha-tropomyosin gene Journal of the American College of Cardiology 29 635 640 10.1016/S0735-1097(96)00538-4 1:STN:280:DyaK2s3hsVGhtg%3D%3D 9060904 (Pubitemid 27116108)
-
(1997)
Journal of the American College of Cardiology
, vol.29
, Issue.3
, pp. 635-640
-
-
Coviello, D.A.1
Maron, B.J.2
Spirito, P.3
Watkins, H.4
Vosberg, H.-P.5
Thierfelder, L.6
Schoen, F.J.7
Seidman, J.G.8
Seidman, C.E.9
-
45
-
-
0033538612
-
Mouse model of a familial hypertrophic cardiomyopathy mutation in α-tropomyosin manifests cardiac dysfunction
-
1:CAS:528:DyaK1MXktlOhu7s%3D 10400910
-
M Muthuchamy K Pieples P Rethinasamy B Hoit IL Grupp GP Boivin, et al. 1999 Mouse model of a familial hypertrophic cardiomyopathy mutation in α-tropomyosin manifests cardiac dysfunction Circulation Research 85 47 56 1:CAS:528:DyaK1MXktlOhu7s%3D 10400910
-
(1999)
Circulation Research
, vol.85
, pp. 47-56
-
-
Muthuchamy, M.1
Pieples, K.2
Rethinasamy, P.3
Hoit, B.4
Grupp, I.L.5
Boivin, G.P.6
-
46
-
-
0034781383
-
A familial hypertrophic cardiomyopathy α-tropomyosin mutation causes severe cardiac hypertrophy and death in mice
-
DOI 10.1006/jmcc.2001.1445
-
R Prabhakar GP Boivin IL Grupp B Hoit G Arteaga RJ Solaro, et al. 2001 A familial hypertrophic cardiomyopathy α-tropomyosin mutation causes severe cardiac hypertrophy and death in mice Journal of Molecular and Cellular Cardiology 33 1815 1828 10.1006/jmcc.2001.1445 1:CAS:528:DC%2BD3MXnsFOjtrw%3D 11603924 (Pubitemid 32977135)
-
(2001)
Journal of Molecular and Cellular Cardiology
, vol.33
, Issue.10
, pp. 1815-1828
-
-
Prabhakar, R.1
Boivin, G.P.2
Grupp, I.L.3
Hoit, B.4
Arteaga, G.5
Solaro, R.J.6
Wieczorek, D.F.7
-
47
-
-
0141839860
-
A mouse model of familial hypertrophic cardiomyopathy caused by a α-tropomyosin mutation
-
DOI 10.1023/A:1025409227350
-
R Prabhakar N Petrashevskaya A Schwartz B Aronow GP Boivin JD Molkentin, et al. 2003 A mouse model of familial hypertrophic cardiomyopathy caused by a α-tropomyosin mutation Molecular and Cellular Biochemistry 251 33 42 10.1023/A:1025409227350 1:CAS:528:DC%2BD3sXovFCgtLc%3D 14575301 (Pubitemid 37220706)
-
(2003)
Molecular and Cellular Biochemistry
, vol.251
, Issue.1-2
, pp. 33-42
-
-
Prabhakar, R.1
Petrashevskaya, N.2
Schwartz, A.3
Aronow, B.4
Boivin, G.P.5
Molkentin, J.D.6
Wieczorek, D.F.7
-
48
-
-
10044280728
-
Effects of two familial hypertrophic cardiomyopathy mutations in α-tropomyosin, Asp175Asn and Glut180Gly, on the thermal unfolding of actin-bound tropomyosin
-
DOI 10.1529/biophysj.104.048793
-
E Kremneva S Boussouf O Nikolaeva R Maytum MA Geeves DI Levitsky 2004 Effects of two familial hypertrophic cardiomyopathy mutations in α-tropomyosin, Asp175Asn and Glu180Gly, on the thermal unfolding of actin-bound tropomyosin Biophysical Journal 87 3922 3933 10.1529/biophysj.104. 048793 1:CAS:528:DC%2BD2cXhtVOmtbnK 15454401 (Pubitemid 39602898)
-
(2004)
Biophysical Journal
, vol.87
, Issue.6
, pp. 3922-3933
-
-
Kremneva, E.1
Boussouf, S.2
Nikolaeva, O.3
Maytum, R.4
Geeves, M.A.5
Levitsky, D.I.6
-
49
-
-
47849118133
-
Prevalence of the myosin-binding protein C mutation in Maine Coon cats
-
DOI 10.1111/j.1939-1676.2008.0113.x
-
R Fries AM Heaney KM Meurs 2008 Prevalence of the myosin-binding protein C mutation in Maine Coon cats Journal of Veterinary Internal Medicine 22 893 896 10.1111/j.1939-1676.2008.0113.x 1:STN:280:DC%2BD1cvmvVWgsg%3D%3D 18498321 (Pubitemid 352039171)
-
(2008)
Journal of Veterinary Internal Medicine
, vol.22
, Issue.4
, pp. 893-896
-
-
Fries, R.1
Heaney, A.M.2
Meurs, K.M.3
-
50
-
-
0033594889
-
Familial hypertrophic cardiomyopathy in Maine Coon cats: An animal model of human disease
-
1:STN:280:DyaK1MzgslSltg%3D%3D 10377082
-
MD Kittleson KM Meurs MJ Munro JA Kittleson S-K Liu PD Pion, et al. 1999 Familial hypertrophic cardiomyopathy in Maine Coon cats: An animal model of human disease Circulation 99 3172 3180 1:STN:280:DyaK1MzgslSltg%3D%3D 10377082
-
(1999)
Circulation
, vol.99
, pp. 3172-3180
-
-
Kittleson, M.D.1
Meurs, K.M.2
Munro, M.J.3
Kittleson, J.A.4
Liu, S.-K.5
Pion, P.D.6
-
51
-
-
0031471956
-
Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex
-
DOI 10.1073/pnas.94.25.13873
-
A Sakamoto K Ono M Abe G Jasmin T Eki Y Murakami, et al. 1997 Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex Proceedings of the National Academy of Sciences of the United States of America 94 13873 13878 10.1073/pnas.94.25. 13873 1:CAS:528:DyaK2sXotVart7c%3D 9391120 (Pubitemid 28009677)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.25
, pp. 13873-13878
-
-
Sakamoto, A.1
Ono, K.2
Abe, M.3
Jasmin, G.4
Eki, T.5
Murakami, Y.6
Masaki, T.7
Toyo-Oka, T.8
Hanaoka, F.9
-
52
-
-
50649083738
-
Functional effects of the hypertrophic cardiomyopathy R403Q mutation are different in an α- Or β-myosin heavy chain backbone
-
10.1074/jbc.M800554200 1:CAS:528:DC%2BD1cXotlOhs7g%3D 18480046
-
S Lowey LM Lesko AS Rovner AR Hodges SL White RB Low, et al. 2008 Functional effects of the hypertrophic cardiomyopathy R403Q mutation are different in an α- or β-myosin heavy chain backbone Journal of Biological Chemistry 283 20579 20589 10.1074/jbc.M800554200 1:CAS:528: DC%2BD1cXotlOhs7g%3D 18480046
-
(2008)
Journal of Biological Chemistry
, vol.283
, pp. 20579-20589
-
-
Lowey, S.1
Lesko, L.M.2
Rovner, A.S.3
Hodges, A.R.4
White, S.L.5
Low, R.B.6
-
53
-
-
37349042936
-
Dilated and hypertrophic cardiomyopathy mutations in troponin and α-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments
-
DOI 10.1161/CIRCRESAHA.107.156380, PII 0000301220071207000009
-
P Robinson PJ Griffiths H Watkins CS Redwood 2007 Dilated and hypertrophic cardiomyopathy mutations in troponin and α-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments Circulation Research 101 1266 1273 10.1161/CIRCRESAHA.107.156380 1:CAS:528: DC%2BD2sXhtlOjsLzK 17932326 (Pubitemid 350294643)
-
(2007)
Circulation Research
, vol.101
, Issue.12
, pp. 1266-1273
-
-
Robinson, P.1
Griffiths, P.J.2
Watkins, H.3
Redwood, C.S.4
-
54
-
-
0034646743
-
Single-molecular mechanisms of R403Q cardiac isolated from the mouse model of familial hypertrophic cardiomyopathy
-
1:CAS:528:DC%2BD3cXislyns78%3D 10764406
-
M Tyska E Hayes M Giewat C Seidman J Seidman D Warshaw 2000 Single-molecular mechanisms of R403Q cardiac isolated from the mouse model of familial hypertrophic cardiomyopathy Circulation Research 86 737 744 1:CAS:528:DC%2BD3cXislyns78%3D 10764406
-
(2000)
Circulation Research
, vol.86
, pp. 737-744
-
-
Tyska, M.1
Hayes, E.2
Giewat, M.3
Seidman, C.4
Seidman, J.5
Warshaw, D.6
-
56
-
-
23344440434
-
Prevention of cardiac hypertrophy by atorvastatin in a transgenic rabbit model of human hypertrophic cardiomyopathy
-
DOI 10.1161/01.RES.0000177090.07296.ac
-
V Senthil SN Chen N Tsybouleva T Halder SF Nagueh JT Willerson, et al. 2005 Prevention of cardiac hypertrophy by atorvastatin in a transgenic rabbit model of human hypertrophic cardiomyopathy Circulation Research 97 285 292 10.1161/01.RES.0000177090.07296.ac 1:CAS:528:DC%2BD2MXmslelt7c%3D 16020756 (Pubitemid 41105455)
-
(2005)
Circulation Research
, vol.97
, Issue.3
, pp. 285-292
-
-
Senthil, V.1
Chen, S.N.2
Tsybouleva, N.3
Halder, T.4
Nagueh, S.F.5
Willerson, J.T.6
Roberts, R.7
Marian, A.J.8
-
57
-
-
37349119371
-
The effects of biological sex and diet on the development of heart failure
-
DOI 10.1161/CIRCULATIONAHA.106.672006, PII 0000301720071204000016
-
JP Konhilas LA Leinwand 2007 The effects of biological sex and diet on the development of heart failure Circulation 116 23 2747 2759 10.1161/CIRCULATIONAHA.106.672006 18056540 (Pubitemid 350291247)
-
(2007)
Circulation
, vol.116
, Issue.23
, pp. 2747-2759
-
-
Konhilas, J.P.1
Leinwand, L.A.2
-
60
-
-
0042889028
-
Sex is a potent modifier of the cardiovascular system
-
1:CAS:528:DC%2BD3sXmtFemsLc%3D 12897194
-
LA Leinwand 2003 Sex is a potent modifier of the cardiovascular system Journal of Clinical Investigation 112 3 302 307 1:CAS:528:DC%2BD3sXmtFemsLc%3D 12897194
-
(2003)
Journal of Clinical Investigation
, vol.112
, Issue.3
, pp. 302-307
-
-
Leinwand, L.A.1
-
61
-
-
0035201270
-
A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy
-
DOI 10.1006/jmcc.2001.1466
-
C Semsarian MJ Healey D Fatkin M Giewat C Duffy CE Seidman, et al. 2001 A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy Journal of Molecular and Cellular Cardiology 33 2055 2060 10.1006/jmcc.2001.1466 1:CAS:528:DC%2BD3MXot12gsL8%3D 11708849 (Pubitemid 33097283)
-
(2001)
Journal of Molecular and Cellular Cardiology
, vol.33
, Issue.11
, pp. 2055-2060
-
-
Semsarian, C.1
Healey, M.J.2
Fatkin, D.3
Giewat, M.4
Duffy, C.5
Seidman, C.E.6
Seidman, J.G.7
-
62
-
-
13444281662
-
Hypertrophic cardiomyopathy: From 'heart tumour' to a complex molecular genetic disorder
-
DOI 10.1016/j.hlc.2004.01.026
-
A Doolan L Nguyen C Semsarian 2004 Hypertrophic cardiomyopathy: from "heart tumour" to a complex molecular genetic disorder Heart, Lung and Circulation 13 15 25 10.1016/j.hlc.2004.01.026 1:CAS:528:DC%2BD2MXit1WmsL4%3D 16352163 (Pubitemid 40903138)
-
(2004)
Heart Lung and Circulation
, vol.13
, Issue.1
, pp. 15-25
-
-
Doolan, A.1
Nguyen, L.2
Semsarian, C.3
-
63
-
-
32644441228
-
Diltiazem treatment prevents diastolic heart failure in mice with familial hypertrophic cardiomyopathy
-
DOI 10.1016/j.ejheart.2005.07.012, PII S1388984205002138
-
D Westermann BC Knollmann P Steendijk S Rutschow A Riad M Pauschinger, et al. 2006 Diltiazem treatment prevents diastolic heart failure in mice with familial hypertrophic cardiomyopathy European Journal of Heart Failure 8 115 121 10.1016/j.ejheart.2005.07.012 1:CAS:528:DC%2BD28XhsFOju7Y%3D 16214409 (Pubitemid 43240843)
-
(2006)
European Journal of Heart Failure
, vol.8
, Issue.2
, pp. 115-121
-
-
Westermann, D.1
Knollmann, B.C.2
Steendijk, P.3
Rutschow, S.4
Riad, A.5
Pauschinger, M.6
Potter, J.D.7
Schultheiss, H.-P.8
Tschope, C.9
-
64
-
-
0035902491
-
Simvastatin induces regression of cardiac hypertrophy and fibrosis and improves cardiac function in a transgenic rabbit model of human hypertrophic cardiomyopathy
-
10.1161/hc2801.094031 1:CAS:528:DC%2BD3MXlslOmtL0%3D 11457751
-
R Patel SF Nagueh N Tsybouleva M Abdellatif S Lutucuta HA Kopelen, et al. 2001 Simvastatin induces regression of cardiac hypertrophy and fibrosis and improves cardiac function in a transgenic rabbit model of human hypertrophic cardiomyopathy Circulation 104 317 324 10.1161/hc2801.094031 1:CAS:528:DC%2BD3MXlslOmtL0%3D 11457751
-
(2001)
Circulation
, vol.104
, pp. 317-324
-
-
Patel, R.1
Nagueh, S.F.2
Tsybouleva, N.3
Abdellatif, M.4
Lutucuta, S.5
Kopelen, H.A.6
-
65
-
-
35648967680
-
HMG CoA reductase inhibition and left ventricular mass in hypertrophic cardiomyopathy: A randomized placebo-controlled pilot study
-
DOI 10.1111/j.1365-2362.2007.01877.x
-
J Bauersachs S Störk M Kung C Waller F Fidler C Hoyer, et al. 2007 HMG CoA reductase inhibition and left ventricular mass in hypertrophic cardiomyopathy: A randomized placebo-controlled pilot study European Journal of Clinical Investigation 37 852 859 10.1111/j.1365-2362.2007.01877.x 1:CAS:528:DC%2BD2sXhsVSrtr3O 17973781 (Pubitemid 350029212)
-
(2007)
European Journal of Clinical Investigation
, vol.37
, Issue.11
, pp. 852-859
-
-
Bauersachs, J.1
Stork, S.2
Kung, M.3
Waller, C.4
Fidler, F.5
Hoyer, C.6
Frantz, S.7
Weidemann, F.8
Ertl, G.9
Angermann, C.E.10
-
66
-
-
33646757738
-
Compound and double mutations in patients with hypertrophic cardiomyopathy: Implications for genetic testing and counselling
-
10.1136/jmg.2005.033886
-
J Ingles A Doolan C Chiu J Seidman C Seidman C Semsarian 2005 Compound and double mutations in patients with hypertrophic cardiomyopathy: Implications for genetic testing and counselling Journal of Medical Genetics 42 10 59 10.1136/jmg.2005.033886
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.10
, pp. 59
-
-
Ingles, J.1
Doolan, A.2
Chiu, C.3
Seidman, J.4
Seidman, C.5
Semsarian, C.6
-
68
-
-
41949129330
-
Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy
-
10.1161/CIRCULATIONAHA.107.755777 18362229
-
T Tsoutsman M Kelly D Ng J-E Tan E Tu L Lam, et al. 2008 Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathy Circulation 117 1820 1831 10.1161/CIRCULATIONAHA. 107.755777 18362229
-
(2008)
Circulation
, vol.117
, pp. 1820-1831
-
-
Tsoutsman, T.1
Kelly, M.2
Ng, D.3
Tan, J.-E.4
Tu, E.5
Lam, L.6
|