-
1
-
-
4844222283
-
Lifetime risk for development of atrial fibrillation: the Framingham Heart Study
-
Lloyd-Jones, D.M., Wang, T.J., Leip, E.P., Larson, M.G., Levy, D., Vasan, R.S., D'Agostino, R.B., Massaro, J.M., Beiser, A., Wolf, P.A. et al. (2004) Lifetime risk for development of atrial fibrillation: the Framingham Heart Study. Circulation, 110, 1042-1046.
-
(2004)
Circulation
, vol.110
, pp. 1042-1046
-
-
Lloyd-Jones, D.M.1
Wang, T.J.2
Leip, E.P.3
Larson, M.G.4
Levy, D.5
Vasan, R.S.6
D'Agostino, R.B.7
Massaro, J.M.8
Beiser, A.9
Wolf, P.A.10
-
2
-
-
0038037760
-
Familial atrial fibrillation isagenetically heterogeneous disorder
-
Darbar, D., Herron, K.J., Ballew, J.D., Jahangir, A., Gersh, B.J., Shen, W.-K., Hammill, S.C., Packer, D.L. and Olson, T.M. (2003) Familial atrial fibrillation isagenetically heterogeneous disorder.J. Am. Coll. Cardiol., 41, 2185-2192.
-
(2003)
J. Am. Coll. Cardiol.
, vol.41
, pp. 2185-2192
-
-
Darbar, D.1
Herron, K.J.2
Ballew, J.D.3
Jahangir, A.4
Gersh, B.J.5
Shen, W.-K.6
Hammill, S.C.7
Packer, D.L.8
Olson, T.M.9
-
3
-
-
0037428218
-
KCNQ1 gain-of-function mutation in familial atrial fibrillation
-
Chen, Y.H., Xu, S.J., Bendahhou, S., Wang, X.L., Wang, Y., Xu, W.Y., Jin, H.W., Sun, H., Su, X.Y., Zhuang, Q.N. et al. (2003) KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science, 299, 251-254.
-
(2003)
Science
, vol.299
, pp. 251-254
-
-
Chen, Y.H.1
Xu, S.J.2
Bendahhou, S.3
Wang, X.L.4
Wang, Y.5
Xu, W.Y.6
Jin, H.W.7
Sun, H.8
Su, X.Y.9
Zhuang, Q.N.10
-
4
-
-
46949093558
-
Atrial natriuretic peptide frameshift mutationin familial atrial fibrillation
-
Hodgson-Zingman, D.M., Karst, M.L., Zingman, L.V., Heublein, D.M., Darbar, D., Herron, K.J., Ballew, J.B., de Andrade, M., Burnett, J.C. and Olson, T.M. (2008) Atrial natriuretic peptide frameshift mutationin familial atrial fibrillation. New Engl. J. Med., 359, 158-165.
-
(2008)
New Engl. J. Med.
, vol.359
, pp. 158-165
-
-
Hodgson-Zingman, D.M.1
Karst, M.L.2
Zingman, L.V.3
Heublein, D.M.4
Darbar, D.5
Herron, K.J.6
Ballew, J.B.7
de Andrade, M.8
Burnett, J.C.9
Olson, T.M.10
-
5
-
-
57349179985
-
Mutationinnuclear pore component NUP155 leadsto atrialfibrillation and early sudden cardiac death
-
Zhang, X., Chen, S., Yoo, S., Chakrabarti, S., Zhang, T., Ke, T., Oberti, C., Yong, S.L., Fang, F., Li, L. et al. (2008) Mutationinnuclear pore component NUP155 leadsto atrialfibrillation and early sudden cardiac death. Cell, 135, 1017-1027.
-
(2008)
Cell
, vol.135
, pp. 1017-1027
-
-
Zhang, X.1
Chen, S.2
Yoo, S.3
Chakrabarti, S.4
Zhang, T.5
Ke, T.6
Oberti, C.7
Yong, S.L.8
Fang, F.9
Li, L.10
-
6
-
-
43049129979
-
X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by Emerin mutation
-
Karst, M.L., Herron, K.J. and Olson, T.M. (2005) X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by Emerin mutation. J. Cardiovasc. Electrophysiol., 19, 510-515.
-
(2005)
J. Cardiovasc. Electrophysiol.
, vol.19
, pp. 510-515
-
-
Karst, M.L.1
Herron, K.J.2
Olson, T.M.3
-
7
-
-
12544257550
-
Sodium channel mutations and susceptibility to heart failure and atrial fibrillation
-
Olson, T.M., Michels, V.V., Ballew, J.D., Reyna, S.P., Karst, M.L., Herron, K.J., Horton, S.C., Rodeheffer, R.J. and Anderson, J.L. (2005) Sodium channel mutations and susceptibility to heart failure and atrial fibrillation. JAMA, 293, 447-454.
-
(2005)
JAMA
, vol.293
, pp. 447-454
-
-
Olson, T.M.1
Michels, V.V.2
Ballew, J.D.3
Reyna, S.P.4
Karst, M.L.5
Herron, K.J.6
Horton, S.C.7
Rodeheffer, R.J.8
Anderson, J.L.9
-
8
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
-
Fatkin, D., MacRae, C., Sasaki, T., Wolff, M.R., Porcu, M., Frenneaux, M., Atherton, J., Vidaillet, H.J., Spudich, S., De Girolami, U. et al. (1999) Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N. Engl. J. Med., 341, 1715-1724.
-
(1999)
N. Engl. J. Med.
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
MacRae, C.2
Sasaki, T.3
Wolff, M.R.4
Porcu, M.5
Frenneaux, M.6
Atherton, J.7
Vidaillet, H.J.8
Spudich, S.9
De Girolami, U.10
-
9
-
-
84856079178
-
Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy
-
Theis, J.L., Sharpe, K.M., Matsumoto, M.E., Chai, H.S., Nair, A.A., Theis, J.D., de Andrade, M., Wieben, E.D., Michels, V.V. and Olson, T.M. (2011) Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy. Circ. Cardiovasc. Genet., 4, 585-594.
-
(2011)
Circ. Cardiovasc. Genet.
, vol.4
, pp. 585-594
-
-
Theis, J.L.1
Sharpe, K.M.2
Matsumoto, M.E.3
Chai, H.S.4
Nair, A.A.5
Theis, J.D.6
de Andrade, M.7
Wieben, E.D.8
Michels, V.V.9
Olson, T.M.10
-
10
-
-
0038275985
-
Cloning and characterization of a novel cardiac-specific kinase that interacts specifically with cardiac troponin I
-
Zhao, Y., Meng, X.M., Wei, Y.J., Zhao, X.W., Liu, D.Q., Cao, H.Q., Liew, C.C. and Ding, J.F. (2003) Cloning and characterization of a novel cardiac-specific kinase that interacts specifically with cardiac troponin I. J. Mol. Med., 81, 297-304.
-
(2003)
J. Mol. Med.
, vol.81
, pp. 297-304
-
-
Zhao, Y.1
Meng, X.M.2
Wei, Y.J.3
Zhao, X.W.4
Liu, D.Q.5
Cao, H.Q.6
Liew, C.C.7
Ding, J.F.8
-
11
-
-
70349684832
-
TNNI3K modifies disease progression in murine models of cardiomyopathy
-
Wheeler, F.C., Tang, H., Marks, O.A., Hadnott, T.N., Chu, P.L., Mao, L., Rockman, H.A. and Marchuk, D.A. (2009) TNNI3K modifies disease progression in murine models of cardiomyopathy. PLoS Genet., 5, 1-11.
-
(2009)
PLoS Genet
, vol.5
, pp. 1-11
-
-
Wheeler, F.C.1
Tang, H.2
Marks, O.A.3
Hadnott, T.N.4
Chu, P.L.5
Mao, L.6
Rockman, H.A.7
Marchuk, D.A.8
-
12
-
-
84871716646
-
Over expression of TNNI3K, acardiac-specific MAPKKK, promotescardiac dysfunction
-
Tang, H., Xiao, K., Mao, L., Rockman, H.A. and Marchuk, D.A. (2013) Over expression of TNNI3K, acardiac-specific MAPKKK, promotescardiac dysfunction. J. Mol. Cell. Cardiol., 54, 101-111.
-
(2013)
J. Mol. Cell. Cardiol.
, vol.54
, pp. 101-111
-
-
Tang, H.1
Xiao, K.2
Mao, L.3
Rockman, H.A.4
Marchuk, D.A.5
-
13
-
-
84886416217
-
Inhibition of the cardiomyocyte-specific kinase TNNI3K limits oxidative stress, injury, and adverse remodeling in the ischemic heart
-
Vagnozzi, R.J., Gatto, G.J. Jr, Kallander, L.S., Hoffman, N.E., Mallilankaraman, K., Ballard, V.L.T., Lawhorn, B.G., Stoy, P., Philp, J., Graves, A.P. et al. (2013) Inhibition of the cardiomyocyte-specific kinase TNNI3K limits oxidative stress, injury, and adverse remodeling in the ischemic heart. Sci. Transl. Med., 5, 1-12.
-
(2013)
Sci. Transl. Med.
, vol.5
, pp. 1-12
-
-
Vagnozzi, R.J.1
Gatto, G.J.2
Kallander, L.S.3
Hoffman, N.E.4
Mallilankaraman, K.5
Ballard, V.L.T.6
Lawhorn, B.G.7
Stoy, P.8
Philp, J.9
Graves, A.P.10
-
14
-
-
84872010658
-
Dissection of a quantitative trait locus for PR interval duration identifies TNNI3K as a novel modulator of cardiac conduction
-
Lodder, E.M., Scicluna, B.P., Milano, A., Sun, A.Y., Tang, H., Remme, C.A.,Moerland,P.D.,Tanck,M.W.T.,Pitt,G.S.,Marchuk, D.A.etal.(2012) Dissection of a quantitative trait locus for PR interval duration identifies TNNI3K as a novel modulator of cardiac conduction. PLoS Genet., 8, 1-8.
-
(2012)
PLoS Genet
, vol.8
, pp. 1-8
-
-
Lodder, E.M.1
Scicluna, B.P.2
Milano, A.3
Sun, A.Y.4
Tang, H.5
Remme, C.A.6
Moerland, P.D.7
Tanck, M.W.T.8
Pitt, G.S.9
Marchuk, D.A.10
-
15
-
-
84911377107
-
Mutation of TNNI3K gene increased incidence of arrhythmias in culture cardiomyocytes and in vivo mouse hearts
-
A31. Resuscitation Science Symposium. Abstract
-
Lai, Z.F., Chen, Y.Z., Chen, J., Tsuda, H., Kitamoto, Y. and Kim-Mitsuyama, S. (2012) Mutation of TNNI3K gene increased incidence of arrhythmias in culture cardiomyocytes and in vivo mouse hearts. Circulation, 126, A31. Resuscitation Science Symposium. Abstract.
-
(2012)
Circulation
, vol.126
-
-
Lai, Z.F.1
Chen, Y.Z.2
Chen, J.3
Tsuda, H.4
Kitamoto, Y.5
Kim-Mitsuyama, S.6
-
16
-
-
0035026704
-
Predicting deleterious amino acid substitutions
-
Ng, P.C. and Henikoff, S. (2001) Predicting deleterious amino acid substitutions. Genome Res., 11, 863-874.
-
(2001)
Genome Res
, vol.11
, pp. 863-874
-
-
Ng, P.C.1
Henikoff, S.2
-
17
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei, I.A., Schmidt, S., Peshkin, L., Ramensky, V.E., Gerasimova, A., Bork, P., Kondrashov, A.S. and Sunyaev, S.R. (2010) A method and server for predicting damaging missense mutations. Nat. Methods, 7, 248-249.
-
(2010)
Nat. Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
Kondrashov, A.S.7
Sunyaev, S.R.8
-
18
-
-
52449132084
-
OverexpressionofTNNI3K, a cardiac-specific MAP kinase, promotes P19CL6-derived cardiac myogenesis and prevents myocardial infarction-induced injury
-
Lai, Z.F.,Chen,Y.Z.,Feng, L.P.,Meng,X.M.,Ding, J.F.,Wang,L.Y., Ye, J., Li, P., Cheng, X.S., Kitamoto,Y. et al. (2008) OverexpressionofTNNI3K, a cardiac-specific MAP kinase, promotes P19CL6-derived cardiac myogenesis and prevents myocardial infarction-induced injury. Am. J. Physiol. Heart Circ. Physiol., 295, H708-H716.
-
(2008)
Am. J. Physiol. Heart Circ. Physiol.
, vol.295
, pp. H708-H716
-
-
Lai, Z.F.1
Chen, Y.Z.2
Feng, L.P.3
Meng, X.M.4
Ding, J.F.5
Wang, L.Y.6
Ye, J.7
Li, P.8
Cheng, X.S.9
Kitamoto, Y.10
-
19
-
-
84874587157
-
TNNI3K, a cardiac-specific kinase, promotes physiological cardiac hypertrophy in transgenic mice
-
Wang, X., Wang, J., Su, M., Wang, C., Chen, J., Wang, H., Song, L., Zou, Y., Zhang, L., Zhang, Y. et al. (2013) TNNI3K, a cardiac-specific kinase, promotes physiological cardiac hypertrophy in transgenic mice. PLoS One, 8, 1-11.
-
(2013)
PLoS One
, vol.8
, pp. 1-11
-
-
Wang, X.1
Wang, J.2
Su, M.3
Wang, C.4
Chen, J.5
Wang, H.6
Song, L.7
Zou, Y.8
Zhang, L.9
Zhang, Y.10
-
20
-
-
84884592445
-
Genic intolerance to functional variation and the interpretation of personal genomes
-
Petrovski, S., Wang, Q., Heinzen, E.L., Allen, A.S. and Goldstein, D.B. (2013) Genic intolerance to functional variation and the interpretation of personal genomes. PLoS Genet., 9, 1-13.
-
(2013)
PLoS Genet
, vol.9
, pp. 1-13
-
-
Petrovski, S.1
Wang, Q.2
Heinzen, E.L.3
Allen, A.S.4
Goldstein, D.B.5
-
21
-
-
0035964342
-
Electrostaticsofnanosystems:applicationtomicrotubulesand theribosome
-
Baker, N.A., Sept, D., Joseph, S., Holst, M.J. and McCammon, J.A. (2001) Electrostaticsofnanosystems:applicationtomicrotubulesand theribosome. Proc. Natl. Acad. Sci. USA, 98, 10037-10041.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 10037-10041
-
-
Baker, N.A.1
Sept, D.2
Joseph, S.3
Holst, M.J.4
McCammon, J.A.5
-
22
-
-
34548789645
-
Identification of the dual specificity and the functional domains of the cardiac-specific protein kinase TNNI3K
-
Feng, Y., Cao, H.Q.,Liu, Z., Ding,J.F. andMeng,X.M. (2007) Identification of the dual specificity and the functional domains of the cardiac-specific protein kinase TNNI3K. Gen. Physiol. Biophys., 26, 104-109.
-
(2007)
Gen. Physiol. Biophys.
, vol.26
, pp. 104-109
-
-
Feng, Y.1
Cao, H.Q.2
Liu, Z.3
Ding, J.F.4
Meng, X.M.5
-
23
-
-
79958140522
-
A graphical interface for the FoldX forcefield
-
Van Durme, J., Delgado, J., Stricher, F., Serrano, L., Schymkowitz, J. and Rousseau, F. (2011) A graphical interface for the FoldX forcefield. Bioinformatics, 27, 1711-1712.
-
(2011)
Bioinformatics
, vol.27
, pp. 1711-1712
-
-
Van Durme, J.1
Delgado, J.2
Stricher, F.3
Serrano, L.4
Schymkowitz, J.5
Rousseau, F.6
-
24
-
-
33846517015
-
KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation
-
Olson, T.M., Alekseev, A.E., Moreau, C., Liu, X.K., Zingman, L.V., Miki, T., Seino, S., Asirvatham, S.J., Jahangir, A. and Terzic, A. (2007) KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation. Nat. Clin. Pract. Cardiovasc. Med., 4, 110-116.
-
(2007)
Nat. Clin. Pract. Cardiovasc. Med.
, vol.4
, pp. 110-116
-
-
Olson, T.M.1
Alekseev, A.E.2
Moreau, C.3
Liu, X.K.4
Zingman, L.V.5
Miki, T.6
Seino, S.7
Asirvatham, S.J.8
Jahangir, A.9
Terzic, A.10
-
25
-
-
84873855851
-
Genetic mutations and mechanisms in dilated cardiomyopathy
-
McNally, E.M., Golbus, J.R. and Puckelwartz, M.J. (2013) Genetic mutations and mechanisms in dilated cardiomyopathy. J. Clin. Invest., 123, 19-26.
-
(2013)
J. Clin. Invest.
, vol.123
, pp. 19-26
-
-
McNally, E.M.1
Golbus, J.R.2
Puckelwartz, M.J.3
-
26
-
-
84866279645
-
Loss of proteostatic control as a substrate for atrial fibrillation:anovel targetfor upstreamtherapybyheat shock proteins
-
Meijering, R.A.M., Zhang, D., Hoogstra-Berends, F., Henning, R.H. and Brundel, B.J.J.M. (2012) Loss of proteostatic control as a substrate for atrial fibrillation:anovel targetfor upstreamtherapybyheat shock proteins.Front. Physiol., 3, 1-11.
-
(2012)
Front. Physiol.
, vol.3
, pp. 1-11
-
-
Meijering, R.A.M.1
Zhang, D.2
Hoogstra-Berends, F.3
Henning, R.H.4
Brundel, B.J.J.M.5
-
27
-
-
34547681313
-
Human ab-crystallin mutation causes oxido-reductive stress and protein aggregation in cardiomyopathy in mice
-
Rajasekaran, N.S., Connell, P., Christians, E.S., Yan, L.J., Taylor, R.P., Orosz, A., Zhang, X.Q., Stevenson, T.J., Peshock, R.M., Leopold, J.A. et al. (2007) Human ab-crystallin mutation causes oxido-reductive stress and protein aggregation in cardiomyopathy in mice. Cell, 130, 427-439.
-
(2007)
Cell
, vol.130
, pp. 427-439
-
-
Rajasekaran, N.S.1
Connell, P.2
Christians, E.S.3
Yan, L.J.4
Taylor, R.P.5
Orosz, A.6
Zhang, X.Q.7
Stevenson, T.J.8
Peshock, R.M.9
Leopold, J.A.10
-
28
-
-
0019165493
-
Echocardiographic measurements in normal subjects from infancy to old age
-
Henry, W.L., Gardin, J.M. and Ware, J.H. (1980) Echocardiographic measurements in normal subjects from infancy to old age. Circulation, 62, 1056-1061.
-
(1980)
Circulation
, vol.62
, pp. 1056-1061
-
-
Henry, W.L.1
Gardin, J.M.2
Ware, J.H.3
-
29
-
-
0029945706
-
Descent graphs in pedigree analysis: application to haplotyping, location scores, and marker sharing statistics
-
Sobel, E. and Lange, K. (1996) Descent graphs in pedigree analysis: application to haplotyping, location scores, and marker sharing statistics. Am. J. Hum. Genet., 58, 1323-1337.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
30
-
-
77956295988
-
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M. et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res., 20, 1297- 1303.
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
Kernytsky, A.6
Garimella, K.7
Altshuler, D.8
Gabriel, S.9
Daly, M.10
-
31
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo, M.A., Banks, E., Poplin, R.E., Garimella, K.V., Maquire, J.R., Hartl, C., Philippakis, A.A., del Angel, G., Rivas, M.A., Hanna, M. et al.(2011) A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet., 43, 491-498.
-
(2011)
Nat. Genet.
, vol.43
, pp. 491-498
-
-
DePristo, M.A.1
Banks, E.2
Poplin, R.E.3
Garimella, K.V.4
Maquire, J.R.5
Hartl, C.6
Philippakis, A.A.7
del Angel, G.8
Rivas, M.A.9
Hanna, M.10
-
32
-
-
84975795680
-
An integrated map of genetic variation from 1092 human genomes
-
The 1000 Genomes Consortium
-
The 1000 Genomes Consortium. (2012) An integrated map of genetic variation from 1092 human genomes. Nature, 491, 56-65.
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
-
33
-
-
84911377425
-
-
Exome Variant Server, NHLBI GO Exome Sequencing Project (ESP), Seattle, WA [October 2013]
-
Exome Variant Server, NHLBI GO Exome Sequencing Project (ESP), Seattle,WA (URL: http://eversusgs.washington.edu/EVS/) [October 2013].
-
-
-
-
34
-
-
74949138753
-
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
-
Drmanac, R., Sparks, A.B., Callow, M.J., Halpern, A.L., Burns, N.L., Kermani, B.G., Carnevali, P., Nazarenko, I., Nilsen, G.B., Yeung, G. et al. (2010) Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays. Science, 327, 78-81.
-
(2010)
Science
, vol.327
, pp. 78-81
-
-
Drmanac, R.1
Sparks, A.B.2
Callow, M.J.3
Halpern, A.L.4
Burns, N.L.5
Kermani, B.G.6
Carnevali, P.7
Nazarenko, I.8
Nilsen, G.B.9
Yeung, G.10
-
35
-
-
58149193233
-
The SWISS-MODEL Repository and associated resources
-
Kiefer, F., Arnold, K., Kunzli, M., Bordoli, L. and Schwede, T. (2009) The SWISS-MODEL Repository and associated resources. Nucleic Acids Res., 37, D387-D392.
-
(2009)
Nucleic Acids Res
, vol.37
, pp. D387-D392
-
-
Kiefer, F.1
Arnold, K.2
Kunzli, M.3
Bordoli, L.4
Schwede, T.5
-
36
-
-
3242877815
-
ClusPro: a fully automated algorithm for protein-protein docking
-
Comeau, S.R., Gatchell, D.W., Vajda,S.and Camacho, C.J. (2004) ClusPro: a fully automated algorithm for protein-protein docking. Nucleic Acids Res., 32, W96-W99.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. W96-W99
-
-
Comeau, S.R.1
Gatchell, D.W.2
Vajda, S.3
Camacho, C.J.4
-
37
-
-
84888295075
-
How good is automated protein docking?
-
Kozakov, D., Beglov, D., Bohnuud, T., Mottarella, S.E., Xia, B., Hall, D.R. and Vajda, S. (2013) How good is automated protein docking? Proteins, 81, 2159-2166.
-
(2013)
Proteins
, vol.81
, pp. 2159-2166
-
-
Kozakov, D.1
Beglov, D.2
Bohnuud, T.3
Mottarella, S.E.4
Xia, B.5
Hall, D.R.6
Vajda, S.7
-
38
-
-
0034971165
-
Mutations that alter the surface of alpha-tropomyosin are associated with dilated cardiomyopathy
-
Olson, T.M., Kishimoto, N.Y., Whitby, F.G. and Michels, V.V. (2001) Mutations that alter the surface of alpha-tropomyosin are associated with dilated cardiomyopathy. J. Mol. Cell Cardiol., 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
-
39
-
-
68949191192
-
Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy
-
Brauch, K.M., Karst, M.L., Herron, K.J., de Andrade, M., Pellikka, P.A., Rodeheffer, R.J., Michels, V.V. and Olson, T.M. (2009) Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy. J. Am. Coll. Cardiol., 54, 930-941.
-
(2009)
J. Am. Coll. Cardiol.
, vol.54
, pp. 930-941
-
-
Brauch, K.M.1
Karst, M.L.2
Herron, K.J.3
de Andrade, M.4
Pellikka, P.A.5
Rodeheffer, R.J.6
Michels, V.V.7
Olson, T.M.8
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