The DOI matches its Crossref record; 24 of the 25 references it cites were found in a registry or an index.
Metavinculin Mutations Alter Actin Interaction in Dilated Cardiomyopathy
Abstract
BACKGROUND: Vinculin and its isoform metavinculin are protein components of intercalated discs, structures that anchor thin filaments and transmit contractile force between cardiac myocytes. We tested the hypothesis that heritable dysfunction of metavinculin may contribute to the pathogenesis of dilated cardiomyopathy (DCM). METHODS AND RESULTS: We performed mutational analyses of the metavinculin-specific exon of vinculin in 350 unrelated patients with DCM. One missense mutation (Arg975Trp) and one 3-bp deletion (Leu954del) were identified. These mutations involved conserved amino acids, were absent in 500 control individuals, and significantly altered metavinculin-mediated cross-linking of actin filaments in an in vitro assay. Ultrastructural examination was performed in one patient (Arg975Trp), revealing grossly abnormal intercalated discs. A potential risk-conferring polymorphism (Ala934Val), identified in one DCM patient and one control individual, had a less pronounced effect on actin filament cross-linking. CONCLUSIONS: These data provide genetic and functional evidence for vinculin as a DCM gene and suggest that metavinculin plays a critical role in cardiac structure and function. Disruption of force transmission at the thin filament-intercalated disc interface is the likely mechanism by which mutations in metavinculin may lead to DCM.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Defects in VCL are associated with dilated cardiomyopathy in humans (Olson et al., 2002).”
From Population genomics reveal recent speciation and rapid evolutionary adaptation in polar bears (2014) · cites this paper as Olson et al., 2002
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Fatkin, D., MacRae, C. A., Sasaki, T., Wolff, M. R., Porcu, M., Frenneaux, M. P., Atherton, J. J., Vidaillet, H. J., Jr., Spudich, S., Girolami, U. D., et al. (1999) · New England Journal of Medicine · doi:10.1056/nejm199912023412302 · Cited by 1,366
Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy
Kamisago, M., Sharma, S. D., DePalma, S. R., Solomon, S., Sharma, P., McDonough, B., Smoot, L., Mullen, M. P., Woolf, P. K., Wigle, E. D., et al. (2000) · New England Journal of Medicine · doi:10.1056/nejm200012073432304 · Cited by 720
Michels, V. V., Moll, P. P., Miller, F. A., Tajik, A. J., Chu, J. S., Driscoll, D. J. O., Burnett, J. C. J., Rodeheffer, R. J., Chesebro, J. H., & Tazelaar, H. D. (1992) · New England Journal of Medicine · doi:10.1056/nejm199201093260201 · Cited by 695
Echocardiographic measurements in normal subjects from infancy to old age.
Henry, W. L., Gardin, J. M., & Ware, J. H. (1980) · Circulation · doi:10.1161/01.cir.62.5.1054 · Cited by 632
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. (1998) · Science · doi:10.1126/science.280.5364.750 · Cited by 621
Self-citationVinculin knockout results in heart and brain defects during embryonic development
Xu, W., Baribault, H., & Adamson, E. D. (1998) · Development · doi:10.1242/dev.125.2.327 · Cited by 538
Desmin Mutation Responsible for Idiopathic Dilated Cardiomyopathy
Li, D., Tapscoft, T., Gonzalez, O., Burch, P. E., Quiñones, M. A., Zoghbi, W. A., Hill, R., Bachinski, L. L., Mann, D. L., & Roberts, R. (1999) · Circulation · doi:10.1161/01.cir.100.5.461 · Cited by 445
Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
Francesco Muntoni, A., Cau, M., Ganau, A., Congiu, R., Arvedi, G., Mateddu, A., Marrosu, M. G., Cianchetti, C., Realdi, G., Cao, A., et al. (1993) · New England Journal of Medicine · doi:10.1056/nejm199309233291304 · Cited by 412
Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
Tsubata, S., Bowles, K. R., Vatta, M., Zintz, C., Titus, J. L., Muhonen, L. E., Bowles, N. E., & Towbin, J. A. (2000) · Journal of Clinical Investigation · doi:10.1172/jci9224 · Cited by 340
Brodsky, G. L., Francesco Muntoni, A., Miočiċ, S., Sinagra, G., Sewry, C. A., & Mestroni, L. (2000) · Circulation · doi:10.1161/01.cir.101.5.473 · Cited by 329
Research works printed but not linked: 5
- 10.1161/circ.100.5.461 · DOI
- 10.1161/circ.101.5.473 · DOI
- Cormack B. Mutagenesis by the polymerase chain reaction.In: Ausubel F Brent R Kingston R et al eds. Current Protocols in Molecular Biology. New York NY: John Wiley and Sons; 1991: 8.5.1–8.5.9.
- 10.1161/circ.95.1.17 · DOI
- 10.1161/res.86.8.846 · DOI
Cited by
Sorted by citations
McCrohon, J. A., Moon, J., Prasad, S. K., McKenna, W. J., Lorenz, C. H., Coats, A. J. S., & Pennell, D. J. (2003) · Circulation · doi:10.1161/01.cir.0000078641.19365.4c · Cited by 1,154
Dilated cardiomyopathy: the complexity of a diverse genetic architecture
Hershberger, R. E., Hedges, D. J., & Morales, A. (2013) · Nature Reviews Cardiology · doi:10.1038/nrcardio.2013.105 · Cited by 1,036
Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline
Hershberger, R. E., Lindenfeld, J. M., Mestroni, L., Seidman, C. E., Taylor, M. R. G., & Towbin, J. A. (2009) · Journal of Cardiac Failure · doi:10.1016/j.cardfail.2009.01.006 · Cited by 700
Striated Muscle Cytoarchitecture: An Intricate Web of Form and Function
Clark, K. A., McElhinny, A., Beckerle, M. C., & Gregorio, C. C. (2002) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.18.012502.105840 · Cited by 705
The integrin adhesome: from genes and proteins to human disease
Winograd-Katz, S. E., Fässler, R., Geiger, B., & Legate, K. R. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3769 · Cited by 641
Targeted deletion of Dicer in the heart leads to dilated cardiomyopathy and heart failure
Chen, J., Murchison, E. P., Tang, R., Callis, T. E., Tatsuguchi, M., Deng, Z., Rojas, M., Hammond, S. M., Schneider, M. D., Selzman, C. H., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710228105 · Cited by 576
Sodium Channel Mutations and Susceptibility to Heart Failure and Atrial Fibrillation
Olson, T. M. (2005) · JAMA · doi:10.1001/jama.293.4.447 · Cited by 552
Self-citationJefferies, J. L., & Towbin, J. A. (2010) · The Lancet · doi:10.1016/s0140-6736(09)62023-7 · Cited by 580
Mutations in Cypher/ZASPin patients with dilated cardiomyopathy and left ventricular non-compaction
Vatta, M., Mohapatra, B., Jimenez, S., Sánchez, X., Faulkner, G., Perles, Z., Sinagra, G., Lin, J.-H. I., Vu, T. M., Zhou, Q., et al. (2003) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2003.10.021 · Cited by 520
Clinical and genetic issues in familial dilated cardiomyopathy
Burkett, E., & Hershberger, R. E. (2005) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2004.11.066 · Cited by 467
Population genomics reveal recent speciation and rapid evolutionary adaptation in polar bears
Liu, S., Lorenzen, E. D., Fumagalli, M., Li, B., Harris, K., Xiong, Z., Zhou, L., Korneliussen, T. S., Somel, M., Babbitt, C., et al. (2014) · Cell · doi:10.1016/j.cell.2014.03.054 · Cited by 411
Mediation, Modulation, and Consequences of Membrane-Cytoskeleton Interactions
Doherty, G. J., & McMahon, H. T. (2008) · Annual Review of Biophysics · doi:10.1146/annurev.biophys.37.032807.125912 · Cited by 378
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing
Pugh, T. J., Kelly, M., Gowrisankar, S., Hynes, E. D., Seidman, M. A., Baxter, S. M., Bowser, M., Harrison, B., Aaron, D., Mahanta, L., et al. (2014) · Genetics in Medicine · doi:10.1038/gim.2013.204 · Cited by 370
Single and collective cell migration: the mechanics of adhesions
Pascalis, C. D., & Etienne‐Manneville, S. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-03-0134 · Cited by 363
Mechanotransduction in Cardiac Hypertrophy and Failure
Lyon, R. C., Zanella, F., Omens, J. H., & Sheikh, F. (2015) · Circulation Research · doi:10.1161/circresaha.116.304937 · Cited by 356
Kostetskii, I., Li, J., Xiong, Y., Zhou, R., Ferrari, V. A., Patel, V. V., Molkentin, J. D., & Radice, G. L. (2005) · Circulation Research · doi:10.1161/01.res.0000156274.72390.2c · Cited by 325
Molecular Mechanisms of Inherited Cardiomyopathies
Fatkin, D., & Graham, R. M. (2002) · Physiological Reviews · doi:10.1152/physrev.00012.2002 · Cited by 328
Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy
Hershberger, R. E., & Siegfried, J. D. (2011) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2011.01.015 · Cited by 322
THE GENETIC BASIS FOR CARDIAC REMODELING
Ahmad, F., Seidman, J. G., & Seidman, C. E. (2005) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.6.080604.162132 · Cited by 305
Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals
Hershberger, R. E., Morales, A., & Siegfried, J. D. (2010) · Genetics in Medicine · doi:10.1097/gim.0b013e3181f2481f · Cited by 289
Mohapatra, B., Jimenez, S., Lin, J.-H. I., Bowles, K. R., Coveler, K. J., Marx, J. G., Chrisco, M. A., Murphy, R. T., Lurie, P. R., Schwartz, R. J., et al. (2003) · Molecular Genetics and Metabolism · doi:10.1016/s1096-7192(03)00142-2 · Cited by 269
Pirruccello, J. P., Bick, A., Wang, M., Chaffin, M., Friedman, S., Yao, J., Guo, X., Venkatesh, B. A., Taylor, K. D., Post, W. S., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15823-7 · Cited by 267
Genetic causes of human heart failure
Morita, H., Seidman, J. G., & Seidman, C. E. (2005) · Journal of Clinical Investigation · doi:10.1172/jci24351 · Cited by 264
Alcalai, R., Metzger, S., Rosenheck, S., Meiner, V., & Chajek-Shaul, T. (2003) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(03)00628-4 · Cited by 241
Integrins and Integrin-Associated Proteins in the Cardiac Myocyte
Israeli‐Rosenberg, S., Manso, A. M., Okada, H., & Ross, R. S. (2014) · Circulation Research · doi:10.1161/circresaha.114.301275 · Cited by 239
Genetics of dilated cardiomyopathy: practical implications for heart failure management
Rosenbaum, A. N., Agre, K. E., & Pereira, N. L. (2019) · Nature Reviews Cardiology · doi:10.1038/s41569-019-0284-0 · Cited by 221
Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy
Hassel, D., Dahme, T., Erdmann, J., Meder, B., Huge, A., Stoll, M., Just, S., Heß, A., Ehlermann, P., Weichenhan, D., et al. (2009) · Nature Medicine · doi:10.1038/nm.2037 · Cited by 211
Zemljic‐Harpf, A. E., Miller, J. C., Henderson, S. A., Wright, A. T., Manso, A. M., Elsherif, L., Dalton, N. D., Thor, A., Perkins, G. A., McCulloch, A. D., et al. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00728-07 · Cited by 208
Spatial distribution and functional significance of activated vinculin in living cells
Chen, H. A., Cohen, D. M., Choudhury, D. M., Kioka, N., & Craig, S. W. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200410100 · Cited by 197
Hershberger, R. E., Parks, S. B., Kushner, J. D., Li, D., Ludwigsen, S., Jakobs, P. M., Nauman, D. J., Burgess, D., Partain, J., & Litt, M. J. (2008) · Clinical and Translational Science · doi:10.1111/j.1752-8062.2008.00017.x · Cited by 196
The physiological role of cardiac cytoskeleton and its alterations in heart failure
Sequeira, V., Nijenkamp, L. L. A. M., Regan, J. A., & van der Velden, J. (2013) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2013.07.011 · Cited by 198
αB-crystallin mutation in dilated cardiomyopathy
Inagaki, N., Hayashi, T., Arimura, T., Koga, Y., Takahashi, M., Shibata, H., Teraoka, K., Chikamori, T., Yamashina, A., & Kimura, A. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.01.154 · Cited by 190
Integrin signalling: The tug-of-war in heart hypertrophy
Brancaccio, M., Hirsch, E., Notte, A., Selvetella, G., Lembo, G., & Tarone, G. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2005.12.015 · Cited by 191
Cooperative coupling of cell-matrix and cell–cell adhesions in cardiac muscle
McCain, M. L., Lee, H., Aratyn-Schaus, Y., Kléber, A. G., & Parker, K. K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203007109 · Cited by 187
Dilated Cardiomyopathy A Disease of the Intercalated Disc?
Perriard, J. (2003) · Trends in Cardiovascular Medicine · doi:10.1016/s1050-1738(02)00209-8 · Cited by 181
Between Rho(k) and a Hard Place
Huveneers, S., Daemen, M. J. A. P., & Hordijk, P. L. (2015) · Circulation Research · doi:10.1161/circresaha.116.305720 · Cited by 175
New Insights into Vinculin Function and Regulation
Peng, X. L., Nelson, E. S., Maiers, J. L., & DeMali, K. A. (2011) · International review of cytology · doi:10.1016/b978-0-12-386043-9.00005-0 · Cited by 179
Genetics of inherited cardiomyopathy
Jacoby, D. L., & McKenna, W. J. (2011) · European Heart Journal · doi:10.1093/eurheartj/ehr260 · Cited by 173
Sébillon, P., Bouchier, C., Duboscq-Bidot, L., Bonne, G., Ahamed, K., Charron, P., Drouin-Garraud, V., Millaire, A., Desrumeaux, G., Benaïche, A., et al. (2003) · Journal of Medical Genetics · doi:10.1136/jmg.40.8.560 · Cited by 171
Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene
Villard, E., Duboscq-Bidot, L., Charron, P., Benaiche, A., Conraads, V. M., Sylvius, N. B., & Michel Komajda, N. (2005) · European Heart Journal · doi:10.1093/eurheartj/ehi193 · Cited by 167
Current treatment of adult Duchenne muscular dystrophy
Wagner, K. R., Lechtzin, N., & Judge, D. P. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2006.06.009 · Cited by 152
Coincidence of Actin Filaments and Talin Is Required to Activate Vinculin
Chen, H. A., Choudhury, D. M., & Craig, S. W. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m607324200 · Cited by 151
Arimura, T., Hayashi, T., Terada, H., Lee, S.-Y., Zhou, Q., Takahashi, M., Ueda, K., Nouchi, T., Hohda, S., Shibutani, M., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311849200 · Cited by 151
Cell-Cell Connection to Cardiac Disease
Sheikh, F., Ross, R. S., & Chen, J. (2009) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2009.12.001 · Cited by 156
Three-Dimensional Structure of Vinculin Bound to Actin Filaments
Janssen, M. E. W., Kim, E., Liu, H., Fujimoto, L. M., Bobkov, A. A., Volkmann, N., & Hanein, D. (2006) · Molecular Cell · doi:10.1016/j.molcel.2005.11.020 · Cited by 149
The costamere bridges sarcomeres to the sarcolemma in striated muscle
Peter, A. K., Cheng, H., Ross, R. S., Knowlton, K. U., & Chen, J. (2011) · Progress in Pediatric Cardiology · doi:10.1016/j.ppedcard.2011.02.003 · Cited by 143
Sarcomeric Protein Mutations in Dilated Cardiomyopathy
Chang, A. N., & Potter, J. D. (2005) · Heart Failure Reviews · doi:10.1007/s10741-005-5252-6 · Cited by 142
Borrmann, C. M., Gründ, C., Kuhn, C., Hofmann, I., Pieperhoff, S., & Franke, W. W. (2006) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2006.02.009 · Cited by 141
Genetics of dilated cardiomyopathy
Kärkkäinen, S., & PEUHKURINEN, K. J. (2007) · Annals of Medicine · doi:10.1080/07853890601145821 · Cited by 141
Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy
Stark, K. J., Esslinger, U. B., Reinhard, W., Petrov, G., Winkler, T. W., Michel Komajda, N., Isnard, R., Charron, P., Villard, E., Cambien, F., et al. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001167 · Cited by 130
Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era
Norton, N., Robertson, P. D., Rieder, M. J., Zuchner, S. L., Rampersaud, E., Martin, E. R., Li, D., Nickerson, D. A., & Hershberger, R. E. (2012) · Circulation Cardiovascular Genetics · doi:10.1161/circgenetics.111.961805 · Cited by 119
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
Theis, J. L., Bos, J. M., Bartleson, V. B., Will, M. L., Binder, J. S., Vatta, M., Towbin, J. A., Gersh, B. J., Ommen, S. R., & Ackerman, M. J. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.10.119 · Cited by 118
The Genetic Bases of Cardiomyopathies
Richard, P., Villard, E., Charron, P., & Isnard, R. (2006) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2006.09.014 · Cited by 116
Heterozygous Inactivation of the Vinculin Gene Predisposes to Stress-Induced Cardiomyopathy
Zemljic‐Harpf, A. E., Ponrartana, S., Avalos, R. T., Jordan, M. C., Roos, K. P., Dalton, N. D., Phan, V. Q., Adamson, E. D., & Ross, R. S. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63364-0 · Cited by 114
Goossens, S., Janssens, B., Bonné, S., Rycke, R. M. D., Braet, F., van Hengel, J., & Roy, F. M. V. (2007) · Journal of Cell Science · doi:10.1242/jcs.004713 · Cited by 113
Vasile, V. C., WILL, M., Ommen, S. R., Edwards, W. D., Olson, T. M., & Ackerman, M. J. (2005) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2005.08.006 · Cited by 112
Self-citationVasile, V. C., Ommen, S. R., Edwards, W. D., & Ackerman, M. J. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.04.151 · Cited by 102
Myocyte-Restricted Focal Adhesion Kinase Deletion Attenuates Pressure Overload–Induced Hypertrophy
DiMichele, L. A., Doherty, J. T., Rojas, M., Beggs, H. E., Reichardt, L. F., Mack, C. P., & Taylor, J. M. (2006) · Circulation Research · doi:10.1161/01.res.0000240498.44752.d6 · Cited by 102
Zheng, M., Cheng, H., Li, X., Zhang, J., Cui, L., Ouyang, K., Han, L., Zhao, T. S., Gu, Y., Dalton, N. D., et al. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn400 · Cited by 100
Molecular genetics and pathogenesis of cardiomyopathy
Kimura, A. (2015) · Journal of Human Genetics · doi:10.1038/jhg.2015.83 · Cited by 99
Sussman, M. A., McCulloch, A. D., & Borg, T. K. (2002) · Circulation Research · doi:10.1161/01.res.0000041680.43270.f8 · Cited by 98
Sheikh, F., Chen, Y., Liang, X., Hirschy, A., Stenbit, A. E., Gu, Y., Dalton, N. D., Yajima, T., Lu, Y., Knowlton, K. U., et al. (2006) · Circulation · doi:10.1161/circulationaha.106.634469 · Cited by 93
The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy
Møller, D. V., Andersen, P. S., Hedley, P. L., Ersbøll, M. K., Bundgaard, H., Moolman‐Smook, J. C., Christiansen, M., & Køber, L. (2009) · European Journal of Human Genetics · doi:10.1038/ejhg.2009.34 · Cited by 92
de Morrée, A., Hensbergen, P. J., van Haagen, H. H. H. B. M., Dragan, I., Deelder, A. M., Hoen, P. A. C. ’., Frants, R. R., & van der Maarel, S. M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013854 · Cited by 85
Genetics of hypertrophic cardiomyopathy: one, two, or more diseases?
Bos, J. M., Ommen, S. R., & Ackerman, M. J. (2007) · Current Opinion in Cardiology · doi:10.1097/hco.0b013e3280e1cc7f · Cited by 82
A novel custom resequencing array for dilated cardiomyopathy
Zimmerman, R., Cox, S. W., Lakdawala, N. K., Cirino, A. L., Mancini‐DiNardo, D., Clark, E. H., Leon, A., Hynes, E. D., White, E. T., Baxter, S., et al. (2010) · Genetics in Medicine · doi:10.1097/gim.0b013e3181d6f7c0 · Cited by 82
Genetics of Dilated Cardiomyopathy
Fatkin, D., Otway, R., & Richmond, Z. (2010) · Heart Failure Clinics · doi:10.1016/j.hfc.2009.11.003 · Cited by 77
Kimura, A. (2010) · Journal of Human Genetics · doi:10.1038/jhg.2009.138 · Cited by 76
Francone, M. (2014) · ISRN Radiology · doi:10.1155/2014/365404 · Cited by 76
Molecular mechanisms in cardiomyopathy
Dadson, K., Hauck, L., & Billia, F. (2017) · Clinical Science · doi:10.1042/cs20160170 · Cited by 81
Zemljic‐Harpf, A. E., Godoy, J. C., Platoshyn, O., Asfaw, E. K., Busija, A. R., Domenighetti, A. A., & Ross, R. S. (2014) · Journal of Cell Science · doi:10.1242/jcs.143743 · Cited by 75
Mechanisms and Functions of Vinculin Interactions with Phospholipids at Cell Adhesion Sites
Izard, T., & Brown, D. T. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.r115.686493 · Cited by 71
Mechanical Regulation of Cardiac Aging in Model Systems
Sessions, A. O., & Engler, A. J. (2016) · Circulation Research · doi:10.1161/circresaha.116.307472 · Cited by 73
Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies
Brodehl, A., Ebbinghaus, H., Deutsch, M.-A., Gummert, J. F., Gärtner, A., Ratnavadivel, S., & Milting, H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20184381 · Cited by 73
A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy
Posch, M. G., Posch, M. J., Geier, C., Erdmann, B., Mueller, W., Richter, A., Ruppert, V., Pankuweit, S., Maisch, B., Perrot, A., et al. (2008) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2008.06.005 · Cited by 68
Effect of Epigallocatechin-3-Gallate on EGFR Signaling and Migration in Non-Small Cell Lung Cancer
Minnelli, C., Cianfruglia, L., Laudadio, E., Mobbili, G., Galeazzi, R., & Armeni, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111833 · Cited by 66
Shen, K., Tolbert, C. E., Guilluy, C., Swaminathan, V., Berginski, M. E., Burridge, K., Superfine, R., & Campbell, S. L. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.244293 · Cited by 65
The Structural Basis of Actin Organization by Vinculin and Metavinculin
Kim, L. Y., Thompson, P. M., Lee, H. T., Pershad, M., Campbell, S. L., & Alushin, G. M. (2015) · Journal of Molecular Biology · doi:10.1016/j.jmb.2015.09.031 · Cited by 62
Molecular Etiology and Pathogenesis of Hereditary Cardiomyopathy
Kimura, A. (2008) · Circulation Journal · doi:10.1253/circj.cj-08-0050 · Cited by 62
The intercalated disc: a unique organelle for electromechanical synchrony in cardiomyocytes
Nielsen, M. S., van Opbergen, C. J. M., van Veen, T. A. B., & Delmar, M. (2023) · Physiological Reviews · doi:10.1152/physrev.00021.2022 · Cited by 62
Vinculin and Talin: Focus on the Myocardium
Zemljic‐Harpf, A. E., Manso, A. M., & Ross, R. S. (2009) · Journal of Investigative Medicine · doi:10.2310/jim.0b013e3181c5e074 · Cited by 56
Genotype, phenotype: upstairs, downstairs in the family of cardiomyopathies
Chien, K. R. (2003) · Journal of Clinical Investigation · doi:10.1172/jci17612 · Cited by 57
Costamere proteins and their involvement in myopathic processes
Jaka, O., Casas-Fraile, L., de Munaín, A. L., & Sáenz, A. (2015) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2015.9 · Cited by 56
Dysregulation of Cell Adhesion Proteins and Cardiac Arrhythmogenesis
Li, J., Patel, V. V., & Radice, G. L. (2006) · Clinical Medicine & Research · doi:10.3121/cmr.4.1.42 · Cited by 55
Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy
Long, P. A., Evans, J. M., & Olson, T. M. (2017) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd4030011 · Cited by 55
Self-citationFamilial Dilated Cardiomyopathy
Peters, S. A., Johnson, R., Birch, S. C. M., Zentner, D., Hershberger, R. E., & Fatkin, D. (2019) · Heart Lung and Circulation · doi:10.1016/j.hlc.2019.11.018 · Cited by 53
Drosophila Heart as a Model for Cardiac Development and Diseases
Souidi, A., & Jagla, K. (2021) · Cells · doi:10.3390/cells10113078 · Cited by 53
Dilated Cardiomyopathy: A Tale of Cytoskeletal Proteins and Beyond
Towbin, J. A., & Bowles, N. E. (2006) · Journal of Cardiovascular Electrophysiology · doi:10.1111/j.1540-8167.2006.00530.x · Cited by 53
Donahue, M., Marchuk, D. A., & Rockman, H. A. (2006) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2006.05.062 · Cited by 53
Genetics of Human and Canine Dilated Cardiomyopathy
Simpson, S., Edwards, J., Mignan, T., Cobb, M., Mongan, N. P., & Rutland, C. S. (2015) · International Journal of Genomics · doi:10.1155/2015/204823 · Cited by 49
Cardiomyopathy in α-Kinase 3 (ALPK3)-Deficient Mice
Van Sligtenhorst, I., Ding, Z.-M., Shi, Z.-Z., Read, R. W., Hansen, G., & Vogel, P. (2012) · Veterinary Pathology · doi:10.1177/0300985811402841 · Cited by 48
A novel mutation, Arg71Thr, in the ?-sarcoglycan gene is associated with dilated cardiomyopathy
K�rkk�inen, S., Miettinen, R., Tuomainen, P. O., K�rkk�inen, P., Heli�, T., Reissell, E., Kaartinen, M., Toivonen, L. K., Nieminen, M. S., Kuusisto, J., et al. (2003) · Journal of Molecular Medicine · doi:10.1007/s00109-003-0480-5 · Cited by 48
Marg, S., Winkler, U., Sestu, M., Himmel, M., Schönherr, M., Bär, J., Mann, A., Moser, M., Mierke, C. T., Rottner, K., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011530 · Cited by 48
Genotype, phenotype: upstairs, downstairs in the family of cardiomyopathies
Chien, K. R. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200317612 · Cited by 48
Witt, S., Zieseniß, A., Fock, U., Jockusch, B. M., & Illenberger, S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m314245200 · Cited by 47
Self-citationLesurf, R., Said, A., Akinrinade, O., Breckpot, J., Delfosse, K., Liu, T., Yao, R., Persad, G., McKenna, F., Noche, R. R., et al. (2022) · npj Genomic Medicine · doi:10.1038/s41525-022-00288-y · Cited by 49
Paxillin and Focal Adhesion Kinase (FAK) Regulate Cardiac Contractility in the Zebrafish Heart
Hirth, S., Bühler, A., Bührdel, J. B., Rudeck, S., Dahme, T., Rottbauer, W., & Just, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0150323 · Cited by 46
Chang, A. N., Parvatiyar, M. S., & Potter, J. D. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.12.081 · Cited by 46
Dilated cardiomyopathy: a genetically heterogeneous disease
Shaw, T., Elliot, P. M., & McKenna, W. J. (2002) · The Lancet · doi:10.1016/s0140-6736(02)09879-3 · Cited by 45
Paxillin and Ponsin Interact in Nascent Costameres of Muscle Cells
Gehmlich, K., Pinotsis, N., Hayeß, K., van der Ven, P. F. M., Milting, H., Banayosy, A. E., Körfer, R., Wilmanns, M., Ehler, E., & Fürst, D. O. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.03.050 · Cited by 44
Metadata
- Authors
- Olson, T. M., Illenberger, S., Kishimoto, N. Y., Huttelmaier, S., Keating, M. T., & Jockusch, B. M.
- Affiliations
- Howard Hughes Medical Institute (US)
- From the Department of Pediatrics and the Division of Cardiology (T.M.O., N.Y.K.) and the Departments of Human Genetics and Medicine, Division of Cardiology, and Howard Hughes Medical Institute (M.T.K.), University of Utah, Salt Lake City, Utah; and Cell Biology, Zoological Institute (S.I., S.H., B.M.J.), Technical University of Braunschweig, Braunschweig, Germany. Dr Keating currently is at the Department of Cell Biology, Harvard Medical School and the Department of Cardiology, Children’s Hospital,...
- ORCID
- Olson, Timothy M.
- Venue
- Circulation
- Published
- 2002-01-29
- Volume
- 105
- Issue
- 4
- Pages
- 431-437
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- OpenAlex
- W1991072112
- Cited by
- 278
- References
- 25
- Citations by year
- 2026: 1 · 2025: 7 · 2024: 9 · 2023: 8 · 2022: 7 · 2021: 7 · 2020: 7 · 2019: 14 · 2018: 3 · 2017: 9 · 2016: 16 · 2015: 11 · 2014: 8 · 2013: 10 · 2012: 13
- FWCI
- 11.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Circulation (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Heart Association
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiomyopathy and Myosin Studies
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Effects of Exercise
- Keywords
- metavinculin, dilated cardiomyopathy, vinculin, intercalated discs, actin filament cross-linking, thin filament, missense mutations, force transmission
- MeSH terms
- Actins, Adult, Aged, Amino Acid Sequence, Cardiomyopathy, Dilated, DNA Mutational Analysis, Humans, Actin Cytoskeleton, Middle Aged, Molecular Sequence Data, Mutation, Myocardium, Pedigree, Sequence Alignment, Vinculin, Conserved Sequence
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review