Non-sarcomeric causes of heart failure by Gehmlich, K, Ehler, E

Genetics of and pathogenic mechanisms in arrhythmogenic right ventricular cardiomyopathy by Vimalanathan, A, Ehler, E, Gehmlich, K

Back to square one: what do we know about the functions of muscle LIM protein in the heart? by Gehmlich, K, Geier, C, Milting, H, Fürst, D, Ehler, E

"MLP: A Stress Sensor Goes Nuclear" by Sylvia Gunkel, Jorg Heineke, Denise Hilfiker-Kleiner, Ralph Knoll, J Mol Cell Cardiol. 2009;47(4):423-5. by Gehmlich, K, Ehler, E, Perrot, A, Fürst, DO, Geier, C

Ponsin interacts with Nck adapter proteins: implications for a role in cytoskeletal remodelling during differentiation of skeletal muscle cells. by Gehmlich, K, Hayess, K, Legler, C, Haebel, S, Van der Ven, P, Ehler, E, Fürst, DO

Thymosin beta4 facilitates epicardial neovascularization of the injured adult heart. by Smart, N, Risebro, C, Clark, J, Ehler, E, Miquerol, L, Rossdeutsch, A, Marber, MS, Riley, P

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions. by Gehmlich, K, Lambiase, P, Asimaki, A, Ciaccio, E, Ehler, E, Syrris, P, Saffitz, J, McKenna, W

Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele. by Gehmlich, K, Syrris, P, Reimann, M, Asimaki, A, Ehler, E, Evans, A, Quarta, G, Pantazis, A, Saffitz, J, McKenna, W

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy? by Gehmlich, K, Asimaki, A, Cahill, T, Ehler, E, Syrris, P, Zachara, E, Re, F, Avella, A, Monserrat, L, Saffitz, J, McKenna, W

Paxillin and ponsin interact in nascent costameres of muscle cells. by Gehmlich, K, Pinotsis, N, Hayess, K, van der Ven, P, Milting, H, El Banayosy, A, Körfer, R, Wilmanns, M, Ehler, E, Fürst, DO

Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathy. by Hoskins, A, Jacques, A, Bardswell, S, McKenna, W, Tsang, V, dos Remedios, C, Ehler, E, Adams, K, Jalilzadeh, S, Avkiran, M, Watkins, H, Redwood, C, Marston, S, Kentish, J

Prox1 maintains muscle structure and growth in the developing heart. by Risebro, C, Searles, R, Melville, A, Ehler, E, Jina, N, Shah, S, Pallas, J, Hubank, M, Dillard, M, Harvey, N, Schwartz, R, Chien, K, Oliver, G, Riley, P

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations. by Gehmlich, K, Syrris, P, Peskett, E, Evans, A, Ehler, E, Asimaki, A, Anastasakis, A, Tsatsopoulou, A, Vouliotis, A, Stefanadis, C, Saffitz, J, Protonotarios, N, McKenna, W

MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy by Gehmlich, K, Lange, S, Lun, A, Blondelle, J, Hooper, C, Dalton, N, Alvarez, E, Zhang, X, Bang, M, Abassi, Y, dos Remedios, C, Peterson, K, Chen, J, Ehler, E

Mutant muscle LIM protein C58G causes cardiomyopathy through protein depletion by Ehsan, M, Kelly, M, Hooper, C, Yavari, A, Beglov, J, Bellahcene, M, Ghataorhe, K, Poloni, G, Goel, A, Kyriakou, T, Fleischanderl, K, Ehler, E, Makeyev, E, Lange, S, Ashrafian, H, Redwood, C, Davies, B, Watkins, H, Gehmlich, K

Combination of Whole Genome Sequencing, Linkage and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy with Features of Left... by Hastings, R, de Villiers, C, Hooper, C, Ormondroyd, L, Pagnamenta, A, Lise, S, Salatino, S, Knight, S, Taylor, J, Thompson, K, Arnold, L, Chatziefthimiou, S, Konarev, P, Wilmanns, M, Ehler, E, Ghisleni, A, Gautel, M, Blair, E, Watkins, H, Gehmlich, K

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy. by Geier, C, Gehmlich, K, Ehler, E, Hassfeld, S, Perrot, A, Hayess, K, Cardim, N, Wenzel, K, Erdmann, B, Krackhardt, F, Posch, MG, Osterziel, K, Bublak, A, Nägele, H, Scheffold, T, Dietz, R, Chien, K, Spuler, S, Fürst, DO, Nürnberg, P, Ozcelik, C

Erratum: Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy (Human Molecular Genetics (2008) vol. 17 (18) (2753-2765) 10.1093/hmg/ddn160) by Geier, C, Gehmlich, K, Ehler, E, Hassfeld, S, Perrot, A, Hayess, K, Cardim, N, Wenzel, K, Erdmann, B, Krackhardt, F, Posch, MG, Osterziel, K, Bublak, A, Nägele, H, Scheffold, T, Dietz, R, Chien, K, Spuler, S, Fürst, DO, Nürnberg, P, Özcelik, C

Insights into the role of a cardiomyopathy-causing genetic variant in ACTN2 by Broadway-Stringer, S, Jiang, H, Wadmore, K, Hooper, C, Douglas, G, Steeples, V, Azad, A, Singer, E, Rayet, J, Galatik, F, Ehler, E, Bennett, P, Kalisch-Smith, J, Sparrow, D, Davies, B, Djinovic-Carugo, K, Gautel, M, Watkins, H, Gehmlich, K

Functional analysis of a gene-edited mouse to gain insights into the disease mechanisms of a titin missense variant by Jiang, H, Hooper, C, Kelly, M, Steeples, V, Simon, J, Beglova, J, Azad, AJ, Leinhos, L, Bennett, P, Ehler, E, Kalisch-Smith, J, Sparrow, D, Fischer, R, Heilig, R, Isackson, H, Ehsan, M, Patone, G, Huebner, N, Davies, B, Watkins, H, Gehmlich, K