Universität zu Köln

Journal Article

Brodehl, Andreas ORCID: 0000-0001-9202-2343, Dieding, Mareike, Klauke, Baerbel, Dec, Eric, Madaan, Shrestha, Huang, Taosheng ORCID: 0000-0001-6601-6687, Gargus, John, Fatima, Azra, Saric, Tomo ORCID: 0000-0001-8344-1095, Cakar, Hamdin, Walhorn, Volker, Toensing, Katja, Skrzipczyk, Tim, Cebulla, Ramona, Gerdes, Desiree, Schulz, Uwe, Gummert, Jan, Svendsen, Jesper Hastrup ORCID: 0000-0001-8466-8515, Olesen, Morten Salling ORCID: 0000-0001-9477-5322, Anselmetti, Dario ORCID: 0000-0002-8720-4369, Christensen, Alex Horby, Kimonis, Virginia and Milting, Hendrik (2013). The Novel Desmin Mutant p.A120D Impairs Filament Formation, Prevents Intercalated Disk Localization, and Causes Sudden Cardiac. Circ.-Cardiovasc. Genet., 6 (6). S. 615 - 624. PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 1942-3268

Buyandelger, Byambajav, Mansfield, Catherine ORCID: 0000-0002-5063-5181, Kostin, Sawa, Choi, Onjee, Roberts, Angharad M., Ware, James S., Mazzarotto, Francesco ORCID: 0000-0002-6159-9980, Pesce, Francesco ORCID: 0000-0002-2882-4226, Buchan, Rachel, Isaacson, Rivka L., Vouffo, Josee, Gunkel, Sylvia, Knoll, Gudrun, McSweeney, Sara J., Wei, Heming, Perrot, Andreas ORCID: 0000-0002-8800-342X, Pfeiffer, Conny, Toliat, Mohammad Reza, Ilieva, Kristina, Krysztofinska, Ewelina, Lopez-Olaneta, Marina M., Gomez-Salinero, Jesus M., Schmidt, Albrecht, Ng, Keat-Eng, Teucher, Niels, Chen, Ju, Teichmann, Martin ORCID: 0000-0002-5257-0510, Eilers, Martin ORCID: 0000-0002-0376-6533, Haverkamp, Wilhelm, Regitz-Zagrosek, Vera, Hasenfuss, Gerd, Braun, Thomas ORCID: 0000-0002-6165-4804, Pennell, Dudley J., Gould, Ian, Barton, Paul J. R., Lara-Pezzi, Enrique ORCID: 0000-0002-2743-1033, Schaefer, Sebastian, Huebner, Norbert, Felkin, Leanne E., O'Regan, Declan P., Brand, Thomas, Milting, Hendrik, Nuernberg, Peter, Schneider, Michael D., Prasad, Sanjay, Petretto, Enrico and Knoll, Ralph (2015). ZBTB17 (MIZ1) Is Important for the Cardiac Stress Response and a Novel Candidate Gene for Cardiomyopathy and Heart Failure. Circ.-Cardiovasc. Genet., 8 (5). S. 643 - 653. PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 1942-3268

Fatima, Azra, Dittmann, Sven, Xu, Guoxing, Gupta, Manoj K., Linke, Matthias, Zechner, Ulrich, Nguemo, Filomain, Milting, Hendrik, Farr, Martin, Hescheler, Juergen and Saric, Tomo ORCID: 0000-0001-8344-1095 (2013). The Disease-Specific Phenotype in Cardiomyocytes Derived from Induced Pluripotent Stem Cells of Two Long QT Syndrome Type 3 Patients. PLoS One, 8 (12). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

Hassoun, Roua, Budde, Heidi, Mannherz, Hans Georg, Lodi, Maria ORCID: 0000-0002-6533-770X, Fujita-Becker, Setsuko, Laser, Kai Thorsten, Gaertner, Anna ORCID: 0000-0001-6899-7693, Klingel, Karin, Moehner, Desiree, Stehle, Robert, Sultana, Innas, Schaaf, Thomas, Majchrzak, Mario, Krause, Verena, Herrmann, Christian, Nowaczyk, Marc M., Muegge, Andreas, Pfitzer, Gabriele, Schroder, Rasmus R., Hamdani, Nazha, Milting, Hendrik, Jaquet, Kornelia and Cimiotti, Diana (2021). De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents. Int. J. Mol. Sci., 22 (17). BASEL: MDPI. ISSN 1422-0067

Muller, Marion, Bischof, Cornelius, Kapries, Torben, Wollnitza, Sophie, Liechty, Chiara, Geissen, Simon, Schubert, Torben, Opacic, Dragan, Gercek, Muhammed, Fortmeier, Vera, Dumitrescu, Daniel, Schlomann, Uwe, Sydykov, Akylbek, Petrovic, Aleksandar, Gnatzy-Feik, Leoni, Milting, Hendrik, Schermuly, Ralph T., Friedrichs, Kai, Rudolph, Volker and Klinke, Anna (2022). Right Heart Failure in Mice Upon Pressure Overload Is Promoted by Mitochondrial Oxidative Stress. JACC-Basic Transl. Sci., 7 (7). S. 658 - 678. NEW YORK: ELSEVIER SCIENCE INC. ISSN 2452-302X

Ratnavadivel, Sandra, de Toledo, Marcelo Szymanski, Rasmussen, Torsten Bloch ORCID: 0000-0003-1468-7248, Saric, Tomo, Gummert, Jan, Zenke, Martin and Milting, Hendrik (2020). Human pluripotent stem cell line (HDZi001-A) derived from a patient carrying the ARVC-5 associated mutation TMEM43-p.S358L. Stem Cell Res., 48. AMSTERDAM: ELSEVIER. ISSN 1876-7753