 | Up a level |
Frank, Derk, Rangrez, Ashraf Yusuf, Friedrich, Corinna, Dittmann, Sven, Stallmeyer, Birgit, Yadav, Pankaj 
ORCID: 0000-0001-7160-9209, Bernt, Alexander, Borlepawar, Ellen Schulze-Bahr Ankush, Zimmermann, Wolfram-Hubertus, Peischard, Stefan, Seebohm, Guiscard, Linke, Wolfgang A., Baba, Hideo A., Krueger, Marcus ORCID: 0000-0003-2008-4582, Unger, Andreas, Usinger, Philip, Frey, Norbert ORCID: 0000-0001-7611-378X and Schulze-Bahr, Eric
(2019).
Cardiac alpha-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy.
Circ.-Genom. Precis. Med., 12 (8).
PHILADELPHIA:
LIPPINCOTT WILLIAMS & WILKINS.
ISSN 1942-325X
Kimura, Kenichi ORCID: 0000-0002-0363-8865, Ooms, Astrid, Graf-Riesen, Kathrin, Kuppusamy, Maithreyan ORCID: 0000-0001-6866-0417, Unger, Andreas, Schuld, Julia, Daerr, Jan, Lother, Achim, Geisen, Caroline, Hein, Lutz ORCID: 0000-0003-1297-0007, Takahashi, Satoru, Li, Guang, Roell, Wilhelm ORCID: 0000-0002-2213-5024, Bloch, Wilhelm, van der Ven, Peter F. M., Linke, Wolfgang A., Wu, Sean M., Huesgen, Pitter F., Hoehfeld, Jorg, Fuerst, Dieter O., Fleischmann, Bernd K. and Hesse, Michael ORCID: 0000-0002-7518-0224
(2021).
Overexpression of human BAG3(P209L) in mice causes restrictive cardiomyopathy.
Nat. Commun., 12 (1).
BERLIN:
NATURE RESEARCH.
ISSN 2041-1723
Loescher, Christine M., Breitkreuz, Martin, Li, Yong, Nickel, Alexander, Unger, Andreas, Dietl, Alexander, Schmidt, Andreas, Mohamed, Belal A., Koetter, Sebastian, Schmitt, Joachim P., Krueger, Marcus ORCID: 0000-0003-2008-4582, Kruger, Martina, Toischer, Karl, Maack, Christoph, Leichert, Lars, I, Hamdani, Nazha and Linke, Wolfgang A.
(2020).
Regulation of titin-based cardiac stiffness by unfolded domain oxidation (UnDOx).
Proc. Natl. Acad. Sci. U. S. A., 117 (39).
S. 24545 - 24557.
WASHINGTON:
NATL ACAD SCIENCES.
ISSN 0027-8424
Schuld, Julia, Orfanos, Zacharias, Chevessier, Frederic, Eggers, Britta ORCID: 0000-0002-6553-4631, Heil, Lorena, Uszkoreit, Julian, Unger, Andreas, Kirfel, Gregor, van der Ven, Peter F. M., Marcus, Katrin, Linke, Wolfgang A., Clemen, Christoph S., Schroeder, Rolf and Fuerst, Dieter O.
(2020).
Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation.
Acta Neuropathol. Commun., 8 (1).
LONDON:
BMC.
ISSN 2051-5960
Storbeck, Markus, Eriksen, Beate Horsberg, Unger, Andreas, Hoelker, Irmgard, Aukrust, Ingvild, Martinez-Carrera, Lilian A., Linke, Wolfgang A., Ferbert, Andreas, Heller, Raoul, Vorgerd, Matthias, Houge, Gunnar and Wirth, Brunhilde ORCID: 0000-0003-4051-5191
(2017).
Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features.
Eur. J. Hum. Genet., 25 (9).
S. 1040 - 1049.
LONDON:
NATURE PUBLISHING GROUP.
ISSN 1476-5438
Unger, Andreas, Dekomien, Gabriele, Guettsches, Anne, Dreps, Thomas, Kley, Rudolf, Tegenthoff, Martin, Ferbert, Andreas, Weis, Joachim, Heyer, Christoph, Linke, Wolfgang A., Martinez-Carrera, Lilian, Storbeck, Markus, Wirth, Brunhilde ORCID: 0000-0003-4051-5191, Hoffjan, Sabine and Vorgerd, Matthias
(2016).
Expanding the phenotype of BICD2 mutations toward skeletal muscle involvement.
Neurology, 87 (21).
S. 2235 - 2244.
PHILADELPHIA:
LIPPINCOTT WILLIAMS & WILKINS.
ISSN 1526-632X