Zobrazeno 1 - 10
of 12
pro vyhledávání: '"P. F. M. Van Der Ven"'
Autor:
Alexander Schaiter, Andreas Hentschel, Felix Kleefeld, Julia Schuld, Vincent Umathum, Tara Procida-Kowalski, Christopher Nelke, Angela Roth, Andreas Hahn, Heidrun H. Krämer, Tobias Ruck, Rita Horvath, Peter F. M. van der Ven, Marek Bartkuhn, Andreas Roos, Anne Schänzer
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-18 (2024)
Abstract To gain a deeper understanding of skeletal muscle function in younger age and aging in elderly, identification of molecular signatures regulating these functions under physiological conditions is needed. Although molecular studies of healthy
Externí odkaz:
https://doaj.org/article/194ae0f583e44868afbde68598f4c31c
Autor:
Keerthika Lohanadan, Marvin Assent, Anja Linnemann, Julia Schuld, Lukas C. Heukamp, Karsten Krause, Matthias Vorgerd, Jens Reimann, Anne Schänzer, Gregor Kirfel, Dieter O. Fürst, Peter F. M. Van der Ven
Publikováno v:
Cells, Vol 13, Iss 1, p 85 (2023)
Synaptopodin-2 (SYNPO2) is a protein associated with the Z-disc in striated muscle cells. It interacts with α-actinin and filamin C, playing a role in Z-disc maintenance under stress by chaperone-assisted selective autophagy (CASA). In smooth muscle
Externí odkaz:
https://doaj.org/article/d61f3e09ff804350af78d9e5e1d5ffbd
Autor:
Kenichi Kimura, Astrid Ooms, Kathrin Graf-Riesen, Maithreyan Kuppusamy, Andreas Unger, Julia Schuld, Jan Daerr, Achim Lother, Caroline Geisen, Lutz Hein, Satoru Takahashi, Guang Li, Wilhelm Röll, Wilhelm Bloch, Peter F. M. van der Ven, Wolfgang A. Linke, Sean M. Wu, Pitter F. Huesgen, Jörg Höhfeld, Dieter O. Fürst, Bernd K. Fleischmann, Michael Hesse
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
An amino acid exchange (P209L) in the human co-chaperone BAG3 gives rise to severe childhood restrictive cardiomyopathy. Here the authors describe humanized transgenic mouse models which phenocopy the disease and provide insight into the pathogenic m
Externí odkaz:
https://doaj.org/article/6cdac892607d45f6a6225c942b322a42
Autor:
Dominik Sellung, Lorena Heil, Nassam Daya, Frank Jacobsen, Janine Mertens-Rill, Heidi Zhuge, Kristina Döring, Misagh Piran, Hendrik Milting, Andreas Unger, Wolfgang A. Linke, Rudi Kley, Corinna Preusse, Andreas Roos, Dieter O. Fürst, Peter F. M. van der Ven, Matthias Vorgerd
Publikováno v:
Cells, Vol 12, Iss 9, p 1321 (2023)
Myofibrillar myopathies (MFM) are a group of chronic muscle diseases pathophysiologically characterized by accumulation of protein aggregates and structural failure of muscle fibers. A subtype of MFM is caused by heterozygous mutations in the filamin
Externí odkaz:
https://doaj.org/article/20add6ba38594b8185ef55298931e823
Autor:
Julia Schuld, Zacharias Orfanos, Frédéric Chevessier, Britta Eggers, Lorena Heil, Julian Uszkoreit, Andreas Unger, Gregor Kirfel, Peter F. M. van der Ven, Katrin Marcus, Wolfgang A. Linke, Christoph S. Clemen, Rolf Schröder, Dieter O. Fürst
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-19 (2020)
Abstract Filamin C (FLNc) is mainly expressed in striated muscle cells where it localizes to Z-discs, myotendinous junctions and intercalated discs. Recent studies have revealed numerous mutations in the FLNC gene causing familial and sporadic myopat
Externí odkaz:
https://doaj.org/article/ba3e1050cbf146d9a4a94ff8ab249a1a
Autor:
Barbara Elsnicova, Daniela Hornikova, Veronika Tibenska, David Kolar, Tereza Tlapakova, Benjamin Schmid, Markus Mallek, Britta Eggers, Ursula Schlötzer-Schrehardt, Viktoriya Peeva, Carolin Berwanger, Bettina Eberhard, Hacer Durmuş, Dorothea Schultheis, Christian Holtzhausen, Karin Schork, Katrin Marcus, Jens Jordan, Thomas Lücke, Peter F. M. van der Ven, Rolf Schröder, Christoph S. Clemen, Jitka M. Zurmanova
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 12020 (2022)
Desmin mutations cause familial and sporadic cardiomyopathies. In addition to perturbing the contractile apparatus, both desmin deficiency and mutated desmin negatively impact mitochondria. Impaired myocardial metabolism secondary to mitochondrial de
Externí odkaz:
https://doaj.org/article/9c11ad5ea2bd4158a3b2fce2b7923011
Autor:
Julius Kostan, Miha Pavšič, Vid Puž, Thomas C Schwarz, Friedel Drepper, Sibylle Molt, Melissa Ann Graewert, Claudia Schreiner, Sara Sajko, Peter F M van der Ven, Adekunle Onipe, Dmitri I Svergun, Bettina Warscheid, Robert Konrat, Dieter O Fürst, Brigita Lenarčič, Kristina Djinović-Carugo
Publikováno v:
PLoS Biology, Vol 19, Iss 4, p e3001148 (2021)
Sarcomeres, the basic contractile units of striated muscle cells, contain arrays of thin (actin) and thick (myosin) filaments that slide past each other during contraction. The Ig-like domain-containing protein myotilin provides structural integrity
Externí odkaz:
https://doaj.org/article/bb2463d4a4ee4d459292729c75f411ce
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e43798 (2012)
The ASB2α protein is the specificity subunit of an E3 ubiquitin ligase complex involved in hematopoietic differentiation and is proposed to exert its effects by regulating the turnover of specific proteins. Three ASB2α substrates have been describe
Externí odkaz:
https://doaj.org/article/1a69d612fff9452299159843097044c9
Autor:
P. F. M. Van Der Ven, Paul H.K. Jap, L.A. Ginsel, G. Schaart, F. C. S. Ramaekers, H.J.E. Croes
Publikováno v:
Journal of Cell Science. 106:749-759
Differentiating human skeletal muscle cell cultures were used to study the association of titin with other sarcomeric and cytoskeletal proteins during myofibrillogenesis. Several developmental stages of these cultures were double stained with antibod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::350c8b7aedc213f000f3459b59415a64
https://doi.org/10.1242/jcs.106.3.749
https://doi.org/10.1242/jcs.106.3.749