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Ion Mobility QTOF-MS Untargeted Lipidomics of Human Serum Reveals a Metabolic Fingerprint for GNE Myopathy Manis, Cristina; Casula, Mattia; Roos, Andreas; Hentschel, Andreas; Vorgerd, Matthias; Pogoryelova, Oksana; Derksen, Alexa; Spendiff, Sally; Lochmueller, Hanns; Caboni, Pierluigi 分享 收藏
Seroprevalence of binding and neutralizing antibodies against 18 adeno-associated virus types in patients with neuromuscular disorders Wang, Xiaoyan; Klann, Patrick Julian; Wiedtke, Ellen; Sano, Yumi; Fischer, Nico; Schiller, Lisa; Elfert, Anna; Guettsches, Anne-Katrin; Weyen, Ute; Grimm, Dirk; Vorgerd, Matthias; Bayer, Wibke 分享 收藏
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Quantitative muscle MRI captures early muscle degeneration in calpainopathy (vol 16, 19676, 2022) Forsting, Johannes; Rohm, Marlena; Froeling, Martijn; Guettsches, Anne-Katrin; Suedkamp, Nicolina; Roos, Andreas; Vorgerd, Matthias; Schlaffke, Lara; Rehmann, Robert 分享 收藏
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Synaptopodin-2 Isoforms Have Specific Binding Partners and Display Distinct, Muscle Cell Type-Specific Expression Patterns Lohanadan, Keerthika; Assent, Marvin; Linnemann, Anja; Schuld, Julia; Heukamp, Lukas C.; Krause, Karsten; Vorgerd, Matthias; Reimann, Jens; Schaenzer, Anne; Kirfel, Gregor; Fuerst, Dieter O.; van der Ven, Peter F. M. 分享 收藏
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Muscle diffusion MRI reveals autophagic buildup in a mouse model for Pompe disease Rohm, Marlena; Russo, Gabriele; Helluy, Xavier; Froeling, Martijn; Umathum, Vincent; Suedkamp, Nicolina; Manahan-Vaughan, Denise; Rehmann, Robert; Forsting, Johannes; Jacobsen, Frank; Roos, Andreas; Shin, Yoon; Schaenzer, Anne; Vorgerd, Matthias; Schlaffke, Lara 分享 收藏
Human skeletal muscle organoids model fetal myogenesis and sustain uncommitted PAX7 myogenic progenitors Mavrommatis, Lampros; Jeong, Hyun-Woo; Kindler, Urs; Gomez-Giro, Gemma; Kienitz, Marie-Cecile; Stehling, Martin; Psathaki, Olympia E.; Zeuschner, Dagmar; Bixel, M. Gabriele; Han, Dong; Morosan-Puopolo, Gabriela; Gerovska, Daniela; Yang, Ji Hun; Kim, Jeong Beom; Arauzo-Bravo, Marcos J.; Schwamborn, Jens C.; Hahn, Stephan A.; Adams, Ralf H.; Scholer, Hans R.; Vorgerd, Matthias; Brand-Saberi, Beate; Zaehres, Holm 分享 收藏
CRISPR/Cas9 Genome Editing in LGMD2A/R1 Patient-Derived Induced Pluripotent Stem and Skeletal Muscle Progenitor Cells Mavrommatis, Lampros; Zaben, Abdul; Kindler, Urs; Kienitz, Marie-Cecile; Dietz, Julienne; Jeong, Hyun-Woo; Boehme, Pierre; Brand-Saberi, Beate; Vorgerd, Matthias; Zaehres, Holm 分享 收藏
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Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects FILIP1的双等位基因变体导致先天性肌病,畸形和神经系统缺陷 Roos, Andreas; van der Ven, Peter F. M.; Alrohaif, Hadil; Koelbel, Heike; Heil, Lorena; Della Marina, Adela; Weis, Joachim; Assent, Marvin; Beck-Woedl, Stefanie; Barresi, Rita; Toepf, Ana; O'Connor, Kaela; Sickmann, Albert; Kohlschmidt, Nicolai; El Gizouli, Magdeldin; Meyer, Nancy; Daya, Nassam; Grande, Valentina; Bois, Karin; Kaiser, Frank J.; Vorgerd, Matthias; Schroeder, Christopher; Schara-Schmidt, Ulrike; Gangfuss, Andrea; Evangelista, Teresinha; Roebisch, Luisa; Hentschel, Andreas; Grueneboom, Anika; Fuerst, Dieter O.; Kuechler, Alma; Tzschach, Andreas; Depienne, Christel; Lochmueller, Hanns 分享 收藏