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nassar aya[Author]
(2 results)?
Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects.
Brain. 2023 Oct 3;146(10):4200-4216. doi: 10.1093/brain/awad152.
Brain. 2023.
PMID: 37163662
Free PMC article.
Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems.
Sellung D, Heil L, Daya N, Jacobsen F, Mertens-Rill J, Zhuge H, Döring K, Piran M, Milting H, Unger A, Linke WA, Kley R, Preusse C, Roos A, Fürst DO, Ven PFMV, Vorgerd M.
Sellung D, et al. Among authors: daya n.
Cells. 2023 May 5;12(9):1321. doi: 10.3390/cells12091321.
Cells. 2023.
PMID: 37174721
Free PMC article.
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Muscle Specific Promotors for Gene Therapy - A Comparative Study in Proliferating and Differentiated Cells.
Dietz J, Jacobsen F, Zhuge H, Daya N, Bigot A, Zhang W, Ehrhardt A, Vorgerd M, Ehrke-Schulz E.
Dietz J, et al. Among authors: daya n.
J Neuromuscul Dis. 2023;10(4):575-592. doi: 10.3233/JND-221574.
J Neuromuscul Dis. 2023.
PMID: 37270809
Free PMC article.
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Proteomic studies in VWA1-related neuromyopathy allowed new pathophysiological insights and the definition of blood biomarkers.
Athamneh M, Daya N, Hentschel A, Gangfuss A, Ruck T, Marina AD, Schara-Schmidt U, Sickmann A, Güttsches AK, Deschauer M, Preusse C, Vorgerd M, Roos A.
Athamneh M, et al. Among authors: daya n.
J Cell Mol Med. 2024 Apr;28(8):e18122. doi: 10.1111/jcmm.18122.
J Cell Mol Med. 2024.
PMID: 38652110
Free PMC article.
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