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المؤلفون: Wilke, Carlo, Haas, Eva, Reetz, Kathrin, Faber, Jennifer, Garcia‐Moreno, Hector, Santana, Magda M, Warrenburg, Bart, Hengel, Holger, Lima, Manuela, Filla, Alessandro, Durr, Alexandra, Melegh, Bela, Masciullo, Marcella, Infante, Jon, Giunti, Paola, Neumann, Manuela, Vries, Jeroen, Pereira de Almeida, Luis, Rakowicz, Maria, Jacobi, Heike, Schüle, Rebecca, Kaeser, Stephan A, Kuhle, Jens, Klockgether, Thomas, Schöls, Ludger, Barro, Christian, Hübener‐Schmid, Jeannette, Synofzik, Matthis, Deuschle, Christian, Stransky, Elke, Brockmann, Kathrin, Schulz, Jörg B, Baliko, Laszlo, Gaalen, Judith, Raposo, Mafalda, Jeromin, Andreas

المصدر: EMBO Molecular Medicine
EMBO molecular medicine 12(7), e11803 (2020). doi:10.15252/emmm.201911803
EMBO Molecular Medicine, 12(7):11803. Wiley

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, FEATURES, chemistry [Intermediate Filaments], Intermediate Filaments, PROTEIN, Prodromal Symptoms, CSF, Severity of Illness Index, Article, blood [Machado-Joseph Disease], Mice, Animals, Humans, ddc:610, knock‐in mouse model, knock-in mouse model, Biomarkers & Diagnostic Imaging, LIGHT-CHAIN, blood [Biomarkers], DISEASE PROGRESSION, presymptomatic stage, MOUSE MODEL, Machado-Joseph Disease, Articles, phosphorylated neurofilament heavy chain, spinocerebellar ataxia type 3, Cross-Sectional Studies, neurofilament light chain, ONSET, Female, NEUROPATHOLOGY, Biomarkers, Neuroscience

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::82c5c841614970207227ce961662fe86