Zobrazeno 1 - 3
of 3
pro vyhledávání: '"metabolism [Fragile X Mental Retardation Protein]"'
Autor:
Anika M. Helferich, Peter M. Andersen, Priyanka Tripathi, Vitaly Zimyanin, Sarah J Brockmann, Axel Freischmidt, Albert C. Ludolph, Hannes Glaß, Joachim Weis, Eleonora Aronica, Andreas Hermann, Peter J. Oefner, Karin M Danzer, Maria Demestre, Karlheinz Holzmann, Alfred Yamoah, Anand Goswami, Tobias M. Böckers, Jörg Reinders, Jochen H. Weishaupt, Katharina Limm, Ina Poser
Publikováno v:
Brain
Brain 144(4), 1214-1229 (2021). doi:10.1093/brain/awab018
Brain, 144(4), 1214-1229. Oxford University Press
Brain 144(4), 1214-1229 (2021). doi:10.1093/brain/awab018
Brain, 144(4), 1214-1229. Oxford University Press
Knowledge about converging disease mechanisms in the heterogeneous syndrome amyotrophic lateral sclerosis (ALS) is rare, but may lead to therapies effective in most ALS cases. Previously, we identified serum microRNAs downregulated in familial ALS, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::691c4d51f5ea8d795f65a3e3483b9bef
https://doi.org/10.1093/brain/awab018
https://doi.org/10.1093/brain/awab018
Autor:
Georg Köhr, Dušica Briševac, Dan Du, Ralf Scholz, Mohammad Nael Elagabani, Hans-Christian Kornau
Publikováno v:
Journal of neurochemistry 157(3), 666-683 (2021). doi:10.1111/jnc.15230
Journal of Neurochemistry : official journal of the International Society for Neurochemistry
Journal of Neurochemistry : official journal of the International Society for Neurochemistry
Fragile X syndrome (FXS), the most common inherited cause of intellectual disability, results from silencing of the fragile X mental retardation gene 1 (FMR1). The analyses of FXS patients’ brain autopsies revealed an increased density of immature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b7c2faee993ea2120f6f513675e9a3e
https://pubmed.ncbi.nlm.nih.gov/33125726
https://pubmed.ncbi.nlm.nih.gov/33125726
Autor:
Carmelo Sgobio, Thomas Koeglsperger, Pan Gao, Felix Machleid, Thomas Arzberger, Kai Bötzel, Tasnim Chakroun, Jochen Herms, Mathias Höllerhage, Yi Tan, Jörg Tost, Elisabeth Findeis, Günter U. Höglinger, Qilin Tang
Publikováno v:
Acta neuropathologica 139(2), 319-345 (2020). doi:10.1007/s00401-019-02099-5
Parkinson's disease (PD) is the most common neurodegenerative movement disorder and is characterized by the progressive loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNc) and the gradual appearance of α-synuclein (α-syn)-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e996d6de49f55b30ce9d8646c655e3f
