Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Aoife Hanet"'
Autor:
Thorsten Schmidt, Inês Morgado Martins, Daniel Weishäupl, Zi‐Jian Wang, Anna Sergeevna Sowa, Olaf Riess, Aoife Hanet
Publikováno v:
CNS Neuroscience & Therapeutics. 24:404-411
Background & aims Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is an autosomal dominantly inherited neurodegenerative disorder and the most common form of SCA worldwide. It is caused by the expansion of a polyglut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64edd45586eed29839b105e5200b0753
https://doi.org/10.1111/cns.12795
https://doi.org/10.1111/cns.12795
Autor:
Dipankar Bhandari, Ramona Weber, Tobias Raisch, Cátia Igreja, Maria Fauser, Aoife Hanet, Duygu Kuzuoğlu-Öztürk, Vincenzo Ruscica, Chung Te Chang, Felix Räsch, Lara Wohlbold
Publikováno v:
Life Science Alliance
The putative UPF1-like SF1 helicase HELZ directly interacts with the CCR4–NOT deadenylase complex to induce translational repression and 5′-to-3′ decay of bound mRNAs.
Eukaryotic superfamily (SF) 1 helicases have been implicated in various
Eukaryotic superfamily (SF) 1 helicases have been implicated in various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7156357f9f72d6482f003742d02cead6
https://doi.org/10.26508/lsa.201900405
https://doi.org/10.26508/lsa.201900405