Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mariia Suslova"'
Autor:
Arnim J. Gaebler, Nilüfer Fakour, Felix Stöhr, Jana Zweerings, Arezoo Taebi, Mariia Suslova, Juergen Dukart, Joerg F. Hipp, Bhim M. Adhikari, Peter Kochunov, Suresh D. Muthukumaraswamy, Anna Forsyth, Thomas Eggermann, Florian Kraft, Ingo Kurth, Michael Paulzen, Gerhard Gründer, Frank Schneider, Klaus Mathiak
Publikováno v:
Translational Psychiatry, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Both, pharmacological and genome-wide association studies suggest N-methyl-D-aspartate receptor (NMDAR) dysfunction and excitatory/inhibitory (E/I)-imbalance as a major pathophysiological mechanism of schizophrenia. The identification of sha
Externí odkaz:
https://doaj.org/article/2a27b92802e64b309b19055bac2f2fa8
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
SLC1A2 and SLC1A3 encode the glial glutamate transporters EAAT2 and EAAT1, which are not only the predominant glutamate uptake carriers in our brain, but also function as anion channels. Two homologous mutations, which predict substitutions of prolin
Externí odkaz:
https://doaj.org/article/f58c2c9fcc4f4e0fab8413c374796c16
Publikováno v:
Human Mutation. 41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b946a7b0688a569768fd60b1dd2d22b
https://doi.org/10.1002/humu.24131
https://doi.org/10.1002/humu.24131
Publikováno v:
Human mutation 41(11), 1892-1905 (2020). doi:10.1002/humu.24089
The episodic ataxias (EA) are a group of inherited neurological diseases characterized by paroxysmal cerebellar incoordination. There exist nine forms of episodic ataxia with distinct neurological symptoms and genetic origins. Episodic ataxia type 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85ce4fa354d5ed4a3c5af2d1d972283d
https://pubmed.ncbi.nlm.nih.gov/32741053
https://pubmed.ncbi.nlm.nih.gov/32741053