Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Visou Ady"'
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Akademický článek
Reliable, Fast and Stable Contrast Response Function Estimation
Autor: Nelson Cortes, Marc Demers, Visou Ady, Lamyae Ikan, Christian Casanova
Publikováno v: Vision, Vol 6, Iss 4, p 62 (2022)
A study was conducted to determine stable cortical contrast response functions (CRFs) accurately and repeatedly in the shortest possible experimentation time. The method consisted of searching for experimental temporal aspects (number and duration of
Externí odkaz: https://doaj.org/article/0d47fefc1c7b44faaed6e78ac9f7d434
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2
Altered synaptic and firing properties of cerebellar Purkinje cells in a mouse model of ARSACS
Autor: Visou Ady, Bernard Brais, R. Anne McKinney, Brenda Toscano-Márquez, Jeanette Hui, Philip K.-Y. Chang, Francois Charron, Moushumi Nath, Alanna J. Watt, Roxanne Larivière, Anna A. Cook
Publikováno v: The Journal of Physiology. 596:4253-4267
Key points Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is an early-onset neurodegenerative human disease characterized in part by ataxia and Purkinje cell loss in anterior cerebellar lobules. A knock-out mouse model has been de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6b98250807d9f3263958a0a62acfa6ec
https://doi.org/10.1113/jp275902
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3
Patterned expression of Pannexin 1 channels in the adult cerebellar Purkinje cells
Autor: Valery I. Shestopalov, David Dubayle, Claude Meunier, Pascale M. Le Blanc, Carole Levenes, Visou Ady
Pannexin1 (PanX1) are recently discovered proteins that can form large pore channels at the cell surface. They have been implicated in ATP-dependent cell-to-cell communication and in several pathophysiological processes such as inflammation, cell dea
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d3e4ad098f55dfc327a60c2a8fcc882
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5
New old drug(s) for spinocerebellar ataxias
Autor: Visou, Ady, Alanna J, Watt
Spinocerebellar ataxia type 1 (SCA1) is a progressive neurodegenerative disease caused by a gene defect, leading to movement disorder such as cerebellar ataxia. It remains largely unknown which functional defect contributes to the cerebellar ataxic p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::934ad47327f2e0d6780382b7c2cef810
https://europepmc.org/articles/PMC5199732/
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10
Type 1 metabotropic glutamate receptors (mGlu1) trigger the gating of GluD2 delta glutamate receptors
Autor: Bertrand Lambolez, Julie Perroy, Claire Piochon, Xiaoru Chen, Visou Ady, Selma Dadak, Carole Levenes, Ludovic Tricoire, Isabelle Dusart, Laurent Fagni
Publikováno v: EMBO Reports
EMBO Reports, EMBO Press, 2014, 15 (1), pp.103-109. ⟨10.1002/embr.201337371⟩
EMBO Reports, 2014, 15 (1), pp.103-109. ⟨10.1002/embr.201337371⟩
International audience; The orphan GluD2 receptor belongs to the ionotropic glutamate receptor family but does not bind glutamate. Ligand-gated GluD2 currents have never been evidenced, and whether GluD2 operates as an ion channel has been a long-sta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39889bdbb7f68752fb77891b4fdbb627
https://hal.archives-ouvertes.fr/hal-02345493
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