Zobrazeno 1 - 10
of 112
pro vyhledávání: '"synaptopathies"'
Autor:
Clive R. Bramham, Volkmar Lessmann, Anthony J. Hannan, Changhe Wang, Alberto Catanese, Tobias Maria Boeckers, Hongyu Zhang
Publikováno v:
Frontiers in Synaptic Neuroscience, Vol 15 (2023)
Externí odkaz:
https://doaj.org/article/438dad54159842b2af11f4fe760ac5bf
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
Externí odkaz:
https://doaj.org/article/30bdfa33638a4b79b52faff1a1e2d8fa
Autor:
Jennifer Cooke, Ciara J. Molloy, Antonia San José Cáceres, Thomas Dinneen, Thomas Bourgeron, Declan Murphy, Louise Gallagher, Eva Loth
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Synaptic gene conditions, i.e., “synaptopathies,” involve disruption to genes expressed at the synapse and account for between 0.5 and 2% of autism cases. They provide a unique entry point to understanding the molecular and biological mechanisms
Externí odkaz:
https://doaj.org/article/8cfd6d1aed9a44a58e08f864e4a56e4f
Autor:
Agnes L. Nishimura, Natalia Arias
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2021)
Amyotrophic Lateral Sclerosis (ALS) is a complex neurodegenerative disease caused by degeneration of motor neurons (MNs). ALS pathogenic features include accumulation of misfolded proteins, glutamate excitotoxicity, mitochondrial dysfunction at dista
Externí odkaz:
https://doaj.org/article/2e0f8818e16741e199a40a669d39b81f
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Davide Pozzi, Elisabetta Menna, Alice Canzi, Genni Desiato, Cristina Mantovani, Michela Matteoli
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 11 (2018)
In the last 15 years, groundbreaking genetic progress has underlined a convergence onto coherent synaptic pathways for most psychiatric and neurodevelopmental disorders, which are now collectively called “synaptopathies.” However, the modest size
Externí odkaz:
https://doaj.org/article/4aaec53989f146ebb80200ea40300ca0
Autor:
Flavia eAntonucci, Irene eCorradini, Giuliana eFossati, Romana eTomasoni, Elisabetta eMenna, Michela eMatteoli
Publikováno v:
Frontiers in Synaptic Neuroscience, Vol 8 (2016)
A hallmark of synaptic specializations is their dependence on highly organized complexes of proteins that interact with each other. The loss or modification of key synaptic proteins directly affects the properties of such networks, ultimately impacti
Externí odkaz:
https://doaj.org/article/7ff4e5aa982545379f8e7f4ff9def2d9
Autor:
Andres Di Paolo, Joaquin Garat, Guillermo Eastman, Joaquina Farias, Federico Dajas-Bailador, Pablo Smircich, José Roberto Sotelo-Silveira
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2021)
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience
Functional genomics studies through transcriptomics, translatomics and proteomics have become increasingly important tools to understand the molecular basis of biological systems in the last decade. In most cases, when these approaches are applied to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::431c3976cef01fc24c06f1b547a7170a
https://www.frontiersin.org/articles/10.3389/fncel.2021.686722/full
https://www.frontiersin.org/articles/10.3389/fncel.2021.686722/full
Autor:
Natalia Arias, Agnes L. Nishimura
Publikováno v:
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience, Vol 15 (2021)
Frontiers in Cellular Neuroscience, Vol 15 (2021)
Amyotrophic Lateral Sclerosis (ALS) is a complex neurodegenerative disease caused by degeneration of motor neurons (MNs). ALS pathogenic features include accumulation of misfolded proteins, glutamate excitotoxicity, mitochondrial dysfunction at dista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75202cbe9af432f0e1b10d8babec5268
https://doi.org/10.3389/fncel.2021.660693
https://doi.org/10.3389/fncel.2021.660693