Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gregory J Wojaczynski"'
Autor:
Nathan P Achilly, Ling-jie He, Olivia A Kim, Shogo Ohmae, Gregory J Wojaczynski, Tao Lin, Roy V Sillitoe, Javier F Medina, Huda Y Zoghbi
Publikováno v:
eLife, Vol 10 (2021)
Rett syndrome is a devastating childhood neurological disorder caused by mutations in MECP2. Of the many symptoms, motor deterioration is a significant problem for patients. In mice, deleting Mecp2 from the cortex or basal ganglia causes motor dysfun
Externí odkaz:
https://doaj.org/article/d3b24f10375f4471b540a38aeb3943f0
Autor:
Wen Li, Lei Chen, Jonathan T. Fleming, Emily Brignola, Kirill Zavalin, Andre Lagrange, Tonia Rex, Shane A. Heiney, Gregory J. Wojaczynski, Javier F. Medina, Chin Chiang
Publikováno v:
J Neurosci
Cerebellar inhibitory interneurons are important regulators of neural circuit activity for diverse motor and nonmotor functions. The molecular layer interneurons (MLIs), consisting of basket cells (BCs) and stellate cells (SCs), provide dendritic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0ef3ccea585709d8efd8a23cee03c67
https://europepmc.org/articles/PMC9236294/
https://europepmc.org/articles/PMC9236294/
Autor:
Fleming Jt, Javier F. Medina, Lagrange Ah, Zavalin K, Li W, Gregory J. Wojaczynski, Chen L, Chiang C, Rex Ts, Heiney Sa, Brignola E
SUMMARYCerebellar inhibitory interneurons are important regulators of neural circuit activity for diverse motor and non-motor functions. The molecular layer interneurons (MLI), consisting of basket cells (BCs) and stellate cells (SCs), provide dendri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::844cafa13a9a376eefc1a6a54ee52aad
https://doi.org/10.1101/2021.04.15.439999
https://doi.org/10.1101/2021.04.15.439999
Autor:
Tao Lin, Olivia A. Kim, Huda Y. Zoghbi, Shogo Ohmae, Ling-jie He, Roy V. Sillitoe, Nathan P. Achilly, Gregory J. Wojaczynski, Javier F. Medina
Publikováno v:
eLife
eLife, Vol 10 (2021)
eLife, Vol 10 (2021)
Rett syndrome is a devastating childhood neurological disorder caused by mutations in MECP2. Of the many symptoms, motor deterioration is a significant problem for patients. In mice, deleting Mecp2 from the cortex or basal ganglia causes motor dysfun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6435bfd16413c11e12125f5ff442c15b
https://doi.org/10.7554/elife.64833
https://doi.org/10.7554/elife.64833
Autor:
Nathan P. Achilly, Roy V. Sillitoe, Shogo Ohmae, Ling-jie He, Gregory J. Wojaczynski, Tao Lin, Olivia A. Kim, Huda Y. Zoghbi, Javier F. Medina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79b06262b3ff816d4ce625fbc012c466
https://doi.org/10.7554/elife.64833.sa2
https://doi.org/10.7554/elife.64833.sa2
Autor:
Tao Lin, Nathan P. Achilly, Shogo Ohmae, Ling-jie He, Roy V. Sillitoe, Olivia A. Kim, Gregory J. Wojaczynski, Huda Y. Zoghbi, Javier F. Medina
Rett syndrome is a devastating childhood neurological disorder caused by mutations in MECP2. Of the many symptoms, motor deterioration is a significant problem for patients. In mice, deleting Mecp2 from the cortex or basal ganglia causes motor dysfun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::792444be3ab1e4d154b80a2178f683fc
https://doi.org/10.1101/2020.11.12.380162
https://doi.org/10.1101/2020.11.12.380162
Publikováno v:
Neuron
Summary The role of the cerebellum in predictive motor control and coordination has been thoroughly studied during movements of a single body part. In the real world, however, actions are often more complex. Here, we show that a small area in the ros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfb5c40342267038260ca6705ecd1cc3
https://doi.org/10.1016/j.neuron.2021.08.017
https://doi.org/10.1016/j.neuron.2021.08.017