Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tyler J. Wishard"'
Autor:
Cory S. Inman, Dawn Eliashiv, Sonja Hiller, Diane Villaroman, Uros Topalovic, Nanthia Suthana, Leonardo Christov-Moore, Tony A. Fields, Matthias Stangl, Tyler J. Wishard, Itzhak Fried, Nicholas R. Hasulak, Zahra M. Aghajan
Current implantable devices that allow for recording and stimulation of brain activity in humans are not inherently designed for research and thus lack programmable control and integration with wearable sensors. We developed a platform that enables w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::505970d8fd3bc21fb2a89e3fef46d875
https://doi.org/10.1101/2020.02.12.946434
https://doi.org/10.1101/2020.02.12.946434
Autor:
Leonardo Christov-Moore, Vikram R. Rao, Uros Topalovic, Diane Villaroman, Itzhak Fried, Sonja Hiller, Nanthia Suthana, Cory S. Inman, Tyler J. Wishard, Tony A. Fields, Dawn Eliashiv, Matthias Stangl, Zahra M. Aghajan, Nicholas R. Hasulak
Publikováno v:
Neuron
Neuron, vol 108, iss 2
Neuron, vol 108, iss 2
Uncovering the neural mechanisms underlying human natural ambulatory behavior is a major challenge for neuroscience. Current commercially available implantable devices that allow for recording and stimulation of deep brain activity in humans can prov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6ac52fe5229a0d3ca75f5babadde2bb
https://doi.org/10.1016/j.neuron.2020.08.021
https://doi.org/10.1016/j.neuron.2020.08.021
Autor:
Mashfiq Hasan, Torrey L.S. Truszkowski, Zhenyu Liu, Hollis T. Cline, Eric J. James, Carlos D. Aizenman, Kara G. Pratt, Tyler J. Wishard
Publikováno v:
Neural Development
Background Fragile X Syndrome is the leading monogenetic cause of autism and most common form of intellectual disability. Previous studies have implicated changes in dendritic spine architecture as the primary result of loss of Fragile X Mental Retar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecc2dfdb10bd2bc7434862d52d2efb36
http://europepmc.org/articles/PMC4977860
http://europepmc.org/articles/PMC4977860
Autor:
Christopher K. Thompson, Regina L. Faulkner, Hollis T. Cline, Han-Hsuan Liu, Tyler J. Wishard
Publikováno v:
eneuro. 1:ENEURO.0055-14.2014
Fragile X Syndrome (FXS) is the leading known monogenic form of autism and the most common form of inherited intellectual disability. FXS results from silencing the FMR1 gene during embryonic development, leading to loss of Fragile X Mental Retardati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d61c80ee279b4a918ec9a5522ebc0dd3
https://doi.org/10.1523/eneuro.0055-14.2014
https://doi.org/10.1523/eneuro.0055-14.2014