Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Lucía Tabares"'
Autor:
Francisca Bermedo-García, Diego Zelada, Esperanza Martínez, Lucía Tabares, Juan Pablo Henríquez
Publikováno v:
BMC Biology, Vol 20, Iss 1, Pp 1-18 (2022)
Abstract Background In a broad variety of species, muscle contraction is controlled at the neuromuscular junction (NMJ), the peripheral synapse composed of a motor nerve terminal, a muscle specialization, and non-myelinating terminal Schwann cells. W
Externí odkaz:
https://doaj.org/article/fd675740d6234605aebb58ddbe690c20
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 11 (2017)
During development, motoneurons experience significant changes in their size and in the number and strength of connections that they receive, which requires adaptive changes in their passive and active electrical properties. Even after reaching matur
Externí odkaz:
https://doaj.org/article/5e40a6cf52dc4888a2b0fc1545c188a2
Neuroprotective effect of adult hematopoietic stem cells in a mouse model of motoneuron degeneration
Publikováno v:
Neurobiology of Disease, Vol 26, Iss 2, Pp 408-418 (2007)
Degenerative spinal motor diseases, like amyotrophic lateral sclerosis, are produced by progressive degeneration of motoneurons. Their clinical manifestations include a progressive muscular weakness and atrophy, which lead to paralysis and premature
Externí odkaz:
https://doaj.org/article/2569d6375d914fe59e37778ea82f4a87
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S309- (2023)
Externí odkaz:
https://doaj.org/article/b610180928284d7a91302654789842f2
Autor:
Francisco Hernandez, Miguel Angel Perez-Castro, Isabel Maria Alonso-Bellido, María De Los Santos Letrán-Sánchez, Eva Maria Perez-Villegas, Joana Vitalle, Luis Miguel Real, Ezequiel Ruiz-Mateos, José Luis Venero, Lucia Tabares, Ángel Carrión Rodríguez, José Ángel Armengol, Sara Bachiller, Rocío Ruiz
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S424- (2023)
Externí odkaz:
https://doaj.org/article/b98d39bd3d7f41388485c4322b10eb38
Autor:
Lucia Tabares, Silvio O. Rizzoli
Publikováno v:
Frontiers in Synaptic Neuroscience, Vol 14 (2022)
Externí odkaz:
https://doaj.org/article/d39bf5d69f6949d7ac1cbe842c0cdeac
Publikováno v:
Frontiers in Synaptic Neuroscience, Vol 14 (2022)
Presynaptic Ca2+ regulation is critical for accurate neurotransmitter release, vesicle reloading of release sites, and plastic changes in response to electrical activity. One of the main players in the regulation of cytosolic Ca2+ in nerve terminals
Externí odkaz:
https://doaj.org/article/85fa2e0d0b9045e1bb9165ab07c71a26
Autor:
Julio Franco-Espin, Alaó Gatius, José Ángel Armengol, Saravanan Arumugam, Mehri Moradi, Michael Sendtner, Jordi Calderó, Lucia Tabares
Publikováno v:
Biomolecules, Vol 12, Iss 10, p 1524 (2022)
Survival motor neuron (SMN) is an essential and ubiquitously expressed protein that participates in several aspects of RNA metabolism. SMN deficiency causes a devastating motor neuron disease called spinal muscular atrophy (SMA). SMN forms the core o
Externí odkaz:
https://doaj.org/article/e83a86571ee14ac9af4a32f71c832cd4
Autor:
Jorge Ojeda, Francisca Bermedo-García, Viviana Pérez, Jessica Mella, Patricia Hanna, Daniel Herzberg, Rocío Tejero, Mario López-Manzaneda, Lucia Tabares, Juan Pablo Henríquez
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
The neuromuscular junction (NMJ) is the peripheral synapse that controls the coordinated movement of many organisms. The NMJ is also an archetypical model to study synaptic morphology and function. As the NMJ is the primary target of neuromuscular di
Externí odkaz:
https://doaj.org/article/eacf05ddf9324bcea91ed9e5988f2756
Autor:
Rocio Tejero, Stefanie Balk, Julio Franco-Espin, Jorge Ojeda, Luisa Hennlein, Hans Drexl, Benjamin Dombert, Jan-Dierk Clausen, Laura Torres-Benito, Lena Saal-Bauernschubert, Robert Blum, Michael Briese, Silke Appenzeller, Lucia Tabares, Sibylle Jablonka
Publikováno v:
iScience, Vol 23, Iss 2, Pp - (2020)
Summary: Neurotransmission defects and motoneuron degeneration are hallmarks of spinal muscular atrophy, a monogenetic disease caused by the deficiency of the SMN protein. In the present study, we show that systemic application of R-Roscovitine, a Ca
Externí odkaz:
https://doaj.org/article/d3b57fc9108d45aa9032e86ae30d3b96