Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rafael Lazo-Gómez"'
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 10 (2023)
Externí odkaz:
https://doaj.org/article/6e9687f0e02e432694bf829bfb8d3625
Autor:
José Manuel Albisua Aguilar, Francisco Ortega Vallado, Orlando Carrillo Torres, Rafael Lazo Gómez, María Elena Pinto Segura
Publikováno v:
Acta Médica Grupo Ángeles. 21:134-139
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa7261325d3127e7d430b46f3c7dea3b
https://doi.org/10.35366/110259
https://doi.org/10.35366/110259
Autor:
Rafael Lazo-Gómez, Ricardo Tapia
Publikováno v:
Translational Neurodegeneration
Translational Neurodegeneration, Vol 6, Iss 1, Pp 1-14 (2017)
Translational Neurodegeneration, Vol 6, Iss 1, Pp 1-14 (2017)
Background Excitotoxicity is a mechanism of foremost importance in the selective motor neuron degeneration characteristic of motor neuron disorders. Effective therapeutic strategies are an unmet need for these disorders. Polyphenols, such as querceti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::450646ea25590e314259931b20dee063
http://europepmc.org/articles/PMC5697078
http://europepmc.org/articles/PMC5697078
Publikováno v:
Neuropharmacology. 82:101-107
In the spinal cord neuronal activity is controlled by the balance between excitatory and inhibitory neurotransmission, mediated mainly by the neurotransmitters glutamate and GABA/glycine, respectively. Alterations of this equilibrium have been associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7414389d50fa9caf3910bbab51b0224c
https://doi.org/10.1016/j.neuropharm.2013.10.003
https://doi.org/10.1016/j.neuropharm.2013.10.003
Autor:
Rafael Lazo-Gómez, Ricardo Tapia
Publikováno v:
Frontiers in Neuroscience, Vol 10 (2016)
Frontiers in Neuroscience
Frontiers in Neuroscience
Motor neuron degeneration is the pathological hallmark of motor neuron diseases, a group of neurodegenerative disorders clinically manifested as muscle fasciculations and hyperreflexia, followed by paralysis, respiratory failure and death. Ample evid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b70447331843782c5ef515eaa895fa64
https://doi.org/10.3389/fnins.2016.00200
https://doi.org/10.3389/fnins.2016.00200
Publikováno v:
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience, Vol 8 (2014)
Frontiers in Cellular Neuroscience, Vol 8 (2014)
Motor neuron physiology and development depend on a continuous and tightly regulated trophic support from a variety of cellular sources. Trophic factors guide the generation and positioning of motor neurons during every stage of the developmental pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef811dd49b3a043f2610d327b88b2726
https://pubmed.ncbi.nlm.nih.gov/24616665
https://pubmed.ncbi.nlm.nih.gov/24616665
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 7 (2013)
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease, characterized by the progressive loss of motor neurons. The cause of this selective neuronal death is unknown, but transcriptional dysregulation is recently emerging as an impo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5601f93597c539f3189cf9c7fddfd34c
https://doi.org/10.3389/fncel.2013.00243
https://doi.org/10.3389/fncel.2013.00243
Autor:
Rafael Lazo-Gomez, Gloria de Lourdes Llamosa-García Velázquez, Diego Mireles-Jacobo, Marco Antonio Sotomayor-Sobrino
Publikováno v:
Clinical Neurophysiology Practice, Vol 4, Iss , Pp 39-46 (2019)
Multiple sclerosis-related neurobehavioral abnormalities are one of the main components of disability in this disease. The same pathological processes that explain demyelination periods and neurodegeneration also allow the comprehension of neurobehav
Externí odkaz:
https://doaj.org/article/dc8a9757238a403c84572ae54ae4d5c0