Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mario Lopez Manzaneda"'
Autor:
Lucia del Prado, Myriam Jaraíz-Rodríguez, Mauro Agro, Marcos Zamora-Dorta, Natalia Azpiazu, Manuel Calleja, Mario Lopez-Manzaneda, Jaime de Juan-Sanz, Alba Fernández-Rodrigo, José A. Esteban, Mònica Girona, Albert Quintana, Eduardo Balsa
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract Deficiencies in the electron transport chain (ETC) lead to mitochondrial diseases. While mutations are distributed across the organism, cell and tissue sensitivity to ETC disruption varies, and the molecular mechanisms underlying this variab
Externí odkaz:
https://doaj.org/article/b2fa9d29c6fd4d769164d81519607546
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
Publikováno v:
Human Molecular Genetics
Spinal muscular atrophy (SMA) is an autosomal recessive degenerative motor neuron disease characterized by symmetrical muscle weakness and atrophy of limb and trunk muscles being the most severe genetic disease in children. In SMA mouse models, motor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ae2d86e18db82682e62c2b0774a361c
https://doi.org/10.1093/hmg/ddab065
https://doi.org/10.1093/hmg/ddab065
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::73fb71e7966b15205095ff9ae730832b
Autor:
Lucia Tabares, Mario Lopez-Manzaneda, Juan Pablo Henríquez, Francisca Bermedo-Garcia, Rocío Tejero, Daniel Herzberg, Patricia Hanna, Jessica Mella, Jorge Ojeda, Viviana Pérez
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::20fe8202af5e342f3935a80606f60255
https://doi.org/10.3389/fncel.2020.00225
https://doi.org/10.3389/fncel.2020.00225
Publikováno v:
Current Opinion in Physiology. 4:1-6
Motor nerve terminals continue to grow and mature several weeks after birth, thus allowing the adaptation of neurotransmitter release to the specific functional requirements of the motor circuit. The presynaptic changes coordinate with the changes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::456662b5d53a9ea2a4bd1db5080549b3
https://doi.org/10.1016/j.cophys.2018.02.009
https://doi.org/10.1016/j.cophys.2018.02.009
Publikováno v:
Human Molecular Genetics. :ddw297
Spinal muscular atrophy (SMA) is the most frequent genetic cause of infant mortality. The disease is characterized by progressive muscle weakness and paralysis of axial and proximal limb muscles. It is caused by homozygous loss or mutation of the SMN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cc0e1fa809b3dee72e3a84096b5f516
https://doi.org/10.1093/hmg/ddw297
https://doi.org/10.1093/hmg/ddw297