Zobrazeno 1 - 5
of 5
pro vyhledávání: '"María eLLorens-Martín"'
Publikováno v:
Frontiers in Neuroscience, Vol 9 (2016)
Newborn neurons are continuously added to the hippocampal dentate gyrus throughout adulthood. In this review, we analyze the maturational stages that newborn granule neurons go through, with a focus on their unique morphological features during each
Externí odkaz:
https://doaj.org/article/f07cafb669dc4fc2804dd93480c89337
Autor:
María eLlorens-Martín, Lidia eBlazquez-Llorca, Ruth eBenavides-Piccione, Alberto eRabano, Felix eHernandez, Jesus eAvila, Javier eDeFelipe
Publikováno v:
Frontiers in Neuroanatomy, Vol 8 (2014)
A progressive loss of episodic memory is a well-known clinical symptom that characterizes Alzheimer’s disease (AD). The beginning of this loss of memory has been associated with the very early, pathological accumulation of tau and neuronal degenera
Externí odkaz:
https://doaj.org/article/60f5d55a3cc34e9a8edc81f8b472ec8b
Autor:
Almudena eFuster-Matanzo, María eLlorens-Martín, Jerónimo eJurado-Arjona, Jesus eAvila, Félix eHernández
Publikováno v:
Frontiers in Neuroscience, Vol 6 (2012)
Tau protein is a microtubule associated protein found in the axonal compartment that stabilizes neuronal microtubules under normal physiological conditions. Tau metabolism has attracted much attention because of its role in neurodegenerative disorder
Externí odkaz:
https://doaj.org/article/4c77217b27c64d62b23dd7996690648b
Publikováno v:
Frontiers in Neuroscience, Vol 5 (2011)
Analyzing the variation in different subpopulations of newborn neurons is central to the study of adult hippocampal neurogenesis. The acclaimed working hypothesis that different subpopulations of newborn, differentiating neurons could be playing diff
Externí odkaz:
https://doaj.org/article/8daec8be9b774c26b3b9f02e98e6a021
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 7 (2014)
Alzheimer disease (AD) is the most common form of age-related dementia. The etiology of AD is considered to be multifactorial as only a negligible percentage of cases have a familial or genetic origin. Glycogen synthase kinase-3 (GSK-3) is regarded a
Externí odkaz:
https://doaj.org/article/b41acf758d6942d4b6cad6df939090d1