about
CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosisThe PI3K signaling pathway as a pharmacological target in Autism related disorders and Schizophrenia.Nomadic AMPA receptors and LTP.GSK3β inhibition promotes synaptogenesis in Drosophila and mammalian neurons.Learning improvement after PI3K activation correlates with de novo formation of functional small spinesActin filaments at the leading edge of cancer cells are characterized by a high mobile fraction and turnover regulation by profilin I.Neurotrophin receptor p75(NTR) mediates Huntington's disease-associated synaptic and memory dysfunction.Hippocampal Dendritic Spines Are Segregated Depending on Their Actin Polymerization.Modulation of aqueous humor outflow by ionic mechanisms involved in trabecular meshwork cell volume regulation.Actin-dependent regulation of neurotransmitter release at central synapses.Profilin induces lamellipodia by growth factor-independent mechanism.Peptides Acting as Cognitive Enhancers.The p.E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time: clinical and genetic characterization of a seven-generation ALS1 Spanish pedigree.Dyrk1A influences neuronal morphogenesis through regulation of cytoskeletal dynamics in mammalian cortical neurons.Presynaptic calcium-channel currents in normal and csp mutant Drosophila peptidergic terminals.PFN1 mutations are also rare in the Catalan population with amyotrophic lateral sclerosis.Identification and functional characterization of ClC-2 chloride channels in trabecular meshwork cellsFocal adhesion kinase regulates actin nucleation and neuronal filopodia formation during axonal growthPhosphoinositide-3-Kinase Activation Controls Synaptogenesis and Spinogenesis in Hippocampal NeuronsSelective antagonism of AMPA receptors unmasks kainate receptor-mediated responses in hippocampal neuronsComparative effects of velnacrine, tacrine and physostigmine on the twitch responses in the rat phrenic-hemidiaphragm preparationHypotensive effect of profilin on rabbit intraocular pressureFUS/TLS gene mutations are the second most frequent cause of familial ALS in the Spanish populationGlaucoma patients present increased levels of diadenosine tetraphosphate, Ap(4)A, in the aqueous humourI112M SOD1 mutation causes ALS with rapid progression and reduced penetrance in four Mediterranean families
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Miguel Morales
@ast
Miguel Morales
@en
Miguel Morales
@es
Miguel Morales
@nl
type
label
Miguel Morales
@ast
Miguel Morales
@en
Miguel Morales
@es
Miguel Morales
@nl
prefLabel
Miguel Morales
@ast
Miguel Morales
@en
Miguel Morales
@es
Miguel Morales
@nl
P106
P1153
57198295386
P21
P31
P496
0000-0002-8885-2333