Results 151 to 160 of about 136,994 (263)
A comprehensive mechanosensory connectome reveals a somatotopically organized neural circuit architecture controlling stimulus-aimed grooming of the <i>Drosophila</i> head. [PDF]
Calle-Schuler SA +4 more
europepmc +1 more source
Tracking Genetic Parkinson's Disease with Molecular Imaging: A Systematic Review
Abstract Background Parkinson's disease (PD) is a worldwide, complex neurodegenerative disorder influenced by both genetic and environmental factors. Around 15–20% of PD cases are linked to genetic mutations, providing insights into the disease's pathogenesis.
Chiara Meneghini +5 more
wiley +1 more source
Low-Grade Papillary Urothelial Carcinoma of the Bladder Presenting as Persistent Genital Arousal Disorder/Genito-Pelvic Dysesthesia: A Case Report. [PDF]
Ponce S +8 more
europepmc +1 more source
Abstract Background The identification of Parkinson's disease (PD) subtypes is crucial for predicting the disease course and designing personalized therapeutic strategies. Objectives The aim of the study was to characterize the heterogeneity of the spatiotemporal evolutionary patterns of striatal dopamine depletion and cerebral hypoperfusion in PD ...
Yeeun Sun +9 more
wiley +1 more source
Molecular continuity between axon guidance and synaptic function. [PDF]
Kim S, Cho HJ, Wang IH, Park SJ.
europepmc +1 more source
An optoelectronic synapse based on Zr‐doped Bi4Ti3O12 exhibits learning/forgetting mimicry and achieves 94.2% accuracy on MNIST, demonstrating a novel pathway for high‐performance neuromorphic computing. ABSTRACT This study enhanced the optoelectronic properties of BIT (Bi4Ti3O12) through Zr doping at the B site, constructing an Au/Bi4Ti2.85Zr0.15O12 ...
Dongping Yang +5 more
wiley +1 more source
SNAP47 Silencing Impairs the Morphology and Neurotransmission of Hippocampal GABAergic Neurons. [PDF]
He Z +6 more
europepmc +1 more source
ABSTRACT Congenital myasthenic syndromes (CMS) are inherited disorders caused by mutations in genes encoding proteins essential for neuromuscular junction (NMJ) function. Pathogenic variants have been identified in more than 35 genes, underscoring the complexity of synaptic biology and the wide range of mechanisms that can compromise neuromuscular ...
Rocio‐Nur Villar‐Quiles +5 more
wiley +1 more source
Synaptic Facilitation Enhances the Reliability and Precision of High-Frequency Neurotransmission. [PDF]
Bernal-Correa AM +3 more
europepmc +1 more source
Presynaptic Congenital Myasthenic Syndromes
ABSTRACT Presynaptic congenital myasthenic syndromes (CMS) encompass a large number of rare neurologic disorders caused by impaired release of acetylcholine (ACh) from motor nerve terminals. There are two main groups of presynaptic CMS: one in which the amount of ACh in synaptic vesicles (SV) is diminished and another in which the mechanism of synaptic
Ricardo A. Maselli
wiley +1 more source

