Results 231 to 240 of about 2,317,385 (378)

Deficiency of the Synaptic Adhesion Protein Leucine‐Rich Repeat Transmembrane Protein 4 Like 1 Affects Anxiety and Aggression in Zebrafish

open access: yesActa Physiologica, Volume 241, Issue 5, May 2025.
ABSTRACT Aim Leucine‐rich repeat transmembrane proteins (LRRTMs) are synaptic adhesion proteins that regulate synapse development and function. They interact transsynaptically with presynaptic binding partners to promote presynaptic differentiation. Polymorphisms of LRRTM4, one of the four members of this protein family, have been linked to multiple ...
Eva Tatzl   +7 more
wiley   +1 more source

Adenosine Receptors in Developing and Adult Mouse Neuromuscular Junctions and Functional Links With Other Metabotropic Receptor Pathways. [PDF]

open access: yesFront Pharmacol, 2018
Tomàs J   +9 more
europepmc   +1 more source

Metabotropic P2Y1 receptor signalling mediates astrocytic hyperactivity in vivo in an Alzheimer’s disease mouse model

open access: yesNature Communications, 2014
Andrea Delekate   +5 more
semanticscholar   +1 more source

Anticonvulsant action of metabotropic glutamate receptor agonists in DBA/2 mice.

open access: gold, 1994
Yoshiko Horikawa   +3 more
openalex   +1 more source

Clinical, Electroencephalogram and Imaging Characteristics of Patients With Anti‐LGI1 Antibody Encephalitis: A Multicenter Cohort Study

open access: yesCNS Neuroscience &Therapeutics, Volume 31, Issue 5, May 2025.
To summarize and analyze the general clinical manifestations, laboratory tests, electroencephalography and imaging characteristics, treatment and prognosis of 88 patients with anti‐leucine‐rich glioma inactivated protein 1 antibody encephalitis (LGI1‐AE) at baseline, discharge, and follow‐up in China, aiming to identify risk factors affecting disease ...
Yang Zhao   +13 more
wiley   +1 more source

Fmr1 deletion enhances and ultimately desensitizes CB1 signaling in autaptic hippocampal neurons

open access: yesNeurobiology of Disease, 2013
Fragile X Syndrome (FXS) is a heritable form of mental retardation caused by a non-coding trinucleotide expansion of the FMR1 gene leading to loss of expression of this RNA binding protein.
Alex Straiker, Kyung-Tai Min, Ken Mackie
doaj  

Translating physiology of the arterial chemoreflex into novel therapeutic interventions targeting carotid bodies in cardiometabolic disorders

open access: yesThe Journal of Physiology, Volume 603, Issue 9, Page 2487-2516, 1 May 2025.
Abstract figure legend The carotid body develops aberrant high activity in chronic heart failure, resistant hypertension, obstructive sleep apnoea (OSA) and diabetes. Hyperactivity of the carotid body leads to both high tonicity and increased sensitivity of the arterial chemoreflex with resultant sympathoexcitation.
Tymoteusz Żera   +7 more
wiley   +1 more source

Home - About - Disclaimer - Privacy