Results 161 to 170 of about 4,781,201 (273)
Gephyrin Neurological Autoimmunity
Gephyrin is a postsynaptic scaffold protein essential for inhibitory neurotransmission. Gephyrin‐immunoglobulin G (IgG) was reported, decades ago, in a single case of paraneoplastic stiff‐person‐like syndrome, but its broader clinical relevance remains unknown.
Maria Chiara Pantuliano +10 more
wiley +1 more source
Impaired Glur2 palmitoylation in cerebellar Purkinje cells of a Friedreich ataxia mouse model. [PDF]
Mercado-Ayón E +7 more
europepmc +1 more source
Objective Spinocerebellar ataxia 1 (SCA1) is a fatal hereditary neurodegenerative disorder with no approved therapies, and gene‐targeting strategies have thus far failed in clinical trials. Exercise remains the only intervention shown to provide clinical benefit in patients with spinocerebellar ataxias (SCAs), yet the underlying mechanisms remain ...
Isabel Soto +12 more
wiley +1 more source
Mice with TLE exhibit significant sleep fragmentation and reduced sleep duration, particularly during non‐rapid eye movement sleep. By employing optogenetic and chemogenetic methods to target CDN glutamatergic neurons, we observed a decrease in sleep fragmentation, an increase in overall sleep duration, and an enhancement in sleep quality among TLE ...
Liang Xia +6 more
wiley +1 more source
HCAR1-mediated lactate signaling modulates motor behavior and regulates spontaneous firing in Purkinje cells. [PDF]
Binda F +4 more
europepmc +1 more source
Abstract Objective Autoimmune epilepsy (AES) is increasingly recognized as a condition in patients with epilepsy of unknown etiology. Early immunotherapy improves outcomes; however, data on its prevalence and the frequency of anti‐neural/neuronal antibodies in Asian populations remain scarce.
Seong Jin Park +14 more
wiley +1 more source
Protocol for sparse labeling of murine Purkinje cells by intracerebroventricular AAV injection using a microelectrode holder. [PDF]
Lillibridge JJ +3 more
europepmc +1 more source
Astrocyte‐enriched and cilia‐related genetic signatures in dementia: A whole‐exome sequencing study
ABSTRACT Background Alzheimer's disease (AD), the most prevalent form of dementia, is highly heritable, yet much of its genetic basis remains unexplained. Most genetic studies have focused on European populations, with limited data from under‐represented groups.
Miaohan Deng +9 more
wiley +1 more source
Purkinje Cells in Crus I and II Encode the Visual Stimulus and the Impending Choice as Monkeys Learn a Reinforcement-Based Visuomotor Association Task. [PDF]
Ipata AE +5 more
europepmc +1 more source
MRI Characterization of Structural Brain Abnormalities in NGLY1 Deficiency
Structural MRI from 11 patients with NGLY1 deficiency, an ultrarare neurodevelopmental disorder, revealed reduced subcortical volume (thalamus and putamen) across ages and reduced cortical surface area in younger patients. These measures tracked with clinical features such as seizures and gait disturbance, supporting brain imaging as a candidate ...
Emily L. Dennis +8 more
wiley +1 more source

