Results 51 to 60 of about 7,018 (220)

Retinal glycoprotein enrichment by concanavalin a enabled identification of novel membrane autoantigen synaptotagmin-1 in equine recurrent uveitis. [PDF]

open access: yes, 2012
Complete knowledge of autoantigen spectra is crucial for understanding pathomechanisms of autoimmune diseases like equine recurrent uveitis (ERU), a spontaneous model for human autoimmune uveitis. While several ERU autoantigens were identified previously,
A Lux   +68 more
core   +2 more sources

Antiepileptic Drugs Elevate Astrocytic Kir4.1 Expression in the Rat Limbic Region

open access: yesFrontiers in Pharmacology, 2018
Inwardly rectifying potassium (Kir) channel subunits Kir4.1 are specifically expressed in astrocytes and regulate neuronal excitability by mediating spatial potassium buffering.
Takahiro Mukai   +12 more
doaj   +1 more source

Kir4.1 Potassium Channel Subunit Is Crucial for Oligodendrocyte Development and In Vivo Myelination [PDF]

open access: yes, 2001
To understand the cellular and in vivo functions of specific K^+ channels in glia, we have studied mice with a null mutation in the weakly inwardly rectifying K^+ channel subunit Kir4.1.
Jacobs, Russell E.   +4 more
core   +1 more source

Morphological plasticity of astroglia: Understanding synaptic microenvironment [PDF]

open access: yes, 2015
Memory formation in the brain is thought to rely on the remodeling of synaptic connections which eventually results in neural network rewiring. This remodeling is likely to involve ultrathin astroglial protrusions which often occur in the immediate ...
Heller, JP, Rusakov, DA
core   +1 more source

Appearance of fast astrocytic component in voltage-sensitive dye imaging of neural activity. [PDF]

open access: yes, 2015
BACKGROUND: Voltage-sensitive dye (VSD) imaging and intrinsic optical signals (IOS) are widely used methods for monitoring spatiotemporal neural activity in extensive networks.
Dobolyi, Arpád   +3 more
core   +1 more source

The central role of aquaporins in the pathophysiology of ischemic stroke [PDF]

open access: yes, 2015
Stroke is a complex and devastating neurological condition with limited treatment options. Brain edema is a serious complication of stroke. Early edema formation can significantly contribute to infarct formation and thus represents a promising target ...
Di Giovanni, Giuseppe   +4 more
core   +6 more sources

Downregulation of Astrocytic Kir4.1 Potassium Channels Is Associated with Hippocampal Neuronal Hyperexcitability in Type 2 Diabetic Mice

open access: yesBrain Sciences, 2020
Epilepsy, characterized by recurrent seizures, affects 1% of the general population. Interestingly, 25% of diabetics develop seizures with a yet unknown mechanism. Hyperglycemia downregulates inwardly rectifying potassium channel 4.1 (Kir4.1) in cultured
Miguel P. Méndez-González   +6 more
doaj   +1 more source

Aquaporin-4 Functionality and Virchow-Robin Space Water Dynamics: Physiological Model for Neurovascular Coupling and Glymphatic Flow. [PDF]

open access: yes, 2017
The unique properties of brain capillary endothelium, critical in maintaining the blood-brain barrier (BBB) and restricting water permeability across the BBB, have important consequences on fluid hydrodynamics inside the BBB hereto inadequately ...
Igarashi, Hironaka   +3 more
core   +1 more source

Regulation of heteromeric Kir4.1‐Kir5.1 channel but not the homomeric Kir4.1 channel by S‐glutathionylation

open access: yesThe FASEB Journal, 2011
The Kir4.1 channel is expressed in the brainstem, retina and kidney. Its heteromerization with Kir5.1 leads to K + currents with distinct properties such as single‐channel conductance, rectification, pH sensitivity and phosphorylation modulations.
Xin Jin   +4 more
openaire   +1 more source

Kir4.1 K+channels are regulated by external cations [PDF]

open access: yesChannels, 2011
The inwardly rectifying potassium channel (Kir), Kir4.1 mediates spatial K(+)-buffering in the CNS. In this process the channel is potentially exposed to a large range of extracellular K(+) concentrations ([K(+)]o). We found that Kir4.1 is regulated by K(+)o.
Johan M, Edvinsson   +2 more
openaire   +2 more sources

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