Results 131 to 140 of about 7,018 (220)
Alzheimer's disease (AD) has complex pathophysiology involving numerous cell types and brain processes. Astrocyte involvement in AD is gaining increased attention, however a complete characterisation of astrocytic changes in the AD human brain is ...
Henry Liu +8 more
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BackgroundRetinal degeneration in transgenic rats that express a mutant cilia gene polycystin-2 (CMV-PKD2(1/703)HA) is characterized by initial photoreceptor degeneration and glial activation, followed by vasoregression and neuronal degeneration (Feng et
Stefanie Vogler +9 more
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The inwardly-rectifying potassium channel Kir4.1 is a major player in the astrocyte-mediated regulation of [K+]o in the brain, which is essential for normal neuronal activity and synaptic functioning.
Federico Sicca +10 more
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Heterozygous KCNJ10 Variants Affecting Kir4.1 Channel Cause Paroxysmal Kinesigenic Dyskinesia
More than 60% of paroxysmal kinesigenic dyskinesia (PKD) cases are of uncertain variants.
Xiaojun Huang +22 more
semanticscholar +1 more source
Роль астроцитів в підтриманні гомеостазу нервової тканини [PDF]
Статтю присвячено огляду даних літератури щодо основних функцій астроцитів, які мають значення для нормального функціонування нервової системи. Йдеться про підтримку вмісту калію в позаклітинній рідині, оскільки астроцити виконують роль буфера для ...
Клопоцький, Г.А. +3 more
core
ALS-like pathology diminishes swelling of spinal astrocytes in the SOD1 animal model
Astrocytes are crucial for the functioning of the nervous system as they maintain the ion homeostasis via volume regulation. Pathological states, such as amyotrophic lateral sclerosis (ALS), affect astrocytes and might even cause a loss of such functions.
Tereza Filipi +12 more
doaj +1 more source
Role of dystrophin and utrophin for assembly and function of the dystrophin glycoprotein complex in non-muscle tissue [PDF]
.: The dystrophin glycoprotein complex (DGC) is a multimeric protein assembly associated with either the X-linked cytoskeletal protein dystrophin or its autosomal homologue utrophin. In striated muscle cells, the DGC links the extracellular matrix to the
Fritschy, J., Haenggi, T.
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