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Astroglial atrophy and loss of function A widespread class of astrocytic changes observed in many neurological diseases and in the majority of neuropsychiatric disorders are represented by structural atrophy and functional asthenia and manifested in the loss of key homoeostatic functions, such as for example glutamate clearance
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PMID: 34687865 Cell Rep Microglial macrophage-derived ds-HMGB1 in DRG orchestrates neuropathic pain through immune-neural signaling
Studies requiring gene expression data, biopsy analysis, inflammatory biomarkers, or multi-tissue effects require GHK-Cus broader biological range
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