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  • Search Condition : Filter (MeSH = Atrophy / pathology)
Species Resource Title
Zebrafish Tg (zCREST2-hsp70:GFP)rw011 A novel homozygous variant of the PIGK gene caused by paternal disomy in a patient with neurodevelopmental disorder, cerebellar atrophy, and seizures.
Human and Animal Cells MG6(RCB2403) Cathepsin H deficiency decreases hypoxia-ischemia-induced hippocampal atrophy in neonatal mice through attenuated TLR3/IFN-β signaling.