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CLN3 Batten disease is a severe pediatric neurodegenerative disorder caused by mutations in the CLN3 gene, most commonly a 1 kb deletion affecting exons 7 and 8. While research has focused on neuronal dysfunction, glial cells are increasingly recognized as key contributors to disease pathology. Amon...
ORGANISM(S): Homo sapiens (Human) 
2026-06-08 | PXD064202 | Pride
A substantial proportion of common variable immunodeficiency (CVID) patients has duodenal inflammation of largely unknown etiology. However, because of its histologic similarities with celiac disease, gluten sensitivity has been proposed as a potential mechanism. We aimed to elucidate the role of th...
ORGANISM(S): Homo sapiens (Human) 
2025-04-29 | PXD063461 | Pride
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