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WD is an autosomal recessive disorder caused by pathogenic variants of the ATP7B gene, which encodes a P-type copper transport ATPase, leading to the accumulation of toxic copper concentrations in various organs, particularly the liver and brain [18]

As an analog of endogenous amylin, it is studied for its receptor-mediated signaling dynamics, sustained activation profile, and downstream neuroendocrine cascades within controlled laboratory environments

HUVEC cells were seeded onto the Matrigel (1 10 4 cells per well) and incubated with different materials for 24 h

J Pediatr Gastroenterol Nutr 2013;56:370-5

Pain Practice , 13 (3), 253257