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1 photyrosine binding domain protein ARH cause autosomal recessive hypercholesterolemia, a disorder cau
3 teracting proteins, including clathrin, AP2, autosomal recessive hypercholesterolemia, and GRASP65, a
5 eritance, and several genetic lesions in the autosomal recessive hypercholesterolemia (ARH) gene on c
11 l, found in the CLASPs beta-arrestin and the autosomal recessive hypercholesterolemia (ARH) protein,
12 common binding site for beta-arrestin or the autosomal recessive hypercholesterolemia (ARH) protein.
13 on cell-surface LDLRs in hepatocytes lacking autosomal recessive hypercholesterolemia (ARH), an adapt
14 photyrosine-binding domain protein ARH cause autosomal recessive hypercholesterolemia (ARH), an inher
15 nd directly to the clathrin adaptor molecule autosomal recessive hypercholesterolemia (ARH), and this
17 ), caused by mutations in the LDLR gene, and autosomal recessive hypercholesterolemia (ARH), of unkno
18 trolling internalization of the LDLR, called autosomal recessive hypercholesterolemia (ARH), remnant
19 -mediated endocytosis depends on the protein autosomal recessive hypercholesterolemia (ARH), which bi
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