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1 e retained in the intracellular membrane are core-glycosylated.
3 Trpm4b, two forms were found, high mannose, core-glycosylated and complex, highly glycosylated (HG),
8 specific manner, processing of CFTR from the core-glycosylated (band B) ER form to the complex-glycos
9 utants at the nonpermissive temperature were core-glycosylated but lacked outer chain carbohydrate, i
10 s that are translocated across the membrane, core-glycosylated, but fail to assemble are dislocated b
11 Glycerol treatment also stabilized immature (core-glycosylated) delta F508 and CFTR molecules that ar
13 ven sequentially increased the processing of core-glycosylated, endoplasmic reticulum-arrested Delta
14 binding to terminally glycosylated Env over core-glycosylated Env precursor in IPs, suggesting that
15 beta4 subunit can be present as an immature, core glycosylated form and a mature, highly glycosylated
16 cretion of invertase, which accumulates as a core-glycosylated form characteristic of the endoplasmic
17 solutes also increased the processing of the core-glycosylated form of green fluorescent protein-Delt
18 h Hsp90 and Hsp70 interact directly with the core-glycosylated form of hERG WT present in the endopla
20 as misprocessed, suggesting inability of the core-glycosylated glycoprotein to traffic to the Golgi.
22 esults indicate that the immature protein is core-glycosylated in the ER, whereas the oligosaccharide
23 cosylated mutants appear to be predominantly core-glycosylated, indicating that mature glycosylation
25 t and glutamate receptor surface expression, core-glycosylated proteins are sufficient to sustain the
26 ds of neuronal surface membrane proteins are core-glycosylated, resulting in the neuronal membrane di
27 d cells with proteasome inhibitors cause the core-glycosylated TCRalpha chains to progressively shift
28 hese studies we show that the degradation of core-glycosylated TCRalpha is blocked by N-acetyl-L-leuc
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