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1 e retained in the intracellular membrane are core-glycosylated.
2              RAMP2-transported receptors are core-glycosylated and are adrenomedullin receptors.
3  Trpm4b, two forms were found, high mannose, core-glycosylated and complex, highly glycosylated (HG),
4   Furthermore, GIRK1 homomultimers reside in core-glycosylated and nonglycosylated states.
5     In US11+cells, MHC class I molecules are core-glycosylated and therefore inserted into the ER.
6      Kidneys of AQP2(T126M/-) mice expressed core-glycosylated AQP2-T126M protein in an endoplasmic r
7  mainly interacts with ER-localized immature core-glycosylated, as well as nascent nonglycosylated, E
8 mediate for up to 5 h without increasing the core glycosylated (band B) form of CFTR.
9 specific manner, processing of CFTR from the core-glycosylated (band B) ER form to the complex-glycos
10 utants at the nonpermissive temperature were core-glycosylated but lacked outer chain carbohydrate, i
11 s that are translocated across the membrane, core-glycosylated, but fail to assemble are dislocated b
12 Glycerol treatment also stabilized immature (core-glycosylated) delta F508 and CFTR molecules that ar
13 contribute to ER quality control of immature core-glycosylated Eag1 proteins, MKRN1, but not CUL7, as
14       Tyrosinase appeared mostly as a 70-kDa core-glycosylated, endoglycosidase H-sensitive, immature
15 ven sequentially increased the processing of core-glycosylated, endoplasmic reticulum-arrested Delta
16  binding to terminally glycosylated Env over core-glycosylated Env precursor in IPs, suggesting that
17 beta4 subunit can be present as an immature, core glycosylated form and a mature, highly glycosylated
18 cretion of invertase, which accumulates as a core-glycosylated form characteristic of the endoplasmic
19 solutes also increased the processing of the core-glycosylated form of green fluorescent protein-Delt
20 h Hsp90 and Hsp70 interact directly with the core-glycosylated form of hERG WT present in the endopla
21 g experiments, we observed that RFFL and the core-glycosylated form of the human ether-a-go-go-relate
22 sfected with delta exon5 CFTR express only a core-glycosylated from (approximately 140 kDa).
23 as misprocessed, suggesting inability of the core-glycosylated glycoprotein to traffic to the Golgi.
24                     Csp associated with both core-glycosylated immature and fully glycosylated mature
25 esults indicate that the immature protein is core-glycosylated in the ER, whereas the oligosaccharide
26 cosylated mutants appear to be predominantly core-glycosylated, indicating that mature glycosylation
27        The cumulative data indicate that the core-glycosylated mucin-like repeats of MUC1 constitute
28 t and glutamate receptor surface expression, core-glycosylated proteins are sufficient to sustain the
29 ds of neuronal surface membrane proteins are core-glycosylated, resulting in the neuronal membrane di
30 d cells with proteasome inhibitors cause the core-glycosylated TCRalpha chains to progressively shift
31 hese studies we show that the degradation of core-glycosylated TCRalpha is blocked by N-acetyl-L-leuc