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1 wild type and mutant forms of human ER alpha-mannosidase I.
2 ncoding the resident Golgi protein alpha-1,2 mannosidase I.
3 e encodes an enzyme previously designated ER mannosidase I.
4                 Interestingly, inhibition of mannosidase I also results in prolonged association betw
5 lycoprotein processing inhibitors that block mannosidase I and increase the amount of protein-bound M
6 me reactions using a combination of human ER mannosidase I and recombinant Golgi mannosidase IA indic
7 proteins as well as vesicle cargo molecules (mannosidase I and sialyltransferase-yellow fluorescent p
8  selective trimming of N-glycans by ER alpha-mannosidase I and subsequent recognition by the ER degra
9 ached to misfolded glycoproteins by ER alpha-mannosidase I and subsequent recognition by the ER degra
10 g five active eukaryotic proteins, including mannosidases I and II, N-acetylglucosaminyl transferases
11 wild type and mutant forms of human ER alpha-mannosidase I as well as by structural analysis of a co-
12 teolytically driven checkpoint control of ER mannosidase I contributes to the establishment of an equ
13 ibition of human endoplasmic reticulum alpha-mannosidase I (ER Man I) and mouse Golgi alpha-mannosida
14 , including endoplasmic reticulum (ER) alpha-mannosidase I (ERManI) and Golgi alpha-mannosidase IA (G
15 d how, modification by endoplasmic reticulum mannosidase I (ERManI) contributes to the preferential s
16                                           ER mannosidase I (ERManI) is a quality control factor that
17               Endoplasmic reticulum alpha1,2 mannosidase I (ERManI), a central component of ER qualit
18 alnexin (CNX) and calreticulin (CRT), and ER mannosidase I in apo(a) intracellular targeting.
19 g the participation of endoplasmic reticulum mannosidase I in the disposal process.
20 rent primary cells or in the presence of the mannosidase I inhibitor deoxymannojirimycin dramatically
21                              In addition, ER mannosidase I inhibitor kifunensine and down-regulation
22  cells cultured in the presence of the alpha-mannosidase-I inhibitor kifunensine.
23 ral serine kinase inhibition implied that ER mannosidase I is subjected to regulated proteolysis.
24 MAN1B1 gene product MAN1B1, also known as ER mannosidase I, is to function within the ER similar to t
25 ene of Drosophila melanogaster encodes Golgi mannosidase I (MAS-1), and flies homozygous for small de
26 d by the sequential action of Golgi alpha1,2-mannosidase I (MIa,b,c), MGAT1, alpha1,2-mannosidase II
27 abidopsis (Arabidopsis thaliana) Golgi alpha-mannosidase I, Nicotiana tabacum beta1,2-N-acetylglucosa
28                                Unexpectedly, mannosidase I redistributed from the Golgi complex to co
29 endent on mannose trimming and inhibition of mannosidase I stabilizes Ii.
30 igosaccharides by endoplasmic reticulum (ER) mannosidase I targets misfolded glycoproteins for disloc
31 haride modification by endoplasmic reticulum mannosidase I, the latter of which occurred as PI Z was
32 sly isolated for Saccharomyces cerevisiae ER mannosidase I, the oligosaccharide in the active site of
33                            Redistribution of mannosidase I was also observed in cells incubated at 15
34    Herein the intracellular fate of human ER mannosidase I was monitored to determine whether a post-
35 in which processing by endoplasmic reticulum mannosidase I, which attenuates the removal of glucose f
36                             Inhibition of ER mannosidase I with deoxymannojirimycin or kifunensine ha

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