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1 ne its relationship to mammalian Golgi alpha-mannosidase II.
2 localized with the medial-Golgi marker alpha-mannosidase II.
3 emical similarities to mammalian Golgi alpha-mannosidase II.
4  the Sf9 enzyme is distinct from Golgi alpha-mannosidase II.
5 es originating from the Golgi and containing mannosidase II.
6 NBCCV was found to be colocalized with alpha-mannosidase II, a marker for the Golgi complex.
7 ndoplasmic reticulum, as well as that due to mannosidase II, a marker for the trans-Golgi network.
8  phosphate concentration in vitro elevated a-mannosidase II activity in the Golgi, enhanced complex-t
9                                   Elevated a-mannosidase II activity was also observed in the aortas
10 noprecipitate betaCOP, Golgi 58K protein, or mannosidase II, all Golgi-resident proteins.
11                  When coexpressed with alpha-mannosidase II, alpha-mannosidase IIx colocalizes with a
12                                        Alpha-mannosidase-II (alphaM-II) catalyzes the first committed
13                                        Alpha-mannosidase-II (alphaM-II) deficiency diminishes complex
14     In contrast to the classical Golgi alpha-mannosidase II (AMAN-2), AMAN-3 displayed a cobalt-depen
15 development consistent with increasing alpha-mannosidase II and core fucosyl-transferase enzyme activ
16  cDNA encoding a protein homologous to alpha-mannosidase II and designated it alpha-mannosidase IIx.
17                                              Mannosidase II and giantin were observed to colocalize w
18 ra and antisera against known Golgi markers (mannosidase-II and furin) revealed that the staining of
19 -GFP fusion colocalized with a Golgi marker, mannosidase II, and retained catalytic activity compared
20     Swainsonine, an inhibitor of Golgi alpha-mannosidase II, blocked beta1,6GlcNAc N-glycan expressio
21 e associated with the Golgi apparatus marker mannosidase II but not with markers to early endosomes (
22 icular stomatitis virus (VSV)-G protein to a mannosidase II-containing Golgi compartment.
23 d for the delivery of a cargo protein to the mannosidase II-containing Golgi compartment.
24                                        alpha-Mannosidase II-deficient autoimmune disease is due to an
25 reen et al. now show that mice lacking alpha-mannosidase II develop an autoimmune disease similar to
26 nnose trimming enzyme drosophila Golgi alpha-mannosidase II (dGMII) complexed with the inhibitors man
27  characterized included inserts in the alpha-mannosidase II (dGMII), ash1, and pumilio genes.
28  glycan M5G0 upon binding to the Golgi alpha-mannosidase II enzyme.
29 of the RER (ribophorin I) and GA (p58, alpha-mannosidase II, galactosyltransferase, and TGN38/41).
30                                        Golgi mannosidase II (GMII) catalyzes the sequential hydrolysi
31                                  Golgi alpha-mannosidase II (GMII), a member of glycoside hydrolase f
32 aminyltransferase I, Arabidopsis Golgi alpha-mannosidase II (GMII), and Arabidopsis beta1,2-xylosyltr
33                    Inhibition of Golgi alpha-mannosidase II (GMII), which acts late in the N-glycan p
34                  In contrast, rab6 and alpha-mannosidase II, Golgi marker proteins, appear unchanged.
35 tegral membrane Golgi proteins called GEARs (mannosidase II, GOS-28, GS15, GPP130, CASP, giantin, and
36 alpha-mannosidase IIx colocalizes with alpha-mannosidase II in COS cells.
37                    The functional role of ER mannosidase II in glycoprotein quality control is discus
38 olgi transport of Rh1, downstream from alpha-mannosidase-II in the medial- Golgi.
39                                  Golgi alpha-mannosidase II is an enzyme that processes the intermedi
40 nto small punctate structures at a time when mannosidase II is still largely localized to Golgi struc
41 nd cosedimented with the Golgi marker, alpha-mannosidase II (Man II).
42 GalT was compared with transfected rat alpha-mannosidase II (medial-Golgi, polyclonal antibody).
43                                        alpha-Mannosidase II (MII) is a key enzyme converting precurso
44 1,2-mannosidase I (MIa,b,c), MGAT1, alpha1,2-mannosidase II (MII, IIx), and MGAT2.
45 several Golgi and vesicle markers, including mannosidase II, p58, trans-Golgi network (TGN)38, and be
46 g kinetics was seen with the HeLa GalT/alpha-mannosidase II pairing.
47 ed oligosaccharides by endoplasmic reticulum mannosidase II partitions variant PI Z away from the con
48                     We report recruitment of mannosidase-II-positive Golgi-derived vesicles during up
49              Brefeldin A treatment inhibited mannosidase-II recruitment and phagocytic uptake of seru
50 on is temporally and spatially distinct from mannosidase II relocation and that FTCD provides a novel
51  its redistribution is distinct from that of mannosidase II relocation.
52 onsisting of the first 117 residues of alpha-mannosidase II tagged with a fluorescent protein and a t
53     Swainsonine, an inhibitor of Golgi alpha-mannosidase II that causes abnormal N-glycosylation, str
54              Mechanistically, recruitment of mannosidase-II vesicles during phagocytic uptake require
55                           The recruitment of mannosidase-II vesicles was an early event mediated by f
56 taining pattern was similar to that of alpha-mannosidase II which is a known resident enzyme of the G
57 at mutation of a single gene, encoding alpha-mannosidase II, which regulates the hybrid to complex br