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1 us and the endoplasmic reticulum, as well as intra-Golgi transport.
2 lved in both endoplasmic reticulum-Golgi and intra-Golgi transport.
3 noglycan sulfation, reflecting disruption of intra-Golgi transport.
4 ay in turn modulate Golgi-plasma membrane or intra-Golgi transport.
5 om the trans-Golgi of machinery required for intra-Golgi transport.
6 of the coatomer-coated vesicles that mediate intra-Golgi transport.
7 t mediate endoplasmic reticulum to Golgi and intra-Golgi transport.
8 t the short isoform of Stx5 is essential for intra-Golgi transport.
9 s of microtubule organization does not block intra-Golgi transport.
10 o the plasma membrane, indicating a block in intra-Golgi transport.
11 through degradation of proteins required for intra-Golgi transport.
12                      In addition, M2 delayed intra-Golgi transport and cell surface delivery of influ
13 ernal progression model posits that both the intra-Golgi transport and Golgi exit of secretory cargos
14 TGN-derived vesicles, like those involved in intra-Golgi transport and in retrograde transport to the
15 ave used a modified version of this in vitro intra-Golgi transport assay to guide purification of a n
16 se-dead PI4Kbeta (PI4Kbeta(D656A)) inhibited intra-Golgi transport but stimulated TGN-to-cell surface
17 se data suggest a model for COPI-independent intra-Golgi transport by cisternal maturation with a shi
18                                      Similar intra-Golgi transport delays were seen at 37 degrees C w
19 gi transport, is homologous to the mammalian intra-Golgi transport factor p115.
20  to visualize the cisternal organization and intra-Golgi transport in nocodazole-induced Golgi minist
21 tion and membrane association is crucial for intra-Golgi transport in vitro and cell homeostasis/surv
22 ic reticulum, the steady-state production of intra-Golgi transport intermediates was not impaired by
23                       The prevailing view of intra-Golgi transport is cisternal progression, which ha
24               It is likely that the block of intra-Golgi transport is imposed by separate actions of
25 might indicate that the in vivo mechanism of intra-Golgi transport is not faithfully reproduced in vi
26  not faithfully reproduced in vitro, or that intra-Golgi transport occurs by a nonvesicular mechanism
27 ibodies are capable of inhibiting vertebrate intra-Golgi transport of a cargo protein in vitro.
28  the molecular organization of the Golgi and intra-Golgi transport of cargos.
29  this, acutely activated M2 had no effect on intra-Golgi transport of HA, but still slowed HA deliver
30  ribbon of mammalian cells strongly inhibits intra-Golgi transport of large cargoes without altering
31   We have pinpointed a role for Gos28 in the intra-Golgi transport of Rh1, downstream from alpha-mann
32 ARARAP, and MAP1-LC3 have been implicated in intra-Golgi transport, receptor sorting, and autophagy,
33 gle quantitative coarse-grained framework of intra-Golgi transport that accounts for both transport m
34 these results, we constructed a new model of intra-Golgi transport that involves rapid partitioning o
35 of the golgin family have been implicated in intra-Golgi transport through tethering coat protein com
36 -induced Golgi ministacks, we found that the intra-Golgi transport velocity of a secretory cargo decr
37 s, TMF, golgin-84, and GMAP-210, can capture intra-Golgi transport vesicles when placed in an ectopic
38       We show that ectopic forms can capture intra-Golgi transport vesicles, but strikingly, the carg
39 ternae where it may participate in tethering intra-Golgi transport vesicles.
40 ) of a p24 protein isolated from COPI-coated intra-Golgi transport vesicles.
41 discriminate between the different models of intra-Golgi transport, we suggest experiments and an ana
42 , whereas endoplasmic reticulum-to-Golgi and intra-Golgi transport were largely unaffected.