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1 lved in both endoplasmic reticulum-Golgi and intra-Golgi transport.
2 noglycan sulfation, reflecting disruption of intra-Golgi transport.
3 ay in turn modulate Golgi-plasma membrane or intra-Golgi transport.
4 s of microtubule organization does not block 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 o the plasma membrane, indicating a block in intra-Golgi transport.
9 through degradation of proteins required for intra-Golgi transport.
10                      In addition, M2 delayed intra-Golgi transport and cell surface delivery of influ
11 TGN-derived vesicles, like those involved in intra-Golgi transport and in retrograde transport to the
12 ave used a modified version of this in vitro intra-Golgi transport assay to guide purification of a n
13 se-dead PI4Kbeta (PI4Kbeta(D656A)) inhibited intra-Golgi transport but stimulated TGN-to-cell surface
14 se data suggest a model for COPI-independent intra-Golgi transport by cisternal maturation with a shi
15 gi transport, is homologous to the mammalian intra-Golgi transport factor p115.
16 tion and membrane association is crucial for intra-Golgi transport in vitro and cell homeostasis/surv
17 ic reticulum, the steady-state production of intra-Golgi transport intermediates was not impaired by
18                       The prevailing view of intra-Golgi transport is cisternal progression, which ha
19               It is likely that the block of intra-Golgi transport is imposed by separate actions of
20 might indicate that the in vivo mechanism of intra-Golgi transport is not faithfully reproduced in vi
21  not faithfully reproduced in vitro, or that intra-Golgi transport occurs by a nonvesicular mechanism
22 ibodies are capable of inhibiting vertebrate intra-Golgi transport of a cargo protein in vitro.
23  this, acutely activated M2 had no effect on intra-Golgi transport of HA, but still slowed HA deliver
24  ribbon of mammalian cells strongly inhibits intra-Golgi transport of large cargoes without altering
25   We have pinpointed a role for Gos28 in the intra-Golgi transport of Rh1, downstream from alpha-mann
26 ARARAP, and MAP1-LC3 have been implicated in intra-Golgi transport, receptor sorting, and autophagy,
27 gle quantitative coarse-grained framework of intra-Golgi transport that accounts for both transport m
28 these results, we constructed a new model of intra-Golgi transport that involves rapid partitioning o
29 of the golgin family have been implicated in intra-Golgi transport through tethering coat protein com
30 ternae where it may participate in tethering intra-Golgi transport vesicles.
31 ) of a p24 protein isolated from COPI-coated intra-Golgi transport vesicles.
32 discriminate between the different models of intra-Golgi transport, we suggest experiments and an ana
33 , whereas endoplasmic reticulum-to-Golgi and intra-Golgi transport were largely unaffected.

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