戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ones and neurotransmitters, enzymes, and the secretory machinery.
2 manipulated individually at the level of the secretory machinery.
3 eedback loop that sensitizes the beta cell's secretory machinery.
4 ld be a limiting component of the platelets' secretory machinery.
5 nals to beta-cell membrane potential and the secretory machinery.
6 f function for an essential component of the secretory machinery.
7 tions between the actin cytoskeleton and the secretory machinery.
8 n by acting directly on the neurotransmitter secretory machinery.
9 w structural and spatial organization of the secretory machinery.
10 cting the functional integrity of the distal secretory machinery.
11 inase A (PKA) through a direct action on the secretory machinery.
12 e correct functioning of the endocytotic and secretory machinery.
13 Syn localizes to the plasma membrane via the secretory machinery.
14 he composition of the extracytoplasmic ESX-1 secretory machinery.
15 tion to maintaining insulin biosynthesis and secretory machinery.
16 on, substrate unfolding, and assembly of the secretory machinery.
17 e of interest as molecular components of the secretory machinery and as major targets of autoimmunity
18 rexin-1alpha is a component of the beta-cell secretory machinery and contributes to secretory granule
19 onized with the expression of genes encoding secretory machinery and signaling factors that regulate
20                 To gain direct access to the secretory machinery and study the regulation, mechanisms
21 naling with the gene expression of the COPII secretory machinery and trafficking.
22 s formation and validate the distal platelet secretory machinery as a potential target for antiplatel
23 because of their differential effects on the secretory machinery, BDNF and CNTF may act cooperatively
24 efined, but the extent of regulation of this secretory machinery by cellular signaling pathways remai
25 ein decreases the Ca2+ responsiveness of the secretory machinery by partially uncoupling Ca2+-sensing
26 taneous release and direct modulation of the secretory machinery by the toxin-bound receptor contribu
27  may constitute an unconventional eukaryotic secretory machinery closely related to the one described
28 erization of Syt isoforms, suggests that the secretory machinery contains a vast repertoire of bioche
29 opodia are dynamic structures that contain a secretory machinery, enabling the delta cell to reach a
30  primary trigger to initiate assembly of the secretory machinery for exocytosis.
31 a specialized collection of cytoskeletal and secretory machinery in apicomplexan parasites, which inc
32                         Here we describe the secretory machinery in axons and its contribution to pla
33                   Discovery of the universal secretory machinery in cells, the porosome, came as no s
34                 Due to the complexity of the secretory machinery in eukaryotic cells, it is difficult
35 nd sufficient for the full biogenesis of the secretory machinery in exocrine cells.
36 ute-phase response, namely, the induction of secretory machinery in hepatocytes.
37 red a specific role for the effector and its secretory machinery in intra- and interspecies bacterial
38                                    While the secretory machinery in mice was similar to humans, mice
39 y be an important component of the regulated secretory machinery in mouse brain.
40 ures for secretion from human platelets, the secretory machinery in single-cell organisms like the se
41 ults demonstrate a new role for the cellular secretory machinery in the control of synaptic function
42 ssion of multiple components of the cellular secretory machinery in the mouse liver, including the en
43 recombinant proteins makes understanding the secretory machinery, including the identification of gly
44 gs indicate that components of the regulated secretory machinery interacts specifically with a signal
45 ve provided insights into how this expansive secretory machinery is built, equipped and maintained.
46 nels in the mouse such that an effect on the secretory machinery is reflected as changes in Ca(2+) cu
47 EA1, clathrin) and the biosynthetic membrane secretory machinery markers p115 (Golgi) and syntaxin 6
48 e in the expression of key components of the secretory machinery of beta-cells, resulting in impaired
49 rs represents an unprecedented burden on the secretory machinery of endothelial cells (ECs).
50 tein synthesis and delivery by targeting the secretory machinery of mature cells.
51 for a novel link between Kin1, Kin2, and the secretory machinery of the budding yeast.
52  VLDL assembly, maturation, degradation, and secretory machinery of the cell, HCV acquires its hepato
53 7a have been identified as components of the secretory machinery of these killer cells.
54  a key role in thrombosis, thus the platelet secretory machinery offers a unique target to modulate h
55 aptic vesicle-associated constituents of the secretory machinery, play a key role in the organization
56 anism coupling dynamic actin assembly to the secretory machinery, producing enhanced ECM degradation
57 nces in the characterization of trypanosomal secretory machinery, provide a unique model system for t
58 may be caused in part by a lack of localized secretory machinery rather than being an intrinsic prope
59 3, which encodes a component of the parasite secretory machinery, reduced susceptibility to the drug.
60  and that PKA modulates an early step in the secretory machinery related to calcium sensing to facili
61 link between such remodeling and the insulin secretory machinery remained unknown and was the major a
62 d to show that one component of the platelet secretory machinery, SNAP-23, is specifically cleaved by
63  a membrane protein, relies on the polarized secretory machinery specific to G1 to be delivered to it
64 ct effect on calcium channels or through the secretory machinery, the effects of cleavage of the SNAR
65 parallels between the synaptic and beta cell secretory machineries to extracellular interactions.
66 ng GTP does not alter the sensitivity of the secretory machinery to Ca2+.
67 E effectors that is recognized by plant cell secretory machinery to redirect these peptides from the
68 irection of a polarized cytoskeleton and the secretory machinery to the damage site.
69 ay have regulatory functions in coupling the secretory machinery to the polarized actin cytoskeleton.
70 yl cyclase, including PKA, ion channels, and secretory machinery, were not affected by disruption of
71 integrated nanoscopy and spectroscopy of the secretory machinery with organelle tracking data in a ma