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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 on, substrate unfolding, and assembly of the secretory machinery.
12 inase A (PKA) through a direct action on the secretory machinery.
13 e correct functioning of the endocytotic and secretory machinery.
14 e of interest as molecular components of the secretory machinery and as major targets of autoimmunity
15 rexin-1alpha is a component of the beta-cell secretory machinery and contributes to secretory granule
16 onized with the expression of genes encoding secretory machinery and signaling factors that regulate
18 s formation and validate the distal platelet secretory machinery as a potential target for antiplatel
19 because of their differential effects on the secretory machinery, BDNF and CNTF may act cooperatively
20 efined, but the extent of regulation of this secretory machinery by cellular signaling pathways remai
21 ein decreases the Ca2+ responsiveness of the secretory machinery by partially uncoupling Ca2+-sensing
22 taneous release and direct modulation of the secretory machinery by the toxin-bound receptor contribu
23 erization of Syt isoforms, suggests that the secretory machinery contains a vast repertoire of bioche
29 red a specific role for the effector and its secretory machinery in intra- and interspecies bacterial
32 ures for secretion from human platelets, the secretory machinery in single-cell organisms like the se
33 ults demonstrate a new role for the cellular secretory machinery in the control of synaptic function
34 ssion of multiple components of the cellular secretory machinery in the mouse liver, including the en
35 recombinant proteins makes understanding the secretory machinery, including the identification of gly
36 gs indicate that components of the regulated secretory machinery interacts specifically with a signal
37 ve provided insights into how this expansive secretory machinery is built, equipped and maintained.
38 nels in the mouse such that an effect on the secretory machinery is reflected as changes in Ca(2+) cu
39 EA1, clathrin) and the biosynthetic membrane secretory machinery markers p115 (Golgi) and syntaxin 6
41 VLDL assembly, maturation, degradation, and secretory machinery of the cell, HCV acquires its hepato
43 a key role in thrombosis, thus the platelet secretory machinery offers a unique target to modulate h
44 aptic vesicle-associated constituents of the secretory machinery, play a key role in the organization
45 anism coupling dynamic actin assembly to the secretory machinery, producing enhanced ECM degradation
46 nces in the characterization of trypanosomal secretory machinery, provide a unique model system for t
47 may be caused in part by a lack of localized secretory machinery rather than being an intrinsic prope
48 and that PKA modulates an early step in the secretory machinery related to calcium sensing to facili
49 link between such remodeling and the insulin secretory machinery remained unknown and was the major a
50 d to show that one component of the platelet secretory machinery, SNAP-23, is specifically cleaved by
51 a membrane protein, relies on the polarized secretory machinery specific to G1 to be delivered to it
52 ct effect on calcium channels or through the secretory machinery, the effects of cleavage of the SNAR
53 parallels between the synaptic and beta cell secretory machineries to extracellular interactions.
56 ay have regulatory functions in coupling the secretory machinery to the polarized actin cytoskeleton.
57 yl cyclase, including PKA, ion channels, and secretory machinery, were not affected by disruption of
58 integrated nanoscopy and spectroscopy of the secretory machinery with organelle tracking data in a ma
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