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1  Golgi integrity and vesiculation during the secretory process.
2 asma membrane but also at the TGN during the secretory process.
3 Na/K-ATPase as an important component of the secretory process.
4  to serve in more specialized aspects of the secretory process.
5 iously been ascribed to dysregulation of the secretory process.
6 rs using a mechanism similar to the neuronal secretory process.
7 AR1 is an indication of the intensity of the secretory process.
8 hed light on how evolution has optimised the secretory process.
9 ting that it may exert multiple roles in the secretory process.
10  in two related but morphologically distinct secretory processes.
11 ated the interconnection between the various secretory processes.
12 ocesses and flux towards the lumen solely by secretory processes.
13 ay, it also participates in biosynthetic and secretory processes.
14 barrier properties and block proinflammatory secretory processes.
15  a critical link between cell activation and secretory processes.
16 to TNF-mediated malabsorption rather than to secretory processes.
17 ing that DHEAS did not directly activate the secretory processes.
18 que model system for the study of eukaryotic secretory processes.
19 es Ca(2+) and Mn(2+) for a variety of normal secretory processes.
20 maS at a concentration sufficient to inhibit secretory processes.
21 cle fusion, cell cycle control, and cellular secretory processes.
22 e Golgi, and shown to be required for normal secretory processes.
23 ng that BAFF signaling can directly regulate secretory processes.
24 esults from a disruption of vesicle-mediated secretory processes.
25 may provide a model relevant to more complex secretory processes.
26 lar body (LB) formation, secretion, and post-secretory processing accelerated significantly following
27 ocated into eukaryotic cells by the type III secretory process and has been hypothesized to function
28 )-dependent absorptive process and a smaller secretory process; and (2) the absorptive process consis
29                     These three steps of the secretory process are thus intimately coordinated.
30 d the molecular mechanisms of unconventional secretory processes are beginning to emerge.
31 model to study the morphologic, genetic, and secretory processes associated with the progression to c
32          This was not due to a defect in the secretory process, because addition of an exogenous secr
33 sma membrane, but it too participates in the secretory process, because expression of catalytically i
34  concept that iodide is subject to an active secretory process by the renal tubule.
35 pancreatic injury, and that blockade of this secretory process could increase autophagy induction.
36 a(++) channels (VDCCs), but not by affecting secretory processes downstream of Ca(++) influx.
37 rmis that require the involvement of unknown secretory processes for mobilizing catharanthine to the
38 c dietary K+ loading stimulates an active K+ secretory process in rat distal colon, which involves an
39 e not a site of Ca2+ release relevant to the secretory process in the pancreatic acinar cell.
40 hat although sharing many common properties, secretory processes in different cells are specialized a
41 be necessary, given their roles in different secretory processes in different tissues, the structural
42 ependence between the actin cytoskeleton and secretory processes in directing cell polarity and growt
43 ion, insulin counter-regulates cholangiocyte secretory processes in the BDL model, which is character
44 e to organelles associated with the cellular secretory process including the endoplasmic reticulum an
45 The intracellular mechanism controlling this secretory process involves cooperative action of two sep
46 sensitive to tetanus toxin, we find that the secretory process is directly up-regulated under conditi
47 s are retained in CF, but the cAMP-dependent secretory process is lost.
48 ur in intracellular compartments late in the secretory process itself, thereby yielding incompletely
49 th the TGN and ISGs also suggests that these secretory processes may be related in mechanism.
50                             This unregulated secretory process occurs only during a limited time wind
51        Self-proteolysis commences during the secretory process of MT1-MMP through the cell compartmen
52 ocated into eukaryotic cells by the type III secretory process of Pseudomonas aeruginosa.
53 st Abeta-induced neurotoxicity and regulates secretory processing of non-amyloidogenic APP via PKC pa
54 is finding exemplifies the potential of post-secretory processing of salivary proteins, which may rep
55 ntains information both about absorptive and secretory processes, regardless of which flux is measure
56 portant part in the functional impairment of secretory processes seen in connection with the autoimmu
57 est that the IDs have a distinct role in the secretory process, separate from the reabsorptive striat
58 oss initiated a pharmacologically actionable secretory process that drove lung adenocarcinoma (LUAD)
59 ely to play a critical role in the active K+ secretory process that typifies this model of colonic K+
60 sults suggest a role for Hrs-2 in regulating secretory processes through calcium- and nucleotide-depe
61 hilst adenosine acts at a later stage of the secretory process to decrease the number of calcium-char
62 f the phagosome and potential connections to secretory processes, toll-like receptor signaling, and a
63  by peroxidase activity, suggesting that the secretory process was altered.
64 e measured if the calcium-dependent chloride secretory process was first maximally stimulated with a
65 le involvement of two types of myosin in the secretory process was investigated, and their distributi