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1 in in secretory vesicles of adrenal medulla (chromaffin granules).
2 retory vesicles of adrenal medulla (known as chromaffin granules).
3 of neuropeptide-containing chromaffin cells (chromaffin granules).
4 S leads to enhanced catecholamine content in chromaffin granules.
5 ells without any detectable association with chromaffin granules.
6 cytosis of neurosecretory vesicles including chromaffin granules.
7 statin radioimmunoassay of size-fractionated chromaffin granules.
8 n 1 of 68-70 kDa was present within isolated chromaffin granules.
9 tivated by endogenous glutathione present in chromaffin granules.
10 rovided by endogenous reduced glutathione in chromaffin granules.
11 e also detected in several systems including chromaffin granules.
12                     Moreover, examination of chromaffin granule abundance in PC12 cells exposed to ba
13  7-fold more sensitive than the conventional chromaffin granule aggregation assay in terms of thresho
14   Sorcin is able to inhibit synexin-mediated chromaffin granule aggregation in a manner saturable wit
15                                        Using chromaffin granules and liposomes we now show that alpha
16 (f) increased catecholamine/ATP ratio in the chromaffin granule; and (g) increased plasma catecholami
17         Furthermore, a size mismatch between chromaffin granules ( approximately 300-nm diameter) and
18 se model led to decreased size and number of chromaffin granules as well as hypertension in these ani
19 nophil granules match the residence times of chromaffin granules at the plasma membrane in intact cel
20 ation of catecholamine-containing dense-core chromaffin granule biogenesis in the adrenal gland and t
21 a coupled relationship between CHGA-mediated chromaffin granule biogenesis, necessary for catecholami
22 myosin II facilitate release from individual chromaffin granules by accelerating dissociation of cate
23  transports electrons across the membrane of chromaffin granules (CG) present in the adrenal medulla,
24 tein (APP) in the lumen of adrenal medullary chromaffin granules (CG).
25 individual natural secretory granules (i.e., chromaffin granules (CGs)) on the single-particle level
26     Stimulated cosecretion of endopin 1 with chromaffin granule components, [Met]enkephalin and a cys
27  co-aggregate efficiently with pituitary and chromaffin granule content proteins at concentrations we
28 f calcium is required for the aggregation of chromaffin granule content.
29 lation of the CHGA gene in the mouse reduced chromaffin granule cotransmitter concentrations by appro
30 stent with the cleavage specificities of the chromaffin granule cysteine protease "PTP" that particip
31  reduction kinetics, similar to those of the chromaffin granule Cyt b(561).
32 le myosin II and cortical actin filaments in chromaffin granule exocytosis were studied by confocal f
33 in L is the responsible cysteine protease of chromaffin granules for converting proenkephalin to the
34 t a full-length CgA/EAP chimera is sorted to chromaffin granules for exocytosis.
35  was present in isolated secretory vesicles (chromaffin granules) from chromaffin cells as a glycopro
36          Our results show that liposomes and chromaffin granules fuse with GUVs containing activated
37 al and non-neuronal cells, and into resealed chromaffin granule ghosts efficiently through passive di
38   While the transport of catecholamines into chromaffin granule ghosts has been extensively character
39       Structure-activity studies with bovine chromaffin granule ghosts show that 3'-hydroxy-MPP(+) is
40 ibition of [3H]dopamine uptake into purified chromaffin granule ghosts showed IC50 values of approxim
41 ation of dopamine (DA) was studied in bovine chromaffin granule ghosts.
42 n addition, we determined that the V-pump of chromaffin granules has only the SFDalpha isoform in its
43 s catecholamines for storage in the lumen of chromaffin granules, has been shown to be involved in DC
44  image analysis to determine the position of chromaffin granules immediately adjacent to the plasma m
45  be biotinylated at the C-terminus in intact chromaffin granules, indicating that it is a transmembra
46                    Surprisingly, the size of chromaffin granules is reduced within few minutes of tre
47 ectrochemical proton gradient created by the chromaffin granule membrane H+-ATPase, and that the accu
48 ) values in the microM range, for the bovine chromaffin granule membrane monoamine transporter(s) (bV
49 phosphatidylinositol 4-kinase is an integral chromaffin granule membrane protein, PtdIns-4,5-P(2) imp
50 have been evaluated for inhibition of bovine chromaffin granule membrane V-ATPase.
51 2) important in exocytosis may reside on the chromaffin granule membrane.
52           Analysis of [125I]TBZ-AIPP-labeled chromaffin granule membranes by SDS-PAGE and autoradiogr
53  in PC12 cells and in a fraction enriched in chromaffin granule membranes from the adrenal medulla.
54 lex with sorcin and recruits this protein to chromaffin granule membranes in a Ca2+-dependent manner.
55    Incubation of [125I]TBZ-AIPP-photolabeled chromaffin granule membranes in the presence of the glyc
56 olar membranes of Neurospora crassa and from chromaffin granule membranes of Bos taurus.
57 ipped clathrin-coated vacuolars and purified chromaffin granule membranes were treated with KI in the
58  synthesized and used to photoaffinity label chromaffin granule membranes.
59                               Neuroendocrine chromaffin granules of adrenal medulla represent regulat
60            Moreover, endopin 1 inhibited the chromaffin granule prohormone thiol protease (involved i
61  is concluded that a significant fraction of chromaffin granules re-seal after exocytosis, and retain
62                            After exocytosis, chromaffin granules release essentially all their catech
63 phenotypic changes, including: (a) decreased chromaffin granule size and number; (b) elevated BP; (c)
64 c vesicles, pancreatic zymogen granules, and chromaffin granules, suggests GAIP's possible involvemen
65 catalytic cysteine protease complex, PTP, in chromaffin granules that may be involved in the proteoly
66                                           In chromaffin granules, the major form of catestatin is cle
67                                              Chromaffin granule ultrastructure revealed a approximate
68  be used to observe destaining of individual chromaffin granules upon exocytosis.
69 associated with the Manduca sexta and bovine chromaffin granule V-ATPase.
70 ar V-ATPase and at 0.4 to >10 microM for the chromaffin granule V-ATPase.
71 ibits the N. crassa V-ATPase better than the chromaffin granule V-ATPase.
72  that secretion of solAPPcyt was mediated by chromaffin granule vesicles.
73 reversible inhibitors for the bovine adrenal chromaffin granule vesicular monoamine transporter (VMAT
74         A decrease in the buoyant density of chromaffin granules was observed after downregulation of
75 well within the physiological range found in chromaffin granules, we conclude that catecholaminergic
76 s with V pump from bovine brain, kidney, and chromaffin granule, whereas an anti-G2 antibody reacts o
77 n catestatin was cleaved in pheochromocytoma chromaffin granules, with the major form, human chromogr