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1 for membrane additions > 100 fF (about fifty large dense-cored vesicles).
2 peroxidase labeling for EM-1 was enriched in large dense core vesicles.
3 malemma, but only DOR-LI was associated with large dense core vesicles.
4 tions containing chromogranin B, a marker of large dense core vesicles.
5 axon terminals and was also associated with large dense core vesicles.
6 erminals that contained both small clear and large dense core vesicles.
7 ally affiliated with either endomembranes or large dense-core vesicles.
8 plasma membranes, but neither is present on large dense-core vesicles.
9 ndicate that NT-3 is packaged in presumptive large dense-core vesicles.
10 DOR was intracellular, often associated with large dense-core vesicles.
11 acid to mimic the proneuropeptides found in large dense-core vesicles.
12 inked by exocytic transport via synaptic and large-dense core vesicles.
13 contained intense peroxidase labeling within large dense core vesicles along the perimeter of the axo
14 Both types contained small clear as well as large dense core vesicles and formed heterogeneous types
15 d that syt I and VII partially colocalize on large dense core vesicles and that upregulation of syt V
16 rine peptide precursor VGF that is stored in large dense core vesicles and undergoes regulated secret
17 rom the NTS contained small, clear, and some large dense-core vesicles and formed heterogeneous synap
18 ls usually contained small clear, as well as large dense-core vesicles and were often apposed to unla
19 electron-lucent vesicles and, occasionally, large, dense-core vesicles) and symmetrical (with small,
20 umerous small pleomorphic vesicles, multiple large dense core vesicles, and several mitochondria, and
21 s, and was associated with plasma membranes, large dense-core vesicles, and cytoplasmic surfaces of s
22 symmetric synapses, contained darkly stained large dense-core vesicles, and displayed gamma-aminobuty
23 both are integral membrane components of the large dense-core vesicles, and that they are closely reg
27 was proposed to be an important regulator of large dense-core vesicle exocytosis from neuroendocrine
28 also been suggested to trigger exocytosis of large dense-core vesicles from neuroendocrine cells.
30 ted calcium entry, the calcium dependence of large dense-cored vesicle fusion under conditions of min
31 nts, and bear varicosities that contain both large dense-core vesicles/granules (120-160 nm) and smal
33 ab3A and rab3B also increased NE uptake into large dense core vesicles in digitonin-permeabilized PC1
34 er with BDNF or its pro-peptide both stained large dense core vesicles in excitatory presynaptic term
35 sicles in nerve terminals or the movement of large dense core vesicles in growth cones and endocrine
36 soluble PCs that are primarily localized to large dense core vesicles in neurons and endocrine cells
38 ionship between Ca2+ entry and exocytosis of large dense-cored vesicles in bovine adrenal chromaffin
39 y in neuronal terminals (which often contain large dense core vesicles) in limbic and basal forebrain
41 sion in behaving mice: a genetically encoded large dense core vesicle (LDCV) sensor that detects pres
42 ently unknown whether the molecular steps of large dense-core vesicle (LDCV) docking and priming are
44 g between divalent cations and exocytosis of large dense-cored vesicles (LDCV) was studied with capac
46 mechanisms responsible for production of the large dense core vesicles (LDCVs) capable of regulated r
48 etion of proteins and neurotransmitters from large dense core vesicles (LDCVs) is a highly regulated
50 VMATs) indicate preferential localization to large dense core vesicles (LDCVs) rather than synaptic-l
52 h targeted to norepinephrine (NE)-containing large dense core vesicles (LDCVs) when stably expressed
56 transmitters fall into two distinct classes, large dense-core vesicles (LDCVs) and small synaptic ves
57 f proteins depends on their inclusion within large dense-core vesicles (LDCVs) capable of regulated e
58 tudied the function of syb in the docking of large dense-core vesicles (LDCVs) in live PC12 cells usi
59 , the presence of estrogen receptor-alpha on large dense-core vesicles (LDCVs) in the hippocampus sug
60 Notably, we found that TRPV1 is present in large dense-core vesicles (LDCVs) that were mobilized to
61 oscopy (TEM) clearly shows that a portion of large dense-core vesicles (LDCVs) with double/multiple c
62 e PC12 cells, VMAT2 localizes exclusively to large dense-core vesicles (LDCVs), and we now show that
63 (CAPS) are priming factors for synaptic and large dense-core vesicles (LDCVs), promoting their entry
64 are required for release at the synapse, and large dense-core vesicles (LDCVs), which mediate extrasy
67 elective role for PICK1 in the biogenesis of large, dense core vesicles (LDCVs) in mouse chromaffin c
71 napin is relatively enriched in the purified large dense-core vesicles of chromaffin cells and associ
73 nd faster events than quanta associated with large dense-core vesicles previously recorded in vertebr
74 between the ways that synaptic vesicles and large dense-core vesicles release their contents have be
76 cells, hormones and neuropeptides stored in large dense core vesicles (secretory granules) are relea
77 rminal signal peptide-containing domain, for large dense core vesicle sorting and regulated secretion
79 quantal size was much less than expected for large dense core vesicles, suggesting that release origi
84 es contained pleomorphic vesicles as well as large dense core vesicles, varied in size and formed het
85 erminals, NT-LI was commonly associated with large, dense-cored vesicles, whereas D2-LI was found alo