| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0014-5793(97)01031-4 |
| P698 | PubMed publication ID | 9315716 |
| P2093 | author name string | G Williams | |
| R D Burgoyne | |||
| P2860 | cites work | SNAP family of NSF attachment proteins includes a brain-specific isoform | Q24323085 |
| A multisubunit particle implicated in membrane fusion | Q24643410 | ||
| Synaptic vesicle membrane fusion complex: action of clostridial neurotoxins on assembly | Q26269962 | ||
| SNAP receptors implicated in vesicle targeting and fusion | Q28131653 | ||
| Mechanisms of intracellular protein transport | Q28131681 | ||
| A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion | Q28255534 | ||
| The N-ethylmaleimide-sensitive fusion protein and alpha-SNAP induce a conformational change in syntaxin | Q28294139 | ||
| SNAPs, a family of NSF attachment proteins involved in intracellular membrane fusion in animals and yeast | Q28299506 | ||
| Sec18p (NSF)-driven release of Sec17p (alpha-SNAP) can precede docking and fusion of yeast vacuoles | Q28609819 | ||
| Tetanus and botulinum-B neurotoxins block neurotransmitter release by proteolytic cleavage of synaptobrevin | Q29619130 | ||
| Purification of an N-ethylmaleimide-sensitive protein catalyzing vesicular transport | Q33658648 | ||
| Vesicle-mediated protein sorting | Q35671061 | ||
| A simple method for the isolation of adrenal chromaffin granules on a large scale | Q39268130 | ||
| Biogenesis of constitutive secretory vesicles, secretory granules and synaptic vesicles | Q40788803 | ||
| Clostridial neurotoxins: new tools for dissecting exocytosis | Q41033673 | ||
| Association of the fusion protein NSF with clathrin-coated vesicle membranes | Q41065573 | ||
| The t-SNAREs syntaxin 1 and SNAP-25 are present on organelles that participate in synaptic vesicle recycling | Q42117532 | ||
| Distinct effects of alpha-SNAP, 14-3-3 proteins, and calmodulin on priming and triggering of regulated exocytosis | Q42771563 | ||
| In adrenal medulla synaptophysin (protein p38) is present in chromaffin granules and in a special vesicle population | Q45044457 | ||
| Homotypic vacuolar fusion mediated by t- and v-SNAREs | Q48049888 | ||
| Colocalization on the same synaptic vesicles of syntaxin and SNAP-25 with synaptic vesicle proteins: a re-evaluation of functional models required? | Q48895901 | ||
| Inhibition of exocytosis in bovine adrenal medullary cells by botulinum toxin type D | Q59098884 | ||
| Is NSF a fusion protein? | Q63383548 | ||
| Subcellular distribution of 65,000 calmodulin-binding protein (p65) and synaptophysin (p38) in adrenal medulla | Q69226282 | ||
| Adrenal chromaffin cells contain functionally different SNAP-25 monomers and SNAP-25/syntaxin heterodimers | Q71618648 | ||
| SNAP-25 is present on chromaffin granules and acts as a SNAP receptor | Q71793372 | ||
| Syntaxin 1 (HPC-1) is associated with chromaffin granules | Q71869167 | ||
| Association of N-ethylmaleimide-sensitive factor with synaptic vesicles | Q72150624 | ||
| SNAP-25 is present in a SNARE complex in adrenal chromaffin cells | Q72180515 | ||
| Blockade by botulinum neurotoxin B of catecholamine release from adrenochromaffin cells correlates with its cleavage of synaptobrevin and a homologue present on the granules | Q72183666 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 349-352 | |
| P577 | publication date | 1997-09-01 | |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | NSF and SNAP are present on adrenal chromaffin granules | |
| P478 | volume | 414 |
| Q40855920 | Analysis of regulated exocytosis in adrenal chromaffin cells: insights into NSF/SNAP/SNARE function |
| Q40757119 | Association of Alpha-Soluble NSF Attachment Protein with Epileptic Seizure |
| Q53917964 | Comparison of cysteine string protein (Csp) and mutant alpha-SNAP overexpression reveals a role for csp in late steps of membrane fusion in dense-core granule exocytosis in adrenal chromaffin cells. |
| Q41995248 | Doc2 is not associated with known regulated exocytotic or endosomal compartments in adrenal chromaffin cells |
| Q77159584 | Docking and fusion in neurosecretion |
| Q42037072 | Early requirement for alpha-SNAP and NSF in the secretory cascade in chromaffin cells |
| Q40780580 | Inhibition of the membrane fusion machinery prevents exit from the TGN and proteolytic processing by furin |
| Q35762171 | Microarray and real-time PCR analysis of adrenal gland gene expression in the 7-day-old rat: effects of hypoxia from birth |
| Q34250652 | N-ethylmaleimide sensitive factor (NSF) structure and function. |
| Q24657428 | Photolysis of a caged peptide reveals rapid action of N-ethylmaleimide sensitive factor before neurotransmitter release |
| Q40855911 | Sorting and storage during secretory granule biogenesis: looking backward and looking forward |
| Q24678373 | Stimulation of NSF ATPase activity by alpha-SNAP is required for SNARE complex disassembly and exocytosis |
| Q44283372 | Transduction of bovine adrenal chromaffin cells using a recombinant adenovirus expressing GFP. |
| Q41823292 | Veratridine induces apoptotic death in bovine chromaffin cells through superoxide production |
| Q42994573 | nSec-1 (munc-18) interacts with both primed and unprimed syntaxin 1A and associates in a dimeric complex on adrenal chromaffin granules |
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