scholarly article | Q13442814 |
P50 | author | Daniel Axelrod | Q88473018 |
Prabhodh S Abbineni | Q90028773 | ||
Ronald W Holz | Q90028777 | ||
P2093 | author name string | Mary A Bittner | |
P2860 | cites work | The chromogranin-secretogranin family | Q28185052 |
A palette of fluorescent proteins optimized for diverse cellular environments | Q28647200 | ||
How proteins produce cellular membrane curvature | Q29618016 | ||
Membrane curvature controls dynamin polymerization | Q30493714 | ||
Localized topological changes of the plasma membrane upon exocytosis visualized by polarized TIRFM. | Q33643745 | ||
Lumenal protein within secretory granules affects fusion pore expansion | Q33990912 | ||
The fusion pores of Ca2+ -triggered exocytosis | Q34037133 | ||
Distinct fusion properties of synaptotagmin-1 and synaptotagmin-7 bearing dense core granules | Q34081432 | ||
Fluorescent cargo proteins in pancreatic beta-cells: design determines secretion kinetics at exocytosis | Q34188253 | ||
Carbocyanine dye orientation in red cell membrane studied by microscopic fluorescence polarization | Q34254410 | ||
Role of the synaptobrevin C terminus in fusion pore formation | Q34276398 | ||
Transmembrane segments of syntaxin line the fusion pore of Ca2+-triggered exocytosis. | Q34305380 | ||
Currents through the fusion pore that forms during exocytosis of a secretory vesicle | Q34397957 | ||
A structural role for the synaptobrevin 2 transmembrane domain in dense-core vesicle fusion pores | Q34470858 | ||
Simultaneous electrical and optical measurements show that membrane fusion precedes secretory granule swelling during exocytosis of beige mouse mast cells | Q34605300 | ||
Secretory granules are recaptured largely intact after stimulated exocytosis in cultured endocrine cells. | Q34763388 | ||
A new role for the dynamin GTPase in the regulation of fusion pore expansion | Q35011226 | ||
Exocytotic fusion pores are composed of both lipids and proteins | Q36589148 | ||
The extended granin family: structure, function, and biomedical implications | Q36666413 | ||
A nibbling mechanism for clathrin-mediated retrieval of secretory granule membrane after exocytosis | Q36725018 | ||
The mystery of the fusion pore | Q37013086 | ||
The molecular function of adrenal chromaffin granules: established facts and unresolved topics | Q39479340 | ||
Mechanisms of dense core vesicle recapture following "kiss and run" ("cavicapture") exocytosis in insulin-secreting cells | Q40522071 | ||
The disulfide-bonded loop of chromogranin B mediates membrane binding and directs sorting from the trans-Golgi network to secretory granules | Q41786528 | ||
Polarized TIRFM reveals changes in plasma membrane topology before and during granule fusion | Q42201429 | ||
Synaptotagmin modulation of fusion pore kinetics in regulated exocytosis of dense-core vesicles | Q43787533 | ||
Identification of a novel sorting determinant for the regulated pathway in the secretory protein chromogranin A. | Q44216719 | ||
Chromogranins A and B are key proteins in amine accumulation, but the catecholamine secretory pathway is conserved without them | Q44482157 | ||
Slow fusion pore expansion creates a unique reaction chamber for co-packaged cargo | Q46310573 | ||
The crucial role of chromogranins in storage and exocytosis revealed using chromaffin cells from chromogranin A null mouse. | Q46681537 | ||
Chromogranin A, the major catecholamine storage vesicle soluble protein. Multiple size forms, subcellular storage, and regional distribution in chromaffin and nervous tissue elucidated by radioimmunoassay. | Q47241345 | ||
Recapture after exocytosis causes differential retention of protein in granules of bovine chromaffin cells. | Q50796308 | ||
Visualization of Membrane Pore in Live Cells Reveals a Dynamic-Pore Theory Governing Fusion and Endocytosis. | Q53833435 | ||
Membrane curvature in synaptic vesicle fusion and beyond. | Q55052659 | ||
The synaptotagmin C2B domain calcium-binding loops modulate the rate of fusion pore expansion. | Q55239707 | ||
The composition of adrenal chromaffin granules: an assessment of controversial results | Q67499091 | ||
Processing of chromogranin A within chromaffin granules starts at C- and N-terminal cleavage sites | Q68325569 | ||
Flux of catecholamines through chromaffin vesicles in cultured bovine adrenal medullary cells | Q71357649 | ||
Intracellular and extracellular processing of chromogranin A. Determination of cleavage sites | Q72563888 | ||
pH-dependent association of chromogranin A with secretory vesicle membrane and a putative membrane binding region of chromogranin A | Q72871525 | ||
The fusion pore, 60 years after the first cartoon | Q89110786 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 2 | |
P304 | page(s) | 118-130 | |
P577 | publication date | 2018-11-30 | |
P1433 | published in | The Journal of General Physiology | Q1092259 |
P1476 | title | Chromogranin A, the major lumenal protein in chromaffin granules, controls fusion pore expansion | |
P478 | volume | 151 |
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