Homotypic fusion of immature secretory granules during maturation in a cell-free assay
about
Rab3D is not required for exocrine exocytosis but for maintenance of normally sized secretory granulesFurin at the cutting edge: from protein traffic to embryogenesis and diseaseThe EARP Complex and Its Interactor EIPR-1 Are Required for Cargo Sorting to Dense-Core VesiclesPhosphoproteome analysis of capacitated human sperm. Evidence of tyrosine phosphorylation of a kinase-anchoring protein 3 and valosin-containing protein/p97 during capacitationSynaptotagmin IV is necessary for the maturation of secretory granules in PC12 cellsPro-hormone secretogranin II regulates dense core secretory granule biogenesis in catecholaminergic cells.In vitro assays of vesicular transport.HID-1, a new component of the peptidergic signaling pathway.Rab3D is critical for secretory granule maturation in PC12 cells.Dense-core secretory granule biogenesis.Discovery and progress in our understanding of the regulated secretory pathway in neuroendocrine cells.Homotypic fusion of immature secretory granules during maturation requires syntaxin 6Role of adaptor proteins in secretory granule biogenesis and maturationSyntaxin-6 SNARE involvement in secretory and endocytic pathways of cultured pancreatic beta-cells.HID-1 is required for homotypic fusion of immature secretory granules during maturation.Modulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autismDynamics of immature secretory granules: role of cytoskeletal elements during transport, cortical restriction, and F-actin-dependent tetheringTwo Rab2 interactors regulate dense-core vesicle maturation.Sorting without a Golgi complex.Syntaxin 6 regulates Glut4 trafficking in 3T3-L1 adipocytes.The trafficking of alpha 1-antitrypsin, a post-Golgi secretory pathway marker, in INS-1 pancreatic beta cells.Roles of myosin Va and Rab3D in membrane remodeling of immature secretory granules.GGA function is required for maturation of neuroendocrine secretory granules.Neuroendocrine transcriptional programs adapt dynamically to the supply and demand for neuropeptides as revealed in NSF mutant zebrafish.Statistical analysis of the quantal basis of secretory granule formation.The dense-core vesicle maturation protein CCCP-1 binds RAB-2 and membranes through its C-terminal domain.Sorting Ourselves Out: Seeking Consensus on Trafficking in the Beta-Cell
P2860
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P2860
Homotypic fusion of immature secretory granules during maturation in a cell-free assay
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
Homotypic fusion of immature secretory granules during maturation in a cell-free assay
@ast
Homotypic fusion of immature secretory granules during maturation in a cell-free assay
@en
type
label
Homotypic fusion of immature secretory granules during maturation in a cell-free assay
@ast
Homotypic fusion of immature secretory granules during maturation in a cell-free assay
@en
prefLabel
Homotypic fusion of immature secretory granules during maturation in a cell-free assay
@ast
Homotypic fusion of immature secretory granules during maturation in a cell-free assay
@en
P2860
P356
P1476
Homotypic fusion of immature secretory granules during maturation in a cell-free assay
@en
P2093
P2860
P304
P356
10.1083/JCB.143.7.1831
P407
P577
1998-12-01T00:00:00Z