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1 cargo prior to its packaging into a nascent transport carrier.
2 ay mechanistic roles in the formation of the transport carrier.
3 e lysosome for degradation by way of an AP-3 transport carrier.
4 l to the ER in coat protein complex I-formed transport carriers.
5 nd fission machineries to produce retrograde transport carriers.
6 assembly, a process essential for generating transport carriers.
7 g by promoting the biogenesis of TGN-derived transport carriers.
8 rt by controlling the biogenesis of specific transport carriers.
9 brane proteins by sorting them into membrane transport carriers.
10 exclude somatodendritic proteins from axonal transport carriers.
11 twork (TGN) of plasma membrane (PM)-destined transport carriers.
12 ed for the biogenesis of TGN to cell surface transport carriers.
13 ve face that seems to match the curvature of transport carriers.
14 iogenesis of cargo-enriched tubulo-vesicular transport carriers.
15 an integral component of some intracellular transport carriers.
16 s of the secretory pathway by membrane-bound transport carriers.
17 BLOC-1-dependent cargo, STX13, or VAMP7 into transport carriers.
18 in transmembrane cargoes with biogenesis of transport carriers.
19 luence BLOC-1 function in generating tubular transport carriers.
20 ocessed cargoes are sorted and packaged into transport carriers.
21 h cargo at tubular microdomains and generate transport carriers.
22 is mediated by interactions between soluble transport carriers and insoluble NPC proteins that conta
23 nterface to locally concentrate COPII-coated transport carriers and link exit sites on the ER to ERGI
24 hondrial proteins functioning as precursors, transport carriers, and gates are preferentially degrade
25 this activity is used to control the size of transport carriers, and to prevent uncontrolled vesicula
27 ur studies define a mechanism by which COPII transport carriers are retained locally at the ER/ERGIC
29 Quinone molecules are intracellular electron-transport carriers, as well as critical intra- and extra
30 This fission reaction is used to generate transport carriers at the TGN that are en route to the c
31 arly endosome, recycling endosome and apical transport carriers before reaching its steady-state apic
33 ble cargo proteins are recognized by nuclear transport carriers, called importins, which mediate thei
34 estrates capture and packaging of cargo into transport carriers coated with sorting nexin BAR domain
35 e assembly of endoplasmic reticulum to Golgi transport carriers commences with the coating of specifi
37 and ligand-receptor binding profile of GABA transport carrier (CsgabP) from the non-model plant, Val
38 s-Golgi network by regulating the fission of transport carriers destined for the plasma membrane.
40 on through cargo adaptors with biogenesis of transport carriers during integral membrane protein traf
43 53)-containing membranes to generate a mega-transport carrier for export of collagens and apolipopro
44 end support to our suggestion that growth of transport carriers for exporting bulky cargoes requires
46 ER exit sites, where they are packaged into transport carriers formed by the highly conserved coat p
47 ed for the membrane fission that separates a transport carrier from its progenitor compartment: the l
48 formation of endoplasmic reticulum to Golgi transport carriers from endoplasmic reticulum sites clos
49 a, PKCeta, and PKD act in series to generate transport carriers from the TGN and their overactivation
51 the secretory pathway, budding of vesicular transport carriers from the trans-Golgi network (TGN) mu
53 released from a TGN block was colocalized in transport carriers in association with PI5K and actin co
54 g melanosomes in melanocytes, is sorted into transport carriers in complex with the tSNARE component
55 was added exogenously to SMG via a membrane-transporting carrier in the presence of PI 3-kinase inhi
57 ays to unambiguously identify TGN46-positive transport carriers involved in protein trafficking betwe
60 f soluble secretory proteins into ER-derived transport carriers occurs via transmembrane cargo recept
61 ing studies indicated that these two nuclear transport carriers of different classes, p10 and Kap-bet
62 nvolves reduced endocytosis and/or increased transport carrier recruitment from an intracellular pool
64 eptor cells is mediated by rhodopsin-bearing transport carriers (RTCs) and regulated by the small GTP
65 i network (TGN) and regulates the fission of transport carriers specifically destined to the cell sur
66 Golgi network (TGN) regulates the fission of transport carriers specifically destined to the cell sur
67 e needed for biogenesis of endosomal tubular transport carriers, strongly inhibits the peroxisome-ass
68 R complexes into clathrin-coated vesicles or transport carriers (TCs) destined for delivery to endoso
70 mediates fusion of melanosomes with tubular transport carriers that also carry the cargo protein TYR
71 at PKD regulates the fission from the TGN of transport carriers that are en route to the cell surface
72 structural evolution of COPII (coat protein) transport carriers that are essential for the transport
73 delivery of melanogenic cargoes via tubular transport carriers that emanate from early endosomes and
74 pical and basolateral proteins into distinct transport carriers that emerge from the trans-Golgi netw
75 hat selects and packages cargo proteins into transport carriers that export cargo from the endosome.
76 pon warming, they exit these compartments in transport carriers that have very different membrane cha
77 sorting of proteins into distinct vesicular transport carriers that mediate secretion and interorgan
78 Intracellular trafficking is mediated by transport carriers that originate by membrane remodeling
79 station for distinct apical and basolateral transport carriers that reach their respective surface d
80 -receptor interactions give rise to distinct transport carriers that regulate the trafficking kinetic
81 m (ER) in two layers to generate cargo-laden transport carriers that ultimately fuse with an adjacent
82 nsfer from trans-Golgi network (TGN)-derived transport carriers to endosomes involves a still undefin
84 cargo proteins are transferred into ESCPE-1 transport carriers to promote endosome-to-plasma membran
85 tes tethering and fusion of endosome-derived transport carriers to the trans-Golgi network (TGN).
88 ver, the role of large COPII vesicles as PC1 transport carriers was not unambiguously demonstrated.
89 GO1 remains at the neck of the newly forming transport carrier, which grows in size by addition of ER
90 e vSNARE for fusing endosome-derived tubular transport carriers with maturing melanosomes in melanocy
91 at VAMP7 mediates fusion of BLOC-1-dependent transport carriers with melanosomes, illuminate SNARE re
93 SNARE-mediated fusion of endosome-derived transport carriers with the trans-Golgi network (TGN) de
94 on to promote the fusion of endosome-derived transport carriers with their corresponding compartments