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1                                   Thus, FcRn transcytotic and recycling sorting steps are distinct.
2 osis in hepatocytes, causing accumulation of transcytotic carriers for the polymeric IgA receptor (pI
3 icle carrier fraction (CVCF), which includes transcytotic carriers.
4  vesicle carrier fraction (CVCF) enriched in transcytotic carriers; (2) slow delivery of [35S]-labele
5                                              Transcytotic commensal penetration may contribute to ini
6 y immunoisolation and found that no uniquely transcytotic elements were present, because recycling re
7  endosomal markers but was distinct from the transcytotic intermediate, the subapical compartment.
8 the polymeric IgA receptor (pIgAR)) but also transcytotic markers (dIgA and the 120-kDa form of pIgAR
9                        Both were enriched in transcytotic markers and depleted in ER and Golgi marker
10  rab11a-containing endosomes and, unlike the transcytotic markers, did not distribute to the plasma m
11 nes that contain apical ABC transporters and transcytotic markers, permitting their targeting to the
12 bendothelial matrix of vascular tissues by a transcytotic mechanism and serves as a catalyst of ECM p
13 li, apical ABC transporters colocalized with transcytotic membrane proteins in rab11a-containing endo
14 K cells promotes a switch from a direct to a transcytotic mode of apical protein delivery and other t
15     Our results suggest that in WIF-B cells, transcytotic molecules pass through a subapical compartm
16                          To characterize the transcytotic passage of albumin through lens epithelial
17                                              Transcytotic passage of albumin was monitored for 4 hour
18 find that sorting of cholera toxin into this transcytotic pathway bypasses retrograde transport to th
19                      Here, we report a novel transcytotic pathway employed by AP-1B-deficient epithel
20 erefore warranting consideration of the FcRn transcytotic pathway for further investigation as a mean
21                                They define a transcytotic pathway important for the physiology of nat
22 vert an infectious outcome, we modulated the transcytotic pathway in polarized Madin-Darby canine kid
23                                          The transcytotic pathway of vitamin B12 has previously been
24 is intermediate in the basolateral-to-apical transcytotic pathway remained functional.
25  suggest the existence of a dendrite-to-axon transcytotic pathway to achieve axonal accumulation.
26 l protein endolyn-78 partially resembled the transcytotic pathway, since anti-endolyn-78 antibodies w
27 n indicate that rab3D is associated with the transcytotic pathway.
28  viral particles may cross the BBB using the transcytotic pathway.
29                         The paracellular and transcytotic pathways of biliary excretion, assessed by
30                The basolateral recycling and transcytotic pathways of epithelial cells were previousl
31 , these data indicate that the secretory and transcytotic pathways remain polarized in cholestatic he
32  on the apical and basolateral recycling and transcytotic pathways, demonstrating that these pathways
33 ptor segregation into distinct recycling and transcytotic pathways.
34 ctively regulate the apical recycling and/or transcytotic pathways.
35  that the density of recycling receptors and transcytotic pIgR in RRC membranes was similar to that i
36 y enriched in recycling receptors and in the transcytotic polymeric Ig receptor (pIgR).
37 on of Wingless that is required for both the transcytotic process and signal transduction in dorsal c
38 caveolae and clathrin-coated vesicles in the transcytotic process.
39                                   However, a transcytotic protein did reach the apical surface after
40  specifically inhibits the caveolae-mediated transcytotic route readily used in the periphery.
41 c tail motif (YRSL) are unable to access the transcytotic route.
42                            We have evaluated transcytotic routes in MDCK cells for their ability to g
43 IgG transport, we examined LIS and endocytic/transcytotic structures from neonatal and weaned animals
44                    This findings confirm the transcytotic targeting of cCAM105 reported in earlier st
45 poles of polarized epithelial cells and that transcytotic traffic is likely to require Rab11a-depende
46                                 Synaptic and transcytotic trafficking thus are restricted to particul
47 red BRE cells by an NOS-dependent process of transcytotic transport in caveolae.
48  that rab17 and syntaxin 2 mediate fusion of transcytotic vesicles at the apical surface.
49 cytoplasmic domain of pIgAR to immunoisolate transcytotic vesicles from a fraction (CV1, rho = 1.146)
50 raction on anti-Rab1a was similar to that of transcytotic vesicles immunoisolated from the same fract
51 R), suggesting that Rab1a is associated with transcytotic vesicles in rat liver.
52                      Fusion of recycling and transcytotic vesicles with the apical and basolateral pl
53  a p22 peptide block the targeting/fusion of transcytotic vesicles with the apical plasma membrane, b
54              However, the association of the transcytotic vesicles with the microtubules was not sens
55 ated with both ER to Golgi and postendosomal transcytotic vesicles, and 2) multiple GTP-binding prote
56                             On endosomes and transcytotic vesicles, FGD6 regulates retromer-dependent
57 b1a appeared to be enriched in postendosomal transcytotic vesicles, whereas those isolated on pIgAR c
58 associated proteins and increased numbers of transcytotic vesicles, which occasionally contained mHtt
59 inuous microvascular endothelium function as transcytotic vesicular carriers for protein molecules >
60 scles) in which they have been identified as transcytotic vesicular carriers.
61  and dibutyryl cAMP (DBcAMP), stimulators of transcytotic vesicular transport, increased the biliary

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