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2 osis in hepatocytes, causing accumulation of transcytotic carriers for the polymeric IgA receptor (pI
4 vesicle carrier fraction (CVCF) enriched in transcytotic carriers; (2) slow delivery of [35S]-labele
6 y immunoisolation and found that no uniquely transcytotic elements were present, because recycling re
8 the polymeric IgA receptor (pIgAR)) but also transcytotic markers (dIgA and the 120-kDa form of pIgAR
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
18 find that sorting of cholera toxin into this transcytotic pathway bypasses retrograde transport to th
20 erefore warranting consideration of the FcRn transcytotic pathway for further investigation as a mean
22 vert an infectious outcome, we modulated the transcytotic pathway in polarized Madin-Darby canine kid
26 l protein endolyn-78 partially resembled the transcytotic pathway, since anti-endolyn-78 antibodies w
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
35 that the density of recycling receptors and transcytotic pIgR in RRC membranes was similar to that i
37 on of Wingless that is required for both the transcytotic process and signal transduction in dorsal c
43 IgG transport, we examined LIS and endocytic/transcytotic structures from neonatal and weaned animals
45 poles of polarized epithelial cells and that transcytotic traffic is likely to require Rab11a-depende
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
53 a p22 peptide block the targeting/fusion of transcytotic vesicles with the apical plasma membrane, b
55 ated with both ER to Golgi and postendosomal transcytotic vesicles, and 2) multiple GTP-binding prote
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 >
61 and dibutyryl cAMP (DBcAMP), stimulators of transcytotic vesicular transport, increased the biliary
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