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1             (ii) Electron microscopy reveals intravesicular 20-nm particles, similar to those formed
2  models are therefore most likely created by intravesicular accumulation of pre-formed liquid amorpho
3 rnal medium stimulated proton efflux and the intravesicular accumulation of radiolabeled gentamicin,
4 cal for pHi regulation as it is activated by intravesicular acid pH.
5  is thought to be pivotal for maintenance of intravesicular acidic pH as well as the maturation, fusi
6 mal tubule was measured from the kinetics of intravesicular acidification in response to rapid mixing
7 I]IUdR in patients with liver metastases and intravesicular administration in patients with bladder c
8  more "protected" routes: intra-arterial and intravesicular administration.
9                             Importantly, the intravesicular alpha-syn is more prone to aggregation th
10 Here we present a metallic pyramid array for intravesicular analysis by combining site-selective diel
11  APP tunes glutamate release, likely through intravesicular and extravesicular interactions with syna
12 y also suggest plausible physical routes for intravesicular, and possibly intracellular, delivery of
13                         Here we show that an intravesicular APP domain interacts with the proteins th
14                                              Intravesicular Asc may also play a role in relieving cat
15 ated with a rapid transmembrane oxidation of intravesicular ascorbate by extravesicular ferricyanide.
16 on of ADP and ATP (rather than exchange with intravesicular ATP) is demonstrated by high pressure liq
17                          Hederagenin induced intravesicular budding but no pore formation.
18 wo types of large vesicles with high and low intravesicular [Ca2+].
19 ntion" process and concentration increase of intravesicular catecholamine.
20 to resist bladder colonization in vivo after intravesicular challenge with type 1-fimbriated E. coli.
21 rug delivery, as their membrane features and intravesicular components may facilitate IT transport.
22 changes in transmitter content such that the intravesicular concentration of transmitter is maintaine
23 -ApoE and betaA suggested presence of stable intravesicular conjugates.
24 vesicles and a target membrane that releases intravesicular content through a transient, nanometer-si
25 o the cytoplasm alters the physical state of intravesicular contents in preparation for release.
26  secretory vesicles dock and fuse to release intravesicular contents to the outside during cell secre
27  can be limited to the bladder urothelium by intravesicular delivery of tamoxifen.
28                        Here we identified an intravesicular domain of APP, called intraluminal SV-APP
29     Direct application of such forces to the intravesicular end of the TM domain resulted in tilting
30 ld be accessible to proteolysis in a soluble intravesicular environment.
31 e FM1-43 and an antibody directed against an intravesicular epitope of synaptotagmin I.
32  cilia with disrupted axonemes and perturbed intravesicular fluid flow in Kupffer's vesicle.
33 ntly underwent cystoscopy, which revealed an intravesicular fluid-filled mass near the left ureteric
34 ntly underwent cystoscopy, which revealed an intravesicular fluid-filled mass near the left ureteric
35 ntaneously, we can dissociate the effects of intravesicular free radical generation on spontaneous ne
36  this study, we acutely probe the effects of intravesicular free radical generation on synaptic vesic
37 llular expression of Gal3-mRuby, which binds intravesicular galactosides and forms puncta upon vesicl
38  presynaptic vesicle release regulation--the intravesicular glutamate fill state of the vesicle.
39 ues within the transmembrane regions and the intravesicular glycosylation of SV2 are required for its
40                                        Thus, intravesicular localization and secretion are part of no
41  acid substitutions occurred in a 56-residue intravesicular loop (IV1 domain) of the vesicle protein
42  but YqkI-dependent Na(+) uptake depended on intravesicular malate and extravesicular lactate.
43    YqkI-dependent lactate uptake depended on intravesicular malate and extravesicular Na(+).
44 icroscopy has shown that, during exocytosis, intravesicular markers escape without collapse of the ve
45 rent vesicles, without causing the mixing of intravesicular material.
46 consistent with chemical dissociation of the intravesicular matrix or gel.
47 ns from the cytosolic ascorbate (Asc) to the intravesicular matrix to provide reducing equivalents fo
48  begins with molecular rearrangements at the intravesicular membrane leaflet and not between the appo
49 ng molecular cargo from the outside into the intravesicular milieu.
50                    Our data suggest that the intravesicular N-glycosylation site of synaptotagmin 1 c
51                   The Ca(2+) uptake requires intravesicular Na(+) and is stimulated by an inside posi
52      IAP is most commonly measured using the intravesicular or "bladder" technique.
53 s indicate that exposure to high pH, whether intravesicular or extracellular, accelerates release of
54 mide, both of which are expected to increase intravesicular pH by inhibiting V-type H+-ATPase, had no
55 her these effects are attributable to raised intravesicular pH due to proton transport through VMATs.
56 ined the effect of ethanol administration on intravesicular pH in intact hepatocytes by applying a fl
57                                     Although intravesicular pH levels in D. discoideum show small aci
58 shown to bind to the vesicle membrane at the intravesicular pH of 5.5 and to be released from it at a
59 ns aggregated in the presence of Ca2+ at the intravesicular pH of 5.5.
60 The effects of extracellular Zn2+ and pH and intravesicular pH on insulin and 5-hydroxytryptamine (5-
61 ng active loading strategies to generate low intravesicular pH to prolong drug retention and increase
62 d these three approaches with measurement of intravesicular pH to show very fast FA binding and trans
63                                          The intravesicular pH was approximately 6.5, supporting only
64               Using pH-sensitive probes, the intravesicular pH was determined and found to be equival
65                  Simulations to estimate the intravesicular pH were conducted to demonstrate that acc
66 r H(+)-ATPase decreased exponentially as the intravesicular pH(in) decreased, suggesting modulation o
67  the conductance of sodium and calcium ions, intravesicular pH, trafficking and excitability.
68 fined conditions allowing extravesicular pH, intravesicular pH, transmembrane pH and membrane potenti
69 tuted M2 using a pH-sensitive dye to monitor intravesicular pH, we conclude that bath pH weakly affec
70 y loaded liposomal formulations having a low intravesicular pH.
71 lease correlated with alterations in the low intravesicular pH.
72 ic weak base ammonium chloride, which raises intravesicular pH.
73 rmeate secretory vesicle membranes and raise intravesicular pH.
74 hibition of G34 cleavage, perhaps by raising intravesicular pH.
75 6 ml h(-)(1)) evoked periodic sharp rises in intravesicular pressure accompanied by rhythmic bursting
76                                   Triplicate intravesicular pressure measurements were performed at l
77  was partly explained by fluctuations in the intravesicular redox concentration in response to osmoti
78 r transporters, and by a highly glycosylated intravesicular sequence.
79 sion in a solution that is hypertonic to the intravesicular solution decreases, and may abolish, chan
80 icles in a solution that is hypotonic to the intravesicular solution increases channel activity where
81 occurred in right-side-out vesicles when the intravesicular space contained either Na+ or K+ but not
82 nded to changes in the osmotically sensitive intravesicular space, and was saturable, exhibiting a Km
83 hen aminoglycosides were present only in the intravesicular space.
84 for K exchange allowing acidification of the intravesicular space.
85                        It was concluded that intravesicular storage conditions and extracellular ions
86 lope that also enclosed the nematode-derived intravesicular structure.
87 f PfCRT, these changes would tend to promote intravesicular trapping of chloroquine (a weak base) and
88      Caspase 3-mediated apoptosis depends on intravesicular trypsinogen activation induced by CTSB, n
89 eteral bladder insertion sites and shortened intravesicular tunnel lengths that correlated with VUR.
90 ontrols; (2) after bladder inflammation with intravesicular turpentine; and (3) after bilateral hypog
91  the percentage of sealed vesicles and their intravesicular volume and sidedness using biochemical ap
92                                              Intravesicular volume estimated by incorporation of radi