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1  significantly decreased the extent of cleft alkalization.
2 r disruption byd-ceramide-C6 causes Golgi pH alkalization.
3 he Rim101 transcription factor upon external alkalization.
4 creasing the voltage sensitivity of internal alkalization.
5 g during acidification and decreasing during alkalization.
6  complex results in defective phagolysosomal alkalization.
7 dependent NHE1-activation and subsequent pHi alkalization.
8      This was potentiated with intracellular alkalization.
9 tion in the ER, were defective for endosomal alkalization.
10 080 led to marked enhancement of the rate of alkalization.
11  H(+)-ATPase activity, leading to apoplastic alkalization.
12 prospectively abandoned hyperventilation and alkalization.
13 the negative effects of hyperventilation and alkalization.
14 g information on chemical changes induced by alkalization.
15  were correlated to the different degrees of alkalization.
16 s patients treated with hyperventilation and alkalization, 13 before and 16 after the availability of
17 ctivation by intracellular and extracellular alkalization(3,8,9), but the mechanistic basis for TASK2
18 w that LT induces a dose-dependent lysosomal alkalization accompanied by an increase in mitochondrial
19                    Ammonia and intracellular alkalization activate TRPV1 through a mechanism that inv
20 n murine sperm, SLO3 mediates a voltage- and alkalization-activated K(+) current essential to male fe
21 Paradoxically, AE3 enhances intracellular re-alkalization after MAc removal in neurons and astrocytes
22                                AE3 speeds re-alkalization after removal of MAc in neurons and astrocy
23 ication of secretin induced a marked urinary alkalization, an effect absent in mice lacking pendrin o
24 lar mechanisms responsible for intracellular alkalization and activation of SLO3 are not completely u
25 of this kinase paralleled or preceded medium alkalization and activation of the defense gene phenylal
26 h a DeltaydcI allele, leads to intracellular alkalization and genetic assimilation of Rho mutant func
27  for pHs decreased to pH 9,8 and 7; however, alkalization and neutralization created casein aggregate
28 in protein and whey protein was suggested in alkalization and neutralization process by non-reducing
29 ression of cell wall elicitor-induced medium alkalization and PAL gene activation, suggesting a regul
30 ubstrate permeability, measurements of media alkalization, and proton decoupling that AQP9 acts as a
31                                     Moderate alkalizations ( approximately 0.5 to 1.0 pH unit alkaliz
32  Intracellular acidification inhibited while alkalization augmented the inward current.
33 ymmetric electrochemical system for seawater alkalization based on a highly reversible and identical
34                               Preventing the alkalization blocked GC ABA-responses and even opened st
35 ortical collecting duct and stimulates urine alkalization by activating the beta -intercalated cells.
36                                              Alkalization by ammonium pre-pulse to pHi 7.78 +/- 0.02
37 vitro and in vivo studies support intestinal alkalization by sodium bicarbonate supplementation as a
38                       Inducing intracellular alkalization by the small molecule JTC801 leads to a dec
39  slower recovery kinetics from intracellular alkalization, consistent with the Cl(-)/HCO3(-) exchange
40                        Hereto, the impact of alkalization degree (none, medium and high) on the poten
41 containing BME were added to chocolates with alkalization degrees (pH 4.5, 6, 7.5) at conching temper
42 liary subunit that helps define the specific alkalization dependence of KSper activation.
43  increase is not attributable to cytoplasmic alkalization; depolarization induces a slight acidificat
44          With physiological ionic gradients, alkalization depolarizes Slo3(-/-) spermatozoa, presumab
45 ow internal pH and low external K, such that alkalization does not reopen the channels unless externa
46 olved in HC feedback but that synaptic cleft alkalization during light-evoked hyperpolarization of HC
47                                              Alkalization enhances pH-sensitive transmitter release a
48 nitiate stomatal closure via rapid cytosolic alkalization followed by Ca(2+) elevation.
49 neralization, desalinization, acidification, alkalization, hardening, and softening) associated with
50                                              Alkalization hyperpolarizes sperm and produces Ca(2+) en
51                      NHE9-mediated endosomal alkalization impairs Rab7 activation, thereby disrupting
52                  The resulting endolysosomal alkalization impedes macrophage antigen processing and p
53 ific potential mood-enhancing compounds upon alkalization, implying a decrease in bitterness and astr
54 lC-K2 blocker, NPPB, caused acidification or alkalization in different subpopulations of intercalated
55 e from the past five years on the effects of alkalization in relation to the conditions applied, the
56  extracellular Cl(-) removal led to a larger alkalization in slc4a10-transfected cells than in contro
57                        The transient urinary alkalization in the postprandial state is suggested to h
58 t is critical for fertility, is activated by alkalization in the range of pH 6.4-7.2 at membrane pote
59                      The results showed that alkalization induced more negative zeta-potential compar
60 A1-dependent lysosomal pathway in inhibiting alkalization-induced cell death and highlight its potent
61 holesterol synthesis, as a key suppressor of alkalization-induced cell death in pancreatic cancer cel
62 ial K(+)/H(+) exchanger, as well as external alkalization inhibited a recovery phase of the reversibl
63                                Intracellular alkalization is a primitive mechanism by which proton pa
64                                              Alkalization is a process to improve color, dispersibili
65                                              Alkalization is an optional process in cocoa powder prod
66 from both sexes, a significant and prolonged alkalization occurred when stimulating the connected ner
67 ments in penumbral cortex and post-ischaemic alkalization of brain.
68 Consistently, we observed that NHE9-mediated alkalization of EEs hindered perinuclear movement.
69 atidylcholine-phospholipase C inhibition and alkalization of endolysosomal compartments blocked its a
70  by a mechanism that probably depends on the alkalization of endolysosomes.
71                                              Alkalization of pH(i) from 7.2 to 7.8 increased gap junc
72 ma membrane Na(+)/Ca(2+) exchanger (NCX) via alkalization of the bath solution, by adding lanthanum,
73 H in yeast, CHX20 elicited acidification and alkalization of the cytosol and vacuole, respectively.
74                       The results reveal the alkalization of the electrolyte close to the oxygen redu
75                                  The ensuing alkalization of the endosomal lumen increased translocat
76 that actin-depolymerizing agents promote the alkalization of the Golgi stack and thetrans-Golgi netwo
77 mentation (5 mg/ml in drinking water) led to alkalization of the intestinal contents.
78 d killing of yeast by primary macrophages by alkalization of the phagosome.
79  Ca(2+) in muscle positively correlated with alkalization of the synaptic cleft, whereas inhibiting P
80 sitive dye pyranine resulted in an immediate alkalization of the vesicle lumen by an average pH chang
81 dles that probe plant vasculature, sense the alkalization of vascular fluid as a biomarker for drough
82 ogether with an NH4Cl-mediated intracellular alkalization (or lesser acidification) of AQP4-expressin
83 ion in the nanocavities during a homogeneous alkalization process driven by chloride-assisted glycido
84                            Moreover, luminal alkalization promotes the recruitment of Rab27b.
85 ds analysis via HS-SPME-GC-MS indicated that alkalization reduced the levels of volatile compounds, r
86                         Hyperventilation and alkalization remain common therapies.
87  during ischemia with glial acidification or alkalization, respectively.
88                            In addition, this alkalization resulted in the reduction of the histopatho
89 controls chemotactic steering; a concomitant alkalization serves as a highly cooperative mechanism th
90                                         Soil alkalization severely affects crop growth and agricultur
91                          Thus, intracellular alkalization stimulates, while intracellular acidificati
92 rents that are less effectively activated by alkalization than are native KSper currents.
93  and pH, and light-induced acidification and alkalization that are asso-ciated with inorganic carbon
94  that high external pH induces intracellular alkalization that directly or indirectly activates plasm
95 ype II approximately 4 Hz) and the degree of alkalization that silenced the cells (type I 7.4-7.6, ty
96 rmation of carbocations is reversible; after alkalization, the ions return to the original neutral fo
97 drial dysfunction is downstream of lysosomal alkalization under lipotoxic conditions and that recover
98 cidification (up to pH 5.0), but also during alkalization (up to pH 8.0), an original and inducible p
99 o investigate the mechanism underlying cleft alkalization, we used muscle-expressed GCaMP3 to monitor
100 lizations ( approximately 0.5 to 1.0 pH unit alkalization) were observed during exposure to inhibitor
101         Na/H exchange (NHE2) results in cell alkalization, whereas intracellular [Na] is regulated by
102 ing cascade involving TGFalpha>PI3K>NHE1>pHi alkalization, which leads to a permissible environment f
103              Experimentally, we achieved the alkalization with an energy consumption of 0.63 kWh/kg N

 
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