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1 high-resolution structure of this ATP-driven ion pump.
2  a threonine, that protein became a chloride ion pump.
3 smitter delivery from the organic electronic ion pump.
4  as well as ion channels and the Na/K-ATPase ion pump.
5 rotein interactions, in addition to being an ion pump.
6 anism may be a progenitor of photobiological ion pumps.
7 realized previously using organic electronic ion pumps.
8 e channel-forming small molecule and protein ion pumps.
9 perometric biosensors and organic electronic ion pumps.
10 opulations that had already evolved distinct ion pumps.
11  while eukaryotic V-type ATPases function as ion pumps.
12 tivation of vision pigments and light-driven ion pumps.
13 a canonical photocycle typical for microbial ion pumps.
14  branch of P-type ATPases, a large family of ion pumps.
15 action cycle of this family of ATP-dependent ion pumps.
16  and a member of the P-type ATPase family of ion pumps.
17 ate sufficient electric fields for effective ion pumping.
18  is performing cellular functions other than ion pumping.
19 all design principles that are necessary for ion pumping.
20                                          The ion pumps (active in the membrane at numbers exceeding 2
21 sequence primarily of the ability to depress ion pumping activities of cells, macromolecular synthesi
22 ession of the mutant a1 protein was low, and ion pumping activity was lost.
23  ring from the vacuolar-type (V-type) sodium ion-pumping adenosine triphosphatase (Na+-ATPase) from E
24                        The simulation of the ion pumping against a proton gradient energized by light
25                             Mutations of the ion pump alpha2-Na/K ATPase cause familial hemiplegic mi
26 By assessing the energy used on postsynaptic ion pumping and action potentials, we show that, instead
27 fferences between the two domains, including ion pumping and DNA replication.
28                                      Primary ion pumps and antiporters exist as multigene families in
29 ) in M6, also play critical roles in related ion pumps and are therefore likely to be common architec
30 ing extensively studied, the central role of ion pumps and carriers is largely ignored in current neu
31 ns is based on the operation of plasmalemmal ion pumps and carriers that establish transmembrane ion
32 s directly regulate the genes of a number of ion pumps and channels, these results suggest that Na(+)
33 f the protein may be the shared mechanism of ion pumps and G-protein related receptors.
34 ers such as inositol trisphosphate, cellular ion pumps and membrane channels has become more clearly
35 dings affirm the alternating-access model of ion pumps and offer the possibility of examining ion occ
36 hy membrane bioenergetics are universal, yet ion pumps and phospholipid membranes arose later and ind
37 ents have not been observed in retinal-based ion pumps and photoreceptors.
38   This may open new avenues for the study of ion pumps and similar electrogenic targets.
39  in this enzyme, a cytochrome c oxidase-type ion-pump and a Q-cycle mechanism, on the basis of the th
40 odopsin (HOP), a light-gated inward chloride ion pump, and measured extracellular receptor potentials
41 ermeation, mechanosensitive channels, active ion pumps, and active stresses in the cortex.
42 th key ion-binding residues of P-type ATPase ion pumps, and N905D was recently identified as one of t
43 hanosensitive ion channels, energy-consuming ion pumps, and the actomyosin cortex, that coordinate to
44 -inspired adsorption-responsive photothermal ion pump (APIP) for enhanced and reversible Li(+) extrac
45                                              Ion pumps are integral membrane proteins responsible for
46 biological entities such as ion channels and ion pumps as a function of ion type and concentration.
47    Th?e atomic structure of the light-driven ion pump bacteriorhodopsin and the surrounding lipid mat
48 umping Ca(2+) (which uses 1 ATP per 2 Ca(2+) ions pumped), but by the 10th and subsequent twitches th
49 s to the previously unknown structure of the ion-pumping channel in the C-type Coxs and provides insi
50       Existing optogenetic silencers include ion pumps, channels, metabotropic receptors, and tools t
51 ons contain open reading frames for a P-type ion pump (CopA) with homology to Cd2+ and Cu2+ ATPases a
52 ly are believed to be bacterial redox-driven ion pumps, coupling an oxidoreduction process to the tra
53 es E1/E2 conformational transition during an ion pumping cycle.
54                  Like many voltage-sensitive ion pumps, cytochrome c oxidase is inhibited by zinc.
55 ase mechanism with strong resemblance to the ion pumps, despite a location of the translocation pathw
56 diverse protein families, including V-ATPase ion pumps, DNA-binding transcription regulators, and ser
57 oth an energy reserve, capable of sustaining ion pumping during periods of transient stress, as well
58 the concentration gradient, demonstrating an ion-pumping effect.
59        Steady-state measurements indicate an ion pumping efficiency of approximately 30%.
60 the spontaneous activator/enzyme release and ion pumping enable enzymes to sufficiently interact with
61 ells that harbor phosphorylases and kinases, ion pumps exhibiting substantial ATPase activity, and my
62 mbrane Ca(2+) ATPase 2 (PMCA2), an essential ion pump expressed exclusively in grey matter and involv
63                                          The ion pump features eight drug reservoirs and channels arr
64 of these structural changes reveals how this ion pump first facilitates ion uptake deep within the ce
65 lymer membrane as a light-powered artificial ion pump for active ion transport, which exhibits potent
66 rotein promise a better understanding of how ion pumps function.
67            Through its classic ATP-dependent ion-pumping function, basolateral Na/K-ATPase (NKA) gene
68 , suggesting that the signal-transducing and ion-pumping functions of Na(+)/K(+)-ATPase cooperate in
69 says confirmed the alkaline induction of two ion pump genes (ENA1 and VMA4), several ion limitation g
70 yo joints strongly expressed the Na/K-ATPase ion pump genes Atp1a1, Atp1b1 and Atp1b3.
71                    Because Rim101p activates ion pump genes, we tested the role of RIM101 in ion home
72              One example compares the inward ion pump halorhodopsin (HR) and the outward proton pump
73   Na(+)/K(+)-ATPase as an energy transducing ion pump has been studied extensively since its discover
74 ynaptic strengths or ionic conductances, and ion pumps have only rarely been demonstrated to play a d
75  of ion homeostasis that can be recovered by ion pumps if the energy supply is adequate.
76 to isolate the energetics of an electrogenic ion pump in an engineered in vitro environment to power
77              Herein, we report light-powered ion pumping in a polystyrene sulfonate anion (PSS) doped
78 appears to be functionally dominant over NKA ion pumping in the control of RPT reabsorption.
79 es hydrolyze ATP in the V1 domain coupled to ion pumping in VO.
80 up of P-type ATPases, an essential family of ion pumps in all kingdoms of life.
81 ach, using the fast generation of functional ion pumps incorporated into nanodiscs and their subseque
82 ating that the Drosophila Na,K-ATPase has an ion-pump-independent role in junction formation and trac
83 odes of action (i.e. CdCl(2) toxicity versus ion pump inhibition by ouabain), a significant advance a
84 lthough halorhodopsin is normally a chloride ion pump, it evidently contains all structural requireme
85 nding proteins that function as light-driven ion pumps, light-gated ion channels, and photosensors, w
86 more likely than a cytochrome c oxidase-type ion-pump mechanism.
87                  Rhodopsins are light-driven ion-pumping membrane proteins found in many organisms an
88  can be realized with water electrolysis and ion pumping membranes, to avoid costly mechanical compre
89                               A microfluidic ion pump (microFIP), capable of delivering a drug withou
90                                          The ion pump Na(+),K(+)-ATPase is a critical determinant of
91                               In the related ion pumps Na(+),K(+)-ATPase and Ca(2+)-ATPase, M4 moves
92 sons: glycolytic enzymes are associated with ion pumps; neurons may increase their energy supply by a
93                                          The ion-pumping NQR complex is an essential respiratory enzy
94                       The organic electronic ion pump (OEIP) provides flow-free and accurate delivery
95 uction of the R109Q mutation into the sodium ion pump of Dokdonia eikasta (KR2) results in passive io
96 ce ion removal, whereas natural light-driven ion pumps offer superior efficiency.
97 alciparum, by targeting PfATP4, an essential ion pump on the parasite surface.
98 r promote active or passive ion transport as ion pumps or directly light-activated channels.
99 l rhodopsins, which function as light-driven ion pumps or photosensors, have been reported.
100 x proteins that function as light-responsive ion pumps or sensory receptors.
101 tion that occlusion/deocclusion reactions of ion pumps perturb the membrane surrounding the protein,
102 stidine-tagged yeast secretory pathway/Golgi ion pump Pmr1 to near homogeneity in one step, using nic
103 nerated in the yeast secretory pathway/Golgi ion pump, Pmr1, targeting oxygen-containing side chains
104 e insight on the structural mechanism of the ion pumping process.
105 -dependent activation of an energy-consuming ion pumping process.
106           We reconstituted a model vectorial ion pump, proteorhodopsin, in liposomes of opposite char
107 d seem to be simply to optimize the enzyme's ion pumping rate under its normal physiological conditio
108  pairs may be a general feature of P2-ATPase ion pumps, reflecting a flexibility of this region that
109 ndicate that PMR1 and PMR2A, encoding P-type ion pumps required for Mn2+ and Na+ tolerance, may also
110 -ATPase are electrogenic and nonelectrogenic ion pumps, respectively.
111         Inactivation of Na+,K+ -ATPases, the ion pumps responsible for maintaining a pH above 6 withi
112     RNA interference of the H(+),K(+)-ATPase ion pump results in membrane hyperpolarization, which ha
113 nnelrhodopsin (BCCR) more closely related to ion pump rhodopsins than other channelrhodopsins.
114 , by primary sequence, more closely resemble ion pump rhodopsins; mechanisms for passive channel cond
115  which is lower than that of other microbial ion pumping rhodopsins.
116                                    Microbial ion-pumping rhodopsins (MRs) are extensively studied ret
117 sting of cyanobacterial chloride and sulfate ion-pumping rhodopsins, the Mastigocladopsis repens rhod
118                            The ATP-dependent ion pump sarco/endoplasmic reticulum Ca(2+)-ATPase (SERC
119                  However, organic electronic ion pumps show high operating voltages and limited trans
120                                     The KdpB ion-pump subunit of KdpFABC is a P-type ATPase, and cata
121 nt, suggesting activation of an electrogenic ion pump such as the H+ pump.
122 sive membrane channels and molecular machine ion pumps such as ATPases.
123 Pase protein family includes, in addition to ion pumps such as Ca(2+)-ATPase and Na(+),K(+)-ATPase, a
124  a single ion channel and the activity of an ion pump suffice to dramatically increase the propensity
125                 Members of the P-type ATPase ion pump superfamily are found in all three branches of
126  recording electrodes via organic electronic ion pump technology.
127                         The MOF serves as an ion pump that continuously provides metal ion activators
128 emical model for the functioning of the V(o) ion pump that is consistent with the known structural fe
129         Na(+)/K(+)-ATPases are transmembrane ion pumps that maintain ion gradients across the basolat
130 e conductors in the form of ion channels and ion pumps that work together to form ion concentration g
131 uces ATP and the cellular processes, such as ion pumping, that consume ATP.
132 espective contributions of NKA signaling and ion pumping to the overall regulation of RPT Na(+) reabs
133 collaborating with the corresponding protein ion pumps to restore physiology.
134 lectrochemical gradients provided by primary ion pumps to translocate metabolites or drugs "uphill" a
135                                P-type ATPase ion pumps translocate their substrates occluded between
136 g proteins, and downstream executors such as ion pumps, transporters, and plasma membrane channels th
137 -ATPase beta-subunit (betaHK) into an active ion pump upon coexpression in Xenopus oocytes.
138 , changes in the expression of several other ion pumps, vesicular proteins, mitochondrial enzymes and
139 or the rational design of novel light-driven ion pumps with optogenetic applications.
140 s some of its molecular machinery, including ion pumps, within lipid bilayer membranes.

 
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