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1  cells optogenetically with halorhodopsin or archaerhodopsin.
2 that the same is true for bacterioruberin in archaerhodopsin.
3  hyperpolarization via the inhibitory opsin, archaerhodopsin.
4 uorescence of a microbial rhodopsin protein, Archaerhodopsin 3 (Arch) from Halorubrum sodomense, expr
5 a detailed spectroscopic characterization of Archaerhodopsin 3 (Arch).
6  the ground (light-adapted) and DA states of Archaerhodopsin-3 (AR3), solved to 1.1 A and 1.3 A resol
7                                     The gene archaerhodopsin-3 (Arch) from Halorubrum sodomense enabl
8             A member of this protein family, Archaerhodopsin-3 (Arch) of halobacterium Halorubrum sod
9                              The proton pump Archaerhodopsin-3 (Arch), an optogenetic tool commonly u
10 activation of a light-activated proton pump, Archaerhodopsin-3 (Arch), proton transients induced ASIC
11 cy tuning of the stimulated neurons, whereas archaerhodopsin-3 (Arch)-mediated inactivation biased de
12  decreased spiking of excitatory neurons, as archaerhodopsin-3 (Arch)-mediated optical silencing of c
13 e optogenetic tools, such as the proton pump archaerhodopsin-3 (Arch).
14  transduced to express either ChR2(E123A) or archaerhodopsin-3 from the Halorubrum sodomense strain T
15 different component opsins: the proton pump, Archaerhodopsin and a chloride channel opsin.
16 ciated virus expressing the inhibitory opsin archaerhodopsin, and fiber-optic cannulae were implanted
17 to and ChR2-EYFP, halorhodopsin eNpHR3.0 and archaerhodopsin Arch-ER2.
18   The light-activated inhibitory proton pump Archaerhodopsin (Arch) was expressed under control of th
19                 Channelrhodopsin-2 (ChR2) or Archaerhodopsin (Arch) were expressed in glycinergic pre
20                                              Archaerhodopsin-(Arch)-transduced RTN neurons were rever
21                   In this work, we show that Archaerhodopsin (ArchT), a light-driven outward proton p
22 pens when both are activated together, using Archaerhodopsin as an optical voltage clamp to provide t
23                              We developed an Archaerhodopsin-based fluorescent voltage sensor whose t
24                                Here, we used Archaerhodopsin-based loss-of-function optogenetics to e
25                               We evolved two archaerhodopsin-based voltage indicators, QuasAr1 and Qu
26                    Here, we demonstrate that Archaerhodopsin can be used to quantitatively image AP w
27  neurons by activating genetically expressed Archaerhodopsin current increased the firing rate and re
28     We used the Photopick platform to evolve archaerhodopsin-derived genetically encoded voltage indi
29 annelrhodopsin, CheRiff, and a near infrared Archaerhodopsin-derived voltage indicator, QuasAr2, via
30         A fluorescent protein is fused to an archaerhodopsin-derived voltage sensor.
31 n contrast, hydrolysis of the Schiff base in archaerhodopsin does not abolish the CD bands of bacteri
32 l-directed behavior, as photoinactivation of archaerhodopsin-expressing neurons in the POm decreased
33 reely behaving mice, whereas inhibition with archaerhodopsin for 30 min suppressed LH pulsatility.
34 ontrast, silencing Npas1(+) GPe neurons with Archaerhodopsin had insignificant effects on Npas1(-) ne
35 based on green fluorescent proteins (FPs) or archaerhodopsin has emerged as a powerful approach for d
36                     Another retinal protein, archaerhodopsin, has been shown to contain a carotenoid,
37 ed mice co-expressing Channelrhodopsin-2 and Archaerhodopsin in pyramidal cells in the hippocampal CA
38 ptogenetic probes, such as halorhodopsin and archaerhodopsin, inhibit transmitter release indirectly
39                               By introducing archaerhodopsin into engrailed-1-positive neurons, we de
40                                     Finally, archaerhodopsin-mediated selective silencing of PV(+) in
41  a pooled high-throughput screen to identify archaerhodopsin mutants with enhanced photoactivation.
42 e transplanted MGE neurons expressing either archaerhodopsin or channelrhodopsin into the visual cort
43 g tdTomato fluorescence, channelrhodopsin-2, archaerhodopsin or GCaMP3.
44 tructing quantum chemical models of a set of Archaerhodopsin reporters in their electronically excite
45  with channelrhodopsin-2, or inhibition with archaerhodopsin, simulated an instantaneous increase or
46 way rats, injected with the inhibitory opsin archaerhodopsin T (ArchT) into the primary auditory cort
47             Finally, in mice transduced with archaerhodopsin-T, semi-chronic optogenetic MCH neuronal
48 et CRF neurons with the optogenetic silencer archaerhodopsin tp009 (CRF-ArchT) to examine the role of