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1 We also show that a blocking antibody antigen-binding fragmen
2 We also show that a lincRNA-specific co-transcriptional RNA c
3 We also show that a S. enterica cobT strain that synthesizes
4 We also show that a very rich mixture of organic aerosols is
5 We also show that a well-established in vivo mild chronic hyp
6 We also show that AAV delivered M-opsin localizes in the dors
7 We also show that an active-site tryptophan, Trp-321, partici
8 We also show that at deep levels of unconsciousness where mov
9 We also show that co-expression of Fat4 and Ds1 in the same c
10 We also show that commendamide is responsible for the previou
11 We also show that CsgB, in the presence of surfactant/LPS, ac
12 We also show that CST unfolds G-quadruplex structures, thus p
13 We also show that disease stage transitions, both reversal an
14 We also show that docking of the sorting platform results in
15 We also show that endonuclease activity of apurinic/apyrimidi
16 We also show that epigenetically driven effects are strongly
17 We also show that identical fluctuations can support multiple
18 We also show that IDGF2 is an abundant haemolymph component,
19 We also show that in nitrate-fed mice there is reduced system
20 We also show that iRFP can be readily detected in 3D organoid
21 We also show that knockdown of TrkB or Bdnf in this brain reg
22 We also show that mutation of Capicua (CIC), a transcriptiona
23 We also show that MYO acts in vivo to inhibit synaptic transm
24 We also show that optix simultaneously acts as a switch gene
25 We also show that phase sensitivity of PSLR can exceed 10(5)
26 We also show that Plk3 in turn suppresses the SIAH2 protein l
27 We also show that reaching a fixed threshold level is not a n
28 We also show that relieving metacognitive task demand improve
29 We also show that reporters harboring stall sequences near th
30 We also show that similar mutagenesis strategies can be used
31 We also show that survival of DTPs is, in part, maintained by
32 We also show that tension stimulation can be translated to a
33 We also show that TEX19.1 likely acts, at least in part, thro
34 We also show that the biogeochemical response of the aquifer
35 We also show that the brine-oil interface jumps from pore-to-
36 We also show that the intrinsically enhanced freedom of motio
37 We also show that the method is significantly faster than the
38 We also show that the presence of barr2 is essential for prop
39 We also show that the same technique applied to the photorece
40 We also show that the senescent phenotype is dynamic, changin
41 We also show that this design strategy is compatible with sev
42 We also show that Tubifex worms retain microplastics for long
43 We also show that Zfp106 knockout mice develop severe motor n
44 We also show that, even in the absence of correlations, for G
45 ering levels of sexually antagonistic selection for colour, we also show that sexual selection leads to greater expansion
46 By direct recording of synaptic currents, we also show that motoneurons are activated by out-of-phase p
49 despread demyelination of the spinal cord and optic nerves, we also show that thinly remyelinated axons with short intern
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