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1 e that one of them, the Cajal body (CB), can be formed de novo.
2 hat the precise patterning of the cortex can be formed de novo.
3 s not adopt canonical conformations and must be modeled de novo.
4  large host and guest molecules can reliably be designed de novo.
5 it reward circuits, dopamine transients must be elicited de novo.
6 ltogether from the shotgun effort and had to be generated de novo.
7 r (CRPC), suggesting that androgens may also be synthesized de novo.
8                          Mitochondria cannot be synthesized de novo.
9 another STAT6-regulated protein(s) that must be synthesized de novo.
10 , but most 9 + 2 architectural proteins must be synthesized de novo.
11 nt in iron-limited cells and did not need to be synthesized de novo.
12 es in various biological processes, and must be biosynthesized de novo.
13 reby increasingly large sequences of DNA can be synthesised de novo, allow an unprecedented ability t
14                               As they cannot be synthesized de novo and are self-replicating, mitocho
15 eplicated in a cell-free system, that it can be generated de novo, and that the strain-specific prope
16 ow mitochondria and organelles, which cannot be formed de novo, are put together.
17                     These channels appear to be induced de novo, because they occur concurrently with
18                    These sequences must then be assembled de novo before most genome analyses can beg
19      Human artificial chromosomes (HACs) can be formed de novo by transfection of large fragments of
20 ts provide evidence that silent synapses can be generated de novo by in vivo experience and thus may
21                         Moreover, [ETA+] can be induced de novo by excess Sup35p, and [ETA+] cells ha
22 vels in PC12 cells exposed to NGF appears to be enhanced de novo DAG synthesis, probably initiated by
23  interaction and the initiation complex must be formed de novo during every round of transcription.
24 sequenced and annotated, transcriptomes must be assembled de novo from the RNA-seq data.
25 ition, we found that PrP(Sc) molecules could be formed de novo from these defined components in the a
26 (reg) cells are absent in the thymus but can be generated de novo from CXCR5(-)Foxp3(+) natural T(reg
27 of the mammalian prion protein (PrP(Sc)) can be produced de novo from a mixture of the normal conform
28 tracellular pyrimidine nucleotides (PyN) can be synthesized de novo from glutamine, CO2, and ATP, or
29 lytically that cytonuclear disequilibria can be generated de novo if the cytoplasmic and nuclear loci
30  we demonstrate that a functional intron can be created de novo in a single step by a segmental genom
31 ule with properties reminiscent of PrPSc can be generated de novo in cultured cells.
32 se (aGVHD) in mice, autoreactive T cells can be generated de novo in the host thymus implying an impa
33  of the more sophisticated activities yet to be generated de novo in the laboratory and sheds light o
34 y expressed only in a few tumor lines, could be induced de novo in all P1A-negative cancer lines of e
35 he embryonic wing primordium and thus has to be induced de novo in the nascent larval wing disc.
36                         Because language can be invented de novo in the manual modality, this offers
37    Moreover, an unmethylated PAI2 gene could be methylated de novo in the suvh4 mutant background.
38   Here, we demonstrate how strictosidine can be produced de novo in a Saccharomyces cerevisiae host f
39                            Neurosteroids can be synthesized de novo in the brain in levels sufficient
40                 A number of sex steroids can be synthesized de novo in the brain, including estrogens
41                        Because the ER cannot be generated de novo, it must be faithfully transmitted
42 al behaviors of these proteins, which cannot be predicted de novo, may play an essential role in rapi
43       Alternative backbone conformations can be generated de novo or by redeploying existing fragment
44      Our data show that novel TSE agents can be generated de novo solely from purified mouse rPrP aft
45 lds and assemblies not observed in nature to be generated de novo, that is, to access the 'dark matte
46                          Mitochondria cannot be generated de novo; they must grow, replicate their ge
47 unusually long and well conserved motifs can be discovered de novo through a comparative genomics app
48 antation tolerance after CD4 Ab blockade can be induced de novo through a TGF-beta-dependent mechanis
49 ining a backbone of sphingoid bases that can be produced de novo through the reaction of palmitate an
50 thetic gene regulatory circuits, as they can be designed de novo to target a given DNA sequence.
51 for engineering these circuits, as TALEs can be designed de novo to target a given DNA sequence.
52 ate that zinc finger DNA-binding domains can be engineered de novo to recognise given DNA sequences.
53  CTL that recognize viral proteins that must be synthesized de novo to be presented as class I Ags.
54 we show that this chromatin architecture can be predicted de novo using epigenetic data derived from
55 ation power, whether an infectious prion can be formed de novo with bacterially expressed recombinant
56 ent establishes that an infectious prion can be formed de novo with bacterially expressed rPrP.
57 s and to determine whether these cells could be infected de novo with HIV-1.
58  that genuinely new enzymatic activities can be created de novo without the need for prior mechanisti

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