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1 ze B-A translocations result from reciprocal interchanges between a supernumerary B chromosome and an
2 associations within human interphase nuclei, interchanges between all possible heterologous pairs of
3      Our results demonstrate that when E3 is interchanged between alphavirus species that belong to t
4                        It involves disulfide interchange between an engineered sulfhydryl group of th
5 ced by bulkier Cp* (Cp*=eta(5) -C5 Me5 ), an interchange between an unsupported radical [Co2 Cp*2 (CO
6 China supports previous hypotheses of faunal interchange between Asia and North America in the early
7 c mammalian fauna during an active period of interchange between Asia and North America.
8                                     However, interchanges between bacteria in these two states have b
9  features are nearly unchanged at either pH, interchange between both conformations is highly reversi
10                 We also show that functional interchange between components of the classical and alte
11 ts with examples that show the potential for interchange between computer science, cognitive science,
12                   DNA repeats are capable of interchanging between different noncanonical and canonic
13  functions, which require rapid and specific interchange between distinct conformations involved in g
14                                      Dynamic interchange between DNA conformations, including metasta
15                           In particular, the interchanges between extended canonical and non-canonica
16 relevant conditions establish that the motif interchanges between flexible (highly populated) and bou
17 ings reveal a RACK7/KDM5C-regulated, dynamic interchange between histone H3K4me1 and H3K4me3 at activ
18 he hypothesis that Rad26 is required for the interchange between holo-TFIIH and a putative repairosom
19            Second is the ubiquity of genetic interchange between human populations, both in terms of
20                                          The interchange between inert dinitrogen gas (N2) in the ext
21 or into murine leukemia L1210 cells via acyl interchange between intracellular glutathione and the ce
22  essential lytic switch gene 50 controls the interchange between lytic and latent gene expression pro
23                                 Such dynamic interchange between metastable and globally stable DNA c
24                                              Interchange between oxidation states is promoted by a "J
25 ese 4H RNAs are interesting because frequent interchanges between parallel and antiparallel conformat
26  system can be used as a model to study gene interchange between primate species that have not achiev
27 cestral mechanism for direct thiol-disulfide interchanges between proteins even in an unfavorable red
28 des the oldest fossil evidence for mammalian interchange between South and North America.
29 NKCC1 chimeras in which N and C termini were interchanged between species.
30 e of the nanocrystals can also be reversibly interchanged between spherical and cubic morphology thro
31                               The reversible interchange between such an inner-sphere complex [ArH,NO
32                                 Notably, the interchange between the amorphous and crystalline forms
33 as shown to be involved in dithiol-disulfide interchange between the Cys-88/Cys-93 and Cys-535/Cys-54
34 rom coeval European ambers, showing a biotic interchange between the eastern and western margins of t
35  binding to the three hosts reveals that the interchange between the isomers is much faster than the
36 o facilitate cell-extrinsic control over the interchange between the lytic and latent cycles.
37                            There is no lipid interchange between the plasma and granule membranes dur
38 s as a dynamic structure with conformational interchange between the pseudoknot and a hairpin with in
39 ent predictions due to the simultaneous mass interchange between the two species.
40 that there is the potential for a functional interchange between the viral proteins expressed by alph
41 rthermore, functional TCR contacts cannot be interchanged between the two epitopes, indicating that t
42 shift to the 888 conformation shows that H27 interchanges between the 885 and 888 conformations on th
43                                  Nutritional interchanges between the partners produce carbohydrates
44 t-protein binding, does not show evidence of interchanging between the apo and Ca(2+)-bound orientati
45 espite the diversification of, and potential interchange between, the spleen and brain Ag-specific T
46                                              Interchange between these states likely explains the var
47 emoval and restoration of Runx1 causes rapid interchanges between these chromatin loops, which reveal

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