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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
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
9 e suggest a system 1.5 of reasoning allowing interchange between Bayesian and logical rules as it fit
10 sembly at the kinetochore, the Ndc80 complex interchanges between bent (auto-inhibited) and open conf
11 features are nearly unchanged at either pH, interchange between both conformations is highly reversi
12 tic representation, the strategy of frequent interchange between captive and wild breeders within ANP
14 ts with examples that show the potential for interchange between computer science, cognitive science,
15 highlight the ability of boron inhibitors to interchange between different hybridization states/bindi
17 functions, which require rapid and specific interchange between distinct conformations involved in g
20 relevant conditions establish that the motif interchanges between flexible (highly populated) and bou
21 ings reveal a RACK7/KDM5C-regulated, dynamic interchange between histone H3K4me1 and H3K4me3 at activ
22 he hypothesis that Rad26 is required for the interchange between holo-TFIIH and a putative repairosom
25 or into murine leukemia L1210 cells via acyl interchange between intracellular glutathione and the ce
27 essential lytic switch gene 50 controls the interchange between lytic and latent gene expression pro
28 des highlights the desirability of continued interchange between magnetism physics and neurobiology.
33 ese 4H RNAs are interesting because frequent interchanges between parallel and antiparallel conformat
34 system can be used as a model to study gene interchange between primate species that have not achiev
35 cestral mechanism for direct thiol-disulfide interchanges between proteins even in an unfavorable red
38 e of the nanocrystals can also be reversibly interchanged between spherical and cubic morphology thro
41 as shown to be involved in dithiol-disulfide interchange between the Cys-88/Cys-93 and Cys-535/Cys-54
42 rom coeval European ambers, showing a biotic interchange between the eastern and western margins of t
43 binding to the three hosts reveals that the interchange between the isomers is much faster than the
47 s as a dynamic structure with conformational interchange between the pseudoknot and a hairpin with in
49 that there is the potential for a functional interchange between the viral proteins expressed by alph
50 rthermore, functional TCR contacts cannot be interchanged between the two epitopes, indicating that t
51 shift to the 888 conformation shows that H27 interchanges between the 885 and 888 conformations on th
53 t-protein binding, does not show evidence of interchanging between the apo and Ca(2+)-bound orientati
54 espite the diversification of, and potential interchange between, the spleen and brain Ag-specific T
55 , supporting the hypothesis that the dynamic interchange between these conformations mediates interfi
58 emoval and restoration of Runx1 causes rapid interchanges between these chromatin loops, which reveal
59 4 T-cell subpopulations, suggesting frequent interchanges between viral reservoir cells in blood and