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1 trnT gene suggests that the two isoforms are interconvertible.
2 of the forms (yellow and pink in color) are interconvertible.
3 These two modes of cell movement are interconvertible.
4 formers of the 1,4 cross-link, which are not interconvertible.
5 We show that these four species are interconvertible.
6 nd after (L2) the native protein, which were interconvertible.
7 redoxins and enzymes that contain reversibly interconvertible [4Fe-4S]2+/+ and [3Fe-4S]+/0 clusters,
8 rs that these two types of spin currents are interconvertible across the interfaces, predicated as th
10 s show that PrPSc molecules are structurally interconvertible and that only a subset of PrPSc conform
14 Foci and homogenous patterns seem freely interconvertible but the prevalence of the uniform stain
21 uc-Leu-Leu-Val-Tyr-AMC and (2) there are two interconvertible conformers of active 20S proteasome.
23 Evidence indicates that CO rebinds to two interconvertible deoxyRmFixL* conformers that are produc
26 XO) and xanthine dehydrogenase (XDH) are two interconvertible forms of the same protein, differing in
27 FAPY base which exists in two separable but interconvertible forms that have been assigned by variou
28 oproteins that exist in two photochromically interconvertible forms, a red light absorbing species, P
29 tase from bovine milk can be prepared in two interconvertible forms, xanthine oxidase (XO) and xanthi
30 ur centres, and FAD as cofactors and has two interconvertible forms, xanthine oxidase and xanthine de
32 onment generates phenotypically distinct but interconvertible malignant cell subpopulations that fuel
33 e, or sphingosine-1-phosphate (S1P) provides interconvertible metabolites with distinct biological ac
34 s weak, we hypothesize that PDI exists as an interconvertible mixture of monomers and dimers in the e
35 ndividual metastatic tumor cells exhibit two interconvertible modes of cell motility during tissue in
36 ctamica strain NL4 revealed two distinct and interconvertible molecular species of LPS with high and
38 ion pattern on the relative stability of the interconvertible N10-C11 carbinolamine, carbinolamine me
40 se two binding sites are independent and non-interconvertible on the time scale of these experiments
45 g that transcription and replication are not interconvertible processes mediated by a common polymera
46 all EML cell subsets exhibit cell-autonomous interconvertible properties, with the capacity to genera
49 n a defined 5'UTR stretch with two predicted interconvertible RNA conformations, as known from ribosw
53 gosine and sphingosine-1-phosphate (SPP) are interconvertible sphingolipid metabolites with opposing
54 models allow for the possibility of multiple interconvertible surface conformations of adsorbed prote
55 preformed stable species or whether they are interconvertible, the fate of band 3 species synthesized
56 apical sulfido diastereomers are potentially interconvertible through a low-lying TBP transition stat
57 7 degrees C), as expected, and that they are interconvertible through peritectic reactions at approxi
58 absence and presence of CD3zeta suggest two interconvertible types of NCR-CD3zeta assemblies: 1) a s
59 ate that the trans and cis diastereomers are interconvertible under reaction conditions with the cis-
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