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1 (III)-(O(2)(*-))] (S), are shown to be redox interconvertible.
2 trnT gene suggests that the two isoforms are interconvertible.
3 of the forms (yellow and pink in color) are interconvertible.
4 These two modes of cell movement are interconvertible.
5 formers of the 1,4 cross-link, which are not interconvertible.
6 We show that these four species are interconvertible.
7 nd after (L2) the native protein, which were interconvertible.
8 redoxins and enzymes that contain reversibly interconvertible [4Fe-4S]2+/+ and [3Fe-4S]+/0 clusters,
9 rs that these two types of spin currents are interconvertible across the interfaces, predicated as th
11 s show that PrPSc molecules are structurally interconvertible and that only a subset of PrPSc conform
15 renders RubyACR bistable (i.e., very slowly interconvertible between two spectrally distinct forms).
16 s studies have shown that B(2)GPI adopts two interconvertible biochemical conformations, oxidized and
17 Foci and homogenous patterns seem freely interconvertible but the prevalence of the uniform stain
25 uc-Leu-Leu-Val-Tyr-AMC and (2) there are two interconvertible conformers of active 20S proteasome.
26 ation sequence in the reaction, in which the interconvertible coordination mode (imino N -> Ru and am
29 Evidence indicates that CO rebinds to two interconvertible deoxyRmFixL* conformers that are produc
32 XO) and xanthine dehydrogenase (XDH) are two interconvertible forms of the same protein, differing in
33 FAPY base which exists in two separable but interconvertible forms that have been assigned by variou
34 oproteins that exist in two photochromically interconvertible forms, a red light absorbing species, P
35 tase from bovine milk can be prepared in two interconvertible forms, xanthine oxidase (XO) and xanthi
36 ur centres, and FAD as cofactors and has two interconvertible forms, xanthine oxidase and xanthine de
38 h agree with experimental structures, reveal interconvertible L and linear conformations likely relat
40 onment generates phenotypically distinct but interconvertible malignant cell subpopulations that fuel
41 e, or sphingosine-1-phosphate (S1P) provides interconvertible metabolites with distinct biological ac
43 s weak, we hypothesize that PDI exists as an interconvertible mixture of monomers and dimers in the e
44 ndividual metastatic tumor cells exhibit two interconvertible modes of cell motility during tissue in
45 ctamica strain NL4 revealed two distinct and interconvertible molecular species of LPS with high and
47 ion pattern on the relative stability of the interconvertible N10-C11 carbinolamine, carbinolamine me
49 se two binding sites are independent and non-interconvertible on the time scale of these experiments
50 t are formally topologically trivial but are interconvertible only by complex, nonphysical multibond
58 g that transcription and replication are not interconvertible processes mediated by a common polymera
59 all EML cell subsets exhibit cell-autonomous interconvertible properties, with the capacity to genera
62 n a defined 5'UTR stretch with two predicted interconvertible RNA conformations, as known from ribosw
66 o overcome energetic differences between the interconvertible species (forced interconversion), the t
67 gosine and sphingosine-1-phosphate (SPP) are interconvertible sphingolipid metabolites with opposing
68 spectrally resolved fluorescence in its two interconvertible states can be assembled in three synthe
69 have been shown to display a high degree of interconvertible states including quiescent, inflammator
70 models allow for the possibility of multiple interconvertible surface conformations of adsorbed prote
71 preformed stable species or whether they are interconvertible, the fate of band 3 species synthesized
72 theoretical investigations suggest that the interconvertible three-redox-state species undergo rever
73 apical sulfido diastereomers are potentially interconvertible through a low-lying TBP transition stat
74 7 degrees C), as expected, and that they are interconvertible through peritectic reactions at approxi
75 dant in the plasma membrane and are directly interconvertible through the action of specific enzymes,
76 absence and presence of CD3zeta suggest two interconvertible types of NCR-CD3zeta assemblies: 1) a s
77 ate that the trans and cis diastereomers are interconvertible under reaction conditions with the cis-
79 attack of PPh(3) on the allenoate generates interconvertible Z-, E-, and twisted adducts: the former