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1 roteases are similar, their FPs are found to be quite different.
2 t the optimum pH and isoelectric point could be quite different.
3 ximodistal axis (base to tip) are thought to be quite different.
4 lecules of cccDNA), and replicating DNAs may be quite different.
5 opulation genetics of sexual populations may be quite different.
6 n patients lacking these lifestyle risks may be quite different.
7 plar for 5-OH-PCB91 and 5-OH-PCB95 proved to be quite different.
8 sion that involves these proteins appears to be quite different.
9 ity in 5-enolexo processes are calculated to be quite different.
10 the linker region that joins the two domains is quite different.
11 trend for the perfluorocarbon (PFC) radicals is quite different.
12 but the reality of DNA's physical existence is quite different.
13 In the germline, however, the situation is quite different.
14 inding to the -152 to -86 bp SPRR1B promoter is quite different.
15 se tissues in energy storage and utilization is quite different.
16 n Fas-deficient autoimmune mice, the picture is quite different.
17 ferases, although the adenine-binding domain is quite different.
18 action of progesterone in these two systems is quite different.
19 rom EXT1 and EXT2, its pattern of expression is quite different.
20 duction of stereoselectivity in DA reactions is quite different.
21 rlying structure of environmental influences is quite different.
22 ngal, and viral keratitis, as the treatments are quite different.
23 series, even when their expression profiles are quite different.
24 ekeeping genes to normalize microarrays that are quite different.
25 e two pathogens, their pathogenic lifestyles are quite different.
26 aternary structures between the heterodimers are quite different.
27 n images, their demands on visual processing are quite different.
28 ude of the binding constant for each complex are quite different.
29 on from pH 7.3 to pH 3.0 for loops CD and EF are quite different.
30 anions and the corresponding neutral species are quite different.
31 ventricular volume between the two patients are quite different.
32 ion machinery, their kinetics of degradation are quite different.
33 on expression during chemoautotrophic growth are quite different.
34 he atomic compositions of the two substances are quite different.
35 The properties of CaMKII labeling are quite different.
36 nslation of prokaryotic and eukaryotic genes are quite different.
37 ffects of KChIP4a and KChIP1-3 on Kv4 gating are quite different.
38 arly identical, their hemichannel properties are quite different.
39 s, the in vivo functions of the two proteins are quite different.
40 olic and sensory effects of these two sugars are quite different.
41 nship between them, their modes of secretion are quite different.
42 The selectivities on the two phases are quite different.
43 ar, their apoptotic and oncogenic properties are quite different.
44 ce because therapeutic options and prognosis are quite different.
45 a of AFGP8 and AFGP1-5 in the amide I region are quite different.
46 of natural selection and breeding structure are quite different.
47 tween those two classes of bis-intercalators are quite different.
48 process is achieved and hence the mechanisms are quite different.
49 atus and final visual outcome in the 2 types are quite different.
50 , the catalytic phenotypes of these isozymes are quite different.
51 fic mechanisms involved in metal recognition are quite different.
52 the class II alleles and genotypes involved are quite different.
53 histories of C. albicans and C. dubliniensis are quite different.
54 e neighborhood ratio between A + T and G + C was quite different.
55 The response of coi1 plants was quite different.
56 s, the chemical composition of these samples was quite different.
57 milar illnesses, the treatment they received was quite different.
58 n-dependent manner; however, the time course was quite different.
59 the freshwater budget at the poles must have been quite different.
60 the experimental water exchange results have been quite different.
61 owever, some of the trigonal tricationic ILs were quite different.
62 tion kinetics in response to interferon-beta were quite different.
63 ts of these proteins on actin polymerization were quite different.
64 ce identity, their responses to Gd@C82(OH)22 were quite different.
65 se, despite the genetic and biological basis being quite different.
66 owever, the surface features of the proteins are quite different, accounting for their different role
67 thy (BSE) infection, the polymorphism effect is quite different although the ARR allotype remains the
68 cytochrome P450 (CYP)1A2 and iron-which can be quite different among inbred strains-are critical in
71 alues of the pKs, 10.5 and 8.5 respectively, are quite different and Mn(2+)SOD's pK affects the coord
72 a bulk nematic phase, the kinematic details are quite different and provide a possible mechanism for
73 e occupied by TcdB bound to the two peptides are quite different and provide valuable insight for the
74 the binding of arachidonate to PGHS-1 and -2 are quite different and that residues within the hydroph
75 key stability determinants for each Cro fold are quite different and that the P22 Cro sequence strong
76 rimary structures of the major coat proteins are quite different and the virions assemble at very dif
77 ay the two repressors cooperatively assemble is quite different and explains in part the differences
78 residues presented by each partner, however, are quite different, and some initial findings concernin
79 t in both molecules, the mechanisms involved are quite different, and this difference resulted in dif
80 ible for phenotypic differences, the picture is quite different, and about 80% of proteins are differ
81 ies that developed in these two environments were quite different, and some indicators (soil salinity
82 imary structures of the two protein subunits are quite different; and the nucleotide/protein subunit
84 signalling molecules and regulatory proteins are quite different between Gram-positives and Gram-nega
85 hanical systems involved in this propagation are quite different between the DHQSs from the two speci
86 ning to host-pathogen numerical dynamics can be quite different between pathogens with frequency-depe
87 ory areas caused by associative learning can be quite different between specialized and nonspecialize
88 onsynonymous, and noncoding sites appears to be quite different between the species, making direct co
91 An edge effect is often observed and can be quite different both qualitatively and quantitatively
93 t monomer-polymer transitions of the mutants are quite different, confirming that the linear polymeri
94 cation procedures of the two proteins, which were quite different, could have contributed to such con
95 composition characteristics of compounds can be quite different depending on whether it is the bulk d
96 able to polycyclic aromatic hydrocarbons may be quite different depending on which other agents are p
97 resentation of mutations in a given gene can be quite different, depending upon the location and type
98 Although the 1976 and 2003 drought extremes were quite different, Douglas fir maintained consistentl
99 -vis absorption spectra of these two isomers are quite different even though their local chromophore
100 gly, the models and interpretation for PEDOT are quite different: film dynamics are determined by fre
101 ts demonstrate that thermodynamic parameters are quite different for paralogous but are quite similar
102 also similar for the two 3,6 derivatives but are quite different for the 2,7 NH and NMe carbazole dic
105 e driven coercivity changes with temperature are quite different for top and bottom CoFeB layers.
106 The changes in ion permeability, however, are quite different for Trp --> Phe and Trp --> 1-methyl
107 owever, the wave morphology of the ictal EEG is quite different for electrodes placed in different an
111 es of Est-6 make up two allele families that are quite different from each other, while there is rela
114 ation properties of the three polar solvents are quite different from one another and from polar solv
119 tions with the NW arenaviruses JUNV and MACV are quite different from responses to infections with th
120 ar distributions of the low energy electrons are quite different from that of simpler targets like Ne
121 ng Li-Li separations in the cycled structure are quite different from the as-prepared material, as re
125 exponents that depend on that rate, and that are quite different from the naive prediction based on t
126 t materials can present novel phenomena that are quite different from the physical properties observe
127 ic mechanisms behind negative signal changes are quite different from those behind positive signal ch
128 elicits a T cell response with features that are quite different from those elicited by the wild-type
129 However, the infrared bands for huPrP23-144 are quite different from those for a synthetic peptide P
130 ed myristate and structure of Ca2+-free Ncs1 are quite different from those in other NCS proteins.
132 between actin and many binding partners and are quite different from those in the Arp2/3 complex.
134 trated that binding behaviors in rodent MCRs are quite different from those in the classical frog ski
136 reveals that the base changes induced by ENU are quite different from those induced by EMS; specifica
138 s building blocks of human intelligence that are quite different from those of artificial intelligenc
140 oxygen affinity and very low cooperativity, are quite different from those of deoxy-Hb A, even in th
141 ins 1 and 3 in our E. coli EF-Tu-GDP complex are quite different from those of EF-Tu with bound GTP f
142 ic structures, but their structural features are quite different from those of genes of both SBEI and
144 dues lining on the active site of TaNAPRTase are quite different from those of QAPRTase, although the
145 cessful coreference resolution in this genre are quite different from those of the general domain, an
146 to be -215 and -240 mV, respectively, which are quite different from those of the holo-E3, suggestin
147 The 2D spectral patterns of the tripeptide are quite different from those of the longer peptides.
148 quilibrium conditions of receptor activation are quite different from those often used to study GABAA
149 al geometry and an oxidation state (+3) that are quite different from those seen in bulk ceria or for
150 values of amino acids that affect catalysis are quite different from those that affect catalysis by
151 The initial retinal responses to defocus are quite different from those when the eye growth patte
152 eal viruses.IMPORTANCE Many archaeal viruses are quite different from viruses infecting bacteria and
155 and Rouse-Zimm models shows the material to be quite different from other thiophene-based conducting
156 e genetic basis of ordinal traits appears to be quite different from regular quantitative traits.
158 ssue-specificity of an isolated enhancer may be quite different from that in the context of its own g
159 As the disease in a new host species may be quite different from that in the original or natural
160 hese cases, clinical signs and pathology can be quite different from the infantile form, raising the
163 egment of the population that is sampled may be quite different from the population variability that
164 hough bacterial sigma factors are thought to be quite different from the specificity factors employed
166 protein, transducin (Gt), and found them to be quite different from those that might be expected fro
167 catalysts induce high enantioselectivity may be quite different from those used by catalysts that rel
169 ed as unique, with speciation and adaptation being quite different from immigration and ecological as
170 eosomes by the ATP-dependent remodeler INO80 is quite different from another remodeler (SWI/SNF) that
172 rotein function from available sequence data is quite different from assigning an EC classification f
173 s were not detected in MHC-II KO mice, which is quite different from CD4 T cell-deficient mice that i
174 s not generally realized that interfacial PT is quite different from conventional PT in bulk water.
175 nocyte cadherins in these individuals, which is quite different from healthy individuals from the Uni
176 t to E3BP of Saccharomyces cerevisiae, which is quite different from its homologous transacetylase in
178 nce dependence of polyol inclusion, however, is quite different from nonpolar alcohol exclusion, sugg
180 The protein adopts a novel structure that is quite different from predicted models and features a
181 ontal lineC double bond was generated, which is quite different from previously reported 1,3-DCs of a
183 tary in adult Teleosts (class: Osteichthyes) is quite different from that in other chordates and is a
185 eous reaction of SP-B(1-25) at the interface is quite different from that in the solution phase.
187 The ApolPBP pH-induced structural change is quite different from that observed for alcohol bindin
191 same kernel, the surface structure of Au103 is quite different from that of Au102, indicating the ma
193 t the evolutionary pattern of these families is quite different from that of concerted evolution but
194 nct ECM distribution pattern of Ang-1, which is quite different from that of fibronectin, laminin, an
195 of release of iron from the N-terminal lobe is quite different from that of its C-terminal counterpa
197 hows its own form of space weathering, which is quite different from that of other airless bodies vis
198 Specifically, residue 773(S) in PI3Kalpha is quite different from that of PI3Kbeta (D), gamma (A),
199 state that the structure of the primate DCN is quite different from that of rodents, with primates l
200 gy landscape from the implicit solvent model is quite different from that of the explicit solvent mod
202 igodendrocytes indicates that their function is quite different from that of the MBPs to which they a
203 erall environment of the CD21/35(-/-) spleen is quite different from that of the wild-type animal per
204 The arrangement of these domains, however, is quite different from that seen in polymerases that us
205 -sites model with variable rates among sites is quite different from that under the infinite-sites mo
210 ssage Toledo strain of human cytomegalovirus is quite different from the corresponding region in the
216 expressed and although its promoter sequence is quite different from the Nt59 and LAT59 promoters, th
218 molecule relative to the poliovirus surface is quite different from the orientation of intercellular
219 lf-bending behavior like a somersault, which is quite different from the previously reported behavior
220 nge of biological and structural studies, it is quite different from the relatively crowded condition
223 to the host cell receptors in a manner that is quite different from the way the natural ligands bind
224 at hybridization for surface immobilized DNA is quite different from the well-studied solution-phase
227 strands flanked by five alpha-helices, which is quite different from those of other known two-compone
228 of the single-headed construct of myosin Vc is quite different from those of other vertebrate myosin
229 Although the split/recombine sampling scheme is quite different from those used in analysis of catego
231 ing of PGSK fluorescence by Fe2+ in vesicles was quite different from that for PGSK and Fe2+ in solut
233 zzling in that the observed reactive pattern was quite different from those seen with TM6 and 12.
235 (DBP) concentration profiles in heated water were quite different from the DBP concentrations in the
237 represented in the samples collected in 2010 were quite different from those collected in 2008 and 20
238 evolved to be adaptive in environments that were quite different from those faced in modern industri
239 o-serine mutant proteins of human ferredoxin were quite different from those of the wild-type protein
240 effects of heroin self-administration itself were quite different from what has been seen during coca
243 af initiation, vascularization, and polarity are quite different in lycophytes and seed plants, consi
244 y against opportunistic infections, but they are quite different in structure from previously studied
245 actions between the large N-terminal domains are quite different in the filament from that observed i
247 e compression characteristics of the fibrils are quite different in the two media, revealing the pres
248 n development and tissue-specific expression are quite different in these organisms, most strikingly
252 anagement approaches to tuberculosis need to be quite different in this country than in other regions
253 mptive evolutionary source of these proteins is quite different in contending models of mitochondrial
256 in the two receptors and across species, but is quite different in the integrin domains, explaining t
262 ges in tumors following treatment with virus were quite different in the presence versus the absence
263 e show that the dynamics of the epidemic can be quite different, in particular, short-term prediction
264 Importantly, fructose and glucose metabolism are quite different; in comparison with glucose, fructos
265 ame for the two isoenzymes, but the S states are quite different, indicating a much larger movement o
266 ptional regulatory elements in these viruses are quite different, indicating that tissue-specific onc
267 In contrast, binding of the globular domain was quite different: it binds much more weakly, with a K
268 nces and innate properties of ABri and Abeta are quite different, notably ABri contains two cysteine
270 g effectors required in each of these models are quite different, quantitating the cellular ratio of
271 between chimpanzees and humans but the shape is quite different, rising more slowly for a longer frac
272 effect, at fw the pattern of differentiation is quite different such that the frequencies of single n
273 their relative location to the 2PG molecule is quite different, suggesting that they probably have d
274 channel activity but the activation kinetics were quite different, suggesting that, even if the chann
275 of characteristics exhibited by Tenuiviruses are quite different than those found for most plant viru
277 acteristics (fluorescence, CD) were found to be quite different than those of natural DNA, apparently
279 This pattern of clearance of filtered fluid is quite different than is seen with the passive capilla
281 assays for individual camptothecin analogues were quite different than those determined for stabiliza
282 ain distributions of PreXMRV-1 and PreXMRV-2 are quite different, the former being found predominantl
283 elaboration of each of these organ types can be quite different, the same general organization of fou
284 , the results with IL-2, a soluble cytokine, are quite different; thus, IL-2 function is markedly inh
286 properties of nanometre-scale materials can be quite different to those of bulk materials due to the
287 Although the spectra of the four peptides are quite different, tyrosine phosphorylation is found t
288 as improved latrines and water treatment can be quite different under conditions of high and low regi
289 The dependence of TOF on etaeff is shown to be quite different upon changing, for instance, the pKa
290 action rate of NO with cell-free Hb and RBCs is quite different, we hypothesize that different reacti
291 xample, the pH dependence of these processes was quite different, with reconstitution being most effi
292 Outcomes for patients with these phenotypes were quite different, with age-adjusted 1-year survival
294 The effects of mutating the two Tyr residues are quite different: Y240F has higher than wild-type act
295 s, functions, and developmental trajectories are quite different, yielding distinctly different tools
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