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1 ated black-hole masses, the components would be separated by 0.007-0.017 parsecs, implying relativist
4 in which PpIX and cobyrinic acid components are separated by 11 atoms chain with the triazole moiety
5 talytic control over reactions at sites that are separated by 11.6, 16.5, and nearly 17.7 A, based on
6 3 identical moving gratings whose directions were separated by 120 degrees were introduced in 3 succe
7 e tunnel when the most C-terminal SA residue was separated by 14 residues from the peptidyl transfera
9 between the two beta-globin paralogs (which are separated by 16.2 kb) is maintained in spite of the
15 types, 5 showed no amino acid changes, and 3 were separated by 21-24 days and were potentially persis
17 ination, provided that their relative spikes are separated by 25 ms or more; remarkably, this elimina
20 (HSO), the heme iron and molybdenum centers are separated by 32 A and the domains containing these c
26 ly followed the first, disappeared when they were separated by 500 ms, and were partly recovered (evi
27 n between two highly conserved elements that are separated by 581 bases within the 1071-base intron 3
29 Two protostars near the centre of the disk are separated by 61 astronomical units and a tertiary pr
33 The transmembrane and periplasmic domains are separated by a 0.9-nm channel constriction composed
34 dule-type II cohesin.dockerin complex, which are separated by a 13-residue linker in an extended conf
35 s encodes two highly polymorphic genes which are separated by a 227 bp intergenic region: first, the
37 n images suggest that the two halves of P-gp are separated by a central cavity that closes upon bindi
39 se in which the pushing and pulling moieties are separated by a conjugated spacer (C horizontal lineX
43 lecular chaperone whose N and middle domains are separated by a disordered region termed the charged
44 wo consecutively-presented scenes, when they are separated by a distractor that masks the transients
45 rils, but not between the beta-sheets, which are separated by a dry interface as in a steric zipper m
47 s two predicted transmembrane helices, which are separated by a highly conserved linker facing the in
48 phate, where the two phosphomonoester groups are separated by a hydroxyl group at the 4-position, the
52 aces of electronic ground and excited states are separated by a large gap of ~20 kcal mol(-1), indica
59 The closed-shell singlet and triplet nitrene are separated by a small energy gap in protic solvents.
61 ) chloroplasts, where the first two cistrons are separated by a spacer region to which no significant
64 ibility of direct transmission when isolates are separated by a substantial number of SNPs; (3) the c
72 hich a stilbene hole acceptor and hole donor are separated by A(3)G(n) diblock polypurine sequences c
74 (2)OH)(2)]Cl and [a-PhobP(CH(2)OH)(2)]Cl can be separated by a selective deformylation with aqueous N
77 pha-helical extracellular domain (TM6a) that is separated by a central, unwound section from a cytopl
81 f these clusters stemmed from 2 classes that were separated by a 13-month period but housed in the sa
82 entical foods provided and free living) that were separated by a 14-d habitual diet washout period.
89 ermini of RNA degradation intermediates that were separated by a length equal to a ribosome-protected
91 le of representing component directions that were separated by a small angle--less than the tuning wi
96 and tetra-histidine-catecholic adducts, that were separated by affinity chromatography and high perfo
97 UCNPs covered by a dye-doped silica shell were separated by agarose gel electrophoresis and scanne
98 sotope ratios of pharmaceuticals that cannot be separated by already existing separation techniques f
99 ugh the C-18 column unretained while the NPs are separated by an ammonium acetate buffered methanol-w
100 ssesses two multibasic cleavage sites, which are separated by an intervening region of 27 amino acids
105 nin-containing fractions in plasma and urine were separated by anion exchange chromatography with a s
106 te species of Pu and Np in different samples were separated by application of an acetate-based electr
107 ighly conserved GnC and TGnnA sequences that are separated by approximately 10 bp, the promoter-dista
109 inucleosomal state where the two nucleosomes are separated by approximately 2 nm face-to-face and rot
111 for ion confinement, where the rf electrodes are separated by arrays of short electrodes, and using t
114 contain discrete functional subregions that are separated by borders that restrict tangential activi
116 Fatty acids containing 14 to 36 carbon atoms are separated by C(8) reversed-phase chromatography usin
117 d by 8-aminopyrene-1,3,6-trisulfonate (APTS) was separated by capillary zone electrophoresis and dete
119 phate (ATP), and adenosine diphosphate (ADP) were separated by capillary electrophoresis, and the dep
128 ometry adopted by the axial TCBD unit, which were separated by chiral high-performance liquid chromat
129 new family of atropisomeric 4,4'-bipyridines were separated by chiral HPLC (high-performance liquid c
131 most potent H4R agonists among 14 racemates were separated by chiral HPLC, yielding eight enantiomer
132 acted from the fabric and the dye components are separated by chromatography prior to mass spectromet
134 [10](1,6)pyrenophane (29c), which could not be separated by column chromatography or crystallization
135 o afford two cyclo-[2]-malonate tethers that were separated by column chromatography in optically pur
140 sized particles melt under high temperature, are separated by defects in reduced graphene oxide and s
143 eemingly redundant transcription factors can be separated by differential degradation and distinct ce
144 lved lineages of KDO8PP orthologs exist, and are separated by diffuse active-site sequence boundaries
145 nt concentrations of bacterial DNA molecules are separated by digitization across 20,000 reactions an
146 using TPEF NSOM reveals that, even when they are separated by distances of several tens of nanometers
151 xa- and azabicyclo[3.2.0]heptane derivatives were separated by enzymatic kinetic resolution with immo
153 ification, chemical and physical information were separated by extended multiplicative signal correct
157 sis of our record's timing, the terminations are separated by four or five precession cycles, support
158 were mixed at a 1:1 ratio, and the proteins were separated by FPLC (fast protein liquid chromatograp
160 ptamers directly from multiple proteins that are separated by gel electrophoresis from a biological m
170 es are mediated by inverted repeats that can be separated by >300 kb, a genomic architecture that app
172 an -1 kJ mol(-1) when the interacting groups were separated by >/=6 rotating bonds, but ranged betwee
173 n classical microscopy, whereby objects that are separated by half a wavelength can no longer be visu
175 ested with trypsin, and the tryptic peptides were separated by high pressure liquid chromatography.
179 All three carpanone diastereoisomers have been separated by HPLC, and their structures have been e
181 Further, the immune reactive LTP of one beer was separated by HPLC and the chromatogram was compared
182 The diastereomeric pairs 11a/11b and 12a/12b were separated by HPLC and the absolute configuration as
183 stituents attached on the six aromatic rings were separated by HPLC using chiral stationary phases.
187 ressure and R-R interval fluctuations, which were separated by intervals that were likely to be too s
189 oligosaccharide precursor or product ions to be separated by ion mobility and independent fragmentati
190 ar mass in the polysorbate formulations have been separated by ion mobility and then fragmented for a
193 a layered electride in which layers of atoms are separated by layers of a 2D electron gas (2DEG), can
199 e c-type heme irons and the nascent TTQ site are separated by long distances over which electron tran
201 ffers, in which the Fab-Fc and Fab-Fab pairs were separated by maximally extended hinge structures.
202 m simultaneously during synthesis and cannot be separated by means of conventional filtration methods
204 the contiguous mesocolon and retroperitoneum are separated by mesothelial and connective tissue layer
205 forms of native GmUreG, purified from seeds, were separated by metal affinity chromatography, and the
208 By perimetry, small central visual islands were separated by midperipheral scotomas from far tempor
210 at the rhodium atom and the chiral center(s) are separated by more than 12 covalent bonds, up to 82%
212 hat 25% of directly coevolving residue pairs are separated by more than 5 A in protein structures and
213 eraction between CDR1 and CDR3 residues that are separated by more than 9 A in the wild-type complex.
216 acclimate to recurring bleaching events that are separated by multiple years, it is currently unknown
217 rmed when metal surfaces with high curvature are separated by nanoscale gaps and an electromagnetic f
218 Other groups or columns of cortical neurons are separated by narrow septa of fibers that reflect dis
219 mixed structural population of RNA molecules is separated by non-denaturing gel electrophoresis and t
222 f inverted repeats (IRs) of 26,819 bp, which were separated by one small single copy (SSC; 18,758 bp)
224 interaction between the nitrogen atoms that are separated by only four sigma bonds if its nitrogens
225 f microfluidic circuits where resonant spots are separated by only one pixel ( approximately 7 mum).
227 al tail peptides (amino acids 1-50, 5-6 kDa) were separated by optimized weak cation exchange/hydroph
229 a prototypical tadpole larval body plan but are separated by over half a billion years of divergent
230 s through interconnected xylem conduits that are separated by partially digested regions in the cell
232 mb and hindlimb compartments of VPL, as they were separated by poorly staining, cell-poor septa.
235 on currently performed procedures when data were separated by procedure, and there was a minimum 1-y
237 xes ([M(mbpy-py)3][PF6]2; M = Ru or Os) that are separated by redox-inactive spacers consisting of 1,
238 equential immunization with variant Ags that are separated by relatively large mutational distances m
240 -soluble protein extracts of SEB-1 sebocytes were separated by reverse-phase high-performance liquid
241 he action of peptidases upon cheese proteins were separated by reverse-phase HPLC to give 28 fraction
242 ource, and peptides in the resultant digests were separated by reverse-phase-HPLC and structurally ch
245 hase extraction (SPE) step, and the analytes were separated by reversed-phase ultra high performance
251 and moisture-stable intermediates can easily be separated by semipreparative chiral HPLC on a gram sc
253 Fusion occurs between inverted repeats that are separated by several kilobases of DNA and share >20
255 dium dodecyl sulfate (SDS)-protein complexes are separated by sieving electrophoresis in a microfluid
256 few final pairings of Cys residues that may be separated by significant intervening primary sequence
257 ighly fluorescent ester derivatives that can be separated by silica normal-phase high-performance liq
261 a-dimer configurations compete some of which are separated by small barriers leading to fluxional str
266 lows the protein and nucleic acid signals to be separated by spectral decomposition such that sedimen
267 ating estimates reveal that myrmecoid clades are separated by substantial phylogenetic distances-as m
268 resulting racemic protected Fmoc-DSA subunit was separated by supercritical fluid chromatography (SFC
269 for analysis, the substrate and the product are separated by surfactant-mediated capillary electroph
273 leucopus indicates two post-glacial lineages are separated by the St. Lawrence River, with a more rec
274 n contrast, when the P3HT chain and TBT unit are separated by the wider bandgap F8 unit, there is lit
279 ar cochlear fluids, endolymph and perilymph, are separated by tight junctions that outline the scala
280 rminal tail both reside in the cytoplasm and are separated by TMH-V, which does not fully span the me
282 e R series, the -NH(2)(+)- recognition sites are separated by trismethylene bridges, whereas in the R
287 of samples with extreme proteolysis indices were separated by two-dimensional electrophoresis and id
288 s of the soluble compartment of the vesicles were separated by two-dimensional gels and subjected to
290 typic peptides shared by all the toxin forms were separated by ultraperformance liquid chromatography
294 "peaks" of high-fitness allele combinations are separated by "valleys" of low-fitness genotypes.
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