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1 readers for MCE and 3 readers for SPECT were collapsed into 1 diagnosis per patient per technique and
2                  Testis ESTs computationally collapsed into 1560 cDNA set used for further analysis.
3                                   These ESTs collapsed into 2,686 and 2,107 EST clusters, respectivel
4 ing clustering and assembly, these sequences collapsed into 5,274 contigs and 6,880 singleton sequenc
5 second, that is, long before the remnant can collapse into a black hole.
6 e cavity-caused the open, conducting pore to collapse into a closed, nonconducting conformation.
7 e renal or Malpighian tubules fails and they collapse into a cyst-like sack.
8 ng by influencing how reaction intermediates collapse into a particular set of stable nucleosomal pos
9 olding conditions initiates a fast molecular collapse into a polyglobular conformation (<20 ms), dete
10 s of an mPE dodecamer induce the foldamer to collapse into a presumed helical conformation.
11                               The real-space collapse into a sharp peak is at odd with the repulsive
12 rocess, through binary black holes and final collapse into a single black hole with gravitational wav
13 h trajectory, the individual travel patterns collapse into a single spatial probability distribution,
14 dependent fitful movement, followed by their collapse into a vacuole and rapid vacuolar lysis.
15                                              Collapsed into a 3-category risk score, major hemorrhage
16 equence tags [ESTs]from these libraries were collapsed into a nonredundant set of 5849 cDNAs, corresp
17 es which have been incorrectly assembled and collapsed into a single copy.
18 he pervasive developmental disorders are now collapsed into a single entity, autism spectrum disorder
19                            The CSF data were collapsed into a single index by the use of weighted mea
20 are variants within a given gene region were collapsed into a single locus and a global P value was c
21 grees ) even when the two one-electron waves collapsed into a single two-electron wave.
22 protect stalled replication forks from being collapsed into a substrate for HR.
23 rs the structure of the Golgi complex, which collapses into a condensed structure near the centrosome
24 in forms a single filamentous structure that collapses into a helix when detached from the cell membr
25 le of reduced denatured conformers initially collapses into a large number of unstructured intermedia
26                 This liberated tyrosine then collapses into a nearby hydrophobic pocket, anchoring a
27  a conductive form, and at low potassium, it collapses into a nonconductive structure with reduced io
28 iC expression independently, and bistability collapses into a predominantly intermediate population i
29 s Fg through a dynamic conformation and then collapses into a register 2-coiled coil as a result of s
30  the IR at 788(2) and 781(2) cm(-)(1), which collapses into a single peak at 784 cm(-1) upon the addi
31  we show here that this behavioral diversity collapses into a single swimming pattern during accelera
32         At a high concentration of Abf2p DNA collapses into a tight nucleoprotein complex.
33 that characterizes the slow die-out dynamics collapses into a unique equilibrium when a constant rate
34 tum character of the environment is reduced, collapsing into a Dirac-delta function in the classical
35 ation of the constituent chromatosome beads, collapsing into a highly condensed form in response to s
36 ze with Past1 in distinct SSR subdomains and collapse into Amphiphysin-dependent membrane nodules in
37 inal release, before the receptor ultimately collapses into an inactive conformation.
38 iation and matter, followed by gravitational collapse into blocks of galactic mass.
39 A five-class latent class analysis model was collapsed into cases and noncases.
40                               Large RNAs can collapse into compact conformations well before the stab
41                                   Large RNAs collapse into compact intermediates in the presence of c
42 elope and underlying laminae, and the nuclei collapsed into condensed, spherical structures.
43  of cell density allow the cells to find and collapse into confining topologies, which are unstable t
44 n interactions, in contrast, are expected to collapse into conformations with long-range order, in th
45 thin sodium nitrate solutions the aggregates collapse into denser clusters, and nanoparticle depositi
46  stage, grade, and ECOG PS were analyzed and collapsed into distinct groups.
47 stalled replication forks and prevents their collapse into DNA double-strand breaks (DSBs).
48  prevents ICL-stalled replication forks from collapsing into double-strand breaks.
49 ation forks that, after prolonged treatment, collapse into DSBs.
50  initial, smooth distribution of dark matter collapses into filaments then into clusters, forming a g
51 vel, a validated 11-point mobility scale was collapsed into four categories: nothing in bed, in-bed a
52                           HCT-CI scores were collapsed into four groups and were evaluated in univari
53 ng (hundreds of microseconds) and involves a collapse into incorrectly folded intermediate population
54   Subsequently, these filamentous structures collapsed into intracellular inclusions that migrated in
55      In a majority of cells, the MT networks collapsed into large bundles.
56 as a key issue in order to prevent them from collapsing into larger aggregates and to provide them pr
57                       Surprisingly, the TFVs collapsed into lipid droplets after entry into the cell
58                               The turbulence collapses into localized three-dimensional nonlinear str
59        The host and guest are prevented from collapsing into more familiar, stable structures by the
60  tend to fold and wrinkle at edges to resist collapsing into multilayers.
61 pendants that induce an intramolecular chain collapse into nanoparticles consisting of one polymer ch
62 tegories 5 (severe disability) and 6 (death) collapsed into one category (severe disability or death)
63                            When proteins are collapsed into orthologous groups (OGs) the resulting me
64 even short hydrophobic polar (HP) chains can collapse into relatively compact structures, exposing hy
65 ovalently cross-linking, can be structurally collapsed into smaller, temporary shapes that permit the
66 mation from CRM and transmittance images was collapsed into straightforward single variables; total i
67   TMEM55B overexpression causes lysosomes to collapse into the cell center, whereas depletion of eith
68 ssion of E-cadherin and beta1-integrin, cell collapse into the central cavity was decreased by uPAR o
69 coli porin OmpF was attributed to loops that collapse into the channel in response to a strong electr
70  was active, and it mediated ERGIC and Golgi collapse into the ER.
71 e globular forms in the gas phase and should collapse into the globular form given enough time.
72 that voltage sensors can act to prevent pore collapse into the intrinsically more stable, closed conf
73                     Docked vesicles fuse and collapse into the membrane within 30 ms of the stimulus.
74 CV docking, fusion-pore opening, and vesicle collapse into the planar membrane.
75  (a) full-collapse fusion, in which vesicles collapse into the plasma membrane, followed by classical
76 n partial actin coat assembly and induces CG collapse into the PM.
77 y coinage metal chalcogen phases, but do not collapse into the solid M(2)E materials owing to the pro
78 cles at the synapse of bipolar cells rapidly collapse into the surface membrane while secretory granu
79                   The side chain of Trp(215) collapses into the active site by shifting > 10 A from i
80                       This intermediate then collapses into the canonical intein fold.
81 rimary cyclobutylmethyl cation spontaneously collapses into the cyclopentyl cation.
82 hat then dilates until the secretory vesicle collapses into the PM; or by "kiss-and-run," where the f
83 according to the new classification and then collapsed into three groups (LEP, ACN/PAP, and MIP/SOL).
84 mains, Eukarya, Archaea, and Bacteria, would collapse into two cellular domains.
85 brium frequency f(eq), we show that all data collapse into two power laws separated by f/f(eq), which

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