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1               The blue PLEDs were repeatedly bent to 1.5 mm radius concave or convex with calculated
2               The needle (with bevel up) was bent to 90 degrees and was inserted in the posterior cor
3                           Because bull sperm bend to a higher curvature after ADP treatment we explor
4 ent modes of thermal deformation from a pure bend to a twist-bend.
5 films with T = 76%) and after 1000 cycles of bending to a 5 mm radius.
6  test and were found insensitive to repeated bending to a small 0.5 cm radius.
7 h flexibility; the nanofiber networks can be bent to a radius of 2 mm with negligible changes in the
8 es are highly flexible and can be repeatedly bent to a radius of 5 mm without significant PCE reducti
9 s suggest a low-barrier isomerization from a bent to a T-shaped isomer that initiates a phosphorus-li
10 nits, an elbow or joint allows the stator to bend to accommodate lateral movements during the activit
11 terlocked alpha-solenoids-about which it can bend to adapt to cages of variable curvature.
12 midline between P6 and P12, and subsequently bends to adopt the ring shape of the mature EB.
13                Deletion analysis mapped this bend to amino acids 611 to 640 of the protein sequence.
14 -responded after return to RT, continuing to bend to an angle greater than wild-type plants.
15 crystals of three N-benzylideneanilines were bent to an arbitrary angle, sliced out from a bundle int
16 n proposed that alphaIIbbeta3 changes from a bent to an extended conformation upon activation, we hyp
17 ositive-definite matrices, we had to employ 'bending' to analyse the G and E matrices with the Flury
18 ones were loaded to failure with three-point bending to assess strength.
19                              We observe such bends to be widely distributed in two-stranded alpha-hel
20 dra share corners in geometries ranging from bent to close to linear Am-O-Fe bonds.
21 a M3 and GluN2B M3' pore-forming helices are bent to dilate the channel pore.
22  indicating the strong coupling of molecular bend to director bend.
23 , there is a shift from midline neural plate bending to dorsolateral bending.
24 ent, via cogwheeling (rotation) and kinking (bending), to effect changes in PHK activities that proba
25 microelectromechanical systems which utilize bending to enhance displacements.
26                After perceiving light, roots bend to escape from light (root light avoidance) and red
27 eral conformations, ranging from compact and bent to extended and open.
28         The IRES rearranges from extended to bent to extended conformations.
29 in adherent cells and that conversion from a bent to extended form takes place at focal adhesions.
30  as well as conversion of the molecules from bent to extended forms.
31 rane, rapidity of changing conformation from bent to extended, affinity for extracellular matrix liga
32                        Double-helical DNA is bent to follow the rounded contours of the target object
33 n and spinal cord begins as the neural plate bends to form the neural folds, which meet and adhere to
34 l elements experiencing combined torsion and bending to gather data on their load-carrying capacity i
35 ation by enabling curvature of the principal bends to increase.
36  degradation system in which membrane sheets bend to isolate portions of the cytoplasm within double-
37 t of the second segment only from inside the bend to its outside.
38  a shift from ancestral reptile-like lateral bending to mammal-like sagittal bending of the vertebral
39 y across the beta-strands, requiring them to bend to match the concavity of the VLR solenoid.
40 at led to a smooth transition from an escape bend to one side into subsequent swimming.
41 cal to an asymmetrical pattern by increasing bending to one side.
42 Ib requires higher forces to transition from bent to open conformational states that is in accordance
43 al transcription factor A (TFAM) employs DNA bending to package mitochondrial DNA (mtDNA) into nucleo
44 is of annulated thiepins designed to undergo bent-to-planar transformation driven by aromatization un
45 lex have been proposed to link protofilament bending to poleward chromosome motion.
46 hoot gravity responses from negative (upward bending) to positive (downward bending), resulting in a
47 of prenatal skin did not reveal the expected bent to proangiogenic molecules, indicating a complex re
48 ription activation is thought to require DNA bending to promote the interaction of upstream activator
49                    We used models of whisker bending to quantify mechanical signals (forces and momen
50 ntaining the consensus Lhx3 binding site are bent to similar angles in complexes containing either wi
51 iability, without performance degradation on bending to small radii of curvature (2.5 mm) for over 2,
52 r growth provides more opportunity for fiber bending to spread domains from their initial 2-fold symm
53 ing highly pliable organic films that can be bent to spread over curved and uneven surfaces.
54 cin-DNA complex may provide a DNA structural bend to stimulate topoisomerase I-mediated DNA cleavage.
55 ve the outer edge of laser written waveguide bends, to suppress radiative bend loss.
56 ns, the rate-limiting step shifts from hinge bending to tertiary contact formati
57 e used gel electrophoretic analysis of helix bending to test the hypothesis that this bulge loop is c
58                              Imparting a tip bend to the guidewire enabled intramyocardial navigation
59 ature, and relate the angle of a gravitropic bend to the magnitude and duration of asymmetric wall so
60          The midline tubular heart begins to bend to the right to form a C-shaped structure around 30
61 418 sits at the neck of the cleft, lending a bend to the volume enclosed by the cleft.
62 bending angle, and shifts the most favorable bending to the direction toward the minor groove.
63 ations, the MD model exhibits concerted axis bending to the extent of 15.5 degrees per A-tract.
64 esting a contribution of protein-induced DNA bending to the function of TCR alpha enhancer.
65 yer geometry and neglect the contribution of bending to the intracellular stresses.
66 g sites of GCN4 transcription factor are pre-bent to the same extent (approximately 12 degrees toward
67 TATA all of the compounds caused significant bending, to values close to or even greater than the A5
68                   All four MBL peptides were bent to varying degrees up to 85(o) in the best-fit mole
69 faciens bacteriophage Milano is flexible and bent to varying degrees, which sets it apart from other
70 ctuation into life-like motions, from simple bending to walking, for example.