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 nits, an elbow or joint allows the stator to
bend to accommodate lateral movements during the activit
10 terlocked alpha-solenoids-about which it can
bend to adapt to cages of variable curvature.
11 midline between P6 and P12, and subsequently
bends to adopt the ring shape of the mature EB.
12 Deletion analysis mapped this
bend to amino acids 611 to 640 of the protein sequence.
13 -responded after return to RT, continuing to
bend to an angle greater than wild-type plants.
14 n proposed that alphaIIbbeta3 changes from a
bent to an extended conformation upon activation, we hyp
15 ositive-definite matrices, we had to employ '
bending' to analyse the G and E matrices with the Flury
16 We observe such
bends to be widely distributed in two-stranded alpha-hel
17 dra share corners in geometries ranging from
bent to close to linear Am-O-Fe bonds.
18 indicating the strong coupling of molecular
bend to director bend.
19 , there is a shift from midline neural plate
bending to dorsolateral bending.
20 ent, via cogwheeling (rotation) and kinking (
bending), to effect changes in PHK activities that proba
21 After perceiving light, roots
bend to escape from light (root light avoidance) and red
22 eral conformations, ranging from compact and
bent to extended and open.
23 The IRES rearranges from extended to
bent to extended conformations.
24 in adherent cells and that conversion from a
bent to extended form takes place at focal adhesions.
25 as well as conversion of the molecules from
bent to extended forms.
26 Double-helical DNA is
bent to follow the rounded contours of the target object
27 n and spinal cord begins as the neural plate
bends to form the neural folds, which meet and adhere to
28 ation by enabling curvature of the principal
bends to increase.
29 t of the second segment only from inside the
bend to its outside.
30 y across the beta-strands, requiring them to
bend to match the concavity of the VLR solenoid.
31 at led to a smooth transition from an escape
bend to one side into subsequent swimming.
32 cal to an asymmetrical pattern by increasing
bending to one side.
33 is of annulated thiepins designed to undergo
bent-to-
planar transformation driven by aromatization un
34 lex have been proposed to link protofilament
bending to poleward chromosome motion.
35 of prenatal skin did not reveal the expected
bent to proangiogenic molecules, indicating a complex re
36 ription activation is thought to require DNA
bending to promote the interaction of upstream activator
37 We used models of whisker
bending to quantify mechanical signals (forces and momen
38 ntaining the consensus Lhx3 binding site are
bent to similar angles in complexes containing either wi
39 iability, without performance degradation on
bending to small radii of curvature (2.5 mm) for over 2,
40 r growth provides more opportunity for fiber
bending to spread domains from their initial 2-fold symm
41 ing highly pliable organic films that can be
bent to spread over curved and uneven surfaces.
42 cin-DNA complex may provide a DNA structural
bend to stimulate topoisomerase I-mediated DNA cleavage.
43 ns, the rate-limiting step shifts from hinge
bending to tertiary contact formati
44 e used gel electrophoretic analysis of helix
bending to test the hypothesis that this bulge loop is c
45 ature, and relate the angle of a gravitropic
bend to the magnitude and duration of asymmetric wall so
46 The midline tubular heart begins to
bend to the right to form a C-shaped structure around 30
47 418 sits at the neck of the cleft, lending a
bend to the volume enclosed by the cleft.
48 bending angle, and shifts the most favorable
bending to the direction toward the minor groove.
49 ations, the MD model exhibits concerted axis
bending to the extent of 15.5 degrees per A-tract.
50 esting a contribution of protein-induced DNA
bending to the function of TCR alpha enhancer.
51 g sites of GCN4 transcription factor are pre-
bent to the same extent (approximately 12 degrees toward
52 TATA all of the compounds caused significant
bending, to values close to or even greater than the A5