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1 stand how it contributes to the overall stem curling.
2 th a marked decrease in root hair growth and curling.
3 ntrast to wild-type plants that exhibit root curling.
4 ubulin-associated GTP promotes protofilament curling.
5 is elegans, egg laying and male ventral tail curling.
6 ntial cell elongation responses such as root curling.
7 w to copulate because of maladroit abdominal curling.
8 tal variations in temperature or humidity by curling.
9 uxin deficient mutant cytokinin induced root curling 2 (ckrc2) in this work reveal that CKRC2 encodes
10 ; P=0.042), prevalence of posterior systolic curling (34 [94%] versus 3 [19%]; P<0.001), and basal to
11 ; P < .001), a higher prevalence of systolic curling (75% [21 of 28] vs 30.7% [35 of 114]; P < .001),
12                             The procedure of curling a ribbon by running it over a sharp blade is com
13 of the leaflets caused by posterior systolic curling accounts for a mechanical stretch of the inferob
14 s had early-onset parkinsonism (dystonic toe curling, action tremor, masked face, bradykinesia, stoop
15   The model identifies factors that optimize curling and clarifies the physical mechanisms underlying
16 ited severe compound leaf defects, including curling and deep serration of leaf margins, shortened pe
17 ng morpholinos, resulted in larvae with tail curling and dystrophic muscle features.
18  males also produces defects in ventral tail curling and enhances the turning defects in ser-1 mutant
19 PS-NPs significantly decreased the appendage curling and heartbeat rate in F0 and reduced reproductio
20 ngs exhibit altered responses to NPA in root curling and hypocotyl elongation.
21 ut use task, step-up task, detour task, tail curling and lying side.
22 ior papillary muscle displacement with basal curling and more impaired inferior-posterior basal strai
23 expressing their targets represses root hair curling and nodule formation, whereas repressing these t
24                                    Efficient curling and packing of the oligomers - or 'curlamers' -
25 s, Drosophila melanogaster larvae generate a curling and rolling response.
26                These phenotypes include leaf curling and the partial conversion of later-arising caul
27 ferential topology recapitulate the observed curling and thickening, in support of an 'inside-to-outs
28            Medium with 2 mM ATP induces root curling, and 3 mM ATP stimulates lateral root growth.
29 let involvement, mitral annular disjunction, curling, and abnormal valvular-myocardial mechanics, as
30 ion and morphological damage (fragmentation, curling, and aggregation).
31 ficient plants exhibited leaf necrosis, leaf curling, and growth stunting symptoms.
32 ciated exaggerated basal myocardial systolic curling, and myocardial longitudinal strain.
33 al abnormalities that include stunting, leaf curling, and the loss of apical dominance.
34 r styling activities, such as straightening, curling, and waving, emit volatile and semivolatile chem
35  a His tag being approximately 65 A long and curling around the base of the structure.
36 odes placed within prey items show that this curling behavior at least doubles the field strength wit
37 pled with limb twitching and stereotyped leg curling behaviors during nocturnal resting in a jumping
38 6 unit cells there is a complex flux-closure curling behaviour resembling an incommensurate phase.
39 he Mtnin mutants undergo excessive root hair curling but are impaired in infection and fail to form n
40 loping leaves, and their feeding causes leaf curling by preventing them from unfurling.
41 itiate 10 to 20 h after the completion of RH curling, by which time major modifications have occurred
42 anding that the direction and extent of stem curling can be partially attributed to stiffness gradien
43  growth and development, like stunting, leaf curling, chlorosis, or necrosis, which we recognize as d
44 rates into the interlayers of h-BN along the curling edge, followed by an immediate drastic gasificat
45      We assessed mitral annular disjunction, curling, global longitudinal strain, segmental peak long
46 tin pentamer, inactive in inducing root hair curling (HAD) or cortical cell division (NOI) in G. soja
47 ll, mitral annulus disjunction, and systolic curling have been recently described by pathological and
48 n uterine muscles, and the reduced abdominal curling in males correlates with alteration in motor neu
49 or extrusion in mated females, and abdominal curling in males during courtship.
50 racterizations of a phot1-5 rcn1-1 (for root curling in n-naphthylphthalamic acid1) double mutant, in
51 played a similar ability to induce root hair curling in response to rhizobia or Nod lipochitooligosac
52 e and a passive layer show rapid, reversible curling in response to stimulus DNA strands added to sol
53 er, it was observed that the absence of root curling in response to touch can be reverted by jasmonic
54  to chemicals used in hair straightening and curling increased the odds that the infant was preterm o
55 tization state in Sm-Co magnets results from curling instabilities and domain-wall pinning effects at
56 ncluding sheltering, sitting on their tails, curling into a ball, or huddling with conspecifics.
57 ence of association between brain tumors and curling iron, heating pad, vibrating massager, electric
58          Finally, we show that the extent of curling is controlled by the interplay between in-plane
59                                              Curling is reversible and involves hierarchical deformat
60                                         Leaf curling is suppressed by sep3 and ft mutations and enhan
61  of axr1, namely, short petioles, downwardly curling leaves, short inflorescence, and reduced fertili
62        A spin vortex consists of an in-plane curling magnetization and a small core region (~10 nm) w
63 ic topological structures characterized by a curling magnetization around a highly stable nanometric
64 terized as a negative regulator of rice root curling mediated by jasmonic acid.
65 is ruled by the geometrical conformations of curling MT-protofilaments entangled in kinetochore fibri
66                                          The curling of a graphitic sheet to form carbon nanotubes pr
67       The interaction between the continuous curling of dipoles and light promotes the conversion of
68 r) sides of lateral organs results in upward curling of leaf blades.
69 red growth, leaf chlorosis, and necrosis and curling of leaf margins.
70 the tips of microtubules, tea1p prevents the curling of microtubules around the cell ends, whereas it
71 ss of EIR1/AGR1/PIN2 function abolishes root curling of mlo4, mlo11, and wild-type seedlings.
72  agl24 svp mutations, the plants show upward curling of rosette and cauline leaves, in addition to ea
73 rature variation initiates the expansion and curling of the bulk h-BN.
74                                          The curling of the leaves provides a protective niche for th
75 al part of the neural tube, which forms by a curling of the neural plate.
76 e elements respond rapidly to temperature by curling or uncurling in about 0.2 s, which in one typica
77 ability of the NodC- mutant to induce marked curlings or infection threads within root hairs.
78                                              Curling originates from an enrichment of myosin in the b
79 d with a higher expression rice ROOT MEANDER CURLING (OsRMC), which encodes a receptor-like kinase ch
80  ends with the ruptured erythrocyte membrane curling outwards, buckling, everting and vesiculating.
81 esults demonstrate that the exaggerated root curling phenotypes of the mlo4 and mlo11 mutants depend
82 tronic devices, it is wise to investigate if curling polarization structures are innate to ferroelect
83                                Protofilament curling presumably drives the transition from tip struct
84 bservations demonstrate how work output from curling protofilaments can be tuned and suggest evolutio
85 g the mechanical and energetic properties of curling protofilaments, but no way to do so has yet been
86 ent of working strokes generated in vitro by curling protofilaments, we show that their mechanical en
87 ly demonstrate the spring-like elasticity of curling protofilaments.
88 ave demonstrated programmable and reversible curling, puffing, and in-plane shrinkage behaviors by em
89 found between mitral annulus disjunction and curling (R=0.85).
90 hylphthalamic acid on the inhibition of root curling, raising the possibility that transport of auxin
91  plastic leachate also reduced the appendage curling rate but increased growth and reproduction.
92 obium-legume interactions, such as root hair curling, rhizobial invasion, infection thread expansion,
93 ype seedlings mimics the rcn1 defect in root curling, root waving and hypocotyl hook formation assays
94 nsertion mutation at this locus impairs root curling, seedling organ elongation and apical hypocotyl
95 nvolves the union in space of two edges of a curling sheet and results in a substantial number of unc
96 ll as shoot phenotypes including upward leaf curling, shortened siliques and narrow lateral branch an
97                                     The long curling tail fibre is formed by the protein YSD1_29, and
98 rius and Apodemus flavicollis) were observed curling their tails inward and positioning it on the bac
99                       Here we use epithelial curling to characterize the out-of-plane mechanics of ep
100 moters, derived from the Cestrum yellow leaf curling virus, drives levels of constitutive transgene e
101 styling techniques, including straightening, curling, waving, and oiling.
102 initiating pore opening and outward membrane curling, we develop a model of the dynamics of the red b
103 ydrogels, structures that undergo reversible curling were produced.

 
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