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1 ate of N-DRC and its attachment to the outer doublet microtubule.
2 the ODA-DC and the outer dynein arm onto the doublet microtubule.
3 ed within the A-tubule of the axonemal outer doublet microtubules.
4 uration of ODAs into a form that can bind to doublet microtubules.
5 ered by dynein ATPases associated with outer doublet microtubules.
6 proteins form crossbridges between the outer doublet microtubules.
7 e confirmed that basal bodies contain mostly doublet microtubules.
8 riven microtubule sliding between subsets of doublet microtubules.
9 RS2, and RS3, repeats every 96 nm along the doublet microtubules.
10 hat the axonemal CKI is located on the outer doublet microtubules.
11 ike projections in the B tubule of the outer doublet microtubules.
12 ke in each 96-nm axoneme repeat on flagellar doublet microtubules.
13 tal part of axonemes before binding to outer doublet microtubules.
14 rdinate dynein arm activity and interconnect doublet microtubules.
15 in the transition of triplet microtubules to doublet microtubules, a defect correlated with failure t
16 a tether linking one I1 motor domain to the doublet microtubule and doublet-specific differences pot
17 on, which comprises part of the wall of each doublet microtubule and is composed of tubulin and three
18 Most dramatically, the space between the doublet microtubules and the flagellar membrane contains
20 tektins, which form coiled-coil filaments in doublet microtubules and which are associated with basal
21 d spoke bases that facilitate docking to the doublet microtubules, and that inner dyneins connect dir
24 nvolves signal-induced severing of the outer doublet microtubules at a precise site in the transition
27 sists of a 9-fold array of remarkably stable doublet microtubules (DMTs), along which motor proteins
29 hanism may mediate the severing of the outer doublet microtubules during Chlamydomonas deflagellation
32 We propose that CKI is anchored on the outer doublet microtubules in position to regulate flagellar d
33 2 genes in the pathway mediating assembly of doublet microtubules in the axoneme from triplet microtu
35 FAP50 is tightly associated with the outer doublet microtubules of the axoneme and appears not to b
36 r to result from defects in either the outer doublet microtubules or the outer arm docking structures
38 flagella have a conserved structure of nine doublet microtubules surrounding a central pair of micro
39 of axoneme architecture, a cylinder of nine doublet microtubules surrounding a central pair of singl
40 metric, with most particles located near the doublet microtubules that face the opposite basal body.
41 lutamylation mainly on the B-tubule of outer doublet microtubules, the site of force production by ci
42 Periodic densities were also observed inside doublet microtubules; these may contribute to doublet st
43 precisely reciprocal to dominant defects in doublet microtubules we observed in a previous study of
44 le distinguishing each one of the nine outer doublet microtubules, we systematically collected and re
45 ar transport, and bound to specific sites on doublet microtubules, where their activity facilitates m
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