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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 e NDRC proximal lobe that binds the adjacent doublet microtubule.
4 -tubule along the length of all nine ciliary doublet microtubules.
5 uration of ODAs into a form that can bind to doublet microtubules.
6  RS2, and RS3, repeats every 96 nm along the doublet microtubules.
7 rdinate dynein arm activity and interconnect doublet microtubules.
8 ed within the A-tubule of the axonemal outer doublet microtubules.
9 ered by dynein ATPases associated with outer doublet microtubules.
10 proteins form crossbridges between the outer doublet microtubules.
11 e confirmed that basal bodies contain mostly doublet microtubules.
12 riven microtubule sliding between subsets of doublet microtubules.
13 hat the axonemal CKI is located on the outer doublet microtubules.
14 ike projections in the B tubule of the outer doublet microtubules.
15 ke in each 96-nm axoneme repeat on flagellar doublet microtubules.
16 tal part of axonemes before binding to outer doublet microtubules.
17 ectively associate with a subset of axonemal doublet microtubules.
18 sting of two central singlets and nine outer doublet microtubules.
19 ferent dynein isoforms on the surface of the doublet microtubules.
20 in the transition of triplet microtubules to doublet microtubules, a defect correlated with failure t
21 la functions as a linker between neighboring doublet microtubules, acts to stabilize the axonemal cor
22  a tether linking one I1 motor domain to the doublet microtubule and doublet-specific differences pot
23 alyses of the Tetrahymena thermophila native doublet microtubule and identify 42 MIPs.
24 on, which comprises part of the wall of each doublet microtubule and is composed of tubulin and three
25   The ciliary skeleton is made of peripheral doublet microtubules and a central pair (CP) with a dist
26 inner and outer dynein arms, but with intact doublet microtubules and central pair.
27 al striations in the B tubule of respiratory doublet microtubules and noncontinuous spirals in sperm
28 latory complex (N-DRC), which links adjacent doublet microtubules and regulates and coordinates the a
29     Most dramatically, the space between the doublet microtubules and the flagellar membrane contains
30 es of IFT particle-like material between the doublet microtubules and the membrane.
31 tektins, which form coiled-coil filaments in doublet microtubules and which are associated with basal
32 d spoke bases that facilitate docking to the doublet microtubules, and that inner dyneins connect dir
33                                      Axoneme doublet microtubules are initiated from the correspondin
34 ODA-associated proteins with tubulins of the doublet microtubules are not known.
35 nvolves signal-induced severing of the outer doublet microtubules at a precise site in the transition
36 yoelectron microscopy and modeling to define doublet microtubules at near-atomic resolution, revealin
37  the linear array of axonemal dyneins to the doublet microtubule by directly interacting with the hea
38 le inhibits the net force imposed on sliding doublet microtubules by inner dynein arms.
39 ssembly and docking of the I1 complex to the doublet microtubule cargo.
40 ned the effect of tubulin acetylation on the doublet microtubule (DMT) in the cilia of Tetrahymena th
41 us with cilia) with axonemes containing nine doublet microtubules (DMTs) and two singlet microtubules
42                             Dynein-decorated doublet microtubules (DMTs) are critical components of t
43                                              Doublet microtubules (DMTs) are flagellar components req
44 resolve the 96-nm modular repeat of axonemal doublet microtubules (DMTs) from both sperm flagella and
45 igh-resolution structures of native axonemal doublet microtubules (DMTs) from sea urchin and bovine s
46  (IFT) trains move bidirectionally along the doublet microtubules (DMTs) of the axoneme within the fl
47 sists of a 9-fold array of remarkably stable doublet microtubules (DMTs), along which motor proteins
48 rotubules (TMTs), the axoneme is composed of doublet microtubules (DMTs), meaning the cilium must con
49  information about the structure of axonemal doublet microtubules (DMTs).
50 microscopy structures of T. brucei flagellar doublet microtubules (DMTs).
51 lum that contains an axoneme of dynein-bound doublet microtubules (DMTs).
52 hanism may mediate the severing of the outer doublet microtubules during Chlamydomonas deflagellation
53  motility require a radially arranged set of doublet microtubules, each decorated in repeating patter
54               Basal bodies organize the nine doublet microtubules found in cilia.
55              Structures of respiratory-cilia doublet microtubules from four individuals with PCD reve
56  and B-tubule singlets from nine ciliary A-B doublet microtubules in cephalic male (CEM) neurons.
57 he major mechanoregulators that bind ciliary doublet microtubules in Chlamydomonas reinhardtii.
58 We propose that CKI is anchored on the outer doublet microtubules in position to regulate flagellar d
59 2 genes in the pathway mediating assembly of doublet microtubules in the axoneme from triplet microtu
60             Axonemal dyneins are tethered to doublet microtubules inside cilia to drive ciliary beati
61 ction of thousands of dynein motors bound to doublet microtubules into a single propulsive waveform.
62 ree-headed axonemal dynein natively bound to doublet microtubules isolated from cilia.
63  that several proteins may interact with the doublet-microtubule lumen [3, 4, 7, 8].
64 roteins establish the unique architecture of doublet microtubules, maintain coherent periodicities al
65  two types of human ciliary microtubule: the doublet microtubules of multiciliated respiratory cells
66   FAP50 is tightly associated with the outer doublet microtubules of the axoneme and appears not to b
67 r to result from defects in either the outer doublet microtubules or the outer arm docking structures
68         The structure uncovers principles of doublet microtubule organization and features specific t
69 iency did not affect the rate of ATP-induced doublet microtubule sliding.
70 n network crosslinking the lumen of axonemal doublet microtubules, suggesting their roles in modulati
71  flagella have a conserved structure of nine doublet microtubules surrounding a central pair of micro
72  of axoneme architecture, a cylinder of nine doublet microtubules surrounding a central pair of singl
73 metric, with most particles located near the doublet microtubules that face the opposite basal body.
74 lutamylation mainly on the B-tubule of outer doublet microtubules, the site of force production by ci
75 Periodic densities were also observed inside doublet microtubules; these may contribute to doublet st
76  precisely reciprocal to dominant defects in doublet microtubules we observed in a previous study of
77 le distinguishing each one of the nine outer doublet microtubules, we systematically collected and re
78 ar transport, and bound to specific sites on doublet microtubules, where their activity facilitates m
79 the repeating structure of a native axonemal doublet microtubule, which reveals the identities, posit
80 veal how mechanoregulatory complexes dock to doublet microtubules with regular 96-nm periodicity and
81 this motor unit to the A-tubule of the outer doublet microtubules within the axoneme.
82                                   Some outer doublet microtubules without arms had a "partial" dockin