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1 mmaplysilla purea, which is known to inhibit axonemal dynein.
2  a specific centrin function associated with axonemal dynein.
3 identified as subunits of cytoplasmic and/or axonemal dyneins.
4 d to be light chains of both cytoplasmic and axonemal dyneins.
5 LCs) have been found in both cytoplasmic and axonemal dyneins.
6 e analogous to the B-link described for some axonemal dyneins.
7  do different things, as is the case for the axonemal dyneins.
8 but not the other components, corresponds to axonemal dyneins.
9  play an essential role in the regulation of axonemal dynein activity and thus of ciliary and flagell
10    The addition of kinase inhibitor restored axonemal dynein activity concomitant with the dephosphor
11                                     In vitro axonemal dynein activity was reduced by the mia1-1 and m
12 amily proteins were originally identified in axonemal dyneins and subsequently found to function in m
13         fd3F regulates genes for Ch-specific axonemal dyneins and TRPV ion channels, which are requir
14                                              Axonemal dyneins are evolutionarily and biochemically di
15                                              Axonemal dyneins are molecular motors that drive the bea
16                                              Axonemal dyneins are multisubunit enzymes that must be p
17                                              Axonemal dyneins are tethered to doublet microtubules in
18 I1) and DNAI2, the first appreciated step in axonemal dynein arm assembly.
19 ilB homologs with presence of genes encoding axonemal dynein arm components.
20 mport into cilia and flagella, multi-subunit axonemal dynein arms are thought to be stabilized and pr
21 unchanged or become elevated, the density of axonemal dynein arms is reduced in reptin(hi2394) mutant
22 cluding the intraflagellar transport system, axonemal dynein arms, radial spokes, the 96-nm ruler, an
23 toplasmic assembly and/or trafficking of the axonemal dynein arms.
24 n and the other essential for assembling the axonemal dynein arms.
25 ized oda mutants, but only a partial loss of axonemal dyneins as shown by both electron microscopy an
26  Assembly Factors; DNAAFs) are necessary for axonemal dynein assembly, although the detailed mechanis
27 nked form of PCD causing disruption of early axonemal dynein assembly.
28                                              Axonemal dynein ATPases direct ciliary and flagellar bea
29 provide direct evidence that mutations in an axonemal dynein can cause hydrocephalus.
30              The slanted conformation of the axonemal dynein causes interaction of its motor domains
31                      These results show that axonemal dynein directly deciphers the tubulin code, whi
32 bules with MTBDs of cytoplasmic dynein-1 and axonemal dynein DNAH7 and determined their cryo-EM struc
33 oward visualizing the ATPase activity of the axonemal dyneins during bending, we have investigated th
34  most of its length, motor proteins from the axonemal dynein family.
35 , and DIS3 as well as DNAH5, a member of the axonemal dynein family.
36  Dense populations of microtubules driven by axonemal dynein form large vortices, providing insights
37 ability of inner dynein arm I1 and wild-type axonemal dynein function.
38 arious cellular transport systems, including axonemal dyneins generating the force for ciliary and fl
39                                      Because axonemal dynein gliding assays are usually done using he
40                          Gliding assays with axonemal dyneins have the unusual feature that the micro
41  allele of the testis-specifically expressed axonemal dynein heavy chain (axDHC) gene, Dnahc8, has be
42 acterized an insertional mutation in a mouse axonemal dynein heavy chain gene (Mdnah5) that reproduce
43                                          The axonemal dynein heavy chain gene Mdnah5 is specifically
44  culture demonstrated that the expression of axonemal dynein heavy chains correlated with the develop
45 fication and partial cloning of seven unique axonemal dynein heavy chains from rat tracheal epithelia
46 cells in culture regulated the expression of axonemal dynein heavy chains in a parallel fashion.
47 r specifically required for the stability of axonemal dynein heavy chains in cytoplasm and suggest th
48 gulate the cell-specific expression of these axonemal dynein heavy chains will further our understand
49 level of conservation does not extend to the axonemal dynein heavy chains, suggesting functional diff
50  Here we report the positional cloning of an axonemal dynein heavy-chain gene, left/right-dynein (lrd
51 ity, can influence the activity of outer arm axonemal dynein in motility assays using purified protei
52                                   We resolve axonemal dyneins in their prestroke states, illuminating
53 Pontin is essential for the stabilization of axonemal dynein intermediate chain 1 (DNAI1) and DNAI2,
54   This allows for the incorporation of these axonemal dyneins into the axoneme directly from the cyto
55                                              Axonemal dynein is the molecular motor responsible for t
56  formation and prevents incorporation of the axonemal dyneins, leading to sterility.
57  motile node cell monocilia and requires the axonemal dynein, left-right dynein (lrd).
58 epends on efficient sperm movement driven by axonemal dynein-mediated microtubule sliding.
59                                An individual axonemal dynein molecule is capable of both unidirection
60  K40 acetylation increases and CTTs decrease axonemal dynein motility.
61 ximal zone axoneme also being decorated with axonemal dynein motor complexes.
62 a novel RNP granule containing the mRNAs for axonemal dynein motor proteins becomes highly polarized
63                                              Axonemal dynein motors drive ciliary motility and can co
64                                  We captured axonemal dynein motors in their pre-power stroke state.
65 noregulatory complexes with their associated axonemal dynein motors provide a mechanism for the long-
66               We address how cytoplasmic and axonemal dynein MTBDs bind microtubules at near atomic r
67 tory beating patterns, the activities of the axonemal dyneins must be coordinated both spatially and
68                                              Axonemal dyneins must be precisely regulated and coordin
69 cle cryo-EM reconstruction of a three-headed axonemal dynein natively bound to doublet microtubules i
70 ubunits, and cytoplasmic factors involved in axonemal dynein preassembly (DNAAFs) are associated with
71                                              Axonemal dyneins produce the motive force for ciliary an
72                           Here, we unveil an axonemal dynein production and assembly hub enriched wit
73                             We show that the axonemal dyneins, radial spokes, and central pair comple
74           To gain a further understanding of axonemal dynein regulation, mutant strains of Chlamydomo
75 these, we identify C16orf71/Daap1 as a novel axonemal dynein regulator.
76 melanogaster that codes for a sperm-specific axonemal dynein subunit.
77 oducts, including constituents of BBSome and axonemal dynein subunit.
78                Ciliary motility is driven by axonemal dyneins that are assembled in the cytoplasm bef
79 tains an 18-residue insertion, found in many axonemal dyneins, that contacts the adjacent protofilame
80                                              Axonemal dynein, the macromolecular machine that powers
81 sity directly influences the activity of the axonemal dyneins, the motors that drive the beating of t
82                Recent work demonstrates that axonemal dyneins, their specific assembly factors, and b
83 to a higher rate of binding of Chlamydomonas axonemal dynein to Chlamydomonas microtubules than to po
84 x specifically localizes the linear array of axonemal dyneins to the doublet microtubule by directly
85 ersity can directly regulate the activity of axonemal dyneins, we asked whether in vitro acetylation