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1  acetylation, we pharmacologically inhibited histone deacetylase 6, a known deacetylase of Hsp90, or
2 DJ-1 serves as a signal for interaction with histone deacetylase 6, an adaptor protein that binds the
3     Tubacin is a small molecule inhibitor of histone deacetylase 6 and blocks aggresome activity.
4 TR) mutant CFTRDeltaF508 and associates with histone deacetylase 6 and dynein, proteins required for
5 ession of the cytoplasmic deacetylase HDAC6 (Histone Deacetylase 6) and that FGFR3 accumulation is co
6 zation was rescued by inhibition of ROCK and histone deacetylase 6 but not by a GAP-mutant form of AR
7    Additionally, a complex of PRR9, TPL, and histone deacetylase 6, can form in vivo, implicating thi
8 he death inducer-obliterator (dido) gene, in histone deacetylase 6 delivery to the primary cilium.
9 t a specific subset of RdDM targets requires HISTONE DEACETYLASE 6 (HDA6) acting upstream of Pol IV r
10                                     Mutating HISTONE DEACETYLASE 6 (HDA6), or the cytosine methyltran
11 d with increased Aurora kinase A (AURKA) and histone deacetylase 6 (HDAC6) activities, which drive di
12 a promoting MT polymerization and inhibiting histone deacetylase 6 (Hdac6) activity to increase MT ac
13 asomes, but also by aggresomes, dependent on histone deacetylase 6 (HDAC6) activity.
14  in up-regulation of the tubulin deacetylase histone deacetylase 6 (HDAC6) and altered spatial distri
15  involves protein kinase C alpha (PKCalpha), histone deacetylase 6 (HDAC6) and beta-catenin (beta-cat
16                   It is highly selective for histone deacetylase 6 (HDAC6) and is 60-fold more active
17 ssion of two known microtubule deacetylases, histone deacetylase 6 (HDAC6) and Sirtuin T2 (SirT2), in
18 e network by a protein complex consisting of histone deacetylase 6 (HDAC6) and the dynein motor compl
19    Here, we have observed that the levels of histone deacetylase 6 (HDAC6) and the related family mem
20                            Here, we identify histone deacetylase 6 (HDAC6) as responsible for abrogat
21                     Furthermore, we identify histone deacetylase 6 (HDAC6) as the enzyme responsible
22                                              Histone deacetylase 6 (HDAC6) catalyzes the removal of a
23 e, we report that the microtubule-associated histone deacetylase 6 (HDAC6) differentially regulates a
24                                  Ablation of histone deacetylase 6 (HDAC6) expression and its activit
25 look at the numerous disease states in which histone deacetylase 6 (HDAC6) has been implicated.
26                 Here, we studied the role of histone deacetylase 6 (HDAC6) in regulating cyst growth
27                 In this report, we show that histone deacetylase 6 (HDAC6) in tumor cells appears to
28 l inhibition as well as genetic silencing of histone deacetylase 6 (HDAC6) increase alpha-tubulin ace
29 stat was recapitulated using the cytoplasmic histone deacetylase 6 (HDAC6) inhibitor tubacin, reveali
30 eport the development of a potent, selective histone deacetylase 6 (HDAC6) inhibitor.
31                                              Histone deacetylase 6 (HDAC6) is a cytoplasmic deacetyla
32                                              Histone deacetylase 6 (HDAC6) is a heat shock protein 90
33                                              Histone deacetylase 6 (HDAC6) is a microtubule-associate
34                                              Histone deacetylase 6 (HDAC6) is a tubulin deacetylase t
35                                              Histone deacetylase 6 (HDAC6) is a tubulin-specific deac
36                                              Histone deacetylase 6 (HDAC6) is structurally and functi
37            We provide evidence that class II histone deacetylase 6 (HDAC6) is the intracellular targe
38                                              Histone deacetylase 6 (HDAC6) is well known for its abil
39                        Herein we report that histone deacetylase 6 (HDAC6) modulates TGF-beta1-mediat
40 acetylation of alpha-tubulin, a substrate of histone deacetylase 6 (HDAC6) occurs.
41                                      Because histone deacetylase 6 (HDAC6) plays an important role in
42  find that the centrosome-associated protein histone deacetylase 6 (HDAC6) promotes the polyubiquitin
43                          Here we report that histone deacetylase 6 (HDAC6) sequentially deacetylates
44 ted by the ubiquitin-proteasome pathway, and histone deacetylase 6 (HDAC6) serves as an ubiquitin E3
45 ate in the cytoplasm and are transported via histone deacetylase 6 (HDAC6) toward the aggresomes.
46           At the same time, the abundance of histone deacetylase 6 (HDAC6) was diminished.
47                                              Histone deacetylase 6 (HDAC6), a class IIb HDAC, plays a
48 so requires input from host microtubules and histone deacetylase 6 (HDAC6), a cytosolic enzyme that,
49                                              Histone deacetylase 6 (HDAC6), a microtubule-associated
50 mpaired in Drosophila melanogaster, and that histone deacetylase 6 (HDAC6), a microtubule-associated
51 ignificant microarray hits was the cytosolic histone deacetylase 6 (HDAC6), a regulator of cell migra
52 of stress responses, we examined the role of histone deacetylase 6 (HDAC6), a unique member of the HD
53  of the tubulin deacetylases, sirtuin 2, and histone deacetylase 6 (HDAC6), blocks EC tube formation
54                Indeed, one of these enzymes, histone deacetylase 6 (HDAC6), influences the acetylatio
55 servations that tau is a direct substrate of histone deacetylase 6 (HDAC6), we sought to map all HDAC
56 e microtubules with paclitaxel or inhibiting histone deacetylase 6 (HDAC6), which destabilizes microt
57 1 inhibits the interaction between TPPP1 and histone deacetylase 6 (HDAC6), which in turn results in
58 ively regulates alternative splicing through histone deacetylase 6 (HDAC6)-mediated deacetylation of
59  RelA in the nucleus, by which MIIP prevents histone deacetylase 6 (HDAC6)-mediated RelA deacetylatio
60 der of ubiquitin zinc finger (BUZ) domain of histone deacetylase 6 (HDAC6).
61 r their ability to selectively inhibit human histone deacetylase 6 (HDAC6).
62  resistance, clonogenicity, and induction of histone deacetylase 6 (HDAC6).
63  cholangiocarcinoma by a mechanism involving histone deacetylase 6 (HDAC6).
64 s, ubiquitinates and regulates expression of histone deacetylase 6 (HDAC6).
65 ted for their ability to inhibit selectively histone deacetylase 6 (HDAC6).
66 ivity of the only known tubulin deacetylase, histone deacetylase 6 (HDAC6).
67                                Knock down of histone deacetylase-6 (HDAC6) increased the acetylation
68  identify the ubiquitin-binding deacetylase, histone deacetylase-6 (HDAC6), as a central component of
69  tissue that is correctable by inhibition of histone deacetylase-6 (HDAC6).
70  attenuate NF-kappaB signaling, and recruits histone deacetylases-6 (HDAC6) to p300-marked promoters
71 Jun dimerization protein 2 [JDP2], ATF2, and histone deacetylase 6 [HDAC6]), as determined by proteom
72 s and cells treated with ethanol or with the histone deacetylase 6 inhibitor trichostatin A (TSA).
73                              Brain-penetrant histone deacetylase 6 inhibitors increase Hsp90 acetylat
74        The cytosolic receptors p62, NBR, and histone deacetylase 6 recognize aggregated ubiquitinated
75                 Administration of ACY-738, a histone deacetylase 6-selective inhibitor, led to Hsp90
76 resome by promoting an iNOS interaction with histone deacetylase 6, which serves as an adaptor betwee

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