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1  dependent on sigB and cshA, which encodes a DEAD box RNA helicase.
2 PNPase), enolase, phosphofructokinase, and a DEAD box RNA helicase.
3 ontain four exons with similarity to a plant DEAD box RNA helicase.
4 lemented the function of Ded1p, an essential DEAD box RNA helicase.
5 ure revealed only one protein, RhlE, another DEAD-box RNA helicase.
6 d positively and negatively by multiple host DEAD-box RNA helicases.
7 t has been observed for many double-stranded DEAD-box RNA helicases.
8 or of SecA is strongly homologous to that in DEAD-box RNA helicases.
9 gous to the "Q motif" recently identified in DEAD-box RNA helicases.
10 ticles, Xp54, which belongs to the family of DEAD-box RNA helicases.
11                                 Among these, DEAD-box RNA helicase 17 (DDX17) was significantly up-re
12           Here we show that the depletion of DEAD-box RNA helicase 3X (DDX3X) triggers a tumor-intrin
13 y, mass spectrometry analysis identified the DEAD-box RNA helicase 6 (DDX6) that interacts with the V
14                   We have identified a novel DEAD box RNA helicase (97 kDa, DP97) from a breast cance
15 visiae is a nucleic acid helicase related to DEAD box RNA helicases and type I DNA helicases.
16          Recently, our group established the DEAD-box RNA helicase and microRNA (miRNA) microprocesso
17 esults confirmed that OsDB10 is a functional DEAD-box RNA helicase and played vital roles in plant de
18 ase polynucleotide phosphorylase (PNPase), a DEAD-box RNA helicase and the Krebs cycle enzyme aconita
19      Mtr4p shares characteristic motifs with DEAD-box RNA helicases and associates with RNA.
20              Taken together, we propose that DEAD-box RNA helicases are directly coupled to transcrip
21                                          The DEAD-box RNA helicases are enzymes involved in many crit
22                   Here, we show that several DEAD-box RNA helicases are sensitive to AMP, which is no
23                                              DEAD-box RNA helicases are vital for the regulation of v
24 tudies and identified DDX5, an ATP-dependent DEAD-box RNA helicase, as a component of the MAML1 prote
25                  Vasa is a broadly conserved DEAD-box RNA helicase associated with germ line developm
26 al activities of human DDX3X are typical for DEAD-box RNA helicases, but diverge quantitatively from
27  this model by identifying such a protein, a DEAD-box RNA helicase called Pitchoune, and show that mo
28       Importantly, we identify the conserved DEAD-box RNA helicase, CGH-1/DDX6, as a key CK2 substrat
29 roteolytic degradation of the cyanobacterial DEAD-box RNA helicase CrhR is conditional, being initiat
30 D-alanine carboxypeptidases (dac1 and dac2), DEAD-box RNA helicases (csdA and Psyc_0943), and energy-
31 s, we identified among multiple proteins the DEAD box RNA helicase CshA (NWMN_1985 or SA1885) by mass
32 iously, our laboratory demonstrated that the DEAD-box RNA helicase Dbp2 in Saccharomyces cerevisiae i
33                                              DEAD-box RNA helicase Dbp4 is required for 18S rRNA synt
34   The adenosine triphosphate (ATP)-dependent DEAD-box RNA helicase DbpA from Escherichia coli functio
35 on of select RNA chaperones, including three DEAD box RNA helicases (DBRHs) (CsdA, SrmB, RhlB) and th
36                                              DEAD-box RNA helicases (DBRHs) modulate RNA secondary st
37                                              DEAD-box RNA helicase DDX21 (also named nucleolar RNA he
38                        Here we show that the DEAD-box RNA helicase DDX21 can sense the transcriptiona
39  In contrast to A52, K7 forms a complex with DEAD box RNA helicase DDX3, thereby suppressing DDX3-med
40 Rev/CRM1 activity utilizes the ATP-dependent DEAD box RNA helicase, DDX3.
41                                          The DEAD-box RNA helicase DDX3X attenuates RNA-RNA interacti
42                                    The human DEAD-box RNA helicase DDX3X is an essential cofactor for
43                                          The DEAD-box RNA helicase DDX3X is frequently mutated in ped
44                                          The DEAD-box RNA helicase DDX3X promotes translation initiat
45 116 colon carcinoma cells, we identified the DEAD-box RNA helicase DDX41 as a novel regulator of p21
46 ocused our analysis on the largely unstudied DEAD box RNA helicase DDX55, and validated its novel rol
47                       Here, we show that the DEAD box RNA helicase, DDX6 is necessary for maintaining
48                             We show that two DEAD-box RNA helicases, DeaD and SrmB, activate csrB/C e
49                                        Yeast DEAD-box RNA helicase Ded1 appears to promote translatio
50                                              DEAD-box RNA helicases, defined by the sequence Asp-Glu-
51 roteins that activate decapping, such as the DEAD-box RNA helicase Dhh1, have been postulated to func
52 eat domain 3 protein (PTCD3), and a putative DEAD-box RNA helicase, DHX30.
53 ions in the HRxGRxxR motif of the prototypal DEAD box RNA helicase eIF-4A abolish or severely inhibit
54                                              DEAD-box RNA helicases eIF4A and Ded1 are believed to pr
55 ranslation initiation involves two conserved DEAD-box RNA helicases, eIF4A and Ded1p.
56        In this study, a virulence-associated DEAD-box RNA helicase-encoding gene (VAD1) was isolated
57       Most aspects of RNA metabolism involve DEAD-box RNA helicases, enzymes that bind and remodel RN
58 ed testicular RNA helicase (GRTH)/DDX25 is a DEAD-box RNA helicase essential for the completion of sp
59                                              DEAD-box RNA helicases eukaryotic translation initiation
60 t least seven nucleus-encoded members of the DEAD box RNA helicase family.
61 nsistent activation of DDX3, a member of the DEAD box RNA helicase family.
62 creen we isolated SUB2, encoding a conserved DEAD-box RNA helicase family member having roles in both
63 n evolutionarily conserved member of the SF2 DEAD-box RNA helicase family that contributes to the reg
64 elicase 5 (DDX5) is a founding member of the DEAD-box RNA helicase family, a group of enzymes that re
65 hat DDX5, one of the founding members of the DEAD-box RNA helicase family, is extremely proficient at
66 egulation by other members of the ubiquitous DEAD-box RNA helicase family.
67                   RCF1 is a highly conserved DEAD-box RNA helicase found in yeast, plants, and mammal
68            We reported earlier that LAF-1, a DEAD box RNA helicase in C. elegans, dynamically interac
69  the gene encoding the sole Asp-Glu-Ala-Asp (DEAD)-box RNA helicase in Synechocystis sp. PCC 6803, cr
70 ependent and ATP-dependent roles of the Has1 DEAD-box RNA helicase in consecutive pre-rRNA processing
71 n this issue of the JCI identifies the first DEAD-box RNA helicase in the pathogenic fungus Cryptococ
72 siRNA) library screen targeting the 58 human DEAD-box RNA helicases in two permissive human cancer ce
73                         DDX3X is a conserved DEAD-box RNA helicase involved in translation initiation
74 lasmic roles as a modulator of ATP-dependent DEAD-box RNA helicases involved in messenger (m)RNA expo
75                                         This DEAD-box RNA helicase is known to be associated with var
76 itiation factor 4A (eIF4A), an ATP-dependent DEAD-box RNA helicase, is a critical component of the eI
77 the single-copy bobcat gene, which encodes a DEAD-box RNA helicase, is embedded within the first Manx
78            In many species examined, Vasa, a DEAD-box RNA helicase, is found in these morphologically
79 itiation factor 4A (eIF4A), an ATP-dependent DEAD-box RNA helicase; its messenger RNA selectivity is
80 tens, PpRH1/PpRH2 are GUCT-domain-containing DEAD-BOX RNA helicases localize to the nucleus.
81                 Unlike a previously reported DEAD box RNA helicase (LOW EXPRESSION OF OSMOTICALLY RES
82                   We show that the conserved DEAD-box RNA helicase Me31B forms viscous P body condens
83                                              DEAD-box RNA helicases mediate all aspects of RNA metabo
84                                              DEAD-box RNA helicases of the bacterial DbpA subfamily a
85           Here we show that DHH1, encoding a DEAD-box RNA helicase orthologous to the human putative
86                             In this study, a DEAD-box RNA helicase OsDB10 was cloned and functionally
87                      Here we showed that the DEAD-box RNA helicase p68 (DDX5) and its associated nonc
88                                          The DEAD-box RNA helicases p68 (DDX5) and p72 (DDX17) have b
89                                          The DEAD box RNA helicase, p68, has been implicated in vario
90                                          The DEAD box RNA helicase, p68, is upregulated in exponentia
91              Here, we show that the abundant DEAD-box RNA helicase p72, but not its close relative p6
92      Here, we functionally characterized the DEAD-box RNA helicase PfDOZI in P. falciparum.
93                                              DEAD box RNA helicases play central roles in RNP biogene
94 es identified frequent mutations in DDX3X, a DEAD-box RNA helicase primarily implicated in translatio
95  is a Saccharomyces cerevisiae mitochondrial DEAD-box RNA helicase protein that is essential for effi
96                                              DEAD-box RNA helicase proteins use the energy of ATP hyd
97                               DDX3 and other DEAD-box RNA helicases regulate nuclear export, translat
98 1 and established that it encodes a putative DEAD-box RNA helicase related to Saccharomycescerevisiae
99 fied as the Kreb's cycle enzyme aconitase, a DEAD-box RNA helicase RhlB and the exoribonuclease polyn
100                       Here, we show that the DEAD box RNA helicase smut-1 functions redundantly in th
101                       Here, we show that the DEAD-box RNA helicase Spb4 with its interacting partner
102 nwinding by DbpA, a non-processive bacterial DEAD-box RNA helicase specifically activated by the pept
103   Eukaryotic initiation factor (eIF) 4A is a DEAD box RNA helicase that works in conjunction with eIF
104  is the second example of a Asp-Glu-Ala-Asp (DEAD) box RNA helicase that unwinds RNA duplexes in a bi
105                                  Gemin3 is a DEAD-box RNA helicase that binds to the Survival of Moto
106                                    Vasa is a DEAD-box RNA helicase that functions in translational re
107                                   DDX3X is a DEAD-box RNA helicase that has been implicated in multip
108       ISE1 encodes a putative plant-specific DEAD-box RNA helicase that localizes specifically to mit
109 soforms of the eIF4A family of ATP-dependent DEAD-box RNA helicases that are required for translation
110 ic initiation factor (eIF)4A, an ATP-powered DEAD-box RNA-helicase that unwinds the messenger RNA sec
111 y RNA-RNA interactions that are modulated by DEAD-box RNA helicases to ensure RNA availability and tr
112                Amplifier is nucleated by the DEAD box RNA helicase Vasa and contains the two Piwi pro
113 rosophila orthologue GUSTAVUS binding to the DEAD-box RNA helicase VASA (DINNNN).
114                 ISE1 encodes a mitochondrial DEAD-box RNA helicase, whereas ISE2 encodes a DEVH-type
115                                              DEAD-box RNA helicases, which are involved in virtually
116                                    DDX3 is a DEAD box RNA helicase with oncogenic properties.
117                    DDX3X encodes an X-linked DEAD-box RNA helicase with a Y-linked paralog, DDX3Y.
118                                    Ded1 is a DEAD-box RNA helicase with essential roles in translatio
119  Gle1 is a conserved, essential regulator of DEAD-box RNA helicases, with critical roles defined in m
120                                          The DEAD-box RNA helicase Xp54 is an integral component of t

 
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