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1 ar 'address' (nuclear localization signal or nuclear export sequence).
2 h was further augmented by removal of FMRP's nuclear export sequence.
3 HDAC4 reversal depended on the HDAC4 nuclear export sequence.
4 hift, unmasking an additional CRM1-dependent nuclear export sequence.
5 ctional HCF-binding motif and a leucine-rich nuclear export sequence.
6 ed mTOR nuclear export with the tagging of a nuclear export sequence.
7 omycin B, despite the absence of a classical nuclear export sequence.
8 of IkappaBalpha is mediated by an N-terminal nuclear export sequence.
9 del for the intermolecular regulation of the nuclear export sequence.
10 -export is attributable to its nonfunctional nuclear-export sequence.
11 RCA1 contains at least two leucine-dependent nuclear export sequences.
12 ts demonstrated that Cdc25 contains multiple nuclear export sequences.
13 at functions as cytoplasmic retention and/or nuclear export sequences.
14 uncated Ssd1 proteins, which presumably lack nuclear export sequences, accumulate in the nucleus.
17 nd COS-7 cells as did deletion of a putative nuclear export sequence (amino acids 224 to 233) or muta
18 accumulation in the nucleus involves both a nuclear export sequence and a nuclear localization signa
19 orted from the nucleus in the absence of its nuclear export sequence and in the presence of a strong
20 is serine lies directly within the cyclin B1 nuclear export sequence and, when phosphorylated, preven
21 inase: a mitochondrial targeting sequence, a nuclear export sequence, and a nuclear localization sequ
23 Additionally, ORF 3b contains a consensus nuclear export sequence, and we demonstrate that nuclear
24 m, using typical hydrophobic amino acid-rich nuclear export sequences, and nuclear localization seque
25 ber of other tumor suppressors have multiple nuclear export sequences, and we sought to determine whe
27 conserved nuclear localization sequences or nuclear export sequences but can accumulate in the nucle
28 smic localization, is actually an autonomous nuclear export sequence, capable of directing nuclear ex
30 th the addition of a nuclear localization or nuclear export sequence demonstrates that nuclear accumu
31 distinct from the LMB-inhibited leucine-rich nuclear export sequence-dependent CRM1 pathway, which is
34 The nuclear export of MPF is mediated by a nuclear export sequence in cyclin B1, and an export-defe
35 oth RGS4 and RGS16, a domain identified as a nuclear export sequence in HIV Rev and other proteins, p
36 wever, the presence of a functional Rev-like nuclear export sequence in hRPF1/Nedd4 ensures a predomi
37 that NPM utilizes a conserved CRM1-dependent nuclear export sequence in its amino terminus to enable
38 show that mutation or deletion of a putative nuclear export sequence in LTV1 is strongly dominant neg
39 , we identified a previously uncharacterized nuclear export sequence in residues 45-54 of IkappaBalph
40 ctopic expression of Cyclin B1 with a mutant nuclear export sequence induced chromosome condensation,
41 osition 71 between the known RNA-binding and nuclear export sequences interfered with GFPRem accumula
42 the nucleus, possibly due to disruption of a nuclear export sequence located downstream of the FERM-a
45 functional nuclear localization sequence and nuclear export sequence motifs in ILK, delineated an app
49 RAK shows that PRAK contains both a putative nuclear export sequence (NES) and a nuclear localization
50 DAC4 and -5 each contain a signal-responsive nuclear export sequence (NES) at their extreme carboxy t
52 that the dsRBD of ILF3 functions as a novel nuclear export sequence (NES) in intact cells, and its a
53 ion repressor of Nrf2 and demonstrate that a nuclear export sequence (NES) in Keap1 is required for t
54 as a leptomycin B-sensitive, CRM1-dependent nuclear export sequence (NES) in the AMPK catalytic subu
55 tative nuclear localization signal (NLS) and nuclear export sequence (NES) of FAC1, using deletion mu
58 cts of RXRalpha are attributed to a putative nuclear export sequence (NES) present in its carboxyl-te
59 st Gle1p, a protein with a leucine-rich (LR) nuclear export sequence (NES) that is essential for poly
61 s identified in ICP27 include a leucine-rich nuclear export sequence (NES), a nuclear localization si
62 n of these cells, we found that a functional nuclear export sequence (NES), ATP, and fractionated cyt
63 ation which contains a dominant leucine-rich nuclear export sequence (NES), the previously defined cy
64 actors interacting with the Rev leucine-rich nuclear export sequence (NES), we identified a kinesin-l
65 Bepsilon is mediated by a short leucine-rich nuclear export sequence (NES)-like sequence ((343)VLLPFD
66 clear in a crm1 mutant, and Crm1p binds to a nuclear export sequence (NES)-like sequence in Yap1p in
70 xport of Upf3p is mediated by a leucine-rich nuclear export sequence (NES-A), but export is not depen
71 ize nuclear localization sequences (NLSs) or nuclear export sequences (NESs) and target the NLS-beari
72 e RRE assembles a Rev oligomer that displays nuclear export sequences (NESs) for recognition by the C
76 Cdc25, allowing nuclear export mediated by a nuclear export sequence present in the N-terminus of Cdc
77 ility of hydrophobic residues (including the nuclear export sequence), providing a rationale for the
80 Although nuclear localization sequence- and nuclear export sequence-targeted proteins both activated
81 Here, we report that BRCA1 contains a second nuclear export sequence that comprises amino acid residu
83 RM1, through a specific leucine-rich domain (nuclear export sequence) that regulates its export to th
85 xport of a protein containing a leucine-rich nuclear export sequence, whereas nuclear import of a pro
87 ional nuclear localization signals (NLS) and nuclear export sequences, yet nuclear import depended on
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