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1  the export factor Aly/REF to access the TAP export pathway.
2 iring Mob2p, Cbk1p, and a functional nuclear export pathway.
3 function in a Los1p-independent tRNA nuclear export pathway.
4  exporter or an adapter in this tRNA nuclear export pathway.
5 ly involved in the CRM1-mediated Rev nuclear export pathway.
6 he SecA component of the bacterium's protein export pathway.
7 orted viral mRNAs to access the TAP-mediated export pathway.
8 -7 is exerted through a CRM-1-dependent mRNA export pathway.
9 in component, one involving the nonclassical export pathway.
10 NXT1 in the context of the Tap-dependent RNA export pathway.
11 of NXT1 in the context of the Crm1-dependent export pathway.
12 omain and a competent Crm1-dependent nuclear export pathway.
13 ins out of the nucleus via the CRM1-mediated export pathway.
14 ticoid receptor (GR) and to characterize the export pathway.
15 g 10 that have counterparts in the flagellar export pathway.
16 fficulty in capturing "snapshots" during the export pathway.
17 peration of this major new bacterial protein export pathway.
18 SV DR element uses a novel nucleocytoplasmic export pathway.
19 eins are general components of the flagellar export pathway.
20 P2 emerges as a key component of the nuclear export pathway.
21  Exd is exported by a CRM1/exportin1-related export pathway.
22 ssion of RNAs dependent on the cellular mRNA export pathway.
23 t prefolded proteins to an alternate protein export pathway.
24 protein export, which proceeds by a type III export pathway.
25 1p is a carrier for the NES-mediated protein export pathway.
26 ev ARM and the successive Rev-dependent mRNA export pathway.
27 ences share a common specialization in their export pathway.
28 ows viral mRNAs to access a cellular protein export pathway.
29 eriplasm of Escherichia coli via the general export pathway.
30 er of a protein to the next component in the export pathway.
31 on budgets challenge this as a sole particle export pathway.
32 ecruits components of the TREX-NXF1/NXT1 RNA export pathway.
33 ecretion of proteins destined to travel this export pathway.
34 P/NXF, providing a link to the cellular mRNA export pathway.
35 rtin 3 import pathways and the Crm1-mediated export pathway.
36 of parasite proteins via a dedicated protein export pathway.
37 t of the endoplasmic reticulum-Golgi protein export pathway.
38 ds to the mRNP at several stages of the mRNA export pathway.
39 y for secretion and a downstream step in the export pathway.
40 ed from cells by a specialized, nonclassical export pathway.
41 nism of this new type of specialized protein export pathway.
42 on in the proper function of the Tat protein export pathway.
43 15 proteases were more effective against the export pathway.
44 vered to the growing flagellum by a type III export pathway.
45 ort of nsP2 is mediated via the CRM1 nuclear export pathway.
46 by inhibiting the Exportin1-mediated nuclear export pathway.
47  that participated in CRM1-dependent nuclear export pathway.
48 mponent of the general Sec-dependent protein export pathway.
49 on is sufficient for mediating the Gle1-mRNA export pathway.
50 egion maintenance-1 (CRM1)-dependent nuclear export pathway.
51  instead, are secreted through the flagellar export pathway.
52 he cell periphery via the classical Golgi/ER export pathway.
53 import receptor and a competent CRM1-nuclear export pathway.
54 ing that native Tax utilizes another nuclear export pathway.
55 that DsbAss directs thioredoxin 1 to the SRP export pathway.
56 nuclear RNA export, they do so via unrelated export pathways.
57 r import and previously unrecognized nuclear export pathways.
58  involved at a vital juncture point in their export pathways.
59  of Xpo1p in at least one of several nuclear export pathways.
60 st cell requirements of these two viral mRNA export pathways.
61 as GR and hnRNP A1 that use distinct nuclear export pathways.
62 eoporin functions and specialized import and export pathways.
63 to be an essential component of multiple RNA export pathways.
64 t alternately exposes sugar import and sugar export pathways.
65 de a key link between the nuclear import and export pathways.
66 imultaneously exposes sugar import and sugar export pathways.
67 model that implicitly accounts for all known export pathways.
68 eal additional, previously unsuspected, mRNA export pathways.
69 ral RNA to the cellular CRM1 or NXF1 nuclear export pathways.
70 ess splicing-dependent cellular mRNA nuclear export pathways.
71 ent tissues via at least 2 SID-1 independent export pathways.
72  plays a functional role in multiple nuclear export pathways.
73 tion of MNK1 suppresses endogenous HDM2 mRNA export pathways.
74 ncreased diversification of these organisms' export pathways.
75 trols the entry of virtually all proteins to export pathways.
76 e evolutionary divergence of eukaryotic mRNA export pathways.
77 ting these enzymes are secreted by different export pathways.
78 that disrupt different Ran-dependent nuclear export pathways.
79  limited representations of the known carbon export pathways(3).
80                                  The nuclear export pathway accessed by NTD is insensitive to leptomy
81  rev-mediated transport, suggesting that the export pathways accessed by the adenoviral and retrovira
82                Furthermore, choice of proper export pathway affects tra-2 translational control.
83          These viruses interfere with import-export pathways, allowing for the cytoplasmic accumulati
84 east one-and perhaps several-additional tRNA export pathways also exist.
85 udding is a nuclear pore-independent nuclear export pathway, analogous to the egress of herpesviruses
86 RNA helicase which functions in the CRM1 RNA export pathway analogously to the postulated role for Db
87  suggested that Rae1 is involved in the mRNA export pathway and Bub3 in the mitotic checkpoint.
88 spatio-temporal aspects of this nonclassical export pathway and demonstrate that heat shock stimulate
89 sm of leukemogenesis mediated by the nuclear export pathway and support further investigation of the
90 and budding are regulated by the RNA nuclear export pathway and that alternative cellular pathways ca
91 Rev and PKI act through an identical nuclear export pathway and that Rev, rather than using a dedicat
92               In Pseudomonas aeruginosa this export pathway and type IV pilus biogenesis are dependen
93 smic RNP complexes, providing a link between export pathways and cytoplasmic fate.
94 ideless proteins occurs through nonclassical export pathways and the release of fibroblast growth fac
95  Tax translocation required the CRM1 nuclear export pathway, and a transient interaction between Tax
96 ly inhibits protein translation, key nuclear export pathways, and cellular mRNA localization early in
97            Components of this unconventional export pathway are highly conserved, suggesting that thi
98 e flagellar apparatus and associated protein export pathway are well conserved in evolution.
99 icularly in oligotrophic oceans where carbon export pathways are limited.
100 pendent on the presence of an intact nuclear export pathway as c-Jun is stabilized and localized to t
101  sugar sensor to regulate an inducible sugar export pathway as leaves develop under high light condit
102 yeast Gle1 involved in the same poly(A) mRNA export pathway as Nup159, also result in seed abortion.
103 ant and reveals a role for the Crm1-mediated export pathway at a late step in viral infection.
104  out of the nucleus through the CRM1 nuclear export pathway, based on observations that treatment of
105 ascent chains that monitor different protein export pathways by a shared molecular mechanism.
106 folded GPI-APs traffic to the Golgi by an ER-export pathway called Rapid ER stress-induced Export (RE
107 agella at different stages of assembly, each export pathway can discriminate and sort unchaperoned ea
108  capacities of the folding, degradation, and export pathways, collectively dictate an adaptable stand
109          Type III secretion (T3S), a protein export pathway common to Gram-negative pathogens, compri
110 mplicate IPMK in a transcript-selective mRNA export pathway controlled by phosphoinositide turnover t
111 53, suggesting that the Tap and CRM1 nuclear export pathways converge at the cytoplasmic periphery of
112                              The second acid-export pathway does not require extracellular anions or
113 rge numbers of PE/PPE proteins via the major export pathway, ESX-5.
114 (with no lysine [K] 1) in the mammalian mRNA export pathway even though it was previously established
115 ifferentially regulated, hnRNP-specific mRNA export pathways exist.
116 Notably, protein secretion through the curli export pathway facilitates acquisition of the amyloid fo
117 smic membrane of many bacteria, is a general export pathway for folded proteins.
118 ical machineries of this alternative nuclear export pathway for large cargos during cell differentiat
119 ar envelope budding is an endogenous nuclear export pathway for large RNP granules.
120  results imply remarkable flexibility in the export pathway for the 60S subunit and help explain how
121 2 complex reflects a defect in the bona fide export pathway for the 60S subunit.
122  mechanisms and reveal a long-sought nuclear export pathway for transcripts with GC-rich sequences.
123 ve inhibitor of rev export, arguing that the export pathways for hdm2 and rev are either overlapping
124                         Two distinct nuclear export pathways for retroviral mRNA have been described:
125 ngly suggest that there are multiple nuclear export pathways for these small RNAs in Arabidopsis.
126 e an alternative to the Sec (general protein export) pathway for translocation across the inner membr
127 endent, suggesting that RSV uses a different export pathway from that of HIV-1 and other complex retr
128 NA to Tap, suggesting it may use a different export pathway from that of the simian retroviruses.
129 cretory, or Sec, system is a primary protein export pathway from the cytosol of Escherichia coli and
130                        These are the general export pathway (GEP), a twin-arginine translocase (TAT)
131 spective, and the definitions of the general export pathway (GEP), the main terminal branch (MTB) of
132                    The Sec-dependent protein export pathway has been well characterized in Escherichi
133 , and provides insight into a divergent mRNA export pathway in apicomplexans.
134 hus allowing direct visualization of the Rev export pathway in living cells.
135 o determine the functional nature of the Tat export pathway in mycobacteria.
136 lved to take advantage of a cellular protein export pathway in order to allow the nucleocytoplasmic t
137 irecting messages into a CRM1-dependent mRNA export pathway in somatic mammalian cells.
138                  We identify a dedicated ISC/export pathway in which augmenter of liver regeneration,
139 ssibility that TRalpha follows a cooperative export pathway in which both calreticulin and CRM1 play
140 cts in the classical protein import and mRNA export pathways in affected cells.
141 and reveal a hierarchical network of protein export pathways in bacteria.
142 on assay to show that there are two cytokine export pathways in T helper cells.
143 cted cells, implicating altered lipid import/export pathways in these cells.
144 d in vivo with other components of the CRM 1 export pathway, including the small GTPase Ran and the n
145                      Further progress on the export pathway, including the terminal step of Crm1 and
146 , which inhibits the Crm1- dependent nuclear export pathway, induces an accumulation of epsin 1 in th
147  and CucA have signal peptides for different export pathways into the periplasm, Tat and Sec respecti
148 may access the same constitutive RNA nuclear export pathway involving RHA, Tap and Sam68, even though
149                           Saturation of tRNA export pathway is a possible explanation of this phenome
150          it is likely that this constitutive export pathway is also used by cellular mRNA, but at a d
151                               This dedicated export pathway is comprised of seven components (SecA2,
152 subtilis can export Ply, suggesting that the export pathway is conserved.
153                                     This RNA export pathway is CRM1 dependent and can be blocked by t
154                       This androgen receptor export pathway is dependent on ATP hydrolysis and is enh
155                    We show that this protein export pathway is highly conserved by demonstrating that
156                      Since this mRNA nuclear export pathway is key for expression of M1 and M2 protei
157  that Rev, rather than using a dedicated RNA export pathway, is instead acting as an adaptor that all
158 ially requires a Sub2-mediated mRNP assembly/export pathway linked to transcription via Rlr1.
159 These findings suggest that the CRM1 nuclear export pathway may be important in the functional regula
160                         Thus the rev nuclear export pathway may be used to regulate an oncogene produ
161                             Atypical nuclear export pathways may thus exist that regulate the compart
162 B, an inhibitor of CRM-1, indicates that the export pathways mediated by Rev and Sam68 are distinct.
163 xiliary protein in the Sec-dependent protein export pathway of Escherichia coli.
164 mbrane protein, gates the type III flagellar export pathway of Salmonella.
165 dressed the relationship between the nuclear export pathway of SNV RU5-reporter RNA and translational
166 ed S(0) in soils, vegetation, and hydrologic export pathways of Napa Valley, CA vineyards, documentin
167 te that the ER-associated degradation (ERAD) export pathway operates in the phagosomes of dendritic c
168 aminoacylation and Los1p operate in the same export pathway or there are more than two pathways for t
169 sport of bacterial proteins across a non-Sec export pathway possess an N domain RRXFLK consensus moti
170  that protein secretion via this specialized export pathway promotes acquisition of the amyloid fold
171               However, the mechanism of this export pathway remains unclear.
172 e, suggesting the presence of redundant tRNA export pathway(s) in Arabidopsis.
173 Nup153 antibodies also block the NES protein export pathway, specifically the export of the HIV Rev p
174                                Prediction of export pathway specificity in prokaryotes is a challengi
175 lensis expresses a complete hexose phosphate export pathway, suggesting deeper metabolic integration,
176          Although effector architectures and export pathways tend to be clade specific, phylogenetica
177 the proinflammatory cytokine IL-1beta via an export pathway that depends on Atg5, inflammasome, at le
178  directs unspliced viral RNAs into a nuclear export pathway that is congruent with the pathway used b
179 indicate that RU5 gag RNA accesses a nuclear export pathway that is distinct from the LMB-inhibited l
180 irects SNV RU5-containing RNAs to a distinct export pathway that is not inhibited by LMB and programs
181                            CRT defines a new export pathway that may regulate the transcriptional act
182 Here, we identify a novel host cell effector export pathway that requires the Golgi-resident aspartyl
183 e the existence of ICP27-independent nuclear export pathways that are accessible to many viral transc
184 n the requirement for Npl3p defines the mRNA export pathway, the requirement for Rip1p defines a path
185 tors associated with the two recognized mRNA export pathways, these results suggest that RTE function
186      Thus, NXT1 regulates the Crm1-dependent export pathway through its direct interaction with Ran-G
187 the function of multiple important bacterial export pathways, through direct allosteric control of ex
188 ponse Element (RRE) through the Crm1 nuclear export pathway to the cytoplasm where viral proteins are
189         HIV-1 requires a specialized nuclear export pathway to transport unspliced and partially spli
190             These data show that the nuclear export pathway used by steroid hormone receptors such as
191 t, suggesting that the ability to follow the export pathway used by TRalpha has been lost by the onco
192 nsferase pull-down assays to investigate the export pathway used by TRalpha.
193 nd demonstrate that the MPMV CTE nuclear RNA export pathway uses a distinct, Crm1-independent mechani
194 o reveal which steps, if any, in the nuclear export pathway utilized by steroid receptors require ATP
195 go nucleocytoplasmic shuttling when the CRM1 export pathway was blocked by LMB treatment, suggesting
196 ag rapidly became intranuclear when the CRM1 export pathway was blocked, implying that most if not al
197                                 Finally, the export pathway was further defined by the ability of spe
198 hat use other karyopherin-mediated import or export pathways was not affected in a kap119Delta strain
199 characterize elements of the vertebrate mRNA export pathway, we identified a human homologue of yeast
200 presented indicating that nuclear import and export pathways were not adversely affected by vaccinia
201  Rev and RanBP1 compete for the same nuclear export pathway, whereas Rev- and the CTE-mediated pathwa
202 tling protein that utilizes the CRM1 nuclear export pathway, while HIV-1 Gag is excluded from the nuc
203 he viral proteins utilize the CRM1-dependent export pathway, while the cellular factors generally fun
204 scovered that inhibition of the CRM1 nuclear export pathway with leptomycin B causes FIV Gag but not
205 mplex and widespread gram-negative bacterial export pathway with the capacity to translocate protein
206 translocation) system is a bacterial protein export pathway with the remarkable ability to transport
207    We propose the existence of multiple mRNA export pathways, with export of Nab2p-associated mRNAs d
208 uence the magnitude and seasonality of these export pathways, with implications for carbon sequestrat

 
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