scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | B R Cullen | |
P2860 | cites work | RAE1 is a shuttling mRNA export factor that binds to a GLEBS-like NUP98 motif at the nuclear pore complex through multiple domains | Q22009429 |
Processing of intervening sequences: a new yeast mutant which fails to excise intervening sequences from precursor tRNAs | Q71156037 | ||
The human tap nuclear RNA export factor contains a novel transportin-dependent nuclear localization signal that lacks nuclear export signal function | Q73133774 | ||
Definition of a consensus transportin-specific nucleocytoplasmic transport signal | Q74638201 | ||
Dbp5, a DEAD-box protein required for mRNA export, is recruited to the cytoplasmic fibrils of nuclear pore complex via a conserved interaction with CAN/Nup159p | Q22010452 | ||
Transport between the cell nucleus and the cytoplasm | Q22065411 | ||
A nuclear export signal in hnRNP A1: a signal-mediated, temperature-dependent nuclear protein export pathway | Q24309825 | ||
Catalysis of guanine nucleotide exchange on Ran by the mitotic regulator RCC1 | Q24311327 | ||
Transportin-mediated nuclear import of heterogeneous nuclear RNP proteins | Q24312051 | ||
Identification of a tRNA-specific nuclear export receptor | Q24314506 | ||
mRNA binding protein mrnp 41 localizes to both nucleus and cytoplasm | Q24322800 | ||
A cap-binding protein complex mediating U snRNA export | Q24336104 | ||
Inhibition of human immunodeficiency virus Rev and human T-cell leukemia virus Rex function, but not Mason-Pfizer monkey virus constitutive transport element activity, by a mutant human nucleoporin targeted to Crm1 | Q24523655 | ||
The role of exportin-t in selective nuclear export of mature tRNAs | Q24533485 | ||
TAP binds to the constitutive transport element (CTE) through a novel RNA-binding motif that is sufficient to promote CTE-dependent RNA export from the nucleus | Q24534064 | ||
The Mex67p-mediated nuclear mRNA export pathway is conserved from yeast to human | Q24534127 | ||
The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates | Q24539652 | ||
Identification of different roles for RanGDP and RanGTP in nuclear protein import | Q24561933 | ||
RanGAP1 induces GTPase activity of nuclear Ras-related Ran | Q24564044 | ||
Amphibian transcription factor IIIA proteins contain a sequence element functionally equivalent to the nuclear export signal of human immunodeficiency virus type 1 Rev | Q24568152 | ||
CRM1 is an export receptor for leucine-rich nuclear export signals | Q27860453 | ||
Nuclear export of the small ribosomal subunit requires the ran-GTPase cycle and certain nucleoporins. | Q27931933 | ||
GLE2, a Saccharomyces cerevisiae homologue of the Schizosaccharomyces pombe export factor RAE1, is required for nuclear pore complex structure and function | Q27933501 | ||
The yeast nucleoporin rip1p contributes to multiple export pathways with no essential role for its FG-repeat region. | Q27934181 | ||
Dbp5p, a cytosolic RNA helicase, is required for poly(A)+ RNA export | Q27934203 | ||
Nuclear mRNA export requires complex formation between Mex67p and Mtr2p at the nuclear pores. | Q27934517 | ||
Dbp5p/Rat8p is a yeast nuclear pore-associated DEAD-box protein essential for RNA export | Q27937989 | ||
A novel in vivo assay reveals inhibition of ribosomal nuclear export in ran-cycle and nucleoporin mutants | Q27939245 | ||
Exportin 1 (Crm1p) is an essential nuclear export factor | Q27939696 | ||
Mex67p, a novel factor for nuclear mRNA export, binds to both poly(A)+ RNA and nuclear pores | Q27940054 | ||
The human RAE1 gene is a functional homologue of Schizosaccharomyces pombe rae1 gene involved in nuclear export of Poly(A)+ RNA | Q28116098 | ||
The HIV-1 Rev activation domain is a nuclear export signal that accesses an export pathway used by specific cellular RNAs | Q28131708 | ||
Nucleocytoplasmic transport: the soluble phase | Q28131723 | ||
Protein import into nuclei: association and dissociation reactions involving transport substrate, transport factors, and nucleoporins | Q28131733 | ||
The nuclear pore complex: from molecular architecture to functional dynamics | Q28138909 | ||
The importin-beta family member Crm1p bridges the interaction between Rev and the nuclear pore complex during nuclear export | Q28254641 | ||
Identification of a nuclear export receptor for tRNA | Q28265348 | ||
TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus | Q28276214 | ||
The HIV-1 rev trans-activator acts through a structured target sequence to activate nuclear export of unspliced viral mRNA | Q28279502 | ||
The human Tap protein is a nuclear mRNA export factor that contains novel RNA-binding and nucleocytoplasmic transport sequences | Q28646657 | ||
HIV-1 structural gene expression requires the binding of multiple Rev monomers to the viral RRE: implications for HIV-1 latency | Q28646762 | ||
Evidence that HIV-1 Rev directly promotes the nuclear export of unspliced RNA | Q28646843 | ||
Identification of a signal for rapid export of proteins from the nucleus | Q29547742 | ||
CRM1 is responsible for intracellular transport mediated by the nuclear export signal | Q29547861 | ||
The asymmetric distribution of the constituents of the Ran system is essential for transport into and out of the nucleus | Q29616325 | ||
Nuclear export of different classes of RNA is mediated by specific factors | Q29618449 | ||
Shuttling of pre-mRNA binding proteins between nucleus and cytoplasm | Q29618907 | ||
Transport of proteins and RNAs in and out of the nucleus | Q29619554 | ||
The GTP-binding protein Ran/TC4 is required for protein import into the nucleus | Q29620192 | ||
Evidence for a role of CRM1 in signal-mediated nuclear protein export | Q29620231 | ||
The constitutive transport element (CTE) of Mason-Pfizer monkey virus (MPMV) accesses a cellular mRNA export pathway | Q30448360 | ||
A small element from the Mason-Pfizer monkey virus genome makes human immunodeficiency virus type 1 expression and replication Rev-independent | Q30454030 | ||
Leptomycin B inhibits equine infectious anemia virus Rev and feline immunodeficiency virus rev function but not the function of the hepatitis B virus posttranscriptional regulatory element | Q33784046 | ||
The K nuclear shuttling domain: a novel signal for nuclear import and nuclear export in the hnRNP K protein | Q33886877 | ||
A second post-transcriptional trans-activator gene required for HTLV-III replication | Q34162178 | ||
The hnRNP C proteins contain a nuclear retention sequence that can override nuclear export signals | Q36237427 | ||
Nuclear tRNA aminoacylation and its role in nuclear export of endogenous tRNAs in Saccharomyces cerevisiae | Q36745203 | ||
Splicing is required for rapid and efficient mRNA export in metazoans | Q36776804 | ||
tRNA transport from the nucleus in a eukaryotic cell: carrier-mediated translocation process | Q37512771 | ||
The arginine-rich domains present in human immunodeficiency virus type 1 Tat and Rev function as direct importin beta-dependent nuclear localization signals | Q39610897 | ||
A functional homologue of the RNA1 gene product in Schizosaccharomyces pombe: purification, biochemical characterization, and identification of a leucine-rich repeat motif | Q40365606 | ||
A look at messenger RNP moving through the nuclear pore | Q41367422 | ||
RNA transport | Q41369752 | ||
Facilitated nuclear transport of histone H1 and other small nucleophilic proteins | Q41740214 | ||
Regulation by HIV Rev depends upon recognition of splice sites | Q41758926 | ||
Coordination of tRNA nuclear export with processing of tRNA. | Q41845245 | ||
The NES-Crm1p export pathway is not a major mRNA export route in Saccharomyces cerevisiae | Q42676980 | ||
The simian retrovirus-1 constitutive transport element, unlike the HIV-1 RRE, uses factors required for cellular mRNA export | Q44103395 | ||
Retroviruses as model systems for the study of nuclear RNA export pathways | Q45345414 | ||
A pre-mRNA-binding protein accompanies the RNA from the gene through the nuclear pores and into polysomes | Q48066850 | ||
Proofreading and aminoacylation of tRNAs before export from the nucleus. | Q50741048 | ||
Monomethylated cap structures facilitate RNA export from the nucleus. | Q50804073 | ||
Intranuclear location of the tRNA splicing enzymes | Q57385024 | ||
Functional dissection of the HIV-1 Rev trans-activator—Derivation of a trans-dominant repressor of Rev function | Q58611466 | ||
Some cis- and trans-acting mutants for splicing target pre-mRNA to the cytoplasm | Q69502444 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 4181-4187 | |
P577 | publication date | 2000-06-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | Nuclear RNA export pathways. | |
P478 | volume | 20 |
Q50719993 | A Ran-independent pathway for export of spliced mRNA. |
Q28364824 | A cis-acting element known to block 3' mRNA degradation enhances expression of polyA-minus mRNA in wild-type yeast cells and phenocopies a ski mutant |
Q34354274 | A new view of mRNA export: separating the wheat from the chaff |
Q24683176 | A nuclear kinesin-like protein interacts with and stimulates the activity of the leucine-rich nuclear export signal of the human immunodeficiency virus type 1 rev protein |
Q24675650 | An essential role for hGle1 nucleocytoplasmic shuttling in mRNA export |
Q39775287 | Analysis of bovine foamy virus btas mRNA transcripts during persistent infection |
Q34077876 | Box C/D small nucleolar RNA trafficking involves small nucleolar RNP proteins, nucleolar factors and a novel nuclear domain |
Q44030629 | Cajal body dynamics and association with chromatin are ATP-dependent |
Q38302290 | Control of nuclear export of hnRNP A1. |
Q45383937 | DNA constructs expressing long-hairpin RNA (lhRNA) protect Penaeus monodon against White Spot Syndrome Virus |
Q22242227 | Destiny of Unspliced Retroviral RNA: Ribosome and/or Virion? |
Q30493932 | Diffusion-based transport of nascent ribosomes in the nucleus |
Q38212068 | Dynamic Post-Transcriptional Regulation of HIV-1 Gene Expression |
Q34347652 | Epstein-Barr virus mRNA export factor EB2 is essential for production of infectious virus |
Q44638975 | Evaluating the role of CRM1-mediated export for adenovirus gene expression |
Q39586522 | Evidence for a posttranscriptional role of a TFIIICalpha-like protein in Chironomus tentans |
Q24538228 | Formation of Tap/NXT1 heterodimers activates Tap-dependent nuclear mRNA export by enhancing recruitment to nuclear pore complexes |
Q28209036 | Functional analysis of the interaction of the human immunodeficiency virus type 1 Rev nuclear export signal with its cofactors |
Q39683279 | Genomic but not antigenomic hepatitis delta virus RNA is preferentially exported from the nucleus immediately after synthesis and processing |
Q36363829 | Human CRM1 augments production of infectious human and feline immunodeficiency viruses from murine cells |
Q34856375 | Human immunodeficiency virus type 1 genetic recombination is more frequent than that of Moloney murine leukemia virus despite similar template switching rates |
Q42800068 | Human p32 protein relieves a post-transcriptional block to HIV replication in murine cells |
Q24538841 | ICP27 interacts with the RNA export factor Aly/REF to direct herpes simplex virus type 1 intronless mRNAs to the TAP export pathway |
Q34552631 | ICP27 selectively regulates the cytoplasmic localization of a subset of viral transcripts in herpes simplex virus type 1-infected cells |
Q64065729 | Identification of charged amino acids required for nuclear localization of human L1 ORF1 protein |
Q36859268 | Imaging and characterizing influenza A virus mRNA transport in living cells |
Q28215961 | In vitro analysis of nuclear transport mediated by the C-terminal shuttle domain of Tap |
Q24529536 | Influenza B and C virus NEP (NS2) proteins possess nuclear export activities |
Q39601251 | Interaction of the influenza virus nucleoprotein with the cellular CRM1-mediated nuclear export pathway |
Q28587170 | Members of the tristetraprolin family of tandem CCCH zinc finger proteins exhibit CRM1-dependent nucleocytoplasmic shuttling |
Q35786108 | Minimal introns are not "junk". |
Q24674855 | NXT1 is necessary for the terminal step of Crm1-mediated nuclear export |
Q35079139 | New insights into the nuclear localization of retroviral Gag proteins |
Q35241432 | Nuclear Factor 90, a cellular dsRNA binding protein inhibits the HIV Rev-export function |
Q34021302 | Nuclear entry and CRM1-dependent nuclear export of the Rous sarcoma virus Gag polyprotein. |
Q34286048 | Nuclear export of mRNA. |
Q30453281 | Nuclear interactions are necessary for translational enhancement by spleen necrosis virus RU5. |
Q46948332 | Nucleocytoplasmic transport of fluorescent mRNA in living mammalian cells: nuclear mRNA export is coupled to ongoing gene transcription. |
Q33338619 | PAUSED, a putative exportin-t, acts pleiotropically in Arabidopsis development but is dispensable for viability |
Q35920650 | PSF acts through the human immunodeficiency virus type 1 mRNA instability elements to regulate virus expression |
Q59132651 | Posttranscriptional Regulation of HIV-1 Gene Expression during Replication and Reactivation from Latency by Nuclear Matrix Protein MATR3 |
Q40196922 | RNA binding by the herpes simplex virus type 1 nucleocytoplasmic shuttling protein UL47 is mediated by an N-terminal arginine-rich domain that also functions as its nuclear localization signal |
Q37997897 | RNA polymerase II transcription on the fast lane |
Q33854295 | RNA splicing at human immunodeficiency virus type 1 3' splice site A2 is regulated by binding of hnRNP A/B proteins to an exonic splicing silencer element |
Q34348421 | RU5 of Mason-Pfizer monkey virus 5' long terminal repeat enhances cytoplasmic expression of human immunodeficiency virus type 1 gag-pol and nonviral reporter RNA. |
Q47965509 | Rae1-mediated nuclear export of Rnc1 is an important determinant in controlling MAPK signaling. |
Q28646696 | Recruitment of the Crm1 nuclear export factor is sufficient to induce cytoplasmic expression of incompletely spliced human immunodeficiency virus mRNAs |
Q34323793 | Regulation of nuclear gamma interferon gene expression by interleukin 12 (IL-12) and IL-2 represents a novel form of posttranscriptional control |
Q39536459 | Rhesus monkey rhadinovirus ORF57 induces gH and gL glycoprotein expression through posttranscriptional accumulation of target mRNAs |
Q34351276 | Robust growth of human immunodeficiency virus type 1 (HIV-1) |
Q36460462 | Robust suppression of HIV replication by intracellularly expressed reverse transcriptase aptamers is independent of ribozyme processing |
Q27640483 | Structural basis for the interaction between the Tap/NXF1 UBA domain and FG nucleoporins at 1A resolution |
Q41836703 | The Ref/Aly proteins are dispensable for mRNA export and development in Caenorhabditis elegans |
Q27637917 | The crystal structure and mutational analysis of a novel RNA-binding domain found in the human Tap nuclear mRNA export factor |
Q33292323 | The human endogenous retrovirus K Rev response element coincides with a predicted RNA folding region |
Q24291654 | Two closely related human nuclear export factors utilize entirely distinct export pathways |
Q28365327 | Using viral species specificity to define a critical protein/RNA interaction surface |
Q27931437 | Utp8p is an essential intranuclear component of the nuclear tRNA export machinery of Saccharomyces cerevisiae |
Q40763108 | Viral regulation of mRNA export |
Q36119000 | eIF4E is a central node of an RNA regulon that governs cellular proliferation |
Q34169710 | mRNA quality control: Marking the message for life or death. |
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