| P2093 | author name string | Domenico Libri | |
| | Mathieu Rougemaille | |
| | Tommaso Villa | |
| | Rajani Kanth Gudipati | |
| P2860 | cites work | The role of nuclear cap binding protein Cbc1p of yeast in mRNA termination and degradation | Q39452112 |
| | Nuclear export of heat shock and non-heat-shock mRNA occurs via similar pathways | Q39453461 |
| | Hpr1 is preferentially required for transcription of either long or G+C-rich DNA sequences in Saccharomyces cerevisiae. | Q39528577 |
| | A nuclear surveillance pathway for mRNAs with defective polyadenylation. | Q39613458 |
| | Nuclear export of mRNA by TAP/NXF1 requires two nucleoporin-binding sites but not p15. | Q39675094 |
| | Intron status and 3'-end formation control cotranscriptional export of mRNA. | Q39864388 |
| | HPR1 encodes a global positive regulator of transcription in Saccharomyces cerevisiae | Q40015882 |
| | Yra1p, a conserved nuclear RNA-binding protein, interacts directly with Mex67p and is required for mRNA export | Q40386970 |
| | The yeast HPR1 gene has a functional role in transcriptional elongation that uncovers a novel source of genome instability | Q40444246 |
| | The RNA processing exosome is linked to elongating RNA polymerase II in Drosophila | Q40682391 |
| | Inefficient processing impairs release of RNA from the site of transcription | Q40954153 |
| | Biochemical analysis of TREX complex recruitment to intronless and intron-containing yeast genes | Q41062668 |
| | NOP3 is an essential yeast protein which is required for pre-rRNA processing | Q41948335 |
| | Recombination between DNA repeats in yeast hpr1delta cells is linked to transcription elongation | Q41950317 |
| | Uncoupling yeast intron recognition from transcription with recursive splicing | Q41961425 |
| | 3'-end formation signals modulate the association of genes with the nuclear periphery as well as mRNP dot formation | Q42076115 |
| | Crystal structure of UAP56, a DExD/H-box protein involved in pre-mRNA splicing and mRNA export | Q42632936 |
| | The DExH/D box protein HEL/UAP56 is essential for mRNA nuclear export in Drosophila | Q43790549 |
| | Processing of 3'-extended read-through transcripts by the exosome can generate functional mRNAs. | Q44042962 |
| | Genome-wide analysis of mRNAs regulated by the THO complex in Drosophila melanogaster | Q47072314 |
| | Molecular evidence that the eukaryotic THO/TREX complex is required for efficient transcription elongation | Q50336100 |
| | Relationship between G+C content, ORF-length and mRNA concentration in Saccharomyces cerevisiae. | Q53860842 |
| | A nuclear cap-binding complex facilitates association of U1 snRNP with the cap-proximal 5' splice site. | Q55066526 |
| | Modulation of Transcription Affects mRNP Quality | Q57024543 |
| | The Yeast Nuclear Cap Binding Complex Can Interact with Translation Factor eIF4G and Mediate Translation Initiation | Q57378139 |
| | Structural basis for the recognition of a nucleoporin FG repeat by the NTF2-like domain of the TAP/p15 mRNA nuclear export factor | Q24291748 |
| | TREX is a conserved complex coupling transcription with messenger RNA export | Q24295211 |
| | Recruitment of the human TREX complex to mRNA during splicing | Q24306879 |
| | Biochemical characterization of the ATPase and helicase activity of UAP56, an essential pre-mRNA splicing and mRNA export factor | Q24309374 |
| | A nuclear cap binding protein complex involved in pre-mRNA splicing | Q24318104 |
| | A cap-binding protein complex mediating U snRNA export | Q24336104 |
| | Human mRNA export machinery recruited to the 5' end of mRNA | Q24338302 |
| | The Mex67p-mediated nuclear mRNA export pathway is conserved from yeast to human | Q24534127 |
| | Formation of Tap/NXT1 heterodimers activates Tap-dependent nuclear mRNA export by enhancing recruitment to nuclear pore complexes | Q24538228 |
| | NXT1 (p15) is a crucial cellular cofactor in TAP-dependent export of intron-containing RNA in mammalian cells | Q24550980 |
| | The structure of the mRNA export factor TAP reveals a cis arrangement of a non-canonical RNP domain and an LRR domain | Q27627787 |
| | Structure of the C-terminal FG-nucleoporin binding domain of Tap/NXF1 | Q27638140 |
| | Structural basis for the interaction between the Tap/NXF1 UBA domain and FG nucleoporins at 1A resolution | Q27640483 |
| | Structural similarity in the absence of sequence homology of the messenger RNA export factors Mtr2 and p15. | Q27641540 |
| | The Mtr2-Mex67 NTF2-like domain complex. Structural insights into a dual role of Mtr2 for yeast nuclear export | Q27642213 |
| | A protein complex containing Tho2, Hpr1, Mft1 and a novel protein, Thp2, connects transcription elongation with mitotic recombination in Saccharomyces cerevisiae | Q27929512 |
| | The yeast THO complex and mRNA export factors link RNA metabolism with transcription and genome instability | Q27929526 |
| | Stable mRNP formation and export require cotranscriptional recruitment of the mRNA export factors Yra1p and Sub2p by Hpr1p | Q27929754 |
| | Differential export requirements for shuttling serine/arginine-type mRNA-binding proteins | Q27930601 |
| | Nab2p and the Thp1p-Sac3p complex functionally interact at the interface between transcription and mRNA metabolism | Q27930687 |
| | Binding of the Mex67p/Mtr2p heterodimer to FXFG, GLFG, and FG repeat nucleoporins is essential for nuclear mRNA export. | Q27931219 |
| | Identification of a regulated pathway for nuclear pre-mRNA turnover. | Q27931532 |
| | A protein that shuttles between the nucleus and the cytoplasm is an important mediator of RNA export | Q27931607 |
| | Mtr10p functions as a nuclear import receptor for the mRNA-binding protein Npl3p | Q27931616 |
| | The mRNA export machinery requires the novel Sac3p-Thp1p complex to dock at the nucleoplasmic entrance of the nuclear pores | Q27931766 |
| | Mex67p mediates nuclear export of a variety of RNA polymerase II transcripts. | Q27932044 |
| | Cryptic pol II transcripts are degraded by a nuclear quality control pathway involving a new poly(A) polymerase | Q27932117 |
| | Phosphorylation by Sky1p promotes Npl3p shuttling and mRNA dissociation. | Q27932171 |
| | Dissecting mechanisms of nuclear mRNA surveillance in THO/sub2 complex mutants | Q27932830 |
| | The C-terminal domain of myosin-like protein 1 (Mlp1p) is a docking site for heterogeneous nuclear ribonucleoproteins that are required for mRNA export | Q27932831 |
| | Quality control of mRNA 3'-end processing is linked to the nuclear exosome | Q27932977 |
| | The yeast splicing factor Mud13p is a commitment complex component and corresponds to CBP20, the small subunit of the nuclear cap-binding complex | Q27933398 |
| | Identification and characterization of yUAP/Sub2p, a yeast homolog of the essential human pre-mRNA splicing factor hUAP56 | Q27933901 |
| | Perinuclear Mlp proteins downregulate gene expression in response to a defect in mRNA export | Q27933999 |
| | A nuclear 3'-5' exonuclease involved in mRNA degradation interacts with Poly(A) polymerase and the hnRNA protein Npl3p | Q27934140 |
| | Yeast poly(A)-binding protein, Pab1, and PAN, a poly(A) nuclease complex recruited by Pab1, connect mRNA biogenesis to export | Q27934476 |
| | Nuclear mRNA export requires complex formation between Mex67p and Mtr2p at the nuclear pores. | Q27934517 |
| | Dual requirement for yeast hnRNP Nab2p in mRNA poly(A) tail length control and nuclear export | Q27934522 |
| | NAB2: a yeast nuclear polyadenylated RNA-binding protein essential for cell viability | Q27934906 |
| | Cotranscriptional recruitment of the serine-arginine-rich (SR)-like proteins Gbp2 and Hrb1 to nascent mRNA via the TREX complex | Q27935984 |
| | A novel yeast gene, THO2, is involved in RNA pol II transcription and provides new evidence for transcriptional elongation-associated recombination. | Q27936954 |
| | Sus1, a functional component of the SAGA histone acetylase complex and the nuclear pore-associated mRNA export machinery | Q27937843 |
| | SAGA interacting factors confine sub-diffusion of transcribed genes to the nuclear envelope | Q27937982 |
| | Functional specificity of shuttling hnRNPs revealed by genome-wide analysis of their RNA binding profiles | Q27938114 |
| | Genome-wide analysis of RNA-protein interactions illustrates specificity of the mRNA export machinery | Q27938364 |
| | A distinct and parallel pathway for the nuclear import of an mRNA-binding protein | Q27938430 |
| | Messenger RNAs are recruited for nuclear export during transcription | Q27938581 |
| | Interactions between mRNA export commitment, 3'-end quality control, and nuclear degradation | Q27938985 |
| | Splicing factor Sub2p is required for nuclear mRNA export through its interaction with Yra1p | Q27939091 |
| | The DECD box putative ATPase Sub2p is an early mRNA export factor | Q27939448 |
| | Nuclear retention of unspliced mRNAs in yeast is mediated by perinuclear Mlp1. | Q27939910 |
| | Degradation of normal mRNA in the nucleus of Saccharomyces cerevisiae | Q35169986 |
| | Cotranscriptional mRNP assembly: from the DNA to the nuclear pore | Q36131482 |
| | TREX, SR proteins and export of mRNA. | Q36131499 |
| | Process or perish: quality control in mRNA biogenesis | Q36149583 |
| | Yeast cap binding complex impedes recruitment of cleavage factor IA to weak termination sites. | Q36177468 |
| | HPR1, a novel yeast gene that prevents intrachromosomal excision recombination, shows carboxy-terminal homology to the Saccharomyces cerevisiae TOP1 gene. | Q36755129 |
| | A mutant nuclear protein with similarity to RNA binding proteins interferes with nuclear import in yeast | Q37373645 |
| | Genome-wide mRNA surveillance is coupled to mRNA export | Q37598853 |
| | Yeast shuttling SR proteins Npl3p, Gbp2p, and Hrb1p are part of the translating mRNPs, and Npl3p can function as a translational repressor | Q37622680 |
| | The role of poly(A) in the translation and stability of mRNA. | Q37803773 |
| | The yeast hnRNP-Like proteins Yra1p and Yra2p participate in mRNA export through interaction with Mex67p | Q27939919 |
| | Mex67p, a novel factor for nuclear mRNA export, binds to both poly(A)+ RNA and nuclear pores | Q27940054 |
| | U2AF65 recruits a novel human DEAD box protein required for the U2 snRNP-branchpoint interaction | Q28245108 |
| | RNA-quality control by the exosome | Q28251052 |
| | TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus | Q28276214 |
| | The polymyositis-scleroderma autoantigen interacts with the helix-loop-helix proteins E12 and E47 | Q28566852 |
| | REF, an evolutionary conserved family of hnRNP-like proteins, interacts with TAP/Mex67p and participates in mRNA nuclear export. | Q28587508 |
| | Transitions in RNA polymerase II elongation complexes at the 3' ends of genes | Q29614767 |
| | Distinction and relationship between elongation rate and processivity of RNA polymerase II in vivo | Q29619233 |
| | A single gene from yeast for both nuclear and cytoplasmic polyadenylate-binding proteins: domain structure and expression | Q29620266 |
| | Crystal structure of the human ATP-dependent splicing and export factor UAP56. | Q33581257 |
| | Poly(A) tail length control in Saccharomyces cerevisiae occurs by message-specific deadenylation. | Q33781517 |
| | A block to mRNA nuclear export in S. cerevisiae leads to hyperadenylation of transcripts that accumulate at the site of transcription | Q33945461 |
| | The Saccharomyces cerevisiae hyperrecombination mutant hpr1Delta is synthetically lethal with two conditional alleles of the acetyl coenzyme A carboxylase gene and causes a defect in nuclear export of polyadenylated RNA. | Q33957885 |
| | A synthetic A tail rescues yeast nuclear accumulation of a ribozyme-terminated transcript | Q33983114 |
| | Formation of export-competent mRNP: escaping nuclear destruction | Q33987252 |
| | A nuclear degradation pathway controls the abundance of normal mRNAs in Saccharomyces cerevisiae | Q34048174 |
| | Cotranscriptionally Formed DNA:RNA Hybrids Mediate Transcription Elongation Impairment and Transcription-Associated Recombination | Q34267573 |
| | T7 RNA polymerase-directed transcripts are processed in yeast and link 3' end formation to mRNA nuclear export | Q34364453 |
| | UAP56 levels affect viability and mRNA export in Caenorhabditis elegans | Q34365217 |
| | Localization of nuclear retained mRNAs in Saccharomyces cerevisiae | Q34365269 |
| | Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors | Q34419716 |
| | mRNA export: travelling with DEAD box proteins | Q34453016 |
| | Nuclear localization of poly(A)+ mRNA following siRNA reduction of expression of the mammalian RNA helicases UAP56 and URH49. | Q34562813 |
| | Nuclear RNA turnover | Q34574303 |
| | Quality control of eukaryotic mRNA: safeguarding cells from abnormal mRNA function | Q34658630 |
| | Genome-wide analysis of nuclear mRNA export pathways in Drosophila | Q35016875 |
| | Polyadenylation: a tail of two complexes. | Q35033251 |
| | Deletion of MUD2, the yeast homolog of U2AF65, can bypass the requirement for sub2, an essential spliceosomal ATPase | Q35076313 |
| | Multiple roles for the yeast SUB2/yUAP56 gene in splicing | Q35076347 |
| | Genes with internal repeats require the THO complex for transcription | Q35080678 |
| | Cotranscriptional recruitment to the mRNA export receptor Mex67p contributes to nuclear pore anchoring of activated genes | Q35131387 |
| | Ubiquitin-associated domain of Mex67 synchronizes recruitment of the mRNA export machinery with transcription | Q35133832 |
| | Early formation of mRNP: license for export or quality control? | Q35137961 |
| | The interplay of nuclear mRNP assembly, mRNA surveillance and export | Q35147368 |
| P433 | issue | 6 | |
| P921 | main subject | cytoplasm | Q79899 |
| P1104 | number of pages | 16 | |
| P304 | page(s) | 327-342 | |
| P577 | publication date | 2008-06-01 | |
| P1433 | published in | Biology of the Cell | Q1254604 |
| P1476 | title | mRNA journey to the cytoplasm: attire required | |
| P478 | volume | 100 | |