| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Katrin Karbstein | Q55172448 |
| P2093 | author name string | Bethany S Strunk | |
| P2860 | cites work | A conserved rRNA methyltransferase regulates ribosome biogenesis | Q81026237 |
| FLO11 mediated filamentous growth of the yeast Saccharomyces cerevisiae depends on the expression of the ribosomal RPS26 genes | Q83834994 | ||
| Functional organization of the yeast proteome by systematic analysis of protein complexes | Q24292209 | ||
| The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction | Q24292709 | ||
| 90S pre-ribosomes include the 35S pre-rRNA, the U3 snoRNP, and 40S subunit processing factors but predominantly lack 60S synthesis factors | Q24302526 | ||
| Parvulin (Par14), a peptidyl-prolyl cis-trans isomerase, is a novel rRNA processing factor that evolved in the metazoan lineage | Q24315973 | ||
| Roles of the HEAT repeat proteins Utp10 and Utp20 in 40S ribosome maturation | Q24321927 | ||
| Nog2p, a putative GTPase associated with pre-60S subunits and required for late 60S maturation steps | Q24535952 | ||
| Mutational analysis of human eIF4AIII identifies regions necessary for exon junction complex formation and nonsense-mediated mRNA decay | Q24541400 | ||
| Functional link between ribosome formation and biogenesis of iron-sulfur proteins | Q24556663 | ||
| The rRNA-processing function of the yeast U14 small nucleolar RNA can be rescued by a conserved RNA helicase-like protein | Q24645774 | ||
| ATP hydrolysis is required for DEAD-box protein recycling but not for duplex unwinding | Q24646651 | ||
| Negative regulation of calcineurin signaling by Hrr25p, a yeast homolog of casein kinase I | Q24646875 | ||
| Analysis of phosphorylation sites on proteins from Saccharomyces cerevisiae by electron transfer dissociation (ETD) mass spectrometry | Q24671750 | ||
| Sequential protein association with nascent 60S ribosomal particles | Q24683118 | ||
| Phosphorylation of mammalian eukaryotic translation initiation factor 6 and its Saccharomyces cerevisiae homologue Tif6p: evidence that phosphorylation of Tif6p regulates its nucleocytoplasmic distribution and is required for yeast cell growth | Q24684104 | ||
| The comparative RNA web (CRW) site: an online database of comparative sequence and structure information for ribosomal, intron, and other RNAs | Q24802442 | ||
| A role for ubiquitin in the clearance of nonfunctional rRNAs | Q27939416 | ||
| Comprehensive mutational analysis of yeast DEXD/H box RNA helicases required for small ribosomal subunit synthesis | Q27939616 | ||
| The tails of ubiquitin precursors are ribosomal proteins whose fusion to ubiquitin facilitates ribosome biogenesis | Q27939801 | ||
| Hrr25-dependent phosphorylation state regulates organization of the pre-40S subunit | Q27939836 | ||
| Esf2p, a U3-associated factor required for small-subunit processome assembly and compaction | Q27939988 | ||
| Quantitative analysis of snoRNA association with pre-ribosomes and release of snR30 by Rok1 helicase | Q27940047 | ||
| The Putative RNA Helicase Dbp4p Is Required for Release of the U14 snoRNA from Preribosomes in Saccharomyces cerevisiae | Q27940128 | ||
| The economics of ribosome biosynthesis in yeast | Q28131645 | ||
| Pseudouridine in RNA: what, where, how, and why | Q28141248 | ||
| The ATPase reaction cycle of yeast DNA topoisomerase II. Slow rates of ATP resynthesis and P(i) release | Q28189142 | ||
| Evolution of protein kinase signaling from yeast to man | Q28205635 | ||
| Nucleotide dependent motion and mechanism of action of p97/VCP | Q28237554 | ||
| Modification of proteins by ubiquitin and ubiquitin-like proteins | Q28244250 | ||
| The post-transcriptional steps of eukaryotic ribosome biogenesis | Q28276470 | ||
| SUMO and ubiquitin in the nucleus: different functions, similar mechanisms? | Q28280175 | ||
| Acid catalysis of the formation of the slow-folding species of RNase A: Evidence that the reaction is proline isomerization | Q28280847 | ||
| Inactivation of the RRB1-Pescadillo pathway involved in ribosome biogenesis induces chromosomal instability | Q28286418 | ||
| The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia | Q28297163 | ||
| Origin of the genetic code: a testable hypothesis based on tRNA structure, sequence, and kinetic proofreading | Q28776301 | ||
| A proteomics approach to understanding protein ubiquitination | Q29547312 | ||
| Classification and evolution of P-loop GTPases and related ATPases | Q29547655 | ||
| Structure of the 80S ribosome from Saccharomyces cerevisiae--tRNA-ribosome and subunit-subunit interactions | Q29614569 | ||
| Global analysis of protein phosphorylation in yeast | Q29615057 | ||
| Ribosome assembly in eukaryotes | Q29615231 | ||
| The DEAD-box protein family of RNA helicases | Q29615303 | ||
| DExD/H box RNA helicases: from generic motors to specific dissociation functions | Q29615304 | ||
| Toward a comprehensive atlas of the physical interactome of Saccharomyces cerevisiae | Q29615775 | ||
| Evolutionary relationships and structural mechanisms of AAA+ proteins | Q29617454 | ||
| Phosphoproteome analysis by mass spectrometry and its application to Saccharomyces cerevisiae | Q29618445 | ||
| Depletion of U14 small nuclear RNA (snR128) disrupts production of 18S rRNA in Saccharomyces cerevisiae | Q29618484 | ||
| Precision and functional specificity in mRNA decay | Q29618689 | ||
| A DNA integrity network in the yeast Saccharomyces cerevisiae | Q29618912 | ||
| A yeast small nuclear RNA is required for normal processing of pre-ribosomal RNA | Q29620542 | ||
| Yeast snR30 is a small nucleolar RNA required for 18S rRNA synthesis | Q29620872 | ||
| Pre-18S ribosomal RNA is structurally compacted into the SSU processome prior to being cleaved from nascent transcripts in Saccharomyces cerevisiae | Q30435434 | ||
| TOR regulates the subcellular distribution of DIM2, a KH domain protein required for cotranscriptional ribosome assembly and pre-40S ribosome export | Q30439960 | ||
| The nuclear poly(A) polymerase and Exosome cofactor Trf5 is recruited cotranscriptionally to nucleolar surveillance | Q30440025 | ||
| Ribosome biogenesis is sensed at the Start cell cycle checkpoint | Q30479027 | ||
| Structure of the Mammalian 80S Ribosome at 8.7 Å Resolution | Q27650283 | ||
| The GTPase superfamily: conserved structure and molecular mechanism | Q27860524 | ||
| Genomic expression programs in the response of yeast cells to environmental changes | Q27860823 | ||
| Systematic identification of protein complexes in Saccharomyces cerevisiae by mass spectrometry | Q27861116 | ||
| Analysis of the yeast kinome reveals a network of regulated protein localization during filamentous growth | Q27901593 | ||
| Roles of eukaryotic ribosomal proteins in maturation and transport of pre-18S rRNA and ribosome function | Q27929504 | ||
| Proteome survey reveals modularity of the yeast cell machinery | Q27929510 | ||
| Rok1p is a putative RNA helicase required for rRNA processing | Q27929771 | ||
| The Saccharomyces cerevisiae 60 S ribosome biogenesis factor Tif6p is regulated by Hrr25p-mediated phosphorylation | Q27929856 | ||
| TOR regulates late steps of ribosome maturation in the nucleoplasm via Nog1 in response to nutrients | Q27930104 | ||
| The novel ATP-binding cassette protein ARB1 is a shuttling factor that stimulates 40S and 60S ribosome biogenesis | Q27930124 | ||
| Absence of Dbp2p alters both nonsense-mediated mRNA decay and rRNA processing | Q27930125 | ||
| Dbp9p, a putative ATP-dependent RNA helicase involved in 60S-ribosomal-subunit biogenesis, functionally interacts with Dbp6p | Q27930128 | ||
| The essential ATP-binding cassette protein RLI1 functions in translation by promoting preinitiation complex assembly | Q27930137 | ||
| Nop53p is a novel nucleolar 60S ribosomal subunit biogenesis protein | Q27930263 | ||
| Spb4p, an essential putative RNA helicase, is required for a late step in the assembly of 60S ribosomal subunits in Saccharomyces cerevisiae. | Q27930317 | ||
| The NUG1 GTPase reveals and N-terminal RNA-binding domain that is essential for association with 60 S pre-ribosomal particles | Q27930393 | ||
| Characterization and mutational analysis of yeast Dbp8p, a putative RNA helicase involved in ribosome biogenesis | Q27930433 | ||
| RNA unwinding in U4/U6 snRNPs requires ATP hydrolysis and the DEIH-box splicing factor Brr2 | Q27930438 | ||
| The carboxy-terminal extension of yeast ribosomal protein S14 is necessary for maturation of 43S preribosomes. | Q27930542 | ||
| The small nucleolar RNP protein NOP1 (fibrillarin) is required for pre-rRNA processing in yeast | Q27931405 | ||
| Utp8p is an essential intranuclear component of the nuclear tRNA export machinery of Saccharomyces cerevisiae | Q27931437 | ||
| The essential protein fap7 is involved in the oxidative stress response of Saccharomyces cerevisiae | Q27931493 | ||
| Bms1p, a novel GTP-binding protein, and the related Tsr1p are required for distinct steps of 40S ribosome biogenesis in yeast | Q27931503 | ||
| Fal1p is an essential DEAD-box protein involved in 40S-ribosomal-subunit biogenesis in Saccharomyces cerevisiae | Q27931519 | ||
| SnR30: a new, essential small nuclear RNA from Saccharomyces cerevisiae | Q27931753 | ||
| The AAA ATPase Rix7 powers progression of ribosome biogenesis by stripping Nsa1 from pre-60S particles | Q27931771 | ||
| Mrd1p binds to pre-rRNA early during transcription independent of U3 snoRNA and is required for compaction of the pre-rRNA into small subunit processomes | Q27932039 | ||
| Yeast Rio1p is the founding member of a novel subfamily of protein serine kinases involved in the control of cell cycle progression | Q27932332 | ||
| Dhr1p, a putative DEAH-box RNA helicase, is associated with the box C+D snoRNP U3. | Q27932355 | ||
| Genetic and biochemical interactions among Yar1, Ltv1 and Rps3 define novel links between environmental stress and ribosome biogenesis in Saccharomyces cerevisiae | Q27932544 | ||
| Potential interface between ribosomal protein production and pre-rRNA processing | Q27932630 | ||
| A genetic interaction map of RNA-processing factors reveals links between Sem1/Dss1-containing complexes and mRNA export and splicing | Q27932638 | ||
| A cold-sensitive mutation in 16S rRNA provides evidence for helical switching in ribosome assembly | Q46065755 | ||
| Autophosphorylation of Archaeoglobus fulgidus Rio2 and crystal structures of its nucleotide-metal ion complexes | Q46534829 | ||
| Structure and activity of the atypical serine kinase Rio1. | Q46594066 | ||
| A family portrait of the RIO kinases | Q46720404 | ||
| Pi release from eIF2, not GTP hydrolysis, is the step controlled by start-site selection during eukaryotic translation initiation | Q46772123 | ||
| Assembly mapping of 30S ribosomal proteins from E. coli | Q47773479 | ||
| Comprehensive comparison of structural characteristics in eukaryotic cytoplasmic large subunit (23 S-like) ribosomal RNA. | Q48065638 | ||
| Architecture of the protein-conducting channel associated with the translating 80S ribosome | Q49485686 | ||
| Protein kinase CK2 activates the atypical Rio1p kinase and promotes its cell-cycle phase-dependent degradation in yeast. | Q53531835 | ||
| Probing the secondary structure of expansion segment ES6 in 18S ribosomal RNA. | Q53615525 | ||
| The DnaK chaperone system facilitates 30S ribosomal subunit assembly. | Q54540763 | ||
| RIO1, an extraordinary novel protein kinase. | Q54541475 | ||
| Incorporation of six additional proteins to complete the assembly map of the 50 S subunit from Escherichia coli ribosomes. | Q54764108 | ||
| Formation and Nuclear Export of Preribosomes Are Functionally Linked to the Small-Ubiquitin-Related Modifier Pathway | Q56479771 | ||
| The synthetic genetic interaction spectrum of essential genes | Q56880004 | ||
| Functional base-pairing interaction between highly conserved elements of U3 small nucleolar RNA and the small ribosomal subunit RNA | Q56903372 | ||
| A Proteome-wide Approach Identifies Sumoylated Substrate Proteins in Yeast | Q58001295 | ||
| Going through the motions: The ATPase cycle of p97 | Q61863733 | ||
| Pyruvate kinase: is the mechanism of phospho transfer associative or dissociative? | Q70537556 | ||
| Crystal structure of unmodified tRNA(Gln) complexed with glutaminyl-tRNA synthetase and ATP suggests a possible role for pseudo-uridines in stabilization of RNA structure | Q72015576 | ||
| Ribosome synthesis during the growth cycle of Saccharomyces cerevisiae | Q72515066 | ||
| Overexpression of mitogen-activated protein kinase kinase kinase reversed cAMP inhibition of NF-kappaB in T cells | Q73043289 | ||
| In vitro reconstitution of 30S ribosomal subunits using complete set of recombinant proteins | Q73979825 | ||
| Modeling a minimal ribosome based on comparative sequence analysis | Q74529126 | ||
| Ria1p (Ynl163c), a protein similar to elongation factors 2, is involved in the biogenesis of the 60S subunit of the ribosome in Saccharomyces cerevisiae | Q77193691 | ||
| rRNA modifications in an intersubunit bridge of the ribosome strongly affect both ribosome biogenesis and activity | Q80407834 | ||
| A large nucleolar U3 ribonucleoprotein required for 18S ribosomal RNA biogenesis | Q27937306 | ||
| Dbp6p is an essential putative ATP-dependent RNA helicase required for 60S-ribosomal-subunit assembly in Saccharomyces cerevisiae | Q27937592 | ||
| High-definition macromolecular composition of yeast RNA-processing complexes | Q27937860 | ||
| Translation initiation and ribosomal biogenesis: involvement of a putative rRNA helicase and RPL46. | Q27937908 | ||
| Temperature-sensitive mutations demonstrate roles for yeast fibrillarin in pre-rRNA processing, pre-rRNA methylation, and ribosome assembly | Q27938039 | ||
| SUMO mediates interaction of Ebp2p, the yeast homolog of Epstein-Barr virus nuclear antigen 1-binding protein 2, with a RING finger protein Ris1p | Q27938373 | ||
| The nucle(ol)ar Tif6p and Efl1p are required for a late cytoplasmic step of ribosome synthesis. | Q27938566 | ||
| The nucleolar protein Esf2 interacts directly with the DExD/H box RNA helicase, Dbp8, to stimulate ATP hydrolysis | Q27938659 | ||
| Global landscape of protein complexes in the yeast Saccharomyces cerevisiae | Q27938796 | ||
| RNA polymerase I transcription and pre-rRNA processing are linked by specific SSU processome components | Q27938887 | ||
| Yph1p, an ORC-interacting protein: potential links between cell proliferation control, DNA replication, and ribosome biogenesis. | Q27938890 | ||
| Dob1p (Mtr4p) is a putative ATP-dependent RNA helicase required for the 3' end formation of 5.8S rRNA in Saccharomyces cerevisiae | Q27939006 | ||
| The putative NTPase Fap7 mediates cytoplasmic 20S pre-rRNA processing through a direct interaction with Rps14. | Q27939042 | ||
| The Saccharomyces cerevisiae homologue of mammalian translation initiation factor 6 does not function as a translation initiation factor | Q27939061 | ||
| Biogenesis of cytosolic ribosomes requires the essential iron-sulphur protein Rli1p and mitochondria | Q27939225 | ||
| Rea1, a dynein-related nuclear AAA-ATPase, is involved in late rRNA processing and nuclear export of 60 S subunits | Q27932924 | ||
| A nuclear AAA-type ATPase (Rix7p) is required for biogenesis and nuclear export of 60S ribosomal subunits | Q27932993 | ||
| Dbp7p, a putative ATP-dependent RNA helicase from Saccharomyces cerevisiae, is required for 60S ribosomal subunit assembly | Q27933064 | ||
| Dbp3p, a putative RNA helicase in Saccharomyces cerevisiae, is required for efficient pre-rRNA processing predominantly at site A3. | Q27933096 | ||
| Cytoplasmic recycling of 60S preribosomal factors depends on the AAA protein Drg1. | Q27933234 | ||
| RRP5 is required for formation of both 18S and 5.8S rRNA in yeast | Q27933500 | ||
| Rio2p, an evolutionarily conserved, low abundant protein kinase essential for processing of 20 S Pre-rRNA in Saccharomyces cerevisiae | Q27933528 | ||
| Genetic evidence for 18S rRNA binding and an Rps19p assembly function of yeast nucleolar protein Nep1p | Q27933577 | ||
| An essential GTPase promotes assembly of preribosomal RNA processing complexes | Q27933643 | ||
| Mak5p, which is required for the maintenance of the M1 dsRNA virus, is encoded by the yeast ORF YBR142w and is involved in the biogenesis of the 60S subunit of the ribosome | Q27933744 | ||
| Monopolar attachment of sister kinetochores at meiosis I requires casein kinase 1. | Q27934088 | ||
| The putative RNA helicase Dbp6p functionally interacts with Rpl3p, Nop8p and the novel trans-acting Factor Rsa3p during biogenesis of 60S ribosomal subunits in Saccharomyces cerevisiae | Q27934110 | ||
| The splicing factor Prp43p, a DEAH box ATPase, functions in ribosome biogenesis | Q27934180 | ||
| Surveillance of nuclear-restricted pre-ribosomes within a subnucleolar region of Saccharomyces cerevisiae | Q27934309 | ||
| Comprehensive analysis of diverse ribonucleoprotein complexes. | Q27934310 | ||
| Differential RNA-dependent ATPase activities of four rRNA processing yeast DEAD-box proteins | Q27934397 | ||
| The splicing ATPase prp43p is a component of multiple preribosomal particles | Q27934798 | ||
| HRR25, a putative protein kinase from budding yeast: association with repair of damaged DNA. | Q27934909 | ||
| Late cytoplasmic maturation of the small ribosomal subunit requires RIO proteins in Saccharomyces cerevisiae | Q27935036 | ||
| Ribosome synthesis in Saccharomyces cerevisiae | Q27935371 | ||
| The path from nucleolar 90S to cytoplasmic 40S pre-ribosomes | Q27935442 | ||
| DRS1 to DRS7, novel genes required for ribosome assembly and function in Saccharomyces cerevisiae | Q27935888 | ||
| Bms1p, a G-domain-containing protein, associates with Rcl1p and is required for 18S rRNA biogenesis in yeast. | Q27935958 | ||
| The putative GTPases Nog1p and Lsg1p are required for 60S ribosomal subunit biogenesis and are localized to the nucleus and cytoplasm, respectively | Q27935997 | ||
| Dbp10p, a putative RNA helicase from Saccharomyces cerevisiae, is required for ribosome biogenesis | Q27936135 | ||
| The helicase Has1p is required for snoRNA release from pre-rRNA. | Q27936348 | ||
| Prp43p is a DEAH-box spliceosome disassembly factor essential for ribosome biogenesis | Q27936468 | ||
| Dual function of eIF3j/Hcr1p in processing 20 S pre-rRNA and translation initiation | Q27936588 | ||
| An in vivo map of the yeast protein interactome | Q27936680 | ||
| Has1p, a member of the DEAD-box family, is required for 40S ribosomal subunit biogenesis in Saccharomyces cerevisiae. | Q27936868 | ||
| The PINc domain protein Utp24, a putative nuclease, is required for the early cleavage steps in 18S rRNA maturation | Q27936907 | ||
| The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast | Q27936929 | ||
| Ntr1 activates the Prp43 helicase to trigger release of lariat-intron from the spliceosome | Q27936960 | ||
| Regulation of ribosome biogenesis by the rapamycin-sensitive TOR-signaling pathway in Saccharomyces cerevisiae | Q27937080 | ||
| RNA helicases--one fold for many functions | Q36851634 | ||
| Regulation of Sli15/INCENP, kinetochore, and Cdc14 phosphatase functions by the ribosome biogenesis protein Utp7 | Q36890081 | ||
| The long unwinding road of RNA helicases | Q36902461 | ||
| Deconstructing ribosome construction | Q37013926 | ||
| DEAD-box proteins can completely separate an RNA duplex using a single ATP. | Q37068571 | ||
| The EF-G-like GTPase Snu114p regulates spliceosome dynamics mediated by Brr2p, a DExD/H box ATPase | Q37183473 | ||
| Concurrent nucleation of 16S folding and induced fit in 30S ribosome assembly | Q37289162 | ||
| The fast-growing business of SUMO chains | Q37321368 | ||
| A role for ubiquitin in the spliceosome assembly pathway | Q37332858 | ||
| Two mutant forms of the S1/TPR-containing protein Rrp5p affect the 18S rRNA synthesis in Saccharomyces cerevisiae | Q38330560 | ||
| The NOG1 GTP-binding protein is required for biogenesis of the 60 S ribosomal subunit | Q38353907 | ||
| Ribosome performance is enhanced by a rich cluster of pseudouridines in the A-site finger region of the large subunit | Q40420065 | ||
| Secondary structure model for bacterial 16S ribosomal RNA: phylogenetic, enzymatic and chemical evidence | Q40481405 | ||
| The ubiquitin-mediated proteolytic pathway: mechanisms of recognition of the proteolytic substrate and involvement in the degradation of native cellular proteins. | Q40720516 | ||
| DbpA: a DEAD box protein specifically activated by 23s rRNA. | Q40873887 | ||
| Protein folding. Prolyl isomerases join the fold | Q40935542 | ||
| Utp8p is a nucleolar tRNA-binding protein that forms a complex with components of the nuclear tRNA export machinery in Saccharomyces cerevisiae | Q41312753 | ||
| Reconstitution of functional 50S ribosomes from in vitro transcripts of Bacillus stearothermophilus 23S rRNA. | Q41608299 | ||
| 18S rRNA processing requires base pairings of snR30 H/ACA snoRNA to eukaryote-specific 18S sequences | Q42049785 | ||
| The Saccharomyces homolog of mammalian RACK1, Cpc2/Asc1p, is required for FLO11-dependent adhesive growth and dimorphism | Q42517635 | ||
| Loss of rRNA modifications in the decoding center of the ribosome impairs translation and strongly delays pre-rRNA processing | Q42554055 | ||
| The roles of Rrp5p in the synthesis of yeast 18S and 5.8S rRNA can be functionally and physically separated | Q42599827 | ||
| ROK1, a high-copy-number plasmid suppressor of kem1, encodes a putative ATP-dependent RNA helicase in Saccharomyces cerevisiae | Q42624322 | ||
| Mechanistic insight into the ribosome biogenesis functions of the ancient protein KsgA. | Q42921023 | ||
| S16 throws a conformational switch during assembly of 30S 5' domain | Q43078958 | ||
| A possible tertiary rRNA interaction between expansion segments ES3 and ES6 in eukaryotic 40S ribosomal subunits | Q43207023 | ||
| Secondary structure of two regions in expansion segments ES3 and ES6 with the potential of forming a tertiary interaction in eukaryotic 40S ribosomal subunits | Q43207560 | ||
| A pre-ribosome with a tadpole-like structure functions in ATP-dependent maturation of 60S subunits | Q44984067 | ||
| Crystal structure of A. fulgidus Rio2 defines a new family of serine protein kinases | Q30955879 | ||
| Yeast 18S rRNA dimethylase Dim1p: a quality control mechanism in ribosome synthesis? | Q32075110 | ||
| Release of the export adapter, Nmd3p, from the 60S ribosomal subunit requires Rpl10p and the cytoplasmic GTPase Lsg1p | Q33840719 | ||
| The regulation of protein function by multisite phosphorylation--a 25 year update | Q33928103 | ||
| A definition of the domains Archaea, Bacteria and Eucarya in terms of small subunit ribosomal RNA characteristics | Q34089680 | ||
| Ribosome structure and activity are altered in cells lacking snoRNPs that form pseudouridines in the peptidyl transferase center | Q34181714 | ||
| Assembly mapping of 30 S ribosomal proteins from Escherichia coli. Further studies. | Q34214234 | ||
| The 18S rRNA dimethylase Dim1p is required for pre-ribosomal RNA processing in yeast. | Q34297937 | ||
| Comprehensive mutational analysis of yeast DEXD/H box RNA helicases involved in large ribosomal subunit biogenesis | Q34353602 | ||
| The ATP switch model for ABC transporters | Q34353789 | ||
| Structural and mutational analysis of the SBDS protein family. Insight into the leukemia-associated Shwachman-Diamond Syndrome | Q34392501 | ||
| 18S rRNA processing requires the RNA helicase-like protein Rrp3. | Q34608155 | ||
| The essential Drosophila ATP-binding cassette domain protein, pixie, binds the 40 S ribosome in an ATP-dependent manner and is required for translation initiation | Q34613325 | ||
| DEAD-box proteins unwind duplexes by local strand separation | Q34707215 | ||
| Potential roles for ubiquitin and the proteasome during ribosome biogenesis | Q34718323 | ||
| Linear ubiquitin fusion to Rps31 and its subsequent cleavage are required for the efficient production and functional integrity of 40S ribosomal subunits | Q34942783 | ||
| Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome | Q34982627 | ||
| RNA-guided nucleotide modification of ribosomal and other RNAs | Q34997177 | ||
| DEAD-box RNA helicases in Escherichia coli | Q35100595 | ||
| Total reconstitution of functionally active 50S ribosomal subunits from Escherichia coli | Q35118896 | ||
| Rad50/SMC proteins and ABC transporters: unifying concepts from high-resolution structures. | Q35119766 | ||
| A superfamily of protein tags: ubiquitin, SUMO and related modifiers | Q35162583 | ||
| The F-box protein Dia2 overcomes replication impedance to promote genome stability in Saccharomyces cerevisiae. | Q35221545 | ||
| Identification of novel Escherichia coli ribosome-associated proteins using isobaric tags and multidimensional protein identification techniques | Q35759723 | ||
| Ribosome synthesis meets the cell cycle | Q35958186 | ||
| Crosstalk in gene expression: coupling and co-regulation of rDNA transcription, pre-ribosome assembly and pre-rRNA processing | Q36131510 | ||
| Rapid, transcript-specific changes in splicing in response to environmental stress | Q36151037 | ||
| Assembly map of the large subunit (50S) of Escherichia coli ribosomes | Q36279594 | ||
| Large-scale analysis of yeast filamentous growth by systematic gene disruption and overexpression. | Q36325980 | ||
| Association of yeast RNA polymerase I with a nucleolar substructure active in rRNA synthesis and processing | Q36327643 | ||
| Structure and function of E. coli ribosomes. V. Reconstitution of functionally active 30S ribosomal particles from RNA and proteins | Q36468269 | ||
| The yeast nucleolar protein Cbf5p is involved in rRNA biosynthesis and interacts genetically with the RNA polymerase I transcription factor RRN3. | Q36573301 | ||
| A surfeit of factors: why is ribosome assembly so much more complicated in eukaryotes than bacteria? | Q36694778 | ||
| Role of GTPases in ribosome assembly | Q36827375 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 2083-2104 | |
| P577 | publication date | 2009-10-22 | |
| P1433 | published in | RNA | Q7277164 |
| P1476 | title | Powering through ribosome assembly | |
| P478 | volume | 15 |
| Q41417382 | 18S rRNA: A Tale of the Tail |
| Q27689601 | 60S ribosome biogenesis requires rotation of the 5S ribonucleoprotein particle |
| Q34169572 | A RanGTP-independent mechanism allows ribosomal protein nuclear import for ribosome assembly |
| Q27930981 | A protein interaction map of the LSU processome |
| Q27931602 | A ribosome-anchored chaperone network that facilitates eukaryotic ribosome biogenesis |
| Q42547174 | A single acetylation of 18 S rRNA is essential for biogenesis of the small ribosomal subunit in Saccharomyces cerevisiae |
| Q35967994 | A temperature-sensitive allele of a putative mRNA splicing helicase down-regulates many cell wall genes and causes radial swelling in Arabidopsis thaliana. |
| Q27932368 | A translation-like cycle is a quality control checkpoint for maturing 40S ribosome subunits |
| Q41338625 | An RNA conformational switch regulates pre-18S rRNA cleavage. |
| Q43189145 | Arabidopsis sensitivity to protein synthesis inhibitors depends on 26S proteasome activity |
| Q34020217 | Arabidopsis thaliana XRN2 is required for primary cleavage in the pre-ribosomal RNA. |
| Q40014302 | Chaperoning ribosome assembly |
| Q52324603 | Characterization of mitochondrion-targeted GTPases in Plasmodium falciparum. |
| Q27937424 | Co-translational capturing of nascent ribosomal proteins by their dedicated chaperones |
| Q27936880 | Coupled GTPase and remodelling ATPase activities form a checkpoint for ribosome export |
| Q27684829 | Crucial role of the Rcl1p-Bms1p interaction for yeast pre-ribosomal RNA processing |
| Q61805385 | Cryo-EM structure of the essential ribosome assembly AAA-ATPase Rix7 |
| Q27678270 | Cryo-EM structures of the late-stage assembly intermediates of the bacterial 50S ribosomal subunit. |
| Q27675379 | Crystal structure of the eukaryotic 60S ribosomal subunit in complex with initiation factor 6 |
| Q33971823 | DEAD-box protein CYT-19 is activated by exposed helices in a group I intron RNA. |
| Q27937619 | Defining the pathway of cytoplasmic maturation of the 60S ribosomal subunit. |
| Q64106232 | Depletion of S-adenosylmethionine impacts on ribosome biogenesis through hypomodification of a single rRNA methylation |
| Q36931465 | Disruption of ribosome assembly in yeast blocks cotranscriptional pre-rRNA processing and affects the global hierarchy of ribosome biogenesis |
| Q33853137 | Dominant mutations in the late 40S biogenesis factor Ltv1 affect cytoplasmic maturation of the small ribosomal subunit in Saccharomyces cerevisiae |
| Q36010663 | Dynamics of oscillatory phenotypes in Saccharomyces cerevisiae reveal a network of genome-wide transcriptional oscillators |
| Q27934691 | Dynamics of the putative RNA helicase Spb4 during ribosome assembly in Saccharomyces cerevisiae |
| Q40103944 | Embryo defective 14 encodes a plastid-targeted cGTPase essential for embryogenesis in maize |
| Q37191855 | Essential ribosome assembly factor Fap7 regulates a hierarchy of RNA-protein interactions during small ribosomal subunit biogenesis |
| Q36849229 | Free energy rhythms in Saccharomyces cerevisiae: a dynamic perspective with implications for ribosomal biogenesis |
| Q35350030 | Functional interaction between ribosomal protein L6 and RbgA during ribosome assembly |
| Q34403421 | Functional ultrastructure of the plant nucleolus |
| Q34471561 | Genetic analysis of the ribosome biogenesis factor Ltv1 of Saccharomyces cerevisiae |
| Q84943272 | Getting ready to commit: ribosomes rehearse translation |
| Q39012254 | Hold on to your friends: Dedicated chaperones of ribosomal proteins: Dedicated chaperones mediate the safe transfer of ribosomal proteins to their site of pre-ribosome incorporation. |
| Q47782255 | How Ribosomes Translate Cancer. |
| Q27930417 | Hrr25/CK1δ-directed release of Ltv1 from pre-40S ribosomes is necessary for ribosome assembly and cell growth |
| Q28941757 | Human RioK3 is a novel component of cytoplasmic pre-40S pre-ribosomal particles |
| Q35770695 | Human nucleolar protein Nop52 (RRP1/NNP-1) is involved in site 2 cleavage in internal transcribed spacer 1 of pre-rRNAs at early stages of ribosome biogenesis |
| Q37921470 | Inside the 40S ribosome assembly machinery |
| Q38925007 | Insights into remodeling events during eukaryotic large ribosomal subunit assembly provided by high resolution cryo-EM structures |
| Q36079250 | Insights into the roles of local translation from the axonal transcriptome |
| Q43029071 | Interaction network of the ribosome assembly machinery from a eukaryotic thermophile. |
| Q90029511 | LYAR potentiates rRNA synthesis by recruiting BRD2/4 and the MYST-type acetyltransferase KAT7 to rDNA |
| Q34056383 | MDM2 mediates nonproteolytic polyubiquitylation of the DEAD-Box RNA helicase DDX24 |
| Q35061568 | Mak5 and Ebp2 act together on early pre-60S particles and their reduced functionality bypasses the requirement for the essential pre-60S factor Nsa1. |
| Q33877560 | Mammalian DEAD box protein Ddx51 acts in 3' end maturation of 28S rRNA by promoting the release of U8 snoRNA. |
| Q33838140 | Maturation of eukaryotic ribosomes: acquisition of functionality |
| Q41492546 | Mms21 SUMO Ligase Activity Promotes Nucleolar Function in Saccharomyces cerevisiae |
| Q91787698 | MoFap7, a ribosome assembly factor, is required for fungal development and plant colonization of Magnaporthe oryzae |
| Q41867681 | Monosome formation during translation initiation requires the serine/arginine-rich protein Npl3. |
| Q48269036 | Motoring toward pre-60S-ribosome export |
| Q37081615 | New twist to nuclear import: When two travel together |
| Q41599068 | Nmd3 is a structural mimic of eIF5A, and activates the cpGTPase Lsg1 during 60S ribosome biogenesis |
| Q37197869 | Non-FG mediated transport of the large pre-ribosomal subunit through the nuclear pore complex by the mRNA export factor Gle2 |
| Q38309688 | Noncoding RNAs in eukaryotic ribosome biogenesis and function |
| Q33682503 | Nucleating the assembly of macromolecular complexes. |
| Q58577976 | Nucleoli in embryos: a central structural platform for embryonic chromatin remodeling? |
| Q34278932 | One core, two shells: bacterial and eukaryotic ribosomes. |
| Q40603375 | Physical and functional interaction between the methyltransferase Bud23 and the essential DEAH-box RNA helicase Ecm16 |
| Q37490611 | Prefabrication of a ribosomal protein subcomplex essential for eukaryotic ribosome formation. |
| Q39071877 | Principles of 60S ribosomal subunit assembly emerging from recent studies in yeast. |
| Q33809292 | Protein-protein interactions within late pre-40S ribosomes. |
| Q38078677 | Quality control mechanisms during ribosome maturation |
| Q27025517 | RNA helicase proteins as chaperones and remodelers |
| Q24603646 | RNA helicases at work: binding and rearranging |
| Q27935945 | Rcl1 protein, a novel nuclease for 18 S ribosomal RNA production |
| Q36784712 | Regulation of ribosome biogenesis by nucleostemin 3 promotes local and systemic growth in Drosophila |
| Q36056785 | Ribosomal RNA of Hyacinthus orientalis L. female gametophyte cells before and after fertilization |
| Q24322643 | Ribosomal protein S3 interacts with the NF-κB inhibitor IκBα |
| Q33602516 | Ribosome assembly factors Pwp1 and Nop12 are important for folding of 5.8S rRNA during ribosome biogenesis in Saccharomyces cerevisiae |
| Q41615171 | Ribosome assembly factors prevent premature translation initiation by 40S assembly intermediates |
| Q47344527 | Ribosome biogenesis in cancer: new players and therapeutic avenues |
| Q97644685 | Ribosomes: An Exciting Avenue in Stem Cell Research |
| Q34457472 | Ribosomopathies and the paradox of cellular hypo- to hyperproliferation. |
| Q27934183 | Role of Mex67-Mtr2 in the nuclear export of 40S pre-ribosomes |
| Q36909178 | Rps14 haploinsufficiency causes a block in erythroid differentiation mediated by S100A8 and S100A9 |
| Q34485744 | RsgA releases RbfA from 30S ribosome during a late stage of ribosome biosynthesis |
| Q24596016 | SF1 and SF2 helicases: family matters |
| Q37953790 | SUMO routes ribosome maturation. |
| Q33889344 | Strong dependence between functional domains in a dual-function snoRNA infers coupling of rRNA processing and modification events |
| Q38433684 | Structural Heterogeneity in Pre-40S Ribosomes. |
| Q27683859 | Structural and Functional Insights into the Mode of Action of a Universally Conserved Obg GTPase |
| Q34579765 | Structural insights into the function of a unique tandem GTPase EngA in bacterial ribosome assembly |
| Q27937217 | Studies on the assembly characteristics of large subunit ribosomal proteins in S. cerevisae |
| Q57858865 | Surveillance pathways rescuing eukaryotic ribosomes lost in translation |
| Q89701706 | TAK1 signaling regulates p53 through a mechanism involving ribosomal stress |
| Q27927675 | Targeted proteomics reveals compositional dynamics of 60S pre-ribosomes after nuclear export |
| Q64066468 | Thallium(I) treatment induces nucleolar stress to stop protein synthesis and cell growth |
| Q42198200 | The AAA-ATPase Rea1 drives removal of biogenesis factors during multiple stages of 60S ribosome assembly. |
| Q27939534 | The DEAD-box RNA helicase-like Utp25 is an SSU processome component |
| Q42259142 | The G-patch protein NF-κB-repressing factor mediates the recruitment of the exonuclease XRN2 and activation of the RNA helicase DHX15 in human ribosome biogenesis. |
| Q42583695 | The Levinthal paradox of the interactome |
| Q37400206 | The Mutation of Glu at Amino Acid 3838 of AtMDN1 Provokes Pleiotropic Developmental Phenotypes in Arabidopsis |
| Q27937626 | The Roles of Puf6 and Loc1 in 60S Biogenesis Are Interdependent, and Both Are Required for Efficient Accommodation of Rpl43. |
| Q41186443 | The T-cell leukemia related rpl10-R98S mutant traps the 60S export adapter Nmd3 in the ribosomal P site in yeast |
| Q33635932 | The assembly factor Erb1 functions in multiple remodeling events during 60S ribosomal subunit assembly in S. cerevisiae. |
| Q27927674 | The conserved Bud20 zinc finger protein is a new component of the ribosomal 60S subunit export machinery |
| Q27931464 | The evolutionarily conserved protein Las1 is required for pre-rRNA processing at both ends of ITS2 |
| Q34110800 | The human nucleolar protein FTSJ3 associates with NIP7 and functions in pre-rRNA processing |
| Q35690797 | The power of AAA-ATPases on the road of pre-60S ribosome maturation--molecular machines that strip pre-ribosomal particles |
| Q42018255 | The rRNA methyltransferase Bud23 shows functional interaction with components of the SSU processome and RNase MRP. |
| Q36266055 | The sRNAome mining revealed existence of unique signature small RNAs derived from 5.8SrRNA from Piper nigrum and other plant lineages |
| Q34559435 | The small subunit processome in ribosome biogenesis—progress and prospects |
| Q38045141 | Toward a molecular understanding of RNA remodeling by DEAD-box proteins |
| Q27937856 | Trm112 is required for Bud23-mediated methylation of the 18S rRNA at position G1575. |
| Q27934913 | Yar1 protects the ribosomal protein Rps3 from aggregation. |
| Q27935269 | Yeast polypeptide exit tunnel ribosomal proteins L17, L35 and L37 are necessary to recruit late-assembling factors required for 27SB pre-rRNA processing. |
| Q27933804 | Yeast ribosomal protein L40 assembles late into precursor 60 S ribosomes and is required for their cytoplasmic maturation |
| Q92785296 | rRNA expansion segment 27Lb modulates the factor recruitment capacity of the yeast ribosome and shapes the proteome |
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