| scholarly article | Q13442814 |
| P50 | author | Michał Dadlez | Q63859587 |
| William F Marzluff | Q89582047 | ||
| Zbigniew Dominski | Q89582050 | ||
| P2093 | author name string | Xiao-Cui Yang | |
| Aleksandra Skrajna | |||
| Ivan Sabath | |||
| P2860 | cites work | Cell cycle-regulated phosphorylation of p220(NPAT) by cyclin E/Cdk2 in Cajal bodies promotes histone gene transcription | Q24290273 |
| Human pre-mRNA cleavage factor II(m) contains homologs of yeast proteins and bridges two other cleavage factors | Q24290465 | ||
| Purified U7 snRNPs lack the Sm proteins D1 and D2 but contain Lsm10, a new 14 kDa Sm D1-like protein | Q24291730 | ||
| Purification and characterization of human cleavage factor Im involved in the 3' end processing of messenger RNA precursors | Q24309304 | ||
| Human pre-mRNA cleavage factor Im is related to spliceosomal SR proteins and can be reconstituted in vitro from recombinant subunits | Q24313453 | ||
| Ars2 links the nuclear cap-binding complex to RNA interference and cell proliferation | Q24317359 | ||
| Integrator, a multiprotein mediator of small nuclear RNA processing, associates with the C-terminal repeat of RNA polymerase II | Q24338780 | ||
| The gene for histone RNA hairpin binding protein is located on human chromosome 4 and encodes a novel type of RNA binding protein | Q24532107 | ||
| Human Fip1 is a subunit of CPSF that binds to U-rich RNA elements and stimulates poly(A) polymerase | Q24535920 | ||
| Symplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAs | Q24537115 | ||
| U7 snRNA mutations in Drosophila block histone pre-mRNA processing and disrupt oogenesis | Q24541402 | ||
| Complex protein interactions within the human polyadenylation machinery identify a novel component | Q24554306 | ||
| Stem-loop binding protein facilitates 3'-end formation by stabilizing U7 snRNP binding to histone pre-mRNA | Q24554504 | ||
| Two-step affinity purification of U7 small nuclear ribonucleoprotein particles using complementary biotinylated 2'-O-methyl oligoribonucleotides | Q24560046 | ||
| Specific contacts between mammalian U7 snRNA and histone precursor RNA are indispensable for the in vitro 3' RNA processing reaction | Q24564263 | ||
| The site of 3' end formation of histone messenger RNA is a fixed distance from the downstream element recognized by the U7 snRNP | Q24595569 | ||
| Structure of histone mRNA stem-loop, human stem-loop binding protein, and 3'hExo ternary complex | Q24631024 | ||
| The 68 kDa subunit of mammalian cleavage factor I interacts with the U7 small nuclear ribonucleoprotein and participates in 3'-end processing of animal histone mRNAs | Q24632908 | ||
| Ribozyme, antisense RNA, and antisense DNA inhibition of U7 small nuclear ribonucleoprotein-mediated histone pre-mRNA processing in vitro | Q24634140 | ||
| Three proteins of the U7-specific Sm ring function as the molecular ruler to determine the site of 3'-end processing in mammalian histone pre-mRNA | Q24644697 | ||
| Length suppression in histone messenger RNA 3'-end maturation: processing defects of insertion mutant premessenger RNAs can be compensated by insertions into the U7 small nuclear RNA | Q24651408 | ||
| Ars2 promotes proper replication-dependent histone mRNA 3' end formation. | Q40760798 | ||
| Interaction profiling identifies the human nuclear exosome targeting complex | Q41412984 | ||
| A core complex of CPSF73, CPSF100, and Symplekin may form two different cleavage factors for processing of poly(A) and histone mRNAs | Q41656652 | ||
| Interaction between FLASH and Lsm11 is essential for histone pre-mRNA processing in vivo in Drosophila | Q41976272 | ||
| FLASH is required for the endonucleolytic cleavage of histone pre-mRNAs but is dispensable for the 5' exonucleolytic degradation of the downstream cleavage product | Q42073225 | ||
| FLASH, a proapoptotic protein involved in activation of caspase-8, is essential for 3' end processing of histone pre-mRNAs | Q42196795 | ||
| Molecular architecture of the human pre-mRNA 3' processing complex | Q42418612 | ||
| Crosstalk between mRNA 3' end processing and transcription initiation | Q42821628 | ||
| A genome-wide RNA interference screen reveals that variant histones are necessary for replication-dependent histone pre-mRNA processing. | Q47070600 | ||
| NELF interacts with CBC and participates in 3' end processing of replication-dependent histone mRNAs | Q50336087 | ||
| A multisubunit factor, CstF, is required for polyadenylation of mammalian pre-mRNAs | Q68164668 | ||
| The biochemistry of polyadenylation | Q71392048 | ||
| Crystal structure of murine CstF-77: dimeric association and implications for polyadenylation of mRNA precursors | Q27644241 | ||
| Small nucleolar RNAs: an abundant group of noncoding RNAs with diverse cellular functions | Q28217265 | ||
| The U7 snRNP and the hairpin binding protein: Key players in histone mRNA metabolism | Q28274771 | ||
| Polyadenylation factor CPSF-73 is the pre-mRNA 3'-end-processing endonuclease | Q28275724 | ||
| Identification of the human U7 snRNP as one of several factors involved in the 3' end maturation of histone premessenger RNA's | Q28280579 | ||
| The special Sm core structure of the U7 snRNP: far-reaching significance of a small nuclear ribonucleoprotein | Q28291688 | ||
| The C-terminal domain of RNA polymerase II couples mRNA processing to transcription | Q28301744 | ||
| Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis | Q28609911 | ||
| Integrating mRNA processing with transcription | Q28610124 | ||
| Expression of microRNAs and its regulation in plants | Q28749287 | ||
| Formation of the 3' end of histone mRNA: getting closer to the end | Q28751417 | ||
| Dual roles of the nuclear cap-binding complex and SERRATE in pre-mRNA splicing and microRNA processing in Arabidopsis thaliana | Q28757913 | ||
| Small Nucleolar RNAs | Q29300155 | ||
| Mechanism and regulation of mRNA polyadenylation | Q29614774 | ||
| Ars2 regulates both miRNA- and siRNA- dependent silencing and suppresses RNA virus infection in Drosophila | Q33486941 | ||
| Ending the message: poly(A) signals then and now | Q34213955 | ||
| 3' end processing of Drosophila melanogaster histone pre-mRNAs: requirement for phosphorylated Drosophila stem-loop binding protein and coevolution of the histone pre-mRNA processing system | Q34324943 | ||
| Isolation and characterization of polyadenylation complexes assembled in vitro. | Q34362676 | ||
| Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors | Q34419716 | ||
| Interactions of CstF-64, CstF-77, and symplekin: implications on localisation and function. | Q34471019 | ||
| A Subset of Drosophila Integrator Proteins Is Essential for Efficient U7 snRNA and Spliceosomal snRNA 3′-End Formation | Q34485087 | ||
| Variable effects of the conserved RNA hairpin element upon 3' end processing of histone pre-mRNA in vitro. | Q34978310 | ||
| Drosophila stem loop binding protein coordinates accumulation of mature histone mRNA with cell cycle progression | Q35076429 | ||
| Strange bedfellows: polyadenylation factors at the promoter | Q35143449 | ||
| Drosophila histone locus bodies form by hierarchical recruitment of components | Q35196079 | ||
| The link between mRNA processing and transcription: communication works both ways | Q35761821 | ||
| Eukaryotic mRNA 3' processing: a common means to different ends | Q36303654 | ||
| A complex containing the CPSF73 endonuclease and other polyadenylation factors associates with U7 snRNP and is recruited to histone pre-mRNA for 3'-end processing | Q36506583 | ||
| Protein factors in pre-mRNA 3'-end processing. | Q37044967 | ||
| Expression of human snRNA genes from beginning to end. | Q37217738 | ||
| The hunt for the 3' endonuclease | Q37936377 | ||
| Emergence of the β-CASP ribonucleases: highly conserved and ubiquitous metallo-enzymes involved in messenger RNA maturation and degradation | Q38081014 | ||
| Making ends meet: coordination between RNA 3'-end processing and transcription initiation. | Q38085601 | ||
| Differences and similarities between Drosophila and mammalian 3' end processing of histone pre-mRNAs | Q38319470 | ||
| SERRATE: a new player on the plant microRNA scene. | Q38778370 | ||
| Interaction of FLASH with arsenite resistance protein 2 is involved in cell cycle progression at S phase | Q39834723 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Drosophila | Q312154 |
| P304 | page(s) | 1726-1744 | |
| P577 | publication date | 2013-10-21 | |
| P1433 | published in | RNA | Q7277164 |
| P1476 | title | 3'-End processing of histone pre-mRNAs in Drosophila: U7 snRNP is associated with FLASH and polyadenylation factors | |
| P478 | volume | 19 |
| Q34634110 | A conserved interaction that is essential for the biogenesis of histone locus bodies |
| Q91833236 | Composition and processing activity of a semi-recombinant holo U7 snRNP |
| Q36976457 | Concentrating pre-mRNA processing factors in the histone locus body facilitates efficient histone mRNA biogenesis. |
| Q47110577 | Coordinating cell cycle-regulated histone gene expression through assembly and function of the Histone Locus Body |
| Q35058505 | CstF-64 is necessary for endoderm differentiation resulting in cardiomyocyte defects |
| Q33983624 | CstF-64 supports pluripotency and regulates cell cycle progression in embryonic stem cells through histone 3' end processing. |
| Q52718270 | Cstf2t Regulates expression of histones and histone-like proteins in male germ cells. |
| Q90288065 | Depletion of Ars2 inhibits cell proliferation and leukemogenesis in acute myeloid leukemia by modulating the miR-6734-3p/p27 axis |
| Q36189905 | Drosophila Symplekin localizes dynamically to the histone locus body and tricellular junctions |
| Q33568513 | Drosophila melanogaster retrotransposon and inverted repeat-derived endogenous siRNAs are differentially processed in distinct cellular locations. |
| Q33965743 | Eri1: a conserved enzyme at the crossroads of multiple RNA-processing pathways |
| Q35162210 | Generation of plasmid vectors expressing FLAG-tagged proteins under the regulation of human elongation factor-1α promoter using Gibson assembly. |
| Q35875832 | In vivo characterization of the Drosophila mRNA 3' end processing core cleavage complex |
| Q52374660 | Integrator subunit 4 is a 'Symplekin-like' scaffold that associates with INTS9/11 to form the Integrator cleavage module. |
| Q40718700 | Mapping the Interaction Network of Key Proteins Involved in Histone mRNA Generation: A Hydrogen/Deuterium Exchange Study |
| Q27684583 | Molecular mechanisms for the regulation of histone mRNA stem-loop-binding protein by phosphorylation. |
| Q36827118 | Non-coding RNAs, the cutting edge of histone messages |
| Q52359095 | Protein composition of catalytically active U7-dependent processing complexes assembled on histone pre-mRNA containing biotin and a photo-cleavable linker. |
| Q38195095 | Structure and function of pre-mRNA 5'-end capping quality control and 3'-end processing |
| Q89582051 | Structure of an active human histone pre-mRNA 3'-end processing machinery |
| Q42087014 | Transcriptomic comparison of Drosophila snRNP biogenesis mutants reveals mutant-specific changes in pre-mRNA processing: implications for spinal muscular atrophy. |
| Q51100143 | U7 snRNP is recruited to histone pre-mRNA in a FLASH-dependent manner by two separate regions of the stem-loop binding protein. |
| Q102369489 | cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing |
Search more.