scholarly article | Q13442814 |
P50 | author | James L. Manley | Q38362017 |
P2093 | author name string | Scott Millhouse | |
P2860 | cites work | Functional association of U2 snRNP with the ATP-independent spliceosomal complex E | Q22254390 |
Cloning and characterization of PSF, a novel pre-mRNA splicing factor | Q24322621 | ||
Human Tra2 proteins are sequence-specific activators of pre-mRNA splicing | Q24336359 | ||
CUS2, a yeast homolog of human Tat-SF1, rescues function of misfolded U2 through an unusual RNA recognition motif | Q24522636 | ||
Sorting out the complexity of SR protein functions | Q24539813 | ||
Splicing and transcription-associated proteins PSF and p54nrb/nonO bind to the RNA polymerase II CTD | Q24540125 | ||
RNA polymerase II accumulation in the promoter-proximal region of the dihydrofolate reductase and gamma-actin genes | Q24550573 | ||
Relief of two built-In autoinhibitory mechanisms in P-TEFb is required for assembly of a multicomponent transcription elongation complex at the human immunodeficiency virus type 1 promoter | Q24552532 | ||
Functional domains of the human splicing factor ASF/SF2 | Q24564249 | ||
A novel set of spliceosome-associated proteins and the essential splicing factor PSF bind stably to pre-mRNA prior to catalytic step II of the splicing reaction | Q24594778 | ||
The human splicing factors ASF/SF2 and SC35 possess distinct, functionally significant RNA binding specificities | Q24598907 | ||
Capping, splicing, and 3' processing are independently stimulated by RNA polymerase II: different functions for different segments of the CTD | Q24601077 | ||
mRNA capping enzyme is recruited to the transcription complex by phosphorylation of the RNA polymerase II carboxy-terminal domain | Q24602633 | ||
Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei | Q27860728 | ||
Tat modifies the activity of CDK9 to phosphorylate serine 5 of the RNA polymerase II carboxyl-terminal domain during human immunodeficiency virus type 1 transcription | Q28116305 | ||
Different phosphorylated forms of RNA polymerase II and associated mRNA processing factors during transcription | Q28131686 | ||
Three RNA polymerase II carboxyl-terminal domain kinases display distinct substrate preferences | Q28208318 | ||
Stimulatory effect of splicing factors on transcriptional elongation | Q28214807 | ||
Protein-protein interactions and 5'-splice-site recognition in mammalian mRNA precursors | Q28251112 | ||
Specific interactions between proteins implicated in splice site selection and regulated alternative splicing | Q28257351 | ||
Specific commitment of different pre-mRNAs to splicing by single SR proteins | Q28262042 | ||
The C-terminal domain of RNA polymerase II couples mRNA processing to transcription | Q28301744 | ||
A nuclear matrix protein interacts with the phosphorylated C-terminal domain of RNA polymerase II. | Q28509334 | ||
The C-terminal domain of the largest subunit of RNA polymerase II interacts with a novel set of serine/arginine-rich proteins | Q28570708 | ||
Integrating mRNA processing with transcription | Q28610124 | ||
Pre-mRNA splicing: awash in a sea of proteins | Q29547272 | ||
An extensive network of coupling among gene expression machines | Q29547273 | ||
DNA binding provides a signal for phosphorylation of the RNA polymerase II heptapeptide repeats | Q68074474 | ||
Phosphorylation causes a conformational change in the carboxyl-terminal domain of the mouse RNA polymerase II largest subunit | Q68187252 | ||
Complementation by SR proteins of pre-mRNA splicing reactions depleted of U1 snRNP | Q72202030 | ||
Growth-related changes in phosphorylation of yeast RNA polymerase II | Q74192542 | ||
RNA polymerase II and the integration of nuclear events | Q29614772 | ||
RNA polymerase II is an essential mRNA polyadenylation factor | Q29614773 | ||
Reversible phosphorylation of the C-terminal domain of RNA polymerase II | Q29614790 | ||
SR proteins and splicing control | Q29619936 | ||
The structure and function of proteins involved in mammalian pre-mRNA splicing | Q29620286 | ||
Exon Identity Established through Differential Antagonism between Exonic Splicing Silencer-Bound hnRNP A1 and Enhancer-Bound SR Proteins | Q30040281 | ||
Splice site selection, rate of splicing, and alternative splicing on nascent transcripts | Q30461752 | ||
A CTD function linking transcription to splicing | Q33368388 | ||
Protein composition of mammalian spliceosomes assembled in vitro | Q33847099 | ||
Distinct roles for CTD Ser-2 and Ser-5 phosphorylation in the recruitment and allosteric activation of mammalian mRNA capping enzyme | Q33858428 | ||
SF2/ASF binds to a splicing enhancer in the third HIV-1 tat exon and stimulates U2AF binding independently of the RS domain. | Q34092879 | ||
The spliceosome: the most complex macromolecular machine in the cell? | Q34278742 | ||
p54(nrb) associates with the 5' splice site within large transcription/splicing complexes. | Q34310192 | ||
Resolution of the mammalian E complex and the ATP-dependent spliceosomal complexes on native agarose mini-gels | Q34362249 | ||
The nuclear matrix protein p255 is a highly phosphorylated form of RNA polymerase II largest subunit which associates with spliceosomes | Q34620338 | ||
Heat-shock inactivation of the TFIIH-associated kinase and change in the phosphorylation sites on the C-terminal domain of RNA polymerase II. | Q34626147 | ||
The mRNA assembly line: transcription and processing machines in the same factory | Q34688409 | ||
The nuclear matrix phosphoprotein p255 associates with splicing complexes as part of the [U4/Y6.U5]tri-snRNP particle | Q34767752 | ||
The human splicing factor ASF/SF2 can specifically recognize pre-mRNA 5' splice sites | Q35171559 | ||
ATP can be dispensable for prespliceosome formation in yeast | Q35185397 | ||
Phosphorylated RNA polymerase II stimulates pre-mRNA splicing | Q35197241 | ||
Splicing factors associate with hyperphosphorylated RNA polymerase II in the absence of pre-mRNA | Q36254517 | ||
Transcription-dependent redistribution of the large subunit of RNA polymerase II to discrete nuclear domains | Q36382489 | ||
SR proteins promote the first specific recognition of Pre-mRNA and are present together with the U1 small nuclear ribonucleoprotein particle in a general splicing enhancer complex | Q36670430 | ||
A hyperphosphorylated form of the large subunit of RNA polymerase II is associated with splicing complexes and the nuclear matrix | Q37398137 | ||
Tails of RNA polymerase II. | Q38003896 | ||
Participation of the C-terminal domain of RNA polymerase II in exon definition during pre-mRNA splicing | Q38499037 | ||
Split genes and RNA splicing | Q40389967 | ||
U1 snRNP-ASF/SF2 interaction and 5' splice site recognition: characterization of required elements. | Q40395456 | ||
hnRNP A/B proteins are required for inhibition of HIV-1 pre-mRNA splicing | Q41679293 | ||
Identification of phosphorylation sites in the repetitive carboxyl-terminal domain of the mouse RNA polymerase II largest subunit. | Q41695825 | ||
An ATP-independent complex commits pre-mRNA to the mammalian spliceosome assembly pathway | Q44540184 | ||
Purification and characterization of pre-mRNA splicing factor SF2 from HeLa cells | Q44744396 | ||
The splicing factor, Prp40, binds the phosphorylated carboxyl-terminal domain of RNA polymerase II. | Q51075771 | ||
Splicing of Balbiani ring 1 gene pre-mRNA occurs simultaneously with transcription. | Q52544550 | ||
The role of exon sequences in splice site selection. | Q52545848 | ||
Characterization of the Residues Phosphorylated in Vitro by Different C-terminal Domain Kinases | Q63362926 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | phosphorylation | Q242736 |
P304 | page(s) | 533-544 | |
P577 | publication date | 2005-01-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | The C-terminal domain of RNA polymerase II functions as a phosphorylation-dependent splicing activator in a heterologous protein | |
P478 | volume | 25 |