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TCERG1 gene

Known as: Urn1, TATA box-binding protein-associated factor 2S, TCERG1 
National Institutes of Health

Related topics

Related topics

1 relation
TCERG1L gene

Papers overview

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Highly Cited
2011
Highly Cited
2011
TCERG1 Regulates Alternative Splicing of the Bcl-x Gene by Modulating the Rate of RNA Polymerase II Transcription
ABSTRACT Complex functional coupling exists between transcriptional elongation and pre-mRNA alternative splicing. Pausing sites… Expand
Highly Cited
2007
Highly Cited
2007
The arginine methyltransferase CARM1 regulates the coupling of transcription and mRNA processing.
The coactivator-associated arginine methyltransferase CARM1 is recruited by many different transcription factors as a positive… Expand
Highly Cited
2006
Highly Cited
2006
General structural motifs of amyloid protofilaments
Human CA150, a transcriptional activator, binds to and is co-deposited with huntingtin during Huntington's disease. The second WW… Expand
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2006
2006
CA150 Expression Delays Striatal Cell Death in Overexpression and Knock-In Conditions for Mutant Huntingtin Neurotoxicity
Transcriptional dysregulation caused by expanded polyglutamines (polyGlns) in huntingtin (htt) may be central to cell-autonomous… Expand
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Highly Cited
2004
Highly Cited
2004
FF Domains of CA150 Bind Transcription and Splicing Factors through Multiple Weak Interactions
ABSTRACT The human transcription factor CA150 modulates human immunodeficiency virus type 1 gene transcription and contains… Expand
Highly Cited
2002
Highly Cited
2002
Hyperphosphorylated C-terminal Repeat Domain-associating Proteins in the Nuclear Proteome Link Transcription to DNA/Chromatin Modification and RNA Processing*
Using an interaction blot approach to search in the human nuclear proteome, we identified eight novel proteins that bind the… Expand
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Highly Cited
2001
Highly Cited
2001
The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: neuropathologic and genetic evidence for a role in Huntington's disease pathogenesis.
Huntington's disease (HD) is a neurodegenerative disease caused by polyglutamine expansion in the protein huntingtin (htt… Expand
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Highly Cited
2001
Highly Cited
2001
The Transcription Elongation Factor CA150 Interacts with RNA Polymerase II and the Pre-mRNA Splicing Factor SF1
ABSTRACT CA150 represses RNA polymerase II (RNAPII) transcription by inhibiting the elongation of transcripts. The FF repeat… Expand
Highly Cited
2000
Highly Cited
2000
Protein-interaction modules that organize nuclear function: FF domains of CA150 bind the phosphoCTD of RNA polymerase II.
An approach for purifying nuclear proteins that bind directly to the hyperphosphorylated C-terminal repeat domain (CTD) of RNA… Expand
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Highly Cited
1999
Highly Cited
1999
Transcriptional Cofactor CA150 Regulates RNA Polymerase II Elongation in a TATA-Box-Dependent Manner
ABSTRACT Tat protein strongly activates transcription from the human immunodeficiency virus type 1 (HIV-1) long terminal repeat… Expand
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