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UAP56 is an important regulator of protein synthesis and growth in cardiomyocytes
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
title
UAP56 is an important regulator of protein synthesis and growth in cardiomyocytes
(English)
1 reference
stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
author name string
Abha Sahni
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
Nadan Wang
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
Jeffrey D. Alexis
series ordinal
3
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stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
language of work or name
English
0 references
publication date
26 February 2010
1 reference
stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
published in
Biochemical and Biophysical Research Communications
1 reference
stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
volume
393
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stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
page(s)
106–110
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stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
issue
1
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stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
cites work
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Distinct activities of the DExD/H-box splicing factor hUAP56 facilitate stepwise assembly of the spliceosome
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17 March 2017
Biochemical characterization of the ATPase and helicase activity of UAP56, an essential pre-mRNA splicing and mRNA export factor
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PubMed Central
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17 March 2017
A molecular link between SR protein dephosphorylation and mRNA export
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17 March 2017
TREX is a conserved complex coupling transcription with messenger RNA export
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PubMed Central
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17 March 2017
Pre-mRNA splicing and mRNA export linked by direct interactions between UAP56 and Aly
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U2AF65 recruits a novel human DEAD box protein required for the U2 snRNP-branchpoint interaction
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Requirement of the DEAD-Box protein ded1p for messenger RNA translation
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The BAT1 gene in the MHC encodes an evolutionarily conserved putative nuclear RNA helicase of the DEAD family
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ATP hydrolysis by initiation factor 4A is required for translation initiation in Saccharomyces cerevisiae
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7 April 2017
DEAD-box proteins: the driving forces behind RNA metabolism
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The mTOR pathway in the control of protein synthesis
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Nuclear localization of poly(A)+ mRNA following siRNA reduction of expression of the mammalian RNA helicases UAP56 and URH49.
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Cardiac hypertrophy: a matter of translation.
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29 September 2017
A new twist on RNA helicases: DExH/D box proteins as RNPases
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29 September 2017
Signaling pathways for cardiac hypertrophy and failure
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29 September 2017
Protein kinase C-zeta mediates angiotensin II activation of ERK1/2 in vascular smooth muscle cells
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Translation initiation factor 4A from Saccharomyces cerevisiae: analysis of residues conserved in the D-E-A-D family of RNA helicases
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Activation of extracellular signal-regulated kinase 5 reduces cardiac apoptosis and dysfunction via inhibition of a phosphodiesterase 3A/inducible cAMP early repressor feedback loop
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3 June 2018
Binding of ATP to UAP56 is necessary for mRNA export
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PubMed Central
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27 November 2018
UAP56 RNA helicase is required for axis specification and cytoplasmic mRNA localization in Drosophila.
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27 November 2018
The DExH/D box protein HEL/UAP56 is essential for mRNA nuclear export in Drosophila
1 reference
stated in
PubMed Central
reference URL
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27 November 2018
Reduction of cardiovascular risk by regression of electrocardiographic markers of left ventricular hypertrophy by the angiotensin-converting enzyme inhibitor ramipril
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PubMed Central
reference URL
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27 November 2018
The hinge-helix 1 region of peroxisome proliferator-activated receptor gamma1 (PPARgamma1) mediates interaction with extracellular signal-regulated kinase 5 and PPARgamma1 transcriptional activation: involvement in flow-induced PPARgamma activation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20116367
retrieved
12 December 2020
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Identifiers
DOI
10.1016/J.BBRC.2010.01.093
1 reference
stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
PMCID
2862620
0 references
PubMed ID
20116367
1 reference
stated in
PubMed
PubMed ID
20116367
retrieved
31 January 2017
ResearchGate publication ID
41189456
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