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HRS/SRp40-mediated inclusion of the fibronectin EIIIB exon, a possible cause of increased EIIIB expression in proliferating liver
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
title
HRS/SRp40-mediated inclusion of the fibronectin EIIIB exon, a possible cause of increased EIIIB expression in proliferating liver
(English)
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
author name string
K. Du
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
Y. Peng
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2
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
L. E. Greenbaum
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3
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
B. A. Haber
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
R. Taub
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5
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
language of work or name
English
0 references
publication date
1 July 1997
1 reference
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PubMed
PubMed ID
9199345
retrieved
31 January 2017
published in
Molecular and Cellular Biology
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
volume
17
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stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
page(s)
4096–4104
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stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
issue
7
1 reference
stated in
PubMed
PubMed ID
9199345
retrieved
31 January 2017
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High levels of glucose-6-phosphatase gene and protein expression reflect an adaptive response in proliferating liver and diabetes
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The 35-kDa mammalian splicing factor SC35 mediates specific interactions between U1 and U2 small nuclear ribonucleoprotein particles at the 3' splice site
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Alternative splicing mechanism in a cytochrome P-450 (P-450PB-1) gene generates the two mRNAs coding for proteins of different functions.
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3 June 2018
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3 June 2018
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3 June 2018
The inclusion of the type III repeat ED-B in the fibronectin molecule generates conformational modifications that unmask a cryptic sequence
1 reference
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3 June 2018
Distinct functions of SR proteins in alternative pre-mRNA splicing.
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27 November 2018
Patterns of alternative splicing of fibronectin pre-mRNA in human adult and fetal tissues
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9199345
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Coordinate oncodevelopmental modulation of alternative splicing of fibronectin pre-messenger RNA at ED-A, ED-B, and CS1 regions in human liver tumors
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9199345
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Turnover of the photosystem II D1 protein in higher plants under photoinhibitory and nonphotoinhibitory irradiance
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9199345
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Coexpression of liver-specific and growth-induced genes in perinatal and regenerating liver: attainment and maintenance of the differentiated state during rapid proliferation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9199345
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A splicing enhancer in the human fibronectin alternate ED1 exon interacts with SR proteins and stimulates U2 snRNP binding
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9199345
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
General splicing factor SF2/ASF promotes alternative splicing by binding to an exonic splicing enhancer
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9199345
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Fibronectin isoforms in plasma membrane domains of normal and regenerating rat liver
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9199345
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1128/MCB.17.7.4096
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3953856
OpenCitations bibliographic resource ID
3953856
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3953856
PMCID
232263
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3953856
PubMed ID
9199345
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3953856
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