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Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
12971990
retrieved
31 January 2017
title
Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development
(English)
1 reference
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PubMed
PubMed ID
12971990
retrieved
31 January 2017
main subject
Homeobox C8
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GOA release 2020-03-11
author
Dashzeveg Bayarsaihan
series ordinal
1
object named as
Dashzeveg Bayarsaihan
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stated in
PubMed
PubMed ID
12971990
retrieved
31 January 2017
Badam Enkhmandakh
series ordinal
3
object named as
Badam Enkhmandakh
1 reference
stated in
PubMed
PubMed ID
12971990
retrieved
31 January 2017
James F. Leckman
series ordinal
5
object named as
James F. Leckman
1 reference
stated in
PubMed
PubMed ID
12971990
retrieved
31 January 2017
author name string
Natalia Bitchevaia
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
12971990
retrieved
31 January 2017
Maria Isabel Tussie-Luna
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
12971990
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31 January 2017
Ananda Roy
series ordinal
6
1 reference
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PubMed
PubMed ID
12971990
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31 January 2017
Frank Ruddle
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
12971990
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31 January 2017
publication date
1 October 2003
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stated in
PubMed
PubMed ID
12971990
retrieved
31 January 2017
published in
Gene Expression Patterns
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PubMed
PubMed ID
12971990
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31 January 2017
volume
3
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PubMed
PubMed ID
12971990
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31 January 2017
issue
5
1 reference
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PubMed
PubMed ID
12971990
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31 January 2017
page(s)
579–589
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PubMed
PubMed ID
12971990
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31 January 2017
cites work
Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix-loop-helix domains
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic organization of the genes Gtf2ird1, Gtf2i, and Ncf1 at the mouse chromosome 5 region syntenic to the human chromosome 7q11.23 Williams syndrome critical region.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
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Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Williams syndrome and related disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The role of a Williams-Beuren syndrome-associated helix-loop-helix domain-containing transcription factor in activin/nodal signaling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biochemistry and biology of the inducible multifunctional transcription factor TFII-I.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Repression of TFII-I-dependent transcription by nuclear exclusion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Physical and functional interactions of histone deacetylase 3 with TFII-I family proteins and PIASxbeta
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of general transcription factor 3, a transcription factor involved in slow muscle-specific gene expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1567-133X(03)00118-2
0 references
PubMed ID
12971990
1 reference
stated in
PubMed
PubMed ID
12971990
retrieved
31 January 2017
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