Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development (Q28587697)

31 January 2017

title

Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development (English)

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31 January 2017

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GOA release 2020-03-11

author

Dashzeveg Bayarsaihan

1

object named as

Dashzeveg Bayarsaihan

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31 January 2017

3

Badam Enkhmandakh

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31 January 2017

5

James F. Leckman

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31 January 2017

Natalia Bitchevaia

2

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31 January 2017

Maria Isabel Tussie-Luna

4

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31 January 2017

Ananda Roy

6

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31 January 2017

Frank Ruddle

7

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31 January 2017

publication date

1 October 2003

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31 January 2017

published in

Gene Expression Patterns

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31 January 2017

volume

3

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31 January 2017

issue

5

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31 January 2017

page(s)

579–589

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Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix-loop-helix domains

31 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23

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https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

Williams syndrome and related disorders

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7 January 2021

Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome

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https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

The role of a Williams-Beuren syndrome-associated helix-loop-helix domain-containing transcription factor in activin/nodal signaling

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https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

Biochemistry and biology of the inducible multifunctional transcription factor TFII-I.

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https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome

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https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

Repression of TFII-I-dependent transcription by nuclear exclusion

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https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

Physical and functional interactions of histone deacetylase 3 with TFII-I family proteins and PIASxbeta

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https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

Characterization of general transcription factor 3, a transcription factor involved in slow muscle-specific gene expression

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https://api.crossref.org/works/10.1016%2FS1567-133X%2803%2900118-2

7 January 2021

10.1016/S1567-133X(03)00118-2

Identifiers

DOI

0 references

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