(Q28505427)

24 January 2017

title

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

1 reference

General transcription factor II I repeat domain-containing 1

24 January 2017

main subject

1 reference

GOA release 2020-03-11

author name string

D. Bayarsaihan

series ordinal

1

1 reference

24 January 2017

F. H. Ruddle

series ordinal

2

1 reference

24 January 2017

language of work or name

English

0 references

publication date

20 June 2000

1 reference

Proceedings of the National Academy of Sciences of the United States of America

24 January 2017

published in

1 reference

24 January 2017

volume

97

1 reference

24 January 2017

issue

13

1 reference

24 January 2017

page(s)

7342–7347

1 reference

Extracellular signal-regulated kinase binds to TFII-I and regulates its activation of the c-fos promoter

24 January 2017

cites work

1 reference

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Tec family of protein-tyrosine kinases: an overview of their structure and function

19 March 2017

1 reference

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Characterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-I

19 March 2017

2 references

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19 March 2017

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Mlx, a novel Max-like BHLHZip protein that interacts with the Max network of transcription factors

29 September 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

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Dosage requirement of Pitx2 for development of multiple organs

19 March 2017

1 reference

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Regulation of nuclear localization and transcriptional activity of TFII-I by Bruton's tyrosine kinase

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

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

19 March 2017

1 reference

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Identification of a novel slow-muscle-fiber enhancer binding protein, MusTRD1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

TFII-I enhances activation of the c-fos promoter through interactions with upstream elements

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

CLIP-115, a novel brain-specific cytoplasmic linker protein, mediates the localization of dendritic lamellar bodies

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Cloning of an inr- and E-box-binding protein, TFII-I, that interacts physically and functionally with USF1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

A multifunctional DNA-binding protein that promotes the formation of serum response factor/homeodomain complexes: identity to TFII-I

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

BAP-135, a target for Bruton's tyrosine kinase in response to B cell receptor engagement

19 March 2017

1 reference

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Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Direct role for Myc in transcription initiation mediated by interactions with TFII-I

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Structural relationships among genes that control development: sequence homology between the Antennapedia, Ultrabithorax, and fushi tarazu loci of Drosophila

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Cooperative interaction of an initiator-binding transcription initiation factor and the helix-loop-helix activator USF

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

The A.T-DNA-binding domain of mammalian high mobility group I chromosomal proteins. A novel peptide motif for recognizing DNA structure

19 March 2017

1 reference

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A rapid micropreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells

19 March 2017

1 reference

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Hox genes in vertebrate development

7 April 2017

1 reference

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Interpreting cDNA sequences: some insights from studies on translation

7 April 2017

1 reference

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Implications of isoform multiplicity of microphthalmia-associated transcription factor in the pathogenesis of auditory-pigmentary syndromes.

9 May 2017

1 reference

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Craniosynostosis syndromes: from genes to premature fusion of skull bones

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Williams-Beuren syndrome: genes and mechanisms

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder

29 September 2017

1 reference

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Williams-Beuren syndrome: an update and review for the primary physician

29 September 2017

1 reference

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Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

NF-kappa B homodimer binding within the HIV-1 initiator region and interactions with TFII-I

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Combinations of closely situated cis-acting elements determine tissue-specific patterns and anterior extent of early Hoxc8 expression

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Y-box proteins interact with the S1 nuclease-sensitive site in the chicken alpha 2(I) collagen gene promoter

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

A long-range regulatory element of Hoxc8 identified by using the pClasper vector

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Regulation of Hoxc-8 during mouse embryonic development: identification and characterization of critical elements involved in early neural tube expression.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

A homologous protein-coding sequence in Drosophila homeotic genes and its conservation in other metazoans.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Use of a protein-blotting procedure and a specific DNA probe to identify nuclear proteins that recognize the promoter region of the transferrin receptor gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

Natural history of Williams syndrome: physical characteristics

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16547

29 September 2017

Evolution of Hox genes

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.97.13.7342

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.97.13.7342

Two cases of Townes-Brocks syndrome

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/10861001

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.97.13.7342

0 references

0 references

0 references

1 reference