Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome (Q34351354)

1 August 2017

title

Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome (English)

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1 August 2017

4

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1 August 2017

5

May Tassabehji

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1 August 2017

1

Timothy A Hinsley

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1 August 2017

Pamela Cunliffe

2

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1 August 2017

Hannah J Tipney

series ordinal

3

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1 August 2017

publication date

1 October 2004

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1 August 2017

language of work or name

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1 August 2017

volume

13

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1 August 2017

issue

10

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1 August 2017

page(s)

2588-2599

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Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome

1 August 2017

cites work

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6 July 2018

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Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23

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6 July 2018

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A synergy control motif within the attenuator domain of CCAAT/enhancer-binding protein alpha inhibits transcriptional synergy through its PIASy-enhanced modification by SUMO-1 or SUMO-3

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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cGMP-dependent protein kinase I beta physically and functionally interacts with the transcriptional regulator TFII-I

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

6 July 2018

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

6 July 2018

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Repression of TFII-I-dependent transcription by nuclear exclusion

6 July 2018

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JAK2 activates TFII-I and regulates its interaction with extracellular signal-regulated kinase.

6 July 2018

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Identification of TFII-I as the endoplasmic reticulum stress response element binding factor ERSF: its autoregulation by stress and interaction with ATF6.

6 July 2018

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Williams syndrome: from genotype through to the cognitive phenotype

6 July 2018

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Structure-function analysis of TFII-I. Roles of the N-terminal end, basic region, and I-repeats

6 July 2018

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VI. Genome structure and cognitive map of Williams syndrome

6 July 2018

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I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses

6 July 2018

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A common motif within the negative regulatory regions of multiple factors inhibits their transcriptional synergy

6 July 2018

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Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes

6 July 2018

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6 July 2018

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Alternatively spliced isoforms of TFII-I. Complex formation, nuclear translocation, and differential gene regulation

6 July 2018

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

6 July 2018

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6 July 2018

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Williams-Beuren syndrome: genes and mechanisms

6 July 2018

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

6 July 2018

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

6 July 2018

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Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes

6 July 2018

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TFII-I Regulates Vβ Promoter Activity through an Initiator Element

6 July 2018

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TFII-I Enhances Activation of the c-fosPromoter through Interactions with Upstream Elements

6 July 2018

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A duplicated gene in the breakpoint regions of the 7q11.23 Williams- Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK

6 July 2018

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6 July 2018

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

6 July 2018

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6 July 2018

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

6 July 2018

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

6 July 2018

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Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth

6 July 2018

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PEST sequences and regulation by proteolysis

6 July 2018

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Recognition by Max of its cognate DNA through a dimeric b/HLH/Z domain

6 July 2018

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A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

6 July 2018

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

6 July 2018

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The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

6 July 2018

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The neighbor-joining method: a new method for reconstructing phylogenetic trees

6 July 2018

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A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins

6 July 2018

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Natural history of Williams syndrome: physical characteristics

6 July 2018

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6 July 2018

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The protein Id: a negative regulator of helix-loop-helix DNA binding proteins

6 July 2018

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6 July 2018

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

6 July 2018

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A cognitive and behavioural phenotype in williams syndrome

6 July 2018

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extramacrochaetae, a negative regulator of sensory organ development in Drosophila, defines a new class of helix-loop-helix proteins

6 July 2018

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Supravalvular Aortic Stenosis in Association with Mental Retardation and a Certain Facial Appearance

6 July 2018

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Supravalvular Aortic Stenosis

21 January 2018

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Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion.

21 January 2018

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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.

27 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2286546

II. Hypersociability in Williams Syndrome

27 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2286546

High level of unequal meiotic crossovers at the origin of the 22q11. 2 and 7q11.23 deletions.

27 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2286546

Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion

27 October 2018

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Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome

27 October 2018

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Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

27 October 2018

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12 December 2020

An alternative pathway for transcription initiation involving TFII-I

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12 December 2020

The williams elfin facies syndrome: the psychological profile as an aid in syndrome identification

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12 December 2020

Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome

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12 December 2020

Identifiers

DOI

10.1110/PS.04747604

1 reference

1 August 2017

1 reference

1 August 2017

1 reference