(Q34315324)

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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

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Europe PubMed Central

PubMed publication ID

1 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

3

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Europe PubMed Central

PubMed publication ID

1 August 2017

6

object named as

May Tassabehji

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Timothy A Hinsley

2

object named as

Timothy A Hinsley

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Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Hannah J Tipney

1

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Europe PubMed Central

PubMed publication ID

1 August 2017

Kay Metcalfe

4

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1 August 2017

Dian Donnai

5

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Europe PubMed Central

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1 August 2017

publication date

1 July 2004

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Europe PubMed Central

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1 August 2017

European Journal of Human Genetics

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Europe PubMed Central

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1 August 2017

12

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Europe PubMed Central

PubMed publication ID

1 August 2017

7

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Europe PubMed Central

PubMed publication ID

1 August 2017

551-560

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Europe PubMed Central

PubMed publication ID

1 August 2017

Natural history of Williams syndrome: physical characteristics

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

EMBOSS: the European Molecular Biology Open Software Suite

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

The Pfam protein families database

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

A knowledge base for predicting protein localization sites in eukaryotic cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Predicting subcellular localization of proteins based on their N-terminal amino acid sequence

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Beta-turns and their distortions: a proposed new nomenclature

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

The BED finger, a novel DNA-binding domain in chromatin-boundary-element-binding proteins and transposases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Interspersed repeats and other mementos of transposable elements in mammalian genomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Tiggers and DNA transposon fossils in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Evidence for a common evolutionary origin of inverted repeat transposons in Drosophila and plants: hobo, activator, and Tam3

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Residues critical for retroviral integrative recombination in a region that is highly conserved among retroviral/retrotransposon integrases and bacterial insertion sequence transposases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

A novel pseudoautosomal human gene encodes a putative protein similar to Ac-like transposases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Centromeres, CENP-B and Tigger too.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombinational hotspot

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201174

21 January 2018

Identifiers

10.1038/SJ.EJHG.5201174

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

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