Essential role of the N-terminal region of TFII-I in viability and behavior (Q30481565)

20 September 2017

Essential role of the N-terminal region of TFII-I in viability and behavior (English)

1 reference

20 September 2017

Victoria Campuzano

15

0 references

Ester Aso

Ester Aso

3

0 references

José Luis Barbero

José L Barbero

12

0 references

Adriana Sampaio

Adriana Sampaio

7

0 references

Nuno Sousa

Nuno Sousa

11

0 references

Maria Segura-Puimedon

1 reference

ORCID Public Data File 2021

author name string

Jaume Lucena

1

1 reference

20 September 2017

Susana Pezzi

2

1 reference

20 September 2017

Maria C Valero

4

1 reference

20 September 2017

Candelas Carreiro

5

1 reference

20 September 2017

Pierre Dubus

6

1 reference

20 September 2017

Maria Segura

8

1 reference

20 September 2017

Isabel Barthelemy

9

1 reference

20 September 2017

Marc Y Zindel

10

1 reference

20 September 2017

Rafael Maldonado

13

1 reference

20 September 2017

Luis A Pérez-Jurado

14

1 reference

20 September 2017

19 April 2010

1 reference

20 September 2017

1 reference

20 September 2017

11

1 reference

20 September 2017

61

1 reference

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice

20 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Signal-induced functions of the transcription factor TFII-I.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Opposing functions of TFII-I spliced isoforms in growth factor-induced gene expression

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Inhibition of TFII-I-dependent cell cycle regulation by p53.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

GTF2IRD1 in craniofacial development of humans and mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Characterizing the musical phenotype in individuals with Williams Syndrome.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Mutational mechanisms of Williams-Beuren syndrome deletions

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Murine fibroblasts lacking p21 undergo senescence and are resistant to transformation by oncogenic Ras.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Elastin is an essential determinant of arterial morphogenesis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Simian virus 40 transformation and the period of cellular deoxyribonucleic acid synthesis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.

20 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-61

An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-61

How to use the optical fractionator: an example based on the estimation of neurons in the hippocampal CA1 and CA3 regions of tree shrews

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-61

Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-61

21 January 2018

Asymmetrical ability.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865459

Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20403157

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Williams-Beuren syndrome: a model of recurrent genomic mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20403157

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-11-61

1 reference

Dimensions Publication ID

20 September 2017

0 references

1 reference

20 September 2017

PubMed publication ID

20403157

1 reference