(Q43116746)

14 November 2017

Gain of function of Tbx1 affects pharyngeal and heart development in the mouse (English)

1 reference

14 November 2017

3

Antonio Baldini

1 reference

14 November 2017

1

Francesca Vitelli

1 reference

14 November 2017

Tuong Huynh

2

1 reference

14 November 2017

1 March 2009

1 reference

14 November 2017

1 reference

14 November 2017

47

1 reference

14 November 2017

3

1 reference

14 November 2017

188-195

1 reference

Identification of downstream genetic pathways of Tbx1 in the second heart field

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

In vivo response to high-resolution variation of Tbx1 mRNA dosage

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Required, tissue-specific roles for Fgf8 in outflow tract formation and remodeling

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Dissecting contiguous gene defects: TBX1.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Role of TBX1 in human del22q11.2 syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Chromosomal microdeletions: dissecting del22q11 syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Generalized lacZ expression with the ROSA26 Cre reporter strain

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

The 22q11.2 deletion syndrome: a gene dosage perspective.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

Cre-mediated excision of Fgf8 in the Tbx1 expression domain reveals a critical role for Fgf8 in cardiovascular development in the mouse

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

A genetic link between Tbx1 and fibroblast growth factor signaling.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2692027

A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field

15 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19253341

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19253341

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/DVG.20476

1 reference

14 November 2017

1 reference

14 November 2017

1 reference

PMCID

2692027