(Q50701627)

English

Altered Tbx1 gene expression is associated with abnormal oesophageal development in the adriamycin mouse model of oesophageal atresia/tracheo-oesophageal fistula.

scientific article published in February 2014

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

Altered Tbx1 gene expression is associated with abnormal oesophageal development in the adriamycin mouse model of oesophageal atresia/tracheo-oesophageal fistula. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

1 reference

based on heuristic

inferred from title

3

object named as

Prem Puri

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

author name string

Danielle Mc Laughlin

1

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

Paula Murphy

2

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

publication date

1 February 2014

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

Pediatric Surgery International

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

30

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

2

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

143-149

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

https://scigraph.springernature.com/pub.10.1007/s00383-013-3455-9

0 references

Evolution of the mechanisms and molecular control of endoderm formation

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

VACTERL/VATER Association

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Abnormal notochord branching is associated with foregut malformations in the adriamycin treated mouse model

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

The T-box gene family

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

The changing epidemiology of congenital heart disease

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesis

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Esophageal atresia and tracheo-esophageal fistula associated with coarctation of the aorta, CHARGE association, and DiGeorge syndrome: a case report and literature review

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype.

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

VATER and hydrocephalus: distinct syndrome?

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Tbx4-Fgf10 system controls lung bud formation during chicken embryonic development.

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Mesenchymal expression of Tbx4 gene is not altered in Adriamycin mouse model

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Optical projection tomography as a tool for 3D microscopy and gene expression studies

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

3D representation of Wnt and Frizzled gene expression patterns in the mouse embryo at embryonic day 11.5 (Ts19).

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Genetic and environmental factors in the etiology of esophageal atresia and/or tracheoesophageal fistula: an overview of the current concepts

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

TBX1, a DiGeorge syndrome candidate gene, is inhibited by retinoic acid

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

The role of chordin/Bmp signals in mammalian pharyngeal development and DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Wnt signalling mediated by Tbx2b regulates cell migration during formation of the neural plate.

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Regional morphogenesis in the hypothalamus: a BMP-Tbx2 pathway coordinates fate and proliferation through Shh downregulation.

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Tbx1 regulates proliferation and differentiation of multipotent heart progenitors

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Three-dimensional imaging clarifies the process of tracheoesophageal separation in the rat.

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Absence of the vagus nerve in the stomach of Tbx1-/- mutant mice

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular development

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

The level of BMP4 signaling is critical for the regulation of distinct T-box gene expression domains and growth along the dorso-ventral axis of the optic cup

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Sonic hedgehog is essential to foregut development

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Retracted: Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Inactivation of Bmp4 from the Tbx1 expression domain causes abnormal pharyngeal arch artery and cardiac outflow tract remodeling.

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Morphogenesis of the trachea and esophagus: current players and new roles for noggin and Bmps

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

De novo microduplication at 22q11.21 in a patient with VACTERL association

1 reference

https://api.crossref.org/works/10.1007%2FS00383-013-3455-9

21 January 2018

Adriamycin-Induced Models of VACTERL Association

1 reference

https://pubmed.ncbi.nlm.nih.gov/24356861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions

1 reference

https://pubmed.ncbi.nlm.nih.gov/24356861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse.

1 reference

https://pubmed.ncbi.nlm.nih.gov/24356861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated

1 reference

https://pubmed.ncbi.nlm.nih.gov/24356861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00383-013-3455-9

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 March 2018

http://europepmc.org/abstract/MED/24356861

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