(Q57812915)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

main subject

22q11 deletion syndrome

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Peter J Scambler

6

1 reference

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9 January 2020

author name string

Katrina Prescott

1

1 reference

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9 January 2020

Sarah Ivins

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Elizabeth Lindsay

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Antonio Baldini

5

1 reference

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9 January 2020

publication date

19 March 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

116

1 reference

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9 January 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

page(s)

486-496

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00439-005-1274-3

9 January 2020

exact match

0 references

cites work

XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis.

1 reference

12 December 2020

Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region

1 reference

12 December 2020

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

1 reference

12 December 2020

Defective vascular development in connexin 45-deficient mice

1 reference

12 December 2020

Gene targeting reveals a widespread role for the high-mobility-group transcription factor Sox11 in tissue remodeling

1 reference

12 December 2020

A genetic link between Tbx1 and fibroblast growth factor signaling.

1 reference

12 December 2020

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

1 reference

12 December 2020

Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome

1 reference

12 December 2020

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome

1 reference

12 December 2020

Global disruption of the cerebellar transcriptome in a Down syndrome mouse model.

1 reference

12 December 2020

Upregulation of the cochaperone Mdg1 in endothelial cells is induced by stress and during in vitro angiogenesis

1 reference

12 December 2020

Transcriptional compensation for loss of an allele of the Ini1 tumor suppressor

1 reference

12 December 2020

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

12 December 2020

Recovery from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region

1 reference

12 December 2020

Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract

1 reference

12 December 2020

Study of dosage compensation in Drosophila.

1 reference

12 December 2020

Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6.

1 reference

12 December 2020

Loss of connexin45 causes a cushion defect in early cardiogenesis

1 reference

12 December 2020

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation.

1 reference

12 December 2020

Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome

1 reference

12 December 2020

Synthetic matrix metalloproteinase inhibitor decreases early cardiac neural crest migration in chicken embryos

1 reference

12 December 2020

Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes

1 reference

12 December 2020

Direct autoregulation and gene dosage compensation by POU-domain transcription factor Brn3a

1 reference

12 December 2020

Gene expression patterns in cell lines from patients with 18q- syndrome

1 reference

12 December 2020

Causes of the phenotype–genotype dissociation in DiGeorge syndrome: clues from mouse models

1 reference

12 December 2020

The nuclear factor SPBP contains different functional domains and stimulates the activity of various transcriptional activators

1 reference

12 December 2020

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

1 reference

12 December 2020

10.1007/S00439-005-1274-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15778864%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference