(Q28510707)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16870172%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

title

Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis (English)

2 references

25 January 2017

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27 December 2019

1 reference

GOA release 2020-03-11

1 reference

7

1 reference

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27 December 2019

Benoit G. Bruneau

12

1 reference

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27 December 2019

8

J G Seidman

1 reference

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27 December 2019

9

Christine E Seidman

1 reference

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27 December 2019

author name string

Yonghong Zhu

2

2 references

25 January 2017

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27 December 2019

Ilyas Vahora

3

2 references

25 January 2017

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27 December 2019

Brian Nieman

4

2 references

25 January 2017

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27 December 2019

Kazuko Koshiba-Takeuchi

5

2 references

25 January 2017

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27 December 2019

Lorinda Davidson

6

2 references

25 January 2017

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27 December 2019

Alessandro D Mori

1

1 reference

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27 December 2019

X Josette Chen

10

1 reference

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27 December 2019

R Mark Henkelman

11

1 reference

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27 December 2019

language of work or name

English

0 references

publication date

24 May 2006

1 reference

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27 December 2019

published in

Developmental Biology

2 references

25 January 2017

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27 December 2019

volume

297

2 references

25 January 2017

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27 December 2019

page(s)

566-586

1 reference

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27 December 2019

issue

2

2 references

25 January 2017

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Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

27 December 2019

cites work

1 reference

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Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations

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Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

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Expressivity of Holt-Oram syndrome is not predicted by TBX5 genotype

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Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome.

7 January 2021

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

7 January 2021

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Patterning the embryonic heart: identification of five mouse Iroquois homeobox genes in the developing heart

7 January 2021

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Transcriptional regulation of cardiac development: implications for congenital heart disease and DiGeorge syndrome

7 January 2021

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GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

7 January 2021

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Expression of T-box genes Tbx2-Tbx5 during chick organogenesis.

7 January 2021

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An interacting network of T-box genes directs gene expression and fate in the zebrafish mesoderm

7 January 2021

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Development gone awry: congenital heart disease

7 January 2021

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Cooperative action of Tbx2 and Nkx2.5 inhibits ANF expression in the atrioventricular canal: implications for cardiac chamber formation

7 January 2021

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The transcriptional repressor Tbx3 delineates the developing central conduction system of the heart.

7 January 2021

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Causes of clinical diversity in human TBX5 mutations

7 January 2021

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Exploration, normalization, and summaries of high density oligonucleotide array probe level data

7 January 2021

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

7 January 2021

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Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart

7 January 2021

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

7 January 2021

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Formation of multiple hearts in mice following deletion of beta-catenin in the embryonic endoderm

7 January 2021

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Baf60c is essential for function of BAF chromatin remodelling complexes in heart development

7 January 2021

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

7 January 2021

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

7 January 2021

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A regulatory code for neurogenic gene expression in the Drosophila embryo

7 January 2021

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Inhibition of Wnt activity induces heart formation from posterior mesoderm

7 January 2021

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

7 January 2021

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An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination

7 January 2021

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Development of the building plan of the heart.

7 January 2021

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7 January 2021

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A WW domain protein TAZ is a critical coactivator for TBX5, a transcription factor implicated in Holt-Oram syndrome

7 January 2021

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A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family

7 January 2021

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7 January 2021

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A regulatory network of T-box genes and the even-skipped homologue vab-7 controls patterning and morphogenesis in C. elegans

7 January 2021

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Slit and Robo control cardiac cell polarity and morphogenesis

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Direct removal in the mouse of a floxed neo gene from a three-loxP conditional knockout allele by two novel approaches

7 January 2021

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Role of TBX1 in human del22q11.2 syndrome

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

3730810

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16870172%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

3730810

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

3730810