(Q24810253)

3 July 2017

title

Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA) (English)

1 reference

3 July 2017

1 reference

6

Elizabeth Goldmuntz

1 reference

3 July 2017

7

Judith Goodship

1 reference

3 July 2017

Nadja Muncke

1

1 reference

3 July 2017

Beate Niesler

2

1 reference

3 July 2017

Ralph Roeth

3

1 reference

3 July 2017

Karin Schön

4

1 reference

3 July 2017

Heinz-Juergen Rüdiger

5

1 reference

3 July 2017

Gudrun Rappold

8

1 reference

3 July 2017

language of work or name

English

0 references

publication date

12 May 2005

1 reference

3 July 2017

1 reference

3 July 2017

volume

6

1 reference

3 July 2017

issue

1

0 references

page(s)

20

1 reference

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

3 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

X-linked situs abnormalities result from mutations in ZIC3

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

The role of Pitx2 during cardiac development. Linking left-right signaling and congenital heart diseases

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Identification of a Wnt/Dvl/beta-Catenin --> Pitx2 pathway mediating cell-type-specific proliferation during development

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Differential regulation of gene expression by PITX2 isoforms

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Regulation of left-right asymmetry by thresholds of Pitx2c activity

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

The Pitx2 protein in mouse development

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Dosage requirement of Pitx2 for development of multiple organs

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Neural crest cells contribute to normal aorticopulmonary septation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra- and periocular mesoderm and right pulmonary isomerism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Congenital heart malformations: prevalence, severity, survival, and quality of life

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Incidence of congenital heart disease: I. Postnatal incidence.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Incidence of congenital heart disease: II. Prenatal incidence

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Missense mutations and gene interruption in PROSIT240, a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries).

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Role of cardiac neural crest cells in cardiovascular development

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

Autosomal dominant transmission of isolated growth hormone deficiency in iris-dental dysplasia (Rieger's syndrome).

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1142516

X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-6-20

Pitx2 isoforms: involvement of Pitx2c but not Pitx2a or Pitx2b in vertebrate left-right asymmetry

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-6-20

Exclusion of PITX2 mutations as a major cause of CHARGE association.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-6-20

Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15890066

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Report of the New England Regional Infant Cardiac Program

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15890066

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The Rieger anomaly concomitant with multiple dental, craniofacial, and somatic midline anomalies and short stature

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15890066

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-6-20

1 reference

Dimensions Publication ID

3 July 2017

1020880218

0 references

PMC publication ID

1142516

0 references

1 reference