Functional dissection of sequence-specific NKX2-5 DNA binding domain mutations associated with human heart septation defects using a yeast-based system. (Q53621281)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Functional dissection of sequence-specific NKX2-5 DNA binding domain mutations associated with human heart septation defects using a yeast-based system.	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Functional dissection of sequence-specific NKX2-5 DNA binding domain mutations associated with human heart septation defects using a yeast-based system (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Michael A Resnick

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

author name string

Alberto Inga

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Stella Marie Reamon-Buettner

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Juergen Borlak

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

publication date

25 May 2005

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Human Molecular Genetics

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

14

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

14

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1965-1975

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15917268%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Homeodomain factor Nkx2-5 in heart development and disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Intramolecular control of transcriptional activity by the NK2-specific domain in NK-2 homeodomain proteins

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

A genetic blueprint for cardiac development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Transcriptional regulation of vertebrate cardiac morphogenesis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Nkx2.5 and Nkx2.6, homologs of Drosophila tinman, are required for development of the pharynx

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Function follows form: cardiac conduction system defects in Nkx2-5 mutation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Biochemical analyses of eight NKX2.5 homeodomain missense mutations causing atrioventricular block and cardiac anomalies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

The unexpected landscape of in vivo somatic mutation in a human epithelial cell lineage

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Differential transactivation by the p53 transcription factor is highly dependent on p53 level and promoter target sequence.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Mammalian transcription factors in yeast: strangers in a familiar land

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Chromosomal site-specific double-strand breaks are efficiently targeted for repair by oligonucleotides in yeast

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Functional mutants of the sequence-specific transcription factor p53 and implications for master genes of diversity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

NK-2 homeobox genes and heart development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Characterization of homo- and heterodimerization of cardiac Csx/Nkx2.5 homeoprotein

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Identification of novel DNA binding targets and regulatory domains of a murine tinman homeodomain factor, nkx-2.5.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Context-dependent transcriptional cooperation mediated by cardiac transcription factors Csx/Nkx-2.5 and GATA-4.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Congenital heart disease caused by mutations in the transcription factor NKX2-5

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

NKX2.5 mutations in patients with tetralogy of fallot

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Development gone awry: congenital heart disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Common arterial trunk associated with a homeodomain mutation of NKX2.6

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

The cardiac transcription factors Nkx2-5 and GATA-4 are mutual cofactors

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

The cardiac tissue-restricted homeobox protein Csx/Nkx2.5 physically associates with the zinc finger protein GATA4 and cooperatively activates atrial natriuretic factor gene expression

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

GATA-4 and Nkx-2.5 coactivate Nkx-2 DNA binding targets: role for regulating early cardiac gene expression

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

A simple p53 functional assay for screening cell lines, blood, and tumors

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Use of a yeast assay to detect functional alterations in p53 in prostate cancer: review and future directions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI202

21 January 2018

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q53621281&oldid=1466633495"