Gene expression in cardiac tissues from infants with idiopathic conotruncal defects (Q33786282)

29 July 2017

title

Gene expression in cardiac tissues from infants with idiopathic conotruncal defects (English)

1 reference

29 July 2017

Douglas C Bittel

1

1 reference

29 July 2017

Merlin G Butler

2

1 reference

29 July 2017

Nataliya Kibiryeva

3

1 reference

29 July 2017

Jennifer A Marshall

4

1 reference

29 July 2017

Jie Chen

5

1 reference

29 July 2017

Gary K Lofland

6

1 reference

29 July 2017

James E O'Brien

7

1 reference

29 July 2017

publication date

5 January 2011

1 reference

29 July 2017

1 reference

29 July 2017

volume

4

1 reference

29 July 2017

page(s)

1

1 reference

Creative Commons Attribution 2.0 Generic

29 July 2017

copyright license

start time

5 January 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Identification of novel glial genes by single-cell transcriptional profiling of Bergmann glial cells from mouse cerebellum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Genetic mechanisms controlling cardiovascular development

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

The developmental genetics of congenital heart disease.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Whole genome microarray analysis of gene expression in subjects with fragile X syndrome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Waddington's widget: Hsp90 and the inheritance of acquired characters.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Principles for the buffering of genetic variation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Advances in the molecular genetics of congenital structural heart disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Outcomes of pregnancy in women with tetralogy of Fallot

4 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-1

Quantitative epigenetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-1

Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-1

Genome-wide array analysis of normal and malformed human hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-1

Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-1

Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-1

The hypoplastic heart in congenital diaphragmatic hernia: reduced expression of basic fibroblast growth factor and platelet-derived growth factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-1

NKX2.5mutations in patients with congenital heart disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Distinct requirements for extra-embryonic and embryonic bone morphogenetic protein 4 in the formation of the node and primitive streak and coordination of left-right asymmetry in the mouse.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3023653

Epigenetic regulation of translation reveals hidden genetic variation to produce complex traits

30 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-4-1

Congenital Heart Disease in 56,109 Births Incidence and Natural History

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21208432

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of significant congenital heart defects in children of parents with Fallot's tetralogy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21208432

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

DNA microarray analysis for human congenital heart disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21208432

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1755-8794-4-1

1 reference

Dimensions Publication ID

29 July 2017

0 references

1 reference

29 July 2017

1 reference