Microarray analysis reveals key genes and pathways in Tetralogy of Fallot (Q42546611)

2 November 2017

Microarray analysis reveals key genes and pathways in Tetralogy of Fallot (English)

1 reference

2 November 2017

1 reference

Yue-E He

1

1 reference

2 November 2017

Hui-Xian Qiu

2

1 reference

2 November 2017

Jian-Bing Jiang

3

1 reference

2 November 2017

Rong-Zhou Wu

4

1 reference

2 November 2017

Ru-Lian Xiang

5

1 reference

2 November 2017

Yuan-Hai Zhang

6

1 reference

2 November 2017

6 July 2017

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Molecular Medicine Reports

2 November 2017

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2 November 2017

16

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2 November 2017

3

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2 November 2017

2707-2713

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describes a project that uses

2 November 2017

Cytoscape

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9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

inferred from PubMed Central ID database lookup

limma

1 reference

22 June 2022

https://europepmc.org/article/PMC/5548054

inferred from PubMed Central ID database lookup

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Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic Networks

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Identification of differently expressed genes and small molecule drugs for Tetralogy of Fallot by bioinformatics strategy

28 May 2018

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28 May 2018

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Pontocerebellar hypoplasia type 3 with tetralogy of Fallot

28 May 2018

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Hepatic overexpression of SIRT1 in mice attenuates endoplasmic reticulum stress and insulin resistance in the liver

28 May 2018

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Gene expression in cardiac tissues from infants with idiopathic conotruncal defects

28 May 2018

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New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle

28 May 2018

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28 May 2018

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Identification of mutations in the ribosomal protein L5 (RPL5) and ribosomal protein L11 (RPL11) genes in Czech patients with Diamond-Blackfan anemia

28 May 2018

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XBP1 is essential for survival under hypoxic conditions and is required for tumor growth.

28 May 2018

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Development gone awry: congenital heart disease

28 May 2018

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28 May 2018

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Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot

28 May 2018

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28 May 2018

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

28 May 2018

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Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.

28 May 2018

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28 May 2018

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28 May 2018

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28 May 2018

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Myocardial degeneration in congenital heart disease. Comparison of morphologic findings in young and old patients with congenital heart disease associated with muscular obstruction to right ventricular outflow

28 May 2018

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Isolation and analysis of genes mainly expressed in adult mouse heart using subtractive hybridization cDNA library.

28 May 2018

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Noncoding RNA expression in myocardium from infants with tetralogy of Fallot

16 August 2018

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A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect

16 August 2018

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16 August 2018

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A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5548054

16 August 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/28713939

12 December 2020

inferred from PubMed ID database lookup

Frequent association of 22q11.2 deletion with tetralogy of Fallot

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28713939

12 December 2020

inferred from PubMed ID database lookup

Tetralogy of Fallot associated with chromosome 22q11 deletion

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28713939

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.3892/MMR.2017.6933

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tptnusafsbc2zlxn3rqbiaugui

30 July 2022

release_tptnusafsbc2zlxn3rqbiaugui

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tptnusafsbc2zlxn3rqbiaugui

30 July 2022

https://api.fatcat.wiki/v0/release/tptnusafsbc2zlxn3rqbiaugui

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/tptnusafsbc2zlxn3rqbiaugui

PubMed publication ID

1 reference

30 July 2022