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TCF4 gene

Known as: SEF2-1B, Transcription Factor 4 Gene, bHLHb19 
This gene plays a role in transcriptional regulation.
National Institutes of Health

Related topics

Related topics

7 relations
Homo sapiensTCF4 protein, humanTCF7L2 geneTCF7L2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Methyl-mercury induces apoptosis through ROS-mediated endoplasmic reticulum stress and mitochondrial apoptosis pathways activation in rat cortical neurons
Abstract Methyl-mercury (MeHg) is a dangerous environmental contamination biotransformed from mercury or inorganic mercury… 
2016
2016
Partial deletion of TCF4 in three generation family with non-syndromic intellectual disability, without features of Pitt-Hopkins syndrome.
2014
2014
Expression of the E-cadherin/β-catenin/tcf-4 pathway in gastric diseases with relation to Helicobacter pylori infection: clinical and pathological implications.
OBJECTIVE To determine the expression of E-cadherin, β-catenin, and transcription factor 4 (TCF4) proteins in gastric diseases… 
2013
2013
FGF19 (fibroblast growth factor 19) as a novel target gene for activating transcription factor 4 in response to endoplasmic reticulum stress.
FGF19 (fibroblast growth factor 19), expressed in the small intestine, acts as an enterohepatic hormone by mediating inhibitory… 
2013
2013
Antagonizing Wnt Pathway in Diabetic Retinopathy
In this issue, Liu et al. (1) reported that kallistatin, an endogenous Wnt antagonist, exerted antiangiogenic and… 
2013
2013
Secretory Defect and Cytotoxicity
Background: D1080N mutation in interphotoreceptor retinoid-binding protein (IRBP) causes retinitis pigmentosa with unknown… 
2008
2008
General Transcription Factor IIA-γ Increases Osteoblast-specific Osteocalcin Gene Expression via Activating Transcription Factor 4 and Runt-related Transcription Factor 2*
ATF4 (activating transcription factor 4) is an osteoblast-enriched transcription factor that regulates terminal osteoblast… 
Highly Cited
2005
Highly Cited
2005
Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations
Isolated (non-syndromic) congenital cataract may be inherited as an autosomal dominant, autosomal recessive, or X-linked… 
2005
2005
Amino-acid limitation induces transcription from the human C/EBPbeta gene via an enhancer activity located downstream of the protein coding sequence.
For animals, dietary protein is critical for the nutrition of the organism and, at the cellular level, protein nutrition… 
1999
1999
Presence of activating transcription factor 4 (ATF4) in the porcine anterior pituitary
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