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EN2 gene

Known as: engrailed homeobox 2, Engrailed Homeobox 2 Gene, ENGRAILED 2 
This gene is involved in transcriptional regulation.
National Institutes of Health

Related topics

Related topics

9 relations
Cell Differentiation processEmbryonic DevelopmentHomeobox Protein Engrailed-2Homo sapiens

Narrower (1)

EN2 wt Allele

Broader (1)

Genes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
EN2 in Prostate Cancer.
2013
2013
Improving Production Traits for El-Salam and Mandarah Chicken Strains by Crossing II-Estimation of Crossbreeding Effects on Egg Production and Egg Quality Traits
A crossbreeding experiment was carried out between two Egyptian strains of chickens namely Mandarah (MM) and ElSalam (SS). The… 
Highly Cited
2012
Highly Cited
2012
Urinary engrailed‐2 (EN2) levels predict tumour volume in men undergoing radical prostatectomy for prostate cancer
What's known on the subject? and What does the study add? 
2011
2011
Association study of the CNS patterning genes and autism in Han Chinese in Taiwan
2008
2008
Nonclassical secretion of human catalase on the surface of CHO cells is more efficient than classical secretion
2008
2008
Association of the Homeobox Transcription Factor Gene ENGRAILED 2 with Autistic Disorder in Chinese Children
Background: Autism is a neurodevelopmental disorder with a strong genetic component. Previous studies have mapped the disease to… 
2005
2005
Engrailed-ZmOCL1 fusions cause a transient reduction of kernel size in maize
ZmOCL1 is the founding member of the ZmOCL (Outer Cell Layer) family encoding putative transcription factors of the HD-ZIP IV… 
Highly Cited
2003
Highly Cited
2003
No association between the EN2 gene and autistic disorder
A utistic spectrum disorders (MIM 209850), which include autism, Asperger syndrome, and pervasive developmental disorder (PDD… 
2002
2002
Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1.
Joubert syndrome (JS) is a rare autosomal recessive malformation syndrome involving agenesis or dysgenesis of the cerebellar… 
2000
2000
Evaluación de un programa de hospitalización a domicilio para niños con cáncer
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