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NR2F2 gene

Known as: NF-E3, NUCLEAR RECEPTOR SUBFAMILY 2, GROUP F, MEMBER 2, SVP40 
This gene is involved in transcriptional regulation.
National Institutes of Health

Papers overview

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2018
2018
Malformations of cortical development (MCD) are a common cause of intractable seizures in humans. Among these, focal cortical… 
2018
2018
Development of an embryo from a single cell, zygote, to multicellular morulae requires activation of hundreds of genes that were… 
2018
2018
OBJECTIVES Congenital diaphragmatic hernia (CDH) is a developmental defect of the diaphragm that causes high newborn morbidity… 
2016
2016
Bone marrow-derived mesenchymal stem cells (BM-MSCs) are pivotal components of the leukemic microenvironment. BM-MSCs have been… 
2012
2012
Congenital diaphragmatic hernia (CDH) is a developmental defect of the diaphragm that causes high newborn mortality. Isolated or… 
2012
2012
Background The Nuclear Receptor 2F2 (NR2F2/COUP-TFII) heterozygous knockout mice display low basal insulinemia and enhanced… 
2010
2010
Expression of the gene encoding neurotensin/neuromedin N (NT/N) is mostly limited to the brain and specialized enteroendocrine N… 
2003
2003
Summary.  Factor (F)VII plays a critical role in initiation of coagulation. Several segments within the 5′ flanking region of the… 
1975
1975
Poyoma DNA replication is initiated predominatly at a site which is 29% from the EcoRI cleavage site. Molecules replicating from…