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HOXA2 gene

Known as: HOMEOBOX A2, HOXA2 
National Institutes of Health

Papers overview

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2017
2016
2016
AbstractTreacher Collins syndrome is an autosomal dominant craniofacial malformation mainly caused by mutations in the TCOF1 gene… 
2013
2013
In a previous study using transgenic mice ectopically expressing Hoxa2 during chondrogenesis, we associated the animal phenotype… 
2013
2013
Introduction. Using transgenic mice ectopically expressing Hoxa2 all along chondrogenesis, we showed that Hoxa2 exerts a negative… 
2012
2009
2009
Valproic acid (VPA) has been shown to cause neural tube defects in humans and mice, but its mechanism of action has not been… 
2004
2004
Hox genes are evolutionarily conserved transcription factors which act to control important developmental pathways involved in… 
2003
2003
Hoxa2~ a second arch selector gene~ when deleted results in many cranial abnormalities including a cleft plate. The occurrence of… 
2001
2001
Hoxa2 is required for a variety of developmental processes in the branchial arches and in the hindbrain. We have created a Hoxa2…