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Paired Mesoderm Homeobox Protein 2B

Known as: PHOX2B Homeodomain Protein, Paired-Like Homeobox 2B, Neuroblastoma Phox 
Paired mesoderm homeobox protein 2B (314 aa, ~32 kDa) is encoded by the human PHOX2B gene. This protein plays a role in the regulation of gene… 
National Institutes of Health

Papers overview

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2020
2020
Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder of an autonomic nervous disorder that affects… 
2019
2019
ABSTRACT Paired-like homeobox (PHOX)2B is considered to be the causative gene of congenital central hypoventilation syndrome… 
2013
2013
Background: The mechanisms that control the Prrxl1 expression are poorly understood. Results: Several regulatory elements present… 
2011
2011
The generation of neural cell diversity in the developing central nervous system relies on mechanisms that provide spatial and… 
2007
2007
AbstractThe expansion of polyalanine repeats is known to cause at least nine disorders, including congenital central… 
2004
2004
Dilp1 is a semi-dominant mouse mutation that causes dilated pupils when heterozygous and is lethal when homozygous. We report… 
Highly Cited
2000
Highly Cited
2000
The homeodomain transcription factors Arix/Phox2a and NBPhox/Phox2b play a role in the specification of the noradrenergic… 
1999
1999
Homeodomain proteins play essential roles in basic processes during embryogenesis and development. NBPhox, a vertebrate paired…