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PHOX2B wt Allele

Known as: NBLST2, PMX2B, Paired-Like Homeobox 2b wt Allele 
Human PHOX2B wild-type allele is located in the vicinity of 4p12 and is approximately 5 kb in length. This allele, which encodes paired mesoderm… 
National Institutes of Health

Related topics

Related topics

7 relations
4p12Familial NeuroblastomaHomo sapiensPaired Mesoderm Homeobox Protein 2B

Broader (1)

PHOX2B gene

Papers overview

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2019
2019
Analysis of the neuronal network of the medullary respiratory center in transgenic rats expressing archaerhodopsin-3 in Phox2b-expressing cells
Review
2018
Review
2018
Congenital heart disease and aortic arch variants associated with mutation in PHOX2B
Congenital central hypoventilation syndrome (CCHS, OMIM 209880) is a rare autosomal dominant disorder caused by mutation in… 
Review
2016
Review
2016
Author's Reply.
To the Editor, We thank Warren and Shimada for their interest and thoughtful comments on our recent manuscript, “Improving… 
Review
2014
Review
2014
Cytoarchitecture and CO(2) sensitivity of Phox2b-positive Parafacial neurons in the newborn rat medulla.
2012
2012
How does CO2 activate the neurons of the retrotrapezoid nucleus?
In the realm of biology, CO2 usually operates via the proxy of pH and virtually all proteins, ion channels and neurons display… 
2012
2012
NPARM in PHOX2B: why some things just should not be expanded.
Although the neural crest and its derivatives have been studied for a very long time, disorders of derivatives of the crest, the… 
2011
2011
Impaired Ventilatory and Thermoregulatory Responses to Hypoxic Stress in Newborn Phox2b Heterozygous Knock-Out Mice
The Phox2b genesis necessary for the development of the autonomic nervous system, and especially, of respiratory neuronal… 
2011
2011
Region- and cell type-selective expression of the evolutionarily conserved Nolz-1/zfp503 gene in the developing mouse hindbrain.
2007
2007
De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome: unequal sister chromatid exchange during paternal gametogenesis
AbstractThe expansion of polyalanine repeats is known to cause at least nine disorders, including congenital central… 
2004
2004
Sudden infant death syndrome is not associated with the mutation of PHOX2B gene, a major causative gene of congenital central hypoventilation syndrome.
Sudden infant death syndrome (SIDS) is a major cause of infant death, but its etiology is unknown. There are several independent… 
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