PAX9 gene

Known as: PAIRED DOMAIN GENE 9, PAIRED BOX GENE 9, paired box 9 
 
National Institutes of Health

Papers overview

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2010
2010
OBJECTIVES Oligodontia, a congenital lack of six or more teeth, is often associated with mutations in the PAX9 gene; therefore… (More)
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2005
2005
Pax9 belongs to the Pax family of transcriptional regulators that are defined by a highly conserved DNA-binding region, the… (More)
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2005
2005
Missing teeth (hypodontia and oligodontia) are a common developmental abnormality in humans and heterozygous mutations of PAX9… (More)
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Highly Cited
2003
Highly Cited
2003
Mutations in PAX9 have been described for families in which inherited oligodontia characteristically involves permanent molars… (More)
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Highly Cited
2002
Highly Cited
2002
Experimental and animal studies, as well as genetic mutations in man, have indicated that the development of dentition is under… (More)
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Highly Cited
2002
Highly Cited
2002
We recently identified a frame-shift mutation in the PAX9 gene as the underlying cause for hypodontia involving permanent molar… (More)
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Highly Cited
2001
Highly Cited
2001
Development of dentition is controlled by numerous genes, as has been shown by experimental animal studies and mutations that… (More)
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Highly Cited
2000
Highly Cited
2000
We identified a frameshift mutation in the paired domain of PAX9 following genome-wide analysis of a family segregating autosomal… (More)
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Highly Cited
1999
Highly Cited
1999
The paralogous genes Pax1 and Pax9 constitute one group within the vertebrate Pax gene family. They encode closely related… (More)
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Highly Cited
1998
Highly Cited
1998
Pax genes have been shown to play important roles in mammalian development and organogenesis. Pax9, a member of this… (More)
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