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PAX3 gene

Known as: paired box 3, Paired Box Gene 3 (Waardenburg Syndrome 1) Gene, HUP2 
This gene plays a role in the transcriptional activation of target genes. It is involved in melanogenesis, neurogenesis and skeletal muscle… Expand
National Institutes of Health

Papers overview

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Review
2007
Review
2007
Pax genes play key roles in the formation of tissues and organs during embryogenesis. Pax3 and Pax7 mark myogenic progenitor… Expand
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Highly Cited
2007
Highly Cited
2007
Pax3 and Pax7 play distinct but overlapping roles in developmental and postnatal myogenesis. The mechanisms involved in the… Expand
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Highly Cited
2005
Highly Cited
2005
During vertebrate development, successive phases of embryonic and fetal myogenesis lead to the formation and growth of skeletal… Expand
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Highly Cited
2005
Highly Cited
2005
FGF, WNT, and BMP signaling promote neural crest formation at the neural plate boundary in vertebrate embryos. To understand how… Expand
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Highly Cited
2005
Highly Cited
2005
A number of regulatory genes have been implicated in neural crest development. However, the molecular mechanism of how neural… Expand
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Highly Cited
2004
Highly Cited
2004
Pax genes encode evolutionarily conserved transcription factors that play critical roles in development. Pax3 and Pax7 constitute… Expand
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Highly Cited
2000
Highly Cited
2000
Waardenburg syndrome (WS) is an autosomal dominant disorder with an incidence of 1 in 40 000 that manifests with sensorineural… Expand
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Highly Cited
2000
Highly Cited
2000
Abstract. Waardenburg syndrome (WS) is associated with neural crest-derived melanocyte deficiency caused by mutations in either… Expand
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Highly Cited
1996
Highly Cited
1996
Pax3 is a transcription factor whose expression has been used as a marker of myogenic precursor cells arising in the lateral… Expand
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Highly Cited
1993
Highly Cited
1993
Alveolar rhabdomyosarcoma, a malignant tumor of skeletal muscle, is characterized by a chromosomal translocation, t(2;13)(q35;q14… Expand
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