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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… 
National Institutes of Health

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ApoptosisBiologic DevelopmentHomo sapiensOrganogenesis

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PAX3 wt Allele

Papers overview

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2016
2016
PAX3 and Waardenburg Syndrome Type 1
2013
2013
Novel mutations of PAX3, MITF and SOX10 genes found in Waardenburg syndrome types 1 and 2 in Brazilian patients
2012
2012
Regulation of Sensory Neurogenesis in the Trigeminal Placode: Notch Pathway Genes, Pax3 Isoforms, and Wnt Ligands
Regulation of Sensory Neurogenesis in the Trigeminal Placode: Notch Pathway Genes, Pax3 Isoforms, and Wnt Ligands Jason S. Adams… 
2011
2011
Bioinformatic analysis of PAX3 gene and PAX3 protein
Objective: To obtain more information about PAX3 gene and PAX3 protein.Methods: Bioinformatics approach were applied to analyze… 
2011
2011
Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II
Waardenburg syndrome (WS) is an auditory–pigmentary disorder resulting from melanocyte defects, with varying combinations of… 
2006
2006
FISH mapping of 10 canine BAC clones harbouring genes and microsatellites in the arctic fox and the Chinese raccoon dog genomes.
Cytogenetic mapping of the arctic fox and the Chinese raccoon dog were performed using a set of canine probes derived from the… 
2001
2001
„Auditory pigmentary syndromes“ — klinische Erscheinungsbilder und genetischer Hintergrund
ZusammenfassungUnter dem Begriff „Auditory pigmentary syndromes“ werden unterschiedliche Krankheitsbilder zusammengefasst, denen… 
2001
2001
Advances in Brief PAX 3 Is Expressed in Human Melanomas and Contributes to Tumor Cell Survival 1
Deregulated expression of the transcription factor PAX3 was observed previously in several tumors like rhabdomyosarcoma and Ewing… 
1998
1998
The mutation status of PAX3 and p53 genes in medulloblastoma.
The p53 and PAX3 genes were examined by PCR, SSCP and DNA sequencing methods in 50 and 58 paraffinembedded medullablastoma… 
1998
1998
Branchio-oculo-facial syndrome associated with a white forelock.
We report a father and his daughter with branchio-oculo-facial syndrome. Since birth the father, and to a lesser extent his…