paired box gene 3 (Waardenburg syndrome 1), isoform CRA_c [Homo sapien - Protein

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PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids. [Biochem Biophys Res Commun. 2024]
PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids.
Li S, He C, Mei L, Wu X, Feng Y, Song J. Biochem Biophys Res Commun. 2024 Feb 26; 698:149510. Epub 2024 Jan 13.
Restoration of functional PAX3 transcriptional factor enhanced neuronal differentiation in PAX3b isoform-depleted neuroblastoma cells. [Cell Tissue Res. 2023]
Restoration of functional PAX3 transcriptional factor enhanced neuronal differentiation in PAX3b isoform-depleted neuroblastoma cells.
Muralidharan N, Murugan A, Raj PA, Jothi M. Cell Tissue Res. 2023 Jan; 391(1):55-65. Epub 2022 Nov 15.
A Novel Variant in Paired Box 3 Gene-related with Waardenburg Syndrome Type-1 in an Afghan Family. [J Coll Physicians Surg Pak. 2022]
A Novel Variant in Paired Box 3 Gene-related with Waardenburg Syndrome Type-1 in an Afghan Family.
Dogan M, Eroz R. J Coll Physicians Surg Pak. 2022 Aug; 32(8):S110-S112.

RefSeq genomic sequence
See the genomic reference sequence for the PAX3 gene (NG_011632.1).
RefSeq protein isoforms
See 8 reference sequence protein isoforms for the PAX3 gene.

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reagent reviews [ExactAntigen/Labome]
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