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PAX3-NCOA2 fusion gene has a dual role in promoting the proliferation and inhibiting the myogenic differentiation of rhabdomyosarcoma cells | Oncogene
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Transcriptome analyses based on genetic screens for Pax3 myogenic targets in the mouse embryo | BMC Genomics | Full Text
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PAX3 Confers Functional Heterogeneity in Skeletal Muscle Stem Cell Responses to Environmental Stress - ScienceDirect
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Molecules | Free Full-Text | Therapeutic Approaches Targeting PAX3-FOXO1 and Its Regulatory and Transcriptional Pathways in Rhabdomyosarcoma
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Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I - ScienceDirect
![Schematic representation of normal and aberrant splicing of the Pax-3... | Download Scientific Diagram Schematic representation of normal and aberrant splicing of the Pax-3... | Download Scientific Diagram](https://www.researchgate.net/publication/14776996/figure/fig4/AS:601662074941441@1520458825015/Schematic-representation-of-normal-and-aberrant-splicing-of-the-Pax-3-gene-in-wild-type.png)
Schematic representation of normal and aberrant splicing of the Pax-3... | Download Scientific Diagram
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Population genetic signature of positive selection on the PAX3 gene and... | Download Scientific Diagram
![Table 1 from Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome. | Semantic Scholar Table 1 from Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e8f2384dcdd750e00f43fd06427e5952370471ad/3-Figure2-1.png)
Table 1 from Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome. | Semantic Scholar
![Two novel mutations of PAX3 and SOX10 were characterized as genetic causes of Waardenburg Syndrome - Yu - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library Two novel mutations of PAX3 and SOX10 were characterized as genetic causes of Waardenburg Syndrome - Yu - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/2bc1a21f-62f0-4e03-a0c8-e1dca46fabd0/mgg31217-fig-0003-m.jpg)
Two novel mutations of PAX3 and SOX10 were characterized as genetic causes of Waardenburg Syndrome - Yu - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I - Ma - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
![The transcriptional activator PAX3-FKHR rescues the defects of Pax3 mutant mice but induces a myogenic gain-of-function phenotype with ligand-independent activation of Met signaling in vivo The transcriptional activator PAX3-FKHR rescues the defects of Pax3 mutant mice but induces a myogenic gain-of-function phenotype with ligand-independent activation of Met signaling in vivo](https://genesdev.cshlp.org/content/17/23/2950/F1.large.jpg)
The transcriptional activator PAX3-FKHR rescues the defects of Pax3 mutant mice but induces a myogenic gain-of-function phenotype with ligand-independent activation of Met signaling in vivo
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