![Genes | Free Full-Text | Gene Co-Expression Networks Restructured Gene Fusion in Rhabdomyosarcoma Cancers Genes | Free Full-Text | Gene Co-Expression Networks Restructured Gene Fusion in Rhabdomyosarcoma Cancers](https://www.mdpi.com/genes/genes-10-00665/article_deploy/html/images/genes-10-00665-g001.png)
Genes | Free Full-Text | Gene Co-Expression Networks Restructured Gene Fusion in Rhabdomyosarcoma Cancers
![Schematic representation of PAX3 gene, mRNA and protein organization.... | Download Scientific Diagram Schematic representation of PAX3 gene, mRNA and protein organization.... | Download Scientific Diagram](https://www.researchgate.net/publication/324947489/figure/fig1/AS:628734881169408@1526913485115/Schematic-representation-of-PAX3-gene-mRNA-and-protein-organization-The-PAX3-gene.png)
Schematic representation of PAX3 gene, mRNA and protein organization.... | Download Scientific Diagram
![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
![Pax3/7 duplicated and diverged independently in amphioxus, the basal chordate lineage | Scientific Reports Pax3/7 duplicated and diverged independently in amphioxus, the basal chordate lineage | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41598-018-27700-x/MediaObjects/41598_2018_27700_Fig1_HTML.jpg)
Pax3/7 duplicated and diverged independently in amphioxus, the basal chordate lineage | Scientific Reports
![Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I - ScienceDirect Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0378111917310004-fx1.jpg)
Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I - ScienceDirect
![PAX3 Confers Functional Heterogeneity in Skeletal Muscle Stem Cell Responses to Environmental Stress - ScienceDirect PAX3 Confers Functional Heterogeneity in Skeletal Muscle Stem Cell Responses to Environmental Stress - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1934590919301183-fx1.jpg)
PAX3 Confers Functional Heterogeneity in Skeletal Muscle Stem Cell Responses to Environmental Stress - ScienceDirect
![PAX3-NCOA2 fusion gene has a dual role in promoting the proliferation and inhibiting the myogenic differentiation of rhabdomyosarcoma cells | Oncogene PAX3-NCOA2 fusion gene has a dual role in promoting the proliferation and inhibiting the myogenic differentiation of rhabdomyosarcoma cells | Oncogene](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fonc.2013.491/MediaObjects/41388_2014_Article_BFonc2013491_Fig1_HTML.jpg)
PAX3-NCOA2 fusion gene has a dual role in promoting the proliferation and inhibiting the myogenic differentiation of rhabdomyosarcoma cells | Oncogene
Time-dependent Pax3-mediated chromatin remodeling and cooperation with Six4 and Tead2 specify the skeletal myogenic lineage in developing mesoderm | PLOS Biology
![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](http://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
![Pax3 and myogenic regulatory factors. (A)Relative mRNA levels of the... | Download Scientific Diagram Pax3 and myogenic regulatory factors. (A)Relative mRNA levels of the... | Download Scientific Diagram](https://www.researchgate.net/publication/45096906/figure/fig5/AS:486098267840516@1492906266358/Pax3-and-myogenic-regulatory-factors-ARelative-mRNA-levels-of-the-indicated-genes-in.png)
Pax3 and myogenic regulatory factors. (A)Relative mRNA levels of the... | Download Scientific Diagram
![Population genetic signature of positive selection on the PAX3 gene and... | Download Scientific Diagram Population genetic signature of positive selection on the PAX3 gene and... | Download Scientific Diagram](https://www.researchgate.net/profile/Xiaoming-Zhang-2/publication/351153379/figure/fig3/AS:1017895064702976@1619696503025/Population-genetic-signature-of-positive-selection-on-the-PAX3-gene-and-results-of_Q640.jpg)
Population genetic signature of positive selection on the PAX3 gene and... | Download Scientific Diagram
![Mutações existentes no gene PAX3. Localização das mutações existentes... | Download Scientific Diagram Mutações existentes no gene PAX3. Localização das mutações existentes... | Download Scientific Diagram](https://www.researchgate.net/profile/Maria-Naia-2/publication/277191527/figure/fig5/AS:391866748030981@1470439721205/Figura-5-Mutacoes-existentes-no-gene-PAX3-Localizacao-das-mutacoes-existentes-no-gene_Q320.jpg)
Mutações existentes no gene PAX3. Localização das mutações existentes... | Download Scientific Diagram
![Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report | BMC Pediatrics | Full Text Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report | BMC Pediatrics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12887-021-02521-6/MediaObjects/12887_2021_2521_Fig4_HTML.png)