Pax3/7 duplicated and diverged independently in amphioxus, the basal chordate lineage | Scientific Reports
Schematic representation of normal and aberrant splicing of the Pax-3... | Download Scientific Diagram
PAX3 - Wikipedia
![PDF] Down-regulation of PAX3 gene expression in rhabdomyosarcoma and melanoma | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/d57448b6fe842e1d8c1e44508ebf9f5cd3512a3d/77-Figure1.10-1.png "PDF] Down-regulation of PAX3 gene expression in rhabdomyosarcoma and melanoma | Semantic Scholar")
PDF] Down-regulation of PAX3 gene expression in rhabdomyosarcoma and melanoma | Semantic Scholar
Phenotypic diversity and genetic complexity of PAX3‐related Waardenburg syndrome - Somashekar - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Molecules | Free Full-Text | Therapeutic Approaches Targeting PAX3-FOXO1 and Its Regulatory and Transcriptional Pathways in Rhabdomyosarcoma
PAX3 (paired box 3) | Gene Report | BioGPS
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
Schematic representation of PAX3 gene, mRNA and protein organization.... | Download Scientific Diagram
Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I - ScienceDirect
How researchers discovered the genetic origin of the 'unibrow' and other hair traits
Waardenburg Syndrome, Type 3 | Hereditary Ocular Diseases
Elements regulating PAX3 expression. The cis-acting elements, their... | Download Scientific Diagram
Fusion of the Paired Box 3 (PAX3) and Myocardin (MYOCD) Genes in Pediatric Rhabdomyosarcoma | Cancer Genomics & Proteomics
Transcriptome analyses based on genetic screens for Pax3 myogenic targets in the mouse embryo | BMC Genomics | Full Text
Aberrant methylation of Pax3 gene and neural tube defects in association with exposure to polycyclic aromatic hydrocarbons | Clinical Epigenetics | Full Text
Frontiers | Case Report: A Novel Gross Deletion in PAX3 (10.26 kb) Identified in a Chinese Family With Waardenburg Syndrome by Third-Generation Sequencing
PAX3-NCOA2 fusion gene has a dual role in promoting the proliferation and inhibiting the myogenic differentiation of rhabdomyosarcoma cells | Oncogene
Two novel mutations of PAX3 and SOX10 were characterized as genetic causes of Waardenburg Syndrome.,Molecular Genetics & Genomic Medicine - X-MOL
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
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
PAX3 Gene - GeneCards | PAX3 Protein | PAX3 Antibody
Molecules | Free Full-Text | Therapeutic Approaches Targeting PAX3-FOXO1 and Its Regulatory and Transcriptional Pathways in Rhabdomyosarcoma
