https://researchdiscovery.drexel.edu/esploro/outputs/doctoral/Multi-omics-characterization-of-the-loss-of/991021212414304721
Multi-omics characterization of the loss of transcriptomic modulators SOX10 and BAP1 in cutaneous...
Identifying alterations to the transcriptomic networks in cancers is crucial for studying their mechanisms and exploiting their weaknesses. In cutaneous...
https://www.wikidata.org/wiki/Q40432015
Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of...
https://edrn.cancer.gov/data-and-resources/miscellaneous-resources/uniprotkbswiss-prot-entry-for-human-sox10/
UniProtKB/Swiss-Prot entry for human SOX10
This is a miscellaneous resource located at https://www.uniprot.org/uniprot/P56693
for humanswissprotentry
https://experts.umn.edu/en/publications/prdm1a-regulates-sox10-and-islet1-in-the-development-of-neural-cr/
prdm1a Regulates sox10 and islet1 in the development of neural crest and Rohon-Beard sensory...
https://www.frontiersin.org/journals/molecular-neuroscience/articles/10.3389/fnmol.2018.00181/full
Frontiers | Key Genes and Pathways Associated With Inner Ear Malformation in SOX10 p.R109W Mutation...
SOX10 (SRY-box 10) mutation may lead to inner ear deformities. However, its molecular mechanisms on inner ear development are not clear. In this work. The in...
https://researchconnect.buffalo.edu/en/publications/loss-of-sox10-function-contributes-to-the-phenotype-of-human-merl/
Loss of SOX10 function contributes to the phenotype of human Merlin-null schwannoma cells - SUNY...