Homo sapiens SRY-box transcription factor 3 (SOX3), RefSeqGene on chro - Nucleotide

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ROR2 deficit may induce the tetralogy of Fallot via down-regulating of β-catenin/SOX3/HSPA6 in vitro and in vivo. [J Cell Mol Med. 2023]
ROR2 deficit may induce the tetralogy of Fallot via down-regulating of β-catenin/SOX3/HSPA6 in vitro and in vivo.
Guo R, Guo YZ, Zhou Q, Li G, Du Z, Shi Y, Xing Q. J Cell Mol Med. 2023 Nov; 27(22):3539-3552. Epub 2023 Sep 25.
A complex structural variant near SOX3 causes X-linked split-hand/foot malformation. [HGG Adv. 2023]
A complex structural variant near SOX3 causes X-linked split-hand/foot malformation.
de Boer E, Marcelis C, Neveling K, van Beusekom E, Hoischen A, Klein WM, de Leeuw N, Mantere T, Melo US, van Reeuwijk J, et al. HGG Adv. 2023 Jul 13; 4(3):100200. Epub 2023 Apr 25.
ARPC1B promotes mesenchymal phenotype maintenance and radiotherapy resistance by blocking TRIM21-mediated degradation of IFI16 and HuR in glioma stem cells. [J Exp Clin Cancer Res. 2022]
ARPC1B promotes mesenchymal phenotype maintenance and radiotherapy resistance by blocking TRIM21-mediated degradation of IFI16 and HuR in glioma stem cells.
Gao Z, Xu J, Fan Y, Zhang Z, Wang H, Qian M, Zhang P, Deng L, Shen J, Xue H, et al. J Exp Clin Cancer Res. 2022 Nov 16; 41(1):323. Epub 2022 Nov 16.

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Nucleotide