1. Dhekne, Herschel S, Pylypenko, Olena, Overeem, Arend W, Houdusse, Anne, van IJzendoorn, Sven C D. 2018. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. In Human mutation, 39, 333-344. doi:10.1002/humu.23386. https://pubmed.ncbi.nlm.nih.gov/29266534/
2. Nan, Haocheng, Han, Lili, Ma, Jiequn, Su, Rujuan, He, Jianjun. 2018. STX3 represses the stability of the tumor suppressor PTEN to activate the PI3K-Akt-mTOR signaling and promotes the growth of breast cancer cells. In Biochimica et biophysica acta. Molecular basis of disease, 1864, 1684-1692. doi:10.1016/j.bbadis.2018.01.031. https://pubmed.ncbi.nlm.nih.gov/29408595/
3. Motoike, Serika, Taguchi, Kei, Harada, Kana, Irifune, Masahiro, Sakai, Norio. 2021. Syntaxin 3 interacts with serotonin transporter and regulates its function. In Journal of pharmacological sciences, 145, 297-307. doi:10.1016/j.jphs.2021.01.007. https://pubmed.ncbi.nlm.nih.gov/33712280/
4. Janecke, Andreas R, Liu, Xiaoqin, Adam, Rüdiger, Heidelberger, Ruth, Janz, Roger. 2021. Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects. In Human genetics, 140, 1143-1156. doi:10.1007/s00439-021-02284-1. https://pubmed.ncbi.nlm.nih.gov/33974130/
5. Despars, Geneviève, Periasamy, Pravin, Tan, Jonathan, O'Neill, Terence J, O'Neill, Helen C. . Gene signature of stromal cells which support dendritic cell development. In Stem cells and development, 17, 917-27. doi:10.1089/scd.2007.0170. https://pubmed.ncbi.nlm.nih.gov/18564035/
6. Pournami, Femitha, Mk, Alok Kumar, Panackal, Anila V, Prabhakar, Jyothi, Jain, Naveen. 2020. Microvillus Inclusion Disease: A Rare Mutation of STX3 in Exon 9 Causing Fatal Congenital Diarrheal Disease. In Journal of pediatric genetics, 11, 154-157. doi:10.1055/s-0040-1716401. https://pubmed.ncbi.nlm.nih.gov/35769957/