1. Wiertelak, Wojciech, Olczak, Mariusz, Maszczak-Seneczko, Dorota. 2022. An interaction between SLC35A1 and ST3Gal4 is differentially affected by CDG-causing mutations in the SLC35A1 gene. In Biochemical and biophysical research communications, 635, 46-51. doi:10.1016/j.bbrc.2022.10.019. https://pubmed.ncbi.nlm.nih.gov/36257191/
2. Han, Julianna, Perez, Jasmine T, Chen, Cindy, tenOever, Benjamin, Manicassamy, Balaji. . Genome-wide CRISPR/Cas9 Screen Identifies Host Factors Essential for Influenza Virus Replication. In Cell reports, 23, 596-607. doi:10.1016/j.celrep.2018.03.045. https://pubmed.ncbi.nlm.nih.gov/29642015/
3. Zuo, Bin, Yang, Fei, Huang, Lulu, He, Yang, Xia, Lijun. 2024. Endothelial Slc35a1 Deficiency Causes Loss of LSEC Identity and Exacerbates Neonatal Lipid Deposition in the Liver in Mice. In Cellular and molecular gastroenterology and hepatology, 17, 1039-1061. doi:10.1016/j.jcmgh.2024.03.002. https://pubmed.ncbi.nlm.nih.gov/38467191/
4. Szulc, Bożena, Zadorozhna, Yelyzaveta, Olczak, Mariusz, Wiertelak, Wojciech, Maszczak-Seneczko, Dorota. 2020. Novel Insights into Selected Disease-Causing Mutations within the SLC35A1 Gene Encoding the CMP-Sialic Acid Transporter. In International journal of molecular sciences, 22, . doi:10.3390/ijms22010304. https://pubmed.ncbi.nlm.nih.gov/33396746/
5. Wang, Jieru, Liu, Hailong, Yang, Yuqing, Wang, Chonglong, Xie, Shengsong. 2023. Genome-scale CRISPR screen identifies TRIM2 and SLC35A1 associated with porcine epidemic diarrhoea virus infection. In International journal of biological macromolecules, 250, 125962. doi:10.1016/j.ijbiomac.2023.125962. https://pubmed.ncbi.nlm.nih.gov/37499712/
6. Ma, Xiaolin, Li, Yun, Kondo, Yuji, Fu, Jianxin, Xia, Lijun. 2021. Slc35a1 deficiency causes thrombocytopenia due to impaired megakaryocytopoiesis and excessive platelet clearance in the liver. In Haematologica, 106, 759-769. doi:10.3324/haematol.2019.225987. https://pubmed.ncbi.nlm.nih.gov/32303557/
7. Kauskot, Alexandre, Pascreau, Tiffany, Adam, Frédéric, Melki, Judith, Borgel, Delphine. 2018. A mutation in the gene coding for the sialic acid transporter SLC35A1 is required for platelet life span but not proplatelet formation. In Haematologica, 103, e613-e617. doi:10.3324/haematol.2018.198028. https://pubmed.ncbi.nlm.nih.gov/30115659/
8. Yang, Yanling, Wang, Yuchen, Campbell, Danielle E, Baldridge, Megan, López, Carolina B. 2025. SLC35A2 gene product modulates paramyxovirus fusion events during infection. In PLoS pathogens, 21, e1012531. doi:10.1371/journal.ppat.1012531. https://pubmed.ncbi.nlm.nih.gov/39792924/
9. Riemersma, Moniek, Sandrock, Julia, Boltje, Thomas J, van Bokhoven, Hans, Lefeber, Dirk J. 2014. Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal α-dystroglycan O-mannosylation, independent from sialic acid. In Human molecular genetics, 24, 2241-6. doi:10.1093/hmg/ddu742. https://pubmed.ncbi.nlm.nih.gov/25552652/