1. Frey, Laura, Ziętara, Natalia, Łyszkiewicz, Marcin, Somech, Raz, Klein, Christoph. . Mammalian VPS45 orchestrates trafficking through the endosomal system. In Blood, 137, 1932-1944. doi:10.1182/blood.2020006871. https://pubmed.ncbi.nlm.nih.gov/33512427/
2. Mugume, Yosia, Roy, Rahul, Agbemafle, William, Vue, Yee, Bassham, Diane C. 2023. VPS45 is required for both diffuse and tip growth of Arabidopsis thaliana cells. In Frontiers in plant science, 14, 1120307. doi:10.3389/fpls.2023.1120307. https://pubmed.ncbi.nlm.nih.gov/36923123/
3. Cowles, C R, Emr, S D, Horazdovsky, B F. . Mutations in the VPS45 gene, a SEC1 homologue, result in vacuolar protein sorting defects and accumulation of membrane vesicles. In Journal of cell science, 107 ( Pt 12), 3449-59. doi:. https://pubmed.ncbi.nlm.nih.gov/7706396/
4. Stepensky, Polina, Saada, Ann, Cowan, Marianne, Bryant, Nia J, Mevorach, Dror. 2013. The Thr224Asn mutation in the VPS45 gene is associated with the congenital neutropenia and primary myelofibrosis of infancy. In Blood, 121, 5078-87. doi:10.1182/blood-2012-12-475566. https://pubmed.ncbi.nlm.nih.gov/23599270/
5. Zhi, Renhou, Li, Qi, Zhang, Huiqin, Fan, Fan. 2025. VPS45 Contributes to the Progression of Hepatocellular Carcinoma by Triggering the Wnt/β-Catenin Signaling Pathway. In Molecular carcinogenesis, 64, 744-755. doi:10.1002/mc.23884. https://pubmed.ncbi.nlm.nih.gov/39835603/
6. Shadur, Bella, Asherie, Nathalie, Newburger, Peter E, Stepensky, Polina. 2018. How we approach: Severe congenital neutropenia and myelofibrosis due to mutations in VPS45. In Pediatric blood & cancer, 66, e27473. doi:10.1002/pbc.27473. https://pubmed.ncbi.nlm.nih.gov/30294941/
7. Vilboux, Thierry, Lev, Atar, Malicdan, May Christine V, Gahl, William A, Somech, Raz. 2013. A congenital neutrophil defect syndrome associated with mutations in VPS45. In The New England journal of medicine, 369, 54-65. doi:10.1056/NEJMoa1301296. https://pubmed.ncbi.nlm.nih.gov/23738510/
智鼠故事 
