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2. Ha, Chang Man, Park, Daehun, Kim, Yoonju, Rasenick, Mark M, Chang, Sunghoe. 2015. SNX14 is a bifunctional negative regulator for neuronal 5-HT6 receptor signaling. In Journal of cell science, 128, 1848-61. doi:10.1242/jcs.169581. https://pubmed.ncbi.nlm.nih.gov/25795301/
3. Akizu, Naiara, Cantagrel, Vincent, Zaki, Maha S, de Lonlay, Pascale, Gleeson, Joseph G. 2015. Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. In Nature genetics, 47, 528-34. doi:10.1038/ng.3256. https://pubmed.ncbi.nlm.nih.gov/25848753/
4. Huang, Hsien-Sung, Yoon, Bong-June, Brooks, Sherian, Zylka, Mark J, Philpot, Benjamin D. 2014. Snx14 regulates neuronal excitability, promotes synaptic transmission, and is imprinted in the brain of mice. In PloS one, 9, e98383. doi:10.1371/journal.pone.0098383. https://pubmed.ncbi.nlm.nih.gov/24859318/
5. Lv, Sha, Jiang, Hongyan, Yu, Lingyan, Sun, Liangliang, Xu, Junjun. 2024. SNX14 inhibits autophagy via the PI3K/AKT/mTOR signaling cascade in breast cancer cells. In Journal of molecular histology, 55, 391-401. doi:10.1007/s10735-024-10209-1. https://pubmed.ncbi.nlm.nih.gov/38869753/
6. Bryant, Dale, Liu, Yang, Datta, Sanchari, Henne, W Mike, Stanier, Philip. . SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20. In Human molecular genetics, 27, 1927-1940. doi:10.1093/hmg/ddy101. https://pubmed.ncbi.nlm.nih.gov/29635513/
7. Fenn, Joe, Boursnell, Mike, Hitti, Rebekkah J, Mellersh, Cathryn S, Forman, Oliver P. 2016. Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed. In BMC genetics, 17, 123. doi:10.1186/s12863-016-0433-y. https://pubmed.ncbi.nlm.nih.gov/27566131/
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