1. Ravindran, Ethiraj, Arashiki, Nobuto, Becker, Lena-Luise, Nakamura, Fumio, Kaindl, Angela M. 2022. Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. In eLife, 11, . doi:10.7554/eLife.80793. https://pubmed.ncbi.nlm.nih.gov/36511780/
2. Asano, Tetsuya, Nakamura, Haruko, Kawamoto, Yuko, Doi, Hiroshi, Tanaka, Fumiaki. 2022. Inhibition of Crmp1 Phosphorylation at Ser522 Ameliorates Motor Function and Neuronal Pathology in Amyotrophic Lateral Sclerosis Model Mice. In eNeuro, 9, . doi:10.1523/ENEURO.0133-22.2022. https://pubmed.ncbi.nlm.nih.gov/35523582/
3. Li, Jinan, Liu, Chang, Zhao, Bo. 2022. Collapsin Response Mediator Protein 1 (CRMP1) Is Required for High-Frequency Hearing. In The American journal of pathology, 192, 805-812. doi:10.1016/j.ajpath.2022.01.011. https://pubmed.ncbi.nlm.nih.gov/35181334/
4. Da Silva, Jorge Diogo, Soares, Ana Rita, Fortuna, Ana Maria, Tkachenko, Nataliya. 2023. Establishing an objective clinical spectrum, genotype-phenotype correlations, and CRMP1 as a modifier in the Ellis-van Creveld syndrome: The first systematic review of EVC- and EVC2-associated conditions. In Genetics in medicine open, 1, 100781. doi:10.1016/j.gimo.2023.100781. https://pubmed.ncbi.nlm.nih.gov/39669252/
5. Yao, Li, Liu, Yong-Hua, Li, Xiaohong, Wang, You-Hua, Shen, Ai-Guo. 2014. CRMP1 Interacted with Spy1 During the Collapse of Growth Cones Induced by Sema3A and Acted on Regeneration After Sciatic Nerve Crush. In Molecular neurobiology, 53, 879-893. doi:10.1007/s12035-014-9049-2. https://pubmed.ncbi.nlm.nih.gov/25526860/
6. Makihara, Hiroko, Nakai, Shiori, Ohkubo, Wataru, Kolattukudy, Pappachan, Goshima, Yoshio. 2016. CRMP1 and CRMP2 have synergistic but distinct roles in dendritic development. In Genes to cells : devoted to molecular & cellular mechanisms, 21, 994-1005. doi:10.1111/gtc.12399. https://pubmed.ncbi.nlm.nih.gov/27480924/
7. Akinaga, Satoshi, Harada, Sayaka, Takahashi, Miyuki, Goshima, Yoshio, Ohshima, Toshio. 2022. Loss of CRMP1 and CRMP2 results in migration defects of Purkinje cells in the X lobule of the mouse cerebellum. In Brain research, 1783, 147846. doi:10.1016/j.brainres.2022.147846. https://pubmed.ncbi.nlm.nih.gov/35219721/
8. Li, Kay Ka-Wai, Qi, Yan, Xia, Tian, Lau, Kin-Mang, Ng, Ho-Keung. 2015. CRMP1 Inhibits Proliferation of Medulloblastoma and Is Regulated by HMGA1. In PloS one, 10, e0127910. doi:10.1371/journal.pone.0127910. https://pubmed.ncbi.nlm.nih.gov/26009886/
9. Lukomska, Agnieszka, Theune, William C, Xing, Jian, Gupta, Mahit, Trakhtenberg, Ephraim F. 2023. Experimental gene expression of developmentally downregulated Crmp1, Crmp4, and Crmp5 promotes axon regeneration and retinal ganglion cell survival after optic nerve injury. In Brain research, 1809, 148368. doi:10.1016/j.brainres.2023.148368. https://pubmed.ncbi.nlm.nih.gov/37059258/
10. Kawamoto, Yuko, Tada, Mikiko, Asano, Tetsuya, Nakamura, Fumio, Tanaka, Fumiaki. 2022. Phosphorylated CRMP1, axon guidance protein, is a component of spheroids and is involved in axonal pathology in amyotrophic lateral sclerosis. In Frontiers in neurology, 13, 994676. doi:10.3389/fneur.2022.994676. https://pubmed.ncbi.nlm.nih.gov/36237616/
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