Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome

Autor: Kenneth A. Myers, Ebba Alkhunaizi, Michelle M. Morrow, Jiddeke J.P. van de Kamp, Elysa J. Marco, Suma P. Shankar, Harvey B. Sarnat, Marwan Shinawi, Jacqueline L. Steele, Megan Glassford, Colette P. DeFilippo, Tracy Brandt, Amy Waldman, Houda Zghal Elloumi, Holly Dubbs, Ganka Douglas, Sumit Parikh, Kristin G. Monaghan, Cyril Mignot, David Chitayat, Bénédicte Héron, Linda E. Kim, Farrah Rajabi, Shane C. Quinonez, William D. Graf, Mark C. Hannibal, Aravindhan Veerapandiyan

Publikováno v: Steele, J L, Morrow, M M, Sarnat, H B, Alkhunaizi, E, Brandt, T, Chitayat, D A, DeFilippo, C P, Douglas, G V, Dubbs, H A, Elloumi, H Z, Glassford, M R, Hannibal, M C, Héron, B, Kim, L E, Marco, E J, Mignot, C, Monaghan, K G, Myers, K A, Parikh, S, Quinonez, S C, Rajabi, F, Shankar, S P, Shinawi, M S, van de Kamp, J J P, Veerapandiyan, A, Waldman, A T & Graf, W D 2022, ' Semaphorin-Plexin Signaling : From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome ', Pediatric Neurology, vol. 126, pp. 65-73 . https://doi.org/10.1016/j.pediatrneurol.2021.10.008
Pediatric Neurology, 126, 65-73. Elsevier Inc.

Background: Semaphorins and plexins are ligands and cell surface receptors that regulate multiple neurodevelopmental processes such as axonal growth and guidance. PLXNA3 is a plexin gene located on the X chromosome that encodes the most widely expres

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da65a60f3e1ab2780a3d905dd23f1bdf
https://doi.org/10.1016/j.pediatrneurol.2021.10.008