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27 results

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Page 1
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects.
AlAbdi L, Desbois M, Rusnac DV, Sulaiman RA, Rosenfeld JA, Lalani S, Murdock DR, Burrage LC; Undiagnosed Diseases Network; Billie Au PY, Towner S, Wilson WG, Wong L, Brunet T, Strobl-Wildemann G, Burton JE, Hoganson G, McWalter K, Begtrup A, Zarate YA, Christensen EL, Opperman KJ, Giles AC, Helaby R, Kania A, Zheng N, Grill B, Alkuraya FS. AlAbdi L, et al. Among authors: opperman kj. Brain. 2023 Apr 19;146(4):1373-1387. doi: 10.1093/brain/awac364. Brain. 2023. PMID: 36200388 Free PMC article.
Ubiquitin ligase activity inhibits Cdk5 to control axon termination.
Desbois M, Opperman KJ, Amezquita J, Gaglio G, Crawley O, Grill B. Desbois M, et al. Among authors: opperman kj. PLoS Genet. 2022 Apr 14;18(4):e1010152. doi: 10.1371/journal.pgen.1010152. eCollection 2022 Apr. PLoS Genet. 2022. PMID: 35421092 Free PMC article.
Genetic behavioral screen identifies an orphan anti-opioid system.
Wang D, Stoveken HM, Zucca S, Dao M, Orlandi C, Song C, Masuho I, Johnston C, Opperman KJ, Giles AC, Gill MS, Lundquist EA, Grill B, Martemyanov KA. Wang D, et al. Among authors: opperman kj. Science. 2019 Sep 20;365(6459):1267-1273. doi: 10.1126/science.aau2078. Epub 2019 Aug 15. Science. 2019. PMID: 31416932 Free PMC article.
Ubiquitin ligase and signalling hub MYCBP2 is required for efficient EPHB2 tyrosine kinase receptor function.
Chang C, Banerjee SL, Park SS, Zhang X, Cotnoir-White D, Opperman KJ, Desbois M, Grill B, Kania A. Chang C, et al. Among authors: opperman kj. bioRxiv [Preprint]. 2023 Oct 28:2023.06.12.544638. doi: 10.1101/2023.06.12.544638. bioRxiv. 2023. Update in: Elife. 2024 Jan 30;12:RP89176. doi: 10.7554/eLife.89176. PMID: 37693478 Free PMC article. Updated. Preprint.
27 results