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Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases.
Boivin M, Deng J, Pfister V, Grandgirard E, Oulad-Abdelghani M, Morlet B, Ruffenach F, Negroni L, Koebel P, Jacob H, Riet F, Dijkstra AA, McFadden K, Clayton WA, Hong D, Miyahara H, Iwasaki Y, Sone J, Wang Z, Charlet-Berguerand N. Boivin M, et al. Among authors: mcfadden k. Neuron. 2021 Jun 2;109(11):1825-1835.e5. doi: 10.1016/j.neuron.2021.03.038. Epub 2021 Apr 21. Neuron. 2021. PMID: 33887199 Free PMC article.
Neuropathology of 22q11 deletion syndrome in an infant.
Wu P, Teot L, Murdoch G, Monaghan-Nichols AP, McFadden K. Wu P, et al. Among authors: mcfadden k. Pediatr Dev Pathol. 2014 Sep-Oct;17(5):386-92. doi: 10.2350/13-11-1399-CR.1. Epub 2014 Jul 14. Pediatr Dev Pathol. 2014. PMID: 25019421
Safety assessment of intradiscal gene transfer: a pilot study.
Wallach CJ, Kim JS, Sobajima S, Lattermann C, Oxner WM, McFadden K, Robbins PD, Gilbertson LG, Kang JD. Wallach CJ, et al. Among authors: mcfadden k. Spine J. 2006 Mar-Apr;6(2):107-12. doi: 10.1016/j.spinee.2005.05.002. Spine J. 2006. PMID: 16517379
209 results