Browsing by Subject Mutation
Showing results 1 to 6 of 6
Issue Date | Title | Author(s) |
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11-Mar-2023 | Early neurotransmitters changes in prodromal frontotemporal dementia: A GENFI study | Premi, E; Pengo, M; Mattioli, I; Cantoni, V; Dukart, J; Gasparotti, R; Buratti, E; Padovani, A; Bocchetta, M; Todd, EG; Bouzigues, A; Cash, DM; Convery, RS; Russell, LL; Foster, P; Thomas, DL; van Swieten, JC; Jiskoot, LC; Seelaar, H; Galimberti, D; Sanchez-Valle, R; Laforce, R; Moreno, F; Synofzik, M; Graff, C; Masellis, M; Tartaglia, MC; Rowe, JB; Tsvetanov, KA; Vandenberghe, R; Finger, E; Tiraboschi, P; de Mendonça, A; Santana, I; Butler, CR; Ducharme, S; Gerhard, A; Levin, J; Otto, M; Sorbi, S; Le Ber, I; Pasquier, F; Rohrer, JD; Borroni, B |
26-Dec-2017 | Meta-analysis on the association between genetic polymorphisms and prepulse inhibition of the acoustic startle response | Quednow, BB; Ejebe, K; Wagner, M; Giakoumaki, SG; Bitsios, P; Kumari, V; Roussos, P |
2012 | Mitotic chromosomes are compacted laterally by KIF4 and condensin and axially by topoisomerase IIα | Samejima, K; Samejima, I; Vagnarelli, P; Ogawa, H; Vargiu, G; Kelly, DA; de Lima Alves, F; Kerr, A; Green, LC; Hudson, DF; Ohta, S; Cooke, CA; Farr, CJ; Rappsilber, J; Earnshaw, WC |
2008 | Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease | Sugiana, C; Pagliarini, DJ; McKenzie, M; Kirby, DM; Salemi, R; Abu-Amero, KK; Dahl, HH; Hutchison, WM; Vascotto, KA; Newbold, RF |
27-Jul-2016 | The progressive ankyloses protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interface. | Seifert, W; Posor, Y; Schu, P; Stenbeck, G; Mundlos, S; Klaassen, S; Nürnberg, P; Haucke, V; Kornak, U; Kühnisch, J |
2012 | A single residue substitution in the receptor-binding domain of H5N1 hemagglutinin is critical for packaging into pseudotyped lentiviral particles | Tang, DJ; Lam, YM; Siu, YL; Lam, CH; Chu, SL; Peiris, JS; Buchy, P; Nal, B; Bruzzone, R |