Browsing byAuthorBlair, IP
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
| 2018-01-01 | Accumulation of dysfunctional SOD1 protein in Parkinson’s disease is not associated with mutations in the SOD1 gene | Trist, BG; Fifita, JA; Freckleton, SE; Hare, DJ; Lewis, SJG; Halliday, GM; Blair, IP; Double, KL |
| 2022-09-14 | Altered SOD1 maturation and post-translational modification in amyotrophic lateral sclerosis spinal cord. | Trist, BG; Genoud, S; Roudeau, S; Rookyard, A; Abdeen, A; Cottam, V; Hare, DJ; White, M; Altvater, J; Fifita, JA; Hogan, A; Grima, N; Blair, IP; Kysenius, K; Crouch, PJ; Carmona, A; Rufin, Y; Claverol, S; Van Malderen, S; Falkenberg, G; Paterson, DJ; Smith, B; Troakes, C; Vance, C; Shaw, CE; Al-Sarraj, S; Cordwell, S; Halliday, G; Ortega, R; Double, KL |
| 2019-07-03 | The C9orf72 hexanucleotide repeat expansion presents a challenge for testing laboratories and genetic counseling | Crook, A; McEwen, A; Fifita, JA; Zhang, K; Kwok, JB; Halliday, G; Blair, IP; Rowe, DB |
| 2019-11 | CMS-01 Genetic testing for familial amyotrophic lateral sclerosis (ALS): insights and challenges. | Crook, A; Hogden, A; Mumford, V; Blair, IP; Williams, KL; Rowe, DB |
| 2017-07-15 | Expression of ALS/FTD-linked mutant CCNF in zebrafish leads to increased cell death in the spinal cord and an aberrant motor phenotype. | Hogan, AL; Don, EK; Rayner, SL; Lee, A; Laird, AS; Watchon, M; Winnick, C; Tarr, IS; Morsch, M; Fifita, JA; Gwee, SSL; Formella, I; Hortle, E; Yuan, KC; Molloy, MP; Williams, KL; Nicholson, GA; Chung, RS; Blair, IP; Cole, NJ |
