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Issue DateTitleAuthor(s)
8-Apr-2022Invited Perspective: How Relevant Are Mode-of-Action Considerations for the Assessment and Prediction of Mixture Effects?Kortenkamp, A
19-Apr-2022Identification and characterization of novel endolysins targeting Gardnerella vaginalis biofilms to treat bacterial vaginosisArroyo-Moreno, S; Cummings, M; Corcoran, DB; Coffey, A; McCarthy, RR
22-Apr-2022Genetic analysis of over half a million people characterises C-reactive protein lociSaid, S; Pazoki, R; Karhunen, V; Võsa, U; Ligthart, S; Bodinier, B; Koskeridis, F; Welsh, P; Alizadeh, BZ; Chasman, DI; Sattar, N; Chadeau-Hyam, M; Evangelou, E; Jarvelin, M-R; Elliott, P; Tzoulaki, I; Dehghan, A
21-Nov-2018FAST-1 antisense RNA epigenetically alters FXN expressionPook, M; Mikaeili, H; Sandi, M; Bayot, A; Al-Mahdawi, S
23-Mar-2022DNA methylation in Friedreich ataxia silences expression of frataxin isoform ERodden, LN; Gilliam, KM; Lam, C; Rojsajjakul, T; Mesaros, C; Dionisi, C; Pook, M; Pandolfo, M; Lynch, DR; Blair, IA; Bidichandani, SI
2015A novel GAA-repeat-expansion-based mouse model of Friedreich's ataxia.Anjomani Virmouni, S; Ezzatizadeh, V; Sandi, C; Sandi, M; Al-Mahdawi, S; Chutake, Y; Pook, MA
10-Jun-2015Identification of telomere dysfunction in Friedreich ataxia.Anjomani-Virmouni, S; Al-Mahdawi, S; Sandi, C; Yasaei, H; Giunti, P; Slijepcevic, P; Pook, M
21-Nov-2018Large interruptions of GAA repeat expansiopns mutations in Friedreich ataxia are very rarePook, M; Al-Mahdawi, S; Ging, H; Bayot, A; Cavalcanti, F; La Cognata, V; Cavallaro, S; Giunti, P
1-May-2015Identification of telomere dysfunction in Friedreich ataxiaAnjomani-Virmouni, S; Al-Mahdawi, S; Sandi, C; Yasaei, H; Slijepcevic, P; Pook, M
12-Nov-2021Impact of COVID-19 on ‘living well’ with mild-to-moderate dementia in the community: findings from the IDEAL cohortClare, L; Martyr, A; Gamble, L; Pentecost, C; Collins, R; Dawson, E; Hunt, A; Parker, S; Allan, L; Burns, A; Hillman, A; Litherland, R; Quinn, C; Matthews, F; Victor, C