1. Brunel University Research Archive

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Issue DateTitleAuthor(s)
2013Epigenetics in Friedreich's ataxia: Challenges and opportunities for therapySandi, C; Al-Mahdawi, S; Pook, MA
2012Novel frataxin isoforms may contribute to the pathological mechanism of friedreich ataxiaXia, H; Cao, Y; Dai, X; Marelja, Z; Zhou, D; Mo, R; Al-Mahdawi, S; Pook, MA; Leimkühler, S; Rouault, TA; Li, K
2013Pharmacological screening using an FXN-EGFP cellular genomic reporter assay for the therapy of Friedreich ataxiaLi, L; Voullaire, L; Sandi, C; Pook, MA; Ioannou, PA; Delatycki, MB; Sarsero, JP
2014MutLα heterodimers modify the molecular phenotype of Friedreich ataxiaEzzatizadeh, V; Sandi, C; Sandi, M; Anjomani-Virmouni, S; Al-Mahdawi, S; Pook, MA
2014Dyclonine rescues frataxin deficiency in animal models and buccal cells of patients with Friedreich's ataxia.Sahdeo, S; Scott, BD; McMackin, MZ; Jasoliya, M; Brown, B; Wulff, H; Perlman, SL; Pook, MA; Cortopassi, GA
2014Generation and characterisation of Friedreich ataxia YG8R mouse fibroblast and neural stem cell modelsSandi, C; Sandi, M; Jassal, H; Ezzatizadeh, V; Anjomani-Virmouni, S; Al-Mahdawi, S; Pook, MA
2014Cellular, molecular and functional characterisation of YAC transgenic mouse models of Friedreich AtaxiaVirmouni, SA; Sandi, C; Al-Mahdawi, S; Pook, MA
2011Prolonged treatment with pimelic o-aminobenzamide HDAC inhibitors ameliorates the disease phenotype of a Friedreich ataxia mouse modelSandi, C; Pinto, RM; Al-Mahdawi, S; Ezzatizadeh, V; Barnes, G; Jones, S; Rusche, JR; Gottesfeld, JM; Pook, MA
2012The mismatch repair system protects against intergenerational GAA repeat instability in a Friedreich ataxia mouse modelEzzatizadeh, V; Pinto, RM; Sandi, C; Sandi, M; Al-Mahdawi, S; Te Riele, H; Pook, MA

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