Browsing by Author Pook, M

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Showing results 1 to 19 of 19
Issue DateTitleAuthor(s)
2016Cytokine therapy-mediated neuroprotection in a Friedreich's ataxia mouse modelKemp, KC; Cerminara, N; Hares, K; Redondo, J; Cook, AJ; Haynes, HR; Burton, BR; Pook, M; Apps, R; Scolding, NJ; Wilkins, A
2008Deranged calcium signaling and neurodegeneration in spinocerebellar ataxia type 3Chen, X; Tang, TS; Tu, H; Nelson, O; Pook, M; Hammer, R; Nukina, N; Bezprozvanny, I
2012DNA methylation and trinucleotide repeat expansion diseasesPook, M
2018FAST-1 antisense RNA epigenetically alters FXN expressionPook, M; Mikaeili, H; Sandi, M; Bayot, A; Al-Mahdawi, S
2014Frataxin deficiency increases cyclooxygenase 2 and prostaglandins in cell and animal models of Friedreich's ataxiaHayashi, G; Shen, Y; Pedersen, TL; Newman, JW; Pook, M; Cortopassi, G
2012Friedreich ataxia: Investigating the relationships between mismatch repair gene expression, FXN gene expression and GAA repeat instability in human and mouse cells and tissuesEzzatizadeh, Vahid
2015Genotype and phenotype characterisation of enhanced Friedreich’s ataxia GAA repeat expansion mouse modelsAnjomani Virmouni, S; Sandi, C; Ezzatizadeh, V; Sandi, M; Al-Mahdawi, S; Pook, M; Anjomani-Virmouni, S
2013Genotype and phenotype characterisation of Friedreich ataxia mouse models and cellsAnjomani Virmouni, Sara
2015Identification and quantification of FXN antisense transcript 1 (FAST-1) in friedreich ataxiaSandi, Madhavi
2015Identification of telomere dysfunction in Friedreich ataxiaAnjomani-Virmouni, S; Al-Mahdawi, S; Sandi, C; Yasaei, H; Slijepcevic, P; Pook, M
2015Identification of telomere dysfunction in Friedreich ataxia.Anjomani-Virmouni, S; Al-Mahdawi, S; Sandi, S; Yasaei, H; Giunti, P; Slijepcevic, P; Pook, M
2012Interferon gamma upregulates frataxin and corrects the functional deficits in a Friedreich ataxia modelTomassini, B; Arcuri, G; Fortuni, S; Sandi, C; Ezzatizadeh, V; Casali, C; Condò, I; Malisan, F; Al-Mahdawi, S; Pook, M; Testi, R
2018Investigating Friedreich ataxia disease mechanisms and therapySaqlain, Saba
2018Investigating novel therapies for Friedreich’s ataxiaSherzai, Mursal
2010Investigating the pathogenesis and therapy of Friedreich AtaxiaSandi, Chiranjeevi
2017Investigating the role of FXN antisense transcript 1 in Friedreich ataxiaMikaeili, Hajar
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
2015Lentivirus-meditated frataxin gene delivery reverses genome instability in Friedreich ataxia patient and mouse model fibroblastsKhonsari, Hassan
2009Therapeutic testing and epigenetic characterization of Friedreich AtaxiaMouro Pinto, Ricardo