C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci
Mizielinska, Sarah, Lashley, Tammaryn, Norona, Frances E., Clayton, Emma L., Ridler, Charlotte E., Fratta, Pietro, Isaacs, Adrian M.
Published in Acta neuropathologica (01.12.2013)
Published in Acta neuropathologica (01.12.2013)
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C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins
Mizielinska, Sarah, Grönke, Sebastian, Niccoli, Teresa, Ridler, Charlotte E., Clayton, Emma L., Devoy, Anny, Moens, Thomas, Norona, Frances E., Woollacott, Ione O. C., Pietrzyk, Julian, Cleverley, Karen, Nicoll, Andrew J., Pickering-Brown, Stuart, Dols, Jacqueline, Cabecinha, Melissa, Hendrich, Oliver, Fratta, Pietro, Fisher, Elizabeth M. C., Partridge, Linda, Isaacs, Adrian M.
Published in Science (American Association for the Advancement of Science) (05.09.2014)
Published in Science (American Association for the Advancement of Science) (05.09.2014)
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Modulation of learning and memory by the targeted deletion of the circadian clock gene Bmal1 in forebrain circuits
Snider, Kaitlin H., Dziema, Heather, Aten, Sydney, Loeser, Jacob, Norona, Frances E., Hoyt, Kari, Obrietan, Karl
Published in Behavioural brain research (15.07.2016)
Published in Behavioural brain research (15.07.2016)
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Frontotemporal dementia causative CHMP2B impairs neuronal endolysosomal traffic-rescue by TMEM106B knockdown
Clayton, Emma L, Milioto, Carmelo, Muralidharan, Bhavana, Norona, Frances E, Edgar, James R, Soriano, Armand, Jafar-nejad, Paymaan, Rigo, Frank, Collinge, John, Isaacs, Adrian M
Published in Brain (London, England : 1878) (01.12.2018)
Published in Brain (London, England : 1878) (01.12.2018)
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Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology
Clayton, Emma L., Mizielinska, Sarah, Edgar, James R., Nielsen, Troels Tolstrup, Marshall, Sarah, Norona, Frances E., Robbins, Miranda, Damirji, Hana, Holm, Ida E., Johannsen, Peter, Nielsen, Jørgen E., Asante, Emmanuel A., Collinge, John, Isaacs, Adrian M.
Published in Acta neuropathologica (01.10.2015)
Published in Acta neuropathologica (01.10.2015)
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The integration site of the APP transgene in the J20 mouse model of Alzheimer's disease
Tosh, Justin L, Rickman, Matthew, Rhymes, Ellie, Norona, Frances E, Clayton, Emma, Mucke, Lennart, Isaacs, Adrian M, Fisher, Elizabeth M C, Wiseman, Frances K
Published in Wellcome open research (2017)
Published in Wellcome open research (2017)
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The integration site of the APP transgene in the J20 mouse model of Alzheimer’s disease
Tosh, Justin L., Rickman, Matthew, Rhymes, Ellie, Norona, Frances E., Clayton, Emma, Mucke, Lennart, Isaacs, Adrian M., Fisher, Elizabeth M.C., Wiseman, Frances K.
Published in Wellcome open research (10.10.2018)
Published in Wellcome open research (10.10.2018)
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Early microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutation
Clayton, Emma L, Mancuso, Renzo, Nielsen, Troels Tolstrup, Mizielinska, Sarah, Holmes, Holly, Powell, Nicholas, Norona, Frances, Larsen, Jytte Overgaard, Milioto, Carmelo, Wilson, Katherine M, Lythgoe, Mark F, Ourselin, Sebastian, Nielsen, Jörgen E, Johannsen, Peter, Holm, Ida, Collinge, John, Oliver, Peter L, Gomez-Nicola, Diego, Isaacs, Adrian M
Published in Human molecular genetics (01.03.2017)
Published in Human molecular genetics (01.03.2017)
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