Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis von Chen, Han-Jou, Anagnostou, Georgia, Chai, Andrea, Withers, James, Morris, Alex, Adhikaree, Jason, Pennetta, Giuseppa, de Belleroche, Jackie S.

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Overexpression of heat shock protein 27 reduces cortical damage after cerebral ischemia von van der Weerd, Louise, Tariq Akbar, Mohammed, Aron Badin, Romina, Valentim, Lauren M, Thomas, David L, Wells, Dominic J, Latchman, David S, Gadian, David G, Lythgoe, Mark F, de Belleroche, Jackie S

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Neuroprotective effects of HSP70 overexpression after cerebral ischaemia—An MRI study von van der Weerd, Louise, Lythgoe, Mark F., Badin, Romina Aron, Valentim, Lauren M., Akbar, Mohammed Tariq, de Belleroche, Jackie S., Latchman, David S., Gadian, David G.

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Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis von Orell, Richard W., Habgood, James, Rudge, Petter, Lane, Russell J. M., de Belleroche, Jackie S.

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Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis von Hosler, Betsy A., Nicholson, Garth A., Sapp, Peter C., Chin, Wendy, Orrell, Richard W., De Belleroche, Jackie S., Esteban, Jesus, Hayward, Lawrence J., McKenna-Yasek, Diane, Yeung, Leone, Cherryson, Annia K., Dench, Joanne E., Wilton, Steve D., Laing, Nigel G., Horvitz, H.Robert, Brown, Robert H.

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Endoplasmic reticulum stress signalling – from basic mechanisms to clinical applications von Almanza, Aitor, Carlesso, Antonio, Chintha, Chetan, Creedican, Stuart, Doultsinos, Dimitrios, Leuzzi, Brian, Luís, Andreia, McCarthy, Nicole, Montibeller, Luigi, More, Sanket, Papaioannou, Alexandra, Püschel, Franziska, Sassano, Maria Livia, Skoko, Josip, Agostinis, Patrizia, Belleroche, Jackie, Eriksson, Leif A., Fulda, Simone, Gorman, Adrienne M., Healy, Sandra, Kozlov, Andrey, Muñoz‐Pinedo, Cristina, Rehm, Markus, Chevet, Eric, Samali, Afshin

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Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6 von Vance, Caroline, Rogelj, Boris, Hortobágyi, Tibor, De Vos, Kurt J, Nishimura, Agnes Lumi, Sreedharan, Jemeen, Hu, Xun, Smith, Bradley, Ruddy, Deborah, Wright, Paul, Ganesalingam, Jeban, Williams, Kelly L, Tripathi, Vineeta, Al-Saraj, Safa, Al-Chalabi, Ammar, Leigh, P. Nigel, Blair, Ian P, Nicholson, Garth, de Belleroche, Jackie, Gallo, Jean-Marc, Miller, Christopher C, Shaw, Christopher E

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The role of D-serine and glycine as co-agonists of NMDA receptors in motor neuron degeneration and amyotrophic lateral sclerosis (ALS) von Paul, Praveen, de Belleroche, Jackie

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Experimental approaches for elucidating co-agonist regulation of NMDA receptor in motor neurons: Therapeutic implications for amyotrophic lateral sclerosis (ALS) von Paul, Praveen, de Belleroche, Jackie

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Association studies indicate that protein disulfide isomerase is a risk factor in amyotrophic lateral sclerosis von Kwok, Chun Tak, Morris, Alex G., Frampton, Jenny, Smith, Bradley, Shaw, Christopher E., de Belleroche, Jackie

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Heat shock protein 27 protects the heart against myocardial infarction von Efthymiou, Christopher A, Mocanu, Mihaela M, de Belleroche, Jackie, Wells, Dominic J, Latchmann, David S, Yellon, Derek M

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Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays von Malaspina, Andrea, Kaushik, Narendra, De Belleroche, Jackie

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Transcription and pathway analysis of the superior temporal cortex and anterior prefrontal cortex in schizophrenia von Barnes, Michael R., Huxley-Jones, Julie, Maycox, Peter R., Lennon, Mark, Thornber, Amy, Kelly, Fiona, Bates, Stewart, Taylor, Adam, Reid, Juliet, Jones, Neil, Schroeder, Jörn, Scorer, Carol A., Davies, Ceri, Hagan, Jim J., Kew, James N.C., Angelinetta, Claire, Akbar, Tariq, Hirsch, Steven, Mortimer, Ann M., Barnes, Thomas R.E., de Belleroche, Jackie

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A 14‐3‐3 mRNA Is Up‐Regulated in Amyotrophic Lateral Sclerosis Spinal Cord von Malaspina, Andrea, Kaushik, Narendra, Belleroche, Jackie de

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Endoplasmic reticulum stress signalling - from basic mechanisms to clinical applications von Almanza, Aitor, Carlesso, Antonio, Chintha, Chetan, Creedican, Stuart, Doultsinos, Dimitrios, Leuzzi, Brian, Luis, Andreia, McCarthy, Nicole, Montibeller, Luigi, More, Sanket, Papaioannou, Alexandra, Pueschel, Franziska, Sassano, Maria Livia, Skoko, Josip, Agostinis, Patrizia, de Belleroche, Jackie, Eriksson, Leif A, Fulda, Simone, Gorman, Adrienne M, Healy, Sandra, Kozlov, Andrey, Munoz-Pinedo, Cristina, Rehm, Markus, Chevet, Eric, Samali, Afshin

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VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK von Kwok, Chun Tak, Wang, Hsiang-Ya, Morris, Alex G, Smith, Bradley, Shaw, Christopher, de Belleroche, Jackie

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Hsp27 overexpression in the R6/2 mouse model of Huntington's disease: chronic neurodegeneration does not induce Hsp27 activation von Zourlidou, Alexandra, Gidalevitz, Tali, Kristiansen, Mark, Landles, Christian, Woodman, Ben, Wells, Dominic J., Latchman, David S., de Belleroche, Jackie, Tabrizi, Sarah J., Morimoto, Richard I., Bates, Gillian P.

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Patterns of inheritance in familial ALS von BRADLEY, Marcus, BRADLEY, Lloyd, DE BELLEROCHE, Jackie, ORRELL, Richard W

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Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays von Malaspina, Andrea, Kaushik, Narendra, de Belleroche, Jackie

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A survey of trinucleotide/tandem repeat-containing transcripts (TNRTs) isolated from human spinal cord to identify genes containing unstable DNA regions as candidates for disorders... von MALASPINA, Andrea, KAUSHIK, Narendra, DE BELLEROCHE, Jackie

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