Items where Author is "Wood, N W"

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Article

Noyce, A J and Kia, D A and Hemani, G and Nicolas, A and Price, T R and De Pablo-Fernandez, E and Haycock, P C and Lewis, P A and Foltynie, T and Smith, G D and International Parkinson Disease Genomics Consortium and Schrag, A and Lees, A J and Hardy, J and Singleton, A and Nalls, M A and Pearce, N and Lawlor, D A and Wood, N W (2017) Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study. PLOS Medicine, 14 (6).

Deas, E and Cremades, N and Angelova, P R and Ludtmann, M H R and Yao, Z and Chen, S and Horrocks, M H and Banushi, B and Little, D and Devine, M J and Gissen, P and Klenerman, D and Dobson, C M and Wood, N W and Gandhi, S and Abramov, A Y (2016) Alpha-Synuclein Oligomers Interact with Metal Ions to Induce Oxidative Stress and Neuronal Death in Parkinson's Disease. Antioxidants & Redox Signaling, 24 (7). pp. 376-91.

Angelova, P R and Ludtmann, M H R and Horrocks, M H and Negoda, A and Cremades, N and Klenerman, D and Dobson, C M and Wood, N W and Pavlov, E V and Gandhi, S and Abramov, A Y (2016) Ca2+ is a key factor in a-synuclein-induced neurotoxicity. Journal of Cell Science, 129 (9). pp. 1792-801.

Mencacci, N E and Rubio-Agusti, I and Zdebik, A and Asmus, F and Ludtmann, M H R and Ryten, M and Plagnol, V and Hauser, A K and Bandres-Ciga, S and Bettencourt, C and Forabosco, P and Hughes, D and Soutar, M M and Peall, K and Morris, H R and Trabzuni, D and Tekman, M and Stanescu, H C and Kleta, R and Carecchio, M and Zorzi, G and Nardocci, N and Garavaglia, B and Lohmann, E and Weissbach, A and Klein, C and Hardy, J and Pittman, A M and Foltynie, T and Abramov, A Y and Gasser, T and Bhatia, K P and Wood, N W (2015) A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia. American Journal of Human Genetics, 96 (6). pp. 938-47.

Plun-Favreau, H and Burchell, V S and Holmstrom, K M and Yao, Z and Deas, E and Cain, K and Fedele, V and Moisoi, N and Campanella, M and Martins, L M and Wood, N W and Gourine, A V and Abramov, A Y (2012) HtrA2 deficiency causes mitochondrial uncoupling through the F1F0-ATP synthase and consequent ATP depletion. CELL DEATH & DISEASE, 3. e335.

This list was generated on Thu Jul 9 07:08:43 2020 BST.