Elizabeth L. Tudor - Publications

Affiliations: 
King's College London, London, UK 
Area:
Motor Neuron Disease

7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2013 Mitchell JC, McGoldrick P, Vance C, Hortobagyi T, Sreedharan J, Rogelj B, Tudor EL, Smith BN, Klasen C, Miller CC, Cooper JD, Greensmith L, Shaw CE. Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion. Acta Neuropathologica. 125: 273-88. PMID 22961620 DOI: 10.1007/S00401-012-1043-Z  0.432
2012 De Vos KJ, Mórotz GM, Stoica R, Tudor EL, Lau KF, Ackerley S, Warley A, Shaw CE, Miller CC. VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis. Human Molecular Genetics. 21: 1299-311. PMID 22131369 DOI: 10.1093/Hmg/Ddr559  0.361
2010 Tudor EL, Galtrey CM, Perkinton MS, Lau KF, De Vos KJ, Mitchell JC, Ackerley S, Hortobágyi T, Vámos E, Leigh PN, Klasen C, McLoughlin DM, Shaw CE, Miller CC. Amyotrophic lateral sclerosis mutant vesicle-associated membrane protein-associated protein-B transgenic mice develop TAR-DNA-binding protein-43 pathology. Neuroscience. 167: 774-85. PMID 20188146 DOI: 10.1016/J.Neuroscience.2010.02.035  0.454
2008 Manser C, Stevenson A, Banner S, Davies J, Tudor EL, Ono Y, Leigh PN, McLoughlin DM, Shaw CE, Miller CC. Deregulation of PKN1 activity disrupts neurofilament organisation and axonal transport. Febs Letters. 582: 2303-8. PMID 18519042 DOI: 10.1016/J.Febslet.2008.05.034  0.392
2007 De Vos KJ, Chapman AL, Tennant ME, Manser C, Tudor EL, Lau KF, Brownlees J, Ackerley S, Shaw PJ, McLoughlin DM, Shaw CE, Leigh PN, Miller CC, Grierson AJ. Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content. Human Molecular Genetics. 16: 2720-8. PMID 17725983 DOI: 10.1093/Hmg/Ddm226  0.448
2006 Panzeri C, De Palma C, Martinuzzi A, Daga A, De Polo G, Bresolin N, Miller CC, Tudor EL, Clementi E, Bassi MT. The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function. Brain : a Journal of Neurology. 129: 1710-9. PMID 16670179 DOI: 10.1093/Brain/Awl104  0.395
2005 Tudor EL, Perkinton MS, Schmidt A, Ackerley S, Brownlees J, Jacobsen NJ, Byers HL, Ward M, Hall A, Leigh PN, Shaw CE, McLoughlin DM, Miller CC. ALS2/Alsin regulates Rac-PAK signaling and neurite outgrowth. The Journal of Biological Chemistry. 280: 34735-40. PMID 16049005 DOI: 10.1074/Jbc.M506216200  0.378
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