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Loss of TMEM106B exacerbates C9ALS/FTD DPR pathology by disrupting autophagosome maturation by Claudia S. Bauer, Claudia S. Bauer, Christopher P. Webster, Christopher P. Webster, Allan C. Shaw, Allan C. Shaw, Jannigje R. Kok, Jannigje R. Kok, Lydia M. Castelli, Lydia M. Castelli, Ya-Hui Lin, Ya-Hui Lin, Emma F. Smith, Emma F. Smith, Francisco Illanes-Álvarez, Francisco Illanes-Álvarez, Adrian Higginbottom, Adrian Higginbottom, Pamela J. Shaw, Pamela J. Shaw, Mimoun Azzouz, Mimoun Azzouz, Laura Ferraiuolo, Laura Ferraiuolo, Guillaume M. Hautbergue, Guillaume M. Hautbergue, Andrew J. Grierson, Andrew J. Grierson, Kurt J. De Vos, Kurt J. De Vos
Published 2022-12-01
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Pre-clinical development of AP4B1 gene replacement therapy for hereditary spastic paraplegia type 47 by Jessica P Wiseman, Joseph M Scarrott, João Alves-Cruzeiro, Afshin Saffari, Cedric Böger, Evangelia Karyka, Emily Dawes, Alexandra K Davies, Paolo M Marchi, Emily Graves, Fiona Fernandes, Zih-Liang Yang, Ian Coldicott, Jennifer Hirst, Christopher P Webster, J Robin Highley, Neil Hackett, Adrienn Angyal, Thushan de Silva, Adrian Higginbottom, Pamela J Shaw, Laura Ferraiuolo, Darius Ebrahimi-Fakhari, Mimoun Azzouz
Published 2024-10-01
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