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Author/Creator Webster, Christopher P

1. SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction. Issue 16 (21st March 2022)

Authors:
Marrone, Lara; Marchi, Paolo M; Webster, Christopher P; Marroccella, Raffaele; Coldicott, Ian; Reynolds, Steven; Alves-Cruzeiro, João; Yang, Zih-Liang; Higginbottom, Adrian; Khundadze, Mukhran; Shaw, Pamela J; Hübner, Christian A; Livesey, Matthew R; Azzouz, Mimoun
Journal:
Human molecular genetics
Issue:
Volume 31:Issue 16(2022)
Page Start:
2693
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Ap4b1-knockout mouse model of hereditary spastic paraplegia type 47 displays motor dysfunction, aberrant brain morphology and ATG9A mislocalization. Issue 1 (6th January 2023)

Authors:
Scarrott, Joseph M; Alves-Cruzeiro, João; Marchi, Paolo M; Webster, Christopher P; Yang, Zih-Liang; Karyka, Evangelia; Marroccella, Raffaele; Coldicott, Ian; Thomas, Hannah; Azzouz, Mimoun
Journal:
Brain communications
Issue:
Volume 5:Issue 1(2023)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. The C9orf72 protein interacts with Rab1a and the ULK1 complex to regulate initiation of autophagy. (22nd June 2016)

Authors:
Webster, Christopher P; Smith, Emma F; Bauer, Claudia S; Moller, Annekathrin; Hautbergue, Guillaume M; Ferraiuolo, Laura; Myszczynska, Monika A; Higginbottom, Adrian; Walsh, Matthew J; Whitworth, Alexander J; Kaspar, Brian K; Meyer, Kathrin; Shaw, Pamela J; Grierson, Andrew J; De Vos, Kurt J
Journal:
EMBO journal
Issue:
Volume 35:Number 15(2016)
Page Start:
1656
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗