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Endosomal structure and APP biology are not altered in preclinical cellular models of Down syndrome
Claudia Cannavo, Karen Cleverley, Cheryl Maduro, Paige Mumford, Dale Moulding, Elizabeth M. C. Fisher, View ORCID ProfileFrances K. Wiseman
doi: https://doi.org/10.1101/2021.12.30.474570
Claudia Cannavo
1UK Dementia Research Institute at UCL, London, WC1N 3BG UK
2Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, WC1N 3BG UK
Karen Cleverley
2Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, WC1N 3BG UK
Cheryl Maduro
2Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, WC1N 3BG UK
Paige Mumford
2Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, WC1N 3BG UK
Dale Moulding
3Light Microscopy Core Facility, Great Ormond Street Institute of Child Health, University College, London, WC1N 1EH UK
Elizabeth M. C. Fisher
2Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, WC1N 3BG UK
4LonDownS Consortium
Frances K. Wiseman
1UK Dementia Research Institute at UCL, London, WC1N 3BG UK
4LonDownS Consortium
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Posted December 30, 2021.
Endosomal structure and APP biology are not altered in preclinical cellular models of Down syndrome
Claudia Cannavo, Karen Cleverley, Cheryl Maduro, Paige Mumford, Dale Moulding, Elizabeth M. C. Fisher, Frances K. Wiseman
bioRxiv 2021.12.30.474570; doi: https://doi.org/10.1101/2021.12.30.474570
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