Therapeutic Inhibition of the Complement System in Diseases of the Central Nervous System

por Carpanini, Sarah M., Torvell, Megan, Morgan, Bryan Paul
Publicado 2019

27th International Mammalian Genome Conference meeting report

por Gamache, Benjamin, Leist, Sarah R., Bard, Andrew Daniel, Logan, Darren W., Carpanini, Sarah M.
Publicado 2014

Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and disease

por Carpanini, Sarah M, Wishart, Thomas M, Gillingwater, Thomas H, Manson, Jean C, Summers, Kim M
Publicado 2017

Genetic Insights into the Impact of Complement in Alzheimer’s Disease

por Torvell, Megan, Carpanini, Sarah M., Daskoulidou, Nikoleta, Byrne, Robert A. J., Sims, Rebecca, Morgan, B. Paul
Publicado 2021

The Impact of Complement Genes on the Risk of Late-Onset Alzheimer’s Disease

por Carpanini, Sarah M., Harwood, Janet C., Baker, Emily, Torvell, Megan, Sims, Rebecca, Williams, Julie, Morgan, B. Paul
Publicado 2021

Novel Monoclonal Antibodies Against Mouse C1q: Characterisation and Development of a Quantitative ELISA for Mouse C1q

por Byrne, Robert A. J., Torvell, Megan, Daskoulidou, Nikoleta, Fathalla, Dina, Kokkali, Eirini, Carpanini, Sarah M., Morgan, B. Paul
Publicado 2021

Rab18 and a Rab18 GEF complex are required for normal ER structure

por Gerondopoulos, Andreas, Bastos, Ricardo Nunes, Yoshimura, Shin-ichiro, Anderson, Rachel, Carpanini, Sarah, Aligianis, Irene, Handley, Mark T., Barr, Francis A.
Publicado 2014

Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation

por Handley, Mark T., Carpanini, Sarah M., Mali, Girish R., Sidjanin, Duska J., Aligianis, Irene A., Jackson, Ian J., FitzPatrick, David R.
Publicado 2015

Quantitative imaging of tissue sections using infrared scanning technology

por Eaton, Samantha L., Cumyn, Elizabeth, King, Declan, Kline, Rachel A., Carpanini, Sarah M., Del‐Pozo, Jorge, Barron, Rona, Wishart, Thomas M.
Publicado 2015

Alzheimer’s disease-associated complement gene variants influence plasma complement protein levels

por Veteleanu, Aurora, Stevenson-Hoare, Joshua, Keat, Samuel, Daskoulidou, Nikoleta, Zetterberg, Henrik, Heslegrave, Amanda, Escott-Price, Valentina, Williams, Julie, Sims, Rebecca, Zelek, Wioleta M., Carpanini, Sarah M., Morgan, Bryan Paul
Publicado 2023

Terminal complement pathway activation drives synaptic loss in Alzheimer’s disease models

por Carpanini, Sarah M., Torvell, Megan, Bevan, Ryan J., Byrne, Robert A. J., Daskoulidou, Nikoleta, Saito, Takashi, Saido, Takaomi C., Taylor, Philip R., Hughes, Timothy R., Zelek, Wioleta M., Morgan, B. Paul
Publicado 2022

Sideroflexin 3 is an α-synuclein-dependent mitochondrial protein that regulates synaptic morphology

por Amorim, Inês S., Graham, Laura C., Carter, Roderick N., Morton, Nicholas M., Hammachi, Fella, Kunath, Tilo, Pennetta, Giuseppa, Carpanini, Sarah M., Manson, Jean C., Lamont, Douglas J., Wishart, Thomas M., Gillingwater, Thomas H.
Publicado 2017

A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton

por Carpanini, Sarah M., McKie, Lisa, Thomson, Derek, Wright, Ann K., Gordon, Sarah L., Roche, Sarah L., Handley, Mark T., Morrison, Harris, Brownstein, David, Wishart, Thomas M., Cousin, Michael A., Gillingwater, Thomas H., Aligianis, Irene A., Jackson, Ian J.
Publicado 2014

Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1

por McQueen, Jamie, Ryan, Tomás J, McKay, Sean, Marwick, Katie, Baxter, Paul, Carpanini, Sarah M, Wishart, Thomas M, Gillingwater, Thomas H, Manson, Jean C, Wyllie, David J A, Grant, Seth G N, McColl, Barry W, Komiyama, Noboru H, Hardingham, Giles E
Publicado 2017