Search Results - Sarah M. Carpanini

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  1. 1
    Therapeutic Inhibition of the Complement System in Diseases of the Central Nervous System

    Therapeutic Inhibition of the Complement System in Diseases of the Central Nervous System by Sarah M. Carpanini, Megan Torvell, B. Paul Morgan

    Published 2019
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  2. 2
    Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation

    Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation by Mark T. Handley, Sarah M. Carpanini, Girish R. Mali, D.J. Sidjanin, Irene A. Aligianis, Ian J. Jackson, David Fitzpatrick

    Published 2015
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  3. 3
    Rab18 and a Rab18 GEF complex are required for normal ER structure

    Rab18 and a Rab18 GEF complex are required for normal ER structure by Andreas Gerondopoulos, Ricardo Bastos, Shin‐ichiro Yoshimura, Rachel Anderson, Sarah M. Carpanini, Irene A. Aligianis, Mark T. Handley, Francis A. Barr

    Published 2014
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  4. 4
    The complement system in neurodegenerative diseases

    The complement system in neurodegenerative diseases by Jacqui Nimmo, Robert A. J. Byrne, Nikoleta Daskoulidou, Lewis M. Watkins, Sarah M. Carpanini, Wioleta M. Zelek, B. Paul Morgan

    Published 2024
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  5. 5
    Complement receptor 1 is expressed on brain cells and in the human brain

    Complement receptor 1 is expressed on brain cells and in the human brain by Nikoleta Daskoulidou, Bethany Shaw, Megan Torvell, Lewis M. Watkins, Emma L. Cope, Sarah M. Carpanini, Nicholas D. Allen, B. Paul Morgan

    Published 2023
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  6. 6
    Alzheimer’s disease-associated complement gene variants influence plasma complement protein levels

    Alzheimer’s disease-associated complement gene variants influence plasma complement protein levels by Aurora Veteleanu, Joshua Stevenson‐Hoare, Samuel Keat, Nikoleta Daskoulidou, Henrik Zetterberg, Amanda Heslegrave, Valentina Escott‐Price, Julie Williams, Rebecca Sims, Wioleta M. Zelek, Sarah M. Carpanini, B. Paul Morgan

    Published 2023
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  7. 7
    Terminal complement pathway activation drives synaptic loss in Alzheimer’s disease models

    Terminal complement pathway activation drives synaptic loss in Alzheimer’s disease models by Sarah M. Carpanini, Megan Torvell, Ryan J. Bevan, Robert A. J. Byrne, Nikoleta Daskoulidou, Takashi Saito, Takaomi C. Saido, Philip R. Taylor, Timothy R. Hughes, Wioleta M. Zelek, B. Paul Morgan

    Published 2022
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  8. 8
    The schizophrenia-associated gene CSMD1 encodes a complement classical pathway inhibitor predominantly expressed by astrocytes and at synapses in mice and humans

    The schizophrenia-associated gene CSMD1 encodes a complement classical pathway inhibitor predominantly expressed by astrocytes and at synapses in mice and humans by Robert A. J. Byrne, Jacqui Nimmo, Megan Torvell, Sarah M. Carpanini, Nikoleta Daskoulidou, Timothy R. Hughes, Linda J. Noble‐Haeusslein, Aurora Veteleanu, Lewis M. Watkins, Wioleta M. Zelek, Michael O’Donovan, B. Paul Morgan

    Published 2025
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  9. 9
    A novel mouse model of Warburg Micro Syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton

    A novel mouse model of Warburg Micro Syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton by Sarah M. Carpanini, Lisa McKie, Derek Thomson, Ann K. Wright, Sarah L. Gordon, Sarah L. Roche, Mark T. Handley, Harris Morrison, David G. Brownstein, Thomas M. Wishart, Michael A. Cousin, Thomas H. Gillingwater, Irene A. Aligianis, Ian J. Jackson

    Published 2014
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  10. 10
    Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1

    Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1 by Jamie McQueen, Tomás J. Ryan, Sean McKay, Katie Marwick, Paul Baxter, Sarah M. Carpanini, Thomas M. Wishart, Thomas H. Gillingwater, Jean Manson, David J. A. Wyllie, Seth G. N. Grant, Barry W. McColl, Noboru H. Komiyama, Giles E. Hardingham

    Published 2017
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  11. 11
    Loss-of-Function Mutations in TBC1D20 Cause Cataracts and Male Infertility in blind sterile Mice and Warburg Micro Syndrome in Humans

    Loss-of-Function Mutations in TBC1D20 Cause Cataracts and Male Infertility in blind sterile Mice and Warburg Micro Syndrome in Humans by Ryan P. Liegel, Mark T. Handley, Adam Ronchetti, S.D.M. Brown, Lars Langemeyer, Andrea Linford, Bo Chang, Deborah Morris‐Rosendahl, Sarah M. Carpanini, Renata Posmyk, Verity Harthill, Eamonn Sheridan, Ghada M. H. Abdel‐Salam, Paulien A. Terhal, Francesca Faravelli, Patrizia Accorsi, Lucio Giordano, Lorenzo Pinelli, Britta Hartmann, Allison D. Ebert, Francis A. Barr, Irene A. Aligianis, D.J. Sidjanin

    Published 2013
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