Bestrophinopathies: perspectives on clinical disease, Bestrophin-1 function and developing therapies

por Singh Grewal, Simranjeet, Smith, Joseph J., Carr, Amanda-Jayne F.
Publicado 2021

Annexin A8 regulates Wnt signaling to maintain the phenotypic plasticity of retinal pigment epithelial cells

por Lueck, Katharina, Carr, Amanda-Jayne F., Yu, Lu, Greenwood, John, Moss, Stephen E.
Publicado 2020

Regulation of retinal pigment epithelial cell phenotype by Annexin A8

por Lueck, Katharina, Carr, Amanda-Jayne F., Stampoulis, Dimitrios, Gerke, Volker, Rescher, Ursula, Greenwood, John, Moss, Stephen E.
Publicado 2017

Using Stem Cells to Model Diseases of the Outer Retina

por Yvon, Camille, Ramsden, Conor M., Lane, Amelia, Powner, Michael B., da Cruz, Lyndon, Coffey, Peter J., Carr, Amanda-Jayne F.
Publicado 2015

Investigation of PTC124-mediated translational readthrough in a retinal organoid model of AIPL1-associated Leber congenital amaurosis

por Leung, Amy, Sacristan-Reviriego, Almudena, Perdigão, Pedro R.L., Sai, Hali, Georgiou, Michalis, Kalitzeos, Angelos, Carr, Amanda-Jayne F., Coffey, Peter J., Michaelides, Michel, Bainbridge, James, Cheetham, Michael E., van der Spuy, Jacqueline
Publicado 2022

Rescue of the MERTK phagocytic defect in a human iPSC disease model using translational read-through inducing drugs

por Ramsden, Conor M., Nommiste, Britta, R. Lane, Amelia, Carr, Amanda-Jayne F., Powner, Michael B., J. K. Smart, Matthew, Chen, Li Li, Muthiah, Manickam N., Webster, Andrew R., Moore, Anthony T., Cheetham, Michael E., da Cruz, Lyndon, Coffey, Peter J.
Publicado 2017

Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups

por Parfitt, David A., Lane, Amelia, Ramsden, Conor M., Carr, Amanda-Jayne F., Munro, Peter M., Jovanovic, Katarina, Schwarz, Nele, Kanuga, Naheed, Muthiah, Manickam N., Hull, Sarah, Gallo, Jean-Marc, da Cruz, Lyndon, Moore, Anthony T., Hardcastle, Alison J., Coffey, Peter J., Cheetham, Michael E.
Publicado 2016

Mislocalisation of BEST1 in iPSC-derived retinal pigment epithelial cells from a family with autosomal dominant vitreoretinochoroidopathy (ADVIRC)

por Carter, David A., Smart, Matthew J. K., Letton, William V. G., Ramsden, Conor M., Nommiste, Britta, Chen, Li Li, Fynes, Kate, Muthiah, Manickam N., Goh, Pollyanna, Lane, Amelia, Powner, Michael B., Webster, Andrew R., da Cruz, Lyndon, Moore, Anthony T., Coffey, Peter J., Carr, Amanda-Jayne F.
Publicado 2016