Calnexin is not essential for mammalian rod opsin biogenesis

por Kosmaoglou, Maria, Cheetham, Michael E.
Publicado 2008

Molecular chaperones and photoreceptor function

por Kosmaoglou, Maria, Schwarz, Nele, Bett, John S., Cheetham, Michael E.
Publicado 2008

Characterisation of a novel OPA1 splice variant resulting in cryptic splice site activation and mitochondrial dysfunction

por Harvey, Joshua Paul, Yu-Wai-Man, Patrick, Cheetham, Michael Edward
Publicado 2022

Molecular chaperone-mediated rescue of mitophagy by a Parkin RING1 domain mutant

por Rose, Johanna M., Novoselov, Sergey S., Robinson, Philip A., Cheetham, Michael E.
Publicado 2011

Correlative light and immuno-electron microscopy of retinal tissue cryostat sections

por Burgoyne, Thomas, Lane, Amelia, Laughlin, William E., Cheetham, Michael E., Futter, Clare E.
Publicado 2018

The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa

por Athanasiou, Dimitra, Aguila, Monica, Bellingham, James, Kanuga, Naheed, Adamson, Peter, Cheetham, Michael E
Publicado 2017

Suppression of protein aggregation by chaperone modification of high molecular weight complexes

por Labbadia, John, Novoselov, Sergey S., Bett, John S., Weiss, Andreas, Paganetti, Paolo, Bates, Gillian P., Cheetham, Michael E.
Publicado 2012

The Inherited Blindness Protein AIPL1 Regulates the Ubiquitin-Like FAT10 Pathway

por Bett, John S., Kanuga, Naheed, Richet, Emma, Schmidtke, Gunter, Groettrup, Marcus, Cheetham, Michael E., van der Spuy, Jacqueline
Publicado 2012

The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control

por Athanasiou, Dimitra, Bevilacqua, Dalila, Aguila, Monica, McCulley, Caroline, Kanuga, Naheed, Iwawaki, Takao, Paul Chapple, J., Cheetham, Michael E.
Publicado 2014

Symmetric arrangement of mitochondria:plasma membrane contacts between adjacent photoreceptor cells regulated by Opa1

por Meschede, Ingrid P., Ovenden, Nicholas C., Seabra, Miguel C., Futter, Clare E., Votruba, Marcela, Cheetham, Michael E., Burgoyne, Thomas
Publicado 2020

A look into retinal organoids: methods, analytical techniques, and applications

por Afanasyeva, Tess A. V., Corral-Serrano, Julio C., Garanto, Alejandro, Roepman, Ronald, Cheetham, Michael E., Collin, Rob W. J.
Publicado 2021

BiP prevents rod opsin aggregation

por Athanasiou, Dimitra, Kosmaoglou, Maria, Kanuga, Naheed, Novoselov, Sergey S., Paton, Adrienne W., Paton, James C., Chapple, J. Paul, Cheetham, Michael E.
Publicado 2012

Molecular Chaperone Mediated Late-Stage Neuroprotection in the SOD1(G93A) Mouse Model of Amyotrophic Lateral Sclerosis

por Novoselov, Sergey S., Mustill, Wendy J., Gray, Anna L., Dick, James R., Kanuga, Naheed, Kalmar, Bernadett, Greensmith, Linda, Cheetham, Michael E.
Publicado 2013

The Nance–Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphology

por Brooks, Simon P., Coccia, Margherita, Tang, Hao R., Kanuga, Naheed, Machesky, Laura M., Bailly, Maryse, Cheetham, Michael E., Hardcastle, Alison J.
Publicado 2010

Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model

por Patrizi, Clarissa, Llado, Manel, Benati, Daniela, Iodice, Carolina, Marrocco, Elena, Guarascio, Rosellina, Surace, Enrico M., Cheetham, Michael E., Auricchio, Alberto, Recchia, Alessandra
Publicado 2021

Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells

por Sladen, Paul E, Jovanovic, Katarina, Guarascio, Rosellina, Ottaviani, Daniele, Salsbury, Grace, Novoselova, Tatiana, Chapple, J Paul, Yu-Wai-Man, Patrick, Cheetham, Michael E
Publicado 2022

Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosa

por Maubaret, Cécilia, Kosmaoglou, Maria, Low, Sancy, Chakarova, Christina F., Bidot, Samuel, Thauvin-Robinet, Christel, Robson, Anthony G., Waseem, Naushin, Cheetham, Michael E., Bhattacharya, Shomi S.
Publicado 2012

The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosis

por Chen, Han-Jou, Mitchell, Jacqueline C., Novoselov, Sergey, Miller, Jack, Nishimura, Agnes L., Scotter, Emma L., Vance, Caroline A., Cheetham, Michael E., Shaw, Christopher E.
Publicado 2016

Protein kinase CK2 modulates HSJ1 function through phosphorylation of the UIM2 domain

por Ottaviani, Daniele, Marin, Oriano, Arrigoni, Giorgio, Franchin, Cinzia, Vilardell, Jordi, Sandre, Michele, Li, Wenwen, Parfitt, David A., Pinna, Lorenzo A., Cheetham, Michael E., Ruzzene, Maria
Publicado 2017

CRISPR-Cas9 correction of OPA1 c.1334G>A: p.R445H restores mitochondrial homeostasis in dominant optic atrophy patient-derived iPSCs

por Sladen, Paul E., Perdigão, Pedro R.L., Salsbury, Grace, Novoselova, Tatiana, van der Spuy, Jacqueline, Chapple, J. Paul, Yu-Wai-Man, Patrick, Cheetham, Michael E.
Publicado 2021