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Molecular Chaperone Mediated Late-Stage Neuroprotection in the SOD1<sup>G93A</sup> Mouse Model of Amyotrophic Lateral Sclerosis.
Published in:
PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0073944
By:
- Novoselov, Sergey S.;
- Mustill, Wendy J.;
- Gray, Anna L.;
- Dick, James R.;
- Kanuga, Naheed;
- Kalmar, Bernadett;
- Greensmith, Linda;
- Cheetham, Michael E.
Publication type:
Article
The Inherited Blindness Protein AIPL1 Regulates the Ubiquitin-Like FAT10 Pathway.
Published in:
PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0030866
By:
- Bett, John S.;
- Kanuga, Naheed;
- Richet, Emma;
- Schmidtke, Gunter;
- Groettrup, Marcus;
- Cheetham, Michael E.;
- Der Spuy, Jacqueline van
Publication type:
Article
Lovastatin inhibits brain endothelial cell Rho‐mediated lymphocyte migration and attenuates experimental autoimmune encephalomyelitis.
Published in:
FASEB Journal, 2003, v. 17, n. 8, p. 1, doi. 10.1096/fj.02-1014fje
By:
- Greenwood, John;
- Walters, Claire E.;
- Pryce, Gareth;
- Kanuga, Naheed;
- Bemud, Evelyne;
- Baker, David;
- Adamson, Peter
Publication type:
Article
Corrigendum to: The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control.
Published in:
Human Molecular Genetics, 2020, v. 29, n. 19, p. 3338, doi. 10.1093/hmg/ddaa190
By:
- Athanasiou, Dimitra;
- Bevilacqua, Dalila;
- Aguila, Monica;
- McCulley, Caroline;
- Kanuga, Naheed;
- Takao Iwawaki;
- Chapple, J. Paul;
- Cheetham, Michael E.
Publication type:
Article
The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 24, p. 4896, doi. 10.1093/hmg/ddx370
By:
- Athanasiou, Dimitra;
- Aguila, Monica;
- Bellingham, James;
- Kanuga, Naheed;
- Adamson, Peter;
- Cheetham, Michael E.
Publication type:
Article
Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 2, p. 305, doi. 10.1093/hmg/ddw387
By:
- Athanasiou, Dimitra;
- Aguila, Monica;
- Opefi, Chikwado A.;
- South, Kieron;
- Bellingham, James;
- Bevilacqua, Dalila;
- Munro, Peter M.;
- Kanuga, Naheed;
- Mackenzie, Francesca E.;
- Dubis, Adam M.;
- Georgiadis, Anastasios;
- Graca, Anna B.;
- Pearson, Rachael A.;
- Ali, Robin R.;
- Sakami, Sanae;
- Palczewski, Krzysztof;
- Sherman, Michael Y.;
- Reeves, Philip J.;
- Cheetham, Michael E.
Publication type:
Article
Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cells.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 4, p. 972, doi. 10.1093/hmg/ddu509
By:
- Schwarz, Nele;
- Carr, Amanda-Jayne;
- Lane, Amelia;
- Moeller, Fabian;
- Li Li Chen;
- Aguilà, Mònica;
- Nommiste, Britta;
- Muthiah, Manickam N.;
- Kanuga, Naheed;
- Wolfrum, Uwe;
- Nagel-Wolfrum, Kerstin;
- da Cruz, Lyndon;
- Coffey, Peter J.;
- Cheetham, Michael E.;
- Hardcastle, Alison J.
Publication type:
Article
The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 24, p. 6594, doi. 10.1093/hmg/ddu385
By:
- Athanasiou, Dimitra;
- Bevilacqua, Dalila;
- Aguila, Monica;
- McCulley, Caroline;
- Kanuga, Naheed;
- Iwawaki, Takao;
- Paul Chapple, J.;
- Cheetham, Michael E.
Publication type:
Article
Hsp90 inhibition protects against inherited retinal degeneration.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 8, p. 2164
By:
- Aguilà, Mònica;
- Bevilacqua, Dalila;
- McCulley, Caroline;
- Schwarz, Nele;
- Athanasiou, Dimitra;
- Kanuga, Naheed;
- Novoselov, Sergey S.;
- Lange, Clemens A.K.;
- Ali, Robin R.;
- Bainbridge, James W.;
- Gias, Carlos;
- Coffey, Peter J.;
- Garriga, Pere;
- Cheetham, Michael E.
Publication type:
Article
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).
Published in:
Human Molecular Genetics, 2012, v. 21, n. 16, p. 3647, doi. 10.1093/hmg/dds194
By:
- Webb, Tom R.;
- Parfitt, David A.;
- Gardner, Jessica C.;
- Martinez, Ariadna;
- Bevilacqua, Dalila;
- Davidson, Alice E.;
- Zito, Ilaria;
- Thiselton, Dawn L.;
- Ressa, Jacob H.C.;
- Apergi, Marina;
- Schwarz, Nele;
- Kanuga, Naheed;
- Michaelides, Michel;
- Cheetham, Michael E.;
- Gorin, Michael B.;
- Hardcastle, Alison J.
Publication type:
Article
Three Different Cone Opsin Gene Array Mutational Mechanisms with Genotype-Phenotype Correlation and Functional Investigation of Cone Opsin Variants.
Published in:
Human Mutation, 2014, v. 35, n. 11, p. 1354, doi. 10.1002/humu.22679
By:
- Gardner, Jessica C.;
- Liew, Gerald;
- Quan, Ying‐Hua;
- Ermetal, Burcu;
- Ueyama, Hisao;
- Davidson, Alice E.;
- Schwarz, Nele;
- Kanuga, Naheed;
- Chana, Ravinder;
- Maher, Eamonn R.;
- Webster, Andrew R.;
- Holder, Graham E.;
- Robson, Anthony G.;
- Cheetham, Michael E.;
- Liebelt, Jan;
- Ruddle, Jonathan B.;
- Moore, Anthony T.;
- Michaelides, Michel;
- Hardcastle, Alison J.
Publication type:
Article
The Nance–Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphology.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 12, p. 2421, doi. 10.1093/hmg/ddq125
By:
- Brooks, Simon P.;
- Coccia, Margherita;
- Tang, Hao R.;
- Kanuga, Naheed;
- Machesky, Laura M.;
- Bailly, Maryse;
- Cheetham, Michael E.;
- Hardcastle, Alison J.
Publication type:
Article
X-linked cataract and Nance-Horan syndrome are allelic disorders.
Published in:
Human Molecular Genetics, 2009, v. 18, n. 14, p. 2643, doi. 10.1093/hmg/ddp206
By:
- Coccia, Margherita;
- Brooks, Simon P.;
- Webb, Tom R.;
- Christodoulou, Katja;
- Wozniak, Izabella O.;
- Murday, Victoria;
- Balicki, Martha;
- Yee, Harris A.;
- Wangensteen, Teresia;
- Riise, Ruth;
- Saggar, Anand K.;
- Park, Soo-Mi;
- Kanuga, Naheed;
- Francis, Peter J.;
- Maher, Eamonn R.;
- Moore, Anthony T.;
- Russell-Eggitt, Isabelle M.;
- Hardcastle, Alison J.
Publication type:
Article
Gene Transfer into the Mouse Retina Mediated by an Adeno-Associated Viral Vector.
Published in:
Human Molecular Genetics, 1996, v. 5, n. 5, p. 591, doi. 10.1093/hmg/5.5.591
By:
- Ali, Robin R.;
- Reichel, Martin B.;
- Thrasher, Adrian J.;
- Levinsky, Roland J.;
- Kinnon, Christine;
- Kanuga, Naheed;
- Hunt, David M.;
- Bhattacharya, Shomi S.
Publication type:
Article

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