N. Kanuga

发表

Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration

Peter M. G. Munro, K. Palczewski, D. Athanasiou, 2016, Human molecular genetics.

Three Different Cone Opsin Gene Array Mutational Mechanisms with Genotype–Phenotype Correlation and Functional Investigation of Cone Opsin Variants

G. Holder, G. Liew, M. Michaelides, 2014, Human mutation.

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).

T. Webb, M. Gorin, M. Michaelides, 2012, Human molecular genetics.

Hsp90 inhibition protects against inherited retinal degeneration

P. Garriga, C. Gias, P. Coffey, 2013, Human molecular genetics.

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

N. Kanuga, M. Cheetham, M. Bailly, 2010, Human molecular genetics.

A dual role for EDEM1 in the processing of rod opsin

P. Garriga, M. Aguilà, N. Kanuga, 2009, Journal of Cell Science.

Lovastatin inhibits brain endothelial cell Rho‐mediated lymphocyte migration and attenuates experimental autoimmune encephalomyelitis

P. Adamson, J. Greenwood, N. Kanuga, 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

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

D. Athanasiou, M. Aguilà, D. Bevilacqua, 2014, Human molecular genetics.

Oxidative stress affects the junctional integrity of retinal pigment epithelial cells.

P. Luthert, J. Greenwood, N. Kanuga, 2004, Investigative ophthalmology & visual science.

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

N. Kanuga, M. Cheetham, J. Bett, 2012, PloS one.

Adeno-associated virus gene transfer to mouse retina.

D. Hunt, S. Bhattacharya, R. Levinsky, 1998, Human gene therapy.

Gene transfer into the mouse retina mediated by an adeno-associated viral vector.

D. Hunt, R. Levinsky, S. Bhattacharya, 1996, Human molecular genetics.

Basement membrane-dependent modification of phenotype and gene expression in human retinal pigment epithelial ARPE-19 cells.

P. Adamson, J. Greenwood, N. Kanuga, 2004, Investigative ophthalmology & visual science.

Absence of p53 delays apoptotic photoreceptor cell death in the rds mouse.

D. Hunt, Peter M. G. Munro, P. Luthert, 1998, Current eye research.

Cloning the REC1 gene of Ustilago maydis

N. Kanuga, A. Spanos, D. Holden, 1991, Current Genetics.

Molecular Chaperone Mediated Late-Stage Neuroprotection in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis

B. Kalmar, L. Greensmith, N. Kanuga, 2013, PloS one.

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

P. Adamson, D. Athanasiou, M. Aguilà, 2017, Human molecular genetics.

Adeno-associated virus gene transfer to mouse retina. Human Gene Therapy

D. Hunt, S. Bhattacharya, R. Levinsky, 1998 .

Characterization of genetically modified human retinal pigment epithelial cells developed for in vitro and transplantation studies.

R. Lund, S. Halford, P. Coffey, 2002, Investigative ophthalmology & visual science.

Transposon tools for recombinant DNA manipulation: characterization of transcriptional regulators from yeast, Xenopus, and mouse.

R. Krumlauf, F. Conlon, J. Sharpe, 1996, Proceedings of the National Academy of Sciences of the United States of America.

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

Peter M. G. Munro, L. da Cruz, P. Coffey, 2016, Cell stem cell.

X-linked cataract and Nance-Horan syndrome are allelic disorders

Soo-Mi Park, T. Webb, A. Moore, 2009, Human molecular genetics.

The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa

B. Kalmar, L. Greensmith, Peter M. G. Munro, 2014, Cell Death and Disease.

The Ustilago maydis nar 1 gene encoding nitrate reductase activity: sequence and transcriptional regulation

N. Kanuga, A. Spanos, D. Holden, 1993 .

Structural and functional architecture of the yeast cell-cycle transcription factor swi6.

I. Taylor, M. Treiber, S. Howell, 1998, Journal of molecular biology.

X-linked cone dystrophy caused by mutation of the red and green cone opsins.

Caterina Ripamonti, Naheed Kanuga, Michel Michaelides, 2010, American journal of human genetics.

The Ustilago maydis pyr3 gene: sequence and transcriptional analysis.

N. Kanuga, A. Spanos, D. Holden, 1992, Gene.

Blue cone monochromacy: Causative mutations and associated phenotypes

John D. Mollon, Alison J. Hardcastle, Naheed Kanuga, 2009, Molecular vision.

A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5).

A. Stockman, C. Ripamonti, G. Holder, 2012, Advances in experimental medicine and biology.

Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cells

U. Wolfrum, K. Nagel-Wolfrum, L. da Cruz, 2014, Human molecular genetics.

The influence of the Ustilago maydis REC1 gene on plasmid-chromosome recombination

N. Kanuga, A. Spanos, D. Holden, 1992, Current Genetics.

Identification and Correct ion of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups Graphical

Peter R. T. Munro, P. Coffey, A. Moore, 2016 .

BiP prevents rod opsin aggregation

D. Athanasiou, N. Kanuga, M. Cheetham, 2012, Molecular biology of the cell.

Subretinal transplantation of genetically modified human cell lines attenuates loss of visual function in dystrophic rats

R. Lund, Y. Sauve, P. Coffey, 2001, Proceedings of the National Academy of Sciences of the United States of America.