R. E. Kelsell

Characterisation of recombinant rat TRPM2 and a TRPM2-like conductance in cultured rat striatal neurons. (2006)

Hill, K., Tigue, N., Kelsell, R.E., Benham, C.D., McNulty, S., Schaefer, M., ...

Original article can be found at: http://www.sciencedirect.com/science/journal/00283908 Copyright Elsevier Ltd. DOI: 10.1016/j.neuropharm.2005.08.021 [Full text of this article is not available in...

Tissue distribution profiles of the human TRPM cation channel family. (2006)

Fonfria, E., Murdock, P., Cusdin, F.S., Benham, C.D., Kelsell, R.E., McNulty, S.

Original article can be found at: http://www.informaworld.com/smpp/title~content=t713597278 Copyright Informa / Taylor and Francis Group. DOI: 10.1080/10799890600637506 [Full text of this article is...

TRPM2 channel opening in response to oxidative stress is dependent on activation of poly(ADP-ribose) polymerase. (2004)

Fonfria, E., Marshall, I.C.B., Benham, C.D., Boyfield, I., Brown, J.D., Hill, K., ...

Original article can be found at: http://www.nature.com/bjp/index.html Copyright British Pharmacological Society and Nature Publishing Group. DOI: 10.1038/sj.bjp.0705914 [Full text of this article is...

Cloning and functional expression of human short TRP7, a candidate protein for store-operated Ca2+ influx. (2002)

Riccio, A., Mattei, C., Kelsell, R. E., Medhurst, A.D., Calver, A. R., Randall, A. D., ...

mRNA distribution analysis of TRPC family in human CNS and peripheral tissues. (2002)

Riccio, A., Medhurst, A.D., Mattei, C., Kelsell, R. E., Calver, A. R., Randall, A. D., ...

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q.

Kelsell, R E, Gregory-Evans, K, Gregory-Evans, C Y, Holder, G E, Jay, M R, Weber, B H, ...

A retGC-1 mutation in autosomal dominant cone-rod dystrophy.

Perrault, I, Rozet, J M, Gerber, S, Kelsell, R E, Souied, E, Cabot, A, ...

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q.

Kelsell, R E, Gregory-Evans, K, Gregory-Evans, C Y, Holder, G E, Jay, M R, Weber, B H, ...

A retGC-1 mutation in autosomal dominant cone-rod dystrophy.

Perrault, I, Rozet, J M, Gerber, S, Kelsell, R E, Souied, E, Cabot, A, ...

Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss

Francis, P J, Johnson, S, Edmunds, B, Kelsell, R E, Sheridan, E, Garrett, C, ...

Aim: To characterise the phenotype and identify the underlying genetic defect in a family with deafness segregating with a North Carolina-like macular dystrophy (NCMD).

Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).

Gehrig, A, Felbor, U, Kelsell, R E, Hunt, D M, Maumenee, I H, Weber, B H

We have recently characterised the genomic organisation of a novel interphotoreceptor matrix proteoglycan, IMPG1, and have mapped the gene locus to chromosome 6q13-q15 by fluorescence in situ...