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2008 2004 2002 2001 1998

Number of items: 6.

2008

Wilkie, S.E. and Vaclavik, V. and Wu, H.M. and Bujakowska, K. and Chakarova, C.F. and Bhattacharya, S.S. and Warren, M.J. and Hunt, D.M. (2008) Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31. Molecular Vision, 14 (81-83). pp. 683-690. ISSN 1090-0535. The full text of this publication is not available from this repository.

2004

Hunt, D.M. and Wilkie, S.E. and Newbold, R. and Deery, E. and Warren, M.J. and Bhattacharya, S.S. and Zhang, K. (2004) Dominant cone and cone-rod dystrophies: functional analysis of mutations in retGC1 and GCAP1. In: Bock, G. and Chader, G. and Goode, J., eds. Retinal Dystrophies: Functional Genomics to Gene Therapy. Novartis Foundation Symposia, 255 . John Wiley & Sons, pp. 37-49. ISBN 9780470853573. The full text of this publication is not available from this repository.

2002

Deery, E.C. and Vithana, E.N. and Newbold, R.J. and Gallon, V.A. and Bhattacharya, S.S. and Warren, M.J. and Hunt, D.M. and Wilkie, S.E. (2002) Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31. human molecular genetics, 11 (25). pp. 3209-3219. ISSN 0964-6906 . The full text of this publication is not available from this repository.

Wilkie, S.E. and Stinton, I. and Cottrill, P. and Deery, E. and Newbold, R. and Warren, M.J. and Bhattacharya, S.S. and Hunt, D.M. (2002) Characterisation of two genes for guanylate cyclase activator protein (GCAP1 and GCAP2) in the Japanese pufferfish, Fugu rubripes. Biochim Biophys Acta, 1577 (1). pp. 73-80. ISSN 0167-4781 . The full text of this publication is not available from this repository.

2001

Wilkie, S.E. and Li, Y. and Deery, E.C. and Newbold, R.J. and Garibaldi, D. and Bateman, J.B. and Zhang, H. and Lin, W. and Zack, D.J. and Bhattacharya, S.S. and Warren, M.J. and Hunt, D.M. and Zhang, K. (2001) Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy. American Journal Humman Genetics, 69 (3). pp. 471-80. ISSN 0002-9297 . The full text of this publication is not available from this repository.

1998

Sokal, I. and Li, N. and Surgucheva, I. and Warren, M.J. and Payne, A.M. and Bhattacharya, S.S. and Baehr, W. and Palczewski, K. (1998) GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy. Molecular Cell, 2 (1). pp. 129-33. ISSN 1097-2765 . The full text of this publication is not available from this repository.

This list was generated on Sat May 25 14:49:53 2013 BST.