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Number of items: 6.

Article

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 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)

Wilkie, S.E. and Warren, M.J. (1998) Recombinant expression, purification, and characterization of three isoenzymes of aspartate aminotransferase from Arabidopsis thaliana. Protein Expr Purif, 12 (3). pp. 381-9. ISSN 1046-5928 . (The full text of this publication is not available from this repository)

Wilkie, S.E. and Lambert, R. and Warren, M.J. (1996) Chloroplastic aspartate aminotransferase from Arabidopsis thaliana: an examination of the relationship between the structure of the gene and the spatial structure of the protein. Biochemical Journal , 319 (3). pp. 969-976. ISSN 0264-6021 . (The full text of this publication is not available from this repository)

Wilkie, S.E. and Roper, J.M. and Smith, A.G. and Warren, M.J. (1995) Isolation, Characterization and Expression of a Cdna Clone Encoding Plastid Aspartate-Aminotransferase from Arabidopsis-Thaliana. Plant Molecular Biology, 27 (6). pp. 1227-1233. ISSN 0167-4412 . (The full text of this publication is not available from this repository)

Book section

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)

This list was generated on Wed Apr 23 18:29:02 2014 BST.