Browse by Person (creator, editor, contributor, etc.)

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | Date | No Grouping
Number of items: 3.

Article

Lightbody, K.L. and Renshaw, P.S. and Collins, M.L. and Wright, R.L. and Hunt, D.M. and Gordon, S.V. and Hewinson, R.G. and Buxton, R.S. and Williamson, R.A. and Carr, M.D. (2004) Characterisation of complex formation between members of the Mycobacterium tuberculosis complex CFP-10/ESAT-6 protein family: towards an understanding of the rules governing complex formation and thereby functional flexibility. FEMS Microbiol Lett, 238 (1). pp. 255-262. ISSN 0378-1097. (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)

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 Fri Apr 25 09:27:13 2014 BST.