Warren MJ - Search Results

1

Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31.

Wilkie SE, Vaclavik V, Wu H, Bujakowska K, Chakarova CF, Bhattacharya SS, Warren MJ, Hunt DM. Wilkie SE, et al. Among authors: warren mj. Mol Vis. 2008 Apr 18;14:683-90. Mol Vis. 2008. PMID: 18431455 Free PMC article.

2

Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31.

Deery EC, Vithana EN, Newbold RJ, Gallon VA, Bhattacharya SS, Warren MJ, Hunt DM, Wilkie SE. Deery EC, et al. Among authors: warren mj. Hum Mol Genet. 2002 Dec 1;11(25):3209-19. doi: 10.1093/hmg/11.25.3209. Hum Mol Genet. 2002. PMID: 12444105

3

A study of the nuclear trafficking of the splicing factor protein PRPF31 linked to autosomal dominant retinitis pigmentosa (ADRP).

Wilkie SE, Morris KJ, Bhattacharya SS, Warren MJ, Hunt DM. Wilkie SE, et al. Among authors: warren mj. Biochim Biophys Acta. 2006 Mar;1762(3):304-11. doi: 10.1016/j.bbadis.2005.12.004. Epub 2006 Jan 4. Biochim Biophys Acta. 2006. PMID: 16427773 Free article.

4

Characterisation of two genes for guanylate cyclase activator protein (GCAP1 and GCAP2) in the Japanese pufferfish, Fugu rubripes.

Wilkie SE, Stinton I, Cottrill P, Deery E, Newbold R, Warren MJ, Bhattacharya SS, Hunt DM. Wilkie SE, et al. Among authors: warren mj. Biochim Biophys Acta. 2002 Aug 19;1577(1):73-80. doi: 10.1016/s0167-4781(02)00413-x. Biochim Biophys Acta. 2002. PMID: 12151097

5

Dominant cone and cone-rod dystrophies: functional analysis of mutations in retGC1 and GCAP1.

Hunt DM, Wilkie SE, Newbold R, Deery E, Warren MJ, Bhattacharya SS, Zhang K. Hunt DM, et al. Among authors: warren mj. Novartis Found Symp. 2004;255:37-49; discussion 49-50, 177-8. doi: 10.1002/0470092645.ch4. Novartis Found Symp. 2004. PMID: 14750595

6

Functional characterization of missense mutations at codon 838 in retinal guanylate cyclase correlates with disease severity in patients with autosomal dominant cone-rod dystrophy.

Wilkie SE, Newbold RJ, Deery E, Walker CE, Stinton I, Ramamurthy V, Hurley JB, Bhattacharya SS, Warren MJ, Hunt DM. Wilkie SE, et al. Among authors: warren mj. Hum Mol Genet. 2000 Dec 12;9(20):3065-73. doi: 10.1093/hmg/9.20.3065. Hum Mol Genet. 2000. PMID: 11115851

7

Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.

Wilkie SE, Li Y, Deery EC, Newbold RJ, Garibaldi D, Bateman JB, Zhang H, Lin W, Zack DJ, Bhattacharya SS, Warren MJ, Hunt DM, Zhang K. Wilkie SE, et al. Among authors: warren mj. Am J Hum Genet. 2001 Sep;69(3):471-80. doi: 10.1086/323265. Epub 2001 Jul 31. Am J Hum Genet. 2001. PMID: 11484154 Free PMC article.

8

Guanylate cyclase activating proteins, guanylate cyclase and disease.

Newbold RJ, Deery EC, Payne AM, Wilkie SE, Hunt DM, Warren MJ. Newbold RJ, et al. Among authors: warren mj. Adv Exp Med Biol. 2002;514:411-38. doi: 10.1007/978-1-4615-0121-3_25. Adv Exp Med Biol. 2002. PMID: 12596936 Review.

9

Purification, characterisation and intracellular localisation of aryl hydrocarbon interacting protein-like 1 (AIPL1) and effects of mutations associated with inherited retinal dystrophies.

Gallon VA, Wilkie SE, Deery EC, Newbold RJ, Sohocki MM, Bhattacharya SS, Hunt DM, Warren MJ. Gallon VA, et al. Among authors: warren mj. Biochim Biophys Acta. 2004 Oct 14;1690(2):141-9. doi: 10.1016/j.bbadis.2004.06.012. Biochim Biophys Acta. 2004. PMID: 15469903 Free article.

10

Recombinant expression, purification, and characterization of three isoenzymes of aspartate aminotransferase from Arabidopsis thaliana.

Wilkie SE, Warren MJ. Wilkie SE, et al. Among authors: warren mj. Protein Expr Purif. 1998 Apr;12(3):381-9. doi: 10.1006/prep.1997.0845. Protein Expr Purif. 1998. PMID: 9535706

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