Hunter AJ - Search Results

1

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.

Isaacs AM, Davies KE, Hunter AJ, Nolan PM, Vizor L, Peters J, Gale DG, Kelsell DP, Latham ID, Chase JM, Fisher EM, Bouzyk MM, Potter A, Masih M, Walsh FS, Sims MA, Doncaster KE, Parsons CA, Martin J, Brown SD, Rastan S, Spurr NK, Gray IC. Isaacs AM, et al. Among authors: hunter aj. Hum Mol Genet. 2000 Jul 22;9(12):1865-71. doi: 10.1093/hmg/9.12.1865. Hum Mol Genet. 2000. PMID: 10915775

2

Novel ENU-induced eye mutations in the mouse: models for human eye disease.

Thaung C, West K, Clark BJ, McKie L, Morgan JE, Arnold K, Nolan PM, Peters J, Hunter AJ, Brown SD, Jackson IJ, Cross SH. Thaung C, et al. Among authors: hunter aj. Hum Mol Genet. 2002 Apr 1;11(7):755-67. doi: 10.1093/hmg/11.7.755. Hum Mol Genet. 2002. PMID: 11929848

3

Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.

Isaacs AM, Jeans A, Oliver PL, Vizor L, Brown SD, Hunter AJ, Davies KE. Isaacs AM, et al. Among authors: hunter aj. Mol Cell Neurosci. 2002 Sep;21(1):114-25. doi: 10.1006/mcne.2002.1158. Mol Cell Neurosci. 2002. PMID: 12359155

4

Towards new models of disease and physiology in the neurosciences: the role of induced and naturally occurring mutations.

Hunter AJ, Nolan PM, Brown SD. Hunter AJ, et al. Hum Mol Genet. 2000 Apr 12;9(6):893-900. doi: 10.1093/hmg/9.6.893. Hum Mol Genet. 2000. PMID: 10767312 Review.

5

A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.

Isaacs AM, Oliver PL, Jones EL, Jeans A, Potter A, Hovik BH, Nolan PM, Vizor L, Glenister P, Simon AK, Gray IC, Spurr NK, Brown SD, Hunter AJ, Davies KE. Isaacs AM, et al. Among authors: hunter aj. J Neurosci. 2003 Mar 1;23(5):1631-7. doi: 10.1523/JNEUROSCI.23-05-01631.2003. J Neurosci. 2003. PMID: 12629167 Free PMC article.

6

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.

Tsai H, Hardisty RE, Rhodes C, Kiernan AE, Roby P, Tymowska-Lalanne Z, Mburu P, Rastan S, Hunter AJ, Brown SD, Steel KP. Tsai H, et al. Among authors: hunter aj. Hum Mol Genet. 2001 Mar 1;10(5):507-12. doi: 10.1093/hmg/10.5.507. Hum Mol Genet. 2001. PMID: 11181574

7

Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.

Tsipouri V, Curtin JA, Nolan PM, Vizor L, Parsons CA, Clapham CM, Latham ID, Rooke LJ, Martin JE, Peters J, Hunter AJ, Rogers D, Rastan S, Brown SD, Fisher EM, Spurr NK, Gray IC. Tsipouri V, et al. Among authors: hunter aj. Comp Funct Genomics. 2004;5(2):123-7. doi: 10.1002/cfg.382. Comp Funct Genomics. 2004. PMID: 18629060 Free PMC article.

8

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment.

Rogers DC, Fisher EM, Brown SD, Peters J, Hunter AJ, Martin JE. Rogers DC, et al. Among authors: hunter aj. Mamm Genome. 1997 Oct;8(10):711-3. doi: 10.1007/s003359900551. Mamm Genome. 1997. PMID: 9321461

9

Informatics for mutagenesis: the design of mutabase--a distributed data recording system for animal husbandry, mutagenesis, and phenotypic analysis.

Strivens MA, Selley RL, Greenaway SJ, Hewitt M, Liu X, Battershill K, McCormack SL, Pickford KA, Vizor L, Nolan PM, Hunter AJ, Peters J, Brown SD. Strivens MA, et al. Among authors: hunter aj. Mamm Genome. 2000 Jul;11(7):577-83. doi: 10.1007/s003350010110. Mamm Genome. 2000. PMID: 10886026

10

A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.

Hardisty-Hughes RE, Tateossian H, Morse SA, Romero MR, Middleton A, Tymowska-Lalanne Z, Hunter AJ, Cheeseman M, Brown SD. Hardisty-Hughes RE, et al. Among authors: hunter aj. Hum Mol Genet. 2006 Nov 15;15(22):3273-9. doi: 10.1093/hmg/ddl403. Epub 2006 Oct 11. Hum Mol Genet. 2006. PMID: 17035249

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