Fisher EM - Search Results

1

SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice.

Rogers DC, Peters J, Martin JE, Ball S, Nicholson SJ, Witherden AS, Hafezparast M, Latcham J, Robinson TL, Quilter CA, Fisher EM. Rogers DC, et al. Among authors: fisher em. Neurosci Lett. 2001 Jun 22;306(1-2):89-92. doi: 10.1016/s0304-3940(01)01885-7. Neurosci Lett. 2001. PMID: 11403965

2

The mouse lysosomal membrane protein 1 gene as a candidate for the motorneuron degeneration (mnd) locus.

Bermingham NA, Martin JE, Fisher EM. Bermingham NA, et al. Among authors: fisher em. Genomics. 1996 Mar 1;32(2):266-71. doi: 10.1006/geno.1996.0114. Genomics. 1996. PMID: 8833154

3

Phenotypic analysis--making the most of your mouse.

Martin JE, Fisher EM. Martin JE, et al. Among authors: fisher em. Trends Genet. 1997 Jul;13(7):254-6. doi: 10.1016/s0168-9525(97)01193-1. Trends Genet. 1997. PMID: 9242043 No abstract available.

4

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: fisher em. Mamm Genome. 1997 Oct;8(10):711-3. doi: 10.1007/s003359900551. Mamm Genome. 1997. PMID: 9321461

5

Wasted by an elongation factor.

Hafezparast M, Fisher E. Hafezparast M, et al. Trends Genet. 1998 Jun;14(6):215-7. doi: 10.1016/s0168-9525(98)01478-4. Trends Genet. 1998. PMID: 9635401 No abstract available.

6

Transchromosomal mouse embryonic stem cell lines and chimeric mice that contain freely segregating segments of human chromosome 21.

Hernandez D, Mee PJ, Martin JE, Tybulewicz VL, Fisher EM. Hernandez D, et al. Among authors: fisher em. Hum Mol Genet. 1999 May;8(5):923-33. doi: 10.1093/hmg/8.5.923. Hum Mol Genet. 1999. PMID: 10196383

7

The kinesin light chain gene: its mapping and exclusion in mouse and human forms of inherited motor neuron degeneration.

Hafezparast M, Witherden A, Nicholson S, Bermingham N, Mackin J, ten Asbroek A, Ball S, Peters J, Baas F, Martin JE, Fisher EM. Hafezparast M, et al. Among authors: fisher em. Neurosci Lett. 1999 Sep 24;273(1):49-52. doi: 10.1016/s0304-3940(99)00620-5. Neurosci Lett. 1999. PMID: 10505649

8

Genealogies of mouse inbred strains.

Beck JA, Lloyd S, Hafezparast M, Lennon-Pierce M, Eppig JT, Festing MF, Fisher EM. Beck JA, et al. Among authors: fisher em. Nat Genet. 2000 Jan;24(1):23-5. doi: 10.1038/71641. Nat Genet. 2000. PMID: 10615122

9

Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource.

Nolan PM, Peters J, Vizor L, Strivens M, Washbourne R, Hough T, Wells C, Glenister P, Thornton C, Martin J, Fisher E, Rogers D, Hagan J, Reavill C, Gray I, Wood J, Spurr N, Browne M, Rastan S, Hunter J, Brown SD. Nolan PM, et al. Mamm Genome. 2000 Jul;11(7):500-6. doi: 10.1007/s003350010096. Mamm Genome. 2000. PMID: 10886012

10

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: fisher em. Hum Mol Genet. 2000 Jul 22;9(12):1865-71. doi: 10.1093/hmg/9.12.1865. Hum Mol Genet. 2000. PMID: 10915775

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