Fisher EM - Search Results

1

Novel phenotypes identified by plasma biochemical screening in the mouse.

Hough TA, Nolan PM, Tsipouri V, Toye AA, Gray IC, Goldsworthy M, Moir L, Cox RD, Clements S, Glenister PH, Wood J, Selley RL, Strivens MA, Vizor L, McCormack SL, Peters J, Fisher EM, Spurr N, Rastan S, Martin JE, Brown SD, Hunter AJ. Hough TA, et al. Among authors: fisher em. Mamm Genome. 2002 Oct;13(10):595-602. doi: 10.1007/s00335-002-2188-1. Mamm Genome. 2002. PMID: 12420138

2

Localization of the human X-linked gene for chronic granulomatous disease to the mouse X chromosome: implications for X-chromosome evolution.

Brockdorff N, Fisher EM, Orkin SH, Lyon MF, Brown SD. Brockdorff N, et al. Among authors: fisher em. Cytogenet Cell Genet. 1988;48(2):124-5. doi: 10.1159/000132605. Cytogenet Cell Genet. 1988. PMID: 3197451

3

The gene encoding tripeptidyl peptidase II maps to chromosome 1 in the mouse.

Bermingham NA, McKay T, Hoyle J, Hernandez D, Martin JE, Fisher EM. Bermingham NA, et al. Among authors: fisher em. Mamm Genome. 1996 May;7(5):390. doi: 10.1007/BF03035314. Mamm Genome. 1996. PMID: 8661741 No abstract available.

4

Mapping TNNC1, the gene that encodes cardiac troponin I in the human and the mouse.

Bermingham N, Hernandez D, Balfour A, Gilmour F, Martin JE, Fisher EM. Bermingham N, et al. Among authors: fisher em. Genomics. 1995 Dec 10;30(3):620-2. doi: 10.1006/geno.1995.1288. Genomics. 1995. PMID: 8825654

5

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

6

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.

7

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

8

The immunophilin FKBP4 (FKBP52/FKBP59) maps to the distal short arm of human chromosome 12.

Bermingham NA, Rauf S, Katsanis N, Martin JE, Hunter AJ, Fisher EM. Bermingham NA, et al. Among authors: fisher em. Mamm Genome. 1998 Mar;9(3):268. doi: 10.1007/s003359900746. Mamm Genome. 1998. PMID: 9501323 No abstract available.

9

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

10

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

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