Fisher EM - Search Results

1

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.

2

A human SHC-related sequence maps to chromosome 17, the SHC gene maps to chromosome 1.

Yulug IG, Egan SE, See CG, Fisher EM. Yulug IG, et al. Among authors: fisher em. Hum Genet. 1995 Aug;96(2):245-8. doi: 10.1007/BF00207393. Hum Genet. 1995. PMID: 7635484

3

An improved protocol for the analysis of SOD1 gene mutations, and a new mutation in exon 4.

Yulug IG, Katsanis N, de Belleroche J, Collinge J, Fisher EM. Yulug IG, et al. Among authors: fisher em. Hum Mol Genet. 1995 Jun;4(6):1101-4. doi: 10.1093/hmg/4.6.1101. Hum Mol Genet. 1995. PMID: 7655468 No abstract available.

4

The SHB adaptor protein maps to human chromosome 9.

Yulug IG, Hillermann R, Fisher EM. Yulug IG, et al. Among authors: fisher em. Genomics. 1994 Dec;24(3):615-7. doi: 10.1006/geno.1994.1681. Genomics. 1994. PMID: 7713524 No abstract available.

5

Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5.

Bermingham N, Hillermann R, Gilmour F, Martin JE, Fisher EM. Bermingham N, et al. Among authors: fisher em. Hum Genet. 1995 Dec;96(6):671-3. doi: 10.1007/BF00210297. Hum Genet. 1995. PMID: 8522325

6

Paralogy mapping: identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH loci.

Katsanis N, Fitzgibbon J, Fisher EM. Katsanis N, et al. Among authors: fisher em. Genomics. 1996 Jul 1;35(1):101-8. doi: 10.1006/geno.1996.0328. Genomics. 1996. PMID: 8661110

7

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.

8

The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndrome.

Katsanis N, Fisher EM. Katsanis N, et al. Among authors: fisher em. Hum Genet. 1996 Oct;98(4):497-9. doi: 10.1007/s004390050246. Hum Genet. 1996. PMID: 8792829

9

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

10

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

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