Fisher EM - Search Results

1

An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes.

O'Doherty A, Ruf S, Mulligan C, Hildreth V, Errington ML, Cooke S, Sesay A, Modino S, Vanes L, Hernandez D, Linehan JM, Sharpe PT, Brandner S, Bliss TV, Henderson DJ, Nizetic D, Tybulewicz VL, Fisher EM. O'Doherty A, et al. Among authors: fisher em. Science. 2005 Sep 23;309(5743):2033-7. doi: 10.1126/science.1114535. Science. 2005. PMID: 16179473 Free PMC article.

2

Highly polymorphic sequence at D21S1448 mapping close to D21S55, within the Down syndrome critical region.

Hernandez D, Pannett AA, Tybulewicz V, Fisher EM. Hernandez D, et al. Among authors: fisher em. Hum Genet. 1995 Jun;95(6):721-2. doi: 10.1007/BF00209498. Hum Genet. 1995. PMID: 7789964

3

Mapping the gene that encodes phosphatidylinositol-specific phospholipase C-gamma 2 in the human and the mouse.

Hernandez D, Egan SE, Yulug IG, Fisher EM. Hernandez D, et al. Among authors: fisher em. Genomics. 1994 Sep 15;23(2):504-7. doi: 10.1006/geno.1994.1533. Genomics. 1994. PMID: 7835906

4

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.

5

Down syndrome genetics: unravelling a multifactorial disorder.

Hernandez D, Fisher EM. Hernandez D, et al. Among authors: fisher em. Hum Mol Genet. 1996;5 Spec No:1411-6. doi: 10.1093/hmg/5.supplement_1.1411. Hum Mol Genet. 1996. PMID: 8875245 Review.

6

Localisation of receptor interacting protein 140 (RIP140) within 100 kb of D21S13 on 21q11, a gene-poor region of the human genome.

Katsanis N, Ives JH, Groet J, Nizetic D, Fisher EM. Katsanis N, et al. Among authors: fisher em. Hum Genet. 1998 Feb;102(2):221-3. doi: 10.1007/s004390050682. Hum Genet. 1998. PMID: 9521594

7

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

8

Mouse autosomal trisomy: two's company, three's a crowd.

Hernandez D, Fisher EM. Hernandez D, et al. Among authors: fisher em. Trends Genet. 1999 Jun;15(6):241-7. doi: 10.1016/s0168-9525(99)01743-6. Trends Genet. 1999. PMID: 10354585 Review.

9

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics.

Mead S, Stumpf MP, Whitfield J, Beck JA, Poulter M, Campbell T, Uphill JB, Goldstein D, Alpers M, Fisher EM, Collinge J. Mead S, et al. Among authors: fisher em. Science. 2003 Apr 25;300(5619):640-3. doi: 10.1126/science.1083320. Epub 2003 Apr 10. Science. 2003. PMID: 12690204

10

Mutations in dynein link motor neuron degeneration to defects in retrograde transport.

Hafezparast M, Klocke R, Ruhrberg C, Marquardt A, Ahmad-Annuar A, Bowen S, Lalli G, Witherden AS, Hummerich H, Nicholson S, Morgan PJ, Oozageer R, Priestley JV, Averill S, King VR, Ball S, Peters J, Toda T, Yamamoto A, Hiraoka Y, Augustin M, Korthaus D, Wattler S, Wabnitz P, Dickneite C, Lampel S, Boehme F, Peraus G, Popp A, Rudelius M, Schlegel J, Fuchs H, Hrabe de Angelis M, Schiavo G, Shima DT, Russ AP, Stumm G, Martin JE, Fisher EM. Hafezparast M, et al. Among authors: fisher em. Science. 2003 May 2;300(5620):808-12. doi: 10.1126/science.1083129. Science. 2003. PMID: 12730604

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