Rubin EM - Search Results

1

The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression.

Hamilton BA, Smith DJ, Mueller KL, Kerrebrock AW, Bronson RT, van Berkel V, Daly MJ, Kruglyak L, Reeve MP, Nemhauser JL, Hawkins TL, Rubin EM, Lander ES. Hamilton BA, et al. Among authors: rubin em. Neuron. 1997 May;18(5):711-22. doi: 10.1016/s0896-6273(00)80312-8. Neuron. 1997. PMID: 9182797 Free article.

2

Functional screening and complex traits: human 21q22.2 sequences affecting learning in mice.

Smith DJ, Rubin EM. Smith DJ, et al. Among authors: rubin em. Hum Mol Genet. 1997;6(10):1729-33. doi: 10.1093/hmg/6.10.1729. Hum Mol Genet. 1997. PMID: 9300665 Review.

3

Optimizing the mouse to sift sequence for function.

Rubin EM, Smith DJ. Rubin EM, et al. Trends Genet. 1997 Nov;13(11):423-6. doi: 10.1016/s0168-9525(97)01293-6. Trends Genet. 1997. PMID: 9385835 Review. No abstract available.

4

Atherosclerosis in mice: getting to the heart of a polygenic disorder.

Rubin EM, Smith DJ. Rubin EM, et al. Trends Genet. 1994 Jun;10(6):199-203. doi: 10.1016/0168-9525(94)90256-9. Trends Genet. 1994. PMID: 8073533 Review.

5

A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration.

Hodgson JG, Agopyan N, Gutekunst CA, Leavitt BR, LePiane F, Singaraja R, Smith DJ, Bissada N, McCutcheon K, Nasir J, Jamot L, Li XJ, Stevens ME, Rosemond E, Roder JC, Phillips AG, Rubin EM, Hersch SM, Hayden MR. Hodgson JG, et al. Among authors: rubin em. Neuron. 1999 May;23(1):181-92. doi: 10.1016/s0896-6273(00)80764-3. Neuron. 1999. PMID: 10402204 Free article.

6

Construction of a panel of transgenic mice containing a contiguous 2-Mb set of YAC/P1 clones from human chromosome 21q22.2.

Smith DJ, Zhu Y, Zhang J, Cheng JF, Rubin EM. Smith DJ, et al. Among authors: rubin em. Genomics. 1995 Jun 10;27(3):425-34. doi: 10.1006/geno.1995.1073. Genomics. 1995. PMID: 7558023

7

Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome.

Smith DJ, Stevens ME, Sudanagunta SP, Bronson RT, Makhinson M, Watabe AM, O'Dell TJ, Fung J, Weier HU, Cheng JF, Rubin EM. Smith DJ, et al. Among authors: rubin em. Nat Genet. 1997 May;16(1):28-36. doi: 10.1038/ng0597-28. Nat Genet. 1997. PMID: 9140392

8

Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome.

Sago H, Carlson EJ, Smith DJ, Rubin EM, Crnic LS, Huang TT, Epstein CJ. Sago H, et al. Among authors: rubin em. Pediatr Res. 2000 Nov;48(5):606-13. doi: 10.1203/00006450-200011000-00009. Pediatr Res. 2000. PMID: 11044479

9

Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities.

Sago H, Carlson EJ, Smith DJ, Kilbridge J, Rubin EM, Mobley WC, Epstein CJ, Huang TT. Sago H, et al. Among authors: rubin em. Proc Natl Acad Sci U S A. 1998 May 26;95(11):6256-61. doi: 10.1073/pnas.95.11.6256. Proc Natl Acad Sci U S A. 1998. PMID: 9600952 Free PMC article.

10

Initial sequencing and comparative analysis of the mouse genome.

Mouse Genome Sequencing Consortium; Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M, An P, Antonarakis SE, Attwood J, Baertsch R, Bailey J, Barlow K, Beck S, Berry E, Birren B, Bloom T, Bork P, Botcherby M, Bray N, Brent MR, Brown DG, Brown SD, Bult C, Burton J, Butler J, Campbell RD, Carninci P, Cawley S, Chiaromonte F, Chinwalla AT, Church DM, Clamp M, Clee C, Collins FS, Cook LL, Copley RR, Coulson A, Couronne O, Cuff J, Curwen V, Cutts T, Daly M, David R, Davies J, Delehaunty KD, Deri J, Dermitzakis ET, Dewey C, Dickens NJ, Diekhans M, Dodge S, Dubchak I, Dunn DM, Eddy SR, Elnitski L, Emes RD, Eswara P, Eyras E, Felsenfeld A, Fewell GA, Flicek P, Foley K, Frankel WN, Fulton LA, Fulton RS, Furey TS, Gage D, Gibbs RA, Glusman G, Gnerre S, Goldman N, Goodstadt L, Grafham D, Graves TA, Green ED, Gregory S, Guigó R, Guyer M, Hardison RC, Haussler D, Hayashizaki Y, Hillier LW, Hinrichs A, Hlavina W, Holzer T, Hsu F, Hua A, Hubbard T, Hunt A, Jackson I, Jaffe DB, Johnson LS, Jones M, Jones TA, Joy A, Kamal M, Karlsson EK, Karolchik D, Kasprzyk A, Kawai J, Keibler E, Kells C, Kent WJ, Kirby A, Kolbe DL, Korf I, Kucherlapa… See abstract for full author list ➔ Mouse Genome Sequencing Consortium, et al. Among authors: rubin em. Nature. 2002 Dec 5;420(6915):520-62. doi: 10.1038/nature01262. Nature. 2002. PMID: 12466850

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