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Results: 2

1.

Modelling human regulatory variation in mouse: finding the function in genome-wide association studies and whole-genome sequencing.

Schmouth JF, Bonaguro RJ, Corso-Diaz X, Simpson EM.

PLoS Genet. 2012;8(3):e1002544. doi: 10.1371/journal.pgen.1002544. Epub 2012 Mar 1. Review.

PMID:
22396661
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Retina restored and brain abnormalities ameliorated by single-copy knock-in of human NR2E1 in null mice.

Schmouth JF, Banks KG, Mathelier A, Gregory-Evans CY, Castellarin M, Holt RA, Gregory-Evans K, Wasserman WW, Simpson EM.

Mol Cell Biol. 2012 Apr;32(7):1296-311. doi: 10.1128/MCB.06016-11. Epub 2012 Jan 30.

PMID:
22290436
[PubMed - indexed for MEDLINE]
Free PMC Article

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