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Results 11-17 of 17 (Search time: 0.001 seconds).
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PreviewIssue DateTitleAuthor(s)
2011Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseasesLawlor, K.; O'Keefe, L.; Samaraweera, S.; van Eyk, C.; McLeod, C.; Maloney, C.; Dang, T.; Suter, C.; Richards, R.
2012Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat diseasevan Eyk, C.; McLeod, C.; O'Keefe, L.; Richards, R.
2011Identification of SOX3 as an XX male sex reversal gene in mice and humansSutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.
1998PAK3 mutation in nonsyndromic X-linked mental retardationAllen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
2006A conserved supergene locus controls colour pattern diversity in Heliconius butterfliesJoron, M.; Papa, R.; Beltrán, M.; Chamberlain, N.; Mavárez, J.; Baxter, S.; Abanto, M.; Bermingham, E.; Humphray, S.J.; Rogers, J.; Beasley, H.; Barlow, K.; Ffrench-Constant, R.H.; Mallet, J.; McMillan, W.O.; Jiggins, C.D.; Noor, M.A.F.
1998The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.
1995X-Y chromosome dissociation in mice and rats exposed to increased testicular or environmental temperaturesVan Zelst, S.; Zupp, J.; Hayman, D.; Setchell, B.

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