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Results 11-19 of 19 (Search time: 0.001 seconds).
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PreviewIssue DateTitleAuthor(s)
1999DECAY, a novel Drosophila caspase related to mammalian Caspase-3 and Caspase-7Dorstyn, L.; Read, S.; Quinn, L.; Richardson, H.; Kumar, S.
1997Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean FeverAksentijevich, I.; Centola, M.; Deng, Z.; Sood, R.; Balow, J.; Wood, G.; Zaks, N.; Mansfield, E.; Chen, X.; Eisenberg, S.; Vedula, A.; Shafran, N.; Raben, N.; Pras, E.; Pras, M.; Kastner, D.; Blake, T.; Baxevanis, A.; Robbins, C.; Krizman, D.; 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.
1999Systematic relationships within the Dasyurid Marsupial Tribe Sminthopsini - a multigene approachBlacket, M.; Krajewski, C.; Labrinidis, A.; Cambron, B.; Cooper, S.; Westerman, M.
1999Evolution and molecular characterization of a β-globin gene from the Australian Echidna Tachyglossus aculeatus (Monotremata)Lee, M.H.; Shroff, R.; Cooper, S.; Hope, R.
1998The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogasterCoulson, M.; Robert, S.; Eyre, H.; Saint, R.
1998Localisation of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels.Kalsi, G.; Whiting, P.; Bourdelles, B.; Callen, D.; Barnard, E.; Gurling, H.
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.