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PreviewIssue DateTitleAuthor(s)
1998Molecular cloning reveals that the p160 Myb-binding protein is a novel, predominantly necleolar protein which may play a role in transactivation by MybTavner, F.; Simpson, R.; Tashiro, S.; Favier, D.; Jenkins, N.; Gilbert, D.; Copeland, N.; MacMillan, E.; Lutwyche, J.; Keough, R.; Ishii, S.; Gonda, T.
1998Pyruvate carboxylaseWallace, J.; Jitrapakdee, S.; Chapman-Smith, A.
1998Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 geneGibson, M.; Ellis, S.; Ades, L.; Haan, E.; Cleary, E.
1998Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancerWhitmore, S.; Settasatian, C.; Crawford, J.; Lower, K.; McCallum, B.; Seshadri, R.; Cornelisse, C.; Moerland, E.; Cleton-Jansen, A.M.; Tipping, A.; Mathew, C.; Savnio, M.; Savoia, A.; Verlander, P.; Auerbach, A.; Van Berkel, C.; Pronk, J.; Doggett, N.; Callen, D.
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.
1998SOLH, a human homologue of the Drosophila melanogaster small optic lobes gene is a member of the Calpain and Zinc-Finger gene families and maps to human chromosome 16p13.3 near CATM (cataract with microphthalmia)Kamei, M.; Webb, G.; Young, I.; Campbell, H.

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