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Results 21-30 of 36 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Comparison of the levels of intra-specific genetic variation within Giardia muris and Giardia intestinalisAndrews, R.; Monis, P.; Ey, P.; Mayrhofer, G.
1998Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16Cavanaugh, J.; Callen, D.; Wilson, S.; Stanford, P.; Sraml, M.; Gorska, M.; Crawford, J.; Whitmore, S.; Shlegel, C.; Foote, S.; Kohonen-Corish, M.; Pavli, P.
1998A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.Town, M.; Jean, G.; Cherqui, S.; Attard, M.; Forestier, L.; Whitmore, S.; Callen, D.; Gribouval, O.; Broyer, M.; Bates, G.; van't Hoff, W.; Antignac, C.
1998Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.Hollway, G.; Mulley, J.
1998Transcriptional activation of Cytochrome P450 genes by different classes of chemical inducersDogra, S.; Whitelaw, M.; May, B.
1998Repression of basal transcription by vitamin D receptor: evidence for interaction of unliganded vitamin D receptor with two receptor interaction domains in rip13Δ1Dwivedi, P.; Muscat, G.; Bailey, P.; Omdahl, J.; May, B.
1998PAK3 mutation in nonsyndromic X-linked mental retardationAllen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
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 human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.Kremmidiotis, G.; Baker, E.; Crawford, J.; Eyre, H.; Nahmias, J.; Callen, D.
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.