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Results 2871-2880 of 3021 (Search time: 0.008 seconds).
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PreviewIssue DateTitleAuthor(s)
2000Cloning of the cDNA and localization of the gene encoding human NRPB, a ubiquitously expressed, multidomain putative adapter proteinHooper, J.; Baker, E.; Ogbourne, S.; Sutherland, G.; Antalis, T.
2000Molecular cloning and chromosomal mapping of a novel five-span transmembrane protein gene, M83Motohashi, T.; Miyoshi, S.; Osawa, M.; Eyre, H.; Sutherland, G.; Matsuda, Y.; Nakamura, Y.; Shibuya, A.; Iwama, A.; Nakauchi, H.
2017The current state of reproductive biology research in Australia and New Zealand: core themes from the Society for Reproductive Biology Annual Meeting, 2016Akison, L.; Andraweera, P.; Bertoldo, M.; Brown, H.; Cuffe, J.; Fullston, T.; Holland, O.; Schjenken, J.
2003Lysosomal storage disorders: emerging therapeutic options require early diagnosisMeikle, P.; Hopwood, J.
2012Alcohol consumption and pancreatic cancer: a pooled analysis in the International Pancreatic Cancer Case-Control Consortium (PanC4)Lucenteforte, E.; La Vecchia, C.; Silverman, D.; Petersen, G.; Bracci, P.; Ji, B.; Bosetti, C.; Li, D.; Gallinger, S.; Miller, A.; Bueno-de-Mesquita, H.; Talamini, R.; Polesel, J.; Ghadirian, P.; Baghurst, P.; Zatonski, W.; Fontham, E.; Bamlet, W.; Holly, E.; Gao, Y.; et al.
2012Prenatal exposure to selective serotonin reuptake inhibitors and risk of childhood overweightGrzeskowiak, L.; Gilbert, A.; Morrison, J.
2002A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutationShaw, M.; Chiurazzi, P.; Romain, D.; Neri, G.; Gecz, J.
1999Attitudes toward prophylactic oophorectomy and screening utilization in women at increased risk of developing hereditary breast/ovarian cancerMeiser, B.; Butow, P.; Barratt, A.; Friedlander, M.; Gattas, M.; Kirk, J.; Suthers, G.; Walpole, I.; Tucker, K.
1996Molecular Characterization of a Nonneuronal Human Unc18 HomologZiegler, S.; Mortrud, M.; Swartz, A.; Baker, E.; Sutherland, G.; Burmeister, M.; Mulligan, J.
2006Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resourceMann, G.; Thorne, H.; Balleine, R.; Butow, P.; Clarke, C.; Edkins, E.; Evans, G.; Fereday, S.; Haan, E.; Gattas, M.; Giles, G.; Goldblatt, J.; Hopper, J.; Kirk, J.; Leary, J.; Lindeman, G.; Niedermayr, E.; Phillips, K.; Picken, S.; Pupo, G.; et al.

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