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Issue DateTitleAuthor(s)Citation
2004Genetic Testing In Familial Isolated Hyperparathyroidism: Unexpected Results And Their ImplicationsLearoyd, Diana; Robinson, Bruce; Birdsey, P.; Burgess, J.; Epstein, M.; et, al; Hill, P.; Perry-Keene, D.; Singh, D.; Stranks, S.; Sweet, A.; Warner, J.; Northern Clinical School: Medicine; Northern Clinical School: MedicineGenetic Testing In Familial Isolated Hyperparathyroidism: Unexpected Results And Their Implications, Journal of Medical Genetics, vol.41,(3),2004,pp 155-160
2005Measurement of masses and branching ratios of Xi(+)(c) and Xi(0)(c) baryonsBakich, Andrew; Cole, Shoshanna; Parslow, Nicholas; Peak, Lawrence; Varvell, Kevin; Abe, K; Adachi, I; Aihara, H; Asano, Y; Bahinipati, S; Bay, A; Bitenc, U; Bizjak, I.; et, al; Lesiak,; Physics; Physics; Science Faculty Admin; Physics; PhysicsMeasurement of masses and branching ratios of Xi(+)(c) and Xi(0)(c) baryons, Physics Letters B, vol.605,(3-4),2005,pp 237-246
2004A Randomized Trial Of Exemestane After Two To Three Years Of Tamoxifen Therapy In Postmenopausal Women With Primary Breast Cancer.Coates, Alan; Alvarez, Isabel; Bertelli, Gianfilippo; Coombes, R Charles; Delozier, Thierry; et, al; Gibson, Lorna J; Hall, Emma; Jassem, Jacek; Jones, Stephen E; Ortmann, Olaf; Paridaens, Robert; School of Public Health: Public HealthA Randomized Trial Of Exemestane After Two To Three Years Of Tamoxifen Therapy In Postmenopausal Women With Primary Breast Cancer., New England Journal of Medicine, vol.350,(11),2004,pp 1081-1092
2006Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease.Roscioli, Tony; Bell, Christopher G; Bloch, Donald B; Cliffe, Simon T; Donald, Jennifer; et, al; Kirk, Edwin P; Mullan, Glen; Sarris, Maria; Taylor, Peter; Wang, Joanne; Central Clinical School: MedicineMutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease., Nature Genetics, vol.38,(6),2006,pp 620-622
2007Modelling the hepatitis C virus epidemic in AustraliaGeorge, Jacob; Weltman, Martin; Bell, Jane; Cooper-Stanbury, Mark; Dolan, Kate; Dore, Gregory J.; et, al; Kaldore, John; Karvelas, Maria; Li, Jiong; Maher, Lisa; Razali, Karina; Thein, Hla Hla; Western Clinical School: Westmead Millennium Institute; Nepean Clinical School: MedicineModelling the hepatitis C virus epidemic in Australia, Drug and Alcohol Dependence, vol.91,(39509),2007,pp 228-235
2007Long-term control of bone turnover in Paget's disease with zoledronic acid and risedronateHooper, Michael; Brown, Jacques P; Curiel, Manuel Diaz; Devogelaer, Jean-Pierre; et, al; Fraser, William D; Hosking, David; Lyles, Kenneth; Miller, Paul; Su, Guoqin; Zelenakas, Ken; Concord Clinical School: MedicineLong-term control of bone turnover in Paget's disease with zoledronic acid and risedronate, JOURNAL OF BONE AND MINERAL RESEARCH 2005, vol.22,(1),2007,pp 142-148
2004Novel Types Of Mutation Responsible For The Dermatosparactic Type Of Ehlers-Danlos Syndrome (Type Viic) And Common Polymorphisms In The Adamts2 Gene.Ades, Lesley; Colige, Alain; De Paepe, Anne; et, al; Franck, Peter; Hausser, Ingrid; Herens, Christian; Malfait, Fransiska; Nuytinck, Lieve; Thiry, Marc; van Essen, Anthonie J.; Children's Hospital Westmead: Paediatrics & Child HealthNovel Types Of Mutation Responsible For The Dermatosparactic Type Of Ehlers-Danlos Syndrome (Type Viic) And Common Polymorphisms In The Adamts2 Gene., THE JOURNAL OF INVESTIGATIVE DERMATOLOGY 2005, vol.123,(4),2004,pp 656-663
2015Measuring a Cherenkov ring in the radio emission from air showers at 110-190 MHz with LOFARBell, Martin; Buitink, S.; Corstanje, A.; de Vries, Krijn; Enriquez, J; et, al; Falcke, Heino D.; Frieswijk, W.; Horandel, J.R.; Nelles, A.; Schellart, P.; Scholten, Olaf; PhysicsMeasuring a Cherenkov ring in the radio emission from air showers at 110-190 MHz with LOFAR, Astroparticle Physics, vol.65, N/A, 2015,pp 11-21
2012The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvementNicholson, Garth; Ahsan, Budrul; Date, Hidetoshi; et, al; Goto, Jun; Ishiura, Hiroyuki; Kawarai, Toshitaka; Mitsui, Jun; Sako, Wataru; Takahashi, Yuji; Tanabe, Osamu; Yoshida, Mari; Concord Clinical School: ANZAC Research InstituteThe TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement, American Journal of Human Genetics, vol.91, 2, 2012,pp 320-329
2007Secretion of Apolipoprotein E From Macrophages Occurs via a Protein Kinase A and Calcium-Dependent Pathway Along the Microtubule NetworkKritharides, Leonard; Sabaretnam, Tharani; et, al; Gaus, Katharina; Guo, Dongni Lily; Hill, Michael; Huby, Thierry; Jary, Eve; Kay, Jason; Kockx, Maaike; Lesnik, Philippe; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineSecretion of Apolipoprotein E From Macrophages Occurs via a Protein Kinase A and Calcium-Dependent Pathway Along the Microtubule Network, Circulation Research, vol.101,(6),2007,pp 607-616