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Results 1-10 of 136 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2004Rise and fall of the Beringian steppe bisonShapiro, B.; Drummond, A.; Rambaut, A.; Wilson, M.; Matheus, P.; Sher, A.; Pybus, O.; Gilbert, M.; Barnes, I.; Binladen, J.; Willerslev, E.; Hansen, A.; Baryshnikov, G.; Burns, J.; Davydov, S.; Driver, J.; Froese, D.; Harington, C.; Keddie, G.; Kosintsev, P.; et al.
2016CXCR5⁺ follicular cytotoxic T cells control viral infection in B cell folliclesLeong, Y.; Chen, Y.; Ong, H.; Wu, D.; Man, K.; Deleage, C.; Minnich, M.; Meckiff, B.; Wei, Y.; Hou, Z.; Zotos, D.; Fenix, K.; Atnerkar, A.; Preston, S.; Chipman, J.; Beilman, G.; Allison, C.; Sun, L.; Wang, P.; Xu, J.; et al.
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.
1995An integrated physical map of human chromosome 16Doggett, N.; Goodwin, L.; Tesmer, J.; Meincke, L.; Bruce, D.; Clark, L.; Altherr, M.; Ford, A.; Chi, H.C.; Marrone, B.; Longmire, J.; Lane, S.; Whitmore, S.; Lowenstein, N.; Sutherland, G.; Mundt, M.; Knill, E.; Bruno, W.; Macken, C.; Torney, D.; et al.
2004Proceedings of the Oxygen Homeostasis/Hypoxia MeetingKaufman, B.; Scharf, O.; Arbeit, J.; Ashcroft, M.; Brown, J.; Bruick, R.; Chapman, J.; Evans, S.; Giaccia, A.; Harris, A.; Huang, E.; Johnson, R.; Kaelin Jr., W.; Koch, C.; Maxwell, P.; Mitchell, J.; Neckers, L.; Powis, G.; Rajendran, J.; Semenza, G.; et al.
2016TBC1D24 genotype-phenotype correlationBalestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; et al.
2022Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial diseaseLee, R.G.; Balasubramaniam, S.; Stentenbach, M.; Kralj, T.; McCubbin, T.; Padman, B.; Smith, J.; Riley, L.G.; Priyadarshi, A.; Peng, L.; Nuske, M.R.; Webster, R.; Peacock, K.; Roberts, P.; Stark, Z.; Lemire, G.; Ito, Y.A.; Boycott, K.M.; Geraghty, M.T.; Van Klinken, J.B.; et al.
2020Repurposing a neurodegenerative disease drug to treat Gram-negative antibiotic-resistant bacterial sepsisDe Oliveira, D.M.P.; Bohlmann, L.; Conroy, T.; Jen, F.E.-C.; Everest-Dass, A.; Hansford, K.A.; Bolisetti, R.; El-Deeb, I.M.; Forde, B.M.; Phan, M.-D.; Lacey, J.A.; Tan, A.; Rivera-Hernandez, T.; Brouwer, S.; Keller, N.; Kidd, T.J.; Cork, A.J.; Bauer, M.J.; Cook, G.M.; Davies, M.R.; et al.
2017NAD deficiency, congenital malformations, and niacin supplementationShi, H.; Enriquez, A.; Rapadas, M.; Martin, E.; Wang, R.; Moreau, J.; Lim, C.; Szot, J.; Ip, E.; Hughes, J.; Sugimoto, K.; Humphreys, D.; McInerney-Leo, A.; Leo, P.; Maghzal, G.; Halliday, J.; Smith, J.; Colley, A.; Mark, P.; Collins, F.; et al.
2017Dominant protection from HLA-linked autoimmunity by antigen-specific regulatory T cellsOoi, J.; Petersen, J.; Tan, Y.; Huynh, M.; Willett, Z.; Ramarathinam, S.; Eggenhuizen, P.; Loh, K.; Watson, K.; Gan, P.; Alikhan, M.; Dudek, N.; Handel, A.; Hudson, B.; Fugger, L.; Power, D.; Holt, S.; Coates, P.; Gregersen, J.; Purcell, A.; et al.

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