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Results 861-870 of 870 (Search time: 0.007 seconds).
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PreviewIssue DateTitleAuthor(s)
2022Core outcome set for clinical studies of postoperative ileus after intestinal surgeryChapman, S.J.; Lee, M.J.; Blackwell, S.; Arnott, R.; ten Broek, R.P.G.; Delaney, C.P.; Dudi-Venkata, N.N.; Fish, R.; Hind, D.; Jayne, D.G.; Mellor, K.; Mishra, A.; O’Grady, G.; Sammour, T.; Thorpe, G.; Wells, C.I.; Wolthuis, A.M.; Fearnhead, N.S.; Adegbola, S.; Bagaglini, G.; et al.
2023Recommendations for culturally safe clinical kidney care for First Nations Australians: a guideline summaryTunnicliffe, D.J.; Bateman, S.; Arnold-Chamney, M.; Dwyer, K.M.; Howell, M.; Gebadi, A.; Jesudason, S.; Kelly, J.; Lambert, K.; Majoni, S.W.; Oliva, D.; Owen, K.J.; Pearson, O.; Rix, E.; Roberts, I.; Taylor, K.; Wittert, G.A.; Widders, K.; Yip, A.; Craig, J.; et al.
2024The potential of epigenetic therapy to target the 3D epigenome in endocrine-resistant breast cancerAchinger-Kawecka, J.; Stirzaker, C.; Portman, N.; Campbell, E.; Chia, K.-M.; Du, Q.; Laven-Law, G.; Nair, S.S.; Yong, A.; Wilkinson, A.; Clifton, S.; Milioli, H.H.; Alexandrou, S.; Caldon, C.E.; Song, J.; Khoury, A.; Meyer, B.; Chen, W.; Pidsley, R.; Qu, W.; et al.
2020HNF4A and GATA6 loss reveals therapeutically actionable subtypes in pancreatic cancerBrunton, H.; Caligiuri, G.; Cunningham, R.; Upstill-Goddard, R.; Bailey, U.M.; Garner, I.M.; Nourse, C.; Dreyer, S.; Jones, M.; Moran-Jones, K.; Wright, D.W.; Paulus-Hock, V.; Nixon, C.; Thomson, G.; Jamieson, N.B.; McGregor, G.A.; Evers, L.; McKay, C.J.; Gulati, A.; Brough, R.; et al.
2013Somatic point mutation calling in low cellularity tumorsKassahn, K.; Holmes, O.; Nones, K.; Patch, A.; Miller, D.; Christ, A.; Harliwong, I.; Bruxner, T.; Xu, Q.; Anderson, M.; Wood, S.; Leonard, C.; Taylor, D.; Newell, F.; Song, S.; Idrisoglu, S.; Nourse, C.; Nourbakhsh, E.; Manning, S.; Wani, S.; et al.; Jordan, I.
2022Potent Stimulation of the Androgen Receptor Instigates a Viral Mimicry Response in Prostate CancerAlizadeh-Ghodsi, M.; Owen, K.L.; Townley, S.L.; Zanker, D.; Rollin, S.P.G.; Hanson, A.R.; Shrestha, R.; Toubia, J.; Gargett, T.; Chernukhin, I.; Luu, J.; Cowley, K.J.; Clark, A.; Carroll, J.S.; Simpson, K.J.; Winter, J.M.; Lawrence, M.G.; Butler, L.M.; Risbridger, G.P.; Thierry, B.; et al.
2020Mutations disrupting neuritogenesis genes confer risk for cerebral palsyJin, S.C.; Lewis, S.A.; Bakhtiari, S.; Zeng, X.; Sierant, M.C.; Shetty, S.; Nordlie, S.M.; Elie, A.; Corbett, M.A.; Norton, B.Y.; van Eyk, C.L.; Haider, S.; Guida, B.S.; Magee, H.; Liu, J.; Pastore, S.; Vincent, J.B.; Brunstrom-Hernandez, J.; Papavasileiou, A.; Fahey, M.C.; et al.
2023Transient naive reprogramming corrects hiPS cells functionally and epigeneticallyBuckberry, S.; Liu, X.; Poppe, D.; Tan, J.P.; Sun, G.; Chen, J.; Nguyen, T.V.; de Mendoza, A.; Pflueger, J.; Frazer, T.; Vargas-Landín, D.B.; Paynter, J.M.; Smits, N.; Liu, N.; Ouyang, J.F.; Rossello, F.J.; Chy, H.S.; Rackham, O.J.L.; Laslett, A.L.; Breen, J.; et al.
2008Interferon autoantibodies associated with AIRE deficiency decrease the expression of IFN-stimulated genesKisand, K.; Link, M.; Wolff, A.; Meager, A.; Tserel, L.; Org, T.; Murumagi, A.; Uibo, R.; Willcox, N.; Podkrajek, K.; Battelino, T.; Lobell, A.; Kampe, O.; Lima, K.; Meloni, A.; Ergun-Longmire, B.; Maclaren, N.; Perheentupa, J.; Krohn, K.; Scott, H.; et al.
2011Progesterone receptor gene variants and risk of endometrial cancerO'Mara, T.; Fahey, P.; Ferguson, K.; Marquart, L.; Lambrechts, D.; Despierre, E.; Vergote, I.; Amant, F.; Hall, P.; Liu, J.; Czene, K.; SASBAC,; Rebbeck, T.; WISE Study Group,; AOCS Management Group,; SEARCH,; Ahmed, S.; Dunning, A.; Gregory, C.; Shah, M.; et al.

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