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Results 1-10 of 38 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2009Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune PhenotypeHubert, F.; Kinkel, S.; Crewther, P.; Cannon, P.; Webster, K.; Link, M.; Uibo, R.; O'Bryan, M.; Meager, A.; Forehan, S.; Smyth, G.; Mittaz, L.; Antonarakis, S.; Peterson, P.; Heath, W.; Scott, H.
2013Linaclotide inhibits colonic nociceptors and relieves abdominal pain via guanylate cyclase-c and extracellular cyclic guanosine 3′,5′-monophosphateCastro, J.; Harrington, A.; Hughes, P.; Martin, C.; Ge, P.; Shea, C.; Jin, H.; Jacobson, S.; Hannig, G.; Mann, E.; Cohen, M.; MacDougall, J.; Lavins, B.; Kurtz, C.; Silos-Santiago, I.; Johnston, J.; Blackshaw, L.; Brierley, S.
2017Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signallingHughes, J.; Dawson, R.; Tea, M.; McAninch, D.; Piltz, S.; Jackson, D.; Stewart, L.; Ricos, M.; Dibbens, L.; Harvey, N.; Thomas, P.
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.
2003Induction of tolerance to a recombinant human enzyme, acid alpha-glucosidase, in enzyme deficient knockout miceRaben, N.; Nagaraju, K.; Lee, A.; Lu, N.; Rivera, Y.; Jatkar, T.; Hopwood, J.; Plotz, P.
2020Phenotypic characterization and comparison of Phe508del and cystic fibrosis transmembrane conductance regulator (CFTR) knockout rat models of cystic fibrosis generated by CRISPR/Cas9 gene editingMcCarron, A.; Cmielewski, P.; Reyne, N.; McIntyre, C.; Finnie, J.; Craig, F.; Rout-Pitt, N.; Delhove, J.; Schjenken, J.E.; Chan, H.Y.; Boog, B.; Knight, E.; Gilmore, R.C.; O'Neal, W.K.; Boucher, R.C.; Parsons, D.; Donnelley, M.
2019Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in femalesJackson, M.R.; Loring, K.E.; Homan, C.C.; Thai, H.N.; Määttänen, L.; Arvio, M.; Jarvela, I.; Shaw, M.; Gardner, A.; Gecz, J.; Shoubridge, C.
2018Aldosterone deficiency in mice burdens respiration and accentuates diet-induced hyperinsulinemia and obesityLiao, W.-H.; Suendermann, C.; Steuer, A.; Lopez, G.; Odermatt, A.; Henneberg, M.; Faresse, N.; Langhans, W.
2006Dipeptidyl peptidases and inflammatory bowel diseaseAbbott, C.; Yazbek, R.; Geier, M.; Demuth, H.; Howarth, G.; Lendeckel, U.; Reinhold, D.; Bank, U.
2018The osteoprogenitor-specific loss of ephrinB1 results in an osteoporotic phenotype affecting the balance between bone formation and resorptionArthur, A.; Nguyen, T.; Paton, S.; Klisuric, A.; Zannettino, A.; Gronthos, S.

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