1. Adelaide Research & Scholarship

Search


Current filters:



Start a new search
Add filters:

Use filters to refine the search results.

 | 
Results 1-10 of 38 (Search time: 0.003 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2012TGF-β mediates proinflammatory seminal fluid signaling in human cervical epithelial cellsSharkey, D.; Macpherson, A.; Tremellen, K.; Mottershead, D.; Gilchrist, R.; Robertson, S.
2017Targeted insertion of an anti-CD2 monoclonal antibody transgene into the GGTA1 locus in pigs using FokI-dCas9Nottle, M.; Salvaris, E.; Fisicaro, N.; McIlfatrick, S.; Vassiliev, I.; Hawthorne, W.; O'Connell, P.; Brady, J.; Lew, A.; Cowan, P.
2014Modifications of human growth differentiation factor 9 to improve the generation of embryos from low competence oocytesLi, J.; Sugimura, S.; Mueller, T.; White, M.; Martin, G.; Ritter, L.; Liang, X.; Gilchrist, R.; Mottershead, D.
2016Prenatal fish oil supplementation and allergy: 6-year follow-up of a randomized controlled trialBest, K.P.; Sullivan, T.; Palmer, D.; Gold, M.; Kennedy, D.J.; Martin, J.; Makrides, M.
2011Heterologous prime-boost-boost immunisation of Chinese cynomolgus macaques using DNA and recombinant poxvirus vectors expressing HIV-1 virus-like particlesBridge, S.; Sharpe, S.; Dennis, M.; Dowall, S.; Getty, B.; Anson, D.; Skinner, M.; Stewart, J.; Blanchard, T.
2015shRNA off-target effects in vivo: impaired endogenous siRNA expression and spermatogenic defectsSong, H.; Bettegowda, A.; Oliver, D.; Yan, W.; Phan, M.; De Rooij, D.; Corbett, M.; Wilkinson, M.; White-Cooper, H.
2013Macrophages regulate corpus luteum development during embryo implantation in miceCare, A.; Diener, K.; Jasper, M.; Brown, H.; Ingman, W.; Robertson, S.
2013ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J.
2012A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityHuang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.
2016X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesHu, H.; Haas, S.; Chelly, J.; Van Esch, H.; Raynaud, M.; De Brouwer, A.; Weinert, S.; Froyen, G.; Frints, S.; Laumonnier, F.; Zemojtel, T.; Love, M.; Richard, H.; Emde, A.; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; et al.

Discover