1. Adelaide Research & Scholarship

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Results 1-10 of 27 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
2017ProBDNF Accelerates Brain Amyloid-β Deposition and Learning and Memory Impairment in APPswePS1dE9 Transgenic MiceChen, J.; Zhang, T.; Jiao, S.; Zhou, X.; Zhong, J.; Wang, Y.; Liu, J.; Deng, J.; Wang, S.; Xu, Z.
2017An immunogenic phenotype in paternal antigen-specific CD8⁺ T cells at embryo implantation elicits later fetal loss in miceMoldenhauer, L.; Diener, K.; Hayball, J.; Robertson, S.
2012TGF-β mediates proinflammatory seminal fluid signaling in human cervical epithelial cellsSharkey, D.; Macpherson, A.; Tremellen, K.; Mottershead, D.; Gilchrist, R.; Robertson, S.
2012Myb-binding protein 1A (MYBBP1A) is essential for early embryonic development, controls cell cycle and mitosis, and acts as a tumor suppressorMori, S.; Bernardi, R.; Laurent, A.; Resnati, M.; Crippa, A.; Gabrieli, A.; Keough, R.; Gonda, T.; Blasi, F.; Plow, E.
2019Calmodulin-dependent signalling pathways are activated and mediate the acute inflammatory response of injured skeletal muscleHu, J.; Shi, D.; Ding, M.; Huang, T.; Gu, R.; Xiao, J.; Xian, C.J.; Dong, J.; Wang, L.; Liao, H.
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.
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.
2015HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.Jolly, L.; Nguyen, L.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.

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