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Results 11-20 of 45 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(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.
2013Conjunctivitis associated with Chlamydia pecorum in three koalas (Phascolarctos cinereus) in the mount lofty ranges, South AustraliaFunnell, O.; Johnson, L.; Woolford, L.; Boardman, W.; Polkinghorne, A.; McLelland, D.
2013Prokineticin 1 induces a pro-inflammatory response in murine fetal membranes but does not induce preterm deliveryLannagan, T.; Wilson, M.; Denison, F.; Norman, J.; Catalano, R.; Jabbour, H.
2013On the morphology and taxonomy of Griphobilharzia amoena Platt and Blair, 1991 (Schistosomatoidea), a dioecious digenetic trematode parasite of the freshwater crocodile, Crocodylus johnstoni, in AustraliaPlatt, T.; Hoberg, E.; Chisholm, L.
2013Improving metabolic health in obese male mice via diet and exercise restores embryo development and fetal growthMc Pherson, N.; Bakos, H.; Owens, J.; Setchell, B.; Lane, M.; Aguila, M.B.
2013TLR 2 and 4 responsiveness from isolated peripheral blood mononuclear cells from rats and humans as potential chronic pain biomarkersKwok, Y.; Tuke, S.; Nicotra, L.; Grace, P.; Rolan, P.; Hutchinson, M.; Price, T.J.
2013Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horseBellone, R.; Holl, H.; Sealuri, V.; Devi, S.; Maddodi, N.; Archer, S.; Sandmeyer, L.; Ludwig, A.; Foerster, D.; Pruvost, M.; Reissmann, M.; Bortfeldt, R.; Adelson, D.; Lim, S.; Nelson, J.; Haase, B.; Engensteiner, M.; Leeb, T.; Forsyth, G.; Mienaltowski, M.; et al.; Anderson, M.G.
2013Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndromeAoki, Y.; Niihori, T.; Banjo, T.; Okamoto, N.; Mizuno, S.; Kurosawa, K.; Ogata, T.; Takada, F.; Yano, M.; Ando, T.; Hoshika, T.; Barnett, C.; Ohashi, H.; Kawame, H.; Hasegawa, T.; Okutani, T.; Nagashima, T.; Hasegawa, S.; Funayama, R.; Nagashima, T.; et al.
2013SGTA: A new player in the molecular co-chaperone gamePhilp, L.; Butler, M.; Hickey, T.; Butler, L.; Tilley, W.; Day, T.

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