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Results 11-20 of 30 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
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.
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.
2013Sensory neuro-immune interactions differ between Irritable Bowel Syndrome subtypesHughes, P.; Harrington, A.; Castro Kraftchenko, J.; Liebregts, T.; Adam, B.; Grasby, D.; Isaacs, N.; Maldeniya, M.; Martin, C.; Persson, J.; Andrews, J.; Holtmann, G.; Blackshaw, L.; Brierley, S.
2013Circadian variation in gastric vagal afferent mechanosensitivityKentish, S.; Frisby, C.L.; Kennaway, D.; Wittert, G.; Page, A.
2013A transcription factor contributes to pathogenesis and virulence in streptococcus pneumoniaeMahdi, L.; Ebrahimie, E.; Adelson, D.; Paton, J.; Ogunniyi, A.; Skurnik, M.
2013The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowthJolly, L.; Homan, C.; Jacob, R.; Barry, S.; Gecz, J.
2013Lack of high-dose radiation mediated prostate cancer promotion and low-dose radiation adaptive response in the TRAMP mouse modelLawrence, M.; Ormsby, R.; Blyth, B.; Bezak, E.; England, G.; Newman, M.; Tilley, W.; Sykes, P.
2013Tropomyosin regulates cell migration during skin wound healingLees, J.; Ching, Y.; Adams, D.; Bach, C.; Samuel, M.; Kee, A.; Hardeman, E.; Gunning, P.; Cowin, A.; O'Neill, G.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.