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Results 11-20 of 45 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2013AqF026 is a pharmacologic agonist of the water channel aquaporin-1Yool, A.; Morelle, J.; Cnops, Y.; Verbavatz, J.; Campbell, E.; Spencer, E.; Booker, G.; Flynn, G.; Devuyst, O.
2013Mechanotransduction pathways promoting tumor progression are activated in invasive human squamous cell carcinomaIbbetson, S.; Pyne, N.; Pollard, A.; Olson, M.; Samuel, M.
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.
2013Yunis-Varón Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphataseCampeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B.
2013The Guinea Pig as a model for sporadic Alzheimer's Disease (AD): the impact of cholesterol intake on expression of AD-related genesSharman, M.; Moussavi Nik, S.; Chen, M.; Ong, D.; Wijaya, L.; Laws, S.; Taddei, K.; Newman, M.; Lardelli, M.; Martins, R.; Verdile, G.; Götz, J.
2013Targeting amino acid transport in metastatic castration-resistant prostate cancer: Effects on cell cycle, cell growth, and tumor developmentWang, Q.; Tiffen, J.; Bailey, C.; Lehman, M.; Ritchie, W.; Fazli, L.; Metierre, C.; Feng, Y.; Li, E.; Gleave, M.; Buchanan, G.; Nelson, C.; Rasko, J.; Holst, J.
2013Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene regionChidlow, G.; Wood, J.; Sharma, S.; Dimasi, D.; Burdon, K.; Casson, R.; Craig, J.; Mittal, B.
2013Essential developmental, genomic stability, and tumour suppressor functions of the mouse orthologue of hSSB1/NABP2Shi, W.; Bain, A.; Schwer, B.; Al-ejeh, F.; Smith, C.; Wong, L.; Chai, H.; Miranda, M.; Ho, U.; Kawaguchi, M.; Miura, Y.; Finnie, J.; Wall, M.; Heierhorst, J.; Wicking, C.; Spring, K.; Alt, F.; Khanna, K.; McKinnon, P.
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.

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