Search


Current filters:


Start a new search
Add filters:

Use filters to refine the search results.


Results 21-30 of 86 (Search time: 0.002 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2013Renal tubular NEDD4-2 deficiency causes NCC-mediated salt-dependent hypertensionRonzaud, C.; Loffing-Cueni, D.; Hausel, P.; Debonneville, A.; Malsure, S.; Fowler-Jaeger, N.; Boase, N.; Perrier, R.; Maillard, M.; Yang, B.; Stokes, J.; Koesters, R.; Kumar, S.; Hummler, E.; Loffing, J.; Staub, O.
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.
2013A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndromeBuchovecky, C.; Turley, S.; Brown, H.; Kyle, S.; McDonald, J.; Liu, B.; Pieper, A.; Huang, W.; Katz, D.; Russell, D.; Shendure, J.; Justice, M.
2013An empirical approach towards the efficient and optimal production of influenza-neutralizing ovine polyclonal antibodies demonstrates that the novel adjuvant CoVaccine HT™ is functionally superior to Freund's adjuvantStevens, N.; Fraser, C.; Alsharifi, M.; Brown, M.; Diener, K.; Hayball, J.; Ferro, V.A.
2013A tudor domain protein SPINDLIN1 interacts with the mRNA-binding protein SERBP1 and is involved in mouse oocyte meiotic resumptionChew, T.; Peaston, A.; Lim, A.; Lorthongpanich, C.; Knowles, B.; Solter, D.; Sun, Q.-Y.
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.