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Results 1-10 of 44 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3Mitchison, H.; Munroe, P.; O'Rawe, A.; Taschner, P.; De Vos, N.; Kremmidiotis, G.; Lensink, I.; Munk, A.; D'Arigo, K.; Anderson, J.; Lerner, T.; Moyzis, R.; Callen, D.; Breuning, M.; Doggett, N.; Gardiner, R.; Mole, S.
1998Expression and activity of prostoglandin endoperoxide synthase-2 in inflammatory human neutrophilsPouliot, M.; Gilbert, C.; Borgeat, P.; Poubelle, P.; Bourgoin, S.; McColl, S.; Naccache, P.
1996Identification of G-protein binding sites of the human interleukin-8 receptors by functional mapping of the intracellular loopsDamaj, B.; McColl, S.; Neote, K.; Songqing, N.; Ogborn, K.; Hebert, C.; Naccache, P.
1998Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24Phillips, H.; Scheffer, I.; Crossland, K.; Bhatia, K.; Fish, D.; Marsden, C.; Howell, S.; Stephenson, J.; Tolmie, J.; Plazzi, G.; Eeg-Olofsson, O.; Singh, R.; Lopes-Cendes, I.; Andermann, E.; Berkovic, S.; Mulley, J.
1995Comparative toxicity and virulence of Escherichia coli clones expressing variant and chimeric Shiga-like toxin type II operonsPaton, A.; Bourne, A.; Manning, P.; Paton, J.
1998Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3Centola, M.; Chen, X.; Sood, R.; Deng, Z.; Aksentijevich, I.; Blake, T.; Ricke, D.; Chen, X.; Wood, G.; Zaks, N.; Richards, N.; Krizman, D.; Mansfield, E.; Apostolou, S.; Liu, J.; Shafran, N.; Vedula, A.; Hamon, M.; Cercek, A.; Kahan, T.; et al.
1995Primitive human haemopoietic progenitors adhere to P-selectin (CD62P)Zannettino, A.; Berndt, M.; Nuitta, S.; Butcher, C.; Vadas, M.; Simmons, P.
1998Molecular analysis of shiga toxigenic Escherichia coli O111:H proteins which react with sera from patients with hemolytic-uremic syndrome.Voss, E.; Paton, A.; Manning, P.; Paton, J.
1998Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1BWallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
1999Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardaGedeon, A.; Colley, A.; Jamieson, R.; Thompson, E.; Rogers, J.; Sillence, D.; Tiller, G.; Mulley, J.; Gecz, J.