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Results 11-20 of 103 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
1998Translocated intimin receptors (Tir) of Shiga-toxigenic Escherichia coli isolates belonging to serogroups O26, O111, and O157 react with sera from patients with hemolytic-uremic syndrome and exhibit marked sequence heterogeneity.Paton, A.; Manning, P.; Woodrow, M.; Paton, J.; Barbieri, J.T.
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.
1999Molecular recognition in a post-translational modification of exceptional specificityChapman-Smith, A.; Morris, T.; Wallace, J.; Cronan Jr, J.
1999Expression of 25(OH)D3 24-hydroxylase in distal nephron: coordinate regulation by 1,25 (OH)2D3 and cAMP or PTHYang, W.; Friedmen, P.; Sharma, R.; Omdahl, J.; May, B.; Siu-Caldera, M.; Reddy, G.; Christakos, S.
1999Analysis of the 5' portion of the type 19A capsule locus identifies two classes of cpsC, cpsD, and cpsE genes in Streptococcus pneumoniaeMorona, J.; Morona, R.; Paton, J.
1999Comparative genetics of capsular polysaccharide biosynthesis in Streptococcus pneumoniae types beloning to serogroup 19Morona, J.; Morona, R.; 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.