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FEMS Microbiology Letters|November 1, 1993
Synthesis of the K5 (group II) capsular polysaccharide in transport-deficient recombinant Escherichia coliD Bronner, V Sieberth, C Pazzani, et al.Journal of Immunology (Baltimore, Md. : 1950)|November 8, 2001
NKG2D receptors induced by IL-15 costimulate CD28-negative effector CTL in the tissue microenvironmentA I Roberts, L Lee, E Schwarz, et al.European Journal of Immunology|March 31, 2000
Human intestinal lamina propria and intraepithelial lymphocytes express receptors specific for chemokines induced by inflammationW W Agace, A I Roberts, L Wu, et al.British Journal of Haematology|May 1, 1996
Idiopathic myelofibrosis in childrenM Sekhar, H G Prentice, U Popat, et al.The Cochrane Database of Systematic Reviews|April 20, 2007
Methods to increase response rates to postal questionnairesP Edwards, I Roberts, M Clarke, et al.Cancer Genetics and Cytogenetics|March 25, 2000
Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridizationS M Gribble, I Roberts, C Grace, et al.Child: Care, Health and Development|April 26, 2006
Out-of-home day care for families living in a disadvantaged area of London: economic evaluation alongside a RCTR Mujica Mota, P K Lorgelly, M Mugford, et al.Blood|July 27, 2001
Simultaneous fetal cell identification and diagnosis by epsilon-globin chain immunophenotyping and chromosomal fluorescence in situ hybridizationM Choolani, H O'Donnell, C Campagnoli, et al.Health Technology Assessment (Winchester, England)|August 10, 2004
The Social Support and Family Health Study: a randomised controlled trial and economic evaluation of two alternative forms of postnatal support for mothers living in disadvantaged inner-city areasM Wiggins, A Oakley, I Roberts, et al.British Journal of Haematology|June 1, 1996
Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutationsI Dokal, A Chase, N V Morgan, et al.Pageof 42