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Julie Webb

Science Communication Consultant

Bibliography

Recent Work

SolexaTM Genome Analysis System. DNA sequencing application note. Provided text and figure framework.

At the heart of the matter: Matin Wiles. SCRIPS May 2006. (Webb JC, ghost writer).

Safe Delivery: written by Tom McGrath, assisted with script, story, and character development.

Web Publications

Genes Talking Website - www.genestalking.co.uk

Scientific Papers

Webb JC, Golovleva I, Simpkins AH, Kempski H, Reeves B, Sturt N, Chessells JM, Brickell PM. Loss of heterozygosity and microsatellite instability at the MLL locus are common in childhood acute leukemia, but not in infant acute leukemia. Blood. 1999 Jul 1;94(1):283-90.

Kempski H, Chalker J, Chessells J, Sturt N, Brickell P, Webb J, Clink JM, Reeves B. An investigation of the t(12;21) rearrangement in children with B-precursor acute lymphoblastic leukaemia using cytogenetic and molecular methods. Br J Haematol. 1999 Jun;105(3):684-9.

Webb JC, Patel DD, Shoulders CC, Knight BL, Soutar AK. Genetic variation at a splicing branch point in intron 9 of the low density lipoprotein (LDL)-receptor gene: a rare mutation that disrupts mRNA splicing in a patient with familial hypercholesterolaemia and a common polymorphism. Hum Mol Genet. 1996 Sep;5(9):1325-31.

Webb JC, Sun XM, McCarthy SN, Neuwirth C, Thompson GR, Knight BL, Soutar AK. Characterization of mutations in the low density lipoprotein (LDL)-receptor gene in patients with homozygous familial hypercholesterolemia, and frequency of these mutations in FH patients in the United Kingdom. J Lipid Res. 1996 Feb;37(2):368-81.

Shovlin CL, Simmonds HA, Fairbanks LD, Deacock SJ, Hughes JM, Lechler RI, Webster AD, Sun XM, Webb JC, Soutar AK. Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency. J Immunol. 1994 Sep 1;153(5):2331-9.

Morgan K, Wharton J, Webb JC, Keogh BE, Smith PL, Taylor KM, Oakley CM, Polak JM, Cleland JG. Co-expression of renin-angiotensin system component genes in human atrial tissue.J Hypertens Suppl. 1994 Jul;12(4):S11-9.

Webb JC, Patel DD, Jones MD, Knight BL, Soutar AK. Characterization and tissue-specific expression of the human 'very low density lipoprotein (VLDL) receptor' mRNA. Hum Mol Genet. 1994 Apr;3(4):531-7.

Sun XM, Patel DD, Webb JC, Knight BL, Fan LM, Cai HJ, Soutar AK. Familial hypercholesterolemia in China. Identification of mutations in the LDL-receptor gene that result in a receptor-negative phenotype. Arterioscler Thromb. 1994 Jan;14(1):85-94

Feher MD, Webb JC, Patel DD, Lant AF, Mayne PD, Knight BL, Soutar AK. Cholesterol-lowering drug therapy in a patient with receptor-negative homozygous familial hypercholesterolaemia. Atherosclerosis. 1993 Nov;103(2):171-80.

Sun XM, Webb JC, Gudnason V, Humphries S, Seed M, Thompson GR, Knight BL, Soutar AK. Characterization of deletions in the LDL receptor gene in patients with familial hypercholesterolemia in the United Kingdom. Arterioscler Thromb. 1992 Jul;12(7):762-70.

Webb JC, Sun XM, Patel DD, McCarthy SN, Knight BL, Soutar AK. Characterization of two new point mutations in the low density lipoprotein receptor genes of an English patient with homozygous familial hypercholesterolemia. J Lipid Res. 1992 May;33(5):689-98.