Dr Pam Thompson 

2011

• Malcolm Taylor, Tracy L. Bergemann, Adiba Hussain, Pamela D. Thompson, Logan Spector. (2011). Transmission of HLA-DP variants from parents to children with B-cell precursor. Human Immunology, eScholarID:125740 | DOI:10.1016/j.humimm.2011.05.011

2010

• Thompson PD, Tipney H, Brass A, Noyes H, Kemp S, Naessens J, Tassabehji M. (2010). Claudin 13, a member of the claudin family regulated in mouse stress induced erythropoiesis. Plos One, 5(9), eScholarID:90776
• Thompson PD, Wade R, Richards S, Gibson B, Hann I, Eden T, Taylor, M. (2010). No association of HLA-A supertype with outcome in childhood acute lymphoblastic leukaemia: results of the UKALL XI trial. British Journal of Haematology, eScholarID:95605

2009

• Taylor M, Hussain A, Urayama K, Chokkalingam A, Thompson PD, Trachtenberg E, Buffler P. (2009). The human major histocompatibility complex and childhood leukemia: an etiological hypothesis based on molecular mimicry. Blood Cells Mol Dis, 42( 2), 129-35. eScholarID:1d32412 | DOI:10.1016/j.bcmd.2008.10.009
• Taylor, GM, Hussain, A, Verhage, V, Thompson, PD, Fergusson, W, Watkins, G, Lightfoot, T, Harrison, C, Birch, JM, NULL. (2009). Strong association of the HLA-DP6 supertype with childhood leukaemia is due to a single allele, DPB1*0601. Leukemia, 23( 5), 863-9. eScholarID:1d32364 | DOI:10.1038/leu.2008.374

2007

• Thompson PD, Webb M, Beckett W, Hinsley T, Jowitt T, Sharrocks A, Tassabehji M. (2007). GTF2IRD1 regulates transcription by binding an evolutionarily conserved DNA motif 'GUCE'. FEBS Lett, 581( 6), 1233-42. eScholarID:1d15607 | DOI:10.1016/j.febslet.2007.02.040

2005

• Tassabehji, M, Hammond, Peter, Karmiloff-Smith, Annette, Thompson, PD, Thorgiersson, Snorri S., Durkin, Marian E., Popescu, Nicholas C., Hutton, Timothy, Metcalfe, K, Rucka, A, Stewart, Helen, Read, AP, Maconochie, Mark, Donnai, D. (2005). GTF2IRD1 in craniofacial development of humans and mice. Science, 310 (5751), 1184-1187. eScholarID:1d26815 | DOI:10.1126/science.1116142

2004

• HinsleyTA, Thompson PD, Tipney HJ, Brass AA, Tassabehji M. (2004). Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome. Protein Sci, 13(10), eScholarID:1d9694

2001

• Cunliffe, P., Reed, V. and Boyd, Y. (2001). Intragenic Deletions at Atp7a in Mouse Models for Menkes Disease. Genomics, 74, 155-162. eScholarID:90856
• Ohanian, J., Cunliffe, P., Ceppi, E., Alder, A., Heerkens, E. and Ohanian, V. (2001). Activation of p38 Mitogen-Activated Protein Kinases by Endothelin and Noradrenaline in Small Arteries, Regulation by Calcium Influx and Tyrosine Kinases, and Their Role in Contraction. Arterioscler Thromb Vasc Biol, 21, 1921-1927. eScholarID:90859

2000

• Boyd, Y., Blair, H. J., Cunliffe, P., Masson, W. K. and Reed, V. (2000). A Phenotype Map of the Mouse X Chromosome: Models for Human X-linked Disease. Genome Research, 10, 277-292. eScholarID:90858

1998

• Boyd, Y., Blair, H. J., Cunliffe, P., Denny, P., Gormally, E. and Heathcote, G. E. (1998). Mouse Chromosome X. Mammalian Genome, 8, S361-S377. eScholarID:90857