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Preview	Issue Date	Title	Author(s)
	2006	Novel DNA binding by a basic helix-loop-helix protein - The role of the dioxin receptor PAS domain	Chapman-Smith, A.; Whitelaw, M.
	1996	Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow	Fairbairn, L.; Lashford, L.; Spooncer, E.; McDermott, R.; Lebens, G.; Arrand, J.; Arrand, J.; Bellantuono, I.; Holt, R.; Hatton, C.; Cooper, A.; Besley, G.; Wraith, J.; Anson, D.; Hopwood, J.; Dexter, T.
	2001	An orphaned mammalian b-globin gene of ancient evolutionary origin	Wheeler, D.; Hope, R.; Cooper, S.; Dolman, G.; Webb, G.; Bottema, C.; Gooley, A.; Goodman, M.; Holland, R.
	2005	Ancient DNA from the first European farmers in 7500-year-old Neolithic sites	Haak, W.; Forster, P.; Bramanti, B.; Matsumura, S.; Brandt, G.; Tanzer, M.; Villems, R.; Renfrew, C.; Gronenborn, D.; Alt, K.; Burger, J.
	1999	Isolation and characterisation of a cDNA encoding a Zona Pellucida Protein (ZPB) from the marsupial Trichosurus vulpecula (Brushtail Possum)	Haines, B.; Rathjen, P.; Hope, R.; Whyatt, L.; Holland, M.; Breed, W.
	2015	Sequencing and analysis of globally obtained human respiratory syncytial virus A and B genomes	Bose, M.; He, J.; Shrivastava, S.; Nelson, M.; Bera, J.; Halpin, R.; Town, C.; Lorenzi, H.; Noyola, D.; Falcone, V.; Gerna, G.; De Beenhouwer, H.; Videla, C.; Kok, T.; Venter, M.; Williams, J.; Henrickson, K.; Varga, S.M.
	2004	Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV	Ward, T.; Valberg, S.; Adelson, D.; Abbey, C.; Binns, M.; Mickelson, J.
	2012	The Basque paradigm: genetic evidence of a maternal continuity in the Franco-Cantabrian region since pre-neolithic times	Behar, D.; Haak, W.; Adler, C.; Cooper, A.; Dersarkissian, C.
	2004	Absence of Yersinia pestis-specific DNA in human teeth from five European excavations of putative plague victims	Gilbert, T.; Cuccui, J.; White, W.; Lynnerup, N.; Titball, R.; Cooper, A.; Prentice, M.
	2010	Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes	Carmichael, C.; Wilkins, E.; Bengtsson, H.; Horwitz, M.; Speed, T.; Vincent, P.; Young, G.; Hahn, C.; Escher, J.; Scott, H.