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Preview	Issue Date	Title	Author(s)
	2007	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation	Tarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; et al.
	2007	Glycemic load and cardiovascular risk	Clifton, P.
	2007	Diverse signalling mechanisms used by relaxin in natural cells and tissues: the evolution of a "neohormone"	Ivell, R.; Heng, K.; Anand Ivell, R.
	2007	The effect of cutaneous input on intracortical inhibition in focal task-specific dystonia	McDonnell, M.; Thompson, P.; Ridding, M.
	2007	Retinotopic organization of small-field-target-detecting neurons in the insect visual system	Barnett, P.; Nordstrom, K.; O'Carroll, D.
	2007	Intracortical inhibition in the human trigeminal motor system	Jaberzadeh, S.; Pearce, S.; Miles, T.; Turker, K.; Nordstrom, M.
	2007	A pneumococcal MerR-like regulator and S-nitrosoglutathione reductase are required for systemic virulence	Stroeher, U.; Kidd, S.; Stafford, S.; Jennings, M.; Paton, J.; McEwan, A.
	2007	Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines	McRae, A.; Matigian, N.; Vadlamudi, L.; Mulley, J.; Mowry, B.; Martin, N.; Berkovic, S.; Hayward, N.; Visscher, P.
	2007	Temporal lobe epilepsy and GEFS(+) phenotypes associated with SCN1B mutations	Scheffer, I.; Harkin, L.; Grinton, B.; Dibbens, L.; Turner, S.; Zielinski, M.; Xu, R.; Jackson, G.; Adams, J.; Connellan, M.; Petrou, S.; Wellard, R.; Briellmann, R.; Wallace, R.; Mulley, J.; Berkovic, S.
	2007	Buccal micronucleus cytome biomarkers may be associated with Alzheimer's disease	Thomas, P.; Hecker, J.; Faunt, J.; Fenech, M.