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Preview	Issue Date	Title	Author(s)
	2007	Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly	Field, M.; Tarpey, P.; Smith, R.; Edkins, S.; O'Meara, S.; Stevens, C.; Tofts, C.; Teague, J.; Butler, A.; Dicks, E.; Barthorpe, S.; Buck, G.; Cole, J.; Gray, K.; Halliday, K.; Hills, K.; Jenkinson, A.; Jones, D.; Menzies, A.; Mironenko, T.; et al.
	2007	The pneumococcal two-component signal transduction system RR/HK06 regulates CbpA and PspA by two distinct mechanisms	Standish, A.; Stroeher, U.; Paton, J.
	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	Cro’s role in the CI–Cro bistable switch is critical for λ’s transition from lysogeny to lytic development	Schubert, R.; Dodd, I.; Egan, J.; Shearwin, K.
	2007	A review of genome mutation and Alzheimer's disease	Thomas, P.; Fenech, M.
	2007	eneralized epilepsy with febrile seizures plus-associated sodium channel β1 subunit mutations severely reduce beta subunit-mediated modulation of sodium channel function	Xu, R.; Thomas, E.; Gazina, E.; Richards, K.; Quick, M.; Wallace, R.; Harkin, L.; Heron, S.; Berkovic, S.; Scheffer, I.; Mulley, J.; Petrou, S.
	2007	Know thy fly	O'Keefe, L.; Smibert, P.; Colella, A.; Chataway, T.; Saint, R.; Richards, R.
	2007	Conserved Glu40 and Glu433 of the biotin carboxylase domain of yeast pyruvate carboxylase I isoenzyme are essential for the association of tetramers	Jitrapakdee, S.; Surinya, K.; Adina-Zada, A.; Polyak, S.; Stojkoski, C.; Smyth, R.; Booker, G.; Cleland, W.; Attwood, P.; Wallace, J.
	2007	A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channel	Xu, R.; Thomas, E.; Jenkins, M.; Gazina, E.; Chiu, C.; Heron, S.; Mulley, J.; Scheffer, I.; Berkovic, S.; Petrou, S.
	2007	Protein and gene expression analysis of Phf6, the gene mutated in the Borjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity	Voss, A.; Gamble, R.; Collin, C.; Shoubridge, C.; Corbett, M.; Gecz, J.; Thomas, T.