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Preview	Issue Date	Title	Author(s)
	1996	Further characterization of proteins associated with elastic fiber microfibrils including the molecular cloning of MAGP-2 (MP25)	Gibson, M.; Hatzinikolas, G.; Kumaratilake, J.; Sandberg, L.; Nicholl, J.; Sutherland, G.; Cleary, E.
	1999	Highly sensitive sequencing of the sulfated domains of heparan sulfate	Merry, C.; Lyon, M.; Deakin, J.; Hopwood, J.; Gallagher, J.
	1998	Molecular characterization, pharmacological properties and chromosomal localization of the human GALR2 galanin receptor	Fathi, Z.; Battaglino, P.; Iben, L.; Li, H.; Baker, E.; Zhang, D.; McGovern, R.; Mahle, C.; Sutherland, G.; Iismaa, T.; Dickinson, K.; Antal Zimanyi, I.
	1996	DNAM-1, a novel adhesion molecule involved in the cytolytic function of T lymphocytes	Shibuya, A.; Campbell, D.; Hannum, C.; Yssel, H.; Franz-Bacon, K.; McClanahan, T.; Kitamura, T.; Nicholl, J.; Sutherland, G.; Lanier, L.; Phillips, J.
	1996	Type X collagen is colocalized with a proteoglycan epitope to form distinct morphological structures in bovine growth cartilage	Gibson, G.; Lin, D.; Francki, F.; Caterson, B.; Foster, B.
	1997	The gene for the human interleukin-11 receptor alpha chain locus is highly homologous to the murine gene and contains alternatively spliced first exons	Nandurkar, H.; Robb, L.; Nicholl, J.; Hilton, D.; Sutherland, G.; Begley, C.
	1998	Complex organisation of the 5'-end of the human glycine tRNA synthetase gene	Mudge, S.; Williams, J.; Eyre, H.; Sutherland, G.; Cowan, P.; Power, D.
	2004	Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation	Weaving, L.; Christodoulou, J.; Williamson, S.; Friend, K.; McKenzie, O.; Archer, H.; Evans, J.; Clarke, A.; Pelka, G.; Tam, P.; Watson, C.; Lahooti, H.; Ellaway, C.; Bennetts, B.; Leonard, H.; Gecz, J.
	2001	A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda	Tiller, G.; Hannig, V.; Dozier, D.; Carrel, L.; Trevarthen, K.; Wilcox, W.; Mundlos, S.; Haines, J.; Gedeon, A.; Gecz, J.
	1997	The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies	D'Adamo, P.; Fassone, L.; Gedeon, A.; Janssen, E.; Bione, S.; Bolhuis, P.; Barth, P.; Wilson, M.; Haan, E.; Orstavik, H.; Patton, M.; Green, A.; Zammarchi, E.; Donati, M.; Toniolo, D.