Search


Current filters:


Start a new search
Add filters:

Use filters to refine the search results.


Results 11-20 of 30 (Search time: 0.007 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
1995The closely linked genes encoding the myeloid nuclear differentation antigen (MNDA) and IFI16 exhibit contrasting haemopoietic expressionDawson, M.; Trapani, J.; Briggs, R.; Nicholl, J.; Sutherland, G.; Baker, E.
1996The human glycine receptor β subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genesHandford, C.; Lynch, J.; Baker, E.; Webb, G.; Ford, J.; Sutherland, G.; Schofield, P.
1995Assignment of the human neuropeptide Y gene to chromosome 7p15.1 by nonisotopic in situ hybridizationBaker, E.; Hort, Y.; Ball, H.; Sutherland, G.; Shine, J.; Herzog, H.
1995Localisation of the adenosine A2b receptor subtype (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybridsTownsend-Nicholson, A.; Baker, E.; Sutherland, G.; Schofield, P.
1995Localisation of the adenosine A1 receptor subtype gene (ADORA1) to chromosome 1q32.1Townsend-Nicholson, A.; Baker, E.; Schofield, P.; Sutherland, G.
1995Gene duplication of the human peptide YY gene (PYY) generated the pancreatic polypeptide gene (PPY) on chromosome 17q21.1Hort, Y.; Baker, E.; Sutherland, G.; Shine, J.; Herzog, H.
1999Myeloid DAP12-associating lectin (MDL)-1 is a cell surface receptor involved in the activation of myeloid cellsBaker, E.; Sutherland, G.; Phillips, J.; Lanier, L.
1998Molecular characterization, pharmacological properties and chromosomal localization of the human GALR2 galanin receptorFathi, Z.; Battaglino, P.; Iben, L.; Li, H.; Baker, E.; Zhang, D.; McGovern, R.; Mahle, C.; Sutherland, G.; Iismaa, T.; Dickinson, K.; Antal Zimanyi, I.
1997Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeatYu, S.; Mangelsdorf, M.; Hewett, D.; Hobson, L.; Baker, E.; Eyre, H.; Lapsys, N.; Le Paslier, D.; Doggett, N.; Sutherland, G.; Richards, R.
1995Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndromeScott, H.; Blanch, L.; Guo, X.H.; Freeman, C.; Orsborn, A.; Baker, E.; Sutherland, G.; Morris, C.; Hopwood, J.