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Gloyn, AL
Hashim, Y
Ashcroft, SJH
Ashfield, R
Wiltshire, S
Turner, RC
Citation: Al. Gloyn et al., Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53), DIABET MED, 18(3), 2001, pp. 206-212
Authors:
Gribble, FM
Reimann, F
Ashfield, R
Ashcroft, FM
Citation: Fm. Gribble et al., Nucleotide modulation of pinacidil stimulation of the cloned K-ATP channelKir6.2/SUR2A, MOLEC PHARM, 57(6), 2000, pp. 1256-1261
Authors:
Huopio, H
Reimann, F
Ashfield, R
Komulainen, J
Lenko, HL
Rahier, J
Vauhkonen, I
Kere, J
Laakso, M
Ashcroft, F
Otonkoski, T
Citation: H. Huopio et al., Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1, J CLIN INV, 106(7), 2000, pp. 897-906
Authors:
Southam, L
Ashfield, R
Cox, R
Lathrop, M
Ashcroft, SJH
Citation: L. Southam et al., Human islets of Langerhans express the delta(c) isoform of calcium/calmodulin-dependent protein kinase II, DIABET M R, 15(4), 1999, pp. 243-246
Authors:
Ashfield, R
Gribble, FM
Ashcroft, SJH
Ashcroft, FM
Citation: R. Ashfield et al., Identification of the high-affinity tolbutamide site on the SUR1 subunit of the K-ATP channel, DIABETES, 48(6), 1999, pp. 1341-1347
Authors:
Otonkoski, T
Ammala, C
Huopio, H
Cote, GJ
Chapman, J
Cosgrove, K
Ashfield, R
Huang, E
Komulainen, J
Ashcroft, FM
Dunne, MJ
Kere, J
Thomas, PM
Citation: T. Otonkoski et al., A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland, DIABETES, 48(2), 1999, pp. 408-415