A genetic and physiological study of impaired glucose homeostasis control in C57BL/6J mice
TOYE, A. A, LIPPIAT, J. D, QUARTERMAN, J, FREEMAN, H. C, ASHCROFT, F. M, COX, R. D, PROKS, P, SHIMOMURA, K, BENTLEY, L, HUGILL, A, MIJAT, V, GOLDSWORTHY, M, MOIR, L, HAYNES, A
Published in Diabetologia (01.04.2005)
Published in Diabetologia (01.04.2005)
Get full text
Journal Article
Variable phenotypic spectrum of diabetes mellitus in a family carrying a novel KCNJ11 gene mutation
D'Amato, E., Tammaro, P., Craig, T. J., Tosi, A., Giorgetti, R., Lorini, R., Ashcroft, F. M.
Published in Diabetic medicine (01.06.2008)
Published in Diabetic medicine (01.06.2008)
Get full text
Journal Article
Kir6.2 mutation causing severe functional effects in vitro produces neonatal diabetes without the expected neurological complications
Tammaro, P, Flanagan, S. E, Zadek, B, Srinivasan, S, Woodhead, H, Hameed, S, Klimes, I, Hattersley, A. T, Ellard, S, Ashcroft, F. M
Published in Diabetologia (01.05.2008)
Published in Diabetologia (01.05.2008)
Get full text
Journal Article
The first clinical case of a mutation at residue K185 of Kir6.2 (KCNJ11): a major ATP‐binding residue
Shimomura, K., De Nanclares, G. P., Foutinou, C., Caimari, M., Castaño, L., Ashcroft, F. M.
Published in Diabetic medicine (01.02.2010)
Published in Diabetic medicine (01.02.2010)
Get full text
Journal Article
Correlating structure and function in ATP-sensitive K + channels
Ashcroft, Frances M., Gribble, Fiona M.
Published in Trends in neurosciences (Regular ed.) (01.07.1998)
Published in Trends in neurosciences (Regular ed.) (01.07.1998)
Get full text
Journal Article
Truncation of Kir6.2 produces ATP-sensitive K + channels in the absence of the sulphonylurea receptor
Tucker, Stephen J, Gribble, Fiona M, Zhao, Chao, Trapp, Stefan, Ashcroft, Frances M
Published in Nature (London) (08.05.1997)
Published in Nature (London) (08.05.1997)
Get full text
Journal Article
Exocytosis elicited by action potentials and voltage-clamp calcium currents in individual mouse pancreatic B-cells
Ammälä, C, Eliasson, L, Bokvist, K, Larsson, O, Ashcroft, F M, Rorsman, P
Published in The Journal of physiology (01.12.1993)
Published in The Journal of physiology (01.12.1993)
Get full text
Journal Article
A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland
OTONKOSKI, T, ÄMMÄLÄ, C, DUNNE, M. J, KERE, J, THOMAS, P. M, HUOPIO, H, COTE, G. J, CHAPMAN, J, COSGROVE, K, ASHFIELD, R, HUANG, E, KOMULAINEN, J, ASHCROFT, F. M
Published in Diabetes (New York, N.Y.) (01.02.1999)
Published in Diabetes (New York, N.Y.) (01.02.1999)
Get full text
Journal Article
Cloning and functional expression of the cDNA encoding a novel ATP-sensitive potassium channel subunit expressed in pancreatic β-cells, brain, heart and skeletal muscle
Sakura, H., Ämmälä, C., Smith, P.A., Gribble, F.M., Ashcroft, F.M.
Published in FEBS letters (27.12.1995)
Published in FEBS letters (27.12.1995)
Get full text
Journal Article
Gliclazide produces high-affinity block of KATP channels in mouse isolated pancreatic beta cells but not rat heart or arterial smooth muscle cells
LAWRENCE, C. L, PROKS, P, RODRIGO, G. C, JONES, P, HAYABUCHI, Y, STANDEN, N. B, ASHCROFT, F. M
Published in Diabetologia (01.08.2001)
Published in Diabetologia (01.08.2001)
Get full text
Journal Article
Permanent neonatal diabetes: combining sulfonylureas with insulin may be an effective treatment
Misra, S., Vedovato, N., Cliff, E., De Franco, E., Hattersley, A. T., Ashcroft, F. M., Oliver, N. S.
Published in Diabetic medicine (01.09.2018)
Published in Diabetic medicine (01.09.2018)
Get full text
Journal Article