Showing 1 - 20 results of 30 for search 'Shimomura, K', query time: 0.31s
Refine Results
-
1
Xenopus oocytes as a heterologous expression system for studying ion channels with the patch-clamp technique. by Tammaro, P, Shimomura, K, Proks, P
Published 2008Journal article -
2
Nicotinamide nucleotide transhydrogenase: a link between insulin secretion, glucose metabolism and oxidative stress. by Freeman, H, Shimomura, K, Cox, R, Ashcroft, F
Published 2006Journal article -
3
A mutation in KCNJ11 causing human hyperinsulinism (Y12X) results in a glucose-intolerant phenotype in the mouse. by Hugill, A, Shimomura, K, Ashcroft, F, Cox, R
Published 2010Journal article -
4
Mechanism of action of a sulphonylurea receptor SUR1 mutation (F132L) that causes DEND syndrome. by Proks, P, Shimomura, K, Craig, T, Girard, C, Ashcroft, F
Published 2007Journal article -
5
Permanent neonatal diabetes caused by an in-frame deletion in the N-terminus of Kir6.2 by Craig, T, Shimomura, K, Flanagan, S, Ellard, S, Hattersley, A, Ashcroft, F
Published 2008Journal article -
6
Nicotinamide nucleotide transhydrogenase: a key role in insulin secretion. by Freeman, H, Shimomura, K, Horner, E, Cox, R, Ashcroft, F
Published 2006Journal article -
7
An in-frame deletion in Kir6.2 (KCNJ11) causing neonatal diabetes reveals a site of interaction between Kir6.2 and SUR1. by Craig, T, Shimomura, K, Holl, R, Flanagan, SE, Ellard, S, Ashcroft, F
Published 2009Journal article -
8
The first clinical case of a mutation at residue K185 of Kir6.2 (KCNJ11): a major ATP-binding residue. by Shimomura, K, de Nanclares, G, Foutinou, C, Caimari, M, Castaño, L, Ashcroft, F
Published 2010Journal article -
9
-
10
-
11
Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes. by Girard, C, Shimomura, K, Proks, P, Absalom, N, Castano, L, Perez de Nanclares, G, Ashcroft, F
Published 2006Journal article -
12
Essential role of NAADP-evoked calcium release in glucose-mediated depolarization, [Ca2+]i spiking and insulin secretion in mouse pancreatic beta cell by Arredouani, A, Parkesh, R, Pillinger, T, Coltart, G, Clough, F, Shimomura, K, Aschcroft, F, Churchill, G, Galione, A
Published 2009Conference item -
13
A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brain. by Shimomura, K, Horster, F, De Wet, H, Flanagan, SE, Ellard, S, Hattersley, A, Wolf, N, Ashcroft, F, Ebinger, F
Published 2007Journal article -
14
3-D structural and functional characterization of the purified KATP channel complex Kir6.2-SUR1. by Mikhailov, M, Campbell, J, De Wet, H, Shimomura, K, Zadek, B, Collins, R, Sansom, MS, Ford, R, Ashcroft, F
Published 2005Journal article -
15
-
16
-
17
-
18
Role of the transcription factor sox4 in insulin secretion and impaired glucose tolerance. by Goldsworthy, M, Hugill, A, Freeman, H, Horner, E, Shimomura, K, Bogani, D, Pieles, G, Mijat, V, Arkell, R, Bhattacharya, S, Ashcroft, F, Cox, R
Published 2008Journal article -
19
PVHL is a regulator of glucose metabolism and insulin secretion in pancreatic beta cells. by Zehetner, J, Danzer, C, Collins, S, Eckhardt, K, Gerber, P, Ballschmieter, P, Galvanovskis, J, Shimomura, K, Ashcroft, F, Thorens, B, Rorsman, P, Krek, W
Published 2008Journal article -
20
Muon spin spectroscopy by Hillier, AD, Blundell, SJ, McKenzie, I, Umegaki, I, Shu, L, Wright, JA, Prokscha, T, Bert, F, Shimomura, K, Berlie, A, Alberto, H, Watanabe, I
Published 2022Journal article