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The Common Single Nucleotide Polymorphism E23K in KIR6. 2 Sensitizes Pancreatic β- …


C Schwanstecher, B Neugebauer, M Schulz, … - Diabetes, 2002 - Am Diabetes Assoc
E23K, a common polymorphism in the pore-forming subunit K IR 6.2 of pancreatic
β-cell ATP-sensitive K + (K ATP ) channels, is functionally relevant and thus
might play a major role in the pathophysiology of common type 2 diabetes. ...
Cited by 32 - Related articles - BL Direct - All 3 versions

Kir6. 2 Polymorphisms Sensitize β-Cell ATP-Sensitive Potassium Channels to Activation by …

- hivinfosource.org [PDF] 
MJ Riedel, P Boora, D Steckley, G de Vries, … - Diabetes, 2003 - Am Diabetes Assoc
The commonly occurring E23K and I337V Kir6.2 polymorphisms in the ATP-sensitive
potassium (K ATP ) channel are more frequent in Caucasian type 2 diabetic
populations. However, the underlying cellular mechanisms contributing to ...
Cited by 51 - Related articles - BL Direct - All 25 versions

Nucleotide sensitivity of pancreatic ATP-sensitive potassium channels and type 2 diabetes


C Schwanstecher, M Schwanstecher - Diabetes, 2002 - Am Diabetes Assoc
Type 2 diabetes is generally perceived as a polygenic disorder, with disease
development being influenced by both hereditary and environmental factors.
However, despite intensive investigations, little progress has been made in ...
Cited by 39 - Related articles - BL Direct - All 3 versions

The prevalent Glu23Lys polymorphism in the potassium inward rectifier 6.2 (KIR6. 2) gene …


O Tschritter, M Stumvoll, F Machicao, M … - Diabetes, 2002 - Am Diabetes Assoc
Genetic factors play an important role in the pathogenesis of type 2 diabetes.
The relevance to type 2 diabetes of the common polymorphism Glu23Lys in the
potassium inward rectifier 6.2 (KIR6.2) gene is still controversial. The ...
Cited by 44 - Related articles - BL Direct - All 5 versions

Variations in insulin secretion in carriers of the E23K variant in the KIR6. 2 subunit of the ATP …

- diabetesjournals.org
LM t Hart, TW van Haeften, JM Dekker, M Bot … - Diabetes, 2002 - Am Diabetes Assoc
An association between type 2 diabetes and genetic variation in the KIR6.2 gene
has been reported in several populations. Based on in vitro studies with cell
lines expressing the Glu 23 Lys (E23K) mutation, it was recently suggested ...
Cited by 19 - Related articles - BL Direct - All 6 versions

KIR6. 2 polymorphism predisposes to type 2 diabetes by inducing overactivity of pancreatic …

- diabetesjournals.org
C Schwanstecher, U Meyer, M … - Diabetes, 2002 - Am Diabetes Assoc
E23K, a common single nucleotide polymorphism in K IR 6.2, the pore-forming
subunit of pancreatic β-cell ATP-sensitive K + channels, significantly enhanced
open probability of these channels, thus reducing their sensitivity toward ...
Cited by 124 - Related articles - BL Direct - All 18 versions

Sequence variations in the human Kir6. 2 gene, a subunit of the beta-cell ATP-sensitive K- …


H Sakura, N Wat, V Horton, H Millns, RC … - Diabetologia, 1996 - Springer
Summary The ATP-sensitive K-channel plays a cen- tral role in insulin release
from pancreatic beta cells. This channel consists of two subunits: a sulphonyl-
urea receptor, SUR1, and an inwardly rectifying K- channel subunit, Kir6.2. ...
Cited by 71 - Related articles - BL Direct - All 3 versions

An E23K single nucleotide polymorphism in the islet ATP-sensitive potassium channel gene ( …


L Love-Gregory, J Wasson, J Lin, G Skolnick, … - Diabetologia, 2003 - Springer
2. Wren A, Seal L, Cohen M et al. (2001) Ghrelin enhances appetite and increases
food intake in humans. J Clin Endo- crinol Metab 86: 5992–5995 3. Tschop M,
Weyer C, Tataranni P, Devanarayan V, Ravussin E, Heiman M (2001) ...
Cited by 70 - Related articles - BL Direct - All 3 versions

Activating mutations in the KCNJ11 gene encoding the ATP-sensitive K+ channel subunit Kir6. …

- diabetesjournals.org
EL Edghill, AL Gloyn, KM Gillespie, AP … - Diabetes, 2004 - Am Diabetes Assoc
We have recently shown that permanent neonatal diabetes can be caused by
activating mutations in KCNJ11 that encode the Kir6.2 subunit of the ß-cell
ATP-sensitive K + channel. Some of these patients were diagnosed after 3 ...
Cited by 25 - Related articles - BL Direct - All 4 versions

Permanent Neonatal Diabetes due to Paternal Germline Mosaicism for an Activating …

- endojournals.org
AL Gloyn, EA Cummings, EL Edghill, LW Harries … - Journal of Clinical Endocrinology & Metabolism, 2004 - Endocrine Soc
Activating mutations in the KCNJ11 gene encoding for the Kir6.2 subunit of the
ß-cell ATP-sensitive potassium channel have recently been shown to be a common
cause of permanent neonatal diabetes. In 80% of probands, these are ...
Cited by 42 - Related articles - BL Direct - All 7 versions


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