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Single Nucleotide Polymorphisms in KATP Channels

- diabetesjournals.org
L Li, Y Shi, X Wang, W Shi, C Jiang - Diabetes, 2005 - Am Diabetes Assoc
ATP-sensitive K + channels (K ATP channels) play an important role in glucose
homeostasis. A single nucleotide polymorphism (SNP) in the Kir6.2 subunit causes a point mutation
of Glu23 to lysine and reduces the ATP sensitivity of pancreatic K ATP channels. The SNP ...
Cited by 14 - Related articles - All 5 versions

Quantitative traits associated with the Type 2 diabetes susceptibility allele in Kir6. 2


MN Weedon, AL Gloyn, G Davey Smith, Y Ben-Shlomo, … - Diabetologia, 2003 - Springer
To the editor: K ATP channels are key to insulin secretion by the beta cell; they couple metabolism
to plasma membrane depol- arisation and, hence, insulin release. K ATP channels consist of
two sub-units: Kir6.2 and SUR1, encoded by the genes KCNJ11 and ABCC8, ...
Cited by 10 - Related articles - BL Direct - All 3 versions

[CITATION] S Umit S, Molnes J, Molven A, Sovik O, Matschinsky F: Permanent neonatal …


PR Njolstad, JV Sagen, L Bjorkhaug, S Odili, N … - Diabetes, 2003
Cited by 3 - Related articles

[CITATION] A calpain 一 10 gene polymorphism is associated with reduced muscle inlTla …


LJ BALER, Y PERMANAPA… - The Journal of clinical Investigation, 2000
Cited by 2 - Related articles

[PDF] 2 型糖尿病遗传病因学研究的现状和展望


纪立农 - 中国医学科学院学报, 2006 - actacams.com
ABSTRACT:Type 2 diabetes is the main type of diabetes in diabetic population. Alongwith the
rapid changes of life style and increased life expectancy,the prevalence of type 2 diabetes increases
rapidly world5 wide. However,strong evidences have shown that genetic factors play ...
Cited by 5 - Related articles - View as HTML - All 4 versions

K ATP channel polymorphism is associated with left ventricular size in hypertensive …

- nih.gov
S Reyes, A Terzic, DW Mahoney, MM Redfield, RJ … - Human genetics, 2008 - Springer
Abstract ATP-sensitive K+ (KATP) channel mutations have been identified in individuals with
dilated cardiomy- opathy and overt heart failure. Here, a common E23K func- tional polymorphism
in the Kir6.2 channel pore versus cardiac phenotype was studied in a cross-sectional ...
Cited by 5 - Related articles - All 5 versions

中国人 CAPN10 基因单核苷酸多态性的分布及其在北方汉族 2 型糖尿病人群中的 …


孙红霞, 张奎星 - 中国医学科学院学报, 2002 - cqvip.com
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维普资讯 中文期刊·专业文章. 维普专业检索Google学术. 临床医学 >> 中国医学科学院学报 >>
2002年24卷3期 >> 摘要. 中国人CAPN10基因单核苷酸多态性的分布及其在北方汉族 ...
Cited by 6 - Related articles - All 3 versions

Polymorphisms of KCNJ11 (Kir6. 2 gene) are associated with Type 2 diabetes and …


BK Koo, YM Cho, BL Park, HS Cheong, HD … - Diabetic …, 2007 - interscience.wiley.com
It is also possible that your web browser is not configured or not able to display style sheets.
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functional. We recommend using the latest version of Microsoft or Mozilla web browser to ...
Cited by 6 - Related articles - BL Direct - All 6 versions

[CITATION] Early epileptic encephalopathy and neonatal diabetes, associated with mutation in …


N Nahi-Buisson, C Bellanne-Chantelot, M Eisermann, … - Am J Hum Genet Suppl, 2004
Cited by 6 - Related articles

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

- diabetesjournals.org
LM t Hart, TW van Haeften, JM Dekker, M Bot, RJ Heine … - 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 that this mutation might result in altered insulin ...
Cited by 19 - Related articles - BL Direct - All 6 versions


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