- ►diabetesjournals.org JC Florez, KA Jablonski, SE Kahn, PW … - Diabetes, 2007 - Am Diabetes Assoc The common polymorphisms KCNJ11 E23K and ABCC8 A1369S have been consistently
associated with type 2 diabetes. We examined whether these variants are also
associated with progression from impaired glucose tolerance (IGT) to ... Cited by 32 - Related articles - BL Direct - All 4 versions
JCFKA Jablonski, SE Kahn, PWFD Dabelea, … - 糖尿病学杂志, 2007 - journal.shouxi.net 【摘要】 The common polymorphisms KCNJ11 E23K and ABCC8 A1369S have been
consistently associated with type 2 diabetes. We examined whether these variants
are also associated with progression from impaired glucose tolerance (IGT) ... Related articles - Cached
- ►endojournals.org G Sesti, E Laratta, M Cardellini, F Andreozzi, … - Journal of Clinical Endocrinology & Metabolism, 2006 - Endocrine Soc Context: Several studies suggest that genetic factors may play a role in the
different responses to antidiabetic therapy; however, conclusive evidence is
still lacking. ... Objective: The objective of the study was to ... Cited by 26 - Related articles - BL Direct - All 3 versions
- ►endojournals.org JC Florez, KA Jablonski, MW Sun, N Bayley, … - Journal of Clinical Endocrinology & Metabolism, 2007 - Endocrine Soc Context: The common P12A polymorphism in PPARG (a target for thiazolidinedione
medications) has been consistently associated with type 2 diabetes. ...
Objective: We examined whether PPARG P12A affects progression from impaired ... Cited by 41 - Related articles - BL Direct - All 7 versions
- ►tokushima-u.ac.jp [PDF] Y Sakamoto, H Inoue, P Keshavarz, K … - Journal of Human Genetics, 2007 - Springer Abstract Many genetic association studies support a contribution of genetic
variants in the KCNJ11-ABCC8 gene locus to type 2 diabetes (T2D) susceptibility
in Caucasians. In non-Caucasian populations, however, there have been only ... Cited by 10 - Related articles - BL Direct - All 4 versions
RM Van Dam, B Hoebee, JC Seidell, MM … - Diabet Med, 2005 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 41 - Related articles - All 4 versions
- ►endojournals.org O Laukkanen, J Pihlajamaki, J Lindstrom, J … - Journal of Clinical Endocrinology & Metabolism, 2004 - Endocrine Soc Type 2 diabetes is caused by defective insulin secretion and impaired insulin
action. We investigated whether common polymorphisms in the SUR1 and Kir6.2
genes are associated with increased risk of type 2 diabetes in 490 subjects ... Cited by 34 - Related articles - All 5 versions
T Hansen, L Ambye, N Grarup, L Hansen, SM … - Diabetologia, 2001 - Springer II diabetes have been identified [1±3]. Furthermore, genetic variation in the
gene encoding calpain-10 is associated with late-onset Type II diabetes among
Mexican-Americans [4] and altered glucose metabo- lism among Pima Indians ... Cited by 19 - Related articles - BL Direct - All 4 versions
- ►oxfordjournals.org J Zhao, DH Xiong, Y Guo, TL Yang, RR … - Human Reproduction, 2007 - ESHRE BACKGROUND: The insulin-like growth factor 1 (IGF1) gene, which plays a crucial
role in hypothalamic–pituitary–ovarian hormone-controlled metabolic
processes, may influence the onset of menarche. Our study aimed to test ... Cited by 10 - Related articles - BL Direct - All 7 versions
- ►diabetesjournals.org JC Florez, N Burtt, PIW de Bakker, P Almgren, … - Diabetes, 2004 - Am Diabetes Assoc The genes for the sulfonylurea receptor (SUR1; encoded by ABCC8) and its
associated islet ATP-sensitive potassium channel (Kir6.2; encoded by KCNJ11) are
adjacent to one another on human chromosome 11. Multiple studies have ... Cited by 147 - Related articles - BL Direct - All 7 versions
