- ►endojournals.org SK Hansen, EMD Nielsen, J Ek, G Andersen, C … - Journal of Clinical Endocrinology & Metabolism, 2005 - Endocrine Soc The separate and combined effects of the PPARG Pro 12 Ala polymorphism and the
KCNJ11 Glu 23 Lys polymorphisms on risk of type 2 diabetes were investigated in
relatively large-scale, case-control studies. Separate effects of the ... Cited by 25 - Related articles - All 5 versions
- ►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
H Ikegami, T Fujisawa, T Ogihara - ILAR JOURNAL., 2004 - dels.nas.edu Except for rare subtypes of diabetes, both type 1 and type 2 diabetes are
multifactorial diseases in which genetic factors consisting of multiple
susceptibility genes and environmen- tal factors contribute to the disease ... Cited by 14 - Related articles - View as HTML - BL Direct - All 2 versions
G Hamilton, P Proitsi, L Jehu, A Morgan, J … - AMERICAN JOURNAL OF MEDICAL GENETICS. PART …, 2007 - 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 12 - Related articles - BL Direct - All 3 versions
- ►endojournals.org [PDF] S Noso, H Ikegami, T Fujisawa, Y Kawabata, K … - Journal of Clinical Endocrinology & Metabolism, 2007 - Endocrine Soc Page 1. - 1 - Full title: Association of small ubiquitin-like modifier 4
(SUMO4) variant, located in IDDM5 locus, with type 2 diabetes ... Cited by 12 - Related articles - BL Direct - All 4 versions
EH Leiter, CH Lee - Diabetes, 2005 - Am Diabetes Assoc In humans, both type 1 and type 2 diabetes exemplify genetically heterogeneous
complex diseases in which epigenetic factors contribute to underlying genetic
susceptibility. Extended human pedigrees often show inheritance of both ... Cited by 10 - Related articles - BL Direct - All 6 versions
A Johansen, DP Jensen, R Bergholdt, HB … - Diabetes, Obesity and Metabolism, 2006 - interscience.wiley.com Aims: Type 1 diabetes mellitus (T1DM) is a chronic disorder primarily triggered
by environmental and immunological factors in genetically susceptible
individuals. Despite the fact that there are indications of common ... Cited by 9 - Related articles - All 2 versions
- ►eje-online.org LB Nielsen, KB Ploug, P Swift, C Orskov, I … - European Journal of Endocrinology, 2007 - EFES Objective: The ATP-dependent K + -channel (K ATP ) is critical for glucose
sensing and normal glucagon and insulin secretion from pancreatic endocrine -
and ß-cells. Gastrointestinal endocrine L- and K-cells are also ... Cited by 8 - Related articles - BL Direct - All 6 versions
A Jorsal, L Tarnow, M Lajer, J Ek, T Hansen, … - Molecular genetics and metabolism, 2008 - Elsevier The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor-γ2
gene is suggested to associate with diabetic nephropathy and cardiovascular
disease in type 2 diabetes. The aim of this study was to investigate the ... Cited by 6 - Related articles - All 3 versions
- ►nih.gov SM Raj, JMM Howson, NM Walker, JD Cooper, … - Diabetologia, 2009 - Springer Abstract Aims/hypothesis We used recently confirmed type 2 diabe- tes gene
regions to investigate the genetic relationship between type 1 and type 2
diabetes, in an average of 7,606 type 1 diabetic individuals and 8,218 ... Cited by 1 - Related articles - All 4 versions
