- ►endojournals.org SM Clee, AD Attie - Endocrine reviews, 2007 - Endocrine Soc Inbred mouse strains provide genetic diversity comparable to that of the human population. Like
humans, mice have a wide range of diabetes-related phenotypes. The inbred mouse strains
differ in the response of their critical physiological functions, such as insulin sensitivity, ... Cited by 29 - Related articles - BL Direct - All 4 versions
- ►gemstudy.ca [PDF] Y Yu, DF Wyszynski, DM Waterworth, SD Wilton, … - Science's …, 2005 - stke.sciencemag.org Abstract: We conducted a genome-wide scan using variance components linkage analysis to
localize quantitative-trait loci (QTLs) influencing triglyceride (TG), high density lipoprotein-cholesterol
(HDL-C), low density lipoprotein-cholesterol, and total cholesterol (TC) levels in 3,071 ... Cited by 23 - Related articles - BL Direct - All 7 versions
SH Kim, X Ma, S Weremowicz, T Ercolino, C Powers, W … - Diabetes, 2004 - Am Diabetes Assoc Maturity-onset diabetes of the young (MODY) is a subtype of diabetes defined by an autosomal
dominant inheritance and a young onset. Six MODY genes have been discovered to date. To
identify additional MODY loci, we conducted a genome scan in 21 extended US families ... Cited by 19 - Related articles - BL Direct - All 5 versions
- ►tokushima-u.ac.jp [PDF] H Kato, K Nomura, D Osabe, S Shinohara, O Mizumori, … - Genomics, 2006 - Elsevier Several previous linkage scans in type 2 diabetes (T2D) families indicated a putative susceptibility
locus on chromosome 12q15–q22, while the underlying gene for T2D has not yet been
identified. We performed a region-wide association analysis on 12q15–q22, using a ... Cited by 19 - Related articles - All 5 versions
- ►jgenetgenomics.org [PDF] QY HUANG, MR CHENG, SL JI - Acta Genetica Sinica, 2006 - Elsevier Type 2 diabetes mellitus (T2DM) is a complex disease characterized by hyperglycemia, insulin
resistance, and impaired insulin secretion. T2DM is under strong genetic control. Identification
and characterization of genes involved in determining T2DM will contribute to a greater ... Cited by 10 - Related articles - All 3 versions
JC Engert, M Lemire, J Faith, D Brisson, TM … - European Journal of …, 2007 - nature.com Susceptibility to coronary heart disease (CHD) has long been known to exhibit familial
aggregation, with heritability estimated to be greater than 50%. The French Canadian population
of the Saguenay-Lac Saint-Jean region of Quebec, Canada is descended from a founder ... Cited by 10 - Related articles - BL Direct - All 4 versions
- ►tokushima-u.ac.jp [PDF] M Moritani, K Nomura, T Tanahashi, D Osabe, Y Fujita, … - Diabetologia, 2007 - Springer Page 1. ARTICLE Genetic association of single nucleotide polymorphisms in endonuclease
G-like 1 gene with type 2 diabetes in a Japanese population M. Moritani & K. Nomura & T.
Tanahashi & D. Osabe & Y. Fujita & S. Shinohara & Y. Yamaguchi & P. Keshavarz & ... Cited by 6 - Related articles - BL Direct - All 5 versions
S Chen, H Saiyin, X Zeng, J Xi, X Liu, X Li, L … - Cytogenet Genome …, 2006 - content.karger.com We have identified and isolated a novel human gene, HMBOX1 (homeobox containing 1) from
a pancreatic cDNA library. Human HMBOX1 is widely expressed in 18 tissues, and it is highly
expressed in pancreas. According to the genome database, HMBOX1 is located at the ... Cited by 4 - Related articles - BL Direct - All 5 versions
JS Dunn, WM Mlynarski, MG Pezzolesi, M … - Annals of Human …, 2006 - interscience.wiley.com The product of the PPP1R3B gene (G L ) is the regulatory subunit of PP1 - a serine/threonine
phosphatase involved in the modulation of glycogen synthesis in the liver and skeletal
muscle. The PPP1R3B gene is located on chromosome 8p23 in a region that has been ... Cited by 2 - Related articles - BL Direct - All 3 versions
