- ►diabetesjournals.org JL Mesa, RJF Loos, PW Franks, KK Ong, J Luan … - Diabetes, 2007 - Am Diabetes Assoc Mutations in the LMNA gene, encoding the nuclear envelope protein lamin A/C, are
responsible for a number of distinct disease entities including Dunnigan-type
familial partial lipodystrophy. Dunningan-type lipodystrophy is ... Cited by 9 - Related articles - BL Direct - All 9 versions
K Duesing, G Charpentier, M Marre, J Tichet, … - Diabetologia, 2008 - Springer Page 1. ARTICLE Evaluating the association of common LMNA variants with type 2 diabetes
and quantitative metabolic phenotypes in French Europids ... Cited by 1 - Related articles - BL Direct - All 2 versions
H Liang, Y Murase, Y Katuta, A Asano, J … - CLINICAL ENDOCRINOLOGY-OXFORD-, 2005 - interscience.wiley.com Objective The LMNA 1908C/T polymorphism has been reported to be associated with
dyslipidaemia, metabolic syndrome, adipose tissue metabolism and obesity
phenotypes, suggesting that this polymorphism presents an increased risk of ... Cited by 2 - Related articles - BL Direct - All 4 versions
- ►diabetesjournals.org KR Owen, CJ Groves, RL Hanson, WC Knowler, … - Diabetes, 2007 - Am Diabetes Assoc Mutations in the LMNA gene (encoding lamin A/C) underlie familial partial
lipodystrophy, a syndrome of monogenic insulin resistance and diabetes. LMNA
maps to the well-replicated diabetes-linkage region on chromosome 1q, and ... Cited by 12 - Related articles - BL Direct - All 9 versions
- ►diabetesjournals.org L Wegner, G Andersen, T Sparso, N Grarup, … - Diabetes, 2007 - Am Diabetes Assoc Mutations in LMNA encoding lamin A and C proteins cause monogenic syndromes
characterized by muscular dystrophy and familial partial lipodystrophy. Eight
tag single nucleotide polymorphisms in the LMNA locus were genotyped in ... Cited by 6 - Related articles - BL Direct - All 4 versions
F Mousavinasab, T Tähtinen, J Jokelainen, P … - Endocrine, 2006 - Springer Received June 26, 2006; Revised September 12, 2006; Accepted October 2, 2006.
Author to whom all correspondence and reprint requests should be addressed:
Firoozeh Mousavinasab, MD, Department of Public Health Science and General ... Cited by 6 - Related articles - BL Direct - All 4 versions
JK Wolford, RL Hanson, C Bogardus, M … - Diabetologia, 2001 - Springer Type II (non-insulin-dependent) diabetes mellitus is a complex heterogeneous
disorder and although the underlying causes are not well understood, it is wide-
ly accepted that disease susceptibility has both genet- ic and ... Cited by 27 - Related articles - BL Direct - All 4 versions
JW Stephens, SJ Hurel, GDO Lowe, A Rumley … - Molecular genetics and metabolism, 2007 - Elsevier Elevated plasma interleukin-6 (IL-6) is associated with coronary heart disease
(CHD), impaired glucose tolerance (IGT), and type 2 diabetes (T2DM). We and
others have described an association between the human interleukin-6 ... Cited by 8 - Related articles - All 2 versions
[CITATION] the DESIR Study Group: TCF7L2 variation predicts hyperglycemia incidence in a French …
I Barroso - fusion.sph.umich.edu Beckmann 9,10 , Sonja I. Berndt 11 , The Prostate, Lung, Colorectal, and Ovarian
(PLCO) Cancer Screening Trial 71 , Sven Bergmann 9,12 , Amanda J. Bennett 3,4 ,
Sheila A. Bingham 13 , Murielle ... Bochud 14 , Morris Brown 15 , ... Related articles - View as HTML - All 2 versions
