- ►diabetesjournals.org L Wegner, G Andersen, T Sparso, N Grarup, C Glumer, … - 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 7,495 Danish whites and related to metabolic and ... Cited by 6 - Related articles - BL Direct - All 4 versions
- ►diabetesjournals.org KR Owen, CJ Groves, RL Hanson, WC Knowler, AR … - 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 there are reported associations between LMNA single ... Cited by 12 - Related articles - BL Direct - All 9 versions
K Duesing, G Charpentier, M Marre, J Tichet, S … - Diabetologia, 2008 - Springer Page 1. ARTICLE Evaluating the association of common LMNA variants with type 2 diabetes
and quantitative metabolic phenotypes in French Europids K. Duesing & G. Charpentier
& M. Marre & J. Tichet & S. Hercberg & P. Froguel & F. Gibson ... Cited by 1 - Related articles - BL Direct - All 2 versions
L Wegner, G Andersen, T Sparsø, N Grarup, C Glümer, … - 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 7,495 Danish whites and related to metabolic and ... Cited by 1 - Related articles - All 3 versions
L Wegner, G Andersen, T Sparsø, N Grarup, C Glümer, … - DIABETES, 2007 - Am Diabetes Assoc Page 1. Brief Report Common Variation in LMNA Increases Susceptibility to Type 2
Diabetes and Associates With Elevated Fasting Glycemia and Estimates of Body Fat and
Height in the General Population Studies of 7,495 Danish Whites ... Related articles
- ►ahajournals.org NI Steinle, R Kazlauskaite, IG Imumorin, WC … - … , and vascular biology, 2004 - Am Heart Assoc Methods and Results— We performed DNA sequence analysis of LMNA. Six single-nucleotide
polymorphisms (SNPs) were identified: c.141889C>T (intron 3), c.141906G>T (intron 3), A287A
(c.141253T>C; exon 5), c.140353G>A (intron 6), c.139418C>T (intron 8), and H566H (c. ... Cited by 23 - Related articles - BL Direct - All 10 versions
B Fontaine-Bisson, MC Alessi, N Saut, F Fumeron, M … - Journal of Molecular … - Springer Abstract Laminopathies are rare monogenic diseases, some of them exhibiting features of the
metabolic syndrome. These diseases are mainly due to mutations in LMNA, encoding A-type
lamins. One LMNA polymor- phism, rs4641, has been associated with the metabolic ... Related articles - All 2 versions
- ►diabetesjournals.org KR Owen, CJ Groves, RL Hanson, WC Knowler, AR … - 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 there are reported associations between LMNA single ... Related articles - All 3 versions
- ►endojournals.org [PDF] SJR Meex, MMJ van Greevenbroek, TA Ayoubi, … - Journal of Clinical …, 2007 - Endocrine Soc Page 1. 1 ATF6 polymorphisms and haplotypes are associated with impaired glucose
homeostasis and type 2 diabetes in Dutch Caucasians Abbreviated title: ATF6 is
associated with type 2 diabetes Steven JR Meex A , Marleen ... Cited by 1 - Related articles
