- ►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
- ►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
- ►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
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
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 E Zeggini, CM Damcott, RL Hanson, MA Karim, NW … - Diabetes, 2006 - Am Diabetes Assoc The gene encoding the transcription factor upstream stimulatory factor (USF)1 influences susceptibility
to familial combined hyperlipidemia (FCHL) and triglyceride levels. Phenotypic overlap between
FCHL and type 2 diabetes makes USF1 a compelling positional candidate for the widely ... Cited by 17 - Related articles - BL Direct - All 7 versions
- ►diabetesjournals.org JL Mesa, RJF Loos, PW Franks, KK Ong, J Luan, SO' … - 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 characterized by loss of subcutaneous ... Cited by 9 - Related articles - BL Direct - All 9 versions
- ►diabetesjournals.org VS Farook, RL Hanson, JK Wolford, C Bogardus, M … - Diabetes, 2002 - Am Diabetes Assoc The KCNJ10 gene is located within a region on chromosome 1q linked to type 2 diabetes in
the Pima Indians and six other populations. We therefore investigated this gene as a potential
type 2 diabetes candidate gene in Pima Indians. KCNJ10 consists of two exons, spans ... Cited by 15 - Related articles - BL Direct - All 5 versions
H Liang, Y Murase, Y Katuta, A Asano, J … - CLINICAL …, 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 atherosclerosis and vascular ... Cited by 2 - Related articles - BL Direct - All 4 versions
Y Murase, K Yagi, Y Katsuda, A Asano, J Koizumi, H … - Metabolism, 2002 - Elsevier Nuclear lamins A and C are encoded by LMNA and are present in terminally differentiated
cells. Rare mutations in LMNA were shown to cause familial partial lipodystrophy, a syndrome
characterized by regional loss of adipose tissue, glucose intolerance, and dyslipidemia, ... Cited by 20 - Related articles - BL Direct - All 8 versions
