Lamines A : deux autres affections pour un même gène = A lamines: two affections for the same geneDEREURE, O.Annales de dermatologie et de vénéréologie. 2004, Vol 131, Num 6-7, issn 0151-9638, p. 611, CAH1Article

A conserved splicing mechanism of the LMNA gene controls premature agingLOPEZ-MEJIA, Isabel C; VAUTROT, Valentin; LOPEZ-OTIN, Carlos et al.Human molecular genetics (Print). 2011, Vol 20, Num 23, pp 4540-4555, issn 0964-6906, 16 p.Article

A LMNA splicing mutation in two sisters with severe dunnigan-type familial partial lipodystrophy type 2MOREL, Chantal F; THOMAS, Mary Ann; HENIAN CAO et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 7, pp 2689-2695, issn 0021-972X, 7 p.Article

Analysis of the Lamin A/C gene as a candidate for Type II diabetes susceptibility in Pima IndiansWOLFORD, J. K; HANSON, R. L; BOGARDUS, C et al.Diabetologia (Berlin). 2001, Vol 44, Num 6, pp 779-782, issn 0012-186XArticle

Histological and molecular features of lipomatous and nonlipomatous adipose tissue in familial partial lipodystrophy caused by LMNA mutationsARAUJO-VILAR, D; VICTORIA, B; GONZALEZ-MENDEZ, B et al.Clinical endocrinology (Oxford. Print). 2012, Vol 76, Num 6, pp 816-824, issn 0300-0664, 9 p.Article

LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscleDIALYNAS, George; FLANNERY, Kaitlin M; ZIRBEL, Luka N et al.Human molecular genetics (Print). 2012, Vol 21, Num 7, pp 1544-1556, issn 0964-6906, 13 p.Article

Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotypeLOMBARDI, Francesca; GULLOTTA, Francesca; LATTANZI, Giovanna et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 11, pp 4467-4471, issn 0021-972X, 5 p.Article

Genotype of the LMNA 1908C>Tvariant is associated with generalized obesity in Asian Indians in North IndiaSHARMA, Mukti; MISRA, Anoop; VIKRAM, Naval et al.Clinical endocrinology (Oxford. Print). 2011, Vol 75, Num 5, pp 642-649, issn 0300-0664, 8 p.Article

Patients with familial partial lipodystrophy of the dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesVANTYGHEM, M. C; PIGNY, P; CAPEAU, J et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 11, pp 5337-5346, issn 0021-972X, 10 p.Article

Recapitulation of premature ageing with iPSCs from Hutchinson―Gilford progeria syndromeLIU, Guang-Hui; BARKHO, Basam Z; THOMPSON, James et al.Nature (London). 2011, Vol 472, Num 7342, pp 221-225, issn 0028-0836, 5 p.Article

Restrictive dermopathy―a lethal congenital laminopathy. Case report and review of the literatureMORAIS, Paulo; MAGINA, Sofia; DO CEU RIBEIRO, Maria et al.European journal of pediatrics. 2009, Vol 168, Num 8, pp 1007-1012, issn 0340-6199, 6 p.Article

Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronismVANTYGHEM, M. C; FAIVRE-DEFRANCE, F; MARCELLI -TOURVIEILLE, S et al.Clinical endocrinology (Oxford. Print)). 2007, Vol 67, Num 2, pp 247-249, issn 0300-0664, 3 p.Article

Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetesHUA LIANG; MURASE, Yuko; KATUTA, Yuko et al.Clinical endocrinology (Oxford. Print). 2005, Vol 63, Num 3, pp 317-322, issn 0300-0664, 6 p.Article

A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathyARAUJO-VILAR, David; LADO-ABEAL, Joaquin; MARTINEZ-SANCHEZ, Noelia et al.Clinical endocrinology (Oxford. Print). 2008, Vol 69, Num 1, pp 61-68, issn 0300-0664, 8 p.Article

An LMNA variant is associated with dyslipidemia and insulin resistance in the JapaneseMURASE, Yuko; YAGI, Kunimasa; KATSUDA, Yuko et al.Metabolism, clinical and experimental. 2002, Vol 51, Num 8, pp 1017-1021, issn 0026-0495Article

Fertility and Obstetrical Complications in Women with LMNA-Related Familial Partial LipodystrophyVANTYGHEM, M. C; VINCENT-DESPLANQUES, D; VIGOUROUX, C et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 6, pp 2223-2229, issn 0021-972X, 7 p.Article

New Metabolic Phenotypes in Laminopathies : LMNA Mutations in Patients with Severe Metabolic SyndromeDECAUDAIN, Aurélie; VANTYGHEM, Marie-Christine; BEREZIAT, Véronique et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 12, pp 4835-4844, issn 0021-972X, 10 p.Article

Multisystem dystrophy syndrome due to Novel missense Mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C geneGARG, Abhimanyu; SPECKMAN, Rebecca A; BOWCOCK, Anne M et al.The American journal of medicine. 2002, Vol 112, Num 7, pp 549-555, issn 0002-9343Article

A progeroid syndrome in mice is caused by defect in A-type laminsMOUNKES, Leslie C; KOZLOV, Serguei; HERNANDEZ, Lidia et al.Nature (London). 2003, Vol 423, Num 6937, pp 298-301, issn 0028-0836, 4 p.Article