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4. [Mutations of the lamin A/C gene causing familial partial lipodystrophy: significance for the development of hyperlipidemia and insulin resistant diabetes mellitus]. Genschel J; Lochs H; Schmidt HH Z Gastroenterol; 2000 Apr; 38(4):341-3. PubMed ID: 10820868 [No Abstract] [Full Text] [Related]
5. Single-nucleotide polymorphisms of the nuclear lamina proteome. Hegele RA; Yuen J; Cao H J Hum Genet; 2001; 46(6):351-4. PubMed ID: 11393540 [TBL] [Abstract][Full Text] [Related]
6. Familial partial lipodystrophy: a monogenic form of the insulin resistance syndrome. Hegele RA Mol Genet Metab; 2000 Dec; 71(4):539-44. PubMed ID: 11136544 [TBL] [Abstract][Full Text] [Related]
7. The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin. Holt I; Clements L; Manilal S; Brown SC; Morris GE Eur J Hum Genet; 2001 Mar; 9(3):204-8. PubMed ID: 11313760 [TBL] [Abstract][Full Text] [Related]
11. Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians. Weyer C; Wolford JK; Hanson RL; Foley JE; Tataranni PA; Bogardus C; Pratley RE Mol Genet Metab; 2001 Mar; 72(3):231-8. PubMed ID: 11243729 [TBL] [Abstract][Full Text] [Related]
12. Heterogeneity of nuclear lamin A mutations in Dunnigan-type familial partial lipodystrophy. Hegele RA; Cao H; Anderson CM; Hramiak IM J Clin Endocrinol Metab; 2000 Sep; 85(9):3431-5. PubMed ID: 10999845 [TBL] [Abstract][Full Text] [Related]
13. Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene. Garg A; Vinaitheerthan M; Weatherall PT; Bowcock AM J Clin Endocrinol Metab; 2001 Jan; 86(1):59-65. PubMed ID: 11231979 [TBL] [Abstract][Full Text] [Related]
14. Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene. Vigouroux C; Auclair M; Dubosclard E; Pouchelet M; Capeau J; Courvalin JC; Buendia B J Cell Sci; 2001 Dec; 114(Pt 24):4459-68. PubMed ID: 11792811 [TBL] [Abstract][Full Text] [Related]
15. Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies. Maraldi NM; Lattanzi G; Capanni C; Columbaro M; Merlini L; Mattioli E; Sabatelli P; Squarzoni S; Manzoli FA Eur J Histochem; 2006; 50(1):1-8. PubMed ID: 16584978 [TBL] [Abstract][Full Text] [Related]
16. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease. Jakobs PM; Hanson EL; Crispell KA; Toy W; Keegan H; Schilling K; Icenogle TB; Litt M; Hershberger RE J Card Fail; 2001 Sep; 7(3):249-56. PubMed ID: 11561226 [TBL] [Abstract][Full Text] [Related]
17. Lessons from human mutations in PPARgamma. Hegele RA Int J Obes (Lond); 2005 Mar; 29 Suppl 1():S31-5. PubMed ID: 15711581 [TBL] [Abstract][Full Text] [Related]
20. Life at the edge: the nuclear envelope and human disease. Burke B; Stewart CL Nat Rev Mol Cell Biol; 2002 Aug; 3(8):575-85. PubMed ID: 12154369 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]