These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
9. A lamin A/C variant causing striated muscle disease provides insights into filament organization. Kronenberg-Tenga R; Tatli M; Eibauer M; Wu W; Shin JY; Bonne G; Worman HJ; Medalia O J Cell Sci; 2021 Mar; 134(6):. PubMed ID: 33536248 [TBL] [Abstract][Full Text] [Related]
10. Laminopathies and the long strange trip from basic cell biology to therapy. Worman HJ; Fong LG; Muchir A; Young SG J Clin Invest; 2009 Jul; 119(7):1825-36. PubMed ID: 19587457 [TBL] [Abstract][Full Text] [Related]
11. Complex effects of laminopathy mutations on nuclear structure and function. Ho R; Hegele RA Clin Genet; 2019 Feb; 95(2):199-209. PubMed ID: 30280378 [TBL] [Abstract][Full Text] [Related]
12. Elevated dual specificity protein phosphatase 4 in cardiomyopathy caused by lamin A/C gene mutation is primarily ERK1/2-dependent and its depletion improves cardiac function and survival. Choi JC; Wu W; Phillips E; Plevin R; Sera F; Homma S; Worman HJ Hum Mol Genet; 2018 Jul; 27(13):2290-2305. PubMed ID: 29668927 [TBL] [Abstract][Full Text] [Related]
13. Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy. Wang Y; Herron AJ; Worman HJ Hum Mol Genet; 2006 Aug; 15(16):2479-89. PubMed ID: 16825283 [TBL] [Abstract][Full Text] [Related]
14. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation. Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843 [TBL] [Abstract][Full Text] [Related]
15. Emerin and the nuclear lamina in muscle and cardiac disease. Holaska JM Circ Res; 2008 Jul; 103(1):16-23. PubMed ID: 18596264 [TBL] [Abstract][Full Text] [Related]
16. Distinct features of lamin A-interacting chromatin domains mapped by ChIP-sequencing from sonicated or micrococcal nuclease-digested chromatin. Lund EG; Duband-Goulet I; Oldenburg A; Buendia B; Collas P Nucleus; 2015; 6(1):30-9. PubMed ID: 25602132 [TBL] [Abstract][Full Text] [Related]
17. Nuclear lamin phosphorylation: an emerging role in gene regulation and pathogenesis of laminopathies. Liu SY; Ikegami K Nucleus; 2020 Dec; 11(1):299-314. PubMed ID: 33030403 [TBL] [Abstract][Full Text] [Related]
18. Nuclear Lamins: Thin Filaments with Major Functions. de Leeuw R; Gruenbaum Y; Medalia O Trends Cell Biol; 2018 Jan; 28(1):34-45. PubMed ID: 28893461 [TBL] [Abstract][Full Text] [Related]
19. From gene to mechanics: a comprehensive insight into the mechanobiology of LMNA mutations in cardiomyopathy. Veltrop RJA; Kukk MM; Topouzidou K; Didden L; Muchir A; van Steenbeek FG; Schurgers LJ; Harakalova M Cell Commun Signal; 2024 Mar; 22(1):197. PubMed ID: 38539233 [TBL] [Abstract][Full Text] [Related]
20. Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy. Motsch I; Kaluarachchi M; Emerson LJ; Brown CA; Brown SC; Dabauvalle MC; Ellis JA Eur J Cell Biol; 2005 Sep; 84(9):765-81. PubMed ID: 16218190 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]