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Items: 1 to 20 of 70

1.

Nuclear damages and oxidative stress: new perspectives for laminopathies.

Lattanzi G, Marmiroli S, Facchini A, Maraldi NM.

Eur J Histochem. 2012 Oct 18;56(4):e45. doi: 10.4081/ejh.2012.e45. Review.

2.

Lipodystrophy-linked LMNA p.R482W mutation induces clinical early atherosclerosis and in vitro endothelial dysfunction.

Bidault G, Garcia M, Vantyghem MC, Ducluzeau PH, Morichon R, Thiyagarajah K, Moritz S, Capeau J, Vigouroux C, Béréziat V.

Arterioscler Thromb Vasc Biol. 2013 Sep;33(9):2162-71. doi: 10.1161/ATVBAHA.113.301933. Epub 2013 Jul 11.

3.

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 Jan-Mar;50(1):1-8. Review.

PMID:
16584978
4.

Sustained accumulation of prelamin A and depletion of lamin A/C both cause oxidative stress and mitochondrial dysfunction but induce different cell fates.

Sieprath T, Corne TD, Nooteboom M, Grootaert C, Rajkovic A, Buysschaert B, Robijns J, Broers JL, Ramaekers FC, Koopman WJ, Willems PH, De Vos WH.

Nucleus. 2015;6(3):236-46. doi: 10.1080/19491034.2015.1050568. Epub 2015 May 21.

5.

Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescence.

Caron M, Auclair M, Donadille B, Béréziat V, Guerci B, Laville M, Narbonne H, Bodemer C, Lascols O, Capeau J, Vigouroux C.

Cell Death Differ. 2007 Oct;14(10):1759-67. Epub 2007 Jul 6.

6.

Laminopathies and lamin-associated signaling pathways.

Maraldi NM, Capanni C, Cenni V, Fini M, Lattanzi G.

J Cell Biochem. 2011 Apr;112(4):979-92. doi: 10.1002/jcb.22992. Review.

PMID:
21400569
7.

A homozygous mutation of prelamin-A preventing its farnesylation and maturation leads to a severe lipodystrophic phenotype: new insights into the pathogenicity of nonfarnesylated prelamin-A.

Le Dour C, Schneebeli S, Bakiri F, Darcel F, Jacquemont ML, Maubert MA, Auclair M, Jeziorowska D, Reznik Y, Béréziat V, Capeau J, Lascols O, Vigouroux C.

J Clin Endocrinol Metab. 2011 May;96(5):E856-62. doi: 10.1210/jc.2010-2234. Epub 2011 Feb 23.

PMID:
21346069
8.

Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells.

Kandert S, Lüke Y, Kleinhenz T, Neumann S, Lu W, Jaeger VM, Munck M, Wehnert M, Müller CR, Zhou Z, Noegel AA, Dabauvalle MC, Karakesisoglou I.

Hum Mol Genet. 2007 Dec 1;16(23):2944-59. Epub 2007 Sep 19. Erratum in: Hum Mol Genet. 2008 Feb 1;17(3):468.

PMID:
17881656
9.

Lamins as mediators of oxidative stress.

Sieprath T, Darwiche R, De Vos WH.

Biochem Biophys Res Commun. 2012 May 18;421(4):635-9. doi: 10.1016/j.bbrc.2012.04.058. Epub 2012 Apr 17. Review. Erratum in: Biochem Biophys Res Commun. 2012 Jul 20;424(1):201-2.

PMID:
22538370
10.

Hutchinson-Gilford progeria syndrome through the lens of transcription.

Prokocimer M, Barkan R, Gruenbaum Y.

Aging Cell. 2013 Aug;12(4):533-43. doi: 10.1111/acel.12070. Epub 2013 Apr 19. Review.

11.

Embryonic senescence and laminopathies in a progeroid zebrafish model.

Koshimizu E, Imamura S, Qi J, Toure J, Valdez DM Jr, Carr CE, Hanai J, Kishi S.

PLoS One. 2011 Mar 30;6(3):e17688. doi: 10.1371/journal.pone.0017688.

12.

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Cau P, Navarro C, Harhouri K, Roll P, Sigaudy S, Kaspi E, Perrin S, De Sandre-Giovannoli A, Lévy N.

Semin Cell Dev Biol. 2014 May;29:125-47. doi: 10.1016/j.semcdb.2014.03.021. Epub 2014 Mar 22. Review.

PMID:
24662892
13.

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.

Muchir A, Medioni J, Laluc M, Massart C, Arimura T, van der Kooi AJ, Desguerre I, Mayer M, Ferrer X, Briault S, Hirano M, Worman HJ, Mallet A, Wehnert M, Schwartz K, Bonne G.

Muscle Nerve. 2004 Oct;30(4):444-50.

PMID:
15372542
14.

Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress.

Paradisi M, McClintock D, Boguslavsky RL, Pedicelli C, Worman HJ, Djabali K.

BMC Cell Biol. 2005 Jun 27;6:27.

15.

[Laminopathies: one gene, several diseases].

Bertrand AT, Chikhaoui K, Ben Yaou R, Bonne G.

Biol Aujourdhui. 2011;205(3):147-62. doi: 10.1051/jbio/2011017. Epub 2011 Oct 11. Review. French.

PMID:
21982404
16.

Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.

Bakay M, Wang Z, Melcon G, Schiltz L, Xuan J, Zhao P, Sartorelli V, Seo J, Pegoraro E, Angelini C, Shneiderman B, Escolar D, Chen YW, Winokur ST, Pachman LM, Fan C, Mandler R, Nevo Y, Gordon E, Zhu Y, Dong Y, Wang Y, Hoffman EP.

Brain. 2006 Apr;129(Pt 4):996-1013. Epub 2006 Feb 14.

PMID:
16478798
17.

Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells.

Lattanzi G.

Biochem Soc Trans. 2011 Dec;39(6):1698-704. doi: 10.1042/BST20110657. Review.

PMID:
22103510
18.

Dysregulated interactions between lamin A and SUN1 induce abnormalities in the nuclear envelope and endoplasmic reticulum in progeric laminopathies.

Chen ZJ, Wang WP, Chen YC, Wang JY, Lin WH, Tai LA, Liou GG, Yang CS, Chi YH.

J Cell Sci. 2014 Apr 15;127(Pt 8):1792-804. doi: 10.1242/jcs.139683. Epub 2014 Feb 12.

19.

Accumulation of distinct prelamin A variants in human diploid fibroblasts differentially affects cell homeostasis.

Candelario J, Borrego S, Reddy S, Comai L.

Exp Cell Res. 2011 Feb 1;317(3):319-29. doi: 10.1016/j.yexcr.2010.10.014. Epub 2010 Oct 23.

PMID:
20974128
20.

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. doi: 10.1172/JCI37679. Epub 2009 Jul 1. Review.

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