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Truncated prelamin A expression in HGPS-like patients: a transcriptional study.
Eur J Hum Genet. 2015 Aug;23(8):1051-61. doi: 10.1038/ejhg.2014.239. Epub 2015 Feb 4.
Eur J Hum Genet. 2015.
PMID: 25649378
Free PMC article.
Altered splicing in prelamin A-associated premature aging phenotypes.
De Sandre-Giovannoli A, Lévy N.
De Sandre-Giovannoli A, et al. Among authors: levy n.
Prog Mol Subcell Biol. 2006;44:199-232. doi: 10.1007/978-3-540-34449-0_9.
Prog Mol Subcell Biol. 2006.
PMID: 17076270
Review.
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Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation.
Ben Yaou R, Navarro C, Quijano-Roy S, Bertrand AT, Massart C, De Sandre-Giovannoli A, Cadiñanos J, Mamchaoui K, Butler-Browne G, Estournet B, Richard P, Barois A, Lévy N, Bonne G.
Ben Yaou R, et al. Among authors: levy n.
Eur J Hum Genet. 2011 Jun;19(6):647-54. doi: 10.1038/ejhg.2010.256. Epub 2011 Jan 26.
Eur J Hum Genet. 2011.
PMID: 21267004
Free PMC article.
Item in Clipboard
New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update.
Navarro CL, Esteves-Vieira V, Courrier S, Boyer A, Duong Nguyen T, Huong le TT, Meinke P, Schröder W, Cormier-Daire V, Sznajer Y, Amor DJ, Lagerstedt K, Biervliet M, van den Akker PC, Cau P, Roll P, Lévy N, Badens C, Wehnert M, De Sandre-Giovannoli A.
Navarro CL, et al. Among authors: levy n.
Eur J Hum Genet. 2014 Aug;22(8):1002-11. doi: 10.1038/ejhg.2013.258. Epub 2013 Oct 30.
Eur J Hum Genet. 2014.
PMID: 24169522
Free PMC article.
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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.
Cau P, et al. Among authors: levy n.
Semin Cell Dev Biol. 2014 May;29:125-47. doi: 10.1016/j.semcdb.2014.03.021. Epub 2014 Mar 22.
Semin Cell Dev Biol. 2014.
PMID: 24662892
Review.
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Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy.
Navarro CL, De Sandre-Giovannoli A, Bernard R, Boccaccio I, Boyer A, Geneviève D, Hadj-Rabia S, Gaudy-Marqueste C, Smitt HS, Vabres P, Faivre L, Verloes A, Van Essen T, Flori E, Hennekam R, Beemer FA, Laurent N, Le Merrer M, Cau P, Lévy N.
Navarro CL, et al. Among authors: levy n.
Hum Mol Genet. 2004 Oct 15;13(20):2493-503. doi: 10.1093/hmg/ddh265. Epub 2004 Aug 18.
Hum Mol Genet. 2004.
PMID: 15317753
Item in Clipboard
Molecular bases of progeroid syndromes.
Navarro CL, Cau P, Lévy N.
Navarro CL, et al. Among authors: levy n.
Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R151-61. doi: 10.1093/hmg/ddl214.
Hum Mol Genet. 2006.
PMID: 16987878
Review.
Item in Clipboard
HGPS and related premature aging disorders: from genomic identification to the first therapeutic approaches.
Pereira S, Bourgeois P, Navarro C, Esteves-Vieira V, Cau P, De Sandre-Giovannoli A, Lévy N.
Pereira S, et al. Among authors: levy n.
Mech Ageing Dev. 2008 Jul-Aug;129(7-8):449-59. doi: 10.1016/j.mad.2008.04.003. Epub 2008 Apr 12.
Mech Ageing Dev. 2008.
PMID: 18513784
Review.
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[A-type lamins and progeroïd syndromes : persistent farnesylation with dramatic effects].
Navarro CL, Poitelon Y, Lévy N.
Navarro CL, et al. Among authors: levy n.
Med Sci (Paris). 2008 Oct;24(10):833-40. doi: 10.1051/medsci/20082410833.
Med Sci (Paris). 2008.
PMID: 18950579
Free article.
Review.
French.
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High prevalence of laminopathies among patients with metabolic syndrome.
Dutour A, Roll P, Gaborit B, Courrier S, Alessi MC, Tregouet DA, Angelis F, Robaglia-Schlupp A, Lesavre N, Cau P, Lévy N, Badens C, Morange PE.
Dutour A, et al. Among authors: levy n.
Hum Mol Genet. 2011 Oct 1;20(19):3779-86. doi: 10.1093/hmg/ddr294. Epub 2011 Jun 30.
Hum Mol Genet. 2011.
PMID: 21724554
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