De Sandre-Giovannoli A - Search Results

1

miR-376a-3p and miR-376b-3p overexpression in Hutchinson-Gilford progeria fibroblasts inhibits cell proliferation and induces premature senescence.

Frankel D, Delecourt V, Novoa-Del-Toro EM, Robin JD, Airault C, Bartoli C, Carabalona A, Perrin S, Mazaleyrat K, De Sandre-Giovannoli A, Magdinier F, Baudot A, Lévy N, Kaspi E, Roll P. Frankel D, et al. Among authors: de sandre giovannoli a. iScience. 2022 Jan 10;25(2):103757. doi: 10.1016/j.isci.2022.103757. eCollection 2022 Feb 18. iScience. 2022. PMID: 35118365 Free PMC article.

2

Lamin a truncation in Hutchinson-Gilford progeria.

De Sandre-Giovannoli A, Bernard R, Cau P, Navarro C, Amiel J, Boccaccio I, Lyonnet S, Stewart CL, Munnich A, Le Merrer M, Lévy N. De Sandre-Giovannoli A, et al. Science. 2003 Jun 27;300(5628):2055. doi: 10.1126/science.1084125. Epub 2003 Apr 17. Science. 2003. PMID: 12702809 No abstract available.

3

Molecular genetics of autosomal-recessive axonal Charcot-Marie-Tooth neuropathies.

Bernard R, De Sandre-Giovannoli A, Delague V, Lévy N. Bernard R, et al. Neuromolecular Med. 2006;8(1-2):87-106. doi: 10.1385/nmm:8:1-2:87. Neuromolecular Med. 2006. PMID: 16775369 Review.

4

Altered splicing in prelamin A-associated premature aging phenotypes.

De Sandre-Giovannoli A, Lévy N. De Sandre-Giovannoli A, et al. 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.

5

An association of Hutchinson-Gilford progeria and malignancy.

Shalev SA, De Sandre-Giovannoli A, Shani AA, Levy N. Shalev SA, et al. Am J Med Genet A. 2007 Aug 15;143A(16):1821-6. doi: 10.1002/ajmg.a.31803. Am J Med Genet A. 2007. PMID: 17618517

6

Pereira S, Bourgeois P, Navarro C, Esteves-Vieira V, Cau P, De Sandre-Giovannoli A, Lévy N. Pereira S, et al. 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.

7

Novel LMNA mutation in atypical Werner syndrome presenting with ischemic disease.

Renard D, Fourcade G, Milhaud D, Bessis D, Esteves-Vieira V, Boyer A, Roll P, Bourgeois P, Levy N, De Sandre-Giovannoli A. Renard D, et al. Stroke. 2009 Feb;40(2):e11-4. doi: 10.1161/STROKEAHA.108.531780. Epub 2008 Dec 18. Stroke. 2009. PMID: 19095983

8

LBR mutation and nuclear envelope defects in a patient affected with Reynolds syndrome.

Gaudy-Marqueste C, Roll P, Esteves-Vieira V, Weiller PJ, Grob JJ, Cau P, Lévy N, De Sandre-Giovannoli A. Gaudy-Marqueste C, et al. J Med Genet. 2010 Jun;47(6):361-70. doi: 10.1136/jmg.2009.071696. J Med Genet. 2010. PMID: 20522425

9

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. 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.

10

A conserved splicing mechanism of the LMNA gene controls premature aging.

Lopez-Mejia IC, Vautrot V, De Toledo M, Behm-Ansmant I, Bourgeois CF, Navarro CL, Osorio FG, Freije JM, Stévenin J, De Sandre-Giovannoli A, Lopez-Otin C, Lévy N, Branlant C, Tazi J. Lopez-Mejia IC, et al. Hum Mol Genet. 2011 Dec 1;20(23):4540-55. doi: 10.1093/hmg/ddr385. Epub 2011 Aug 29. Hum Mol Genet. 2011. PMID: 21875900

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