Bourgeois P - Search Results

1

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

2

A new lamin a mutation associated with acrogeria syndrome.

Hadj-Rabia S, Mashiah J, Roll P, Boyer A, Bourgeois P, Van Kien PK, Lévy N, De Sandre-Giovannoli A, Bodemer C, Navarro C. Hadj-Rabia S, et al. Among authors: bourgeois p. J Invest Dermatol. 2014 Aug;134(8):2274-2277. doi: 10.1038/jid.2014.158. Epub 2014 Apr 1. J Invest Dermatol. 2014. PMID: 24687084 Free article. No abstract available.

3

Prelamin A accumulation in endothelial cells induces premature senescence and functional impairment.

Bonello-Palot N, Simoncini S, Robert S, Bourgeois P, Sabatier F, Levy N, Dignat-George F, Badens C. Bonello-Palot N, et al. Among authors: bourgeois p. Atherosclerosis. 2014 Nov;237(1):45-52. doi: 10.1016/j.atherosclerosis.2014.08.036. Epub 2014 Aug 28. Atherosclerosis. 2014. PMID: 25200614

4

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. Among authors: bourgeois p. Stroke. 2009 Feb;40(2):e11-4. doi: 10.1161/STROKEAHA.108.531780. Epub 2008 Dec 18. Stroke. 2009. PMID: 19095983

5

Unraveling LMNA Mutations in Metabolic Syndrome: Cellular Phenotype and Clinical Pitfalls.

Desgrouas C, Varlet AA, Dutour A, Galant D, Merono F, Bonello-Palot N, Bourgeois P, Lasbleiz A, Petitjean C, Ancel P, Levy N, Badens C, Gaborit B. Desgrouas C, et al. Among authors: bourgeois p. Cells. 2020 Jan 28;9(2):310. doi: 10.3390/cells9020310. Cells. 2020. PMID: 32012908 Free PMC article.

6

A Rare Mutation in LMNB2 Associated with Lipodystrophy Drives Premature Cell Senescence.

Varlet AA, Desgrouas C, Jebane C, Bonello-Palot N, Bourgeois P, Levy N, Helfer E, Dubois N, Valero R, Badens C, Beliard S. Varlet AA, et al. Among authors: bourgeois p. Cells. 2021 Dec 24;11(1):50. doi: 10.3390/cells11010050. Cells. 2021. PMID: 35011612 Free PMC article.

7

A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated Cardiomyopathy.

Galant D, Gaborit B, Desgrouas C, Abdesselam I, Bernard M, Levy N, Merono F, Coirault C, Roll P, Lagarde A, Bonello-Palot N, Bourgeois P, Dutour A, Badens C. Galant D, et al. Among authors: bourgeois p. Cells. 2016 Apr 25;5(2):21. doi: 10.3390/cells5020021. Cells. 2016. PMID: 27120622 Free PMC article.

8

Differential Brain, Cognitive and Motor Profiles Associated with Partial Trisomy. Modeling Down Syndrome in Mice.

Roubertoux PL, Baril N, Cau P, Scajola C, Ghata A, Bartoli C, Bourgeois P, Christofaro JD, Tordjman S, Carlier M. Roubertoux PL, et al. Among authors: bourgeois p. Behav Genet. 2017 May;47(3):305-322. doi: 10.1007/s10519-017-9835-5. Epub 2017 Feb 15. Behav Genet. 2017. PMID: 28204906

9

Erratum to: Differential Brain, Cognitive and Motor Profiles Associated with Partial Trisomy. Modeling Down Syndrome in Mice.

Roubertoux PL, Baril N, Cau P, Scajola C, Ghata A, Bartoli C, Bourgeois P, di Christofaro J, Tordjman S, Carlier M. Roubertoux PL, et al. Among authors: bourgeois p. Behav Genet. 2017 May;47(3):323. doi: 10.1007/s10519-017-9845-3. Behav Genet. 2017. PMID: 28337630 No abstract available.

10

Tricho-Hepato-Enteric Syndrome mutation update: Mutations spectrum of TTC37 and SKIV2L, clinical analysis and future prospects.

Bourgeois P, Esteve C, Chaix C, Béroud C, Lévy N; THES clinical consortium; Fabre A, Badens C. Bourgeois P, et al. Hum Mutat. 2018 Jun;39(6):774-789. doi: 10.1002/humu.23418. Epub 2018 Mar 25. Hum Mutat. 2018. PMID: 29527791 Review.

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