Bonello-Palot N - Search Results

1

Perilipin 1: a systematic review on its functions on lipid metabolism and atherosclerosis in mice and humans.

Desgrouas C, Thalheim T, Cerino M, Badens C, Bonello-Palot N. Desgrouas C, et al. Among authors: bonello palot n. Cardiovasc Res. 2024 Mar 14;120(3):237-248. doi: 10.1093/cvr/cvae005. Cardiovasc Res. 2024. PMID: 38214891

2

High prevalence of mutations in perilipin 1 in patients with precocious acute coronary syndrome.

Bonello-Palot N, Laine M, Cuisset T, Ronchard T, Desgrouas C, Merono F, Ibrahim-Kosta M, Cerino M, Blanchard A, Bourgeois P, Levy N, Loundou A, Morange PE, Alessi MC, Badens C, Bonello L. Bonello-Palot N, et al. Atherosclerosis. 2020 Jan;293:86-91. doi: 10.1016/j.atherosclerosis.2019.12.002. Epub 2019 Dec 12. Atherosclerosis. 2020. PMID: 31877397 Free article.

3

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. Cells. 2020 Jan 28;9(2):310. doi: 10.3390/cells9020310. Cells. 2020. PMID: 32012908 Free PMC article.

4

A novel SUPT5H variant associated with a beta-thalassaemia trait.

Charnay T, Cerino M, Gonnet K, Bonello-Palot N, Bréchard MP, Badens C. Charnay T, et al. Br J Haematol. 2022 Mar;196(6):e70-e71. doi: 10.1111/bjh.17985. Epub 2021 Dec 1. Br J Haematol. 2022. PMID: 34854076 No abstract available.

5

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: bonello palot n. Cells. 2021 Dec 24;11(1):50. doi: 10.3390/cells11010050. Cells. 2021. PMID: 35011612 Free PMC article.

6

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. Cells. 2016 Apr 25;5(2):21. doi: 10.3390/cells5020021. Cells. 2016. PMID: 27120622 Free PMC article.

7

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. Atherosclerosis. 2014 Nov;237(1):45-52. doi: 10.1016/j.atherosclerosis.2014.08.036. Epub 2014 Aug 28. Atherosclerosis. 2014. PMID: 25200614

8

Refining NGS diagnosis of muscular disorders.

Cerino M, Salort-Campana E, Gorokhova S, Sevy A, Bonello-Palot N, Levy N, Attarian S, Bartoli M, Krahn M. Cerino M, et al. J Neurol Neurosurg Psychiatry. 2021 Feb;92(2):223-225. doi: 10.1136/jnnp-2018-319254. Epub 2020 Sep 15. J Neurol Neurosurg Psychiatry. 2021. PMID: 32934002 No abstract available.

9

Retrospective analysis and reclassification of DYSF variants in a large French series of dysferlinopathy patients.

Charnay T, Blanck V, Cerino M, Bartoli M, Riccardi F, Bonello-Palot N, Pécheux C, Nguyen K, Lévy N, Gorokhova S, Krahn M. Charnay T, et al. Genet Med. 2021 Aug;23(8):1574-1577. doi: 10.1038/s41436-021-01164-3. Epub 2021 Apr 29. Genet Med. 2021. PMID: 33927379 Free article.

10

Co-occurrence of oculocutaneous albinism type 2 and mild sickle cell disease explained by HbS/βthal genotype in an individual from the Democratic Republic of Congo.

Aquaron R, Lasseaux E, Kelekele J, Bonello-Palot N, Badens C, Arveiler B, Tshilolo L. Aquaron R, et al. Among authors: bonello palot n. Eur J Med Genet. 2022 Oct;65(10):104594. doi: 10.1016/j.ejmg.2022.104594. Epub 2022 Aug 12. Eur J Med Genet. 2022. PMID: 35964929

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