Da Silva N - Search Results

1

Hepatitis E virus RNA-dependent RNA polymerase is involved in RNA replication and infectious particle production.

Oechslin N, Da Silva N, Szkolnicka D, Cantrelle FX, Hanoulle X, Moradpour D, Gouttenoire J. Oechslin N, et al. Among authors: da silva n. Hepatology. 2022 Jan;75(1):170-181. doi: 10.1002/hep.32100. Epub 2021 Dec 8. Hepatology. 2022. PMID: 34387882 Free PMC article.

2

Recombinant Hepatitis E Viruses Harboring Tags in the ORF1 Protein.

Szkolnicka D, Pollán A, Da Silva N, Oechslin N, Gouttenoire J, Moradpour D. Szkolnicka D, et al. Among authors: da silva n. J Virol. 2019 Sep 12;93(19):e00459-19. doi: 10.1128/JVI.00459-19. Print 2019 Oct 1. J Virol. 2019. PMID: 31315997 Free PMC article.

3

Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder.

Rochdi K, Cerino M, Da Silva N, Delague V, Bouzidi A, Nahili H, Zouiri G, Kriouile Y, Gorokhova S, Bartoli M, Saïle R, Barakat A, Krahn M. Rochdi K, et al. Among authors: da silva n. Clin Chim Acta. 2022 Jan 1;524:51-58. doi: 10.1016/j.cca.2021.11.020. Epub 2021 Nov 28. Clin Chim Acta. 2022. PMID: 34852264

4

A novel bi-allelic loss-of-function mutation in STIM1 expands the phenotype of STIM1-related diseases.

Salvi A, Skrypnyk C, Da Silva N, Urtizberea JA, Bakhiet M, Robert C, Lévy N, Megarbané A, Delague V, Bartoli M. Salvi A, et al. Among authors: da silva n. Clin Genet. 2021 Jul;100(1):84-89. doi: 10.1111/cge.13959. Epub 2021 Mar 29. Clin Genet. 2021. PMID: 33733462

5

Splicing impact of deep exonic missense variants in CAPN3 explored systematically by minigene functional assay.

Dionnet E, Defour A, Da Silva N, Salvi A, Lévy N, Krahn M, Bartoli M, Puppo F, Gorokhova S. Dionnet E, et al. Among authors: da silva n. Hum Mutat. 2020 Oct;41(10):1797-1810. doi: 10.1002/humu.24083. Epub 2020 Jul 27. Hum Mutat. 2020. PMID: 32668095

6

Novel Exon-Skipping Therapeutic Approach for the DMD Gene Based on Asymptomatic Deletions of Exon 49.

Abaji M, Gorokhova S, Da Silva N, Busa T, Grelet M, Missirian C, Sigaudy S, Philip N, Leturcq F, Lévy N, Krahn M, Bartoli M. Abaji M, et al. Among authors: da silva n. Genes (Basel). 2022 Jul 19;13(7):1277. doi: 10.3390/genes13071277. Genes (Basel). 2022. PMID: 35886062 Free PMC article.

7

Truncated prelamin A expression in HGPS-like patients: a transcriptional study.

Barthélémy F, Navarro C, Fayek R, Da Silva N, Roll P, Sigaudy S, Oshima J, Bonne G, Papadopoulou-Legbelou K, Evangeliou AE, Spilioti M, Lemerrer M, Wevers RA, Morava E, Robaglia-Schlupp A, Lévy N, Bartoli M, De Sandre-Giovannoli A. Barthélémy F, et al. Among authors: da silva n. 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.

8

Towards plant resistance to viruses using protein-only RNase P.

Gobert A, Quan Y, Arrivé M, Waltz F, Da Silva N, Jomat L, Cohen M, Jupin I, Giegé P. Gobert A, et al. Among authors: da silva n. Nat Commun. 2021 Feb 12;12(1):1007. doi: 10.1038/s41467-021-21338-6. Nat Commun. 2021. PMID: 33579946 Free PMC article.

9

Mechanisms of myostatin and activin A accumulation in chronic kidney disease.

Bataille S, Dou L, Bartoli M, Sallée M, Aniort J, Ferkak B, Chermiti R, McKay N, Da Silva N, Burtey S, Poitevin S. Bataille S, et al. Among authors: da silva n. Nephrol Dial Transplant. 2022 Jun 23;37(7):1249-1260. doi: 10.1093/ndt/gfac136. Nephrol Dial Transplant. 2022. PMID: 35333341

10

First characterization of congenital myasthenic syndrome type 5 in North Africa.

Khaoula R, Cerino M, Da Silva N, Delague V, Nahili H, Kriouile Y, Gorokhova S, Bartoli M, Saïle R, Barakat A, Krahn M. Khaoula R, et al. Among authors: da silva n. Mol Biol Rep. 2021 Oct;48(10):6999-7006. doi: 10.1007/s11033-021-06530-7. Epub 2021 Sep 22. Mol Biol Rep. 2021. PMID: 34553317 Free article.

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