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A Genome-Wide CRISPR-Cas9 Screen Identifies the Dolichol-Phosphate Mannose Synthase Complex as a Host Dependency Factor for Dengue Virus Infection.
Labeau A, Simon-Loriere E, Hafirassou ML, Bonnet-Madin L, Tessier S, Zamborlini A, Dupré T, Seta N, Schwartz O, Chaix ML, Delaugerre C, Amara A, Meertens L. Labeau A, et al. Among authors: seta n. J Virol. 2020 Mar 17;94(7):e01751-19. doi: 10.1128/JVI.01751-19. Print 2020 Mar 17. J Virol. 2020. PMID: 31915280 Free PMC article.
[Inherited disorders of protein glycosylation].
Dupré T, Lavieu G, Moore S, Seta N; Réseau de recherche sur les CDG I Inserm/AFM (4MR39F). Dupré T, et al. Among authors: seta n. Med Sci (Paris). 2004 Mar;20(3):331-8. doi: 10.1051/medsci/2004203331. Med Sci (Paris). 2004. PMID: 15067579 Free article. Review. French.
Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations.
Dupré T, Vuillaumier-Barrot S, Chantret I, Sadou Yayé H, Le Bizec C, Afenjar A, Altuzarra C, Barnérias C, Burglen L, de Lonlay P, Feillet F, Napuri S, Seta N, Moore SE. Dupré T, et al. Among authors: seta n. J Med Genet. 2010 Nov;47(11):729-35. doi: 10.1136/jmg.2009.072504. Epub 2010 Aug 2. J Med Genet. 2010. PMID: 20679665 Free article.
Complementarity of electrophoretic, mass spectrometric, and gene sequencing techniques for the diagnosis and characterization of congenital disorders of glycosylation.
Bruneel A, Cholet S, Drouin-Garraud V, Jacquemont ML, Cano A, Mégarbané A, Ruel C, Cheillan D, Dupré T, Vuillaumier-Barrot S, Seta N, Fenaille F. Bruneel A, et al. Among authors: seta n. Electrophoresis. 2018 Dec;39(24):3123-3132. doi: 10.1002/elps.201800021. Epub 2018 Jul 3. Electrophoresis. 2018. PMID: 29869806
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.
Ng BG, Sosicka P, Fenaille F, Harroche A, Vuillaumier-Barrot S, Porterfield M, Xia ZJ, Wagner S, Bamshad MJ, Vergnes-Boiteux MC, Cholet S, Dalton S, Dell A, Dupré T, Fiore M, Haslam SM, Huguenin Y, Kumagai T, Kulik M, McGoogan K, Michot C, Nickerson DA, Pascreau T, Borgel D, Raymond K, Warad D; University of Washington Center for Mendelian Genomics (UW-CMG); Flanagan-Steet H, Steet R, Tiemeyer M, Seta N, Bruneel A, Freeze HH. Ng BG, et al. Among authors: seta n. Am J Hum Genet. 2021 Jun 3;108(6):1040-1052. doi: 10.1016/j.ajhg.2021.04.013. Epub 2021 May 7. Am J Hum Genet. 2021. PMID: 33964207 Free PMC article.
A new insight into PMM2 mutations in the French population.
Le Bizec C, Vuillaumier-Barrot S, Barnier A, Dupré T, Durand G, Seta N. Le Bizec C, et al. Among authors: seta n. Hum Mutat. 2005 May;25(5):504-5. doi: 10.1002/humu.9336. Hum Mutat. 2005. PMID: 15844218
Expanding the Spectrum of PMM2-CDG Phenotype.
Vuillaumier-Barrot S, Isidor B, Dupré T, Le Bizec C, David A, Seta N. Vuillaumier-Barrot S, et al. Among authors: seta n. JIMD Rep. 2012;5:123-5. doi: 10.1007/8904_2011_114. Epub 2011 Dec 25. JIMD Rep. 2012. PMID: 23430927 Free PMC article.
178 results