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Page 1
Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation.
Dangoumau A, Marouillat S, Coelho R, Wurmser F, Brulard C, Haouari S, Laumonnier F, Corcia P, Andres CR, Blasco H, Vourc'h P. Dangoumau A, et al. Among authors: brulard c. Int J Mol Sci. 2021 Feb 11;22(4):1796. doi: 10.3390/ijms22041796. Int J Mol Sci. 2021. PMID: 33670299 Free PMC article.
Mutation in the RRM2 domain of TDP-43 in Amyotrophic Lateral Sclerosis with rapid progression associated with ubiquitin positive aggregates in cultured motor neurons.
Maurel C, Madji-Hounoum B, Thepault RA, Marouillat S, Brulard C, Danel-Brunaud V, Camdessanche JP, Blasco H, Corcia P, Andres CR, Vourc'h P. Maurel C, et al. Among authors: brulard c. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Feb;19(1-2):149-151. doi: 10.1080/21678421.2017.1349152. Epub 2017 Jul 13. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 28705014
Typical bulbar ALS can be linked to GARS mutation.
Corcia P, Brulard C, Beltran S, Marouillat S, Bakkouche SE, Andres CR, Blasco H, Vourc'h P. Corcia P, et al. Among authors: brulard c. Amyotroph Lateral Scler Frontotemporal Degener. 2019 May;20(3-4):275-277. doi: 10.1080/21678421.2018.1556699. Epub 2019 Jan 20. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 30661401
Effect of familial clustering in the genetic screening of 235 French ALS families.
Corcia P, Camu W, Brulard C, Marouillat S, Couratier P, Camdessanché JP, Cintas P, Verschueren A, Soriani MH, Desnuelle C, Fleury MC, Guy N, Cassereau J, Viader F, Pittion-Vouyovitch S, Danel V, Kolev I, Le Masson G, Beltran S, Salachas F, Bernard E, Pradat PF, Blasco H, Lanznaster D, Hergesheimer R, Laumonnier F, Andres CR, Meininger V, Vourc'h P. Corcia P, et al. Among authors: brulard c. J Neurol Neurosurg Psychiatry. 2021 May;92(5):479-484. doi: 10.1136/jnnp-2020-325064. Epub 2021 Jan 6. J Neurol Neurosurg Psychiatry. 2021. PMID: 33408239
A novel mutation in the transmembrane 6 domain of GABBR2 leads to a Rett-like phenotype.
Vuillaume ML, Jeanne M, Xue L, Blesson S, Denommé-Pichon AS, Alirol S, Brulard C, Colin E, Isidor B, Gilbert-Dussardier B, Odent S, Parent P, Donnart A, Redon R, Bézieau S, Rondard P, Laumonnier F, Toutain A. Vuillaume ML, et al. Among authors: brulard c. Ann Neurol. 2018 Feb;83(2):437-439. doi: 10.1002/ana.25155. Epub 2018 Feb 7. Ann Neurol. 2018. PMID: 29369404 Free article. No abstract available.
A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression.
Liu J, Ottaviani D, Sefta M, Desbrousses C, Chapeaublanc E, Aschero R, Sirab N, Lubieniecki F, Lamas G, Tonon L, Dehainault C, Hua C, Fréneaux P, Reichman S, Karboul N, Biton A, Mirabal-Ortega L, Larcher M, Brulard C, Arrufat S, Nicolas A, Elarouci N, Popova T, Némati F, Decaudin D, Gentien D, Baulande S, Mariani O, Dufour F, Guibert S, Vallot C, Rouic LL, Matet A, Desjardins L, Pascual-Pasto G, Suñol M, Catala-Mora J, Llano GC, Couturier J, Barillot E, Schaiquevich P, Gauthier-Villars M, Stoppa-Lyonnet D, Golmard L, Houdayer C, Brisse H, Bernard-Pierrot I, Letouzé E, Viari A, Saule S, Sastre-Garau X, Doz F, Carcaboso AM, Cassoux N, Pouponnot C, Goureau O, Chantada G, de Reyniès A, Aerts I, Radvanyi F. Liu J, et al. Among authors: brulard c. Nat Commun. 2021 Sep 22;12(1):5578. doi: 10.1038/s41467-021-25792-0. Nat Commun. 2021. PMID: 34552068 Free PMC article.
Recurrent TRIO Fusion in Nontranslocation-Related Sarcomas.
Delespaul L, Lesluyes T, Pérot G, Brulard C, Lartigue L, Baud J, Lagarde P, Le Guellec S, Neuville A, Terrier P, Vince-Ranchère D, Schmidt S, Debant A, Coindre JM, Chibon F. Delespaul L, et al. Among authors: brulard c. Clin Cancer Res. 2017 Feb 1;23(3):857-867. doi: 10.1158/1078-0432.CCR-16-0290. Epub 2016 Aug 15. Clin Cancer Res. 2017. PMID: 27528700
24 results