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Page 1
Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett Syndrome.
Int J Mol Sci. 2021 Apr 21;22(9):4316. doi: 10.3390/ijms22094316.
Int J Mol Sci. 2021.
PMID: 33919253
Free PMC article.
[Unexpected link between Huntington disease and Rett syndrome].
Roux JC, Zala D, Panayotis N, Borges-Correia A, Saudou F, Villard L.
Roux JC, et al. Among authors: borges correia a.
Med Sci (Paris). 2012 Jan;28(1):44-6. doi: 10.1051/medsci/2012281016. Epub 2012 Jan 27.
Med Sci (Paris). 2012.
PMID: 22289830
Free article.
French.
No abstract available.
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Modification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathway.
Roux JC, Zala D, Panayotis N, Borges-Correia A, Saudou F, Villard L.
Roux JC, et al. Among authors: borges correia a.
Neurobiol Dis. 2012 Feb;45(2):786-95. doi: 10.1016/j.nbd.2011.11.002. Epub 2011 Nov 15.
Neurobiol Dis. 2012.
PMID: 22127389
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Morphological and functional alterations in the substantia nigra pars compacta of the Mecp2-null mouse.
Panayotis N, Pratte M, Borges-Correia A, Ghata A, Villard L, Roux JC.
Panayotis N, et al. Among authors: borges correia a.
Neurobiol Dis. 2011 Feb;41(2):385-97. doi: 10.1016/j.nbd.2010.10.006. Epub 2010 Oct 14.
Neurobiol Dis. 2011.
PMID: 20951208
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Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.
Milh M, Villeneuve N, Chouchane M, Kaminska A, Laroche C, Barthez MA, Gitiaux C, Bartoli C, Borges-Correia A, Cacciagli P, Mignon-Ravix C, Cuberos H, Chabrol B, Villard L.
Milh M, et al. Among authors: borges correia a.
Epilepsia. 2011 Oct;52(10):1828-34. doi: 10.1111/j.1528-1167.2011.03181.x. Epub 2011 Jul 19.
Epilepsia. 2011.
PMID: 21770924
Free article.
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A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome.
Matagne V, Ehinger Y, Saidi L, Borges-Correia A, Barkats M, Bartoli M, Villard L, Roux JC.
Matagne V, et al. Among authors: borges correia a.
Neurobiol Dis. 2017 Mar;99:1-11. doi: 10.1016/j.nbd.2016.12.009. Epub 2016 Dec 11.
Neurobiol Dis. 2017.
PMID: 27974239
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Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus.
Cacciagli P, Sutera-Sardo J, Borges-Correia A, Roux JC, Dorboz I, Desvignes JP, Badens C, Delepine M, Lathrop M, Cau P, Lévy N, Girard N, Sarda P, Boespflug-Tanguy O, Villard L.
Cacciagli P, et al. Among authors: borges correia a.
Am J Hum Genet. 2013 Sep 5;93(3):579-86. doi: 10.1016/j.ajhg.2013.07.023.
Am J Hum Genet. 2013.
PMID: 24011989
Free PMC article.
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