Fany Bourgois-Rocha
Overview
Explore the profile of Fany Bourgois-Rocha including associated specialties, affiliations and a list of published articles.
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7
Citations
319
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Recent Articles
1.
Hakibilen C, Delort F, Daher M, Joanne P, Cabet E, Cardoso O, et al.
Front Cell Dev Biol
. 2022 Mar;
10:783724.
PMID: 35350386
Cellular adhesion and migration are key functions that are disrupted in numerous diseases. We report that desmin, a type-III muscle-specific intermediate filament, is a novel cell adhesion regulator. Expression of...
2.
Delort F, Segard B, Hakibilen C, Bourgois-Rocha F, Cabet E, Vicart P, et al.
Exp Cell Res
. 2019 Aug;
383(2):111539.
PMID: 31369751
Desminopathies are a type of myofibrillar myopathy resulting from mutations in DES, encoding the intermediate filament protein desmin. They display heterogeneous phenotypes, suggesting environment influences. Patient muscle proteins show oxidative...
3.
Lopes C, Aubert S, Bourgois-Rocha F, Barnat M, Rego A, Deglon N, et al.
PLoS One
. 2016 Feb;
11(2):e0148680.
PMID: 26863614
Mutations of the huntingtin protein (HTT) gene underlie both adult-onset and juvenile forms of Huntington's disease (HD). HTT modulates mitotic spindle orientation and cell fate in mouse cortical progenitors from...
4.
Drouet V, Ruiz M, Zala D, Feyeux M, Auregan G, Cambon K, et al.
PLoS One
. 2014 Jun;
9(6):e99341.
PMID: 24926995
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder resulting from polyglutamine expansion in the huntingtin (HTT) protein and for which there is no cure. Although suppression of both wild...
5.
Nicoleau C, Varela C, Bonnefond C, Maury Y, Bugi A, Aubry L, et al.
Stem Cells
. 2013 Jul;
31(9):1763-74.
PMID: 23818270
Wnt-ligands are among key morphogens that mediate patterning of the anterior territories of the developing brain in mammals. We qualified the role of Wnt-signals in regional specification and subregional organization...
6.
Feyeux M, Bourgois-Rocha F, Redfern A, Giles P, Lefort N, Aubert S, et al.
Hum Mol Genet
. 2012 Jun;
21(17):3883-95.
PMID: 22678061
Huntington's disease (HD) is characterized by a late clinical onset despite ubiquitous expression of the mutant gene at all developmental stages. How mutant huntingtin impacts on signalling pathways in the...
7.
Chamberlain S, Chen P, Ng K, Bourgois-Rocha F, Lemtiri-Chlieh F, Levine E, et al.
Proc Natl Acad Sci U S A
. 2010 Sep;
107(41):17668-73.
PMID: 20876107
Angelman syndrome (AS) and Prader-Willi syndrome (PWS) are neurodevelopmental disorders of genomic imprinting. AS results from loss of function of the ubiquitin protein ligase E3A (UBE3A) gene, whereas the genetic...