Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Fany Bourgois-Rocha"'
Autor:
Coralie Hakibilen, Florence Delort, Marie-Thérèse Daher, Pierre Joanne, Eva Cabet, Olivier Cardoso, Fany Bourgois-Rocha, Cuixia Tian, Eloy Rivas, Marcos Madruga, Ana Ferreiro, Alain Lilienbaum, Patrick Vicart, Onnik Agbulut, Sylvie Hénon, Sabrina Batonnet-Pichon
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
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 p.R406W mutant desmin, identified in
Externí odkaz:
https://doaj.org/article/12b77063322b48c8ba1ebb36cdf0aadb
Autor:
Carla Lopes, Sophie Aubert, Fany Bourgois-Rocha, Monia Barnat, Ana Cristina Rego, Nicole Déglon, Anselme L Perrier, Sandrine Humbert
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0148680 (2016)
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 the ventricular zone. Using human emb
Externí odkaz:
https://doaj.org/article/804b5ee049234073876b67a25959889b
Autor:
Coralie Hakibilen, Florence Delort, Marie-Thérèse Daher, Pierre Joanne, Eva Cabet, Olivier Cardoso, Fany Bourgois-Rocha, Cuixia Tian, Eloy Rivas, Marcos Madruga, Ana Ferreiro, Alain Lilienbaum, Patrick Vicart, Onnik Agbulut, Sylvie Hénon, Sabrina Batonnet-Pichon
Publikováno v:
Frontiers in cell and developmental biology. 10
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 p.R406W mutant desmin, identified in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03def9f6e40dc5163a5740807cd849cd
https://pubmed.ncbi.nlm.nih.gov/35350386
https://pubmed.ncbi.nlm.nih.gov/35350386
Autor:
Valérie Drouet, Marta Ruiz, Diana Zala, Maxime Feyeux, Gwennaëlle Auregan, Karine Cambon, Laetitia Troquier, Johann Carpentier, Sophie Aubert, Nicolas Merienne, Fany Bourgois-Rocha, Raymonde Hassig, Maria Rey, Noëlle Dufour, Frédéric Saudou, Anselme L Perrier, Philippe Hantraye, Nicole Déglon
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e99341 (2014)
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 type and mutant HTT expression by R
Externí odkaz:
https://doaj.org/article/53fb4717c2244083b8f7184a75b42623
Autor:
Meng-Er Huang, Guilhem Clary, Sabrina Batonnet-Pichon, Florence Delort, Fany Bourgois-Rocha, Eva Cabet, Onnik Agbulut, Alain Lilienbaum, Coralie Hakibilen, Patrick Vicart, Bertrand-David Segard
Publikováno v:
Experimental Cell Research
Experimental Cell Research, Elsevier, 2019, 383 (2), pp.111539. ⟨10.1016/j.yexcr.2019.111539⟩
Experimental Cell Research, Elsevier, 2019, 383 (2), pp.111539. ⟨10.1016/j.yexcr.2019.111539⟩
International audience; 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 pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92d36c413405a3476fe717337b0b1a02
https://pubmed.ncbi.nlm.nih.gov/31369751
https://pubmed.ncbi.nlm.nih.gov/31369751
Autor:
Aurore Bugi, Christine Varela, Laetitia Aubry, Camille Nicoleau, Yves Maury, Fany Bourgois-Rocha, Pedro Viegas, Anselme L. Perrier, Marc Peschanski, Caroline Bonnefond
Publikováno v:
STEM CELLS
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 of the human telencephalon using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3c7aa2758848161f8cbca9c9df236f1
Autor:
Fouad Lemtiri-Chlieh, Stormy J. Chamberlain, Fany Bourgois-Rocha, Pin-Fang Chen, Marc Lalande, Khong Y. Ng, Eric S. Levine
Publikováno v:
Proceedings of the National Academy of Sciences. 107:17668-17673
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 defect in PWS is unknown. Althou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58126755004cd15e264b24115cf3cfc5
https://doi.org/10.1073/pnas.1004487107
https://doi.org/10.1073/pnas.1004487107
Autor:
Lesley Jones, Sophie Aubert, Nicole Déglon, Aurore Bugi, Peter Giles, Marta Ruiz, Fany Bourgois-Rocha, Anselme L. Perrier, Nathalie Lefort, Nicholas D. Allen, Marc Peschanski, Amanda Redfern, Caroline Bonnefond, Maxime Feyeux
Publikováno v:
Human molecular genetics. 21(17)
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 pre-symptomatic period has remained essentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d771fe5cd0c04b137d33df72d4470da2
https://pubmed.ncbi.nlm.nih.gov/22678061
https://pubmed.ncbi.nlm.nih.gov/22678061
Autor:
Raymonde Hassig, Diana Zala, Laetitia Troquier, Johann Carpentier, Maxime Feyeux, Sophie Aubert, Karine Cambon, Nicolas Merienne, Anselme L. Perrier, Maria Rey, Nicole Déglon, Gwennaelle Auregan, Fany Bourgois-Rocha, Valérie Drouet, Marta Ruiz, Frédéric Saudou, Noelle Dufour, Philippe Hantraye
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e99341 (2014)
PLoS ONE
PLoS ONE, 2014, 9 (6), pp.e99341. ⟨10.1371/journal.pone.0099341⟩
PLoS ONE, Public Library of Science, 2014, 9 (6), pp.e99341. ⟨10.1371/journal.pone.0099341⟩
Plos One, vol. 9, no. 6, pp. e99341
PloS one
PLoS ONE
PLoS ONE, 2014, 9 (6), pp.e99341. ⟨10.1371/journal.pone.0099341⟩
PLoS ONE, Public Library of Science, 2014, 9 (6), pp.e99341. ⟨10.1371/journal.pone.0099341⟩
Plos One, vol. 9, no. 6, pp. e99341
PloS one
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 type and mutant HTT expression by R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abf80f83973f20ca7735625d37ed68f5
https://doi.org/10.1371/journal.pone.0099341
https://doi.org/10.1371/journal.pone.0099341
Autor:
Drouet, Valérie1,2, Ruiz, Marta1,2, Zala, Diana3,4,5, Feyeux, Maxime6,7, Auregan, Gwennaëlle1,2, Cambon, Karine1,2, Troquier, Laetitia8, Carpentier, Johann1,2, Aubert, Sophie9, Merienne, Nicolas8, Bourgois-Rocha, Fany6,7, Hassig, Raymonde1,2, Rey, Maria8, Dufour, Noëlle1,2, Saudou, Frédéric3,4,5, Perrier, Anselme L.6,7, Hantraye, Philippe1,2, Déglon, Nicole1,2,8 nicole.deglon@chuv.ch
Publikováno v:
PLoS ONE. Jun2014, Vol. 9 Issue 6, p1-13. 13p.