Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rachida Bouarich"'
Autor:
María-Jesús Lobón-Iglesias, Mamy Andrianteranagna, Zhi-Yan Han, Céline Chauvin, Julien Masliah-Planchon, Valeria Manriquez, Arnault Tauziede-Espariat, Sandrina Turczynski, Rachida Bouarich-Bourimi, Magali Frah, Christelle Dufour, Thomas Blauwblomme, Liesbeth Cardoen, Gaelle Pierron, Laetitia Maillot, Delphine Guillemot, Stéphanie Reynaud, Christine Bourneix, Célio Pouponnot, Didier Surdez, Mylene Bohec, Sylvain Baulande, Olivier Delattre, Eliane Piaggio, Olivier Ayrault, Joshua J. Waterfall, Nicolas Servant, Kevin Beccaria, Volodia Dangouloff-Ros, Franck Bourdeaut
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-21 (2023)
Abstract Atypical teratoid rhabdoid tumors (ATRT) are divided into MYC, TYR and SHH subgroups, suggesting diverse lineages of origin. Here, we investigate the imaging of human ATRT at diagnosis and the precise anatomic origin of brain tumors in the R
Externí odkaz:
https://doaj.org/article/6d882cd6286a4142b5077b07cc2ff82d
Autor:
Bujamin H. Vokshi, Guillaume Davidson, Nassim Tawanaie Pour Sedehi, Alexandra Helleux, Marc Rippinger, Alexandre R. Haller, Justine Gantzer, Jonathan Thouvenin, Philippe Baltzinger, Rachida Bouarich, Valeria Manriquez, Sakina Zaidi, Priya Rao, Pavlos Msaouel, Xiaoping Su, Hervé Lang, Thibault Tricard, Véronique Lindner, Didier Surdez, Jean-Emmanuel Kurtz, Franck Bourdeaut, Nizar M. Tannir, Irwin Davidson, Gabriel G. Malouf
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-19 (2023)
Abstract Renal medullary carcinoma (RMC) is an aggressive tumour driven by bi-allelic loss of SMARCB1 and tightly associated with sickle cell trait. However, the cell-of-origin and oncogenic mechanism remain poorly understood. Using single-cell seque
Externí odkaz:
https://doaj.org/article/01f90a34514d4d2a88792568e2a609ad
Autor:
Iva Simeonova, Sara Jaber, Irena Draskovic, Boris Bardot, Ming Fang, Rachida Bouarich-Bourimi, Vincent Lejour, Laure Charbonnier, Claire Soudais, Jean-Christophe Bourdon, Michel Huerre, Arturo Londono-Vallejo, Franck Toledo
Publikováno v:
Cell Reports, Vol 3, Iss 6, Pp 2046-2058 (2013)
Mutations in p53, although frequent in human cancers, have not been implicated in telomere-related syndromes. Here, we show that homozygous mutant mice expressing p53Δ31, a p53 lacking the C-terminal domain, exhibit increased p53 activity and suffer
Externí odkaz:
https://doaj.org/article/686d4f67f2fc40f1a5ee582240159315
Autor:
Iva Simeonova, Vincent Lejour, Boris Bardot, Rachida Bouarich-Bourimi, Aurélie Morin, Ming Fang, Laure Charbonnier, Franck Toledo
Publikováno v:
PLoS Genetics, Vol 8, Iss 6, p e1002731 (2012)
Evolutionary forces that shape regulatory networks remain poorly understood. In mammals, the Rb pathway is a classic example of species-specific gene regulation, as a germline mutation in one Rb allele promotes retinoblastoma in humans, but not in mi
Externí odkaz:
https://doaj.org/article/1d8fff3c538b4d53a41141e9eb573efc
Autor:
Nausica Arnoult, Caroline Schluth-Bolard, Anne Letessier, Irena Drascovic, Rachida Bouarich-Bourimi, Judith Campisi, Sahn-Ho Kim, Amina Boussouar, Alexandre Ottaviani, Frédérique Magdinier, Eric Gilson, Arturo Londoño-Vallejo
Publikováno v:
PLoS Genetics, Vol 6, Iss 4, p e1000920 (2010)
The mechanisms governing telomere replication in humans are still poorly understood. To fill this gap, we investigated the timing of replication of single telomeres in human cells. Using in situ hybridization techniques, we have found that specific t
Externí odkaz:
https://doaj.org/article/3e341172847d40159be7b61dc626ac57
Autor:
Thibault Passeri, Ahmed Dahmani, Julien Masliah-Planchon, Adnan Naguez, Marine Michou, Rania El Botty, Sophie Vacher, Rachida Bouarich, André Nicolas, Marc Polivka, Coralie Franck, Anne Schnitzler, Fariba Némati, Sergio Roman-Roman, Franck Bourdeaut, Homa Adle-Biassette, Hamid Mammar, Sébastien Froelich, Ivan Bièche, Didier Decaudin
Publikováno v:
Cancers; Volume 14; Issue 6; Pages: 1486
Chordomas are rare neoplasms characterized by a high recurrence rate and a poor long-term prognosis. Considering their chemo-/radio-resistance, alternative treatment strategies are strongly required, but their development is limited by the paucity of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f1ba449dc4f69b0c9caa743fb998e27
Autor:
Bujamin Vokshi, Guillaume Davidson, Alexandra Helleux, Marc Rippinger, Alexandre Haller, Justine Gantzer, Philippe Baltzinger, Jonathan Thouvenin, Rachida Bouarich-Bourimi, Valentina Manriquez, Sakina Zaidi, Pavlos Msaouel, Xiaoping Su, Hervé Lang, Thibault Tricard, Véronique Lindner, Didier Surdez, Jean-Emmanuel Kurtz, Franck BOURDEAUT, Nizar Tannir, Irwin Davidson, Gabriel Malouf
Renal medullary carcinoma (RMC) is an aggressive tumour driven by bi-allelic loss of SMARCB1 and tightly associated with sickle cell trait. However, the cell-of-origin and oncogenic mechanism remain poorly understood. Using single-cell sequencing of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf5a58b6653320a21103a472808302ca
https://doi.org/10.21203/rs.3.rs-1178801/v1
https://doi.org/10.21203/rs.3.rs-1178801/v1
Autor:
Thibault Passeri, Ahmed Dahmani, Julien Masliah-Planchon, Adnan Naguez, Marine Michou, Rania El-Botty, Sophie Vacher, Rachida Bouarich, André Nicolas, Marc Polivka, Coralie Franck, Anne Schnitzler, Fariba Némati, Sergio Roman-Roman, Franck Bourdeaut, Homa Adle-Biassette, Hamid Mammar, Sébastien Froelich, Ivan Bièche, Didier Decaudin
Publikováno v:
Cancer Research. 82:LB567-LB567
Background: Chordomas are considered as rare bone neoplasms characterized by a high level of recurrence and a poor long-term prognosis. Considering their chemo-radio-resistance, alternative treatment strategies are therefore strongly requested, but t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e9ad7db3a49b24bcdf4100923ce17a9
https://doi.org/10.1158/1538-7445.am2022-lb567
https://doi.org/10.1158/1538-7445.am2022-lb567
Autor:
Maria Lobon-Iglesias, Mamy Andrianteranagna, Zhi-Yan Han, Julien Masliah-Planchon, Arnault Tauziede-Espariat, Magali Frah, Christelle Dufour, Celine Chauvin, Rachida Bouarich, Valeria Manriquez, Sandrina Turczinski, Olivier Delattre, Sylvain Baulande, Olivier Ayrault, Nicolas Servant, Kevin Beccaria, Volodia Dangouloff-Ros, Franck Bourdeaut
Publikováno v:
Neuro-Oncology. 24:i5-i5
Atypical teratoid rhabdoid tumors (ATRT) are divided in three molecular subgroups, the so-called MYC, TYR and SHH subgroups. This heterogeneity suggests some diversity in the cells of origin, which remain hypothetical thus far. A careful radiological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b2304ec4c839a19e340247d43c6aa49
https://doi.org/10.1093/neuonc/noac079.010
https://doi.org/10.1093/neuonc/noac079.010
Autor:
Sara Jaber, Ming Fang, Michel Huerre, Boris Bardot, Laure Charbonnier, Claire Soudais, Franck Toledo, Rachida Bouarich-Bourimi, Jean-Christophe Bourdon, Iva Simeonova, Irena Draskovic, Vincent Lejour, Arturo Londoño-Vallejo
Publikováno v:
Cell Reports
Cell Reports, Elsevier Inc, 2013, 3 (6), pp.2046-2058. ⟨10.1016/j.celrep.2013.05.028⟩
Cell Reports, 2013, 3 (6), pp.2046-2058. ⟨10.1016/j.celrep.2013.05.028⟩
Cell Reports, Elsevier Inc, 2013, 3 (6), pp.2046-2058. 〈10.1016/j.celrep.2013.05.028〉
Cell Reports, Vol 3, Iss 6, Pp 2046-2058 (2013)
Cell Reports, Elsevier Inc, 2013, 3 (6), pp.2046-2058. ⟨10.1016/j.celrep.2013.05.028⟩
Cell Reports, 2013, 3 (6), pp.2046-2058. ⟨10.1016/j.celrep.2013.05.028⟩
Cell Reports, Elsevier Inc, 2013, 3 (6), pp.2046-2058. 〈10.1016/j.celrep.2013.05.028〉
Cell Reports, Vol 3, Iss 6, Pp 2046-2058 (2013)
International audience; Mutations in p53, although frequent in human cancers , have not been implicated in telomere-related syndromes. Here, we show that homozygous mutant mice expressing p53 D31 , a p53 lacking the C-terminal domain, exhibit increas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eb34a68d35a8c64c7bbff5c8041f82d