Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Julien Vibert"'
Autor:
Jean-Michel Coindre, Antoine Italiano, Maud Toulmonde, Alban Bessede, Florent Peyraud, Jean-Philippe Guégan, Lucile Vanhersecke, Julien Vibert, Mariella Spalato-Ceruso
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 11, Iss Suppl 2 (2023)
Externí odkaz:
https://doaj.org/article/a59f587325c94fa48399e8ad95506c8e
Autor:
Yassine Bouchoucha, Arnault Tauziède‐Espariat, Arnaud Gauthier, Delphine Guillemot, Dorian Bochaton, Julien Vibert, Matthieu Carton, Sarah Watson, Sandrine Grossetête, Chloé Quignot, Daniel Orbach, Nadège Corradini, Gudrun Schleiermacher, Franck Bourdeaut, Marie Simbozel, Christelle Dufour, Véronique Minard‐Colin, Mehdi Brahmi, Franck Tirode, Daniel Pissaloux, Marie Karanian, Marie‐Christine Machet, Julien Masliah‐Planchon, Olivier Delattre, Liesbeth Cardoen, Gaëlle Pierron, François Doz
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 8, Iss 3, Pp 217-232 (2022)
Abstract BCOR‐ITD tumours form an emerging family of aggressive entities with an internal tandem duplication (ITD) in the last exon of the BCOR gene. The family includes cerebral tumours, termed central nervous system BCOR‐ITD (CNS BCOR‐ITD), a
Externí odkaz:
https://doaj.org/article/e02a318f290e402595038192d567159c
Autor:
Julien Vibert, Sarah Watson
Publikováno v:
Cancers, Vol 14, Iss 10, p 2548 (2022)
Soft tissue sarcomas are malignant tumors of mesenchymal origin, encompassing a large spectrum of entities that were historically classified according to their histological characteristics. Over the last decades, molecular biology has allowed a bette
Externí odkaz:
https://doaj.org/article/9c0d6e595b824583bf266baee3096b17
Autor:
Younes Belkouchi, Hugues Talbot, Nathalie Lassau, Littisha Lawrance, Siham Farhane, Rahma Feki-Mkaouar, Joya Hadchiti, Lama Dawi, Julien Vibert, Paul-Henry Cournède, Clara Cousteix, Camille Mazza, Michele Kind, Antoine Italiano, Aurelien Marabelle, Samy Ammari, Stephane Champiat
Publikováno v:
Clinical Cancer Research. 29:1528-1534
Purpose: The objective of the study is to propose the immunotherapy progression decision (iPD) score, a practical tool based on patient features that are available at the first evaluation of immunotherapy treatment, to help oncologists decide whether
Autor:
Stephane Champiat, Samy Ammari, Aurelien Marabelle, Antoine Italiano, Michele Kind, Camille Mazza, Clara Cousteix, Paul-Henry Cournède, Julien Vibert, Lama Dawi, Joya Hadchiti, Rahma Feki-Mkaouar, Siham Farhane, Littisha Lawrance, Nathalie Lassau, Hugues Talbot, Younes Belkouchi
Radiological feature impact on survival. Radiological features include progression of target lesions > 20%, progression of non-target lesions > 50% and the emergence of new lesions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a4ef977c637fc3da83221f2b3740b23
https://doi.org/10.1158/1078-0432.22633108.v1
https://doi.org/10.1158/1078-0432.22633108.v1
Autor:
Stephane Champiat, Samy Ammari, Aurelien Marabelle, Antoine Italiano, Michele Kind, Camille Mazza, Clara Cousteix, Paul-Henry Cournède, Julien Vibert, Lama Dawi, Joya Hadchiti, Rahma Feki-Mkaouar, Siham Farhane, Littisha Lawrance, Nathalie Lassau, Hugues Talbot, Younes Belkouchi
Purpose:The objective of the study is to propose the immunotherapy progression decision (iPD) score, a practical tool based on patient features that are available at the first evaluation of immunotherapy treatment, to help oncologists decide whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3805ff29cc9e2616ab9a2edfaeeb31c
https://doi.org/10.1158/1078-0432.c.6533077
https://doi.org/10.1158/1078-0432.c.6533077
Autor:
Carine Ngo, Benjamin Verret, Julien Vibert, Sophie Cotteret, Antonin Levy, Cécile Le Pechoux, Leila Haddag‐Miliani, Charles Honore, Matthieu Faron, Fabien Quinquis, Axel Le Cesne, Jean‐Yves Scoazec, Gaëlle Pierron
Publikováno v:
Genes, chromosomescancerREFERENCES. 62(1)
Extraskeletal myxoid chondrosarcoma (EMC) is a rare soft tissue neoplasm of uncertain lineage characterized by the pathognomonic rearrangement of the NR4A3 gene, which in most cases is fused with EWSR1. Other NR4A3 fusion partners have been described
Autor:
Nadège Gruel, Chloé Quignot, Julien Vibert, Sylvie Bonvalot, Sophie El Zein, Dimitri Tzanis, Sylvain Baulande, Odette Mariani, Joshua Waterfall, Olivier Delattre, Sarah Watson
Publikováno v:
Cancer Research. 83:96-96
Introduction: Dedifferentiated liposarcomas (DDLPS) are the most frequent high-grade soft tissue sarcoma in adults. From a pathological point of view, these tumors are composed of high-grade undifferentiated tumor cells (DD), often showing an abrupt
Autor:
Yassine Bouchoucha, Arnault Tauziède‐Espariat, Arnaud Gauthier, Delphine Guillemot, Dorian Bochaton, Julien Vibert, Matthieu Carton, Sarah Watson, Sandrine Grossetête, Chloé Quignot, Daniel Orbach, Nadège Corradini, Gudrun Schleiermacher, Franck Bourdeaut, Marie Simbozel, Christelle Dufour, Véronique Minard‐Colin, Mehdi Brahmi, Franck Tirode, Daniel Pissaloux, Marie Karanian, Marie‐Christine Machet, Julien Masliah‐Planchon, Olivier Delattre, Liesbeth Cardoen, Gaëlle Pierron, François Doz
Publikováno v:
The journal of pathology. Clinical research. 8(3)
BCOR-ITD tumours form an emerging family of aggressive entities with an internal tandem duplication (ITD) in the last exon of the BCOR gene. The family includes cerebral tumours, termed central nervous system BCOR-ITD (CNS BCOR-ITD), and sarcomatous
Publikováno v:
Clinical Cancer Research. 28:IA009-IA009
Many cancers are characterized by gene fusions encoding oncogenic chimeric transcription factors (TFs) such as EWS::FLI1 in Ewing sarcoma (EwS). EWS::FLI1 induces a complete reprogramming of mesenchymal stem cells, the putative cell of origin of Ewin