Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Camille Grison"'
Autor:
Zhi-Yan Han, Wilfrid Richer, Paul Fréneaux, Céline Chauvin, Carlo Lucchesi, Delphine Guillemot, Camille Grison, Delphine Lequin, Gaelle Pierron, Julien Masliah-Planchon, André Nicolas, Dominique Ranchère-Vince, Pascale Varlet, Stéphanie Puget, Isabelle Janoueix-Lerosey, Olivier Ayrault, Didier Surdez, Olivier Delattre, Franck Bourdeaut
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
SMARCB1 inactivation is prevalent in human atypical teratoid/rhabdoid tumours but a mouse model that accurately phenocopies the human disease is lacking. Here, the authors show that inactivation of SMARCB1between E6 and E10 in mice results in tumours
Externí odkaz:
https://doaj.org/article/db7502ce51b84400a57d9b5dd944a70e
Autor:
Noé Palmic, Joël Acker, Pascale Lesage, Christine Conesa, Rachid Menouni, Amandine Bonnet, Hélène Fayol, Camille Grison, Amna Asif-Laidin, Indranil Adhya
SUMMARYIntegration of transposable elements into the genome is mutagenic. Mechanisms that target integration into relatively safe locations and minimize deleterious consequences for cell fitness have emerged during evolution. In budding yeast, the in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a84d2596ca0c3f9c58894f500e0368c6
https://doi.org/10.1101/2019.12.18.879569
https://doi.org/10.1101/2019.12.18.879569
Autor:
Julia Cruz, Jorge Campos, Virginie Chene, Gaëlle Pierron, Javier Lavernia, Antonio Llombart-Bosch, Camille Grison, Luis Rubio, Isidro Machado, María Barrios, Olivier Delattre
Publikováno v:
Virchows Archiv. 463:837-842
The present study describes a new case of EWSR1-negative undifferentiated sarcoma with CIC/DUX4 gene fusion. This case is similar to tumors described as primitive undifferentiated round cell sarcomas that occur mainly in the trunk and display an aggr
Autor:
Jacques Grill, Franck Bourdeaut, Camille Grison, Catherine Miquel, Wilfrid Richer, Clémentine Krucker, Gaëlle Pierron, François Radvanyi, Laurence Brugières, Michel Zerah, Olivier Delattre, Jeanne Amiel
Publikováno v:
Pediatric Blood & Cancer. 61:383-386
Medulloblastomas (MB) are classified in four subgroups: the well defined WNT and Sonic Hedgehog (SHH) subgroups, and the less defined groups 3 and 4. They occasionally occur in the context of a cancer predisposition syndrome. While germline APC mutat
Autor:
Annie Laquerrière, Wilfrid Richer, Olivier Delattre, Jérôme Couturier, François Doz, Sophie Michalak, Camille Grison, Claude-Alain Maurage, Alexandre Vasiljevic, Catherine Miquel, Marie-Bernadette Delisle, Franck Bourdeaut, Gaëlle Pierron, Dominique Figarella-Branger
Publikováno v:
Cancer Genetics. 206:124-129
As prognostic factors, MYC and MYCN amplifications are routinely assessed in medulloblastomas. Fluorescence in situ hybridization (FISH) is currently considered as the technique of reference. Recently, array comparative genomic hybridization (aCGH) h
Autor:
Annick Sevely, Franck Bourdeaut, Christelle Dufour, Camille Grison, Marie Bernadette Delisle, Anne Isabelle Bertozzi, Torsten Pietsch, Nicolas Sevenet, Delphine Lafon, Najat Loukh, Catherine Miquel, Aurore Siegfried
Publikováno v:
Clinical Neuropathology
The aim of this study was to better define the clinical and biopathological features of patients with desmoplastic/nodular medulloblastoma (DNMB) and to further characterize this subgroup. 17 children aged < 5 years, with initial DNMB treated accordi
Autor:
André Nicolas, Wilfrid Richer, Camille Grison, Paul Fréneaux, Olivier Delattre, Céline Chauvin, Olivier Ayrault, Gaëlle Pierron, Dominique Ranchère-Vince, Delphine Guillemot, Delphine Lequin, Franck Bourdeaut, Stéphanie Puget, Julien Masliah-Planchon, Pascale Varlet, Carlo Lucchesi, Didier Surdez, Isabelle Janoueix-Lerosey, Zhi-Yan Han
Publikováno v:
Nature Communications
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
Rhabdoid tumours (RTs) are highly aggressive tumours of infancy, frequently localized in the central nervous system (CNS) where they are termed atypical teratoid/rhabdoid tumours (AT/RTs) and characterized by bi-allelic inactivation of the SMARCB1 tu
Autor:
Pascale Soyeux, J. Moroch, Annick Vieillefond, Gaëlle Pierron, Julien Calderaro, Florence Pedeutour, Yves Allory, Jérôme Couturier, Pascale Maillé, Camille Grison, Olivier Delattre, Marie Christine Rousselet, Alexandre de la Taille
Publikováno v:
Histopathology. 61:428-435
Calderaro J, Moroch J, Pierron G, Pedeutour F, Grison C, Maille P, Soyeux P, de la Taille A, Couturier J, Vieillefond A, Rousselet M C, Delattre O & Allory Y (2012) Histopathology 61, 428–435 SMARCB1/INI1 inactivation in renal medullary carcinoma A
Autor:
Franck, Bourdeaut, Catherine, Miquel, Wilfrid, Richer, Jacques, Grill, Michel, Zerah, Camille, Grison, Gaelle, Pierron, Jeanne, Amiel, Clementine, Krucker, Francois, Radvanyi, Laurence, Brugieres, Olivier, Delattre
Publikováno v:
Pediatric bloodcancer. 61(2)
Medulloblastomas (MB) are classified in four subgroups: the well defined WNT and Sonic Hedgehog (SHH) subgroups, and the less defined groups 3 and 4. They occasionally occur in the context of a cancer predisposition syndrome. While germline APC mutat
Autor:
Julien, Calderaro, Julien, Moroch, Gaelle, Pierron, Florence, Pedeutour, Camille, Grison, Pascale, Maillé, Pascale, Soyeux, Alexandre, de la Taille, Jérome, Couturier, Annick, Vieillefond, Marie Christine, Rousselet, Olivier, Delattre, Yves, Allory
Publikováno v:
Histopathology. 61(3)
Renal medullary carcinoma (RMC), a rare and highly aggressive tumour which occurs in patients with sickle-cell disease, shares many clinicopathological features with collecting duct carcinoma (CDC). The molecular mechanisms underlying RMC and CDC are