日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Nanopore sequencing as a cutting-edge technology for medulloblastoma classification.

纳米孔测序作为髓母细胞瘤分类的前沿技术

Filser Mathilde, Torrejon Jacob, Merchadou Kevin, Dufour Christelle, Girard Elodie, Bourneix Christine, Lemaître Elisa, Gharsalli Tarek, Brillet Riwan, Wong Jennifer, Gentien David, Rapinat Audrey, Servant Nicolas, Vasiljevic Alexandre, Bertozzi Anne Isabelle, Raimbault Sandra, Tauziede Espariat Arnault, Lhermitte Benoit, Faure-Conter Cécile, Icher Céline, Berger Claire, Maurage Claude Alain, Bodet Damien, Meyronet David, Uro-Coste Emmanuelle, De Carli Emilie, Forest Fabien, Palenzuela Gilles, Chotard Guillaume, Gauchotte Guillaume, Sudour Helene, Mansuy Ludovic, Deparis Marianna, Tallegas Matthias, Faisant Maxime, Entz-Werle Natacha, Varlet Pascale, Leblond Pierre, Michalak-Provost Sophie, Proust Houdemont Stéphanie, Rigau Valérie, Doz François, Delattre Olivier, Bourdeaut Franck, Ayrault Olivier, Masliah-Planchon Julien

A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript

BRCA1 基因的创始外显子重复,其断点位于 T2T 参考基因组特异性区域,导致产生构成性融合转录本。

Schwartz, Mathias; Filser, Mathilde; Merchadou, Kevin; Lemaitre, Elisa; Abidallah, Khadija; Tenreiro, Henrique; Dubois D'enghien, Catherine; Rapinat, Audrey; Pierre-Noel, Elise; Suybeng, Voreak; Espenel, Marion; Baulande, Sylvain; Adams, Séverine; Remenieras, Audrey; Renaud, Crystal; Aucouturier, Camille; Delnatte, Capucine; Garrec, Céline; Renault, Victor; Golmard, Lisa; Fourme, Emmanuelle; Masliah-Planchon, Julien; Caputo, Sandrine M

Author Correction: A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript

作者更正:BRCA1 基因创始人外显子重复导致 T2T 参考基因组特异性区域断点,从而产生构成性融合转录本。

Schwartz, Mathias; Filser, Mathilde; Merchadou, Kevin; Lemaitre, Elisa; Abidallah, Khadija; Tenreiro, Henrique; Dubois D'enghien, Catherine; Rapinat, Audrey; Pierre-Noel, Elise; Suybeng, Voreak; Espenel, Marion; Baulande, Sylvain; Adams, Séverine; Remenieras, Audrey; Renaud, Crystal; Aucouturier, Camille; Delnatte, Capucine; Garrec, Céline; Renault, Victor; Golmard, Lisa; Fourme, Emmanuelle; Masliah-Planchon, Julien; Caputo, Sandrine M

MDB-12. NANOPORE SEQUENCING AS A CUTTING-EDGE TECHNOLOGY FOR MEDULLOBLASTOMA CLASSIFICATION

MDB-12.纳米孔测序作为髓母细胞瘤分类的前沿技术

Zhou, Xiaoyu; Zhang, Jianli; Xu, Liwei; Jin, Aiyun; Filser, Mathilde; Torrejon, Jacob; Merchadou, Kevin; Girard, Elodie; Bourneix, Christine; Lemaître, Elisa; Brillet, Riwan; Wong, Jennifer; Gentien, David; Rapinat, Audrey; Servant, Nicolas; Vasiljevic, Alexandre; Bertozzi, Anne-Isabelle; Raimbault, Sandra; Tauziède-Espariat, Arnault; Lhermitte, Benoit; Faure-Conter, Cécile; Icher, Céline; Berger, Claire; Maurage, Claude-Alain; Bodet, Damien; Meyronet, David; Uro-Coste, Emmanuelle; De Carli, Emilie; Forest, Fabien; Palenzuela, Gilles; Chotard, Guillaume; Gauchotte, Guillaume; Sudour, Hélène; Mansuy, Ludovic; Deparis, Mariana; Machet, Marie-Christine; Faisant, Maxime; Entz-Werle, Natacha; Varlet, Pascale; Leblond, Pierre; Michalak-Provost, Sophie; Houdemont, Stéphanie Proust; Rigau, Valérie; Doz, François; Bourdeaut, Franck; Delattre, Olivier; Ayrault, Olivier; Masliah-Planchon, Julien

Intratumor CMS Heterogeneity Impacts Patient Prognosis in Localized Colon Cancer

肿瘤内CMS异质性影响局限性结肠癌患者的预后

Marisa, Laetitia; Blum, Yuna; Taieb, Julien; Ayadi, Mira; Pilati, Camilla; Le Malicot, Karine; Lepage, Côme; Salazar, Ramon; Aust, Daniela; Duval, Alex; Blons, Hélène; Taly, Valérie; Gentien, David; Rapinat, Audrey; Selves, Janick; Mouillet-Richard, Sophie; Boige, Valérie; Emile, Jean-François; de Reyniès, Aurélien; Laurent-Puig, Pierre

Decentralization of Next-Generation RNA Sequencing-Based MammaPrint® and BluePrint® Kit at University Hospitals Leuven and Curie Institute Paris

鲁汶大学医院和巴黎居里研究所的下一代RNA测序MammaPrint®和BluePrint®试剂盒的去中心化应用

Slembrouck, Laurence; Darrigues, Lauren; Laurent, Cecile; Mittempergher, Lorenza; Delahaye, Leonie Jmj; Vanden Bempt, Isabelle; Vander Borght, Sara; Vliegen, Liesbet; Sintubin, Petra; Raynal, Virginie; Bohec, Mylene; Reyes, Cécile; Rapinat, Audrey; Helsmoortel, Céline; Jongen, Lynn; Hoste, Griet; Neven, Patrick; Wildiers, Hans; Smeets, Ann; Nevelsteen, Ines; Punie, Kevin; Van Nieuwenhuysen, Els; Han, Sileny; Vincent Salomon, Anne; Laas Faron, Enora; Cynober, Timothé; Gentien, David; Baulande, Sylvain; Snel, Mireille Hj; Witteveen, Anke T; Neijenhuis, Sari; Glas, Annuska M; Reyal, Fabien; Floris, Giuseppe

Reference-free transcriptome exploration reveals novel RNAs for prostate cancer diagnosis

无需参考序列的转录组探索揭示了用于前列腺癌诊断的新型RNA

Pinskaya, Marina; Saci, Zohra; Gallopin, Mélina; Gabriel, Marc; Nguyen, Ha Tn; Firlej, Virginie; Descrimes, Marc; Rapinat, Audrey; Gentien, David; Taille, Alexandre de la; Londoño-Vallejo, Arturo; Allory, Yves; Gautheret, Daniel; Morillon, Antonin

Patient-derived xenografts recapitulate molecular features of human uveal melanomas.

患者来源的异种移植瘤重现了人类葡萄膜黑色素瘤的分子特征

Laurent Cécile, Gentien David, Piperno-Neumann Sophie, Némati Fariba, Nicolas André, Tesson Bruno, Desjardins Laurence, Mariani Pascale, Rapinat Audrey, Sastre-Garau Xavier, Couturier Jérôme, Hupé Philippe, de Koning Leanne, Dubois Thierry, Roman-Roman Sergio, Stern Marc-Henri, Barillot Emmanuel, Harbour J William, Saule Simon, Decaudin Didier

Sperm transcriptome profiling in oligozoospermia

少精症患者的精子转录组分析

Montjean, Debbie; De La Grange, Pierre; Gentien, David; Rapinat, Audrey; Belloc, Stéphanie; Cohen-Bacrie, Paul; Menezo, Yves; Benkhalifa, Moncef