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

Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.

白细胞中人类 E3 泛素连接酶 CBL 的体细胞缺陷会损害 B 细胞的发育和功能,但不会影响 T 细胞的发育和功能。

Vatovec Taja, Neehus Anna-Lena, Jackson Katherine J L, Avery Danielle T, Bagarić Ivan, Erazo Lucia, Arango-Franco Carlos A, Ogishi Masato, Ahmed Syed F, Cederholm Axel, Russell Amanda J, Della Mina Erika, Al-Rifai Dena, Bull Rowena, Buetow Lori, Sobrino Steicy, Zhang Allison, Wahlster Lara, Michelet Marine, Parvaneh Nima, Peel Jessica, Barzaghi Federica, Leardini Davide, Philippot Quentin, Saettini Francesco, Dutrieux Jacques, de Muylder Benedicte, Vendemini Francesca, Baccelli Francesco, Catala Albert, Gambineri Eleonora, Veltroni Marinella, Pandiarajan Vignesh, Aguilar Yurena, Haerynck Filomeen, Elliott Michael, Turville Stuart, Brillot Fabienne, Khan Taushif, Consonni Filippo, Berteloot Laureline, Sewell William A, Rao Geetha, Largeaud Laetitia, Conti Francesca, Roullion Cecile, Masson Cécile, Pegoraro Francesco, Ye Tianyi, Joubran Samantha, Villalpando Emily, Bessot Boris, Seeleuthner Yoann, Le Voyer Tom, Rosain Jérémie, Li Hailun, Janda Zarah, Muratore Edoardo, Soudée Camille, Delabesse Eric, Goulvestre Claire, Shahrooei Mohammad, Puel Anne, André Isabelle, Bole-Feysot Christine, Abel Laurent, Erlacher Miriam, Béziat Vivien, Lagresle-Peyrou Chantal, Cheynier Remi, Six Emmanuelle, Marr Nico, Pasquet Marlène, Alsina Laia, Goodnow Christopher C, Landegren Nils, Aiuti Alessandro, Zhang Peng, Masetti Riccardo, Huang Danny T, Ma Cindy S, Casanova Jean-Laurent, Sankaran Vijay G, Bustamante Jacinta, Tangye Stuart G, Bohlen Jonathan

Human oncostatin M deficiency underlies an inherited severe bone marrow failure syndrome.

人类抑癌素M缺乏症是遗传性严重骨髓衰竭综合征的根本原因

Garrigue Alexandrine, Kermasson Laëtitia, Susini Sandrine, Fert Ingrid, Mahony Christopher B, Sadek Hanem, Luce Sonia, Chouteau Myriam, Cavazzana Marina, Six Emmanuelle, Le Bousse-Kerdilès Marie-Caroline, Anginot Adrienne, Souraud Jean-Baptiste, Cormier-Daire Valérie, Willems Marjolaine, Sirvent Anne, Russello Jennifer, Callebaut Isabelle, André Isabelle, Bertrand Julien Y, Lagresle-Peyrou Chantal, Revy Patrick

Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation

白细胞性CBL杂合性缺失患者的自身炎症是由组成型ERK介导的单核细胞活化引起的。

Bohlen, Jonathan; Bagarić, Ivan; Vatovec, Taja; Ogishi, Masato; Ahmed, Syed F; Cederholm, Axel; Buetow, Lori; Sobrino, Steicy; Le Floc'h, Corentin; Arango-Franco, Carlos A; Seabra, Luis; Michelet, Marine; Barzaghi, Federica; Leardini, Davide; Saettini, Francesco; Vendemini, Francesca; Baccelli, Francesco; Catala, Albert; Gambineri, Eleonora; Veltroni, Marinella; Aguilar de la Red, Yurena; Rice, Gillian I; Consonni, Filippo; Berteloot, Laureline; Largeaud, Laetitia; Conti, Francesca; Roullion, Cécile; Masson, Cécile; Bessot, Boris; Seeleuthner, Yoann; Le Voyer, Tom; Rinchai, Darawan; Rosain, Jérémie; Neehus, Anna-Lena; Erazo-Borrás, Lucia; Li, Hailun; Janda, Zarah; Cho, En-Jui; Muratore, Edoardo; Soudée, Camille; Lainé, Candice; Delabesse, Eric; Goulvestre, Claire; Ma, Cindy S; Puel, Anne; Tangye, Stuart G; André, Isabelle; Bole-Feysot, Christine; Abel, Laurent; Erlacher, Miriam; Zhang, Shen-Ying; Béziat, Vivien; Lagresle-Peyrou, Chantal; Six, Emmanuelle; Pasquet, Marlène; Alsina, Laia; Aiuti, Alessandro; Zhang, Peng; Crow, Yanick J; Landegren, Nils; Masetti, Riccardo; Huang, Danny T; Casanova, Jean-Laurent; Bustamante, Jacinta

Clonal tracking in gene therapy patients reveals a diversity of human hematopoietic differentiation programs

基因治疗患者的克隆追踪揭示了人类造血分化程序的多样性

Six, Emmanuelle; Guilloux, Agathe; Denis, Adeline; Lecoules, Arnaud; Magnani, Alessandra; Vilette, Romain; Male, Frances; Cagnard, Nicolas; Delville, Marianne; Magrin, Elisa; Caccavelli, Laure; Roudaut, Cécile; Plantier, Clemence; Sobrino, Steicy; Gregg, John; Nobles, Christopher L; Everett, John K; Hacein-Bey-Abina, Salima; Galy, Anne; Fischer, Alain; Thrasher, Adrian J; André, Isabelle; Cavazzana, Marina; Bushman, Frederic D

Extensive multilineage analysis in patients with mixed chimerism after allogeneic transplantation for sickle cell disease: insight into hematopoiesis and engraftment thresholds for gene therapy

对接受异基因移植治疗镰状细胞病后出现混合嵌合体的患者进行广泛的多系分析:深入了解基因治疗的造血和植入阈值

Magnani, Alessandra; Pondarré, Corinne; Bouazza, Naïm; Magalon, Jeremy; Miccio, Annarita; Six, Emmanuelle; Roudaut, Cecile; Arnaud, Cécile; Kamdem, Annie; Touzot, Fabien; Gabrion, Aurélie; Magrin, Elisa; Couzin, Chloé; Fusaro, Mathieu; André, Isabelle; Vernant, Jean-Paul; Gluckman, Eliane; Bernaudin, Françoise; Bories, Dominique; Cavazzana, Marina

T cell dynamics and response of the microbiota after gene therapy to treat X-linked severe combined immunodeficiency

基因治疗治疗X连锁重症联合免疫缺陷后T细胞动力学和微生物群反应

Clarke, Erik L; Connell, A Jesse; Six, Emmanuelle; Kadry, Nadia A; Abbas, Arwa A; Hwang, Young; Everett, John K; Hofstaedter, Casey E; Marsh, Rebecca; Armant, Myriam; Kelsen, Judith; Notarangelo, Luigi D; Collman, Ronald G; Hacein-Bey-Abina, Salima; Kohn, Donald B; Cavazzana, Marina; Fischer, Alain; Williams, David A; Pai, Sung-Yun; Bushman, Frederic D

INSPIIRED: Quantification and Visualization Tools for Analyzing Integration Site Distributions

INSPIIRED:用于分析整合位点分布的量化和可视化工具

Berry, Charles C; Nobles, Christopher; Six, Emmanuelle; Wu, Yinghua; Malani, Nirav; Sherman, Eric; Dryga, Anatoly; Everett, John K; Male, Frances; Bailey, Aubrey; Bittinger, Kyle; Drake, Mary J; Caccavelli, Laure; Bates, Paul; Hacein-Bey-Abina, Salima; Cavazzana, Marina; Bushman, Frederic D

INSPIIRED: A Pipeline for Quantitative Analysis of Sites of New DNA Integration in Cellular Genomes

INSPIIRED:用于定量分析细胞基因组中新DNA整合位点的流程

Sherman, Eric; Nobles, Christopher; Berry, Charles C; Six, Emmanuelle; Wu, Yinghua; Dryga, Anatoly; Malani, Nirav; Male, Frances; Reddy, Shantan; Bailey, Aubrey; Bittinger, Kyle; Everett, John K; Caccavelli, Laure; Drake, Mary J; Bates, Paul; Hacein-Bey-Abina, Salima; Cavazzana, Marina; Bushman, Frederic D

Gene Therapy for X-Linked Severe Combined Immunodeficiency: Where Do We Stand?

X连锁重症联合免疫缺陷的基因治疗:我们目前处于什么阶段?

Cavazzana, Marina; Six, Emmanuelle; Lagresle-Peyrou, Chantal; André-Schmutz, Isabelle; Hacein-Bey-Abina, Salima

Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome

基因治疗对重症Wiskott-Aldrich综合征患者的疗效

Hacein-Bey Abina, Salima; Gaspar, H Bobby; Blondeau, Johanna; Caccavelli, Laure; Charrier, Sabine; Buckland, Karen; Picard, Capucine; Six, Emmanuelle; Himoudi, Nourredine; Gilmour, Kimberly; McNicol, Anne-Marie; Hara, Havinder; Xu-Bayford, Jinhua; Rivat, Christine; Touzot, Fabien; Mavilio, Fulvio; Lim, Annick; Treluyer, Jean-Marc; Héritier, Sébastien; Lefrère, Francois; Magalon, Jeremy; Pengue-Koyi, Isabelle; Honnet, Géraldine; Blanche, Stéphane; Sherman, Eric A; Male, Frances; Berry, Charles; Malani, Nirav; Bushman, Frederic D; Fischer, Alain; Thrasher, Adrian J; Galy, Anne; Cavazzana, Marina