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

Formation of extraterrestrial peptides and their derivatives

地外肽及其衍生物的形成

Krasnokutski, Serge A; Jäger, Cornelia; Henning, Thomas; Geffroy, Claude; Remaury, Quentin B; Poinot, Pauline

Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations

全基因组关联研究发现,在三个不同的群体中,结核分枝杆菌感染的耐药性与10q26.2位点存在关联。

Quistrebert, Jocelyn; Orlova, Marianna; Kerner, Gaspard; Ton, Le Thi; Luong, Nguyễn Trong; Danh, Nguyễn Thanh; Vincent, Quentin B; Jabot-Hanin, Fabienne; Seeleuthner, Yoann; Bustamante, Jacinta; Boisson-Dupuis, Stéphanie; Huong, Nguyen Thu; Ba, Nguyen Ngoc; Casanova, Jean-Laurent; Delacourt, Christophe; Hoal, Eileen G; Alcaïs, Alexandre; Thai, Vu Hong; Thành, Lai The; Abel, Laurent; Schurr, Erwin; Cobat, Aurélie

Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway

贝宁农村布鲁里溃疡的全基因组关联研究揭示了两种长链非编码RNA和自噬通路的作用。

Manry, Jeremy; Vincent, Quentin B; Johnson, Christian; Chrabieh, Maya; Lorenzo, Lazaro; Theodorou, Ioannis; Ardant, Marie-Françoise; Marion, Estelle; Chauty, Annick; Marsollier, Laurent; Abel, Laurent; Alcaïs, Alexandre

Patient-Reported Outcomes/Satisfaction and Spectacle Independence with Blended or Bilateral Multifocal Intraocular Lenses in Cataract Surgery

白内障手术中采用混合型或双侧多焦点人工晶状体的患者报告结果/满意度和脱镜情况

Hovanesian, John A; Lane, Stephen S; Allen, Quentin B; Jones, Michael

Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer

家族性严重布鲁里溃疡中8p23.1染色体上的微缺失

Vincent, Quentin B; Belkadi, Aziz; Fayard, Cindy; Marion, Estelle; Adeye, Ambroise; Ardant, Marie-Françoise; Johnson, Christian R; Agossadou, Didier; Lorenzo, Lazaro; Guergnon, Julien; Bole-Feysot, Christine; Manry, Jeremy; Nitschké, Patrick; Theodorou, Ioannis; Casanova, Jean-Laurent; Marsollier, Laurent; Chauty, Annick; Abel, Laurent; Alcaïs, Alexandre

Dysfunctional tear syndrome: dry eye disease and associated tear film disorders - new strategies for diagnosis and treatment

泪液功能障碍综合征:干眼症及相关泪膜疾病——诊断和治疗的新策略

Milner, Mark S; Beckman, Kenneth A; Luchs, Jodi I; Allen, Quentin B; Awdeh, Richard M; Berdahl, John; Boland, Thomas S; Buznego, Carlos; Gira, Joseph P; Goldberg, Damien F; Goldman, David; Goyal, Raj K; Jackson, Mitchell A; Katz, James; Kim, Terry; Majmudar, Parag A; Malhotra, Ranjan P; McDonald, Marguerite B; Rajpal, Rajesh K; Raviv, Tal; Rowen, Sheri; Shamie, Neda; Solomon, Jonathan D; Stonecipher, Karl; Tauber, Shachar; Trattler, William; Walter, Keith A; Waring, George O 4th; Weinstock, Robert J; Wiley, William F; Yeu, Elizabeth

Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations

人类双等位基因RLTPR突变导致的T细胞和B细胞双重内在缺陷

Yi Wang,Cindy S Ma,Yun Ling,Aziz Bousfiha,Yildiz Camcioglu,Serge Jacquot,Kathryn Payne,Elena Crestani,Romain Roncagalli,Aziz Belkadi,Gaspard Kerner,Lazaro Lorenzo,Caroline Deswarte,Maya Chrabieh,Etienne Patin,Quentin B Vincent,Ingrid Müller-Fleckenstein,Bernhard Fleckenstein,Fatima Ailal,Lluis Quintana-Murci,Sylvie Fraitag,Marie-Alexandra Alyanakian,Marianne Leruez-Ville,Capucine Picard,Anne Puel,Jacinta Bustamante,Stéphanie Boisson-Dupuis,Marie Malissen,Bernard Malissen,Laurent Abel,Alain Hovnanian,Luigi D Notarangelo,Emmanuelle Jouanguy,Stuart G Tangye,Vivien Béziat,Jean-Laurent Casanova

Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage

利用全外显子组测序分析群体结构、亲本近亲繁殖和家族连锁

Belkadi, Aziz; Pedergnana, Vincent; Cobat, Aurélie; Itan, Yuval; Vincent, Quentin B; Abhyankar, Avinash; Shang, Lei; El Baghdadi, Jamila; Bousfiha, Aziz; Alcais, Alexandre; Boisson, Bertrand; Casanova, Jean-Laurent; Abel, Laurent

Deep dermatophytosis and inherited CARD9 deficiency

深部皮肤癣菌病和遗传性 CARD9 缺陷

Lanternier, Fanny; Pathan, Saad; Vincent, Quentin B; Liu, Luyan; Cypowyj, Sophie; Prando, Carolina; Migaud, Mélanie; Taibi, Lynda; Ammar-Khodja, Aomar; Stambouli, Omar Boudghene; Guellil, Boumediene; Jacobs, Frederique; Goffard, Jean-Christophe; Schepers, Kinda; Del Marmol, Véronique; Boussofara, Lobna; Denguezli, Mohamed; Larif, Molka; Bachelez, Hervé; Michel, Laurence; Lefranc, Gérard; Hay, Rod; Jouvion, Gregory; Chretien, Fabrice; Fraitag, Sylvie; Bougnoux, Marie-Elisabeth; Boudia, Merad; Abel, Laurent; Lortholary, Olivier; Casanova, Jean-Laurent; Picard, Capucine; Grimbacher, Bodo; Puel, Anne

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

IFN-γR2 部分缺乏是由于蛋白质错误折叠造成的,可以通过糖基化抑制剂来挽救

Marcela Moncada-Vélez, Rubén Martinez-Barricarte, Dusan Bogunovic, Xiao-Fei Kong, Lizbeth Blancas-Galicia, Cengiz Tirpan, Guzide Aksu, Quentin B Vincent, Bertrand Boisson, Yuval Itan, Noé Ramírez-Alejo, Satoshi Okada, Alexandra Y Kreins, Vanessa L Bryant, Jose Luis Franco, Mélanie Migaud, Sara Espin