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

Surface CD81 supports leukemia stem cell function and reveals a therapeutic vulnerability in acute myeloid leukemia

表面CD81支持白血病干细胞功能,并揭示急性髓系白血病的治疗弱点。

Gonzales, Fanny; Peyrouze, Pauline; Laurent, Djohana; Boyer, Thomas; Boukrout, Nihad; Couturier, Cyril; Houdiard, Soizic; Lisi, Véronique; Barthélémy, Adeline; Sevrin, François; Plesa, Adriana; Bongiovanni, Antonino; Pottier, Nicolas; Preudhomme, Claude; Lavallée, Vincent-Philippe; Geles, Konstantinos; Duployez, Nicolas; Berthon, Céline; Roumier, Christophe; Cheok, Meyling

Aging affects reprogramming of pulmonary capillary endothelial cells after lung injury in male mice.

衰老会影响雄性小鼠肺损伤后肺毛细血管内皮细胞的重编程

Truchi Marin, Gautier-Isola Marine, Savary Grégoire, Scribe Célia, Lingampally Arun, Cadis Hugo, Baeri Alberto, Magnone Virginie, Girard-Riboulleau Cédric, Arguel Marie-Jeanne, de Schutter Clémentine, Fassy Julien, Boukrout Nihad, Larrue Romain, Martin Nathalie, Rezzonico Roger, Pluquet Olivier, Perrais Michael, Hofman Véronique, Marquette Charles-Hugo, Hofman Paul, Günther Andreas, Ricard Nicolas, Barbry Pascal, Leroy Sylvie, Lebrigand Kevin, Bellusci Saverio, Cauffiez Christelle, Vassaux Georges, Pottier Nicolas, Mari Bernard

Correction: Integrating rare genetic variants into DPYD pharmacogenetic testing may help preventing fluoropyrimidine-induced toxicity

更正:将罕见基因变异纳入DPYD药物遗传学检测可能有助于预防氟尿嘧啶类药物引起的毒性。

Larrue, Romain; Fellah, Sandy; Hennart, Benjamin; Sabaouni, Naoual; Boukrout, Nihad; Van der Hauwaert, Cynthia; Delage, Clément; Cheok, Meyling; Perrais, Michaël; Cauffiez, Christelle; Allorge, Delphine; Pottier, Nicolas

Severe hypophosphatemia induced by excessive production of FGF23 in acute hepatitis: from bedside to bench

急性肝炎中FGF23过度生成引起的严重低磷血症:从临床到基础研究

Hamroun, Aghiles; Boukrout, Nihad; Cauffiez, Christelle; Fellah, Sandy; Van der Hauwaert, Cynthia; Pottier, Nicolas; Mentaverri, Romuald; Zaworski, Jeremy; Gnemmi, Viviane; Gibier, Jean-Baptiste; Letavernier, Emmanuel; Louvet, Alexandre; Provôt, François; Lenain, Rémi; Maanaoui, Mehdi; Glowacki, François; Lionet, Arnaud

Whole-genome sequencing revealed a novel structural variant in COL4A4 causing autosomal dominant Alport syndrome: A case report

全基因组测序揭示了COL4A4基因中一种新的结构变异,该变异导致常染色体显性遗传的Alport综合征:病例报告

Delage, Clément; Andreani, Marine; Boukrout, Nihad; Sabaouni, Naoual; Perrais, Michaël; Lefebvre, Bruno; Cauffiez, Christelle; Pottier, Nicolas; Larrue, Romain

Integrating rare genetic variants into DPYD pharmacogenetic testing may help preventing fluoropyrimidine-induced toxicity

将罕见基因变异纳入DPYD药物遗传学检测可能有助于预防氟尿嘧啶类药物引起的毒性。

Larrue, Romain; Fellah, Sandy; Hennart, Benjamin; Sabaouni, Naoual; Boukrout, Nihad; Van der Hauwaert, Cynthia; Delage, Clément; Cheok, Meyling; Perrais, Michaël; Cauffiez, Christelle; Allorge, Delphine; Pottier, Nicolas

TGF-βRII Knock-down in Pancreatic Cancer Cells Promotes Tumor Growth and Gemcitabine Resistance. Importance of STAT3 Phosphorylation on S727.

胰腺癌细胞中TGF-βRII敲低促进肿瘤生长和吉西他滨耐药性STAT3在S727位点的磷酸化至关重要

Drubay Vincent, Skrypek Nicolas, Cordiez Lucie, Vasseur Romain, Schulz Céline, Boukrout Nihad, Duchêne Belinda, Coppin Lucie, Van Seuningen Isabelle, Jonckheere Nicolas