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

Dual inhibition of mTOR and calcineurin pathways mitigates missing self-induced NK cell-mediated microvascular rejection

双重抑制 mTOR 和钙调磷酸酶通路可减轻自身诱导的 NK 细胞介导的微血管排斥反应。

Hamada, Sarah; Beadle, Jack; Koenig, Alice; Sugranes, Basile; Ferdinand, John; Chen, Chien-Chia; Mathias, Virginie; Eloudzeri, Maeva; Barba, Thomas; Paidassi, Helena; Saison, Carole; Dubois, Valérie; Morelon, Emmanuel; Walzer, Thierry; Marcais, Antoine; Rabeyrin, Maud; Rabant, Marion; Bruneval, Patrick; Racapé, Maud; Duong Van Huyen, Jean Paul; Clatworthy, Menna R; Roufosse, Candice; Thaunat, Olivier

Chemotaxis overrides the killing response in alloreactive CTLs, providing vascular immune privilege during cellular rejection.

趋化作用可抑制同种异体反应性 CTL 的杀伤反应,从而在细胞排斥过程中提供血管免疫豁免

Barba Thomas, Oberbarnscheidt Martin, Franck Gregory, Gao Chantal, This Sebastien, Rabeyrin Maud, Roufosse Candice, Moran Linda, Koenig Alice, Mathias Virginie, Saison Carole, Dubois Valérie, Pallet Nicolas, Anglicheau Dany, Lamarthée Baptiste, Hertig Alexandre, Morelon Emmanuel, Hot Arnaud, Paidassi Helena, Defrance Thierry, Nicoletti Antonio, Duong Van Huyen Jean-Paul, Xu-Dubois Yi-Chung, Lakkis Faddi G, Thaunat Olivier

Lack of the nucleoside transporter ENT1 results in the Augustine-null blood type and ectopic mineralization

核苷转运蛋白ENT1的缺失会导致奥古斯丁阴性血型和异位矿化。

Daniels, Geoff; Ballif, Bryan A; Helias, Virginie; Saison, Carole; Grimsley, Shane; Mannessier, Lucienne; Hustinx, Hein; Lee, Edmond; Cartron, Jean-Pierre; Peyrard, Thierry; Arnaud, Lionel

Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior

编码乳腺癌抗性蛋白的ABCG2基因的无效等位基因定义了新的血型系统Junior。

Saison, Carole; Helias, Virginie; Ballif, Bryan A; Peyrard, Thierry; Puy, Hervé; Miyazaki, Toru; Perrot, Sébastien; Vayssier-Taussat, Muriel; Waldner, Mauro; Le Pennec, Pierre-Yves; Cartron, Jean-Pierre; Arnaud, Lionel

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

ABCB6 对红细胞生成并非必需,并且是新的血型系统 Langereis 的标志。

Helias, Virginie; Saison, Carole; Ballif, Bryan A; Peyrard, Thierry; Takahashi, Junko; Takahashi, Hideo; Tanaka, Mitsunobu; Deybach, Jean-Charles; Puy, Hervé; Le Gall, Maude; Sureau, Camille; Pham, Bach-Nga; Le Pennec, Pierre-Yves; Tani, Yoshihiko; Cartron, Jean-Pierre; Arnaud, Lionel

A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia

编码红系转录因子KLF1的基因发生显性突变会导致先天性红细胞生成障碍性贫血。

Arnaud, Lionel; Saison, Carole; Helias, Virginie; Lucien, Nicole; Steschenko, Dominique; Giarratana, Marie-Catherine; Prehu, Claude; Foliguet, Bernard; Montout, Lory; de Brevern, Alexandre G; Francina, Alain; Ripoche, Pierre; Fenneteau, Odile; Da Costa, Lydie; Peyrard, Thierry; Coghlan, Gail; Illum, Niels; Birgens, Henrik; Tamary, Hannah; Iolascon, Achille; Delaunay, Jean; Tchernia, Gil; Cartron, Jean-Pierre