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

CD69 regulates the tissue dynamics of epigenetically imprinted memory CD4(+) T cells

CD69 调控表观遗传印记记忆 CD4(+) T 细胞的组织动态

Hirasawa, Rui; Iwamura, Chiaki; Kiuchi, Masahiro; Hishiya, Takahisa; Sasaki, Atsushi; Kakinuma, Kohei; Ohishi, Kanae; Kurosugi, Akane; Nemoto, Masahiro; Kokubo, Kota; Hiramoto, Takuto; Iinuma, Tomohisa; Yonekura, Syuji; Onodera, Atsushi; Kimura, Motoko Y; Motohashi, Shinichiro; Tumes, Damon J; Hanazawa, Toyoyuki; Nakayama, Toshinori; Ohtori, Seiji; Hirahara, Kiyoshi

Integrated analysis identifies a CXCR6/CD45/PD-1-based risk model for melanoma prognosis and intratumoral CD8+/CD69 + T-cell infiltration correlation

综合分析确定了基于CXCR6/CD45/PD-1的黑色素瘤预后风险模型以及肿瘤内CD8+/CD69+T细胞浸润相关性。

Wang, Hai-Yun; Cai, Hao-Yang; Deng, Ling; Lu, Yi; Huang, Jiali; Hou, Ting; Liu, Ye; Huang, Xin-Yang; Wang, Ze-Meng; Li, Yue; Wang, Fang

Harnessing TAGAP to improve immunotherapy for lung squamous carcinoma treatment by targeting c-Rel in CD4+ T cells

利用 TAGAP 靶向 CD4+ T 细胞中的 c-Rel 改善肺鳞状细胞癌的免疫疗法

Peian Cai #, Haibo Sun #, Tongmeng Jiang, Huawei Li, Dejing Huang, Xiaopei Hao, Wei Wang, Wenqun Xing, Guanghui Liang

Co-expression of CD69, CD49d, CD279 and CD20 in chronic lymphocytic leukemia cells is a new biomarker of active disease before or under therapy

慢性淋巴细胞白血病细胞中CD69、CD49d、CD279和CD20的共表达是治疗前或治疗期间疾病活动性的新型生物标志物。

Cadot, Sarah; Ysebaert, Loïc; Lamy, Sébastien; Laurent, Camille; Quillet-Mary, Anne

Expansion of CD103(+)CD69(+)CD8(+) cytotoxic liver tissue resident memory T cells and inflammatory monocytes in advanced biliary atresia

晚期胆道闭锁中CD103(+)CD69(+)CD8(+)细胞毒性肝组织驻留记忆T细胞和炎症单核细胞的扩增

Sibbertsen, Freya; Dress, Regine J; Weidemann, Sören Alexander; Möller, Katharina; Herden, Uta; Fischer, Lutz; Paul, Kevin; Oh, Jun; Tolosa, Eva; Schulz-Jürgensen, Sebastian; Gersting, Søren W; Muntau, Ania C; Dunay, Gábor A

Multi-omic analysis of PBMCs in sepsis reveals widespread cytotoxic dysfunction and an increased population of CD69 expressing naïve CD4+ T cells

对脓毒症患者外周血单核细胞的多组学分析揭示了广泛的细胞毒性功能障碍以及表达CD69的初始CD4+ T细胞数量增加。

Flynn, Joshua; Baird, Anne Marie; Breen, Eamon; Carty, Michael; McNevin, Ciara S; McDermott, Lisa; Kenny, Elaine M; Coakley, John Davis; Ryan, Thomas; Doherty, Derek G; Sheils, Orla

CD48, CD69, and TIGIT as diagnostic biomarkers for primary Sjögren's syndrome: an integrated machine learning and multi-disease discrimination validation study

CD48、CD69 和 TIGIT 作为原发性干燥综合征的诊断生物标志物:一项整合机器学习和多疾病鉴别验证研究

Xu, Linlin; Jiang, Pingping; Xiao, Yang; Wang, Hongling; Liu, Hongbo; Chen, Huoying

Targets of influenza human T-cell response are mostly conserved in H5N1

流感病毒人类T细胞反应的靶点在H5N1中大多是保守的。

John Sidney # ,A-Reum Kim # ,Rory D de Vries ,Bjoern Peters ,Philip S Meade ,Florian Krammer ,Alba Grifoni ,Alessandro Sette

Enhancing immunotherapy through PD-L1 upregulation: the promising combination of anti-PD-L1 plus mTOR inhibitors

通过上调PD-L1增强免疫疗法:抗PD-L1抑制剂联合mTOR抑制剂的前景广阔

Anna Hernández-Prat ,Alejo Rodriguez-Vida ,Laura Cardona ,Mengjuan Qin ,Oriol Arpí-Llucià ,Luis Soria-Jiménez ,Sílvia Menendez ,Fabricio Gerel Quimis ,Miguel Galindo ,Edurne Arriola ,Marta Salido ,Nuria Juanpere-Rodero ,Federico Rojo ,Aura Muntasell ,Joan Albanell ,Ana Rovira ,Joaquim Bellmunt

Hyperglycemia Induced in Sprague-Dawley Rats Modulates the Expression of CD36 and CD69 During Wound Healing

Sprague-Dawley大鼠高血糖症可调节伤口愈合过程中CD36和CD69的表达

Ho, Vy; Tran, Tommy; Patel, Jaylan; Teshome, Betelhem; Rai, Vikrant