Signal Transduction and Targeted Therapy

Signal Transduction and Targeted Therapy(英文缩写 SIGNAL TRANSDUCT TAR),ISSN 2095-9907,eISSN 2059-3635 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
81.200
JCR 分区
Q1
CAS 分区
B1
近一年发文量
492
本站 PubMed 收录统计

发文量统计区间:2025-09-21 至 2026-09-21,按本站收录文献的发表日期统计。

指标来源:jcr_cas_ifqb

ISSN: 2095-9907 · eISSN: 2059-3635 · 缩写: SIGNAL TRANSDUCT TAR

期刊简介

暂无简介。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
202138.120Q1
202239.300Q1
202340.800Q1
202452.700Q1
202581.200Q1

Signal Transduction and Targeted Therapy 最新收录文献

  1. JCR分区: Q1 CAS分区: B1 影响因子: 81.2
  2. JCR分区: Q1 CAS分区: B1 影响因子: 81.2

    2. Chromosomal instability in cancer: sources, consequences and new therapeutic opportunities.

    作者:
    Angela Flavia Serpico, Domenico Grieco
    日期:
    2026-09-18

    Chromosomal instability (CIN) refers to a high rate of chromosome segregation errors during consecutive cell divisions and is a hallmark of cancers with aggressive behavior and poor prognosis. Cancer cells exhibiting CIN may acquire both numerical (N-CIN) and structural (S-CIN) chromosome alteration…

  3. JCR分区: Q1 CAS分区: B1 影响因子: 81.2

    3. An integrated multiomic single-vesicle atlas delineates graft exosome heterogeneity in chronic lung allograft dysfunction.

    作者:
    Dong Tian, Xiangyun Zheng, Zengwei Yu, Dapeng Wang, Weiyang Chen, Yaling Liu, Zehui Liu, Boyang Xia, Xiaohan Jin, Haoji Yan, Ye Wu, Yongsheng Zhao, Chuanfen Zhang, Qiang Pu, Jingyu Chen, Masaaki Sato, Lunxu Liu
    日期:
    2026-09-17

    The underlying mechanisms of exosomes in chronic lung allograft dysfunction (CLAD) remain poorly understood. The primary challenge lies in the substantial functional heterogeneity of exosomes in CLAD. In this study, lung transplantation was initially performed, followed by the generation of a chroni…

  4. JCR分区: Q1 CAS分区: B1 影响因子: 81.2

    4. Targeting super elongation complex-driven RNA polymerase II elongation reduces plaque vulnerability.

    作者:
    Karoline E Kokot, Sebastian Reichardt, Christian Menedo, Stephan Erbe, Jasmin M Kneuer, Kaylin C A Palm, Julian Hoba, Michael Andritschke, Mirko Katzmann, Annika Reuser, Moritz von Scheidt, Michal Mokry, Junjie Xiao, Bilal N Sheikh, Nora Klöting, Ulrich Laufs, Jes-Niels Boeckel
    日期:
    2026-09-17

    Atherosclerotic plaque rupture is a major cause of myocardial infarction and stroke, yet the mechanisms governing plaque stability remain incompletely understood. Endothelial activation can trigger endothelial-to-mesenchymal transition, a program linked to endothelial dysfunction and lesion vulnerab…

  5. JCR分区: Q1 CAS分区: B1 影响因子: 81.2

    5. {"_":"SCF regulates osteoblast differentiation through targeting RUNX2.","sup":["JFK"]}

    作者:
    Zesen Shang, Yue Zhang, Yang Liu, Xinyi Yuan, Jichuang Wang, Dongwei Fan, Da Zou, Dazhao Tie, Fei Pei, Hongshan Zhao, Shuguo Zheng, Xinjing Tang, Weishi Li, Lin He
    日期:
    2026-09-16

    RUNX2 (Runt-related transcription factor 2) is a master regulator of osteogenesis, and its genetic mutations are associated with ~65% cases of cleidocranial dysplasia (CCD), an autosomal dominant abnormal bone development disorder in humans with defective intramembranous bone formation. However, how…

  6. JCR分区: Q1 CAS分区: B1 影响因子: 81.2

    6. HIF1α-KLF4 signaling dictates extra-erythrocyte expression of hemoglobin conferring sorafenib resistance in hepatocellular carcinoma.

    作者:
    Bo Zhang, Feichang Liu, Xinyue Gao, Yichao Zhu, Tong Chen, Jiahui Hao, Yuexian Wei, Zhuoran Sun, Ruigang Yang, Yalan Yang, He Ren, Yutong Li, Chunxiao Yu, Tianyi Ren, Yinuo Huang, Hong Jiang, Gerry Melino, Li Ma, Hongyan Huang, Qiang Sun
    日期:
    2026-09-16

    Cancer cells must deal with excessive reactive oxygen species (ROS) to survive severe hypoxia and anticancer therapy; however, anti-ROS mechanisms other than the well-known NFE2L2/NRF2 signaling pathway are poorly recognized. Here, we report a ROS scavenging mechanism mediated by HIF1α-KLF4-induced …

  7. JCR分区: Q1 CAS分区: B1 影响因子: 81.2
  8. JCR分区: Q1 CAS分区: B1 影响因子: 81.2

    8. Hepassocin prevents age-related liver senescence and facilitates liver regeneration by activating AMPK.

    作者:
    Yang Yang, Hui Chen, Shensi Xiang, Yujia Wei, Limin Zhang, Aihua Sun, Xiao E, Fan Wu, Ning Luo, Fei Liang, Xiaojie Wu, Chenyu Wang, Zhuo Chen, Qizheng Zhang, Xinrui Chen, Qinlu Wu, Zixuan Han, Changyan Li, Ronghua Yin, Guangming Ren, Jingjing Li, Ke Zhao, Huiying Gao, Ruijia Wang, Miao Yu, Xiaoming Yang
    日期:
    2026-09-15

    Liver aging significantly impairs hepatic function and regenerative capacity, increasing the risk of morbidity and mortality from chronic liver diseases. Identifying molecular regulators of these processes may reveal promising therapeutic targets. Although Hepassocin (HPS), a hepatokine with known h…

  9. JCR分区: Q1 CAS分区: B1 影响因子: 81.2

    9. Interleukin-1 receptor-associated kinase 1 controls chemoresistance and immuno-killing in non-small cell lung cancer.

    作者:
    Sabrina Digiovanni, Claudia Giannotta, Luca Alessandri, Simona Fontana, Angelo Meoli, Paolo Bironzo, Alessandra Merlini, Gabriella Doronzo, Parab Sushant, Elisa Balmas, Muhlis Akman, Joanna Kopecka, Maddalena Arigoni, Francesca Napoli, Julia Wens, Samuele Tarallo, Alessandro Bertero, Stefano Guglielmo, Barbara Rolando, Davide Palma, Luisella Righi, Massimo Massaia, Raffaele Calogero, Federico Bussolino, Silvia Novello, Giorgio Vittorio Scagliotti, Iris Chiara Salaroglio, Chiara Riganti
    日期:
    2026-09-15

    Non-small cell lung cancer (NSCLC) shows partial chemoimmunoresistance, driven by the upregulation of the drug efflux transporters ABCB1 and ABCC1 and the downregulation of the immunosensitizer protein ABCA1. To elucidate the molecular mechanisms underlying this chemoimmunoresistant phenotype, by pe…

  10. JCR分区: Q1 CAS分区: B1 影响因子: 81.2

    10. The histone deacetylase family in health and disease.

    作者:
    Ri Wen, Yu-Hang Yang, Tao Zhang, Sen-Yu Zhang, Xin-Ru Yang, Li-Ying Zhang, Peng-Hui Hao, Yue Zheng, Ni Yang, Tie-Ning Zhang
    日期:
    2026-09-15

    Zinc-dependent classical histone deacetylases, including Classes I, II, and IV, are ubiquitously present in mammals and play vital roles in numerous biological processes. To date, eleven histone deacetylase members have been identified, namely, histone deacetylase 1 through histone deacetylase 11. A…

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