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

Dural ectopic lymphatic structures accumulate during aging and exhibit dysregulation in neurodegenerative diseases

硬脑膜异位淋巴结构在衰老过程中积聚，并在神经退行性疾病中表现出功能紊乱。

期刊:Proceedings of the National Academy of Sciences of the United States of America
影响因子:9.1
doi:10.1073/pnas.2425081122
Fruitman Davidi, Amit; Shirenova, Sophie; Michaelovich, Dolev; Benedetti, Giulio; Shtrasberg, Hadar; Shoval, Irit; Hauschner, Hagit; Oz, Gal; Vardy, Karin; Hirsh, Tamir; Madar, Ravit; Stern, Edward A; Rosenmann, Hanna; Biragyn, Arya; Okun, Eitan
衰老
神经科学
发表日期：2025
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HLH-30/TFEB Rewires the Chaperone Network to Promote Proteostasis Upon Perturbations to the Coenzyme A and Iron-Sulfur Cluster Biosynthesis Pathways.

HLH-30/TFEB 重塑分子伴侣网络，以在辅酶 A 和铁硫簇生物合成途径受到扰动时促进蛋白质稳态

期刊:Aging Cell
影响因子:7.1
doi:10.1111/acel.70038
Shalash Rewayd, Solomon Dror Michael, Levi-Ferber Mor, von Chrzanowski Henrik, Atrash Mohammad Khaled, Nakar Barak, Avivi Matan Yosef, Hauschner Hagit, Swisa Aviya, Meléndez Alicia, Shav-Tal Yaron, Henis-Korenblit Sivan
其它
发表日期：2025
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Integrated transcriptome and cell phenotype analysis suggest involvement of PARP1 cleavage, Hippo/Wnt, TGF-β and MAPK signaling pathways in ovarian cancer cells response to cannabis and PARP1 inhibitor treatment

综合转录组和细胞表型分析表明 PARP1 裂解、Hippo/Wnt、TGF-β 和 MAPK 信号通路参与了卵巢癌细胞对大麻和 PARP1 抑制剂治疗的反应

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2024.1333964
Nurit Shalev, Michelle Kendall, Navin Kumar, Sudeep Tiwari, Seegehalli M Anil, Hagit Hauschner, Savvemala G Swamy, Adi Doron-Faingenboim, Eduard Belausov, Bruce E Kendall, Hinanit Koltai
信号转导
肿瘤
卵巢癌
肿瘤细胞
Hippo
MAPK/ERK
TGF-β
Wnt/β-Catenin
发表日期：2024
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High-risk type-2 diabetes mellitus patients, without prior ischemic events, have normal blood platelet functionality profiles: a cross-sectional study

既往无缺血事件的高危2型糖尿病患者，其血小板功能指标正常：一项横断面研究

期刊:Cardiovascular Diabetology
影响因子:10.6
doi:10.1186/s12933-015-0244-x
Shlomai, Gadi; Haran-Appel, Tal; Sella, Tal; Grossman, Yoni; Hauschner, Hagit; Rosenberg, Nurit; Grossman, Ehud
血小板
糖尿病
代谢
发表日期：2015
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A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia

α(IIb)基因中13个碱基对的缺失是一种创始突变，在患有格氏血小板无力症的巴勒斯坦阿拉伯患者中占主导地位。

期刊:Journal of Thrombosis and Haemostasis
影响因子:5
doi:10.1111/j.1538-7836.2005.01618.x
Rosenberg, N; Hauschner, H; Peretz, H; Mor-Cohen, R; Landau, M; Shenkman, B; Kenet, G; Coller, B S; Awidi, A A; Seligsohn, U
血小板
发表日期：2005
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