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

Bioengineered iPSC-derived human macrophages with increased angiotensin-converting enzyme (ACE) expression suppress solid tumor growth.

生物工程改造的 iPSC 衍生的人类巨噬细胞,其血管紧张素转换酶 (ACE) 表达增加,可抑制实体瘤的生长。

Shibata Tomohiro, Bhat Shabir, Cao DuoYao, Saito Suguru, Khan Noor, Bernstein Ellen A, Tokudome Takeshi, Okwan-Duodu Derick, Tourtellotte Warren G, Bernstein Kenneth E, Khan Zakir

BACE2 tunes lipid uptake through lipid transporters shedding supporting cancer cell proliferation.

BACE2 通过脂质转运蛋白的脱落来调节脂质吸收,从而支持癌细胞增殖。

Matafora Vittoria, Elhagh Alice, Morelli Alessandra, Tronci Laura, Cattaneo Angela, Conti Camilla, Casagrande Francesca, Farris Francesco, Bachi Angela

Angiotensin-Converting Enzyme (ACE) Inhibitors and Statins Mitigate Negative Cardiovascular and Pulmonary Effects of Particulate Matter in a Mouse Exposure Model.

血管紧张素转换酶 (ACE) 抑制剂和他汀类药物可减轻颗粒物在小鼠暴露模型中对心血管和肺部的负面影响。

Junglas Tristan, Daiber Andreas, Kuntic Ivana, Valar Arijan, Zheng Jiayin, Oelze Matthias, Strohm Lea, Ubbens Henning, Hahad Omar, Bayo Jimenez Maria Teresa, Münzel Thomas, Kuntic Marin

BACE1 regulates sleep-wake cycle through both enzymatic and non-enzymatic actions.

BACE1 通过酶促和非酶促作用调节睡眠-觉醒周期。

Heininger Hannah, Feng Xiao, Altunkaya Alp, Zheng Fang, Stockinger Florian, Wefers Benedikt, Müller Stephan A, Giesbertz Pieter, Tschirner Sarah K, Shqau Dorina, Adelsberger Helmuth, Ponomarenko Alexey, Fenzl Thomas, Alzheimer Christian, Lichtenthaler Stefan F, Huth Tobias

Neuroinflammatory and transcriptional dynamics during SARS-CoV-2 infection in KRT18-hACE2 mouse brain.

KRT18-hACE2 小鼠脑内 SARS-CoV-2 感染期间的神经炎症和转录动态。

Ahn Dae-Gyun, Mai Nhu Thi Quynh, Jeong Da-Jin, Moon Byoung-San

Natural Selection-Guided ACE2-Targeted Molecular Imaging: A New Paradigm for PET Tracer Development.

自然选择引导的ACE2靶向分子成像:PET示踪剂开发的新范式。

Li Rou, Li Jie, Xue Shuai, Li Danni, Yang Zixin, Wang Tao, Hai Wangxi, Li Xiao

NRF2 activators and the inhibitor of nuclear export, selinexor, restrict coronaviruses by targeting a network involving ACE2, TMPRSS2, and XPO1 through an NRF2-independent mechanism.

NRF2 激活剂和核输出抑制剂 selinexor 通过一种不依赖于 NRF2 的机制,靶向涉及 ACE2、TMPRSS2 和 XPO1 的网络,从而限制冠状病毒。

Waqas Fakhar H, Silva da Costa Leandro, Zapatero-Belinchón Francisco J, Carter-Timofte Madalina E, Lasswitz Lisa, van der Horst Demi, Möller Rebecca, Dahlmann Julia, Olmer Ruth, Geffers Robert, Gerold Gisa, Olagnier David, Pessler Frank

SAMHD1 depletion restricts SARS-CoV-2 infection by suppressing HNF1-dependent ACE2 expression in lung epithelial cells.

SAMHD1 的缺失通过抑制肺上皮细胞中 HNF1 依赖的 ACE2 表达来限制 SARS-CoV-2 感染。

Cheung Pak-Hin Hinson, Chan Pearl, Yang Hua, Ambrus Krisztina, Honne Shravya, Kim Baek, Perlman Stanley, Wu Li

SARS-CoV-2 Spike Protein Induces Time-Dependent and Brain-Region-Specific Alterations in Ferroptosis Markers: A Preliminary Study in K18-hACE2 Mice.

SARS-CoV-2 刺突蛋白诱导铁死亡标志物发生时间依赖性和脑区特异性改变:K18-hACE2 小鼠的初步研究。

Yehia Asmaa, Toufaily Chirine, Abdel Ghaffar Dalia M, El Wakeel Gehan, Adel Mohamed, Mostafa Abeer F, Abulseoud Osama A

PoMA-10: a dual-action antiviral disrupting SARS-CoV-2 Spike-ACE2 interaction and protecting lung tissue.

PoMA-10:一种双效抗病毒药物,可破坏 SARS-CoV-2 Spike-ACE2 相互作用并保护肺组织。

Lee Soheun, Yoon Suh Jin, Lim Jihae, Oh Ji Hyun, Ryu Jae-Sang, Kim Gahee, Kang Hyunwoo, Jo Nayoon, Lee Sehan, Jang Sunbok, Lee Yoonji, Park Yunjeong, Hwang Eun Sook