文献引用 (80)
The WNK-OXSR1 osmosensing pathway mediates intestinal regeneration via Hippo-YAP signaling.
WNK-OXSR1渗透压感知通路通过Hippo-YAP信号介导肠道再生。
Lithospermic Acid Improves Doxorubicin-Induced Cardiomyopathy Through Sirtuin-3-Mediated Deacetylation of p53.
紫草酸通过Sirtuin-3介导的p53去乙酰化改善阿霉素诱发的心肌病。
Erianin facilitates pyroptosis in endometrial cancer via targeting m6A reader YTHDF1.
Erianin 通过靶向 m6A 阅读器 YTHDF1 促进子宫内膜癌细胞焦亡。
PDCoV NSP5 cleaves the selective autophagy receptor CCDC50 to disrupt autophagic degradation of the viral envelope protein.
PDCoV NSP5 可切割选择性自噬受体 CCDC50，从而破坏病毒包膜蛋白的自噬降解。
PSAT1 Promotes NSCLC Progression via the De Novo Serine Synthesis Pathway and Represents a Therapeutic Vulnerability.
PSAT1 通过从头丝氨酸合成途径促进 NSCLC 进展，并代表治疗弱点。
Engineering HLA-G-targeted extracellular vesicles nanoplatform for enhanced cancer therapy through precise cancer drug delivery.
构建靶向 HLA-G 的细胞外囊泡纳米平台，通过精准的癌症药物递送增强癌症治疗效果。
Transgenerational inheritance of diminished ovarian reserve triggered by prenatal propylparaben exposure in mice.
产前暴露于对羟基苯甲酸丙酯可导致小鼠卵巢储备功能下降，并出现跨代遗传
Cleavage of the selective autophagy receptor NBR1 by the PDCoV main protease NSP5 impairs autophagic degradation of the viral envelope protein
PDCoV主蛋白酶NSP5对选择性自噬受体NBR1的切割会损害病毒包膜蛋白的自噬降解。
AI-identified CD133-targeting natural compounds demonstrate differential anti-tumor effects and mechanisms in pan-cancer models.
AI 识别出的靶向 CD133 的天然化合物在泛癌模型中表现出不同的抗肿瘤效果和机制。
Therapeutic Activation of PPARα Inhibits Transformed Follicular Lymphoma Tumorigenesis via the FOXM1 Signaling Pathway
PPARα的治疗性激活通过FOXM1信号通路抑制转化型滤泡性淋巴瘤的肿瘤发生
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