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Whole genome profiling of whole liver lysates of vehicle and Sorafenib-treated iAST mice

ChEBI2014-06-20 更新2026-07-21 收录

肝脏疾病模型基因组学

靶向药物作用机制

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-54857 数据链接链接失效反馈

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Whole genome profiling of whole liver lysates of vehicle and Sorafenib-treated iAST mice

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创建时间：

2014-06-20

激酶结构域

靶向药物作用机制

Structure of T790M EGFR kinase domain co-crystallized with dacomitinib Descriptor: (2E)-N-{4-[(3-chloro-4-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}-4-(piperidin-1-yl)but-2-enamide, Epidermal growt

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Variables influencing BChE inhibition.

靶向药物作用机制

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Variables influencing BChE inhibition.

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Crystal Structure of KPT-330 bound to CRM1 (537-DLTVK-541 to GLCEQ)

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靶向药物作用机制

Crystal Structure of KPT-330 bound to CRM1 (537-DLTVK-541 to GLCEQ) Descriptor: Exportin-1, GLYCEROL, GTP-binding nuclear protein Ran, ... Authors: Baumhardt, J.M, Chook, Y.M. Deposit date: 2020-12-21

Protein Data Bank Japan2023-10-18 更新20

Modulation of immune system mediated by ibrutinib in chronic lymphocytic leukemia

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靶向药物作用机制

Our project is based on the hypothesis that ibrutinib could interfere with chronic lymphocytic leukemia (CLL) microenvironment, modulating the immune response. The aim of the project is to understand

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Apatinib preferentially inhibits Gefitinib-resistant lung cancer cells by inducing cell cycle arrest and inhibiting VEGFR signaling pathway. Apatinib preferentially inhibits Gefitinib-resistant lung cancer cells by inducing cell cycle arrest and inhibiting VEGFR signaling pathway

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Targeted therapy for patients with EGFR mutations by tyrosine kinase inhibitors (TKIs) has provided a significant benefit to patients. However, gradually developed resistance to the therapy becomes a

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Whole genome profiling of whole liver lysates of vehicle and Sorafenib-treated iAST mice

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