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Classical drugs used in this study.

Figshare2015-12-02 更新2026-04-29 收录

代谢动力学

多药耐药机制

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https://figshare.com/articles/dataset/_Classical_drugs_used_in_this_study_/693634 数据链接链接失效反馈

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资源简介：

Mechanism of action, concentrations, and ABC efflux transporter substrate specificity for classical therapeutics.

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创建时间：

2015-12-02

高通量生物分析

代谢动力学

As the desire for a shortened design/make/test/learn cycle increases in early drug discovery, the pressure to rapidly deliver drug metabolism pharmacokinetic data continues to rise. From a bioanalytic

DataCite Commons2024-05-16 更新90

Structure of HIV-1 RT Q151M mutant

HIV逆转录酶结构解析

多药耐药机制

Structure of HIV-1 RT Q151M mutant Descriptor: RT p51 subunit, RT p66 subunit Authors: Nakamura, A, Tamura, N, Yasutake, Y. Deposit date: 2015-04-27 Release date: 2015-11-11 Last modified: 2023-11-08

Protein Data Bank Japan2023-11-08 更新60

Draft Genome sequencing of Pseudomonas aeruginosa BK1 strain, isolated from keratitis patients.

细菌基因组测序

多药耐药机制

A multidrug resistant Pseudomonas aeruginosa BK1 strain isolated from corneal infection

NIAID Data Ecosystem40

CEFSULODIN LC/MS/MS DATA

代谢动力学

抗生素分布

Plasma and brain concentration profiles following IP administration of 100 mg/kg cefsulodin in C57BL/6J mice.

Mendeley Data70

Changes in the expression of miR-381 and miR-495 are inversely associated with the expression of the MDR1 gene and development of multi-drug resistance. Homo sapiens

多药耐药机制

MicroRNA调控

Multidrug resistance (MDR) frequently develops in cancer patients exposed to chemotherapeutic agents and is usually brought about by over-expression of P-glycoprotein (P-gp) which acts as a drug efflu

NIAID Data Ecosystem60

Classical drugs used in this study.

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