Pre-clinical QT Risk Assessment in Pharmaceutical Companies - Issues of Current QT Risk Assessment --Reference-Cited by-同舟云学术

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Pre-clinical QT Risk Assessment in Pharmaceutical Companies - Issues of Current QT Risk Assessment -

Published:2009-01-31 Issue:1 Volume:17 Page:1-11
ISSN:1976-9148
Container-title:Biomolecules and Therapeutics
language:en
Short-container-title:Biomolecules and Therapeutics

Author:

Takasuna Kiyoshi,Katsuyoshi Chiba,Manabe Sunao

Publisher

The Korean Society of Applied Pharmacology

Subject

Drug Discovery,Pharmacology,Molecular Medicine,Biochemistry

Link

http://ocean.kisti.re.kr/downfile/crosscheck/ksp/JAKO200904751484332.pdf

Reference67 articles.

1. 3,3′,5,5′-Tetramethylbenzidine as an Ames Test Negative Chromogen for Horse-Radish Peroxidase in Enzyme-Immunoassay

2. Artificial cell-microencapsulated phenylalanine ammonia-lyase

3. Effects of Oral Administration of Artificial Cells Immobilized Phenylalanine Ammonia-Lyase on Intestinal Amino Acids of Phenylketonuric Rats

4. A New Theory of Enterorecirculation of Amino Acids and its use for Depleting Unwanted Amino Acids Using Oral Enzyme-Artificial Cells, as in Removing Phenylalanine in Phenylketonuria

5. Protection of phenylalanine ammonia-lyase from proteolytic attack

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1. Modeling time‐delayed concentration‐QT effects with ACT‐1014‐6470, a novel oral complement factor 5a receptor 1 (C5a₁ receptor) antagonist;Pharmacology Research & Perspectives;2023-07-20

2. The Challenges of Predicting Drug-Induced QTc Prolongation in Humans;Toxicological Sciences;2022-02-11

3. Comprehensive Cardiac Safety Assessment using hiPS-cardiomyocytes (Consortium for Safety Assessment using Human iPS Cells: CSAHi);Current Pharmaceutical Biotechnology;2020-06-09

4. Investigation of hERG1b influence on hERG channel pharmacology at physiological temperature;Journal of Pharmacology and Pharmacotherapeutics;2018

5. CSAHi study: Detection of drug-induced ion channel/receptor responses, QT prolongation, and arrhythmia using multi-electrode arrays in combination with human induced pluripotent stem cell-derived cardiomyocytes;Journal of Pharmacological and Toxicological Methods;2017-05

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