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Drug Safety Evaluation

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Cover of 'Drug Safety Evaluation'

Table of Contents

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    Book Overview
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    Chapter 1 Nonclinical Development of Combination Drugs
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    Chapter 2 Juvenile Nonclinical Safety Studies in Support of Pediatric Drug Development
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    Chapter 3 Procedures of Necropsy and Tissue Sampling
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    Chapter 4 Tissue Sampling and Processing for Histopathology Evaluation
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    Chapter 5 Principles and Methods of Immunohistochemistry
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    Chapter 6 Applications of Mass Spectrometry Imaging for Safety Evaluation
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    Chapter 7 In Vivo Rat T-Lymphocyte Pig-a Assay: Detection and Expansion of Cells Deficient in the GPI-Anchored CD48 Surface Marker for Analysis of Mutation in the Endogenous Pig-a Gene
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    Chapter 8 Detection of In Vivo Mutation in the Pig-a Gene of Mouse Bone Marrow Erythroids
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    Chapter 9 The Use of Bacterial Repair Endonucleases in the Comet Assay
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    Chapter 10 Automated Patch-Clamp Methods for the hERG Cardiac Potassium Channel
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    Chapter 11 Impedance Measurement in Induced Pluripotent Stem Cell-Derived Cardiomyocytes
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    Chapter 12 Target Safety Assessment: Strategies and Resources
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    Chapter 13 NMR and MS Methods for Metabolomics
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    Chapter 14 Protocols and Applications of Cellular Metabolomics in Safety Studies Using Precision-Cut Tissue Slices and Carbon 13 NMR
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    Chapter 15 Statistical Analysis of Quantitative RT-PCR Results
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    Chapter 16 Evaluation of Mitochondrial Respiration in Cultured Rat Hepatocytes
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    Chapter 17 FETAX Assay for Evaluation of Developmental Toxicity
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    Chapter 18 Evaluation of Embryotoxicity Using the Zebrafish Model
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    Chapter 19 Absolute Quantification of Toxicological Biomarkers via Mass Spectrometry
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    Chapter 20 Next-Generation Sequencing to Investigate Urinary microRNAs from Macaca fascicularis (Cynomolgus Monkey)
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    Chapter 21 Quantitative RT-PCR for MicroRNAs in Biofluids
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    Chapter 22 Chromogenic In Situ Hybridization Methods for microRNA Biomarker Monitoring of Drug Safety and Efficacy
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    Chapter 23 Urine Exosome Isolation and Characterization
Attention for Chapter 18: Evaluation of Embryotoxicity Using the Zebrafish Model
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Chapter title
Evaluation of Embryotoxicity Using the Zebrafish Model
Chapter number 18
Book title
Drug Safety Evaluation
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7172-5_18
Pubmed ID
Book ISBNs
978-1-4939-7170-1, 978-1-4939-7172-5
Authors

Lisa Truong, Robert L. Tanguay

Abstract

The embryonic zebrafish model offers the power of whole-animal investigations (e.g., intact organism, functional homeostatic feedback mechanisms, and intercellular signaling) with the convenience of cell culture (e.g., cost- and time-efficient, minimal infrastructure, small quantities of solutions required). The model system overcomes many of the current limitations in rapid to high-throughput screening of drugs/compounds and casts a broad net to rapidly evaluate integrated system effects. Additionally, it is an ideal platform to follow up with targeted studies aimed at the mechanisms of toxic action. Exposures are carried out in multi-well plates so minimal solution volumes are required for the assessments. Numerous morphological, developmental, and behavioral endpoints can be evaluated noninvasively due to the transparent nature of the embryos.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 66 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Portugal 1 2%
Unknown 65 98%

Demographic breakdown

Readers by professional status Count As %
Student > Master 14 21%
Student > Bachelor 9 14%
Student > Ph. D. Student 8 12%
Researcher 6 9%
Student > Doctoral Student 5 8%
Other 5 8%
Unknown 19 29%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 18 27%
Agricultural and Biological Sciences 12 18%
Environmental Science 4 6%
Unspecified 3 5%
Pharmacology, Toxicology and Pharmaceutical Science 2 3%
Other 4 6%
Unknown 23 35%