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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 4: Tissue Sampling and Processing for Histopathology Evaluation
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Chapter title
Tissue Sampling and Processing for Histopathology Evaluation
Chapter number 4
Book title
Drug Safety Evaluation
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7172-5_4
Pubmed ID
Book ISBNs
978-1-4939-7170-1, 978-1-4939-7172-5
Authors

Mohamed Slaoui, Anne-Laure Bauchet, Laurence Fiette

Abstract

Histological procedures aim at providing good-quality sections that can be used for a light microscopic evaluation of tissue. These are applicable to identify either spontaneous or diseases-induced changes. Routinely, tissues are fixed with neutral formalin 10%, embedded in paraffin, and manually sectioned with a microtome to obtain 4-5 μm thick paraffin sections. Dewaxed sections are then stained with HE&S (hematoxylin-eosin and saffron) or can be used for other purposes (special stains, immunohistochemistry, in situ hybridization, etc.). During this processing, many steps and procedures are critical to ensure standard and interpretable sections. This chapter provides key recommendations to efficiently achieve this objective.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 88 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 88 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 15 17%
Student > Master 10 11%
Student > Ph. D. Student 5 6%
Student > Doctoral Student 3 3%
Researcher 3 3%
Other 7 8%
Unknown 45 51%
Readers by discipline Count As %
Medicine and Dentistry 18 20%
Biochemistry, Genetics and Molecular Biology 11 13%
Pharmacology, Toxicology and Pharmaceutical Science 5 6%
Veterinary Science and Veterinary Medicine 2 2%
Nursing and Health Professions 2 2%
Other 6 7%
Unknown 44 50%