CRISPR in animals and animal models /

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Bibliographic Details
Imprint:London : Academic Press, an imprint of Elsevier, 2017.
Description:1 online resource
Language:English
Series:Progress in molecular biology and translational science ; volume 152
Progress in molecular biology and translational science ; volume 152.
Subject:
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/12378993
Hidden Bibliographic Details
Other authors / contributors:Torres-Ruiz, Raul, editor.
Roguez-Perales, Sandra, editor.
ISBN:9780128125076
0128125071
9780128125069
0128125063
Notes:Online resource; title from PDF title page (EBSCO, viewed November 14, 2017).
Summary:CRISPR in Animals and Animal Models, Volume 152, the latest release in the Progress in Molecular Biology and Translational Science series, explores the genome editing CRISPR system in cells and animal models, its applications, the uses of the CRISPR system, and the past, present and future of CRISPR genome editing. Topics of interest in this updated volume include a section on CRISPR history, The genome editing revolution, Programming CRISPR and its applications, CRISPR Delivery methods, CRISPR libraries and screening, CRISPR investigation in haploid cells, CRISPR in the generation of transgenic animals, CRISPR therapeutics, and Promising strategies and present challenges.
Other form:Print version: 9780128125069 0128125063

MARC

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505 0 |a Cover -- Title page -- Copyright -- Contents -- Contributors -- Chapter One -- CRISPR History: Discovery, Characterization, and Prosperity -- Abstract -- 1 Introduction -- 2 Discovery of CRISPR-Cas systems -- 2.1 Identification of CRISPR Loci and cas Genes -- 2.2 Prediction of Small RNA-Based Antiviral Functions of CRISPR -- 2.2.1 Identification of CRISPR-Related Small RNAs -- 2.2.2 Origin of Spacers in CRISPR Loci -- 2.3 Experimental Demonstration of the Basic Mechanism of CRISPR-Cas System -- 2.3.1 Adaptation -- 2.3.2 crRNA Biogenesis 
505 8 |a 2.3.3 Interference3 Molecular mechanisms of nucleic acid interference -- 3.1 PAM-Dependent DNA Interference by Type I CRISPR-Cas Systems -- 3.2 Type II CRISPR-Cas System Requires a Unique tracrRNA for DNA Interference -- 3.3 RNA-Activated DNA Interference by Type III CRISPR-Cas Systems -- 4 Discovery of anti-CRISPR system -- 5 Identification of novel CRISPR-Cas systems -- 6 Blooming of CRISPR technology -- References -- Chapter Two -- CRISPR/Cas9 Technology: Applications and Human Disease Modeling -- Abstract -- 1 Genome engineering tools 
505 8 |a 1.1 Genome Engineering Technologies1.1.1 Homologous Recombination (HR) -- 1.1.2 Double-Strand Breaks (DSBs) -- 1.1.3 NHEJ Versus HDR -- 1.1.4 Zinc Finger Nuclease (ZFN) -- 1.1.5 Transcription Activator-Like Effector Nucleases (TALENs) -- 1.1.6 CRISPR/Cas9 -- 1.2 Off Target Effects -- 2 CRISPR applications -- 2.1 CRISPRi and CRISPRa: Regulation of Transcriptional Levels -- 2.2 Epigenome Edition -- 2.3 Genome Imaging -- 2.4 Large-Scale Functional Genomic Studies Using CRISPR/Cas9 -- 2.5 Edition of Single-Stranded RNA 
505 8 |a 3 CRISPR applications in biomedical modeling3.1 Neurological Disease Models -- 3.2 Cancer Models -- 3.3 Cardiovascular Disease Models -- 3.4 Infectious Disease Models -- 3.5 Immunodeficiency Models -- 4 Concluding remarks -- References -- Chapter Three -- Dynamics of Indel Profiles Induced by Various CRISPR/Cas9 Delivery Methods -- Abstract -- 1 Introduction -- 1.1 Genome Editing and DNA Repair -- 1.2 Indel Detection Methodologies -- 1.3 IDAA for Indel Detection and gRNA Selection -- 2 Materials and methods -- 2.1 gRNAs, Plasmid Vectors and Cell Lines 
505 8 |a 2.2 Cas9 and gRNA Delivery Conditions2.3 Efficiency Measurements -- 3 Results -- 3.1 Rationale and Design of the Study -- 3.2 Transfection and Integration Dynamics -- 3.3 Efficiency of Generating Indels Over Time -- 3.4 Indel Profiles Over Time -- 3.5 Dynamic Effect of gRNA Stability on Indel Efficiency -- 3.6 Comparison of IDAA and TIDE Methods -- 4 Concluding remarks -- Acknowledgments -- References -- Chapter Four -- CRISPR Libraries and Screening -- Abstract -- 1 Introduction -- 2 Mouse models of cancer -- 3 CRISPR-Cas9 systems -- 4 CRISPR libraries 
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