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1. Full Text Publisher Correction: Principles of nucleosome organization revealed by single-cell micrococcal nuclease sequencing
by Lai, Binbin and Gao, Weiwu and Cui, Kairong and Xie, Wanli and Tang, Qingsong and Jin, Wenfei and Hu, Gangqing and Ni, Bing and Zhao, Keji
Nature, ISSN 0028-0836, 12/2018, Volume 564, Issue 7735, pp. E17 - E17
Change history: In Fig. 1c of this Letter, the two graphs were duplicates. The right panel of Fig. 1c has been corrected online. 
Nucleases
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2. Full Text Forschung zu Genodermatosen durch neue Genom-Editing-Methoden
by Lehmann, Janin and Seebode, Christina and Emmert, Steffen
JDDG - Journal of the German Society of Dermatology, ISSN 1610-0379, 08/2017, Volume 15, Issue 8, pp. 783 - 790
Nucleases
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3. Full Text Off‐target effects of engineered nucleases
by Yee, Jiing‐Kuan
The FEBS Journal, ISSN 1742-464X, 09/2016, Volume 283, Issue 17, pp. 3239 - 3248
Recent advances in gene editing with engineered nucleases have transformed our ability to manipulate the genome from diverse organisms for applications ranging... 
homology‐directed repair | meganuclease | CRISPR/Cas9 | off‐target effect | transcription activator‐like effector nuclease | zinc finger nuclease | engineered nuclease | gene editing | nonhomologous end‐joining | Engineered nuclease | Transcription activator-like effector nuclease | Gene editing | Off-target effect | Nonhomologous end-joining | Zinc finger nuclease | Homology-directed repair | Meganuclease | transcription activator-like effector nuclease | off-target effect | nonhomologous end-joining | homology-directed repair | STRAND BREAK REPAIR | SPECIFICITY | TALENS | HUMAN-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | RESTRICTION ENZYMES | DNA-CLEAVAGE | ZINC-FINGER NUCLEASES | GENOME | CRISPR-CAS NUCLEASES | HOMING ENDONUCLEASE | Zinc Fingers | Protein Engineering - methods | Humans | Transcription Activator-Like Effector Nucleases - chemistry | Transcription Activator-Like Effector Nucleases - metabolism | Substrate Specificity | Binding Sites - genetics | Transcription Activator-Like Effector Nucleases - genetics | DNA Breaks, Double-Stranded | Deoxyribonucleases - metabolism | Deoxyribonucleases - genetics | Animals | DNA Repair | Gene Editing - methods | Deoxyribonucleases - chemistry | Animal genetics | Nucleases | DNA binding proteins | Analysis | Genomics | Enzymes | Genetic engineering | Genomes | Biomedical research | DNA repair
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4. Full Text Characteristics and application of S1–P1 nucleases in biotechnology and medicine
by Koval, Tomáš and Dohnálek, Jan
Biotechnology Advances, ISSN 0734-9750, 05/2018, Volume 36, Issue 3, pp. 603 - 612
3′–nucleases/nucleotidases of the S1–P1 family (EC 3.1.30.1) are single–strand–specific or non-specific zinc–dependent phosphoesterases present in plants,... 
TILLING | Cancer treatment | Protozoan parasites | Nuclease protection assay | Leishmaniasis | Heteroduplex cleavage | Structure-function relationship | Host-pathogen interaction | S1–P1 nuclease | Single-nucleotide mismatch | MOLECULAR CHARACTERIZATION | PENICILLIUM-CITRINUM | STRAND-SPECIFIC NUCLEASE | EXTRACELLULAR DNA | CRYSTAL-STRUCTURE | MUNG BEAN NUCLEASE | MISMATCH CLEAVAGE | CLASS-I NUCLEASE | AMINO-ACID-SEQUENCE | S1 NUCLEASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | S1-P1 nuclease | Fungal Proteins - chemistry | Humans | Single-Strand Specific DNA and RNA Endonucleases - chemistry | Single-Strand Specific DNA and RNA Endonucleases - pharmacology | Substrate Specificity | Structure-Activity Relationship | DNA Mutational Analysis - methods | Host-Pathogen Interactions | Biotechnology - methods | Nucleotidases - metabolism | Single-Strand Specific DNA and RNA Endonucleases - metabolism | Antineoplastic Agents - pharmacology | Single-Strand Specific DNA and RNA Endonucleases - genetics | Molecular Targeted Therapy - methods | Fungal Proteins - metabolism | Prevention | Enzymes | Biotechnology | Nucleases | DNA binding proteins | Cancer
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5. Full Text ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering
by Gaj, Thomas and Gersbach, Charles A and Barbas, Carlos F
Trends in Biotechnology, ISSN 0167-7799, 2013, Volume 31, Issue 7, pp. 397 - 405
Highlights • ZFNs, TALENs, and CRISPR/Cas-based RNA-guided DNA endonucleases are programmable site-specific nucleases. • Site-specific nucleases induce DNA... 
Internal Medicine | clustered regulatory interspaced short palindromic repeat | transcription activator-like effector nuclease | zinc-finger nuclease | genome engineering | Genome engineering | Zinc-finger nuclease | Transcription activator-like effector nuclease | Clustered regulatory interspaced short palindromic repeat | TRANSCRIPTION FACTORS | DOUBLE-STRAND BREAKS | EMBRYO MICROINJECTION | NICKING ENZYME | ZINC-FINGER NUCLEASES | PLURIPOTENT STEM-CELLS | DNA-SEQUENCE SPECIFICITY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | TARGETED GENE DISRUPTION | EFFECTOR NUCLEASES | Genetic Engineering - methods | Recombinant Proteins - metabolism | Deoxyribonucleases - genetics | Molecular Biology - trends | Zinc Fingers | Biological Therapy - methods | Biological Therapy - trends | Clustered Regularly Interspaced Short Palindromic Repeats | Recombinant Proteins - genetics | Molecular Biology - methods | Deoxyribonucleases - metabolism | Genetic Engineering - trends | Medical research | Genetic engineering | DNA repair | Genes | Methods | zinc-finger | TALE | CRISPR | nuclease
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6. Full Text Use of designer nucleases for targeted gene and genome editing in plants
by Weeks, Donald P and Spalding, Martin H and Yang, Bing
Plant Biotechnology Journal, ISSN 1467-7644, 02/2016, Volume 14, Issue 2, pp. 483 - 495
Summary The ability to efficiently inactivate or replace genes in model organisms allowed a rapid expansion of our understanding of many of the genetic,... 
genome editing | zinc finger nuclease | site‐directed mutagenesis | TAL effector nuclease | CRISPR/Cas9 | designer nucleases | Designer nucleases | Genome editing | Zinc finger nuclease | Site-directed mutagenesis | site-directed mutagenesis | CRISPR | TRANSPOSABLE ELEMENTS | CRISPR-CAS SYSTEM | DOUBLE-STRAND BREAKS | TAL EFFECTOR NUCLEASES | ZINC-FINGER NUCLEASES | DNA-BINDING SPECIFICITY | PLANT SCIENCES | CHLAMYDOMONAS-REINHARDTII | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | Cas9 | HOMOLOGOUS RECOMBINATION | GUIDE RNA DESIGN | SITE-SPECIFIC MUTAGENESIS | Gene Targeting - methods | Crops, Agricultural - genetics | Gene Editing - methods | Endonucleases - metabolism | Plants - genetics | Plants, Genetically Modified | Nucleases | Genes | Genomics | Plant genetics | Genetic research | Plants | DNA binding proteins | Genomes | Deoxyribonucleic acid--DNA | Heart | DNA damage | Homologous recombination | Oligonucleotides | Plant biology | Homology | Organisms | DNA repair | Herbicides | Agricultural production | Agriculture | Zinc finger proteins | Genetic modification | Plants (botany) | Nucleotide sequence | Crops | Plant communities | Food production | Ribonucleic acid--RNA | Zinc | Tobacco | Engineers | Index Medicus | Ribonucleic acids | Breaking | Deoxyribonucleic acid | Plants (organisms) | Nuclease
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7. Full Text Elimination of inter-domain interactions increases the cleavage fidelity of the restriction endonuclease Dra III
by Zhuo, Wei and Lai, Xuhui and Zhang, Liqing and Chan, Siu-Hong and Li, Fengjuan and Zhu, Zhenyu and Yang, Maojun and Sun, Dapeng
Protein & Cell, ISSN 1674-800X, 05/2014, Volume 5, Issue 5, p. 357
DraIII is a type IIP restriction endonucleases (REases) that recognizes and creates a double strand break within the gapped palindromic sequence CAC[right... 
Nucleases
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8. Full Text A beginner's guide to gene editing
by Harrison, Patrick T and Hart, Stephen
Experimental Physiology, ISSN 0958-0670, 04/2018, Volume 103, Issue 4, pp. 439 - 448
New Findings What is the topic of this review? This review summarizes the development of gene editing from early proof‐of‐concept studies in the 1980s to... 
CRISPR | guide RNA | cystic fibrosis | TAL‐effector nuclease | zinc finger nuclease | Cas9 | gene editing | TAL-effector nuclease | STEM-CELLS | PHYSIOLOGY | HUMAN-DISEASE | HUMAN-CELLS | MODEL | IDENTIFICATION | ZINC-FINGER NUCLEASES | DELIVERY | ENDONUCLEASE | DNA | CYSTIC-FIBROSIS GENE | Endonucleases - genetics | Animals | Humans | Genome - genetics | Clustered Regularly Interspaced Short Palindromic Repeats - genetics | Gene Editing - methods | CRISPR-Cas Systems - genetics | Zinc Finger Nucleases - genetics | Nucleases | RNA | Genes | Genomics | Genetic research | Cystic fibrosis | Zinc finger proteins | DNA binding proteins | Nucleotide sequencing | Cells | DNA sequencing | Animal models | RNA editing | Genomes | Ribonucleic acid--RNA
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9. Full Text Designed nucleases for targeted genome editing
by Lee, Junwon and Chung, Jae‐Hee and Kim, Ho Min and Kim, Dong‐Wook and Kim, Hyongbum
Plant Biotechnology Journal, ISSN 1467-7644, 02/2016, Volume 14, Issue 2, pp. 448 - 462
Summary Targeted genome‐editing technology using designed nucleases has been evolving rapidly, and its applications are widely expanding in research, medicine... 
homology‐directed repair | double‐strand break | transcription activator‐like effector nuclease | CRISPR‐Cas9 | zinc‐finger nuclease | nonhomologous end‐joining | Zinc-finger nuclease | Transcription activator-like effector nuclease | Nonhomologous end-joining | Double-strand break | CRISPR-Cas9 | Homology-directed repair | CRISPR-CAS SYSTEMS | PLANT-CELLS | DOUBLE-STRAND BREAKS | ZINC-FINGER NUCLEASES | DNA-BINDING SPECIFICITY | PROGRAMMABLE NUCLEASES | PLANT SCIENCES | PLURIPOTENT STEM-CELLS | transcription activator-like effector nuclease | zinc-finger nuclease | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | nonhomologous end-joining | GENE-EXPRESSION | double-strand break | RNA-GUIDED ENDONUCLEASES | homology-directed repair | Genetic Engineering | Base Sequence | DNA Repair - genetics | Endonucleases - metabolism | Genome, Plant | DNA Breaks, Double-Stranded | Gene Editing | Genetic research | Nucleases | DNA binding proteins | Genomics | Plant genetics | Editing | DNA repair | Genomes | CRISPR | Biotechnology | Transcription | Homology | Research | Ribonucleic acid--RNA | Gene expression | Zinc | Gene sequencing | Efficiency | Technology | Cell cycle | Stem cells | Non-homologous end joining | Genetic engineering | Mutation | Repair | Chromosomes | Deoxyribonucleic acid--DNA | Methods | Technology utilization | Breaking | Bacteria | Nuclease
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