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2018, Methods in Molecular Biology, ISBN 1493977733, Volume 1767
eBook
Nature Methods, ISSN 1548-7091, 02/2019, Volume 16, Issue 2, pp. 147 - 150
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 05/2018, Volume 430, Issue 10, pp. 1426 - 1430
Journal Article
Journal Article
Nature, ISSN 0028-0836, 11/2017, Volume 551, Issue 7681, pp. 464 - 471
The spontaneous deamination of cytosine is a major source of transitions from C·G to T·A base pairs, which account for half of known pathogenic point mutations... 
Directed evolution | Fracture mechanics | Disease | Biological evolution | Genomes | Drug resistance | Experiments | Guanine | Efficiency | Bacteria | Cleavage | Evolution | Cytosine | Nuclease | Deoxyribonucleic acid--DNA | Transfer RNA | CRISPR | Protein engineering | Enzymes | Adenosine | Base pairs | Adenine | Ductile-brittle transition | Adenosine deaminase | Ribonucleic acid--RNA | Studies | Antibiotics | Deamination | Mutation | Index Medicus
Journal Article
2004, ISBN 9781588292421, xiii· 435
Book
Marine Biotechnology, ISSN 1436-2228, 8/2016, Volume 18, Issue 4, pp. 449 - 452
CRISPR/Cas9 system has been used widely in animals and plants to direct mutagenesis. To date, no such method exists for fish somatic cell lines. We describe an... 
Life Sciences | Microbiology | CRISPR/Cas9 | Zoology | Freshwater & Marine Ecology | Genome editing | Engineering, general | FACS | CHSE-214 | EGFP | nCas9n | SYSTEM | KNOCK-IN | ZEBRAFISH | RNA | CRISPR-CAS9 | GENE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | MARINE & FRESHWATER BIOLOGY | Endonucleases - genetics | Green Fluorescent Proteins - genetics | Endonucleases - metabolism | Transfection | Base Sequence | Cloning, Molecular | Clustered Regularly Interspaced Short Palindromic Repeats | Hygromycin B - analogs & derivatives | Genes, Reporter | Genetic Engineering - methods | Cell Line | Green Fluorescent Proteins - metabolism | Genetic Vectors - chemistry | Animals, Genetically Modified | Bacterial Proteins - genetics | Genetic Vectors - metabolism | Plasmids - metabolism | Salmon - genetics | Gentamicins | Animals | CRISPR-Cas Systems | Plasmids - chemistry | Bacterial Proteins - metabolism | Gene Editing - methods | Cinnamates | Anopheles | Analysis | Fishes | Genes | Genomics | Genetically modified organisms | Genetic research | Animal genetic engineering | Genomes | Methods | Flow cytometry | Biotechnology | Methodology | High-throughput screening | Editing | Inactivation | Gene sequencing | Fish | Freshwater fish | Sequencing | Genetic modification | CRISPR | Deactivation | Nucleotide sequence | Salmon | Cloning | Marine biology | Hygromycin | Clones | Cells | Polymerase chain reaction | Amplification | Studies | Geneticin | Mutagenesis | Microscopy | Cellular biology | DNA | Cell lines | In vitro methods and tests | Lines | Index Medicus | Cas9 | Short Communication
Journal Article
Nature Biotechnology, ISSN 1087-0156, 2014, Volume 32, Issue 6, pp. 569 - 576
  Monomeric CRISPR-Cas9 nucleases are widely used for targeted genome editing but can induce unwanted off-target mutations with high frequencies. Here we... 
Genetic research | Nucleases | Genetic aspects | Genetic engineering | Zinc finger proteins | Research | Biotechnology | Enzymes | Mutation | Genomics | Index Medicus
Journal Article
Frontiers in Microbiology, ISSN 1664-302X, 10/2018, Volume 9, pp. 2307 - 2307
Various methods for editing specific sites in the Escherichia coli chromosome are available, and gene-size (similar to 1 kb) integration into a single site or... 
CRISPR-Cas12a | Halomonas | Synthetic biology | Multiplex genome editing | E. Coli | SYSTEM | multiplex genome editing | RECOMBINATION | CRISPR/CAS9 | RNA | LAMBDA-GAM PROTEIN | MICROBIOLOGY | synthetic biology | GENE REPLACEMENT | IN-VIVO | 5-AMINOLEVULINIC ACID | RECBCD ENZYME | CODON USAGE | E. coli
Journal Article
Nature, ISSN 0028-0836, 12/2016, Volume 540, Issue 7631, pp. 144 - 149
Journal Article
Cell, ISSN 0092-8674, 09/2016, Volume 167, Issue 1, pp. 233 - 247.e17
Journal Article