TY  - BOOK
AU  - Storici,Francesca
TI  - Gene correction: methods and protocols 
T2  - Methods in molecular biology,
SN  - 9781627037600 (alk. paper)
U1  - 572.877 23
PY  - 2014///
CY  - New York
PB  - Humana Press
KW  - Genetic recombination
KW  - Genetic regulation
KW  - Mutation (Biology)
KW  - Genetic Therapy
KW  - Laboratory Manuals
KW  - mesh
N1  - Includes bibliographical references and index; RecTEPsy-mediated recombineering in Pseudomonas syringae; Bryan Swingle -; Genome manipulations with bacterial recombineering and site-specific integration in Drosophila; Yi Zhang, William Schreiner, and Yikang S. Rong --; Multiple genetic manipulations of DT40 cell line; Akira Motegi and Minoru Takata --; Gene targeting of human pluripotent stem cells by homologous recombination; Sara E. Howden and James A. Thomson --; Methods for the assessment of ssODN-mediated gene correction frequencies in muscle cells; Carmen Bertoni --; Small fragment homologous replacement (SFHR) : sequence-specific modification of genomic DNA in eukaryotic cells by small DNA fragments; Andrea Luchetti, Arianna Malgieri, and Federica Sangiuolo --; Preparation and application of triple helix forming oligonucleotides and single strand oligonucleotide donors for gene correction; Md. Rowshon Alam ... [et al.] --; Triplex-mediated genome targeting and editing; Faisal Reza and Peter M. Glazer --; Targeting piggyBac transposon integrations in the human genome; Daniel L. Galvan, Claudia S. Kettlun, and Matthew H. Wilson --; Gene targeting in human-induced pluripotent stem cells with adenoviral vectors; Kohnosuke Mitani --; Enhanced gene targeting of adult and pluripotent stem cells using evolved adeno-associated virus; Melissa A. Bartel and David V. Schaffer --; Lentiviral vectors encoding zinc-finger nucleases specific for the model target locus HPRT1; Laetitia P.L. Pelascini and Manuel A.F.V. Gonçalves --; Designing and testing the activities of TAL effector nucleases; Yanni Lin, Thomas J. Cradick, and Gang Bao --; Bacterial one-hybrid system to isolate homing endonuclease variants with altered DNA target specificities; Rakesh Joshi and Frederick S. Gimble --; Design and analysis of site-specific single-strand nicking endonucleases for gene correction; Michael J. Metzger and Michael T. Certo --; CRISPR-Cas-mediated targeted genome editing in human cells; Luhan Yang ... [et al.] --; RNA-guided genome editing of mammalian cells; Neena K. Pyzocha ... [et al.] --; Nuclease-mediated double-strand break (DSB) enhancement of small fragment homologous recombination (SFHR) gene modification in human- induced pluripotent stem cells (hiPSCs); R. Geoffrey Sargent, Shingo Suzuki, and Dieter C. Gruenert --; AAV-mediated gene editing via double-strand break repair; Matthew L. Hirsch and R. Jude Samulski --; Genetic modification stimulated by the induction of a site- specific break distant from the locus of correction in haploid and diploid yeast Saccharomyces cerevisiae; Samantha Stuckey and Francesca Storici --; Southern blot protocol to detect chimeric nuclease- mediated gene repair; Céline J. Rocca ... [et al.] --; High-throughput cellular screening of engineered nuclease activity using the single-strand annealing assay and luciferase reporter; Thomas J. Cradick, Christopher J. Antico, and Gang Bao --; Unbiased method for detection of genome-wide off- target effects in cell lines treated with zinc finger nucleases; Cory R. Lindsay and David B. Roth --; Identification of off-target cleavage sites of zinc finger nucleases and TAL effector nucleases using predictive models; Eli J. Fine, Thomas J. Cradick, and Gang Bao --; Method for retinal gene repair in neonatal mouse; Marilyn Dernigoghossian ... [et al.] --; In utero delivery of oligodeoxynucleotides for gene correction; Lingzhi Cai ... [et al.] --; Portal vein delivery of viral vectors for gene therapy for hemophilia; Alexandra Sherman ... [et al.] --; Gene correction of induced pluripotent stem cells derived from a murine model of x-linked chronic granulomatous disorder; Sayandip Mukherjee and Adrian J. Thrasher --; Efficient transduction of hematopoietic stem cells and its potential for gene correction of hematopoietic diseases; Dolly Thomas and Gustavo Mostoslavsky
ER  -