Stem cell-derived clade F AAVs mediate high-efficiency homologous recombination-based genome editing (Q59356657)

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article published in the Proceedings of the National Academy of Sciences of the United States of America

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English	Stem cell-derived clade F AAVs mediate high-efficiency homologous recombination-based genome editing	article published in the Proceedings of the National Academy of Sciences of the United States of America

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title

Stem cell-derived clade F AAVs mediate high-efficiency homologous recombination-based genome editing (English)

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corrigendum / erratum

Correction for Smith et al., Stem cell-derived clade F AAVs mediate high-efficiency homologous recombination-based genome editing

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author name string

Laura J Smith

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1

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Jason Wright

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2

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Gabriella Clark

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3

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Taihra Ul-Hasan

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4

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Xiangyang Jin

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5

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Abigail Fong

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6

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Manasa Chandra

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7

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Thia St Martin

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8

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Hillard Rubin

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9

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David Knowlton

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10

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Jeff L Ellsworth

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11

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Yuman Fong

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12

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Kamehameha K Wong

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13

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Saswati Chatterjee

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14

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language of work or name

English

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publication date

31 July 2018

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published in

Proceedings of the National Academy of Sciences of the United States of America

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volume

115

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issue

31

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page(s)

E7379-E7388

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cites work

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RAG-1 and RAG-2, adjacent genes that synergistically activate V(D)J recombination

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Altering the genome by homologous recombination

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The double-strand-break repair model for recombination

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Expression of a site-specific endonuclease stimulates homologous recombination in mammalian cells

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Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.

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Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16p13.13-p13.2.

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Ataxia-telangiectasia and cellular responses to DNA damage.

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Integration of adeno-associated virus vectors in CD34+ human hematopoietic progenitor cells after transduction.

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Genetic manipulation of genomes with rare-cutting endonucleases

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Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination

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Adeno-associated virus type 2-mediated transduction in primary human bone marrow-derived CD34+ hematopoietic progenitor cells: donor variation and correlation of transgene expression with cellular differentiation

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Evidence for at Least Eight Fanconi Anemia Genes

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Interstitial deletions and intrachromosomal amplification initiated from a double-strand break targeted to a mammalian chromosome

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Human gene targeting by viral vectors

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DNA breakage and repair

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Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae

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Ubiquitous expression of marker transgenes in mice and rats.

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Design and packaging of adeno-associated virus gene targeting vectors

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Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A

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dbSNP: the NCBI database of genetic variation

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BRCA2 is required for homology-directed repair of chromosomal breaks

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12 December 2020

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Role of BRCA2 in control of the RAD51 recombination and DNA repair protein.

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Targeted chromosomal cleavage and mutagenesis in Drosophila using zinc-finger nucleases

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Nbs1 is essential for DNA repair by homologous recombination in higher vertebrate cells

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12 December 2020

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Efficient gene targeting mediated by adeno-associated virus and DNA double-strand breaks

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Genetic reversion in an acute myelogenous leukemia cell line from a Fanconi anemia patient with biallelic mutations in BRCA2

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12 December 2020

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Roles of BRCA1 and BRCA2 in homologous recombination, DNA replication fidelity and the cellular response to ionizing radiation

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12 December 2020

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X-linked inheritance of Fanconi anemia complementation group B

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Impaired nuclear transport and uncoating limit recombinant adeno-associated virus 2 vector-mediated transduction of primary murine hematopoietic cells.

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Recombinant AAV2 transduction of primitive human hematopoietic stem cells capable of serial engraftment in immune-deficient mice

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12 December 2020

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Homologous recombination is required for AAV-mediated gene targeting

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12 December 2020

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Gene targeting in vivo by adeno-associated virus vectors.

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12 December 2020

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Ubiquitous and uniform in vivo fluorescence in ROSA26-EGFP BAC transgenic mice

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12 December 2020

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The Fanconi anemia pathway promotes homologous recombination repair in DT40 cell line.

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12 December 2020

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Quiescent subpopulations of human CD34-positive hematopoietic stem cells are preferred targets for stable recombinant adeno-associated virus type 2 transduction

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Analysis of AAV serotypes 1-9 mediated gene expression and tropism in mice after systemic injection

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12 December 2020

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Adeno-associated virus site-specific integration is mediated by proteins of the nonhomologous end-joining pathway

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12 December 2020

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Adeno-associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo.

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12 December 2020

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The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway

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12 December 2020

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Differential effects of DNA double-strand break repair pathways on single-strand and self-complementary adeno-associated virus vector genomes

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12 December 2020

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Rad52 inactivation is synthetically lethal with BRCA2 deficiency

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12 December 2020

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A TALE nuclease architecture for efficient genome editing

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Efficient construction of sequence-specific TAL effectors for modulating mammalian transcription

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12 December 2020

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AAV-mediated gene targeting methods for human cells

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12 December 2020

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A capillary electrophoresis sequencing method for the identification of mutations in the inverted terminal repeats of adeno-associated virus

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A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity

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Multiplex genome engineering using CRISPR/Cas systems

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12 December 2020

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RNA-guided human genome engineering via Cas9

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12 December 2020

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High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells

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12 December 2020

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Genome-wide analysis reveals characteristics of off-target sites bound by the Cas9 endonuclease.

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12 December 2020

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Targeted genome editing in human repopulating haematopoietic stem cells

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12 December 2020

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Gene transfer properties and structural modeling of human stem cell-derived AAV.

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12 December 2020

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Promoterless gene targeting without nucleases ameliorates haemophilia B in mice.

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GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases

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Therapeutic genome editing: prospects and challenges

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12 December 2020

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In vivo genome editing using Staphylococcus aureus Cas9

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12 December 2020

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Comparative Study of Liver Gene Transfer With AAV Vectors Based on Natural and Engineered AAV Capsids.

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12 December 2020

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Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system

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12 December 2020

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Efficient modification of CCR5 in primary human hematopoietic cells using a megaTAL nuclease and AAV donor template

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Highly efficient homology-driven genome editing in human T cells by combining zinc-finger nuclease mRNA and AAV6 donor delivery.

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12 December 2020

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Homology-driven genome editing in hematopoietic stem and progenitor cells using ZFN mRNA and AAV6 donors.

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12 December 2020

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Targeted gene addition in human CD34(+) hematopoietic cells for correction of X-linked chronic granulomatous disease

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12 December 2020

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Systematic quantification of HDR and NHEJ reveals effects of locus, nuclease, and cell type on genome-editing

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12 December 2020

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Interplay between Fanconi anemia and homologous recombination pathways in genome integrity

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12 December 2020

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High-Efficiency Transduction of Primary Human Hematopoietic Stem/Progenitor Cells by AAV6 Vectors: Strategies for Overcoming Donor-Variation and Implications in Genome Editing.

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12 December 2020

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CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes

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The control of DNA repair by the cell cycle

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12 December 2020

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Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin Deficiency.

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Identifiers

DOI

10.1073/PNAS.1802343115

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PMC publication ID

6077703

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PubMed publication ID

30018062

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