Repair of DNA double-strand breaks by templated nucleotide sequence insertions derived from distant regions of the genome.
about
Templated Sequence Insertion Polymorphisms in the Human GenomeMobile Bacterial Group II Introns at the Crux of Eukaryotic EvolutionCloning-free CRISPR/Cas system facilitates functional cassette knock-in in mice.Landscape of insertion polymorphisms in the human genomeHigh evolutionary turnover of satellite families in Caenorhabditis.Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3.Discovery and characterization of Alu repeat sequences via precise local read assembly.Transcript RNA supports precise repair of its own DNA gene.A LAIR1 insertion generates broadly reactive antibodies against malaria variant antigens.Transcript-RNA-templated DNA recombination and repairFrequent occurrence of large duplications at reciprocal genomic rearrangement breakpoints in multiple myeloma and other tumors.Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genesNuclear Noncoding RNAs and Genome Stability.Generation of Gross Chromosomal Rearrangements by a Single Engineered DNA Double Strand Break.Non-homologous DNA increases gene disruption efficiency by altering DNA repair outcomes.Genomic rearrangements induced by unscheduled DNA double strand breaks in somatic mammalian cells.Public antibodies to malaria antigens generated by two LAIR1 insertion modalities.A molecular perspective on a complex polymorphic inversion system with cytological evidence of multiply reused breakpoints.Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions.Efficient CRISPR/Cas9-Mediated Genome Editing Using a Chimeric Single-Guide RNA Molecule.RAG1/2 induces genomic insertions by mobilizing DNA into RAG1/2-independent breaksEvolution of Tandem Repeat Satellite Sequences in Two Closely Related Caenorhabditis Species. Diminution of Satellites in Hermaphrodites.The novel fusion transcript NR5A2-KLHL29FT is generated by an insertion at the KLHL29 locus.Thrombopoietin protects hematopoietic stem cells from retrotransposon-mediated damage by promoting an antiviral response.Lateral gene transfer between prokaryotes and eukaryotes.Transcription-associated events affecting genomic integrity.
P2860
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P2860
Repair of DNA double-strand breaks by templated nucleotide sequence insertions derived from distant regions of the genome.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Repair of DNA double-strand br ...... distant regions of the genome.
@ast
Repair of DNA double-strand br ...... distant regions of the genome.
@en
type
label
Repair of DNA double-strand br ...... distant regions of the genome.
@ast
Repair of DNA double-strand br ...... distant regions of the genome.
@en
prefLabel
Repair of DNA double-strand br ...... distant regions of the genome.
@ast
Repair of DNA double-strand br ...... distant regions of the genome.
@en
P2093
P2860
P356
P1476
Repair of DNA double-strand br ...... distant regions of the genome.
@en
P2093
Liat Goldberg
Masahiro Onozawa
P Leif Bergsagel
Peter D Aplan
Tamas Varga
W Michael Kuehl
Yoo Jung Kim
Zhenhua Zhang
P2860
P304
P356
10.1073/PNAS.1321889111
P407
P577
2014-05-12T00:00:00Z