Extensive genomic copy number variation in embryonic stem cells
about
Site specific mutation of the Zic2 locus by microinjection of TALEN mRNA in mouse CD1, C3H and C57BL/6J oocytesA conditional knockout resource for the genome-wide study of mouse gene functionMechanisms of change in gene copy numberZinc-finger nuclease-induced gene repair with oligodeoxynucleotides: wanted and unwanted target locus modificationsA genetic screen using the PiggyBac transposon in haploid cells identifies Parp1 as a mediator of olaparib toxicityCharacterizing complex structural variation in germline and somatic genomesThe human genome puzzle - the role of copy number variation in somatic mosaicismNucleotide, cytogenetic and expression impact of the human chromosome 8p23.1 inversion polymorphism.Early embryonic chromosome instability results in stable mosaic pattern in human tissuesA hyperactive piggyBac transposase for mammalian applicationsLandscape of standing variation for tandem duplications in Drosophila yakuba and Drosophila simulans.Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.DNA template strand sequencing of single-cells maps genomic rearrangements at high resolution.Passage number is a major contributor to genomic structural variations in mouse iPSCs.A practical and efficient cellular substrate for the generation of induced pluripotent stem cells from adults: blood-derived endothelial progenitor cellsGenetics. Genome mosaicism--one human, multiple genomes.Controlled somatic and germline copy number variation in the mouse modelSystematic genome sequence differences among leaf cells within individual trees.Is mouse embryonic stem cell technology obsolete?Isolation of homozygous mutant mouse embryonic stem cells using a dual selection system.Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells.Agouti C57BL/6N embryonic stem cells for mouse genetic resourcesReplication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants.Impact of retrotransposons in pluripotent stem cellsSUN1 and SUN2 play critical but partially redundant roles in anchoring nuclei in skeletal muscle cells in mice.High-Sensitivity Mass Spectrometry for Probing Gene Translation in Single Embryonic Cells in the Early Frog (Xenopus) Embryo.Developmental and environmental variation in genomes.Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood.Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines.Rapid target gene validation in complex cancer mouse models using re-derived embryonic stem cells.Assessing the value of autologous and allogeneic cells for regenerative medicine.Quality control: Genome maintenance in pluripotent stem cells.Cancer quasispecies and stem-like adaptive aneuploidy.Systematic generation of in vivo G protein-coupled receptor mutants in the rat.Aneuploid embryonic stem cells exhibit impaired differentiation and increased neoplastic potential.Achilles' heel of pluripotent stem cells: genetic, genomic and epigenetic variations during prolonged culture.Generating Genetically Modified Mice: A Decision Guide.Behavior genetics and postgenomics.Using the GEMM-ESC strategy to study gene function in mouse models.
P2860
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P2860
Extensive genomic copy number variation in embryonic stem cells
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Extensive genomic copy number variation in embryonic stem cells
@en
type
label
Extensive genomic copy number variation in embryonic stem cells
@en
prefLabel
Extensive genomic copy number variation in embryonic stem cells
@en
P2093
P2860
P356
P1476
Extensive genomic copy number variation in embryonic stem cells
@en
P2093
Allan Bradley
William C Skarnes
P2860
P304
17453-17456
P356
10.1073/PNAS.0805638105
P407
P577
2008-11-06T00:00:00Z