TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.
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EDEM2 initiates mammalian glycoprotein ERAD by catalyzing the first mannose trimming stepSingle-Base Pair Genome Editing in Human Cells by Using Site-Specific EndonucleasesStochastic promoter activation affects Nanog expression variability in mouse embryonic stem cellsPCS/MVA syndrome caused by an Alu insertion in the BUB1B geneCan genome engineering be used to target cancer-associated enhancers?Microhomology-mediated end-joining-dependent integration of donor DNA in cells and animals using TALENs and CRISPR/Cas9Epigenetic mechanisms underlying the pathogenesis of neurogenetic diseasesSimultaneous live imaging of the transcription and nuclear position of specific genes.CAUSEL: an epigenome- and genome-editing pipeline for establishing function of noncoding GWAS variants.Human genome editing as a tool to establish causalityA practical guide to induced pluripotent stem cell research using patient samples.Demystifying the secret mission of enhancers: linking distal regulatory elements to target genes.Emerging links among Chromosome Instability (CIN), cancer, and aging.Mechanisms for nonmitotic activation of Aurora-A at cilia.Prevalence of germline mutations in the spindle assembly checkpoint gene BUB1B in individuals with early-onset colorectal cancer.Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation.Kinetochore Malfunction in Human Pathologies.Ciliopathy in PCS (MVA) syndrome.The future of drug discovery: enabling technologies for enhancing lead characterization and profiling therapeutic potential.Methods for Scarless, Selection-Free Generation of Human Cells and Allele-Specific Functional Analysis of Disease-Associated SNPs and Variants of Uncertain Significance.Site-specific randomization of the endogenous genome by a regulatable CRISPR-Cas9 piggyBac system in human cells.Updated summary of genome editing technology in human cultured cells linked to human genetics studies.Analysis of individual differences in radiosensitivity using genome editing.Wilms tumor accompanied by premature chromatid separation.Exploration of genetic basis underlying individual differences in radiosensitivity within human populations using genome editing technology.
P2860
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P2860
TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 16 December 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
TALEN-mediated single-base-pai ...... usative of PCS (MVA) syndrome.
@en
TALEN-mediated single-base-pai ...... m of BUB1B as causative of PCS
@nl
type
label
TALEN-mediated single-base-pai ...... usative of PCS (MVA) syndrome.
@en
TALEN-mediated single-base-pai ...... m of BUB1B as causative of PCS
@nl
prefLabel
TALEN-mediated single-base-pai ...... usative of PCS (MVA) syndrome.
@en
TALEN-mediated single-base-pai ...... m of BUB1B as causative of PCS
@nl
P2093
P2860
P50
P356
P1476
TALEN-mediated single-base-pai ...... ausative of PCS (MVA) syndrome
@en
P2093
Akihiro Watanabe
Akinori Kanai
Atsushi Ogawa
Keiko Asami
Kosuke Hosoba
Tadashi Kajii
Yoshiki Kudo
P2860
P304
P356
10.1073/PNAS.1317008111
P407
P577
2013-12-16T00:00:00Z