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TKG
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Author Details
Full Name
Kosuke Yusa
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
2003
Papers
71
H Index
39
Expertise
CM4AI Collaborator
Prashant Mali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36717582
B1 SINE-binding ZFP266 impedes mouse iPSC generation through suppression of chromatin opening mediated by reprogramming factors.
Nat Commun
2023
37576222
Transposon delivery for CRISPR-based loss-of-function screen in mice identifies NF2 as a cooperating gene involved with the canonical WNT signaling molecular class of hepatocellular carcinoma.
Heliyon
2023
34638130
The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11.
Blood Adv
2022
36241868
AKT-mTORC1 reactivation is the dominant resistance driver for PI3Kβ/AKT inhibitors in PTEN-null breast cancer and can be overcome by combining with Mcl-1 inhibitors.
Oncogene
2022
36271468
Author Correction: Pooled extracellular receptor-ligand interaction screening using CRISPR activation.
Genome Biol
2022
36228744
Pharmacologic characterization of TBP1901, a prodrug form of aglycone curcumin, and CRISPR-Cas9 screen for therapeutic targets of aglycone curcumin.
Eur J Pharmacol
2022
35171652
Selective targeting of multiple myeloma cells with a monoclonal antibody recognizing the ubiquitous protein CD98 heavy chain.
Sci Transl Med
2022
35333572
Genome-wide screening identifies Polycomb repressive complex 1.3 as an essential regulator of human naïve pluripotent cell reprogramming.
Sci Adv
2022
32764680
KAT7 is a genetic vulnerability of acute myeloid leukemias driven by MLL rearrangements.
Leukemia
2021
34261826
Measurement of the nuclear concentration of α-ketoglutarate during adipocyte differentiation by using a fluorescence resonance energy transfer-based biosensor with nuclear localization signals.
Endocr J
2021
32251294
Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions.
Nat Commun
2020
32005967
Author Correction: ARID1A influences HDAC1/BRD4 activity, intrinsic proliferative capacity and breast cancer treatment response.
Nat Genet
2020
31913353
ARID1A influences HDAC1/BRD4 activity, intrinsic proliferative capacity and breast cancer treatment response.
Nat Genet
2020
30639098
Genome-wide CRISPR Screens in T Helper Cells Reveal Pervasive Crosstalk between Activation and Differentiation.
Cell
2019
31862961
Agreement between two large pan-cancer CRISPR-Cas9 gene dependency data sets.
Nat Commun
2019
31097696
Functional linkage of gene fusions to cancer cell fitness assessed by pharmacological and CRISPR-Cas9 screening.
Nat Commun
2019
31034882
Genome-wide CRISPR-Cas9 screening in mammalian cells.
Methods
2019
30971826
Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens.
Nature
2019
30722791
Structural rearrangements generate cell-specific, gene-independent CRISPR-Cas9 loss of fitness effects.
Genome Biol
2019
30932271
CRISPR-Knockout Screen Identifies Dmap1 as a Regulator of Chemically Induced Reprogramming and Differentiation of Cardiac Progenitors.
Stem Cells
2019
30674557
JACKS: joint analysis of CRISPR/Cas9 knockout screens.
Genome Res
2019
30622252
ATM orchestrates the DNA-damage response to counter toxic non-homologous end-joining at broken replication forks.
Nat Commun
2019
29748565
Genome-wide and high-density CRISPR-Cas9 screens identify point mutations in PARP1 causing PARP inhibitor resistance.
Nat Commun
2018
30103702
Unsupervised correction of gene-independent cell responses to CRISPR-Cas9 targeting.
BMC Genomics
2018
29914970
Genome-scale identification of cellular pathways required for cell surface recognition.
Genome Res
2018
29996108
Genome-wide CRISPR-KO Screen Uncovers mTORC1-Mediated Gsk3 Regulation in Naive Pluripotency Maintenance and Dissolution.
Cell Rep
2018
30568163
SRPK1 maintains acute myeloid leukemia through effects on isoform usage of epigenetic regulators including BRD4.
Nat Commun
2018
30477585
Pooled extracellular receptor-ligand interaction screening using CRISPR activation.
Genome Biol
2018
29728365
A CRISPR knockout screen identifies SETDB1-target retroelement silencing factors in embryonic stem cells.
Genome Res
2018
29643451
Author Correction: Optimised metrics for CRISPR-KO screens with second-generation gRNA libraries.
Sci Rep
2018
28835438
Molecular synergy underlies the co-occurrence patterns and phenotype of <i>NPM1</i>-mutant acute myeloid leukemia.
Blood
2017
28388235
Applications of CRISPR genome editing technology in drug target identification and validation.
Expert Opin Drug Discov
2017
29174331
Constitutively Active SMAD2/3 Are Broad-Scope Potentiators of Transcription-Factor-Mediated Cellular Reprogramming.
Cell Stem Cell
2017
28785007
Optimised metrics for CRISPR-KO screens with second-generation gRNA libraries.
Sci Rep
2017
27054363
Mutational History of a Human Cell Lineage from Somatic to Induced Pluripotent Stem Cells.
PLoS Genet
2016
27760321
A CRISPR Dropout Screen Identifies Genetic Vulnerabilities and Therapeutic Targets in Acute Myeloid Leukemia.
Cell Rep
2016
25378133
Off-target assessment of CRISPR-Cas9 guiding RNAs in human iPS and mouse ES cells.
Genesis
2015
26104701
piggyBac Transposon.
Microbiol Spectr
2015
25408399
piggyBac transposon-based insertional mutagenesis in mouse haploid embryonic stem cells.
Methods Mol Biol
2015
24535568
Genome-wide recessive genetic screening in mammalian cells with a lentiviral CRISPR-guide RNA library.
Nat Biotechnol
2014
25418962
Simulation and estimation of gene number in a biological pathway using almost complete saturation mutagenesis screening of haploid mouse cells.
BMC Genomics
2014
25024429
Removal of reprogramming transgenes improves the tissue reconstitution potential of keratinocytes generated from human induced pluripotent stem cells.
Stem Cells Transl Med
2014
23358416
The piggyBac transposon displays local and distant reintegration preferences and can cause mutations at noncanonical integration sites.
Mol Cell Biol
2013
24071911
Seamless genome editing in human pluripotent stem cells using custom endonuclease-based gene targeting and the piggyBac transposon.
Nat Protoc
2013
23908384
Enhancement of microhomology-mediated genomic rearrangements by transient loss of mouse Bloom syndrome helicase.
Genome Res
2013
23845441
A genetic progression model of Braf(V600E)-induced intestinal tumorigenesis reveals targets for therapeutic intervention.
Cancer Cell
2013
23990560
Nuclear Wave1 is required for reprogramming transcription in oocytes and for normal development.
Science
2013
23702683
Detailed molecular characterisation of acute myeloid leukaemia with a normal karyotype using targeted DNA capture.
Leukemia
2013
22184403
The critical role of histone H2A-deubiquitinase Mysm1 in hematopoiesis and lymphocyte differentiation.
Blood
2012
21992617
Hyperactive piggyBac gene transfer in human cells and in vivo.
Hum Gene Ther
2012
1 - 50 of 71
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Wellcome Sanger Institute
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Peter Ellis
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Keiko Akagi
The University of Texas MD Anderson Cancer Center
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Carlos Caldas
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Jacqueline K White
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