Related references
Note: Only part of the references are listed.Adenine base editing in an adult mouse model of tyrosinaemia
Chun-Qing Song et al.
NATURE BIOMEDICAL ENGINEERING (2020)
Simplified adenine base editors improve adenine base editing efficiency in rice
Kai Hua et al.
PLANT BIOTECHNOLOGY JOURNAL (2020)
'Off-the-shelf' allogeneic CAR T cells: development and challenges
S. Depil et al.
NATURE REVIEWS DRUG DISCOVERY (2020)
Cytosine base editor 4 but not adenine base editor generates off-target mutations in mouse embryos
Hye Kyung Lee et al.
COMMUNICATIONS BIOLOGY (2020)
Expanding the base editing scope in rice by using Cas9 variants
Kai Hua et al.
PLANT BIOTECHNOLOGY JOURNAL (2019)
Transcriptome-wide off-target RNA editing induced by CRISPR-guided DNA base editors
Julian Grunewald et al.
NATURE (2019)
Circularly permuted and PAM-modified Cas9 variants broaden the targeting scope of base editors
Tony P. Huang et al.
NATURE BIOTECHNOLOGY (2019)
Analysis and minimization of cellular RNA editing by DNA adenine base editors
Holly A. Rees et al.
SCIENCE ADVANCES (2019)
Off-target RNA mutation induced by DNA base editing and its elimination by mutagenesis
Changyang Zhou et al.
NATURE (2019)
Development of hRad51-Cas9 nickase fusions that mediate HDR without double-stranded breaks
Holly A. Rees et al.
NATURE COMMUNICATIONS (2019)
CRISPR DNA base editors with reduced RNA off-target and self-editing activities
Julian Grunewald et al.
NATURE BIOTECHNOLOGY (2019)
Adenine base editors catalyze cytosine conversions in human cells
Heon Seok Kim et al.
NATURE BIOTECHNOLOGY (2019)
Targeting specificity of APOBEC-based cytosine base editor in human iPSCs determined by whole genome sequencing
Erica McGrath et al.
NATURE COMMUNICATIONS (2019)
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors
Beau R. Webber et al.
NATURE COMMUNICATIONS (2019)
First-in-Human Assessment of Feasibility and Safety of Multiplexed Genetic Engineering of Autologous T Cells Expressing NY-ESO-1 TCR and CRISPR/Cas9 Gene Edited to Eliminate Endogenous TCR and PD-1 (NYCE T cells) in Advanced Multiple Myeloma (MM) and Sarcoma
Edward A. Stadtmauer et al.
BLOOD (2019)
Highly Efficient A.T to G.C Base Editing by Cas9n-Guided tRNA Adenosine Deaminase in Rice
Fang Yan et al.
MOLECULAR PLANT (2018)
Precise A.T to G.C Base Editing in the Rice Genome
Kai Hua et al.
MOLECULAR PLANT (2018)
Adenine base editing in mouse embryos and an adult mouse model of Duchenne muscular dystrophy
Seuk-Min Ryu et al.
NATURE BIOTECHNOLOGY (2018)
Chimeric Antigen Receptor Therapy
Carl H. June et al.
NEW ENGLAND JOURNAL OF MEDICINE (2018)
In vivo base editing of post-mitotic sensory cells
Wei-Hsi Yeh et al.
NATURE COMMUNICATIONS (2018)
Highly efficient RNA-guided base editing in rabbit
Zhiquan Liu et al.
NATURE COMMUNICATIONS (2018)
Correction of the Marfan Syndrome Pathogenic FBN1 Mutation by Base Editing in Human Cells and Heterozygous Embryos
Yanting Zeng et al.
MOLECULAR THERAPY (2018)
Engineered CRISPR-Cas9 nuclease with expanded targeting space
Hiroshi Nishimasu et al.
SCIENCE (2018)
Increasing targeting scope of adenosine base editors in mouse and rat embryos through fusion of TadA deaminase with Cas9 variants
Lei Yang et al.
PROTEIN & CELL (2018)
Base editing: precision chemistry on the genome and transcriptome of living cells
Holly A. Rees et al.
NATURE REVIEWS GENETICS (2018)
Multiplex Genome Editing to Generate Universal CAR T Cells Resistant to PD1 Inhibition
Jiangtao Ren et al.
CLINICAL CANCER RESEARCH (2017)
Programmable base editing of A.T to G.C in genomic DNA without DNA cleavage
Nicole M. Gaudelli et al.
NATURE (2017)
Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells
Waseem Qasim et al.
SCIENCE TRANSLATIONAL MEDICINE (2017)
Improving the DNA specificity and applicability of base editing through protein engineering and protein delivery
Holly A. Rees et al.
NATURE COMMUNICATIONS (2017)
At least 20% donor myeloid chimerism is necessary to reverse the sickle phenotype after allogeneic HSCT
Courtney D. Fitzhugh et al.
BLOOD (2017)
KLF1 drives the expression of fetal hemoglobin in British HPFH
Beeke Wienert et al.
BLOOD (2017)
ClinVar: public archive of interpretations of clinically relevant variants
Melissa J. Landrum et al.
NUCLEIC ACIDS RESEARCH (2016)
Customizing the genome as therapy for the β-hemoglobinopathies
Matthew C. Canver et al.
BLOOD (2016)
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
Alexis C. Komor et al.
NATURE (2016)
Multiplex Genome-Edited T-cell Manufacturing Platform for Off-the-Shelf Adoptive T-cell Immunotherapies
Laurent Poirot et al.
CANCER RESEARCH (2015)
In vivo genome editing using Staphylococcus aureus Cas9
F. Ann Ran et al.
NATURE (2015)
Chemically modified guide RNAs enhance CRISPR-Cas genome editing in human primary cells
Ayal Hendel et al.
NATURE BIOTECHNOLOGY (2015)
GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases
Shengdar Q. Tsai et al.
NATURE BIOTECHNOLOGY (2015)
ClinVar: public archive of relationships among sequence variation and human phenotype
Melissa J. Landrum et al.
NUCLEIC ACIDS RESEARCH (2014)
A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity
Martin Jinek et al.
SCIENCE (2012)
Miscoding properties of 2'-deoxyinosine, a nitric oxide-derived DNA adduct, during translesion synthesis catalyzed by human DNA polymerases
Manabu Yasui et al.
JOURNAL OF MOLECULAR BIOLOGY (2008)
USER fusion: a rapid and efficient method for simultaneous fusion and cloning of multiple PCR products
Fernando Geu-Flores et al.
NUCLEIC ACIDS RESEARCH (2007)
Specificity and expression of CIITA, the master regulator of MHC class II genes
S LeibundGut-Landmann et al.
EUROPEAN JOURNAL OF IMMUNOLOGY (2004)
Share Paper
