Citation Impact
Citing Papers
Correction of the Marfan Syndrome Pathogenic FBN1 Mutation by Base Editing in Human Cells and Heterozygous Embryos
2018
Fragile X mental retardation protein modulates the stability of its m6A-marked messenger RNA targets
2018
Precision cancer mouse models through genome editing with CRISPR-Cas9
2015
The role of m6A RNA methylation in human cancer
2019 Standout
The promise and challenge of therapeutic genome editing
2020 StandoutNatureNobel
Enhancing extracellular vesicle cargo loading and functional delivery by engineering protein-lipid interactions
2024 StandoutNobel
Selective disruption of an oncogenic mutant allele by CRISPR/Cas9 induces efficient tumor regression
2017
Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects
2020 Standout
Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage
2017 StandoutNature
Genome editing reveals a role for OCT4 in human embryogenesis
2017 Nature
Epitranscriptomic influences on development and disease
2017
Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors
2020 Standout
Where, When, and How: Context-Dependent Functions of RNA Methylation Writers, Readers, and Erasers
2019 Standout
Bridge helix arginines play a critical role in Cas9 sensitivity to mismatches
2020 StandoutNobel
Adeno-associated virus vector as a platform for gene therapy delivery
2019 Standout
Applications of CRISPR technologies in research and beyond
2016 StandoutNobel
Dynamic m6A modification regulates local translation of mRNA in axons
2017
Ubiquitination Regulates the Proteasomal Degradation and Nuclear Translocation of the Fat Mass and Obesity-Associated (FTO) Protein
2017
Reading, writing and erasing mRNA methylation
2019 Standout
The Biology of CRISPR-Cas: Backward and Forward
2018 StandoutNobel
CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes
2016 Standout
Engineering the Delivery System for CRISPR-Based Genome Editing
2018
Efficient delivery of nuclease proteins for genome editing in human stem cells and primary cells
2015
Correction of β-thalassemia mutant by base editor in human embryos
2017
Adenovirus-Mediated Somatic Genome Editing of Pten by CRISPR/Cas9 in Mouse Liver in Spite of Cas9-Specific Immune Responses
2015
In Vivo Delivery of CRISPR/Cas9 for Therapeutic Gene Editing: Progress and Challenges
2017
Inhibition of HIV-1 infection of primary CD4+ T-cells by gene editing of CCR5 using adenovirus-delivered CRISPR/Cas9
2015
Delivery of an Artificial Transcription Regulator dCas9-VPR by Extracellular Vesicles for Therapeutic Gene Activation
2018
Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery
2017 StandoutNobel
CRISPR-Cas guides the future of genetic engineering
2018 StandoutScienceNobel
A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice
2016
SUMOylation of the m6A-RNA methyltransferase METTL3 modulates its function
2018
Works of Lichun Tang being referenced
CRISPR/Cas9-mediated gene editing in human zygotes using Cas9 protein
2017
Efficient gene editing in adult mouse livers via adenoviral delivery of CRISPR/Cas9
2014
Fat mass and obesity-associated (FTO) protein regulates adult neurogenesis
2017