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A PCR based protocol for detecting indel mutations induced by TALENs and CRISPR/Cas9 in zebrafish

PloS one, 2014-06, Vol.9 (6), p.e98282

2014

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Artificial Virus Delivers CRISPR-Cas9 System for Genome Editing of Cells in Mice

ACS nano, 2017-01, Vol.11 (1), p.95-111

2017

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Long Noncoding RNA LINC00092 Acts in Cancer-Associated Fibroblasts to Drive Glycolysis and Progression of Ovarian Cancer

Cancer research (Chicago, Ill.), 2017-03, Vol.77 (6), p.1369-1382

2017

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Recent advances in therapeutic CRISPR-Cas9 genome editing: mechanisms and applications

Molecular biomedicine, 2023-04, Vol.4 (1), p.10-10, Article 10

2023

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CRISPR/Cas9-Mediated Genome Editing of Epigenetic Factors for Cancer Therapy

Human gene therapy, 2015-07, Vol.26 (7), p.463-471

2015

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BE-PIGS: a base-editing tool with deaminases inlaid into Cas9 PI domain significantly expanded the editing scope

Signal transduction and targeted therapy, 2019-09, Vol.4 (1), p.36-36, Article 36

2019

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Case report: A case of delayed cutaneous metastases from signet-ring cell mixed-type gastric cancer

Frontiers in oncology, 2023-02, Vol.13, p.1105080

2023

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Enhancing prime editing via inhibition of mismatch repair pathway

Molecular biomedicine, 2022-02, Vol.3 (1), p.7-7, Article 7

2022

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sgBE: a structure-guided design of sgRNA architecture specifies base editing window and enables simultaneous conversion of cytosine and adenosine

Genome Biology, 2020-08, Vol.21 (1), p.222-222, Article 222

2020

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HDAC inhibitors improve CRISPR-Cas9 mediated prime editing and base editing

Molecular therapy. Nucleic acids, 2022-09, Vol.29, p.36-46

2022

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Recent Advances in CRISPR/Cas9 Directed Base Editing

Current gene therapy, 2021-01, Vol.21 (4), p.327-337

2021

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WT-PE: Prime editing with nuclease wild-type Cas9 enables versatile large-scale genome editing

Signal transduction and targeted therapy, 2022-04, Vol.7 (1), p.108-108, Article 108

2022

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Efficient Gene Targeting in Zebrafish Mediated by a Zebrafish-Codon- Optimized Cas9 and Evaluation of Off-Targeting Effect

Journal of genetics and genomics, 2014-01, Vol.41 (1), p.43-46

2014

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The RNA binding protein SORBS2 suppresses metastatic colonization of ovarian cancer by stabilizing tumor-suppressive immunomodulatory transcripts

Genome Biology, 2018-03, Vol.19 (1), p.35-35, Article 35

2018

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CRISPR/Cas9-mediated correction of human genetic disease

Science China. Life sciences, 2017-05, Vol.60 (5), p.447-457

2017

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Dual-AAV split prime editor corrects the mutation and phenotype in mice with inherited retinal degeneration

Signal transduction and targeted therapy, 2023-02, Vol.8 (1), p.57-57, Article 57

2023

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Wolf–Hirschhorn Syndrome Candidate 1 (whsc1) Functions as a Tumor Suppressor by Governing Cell Differentiation

Neoplasia (New York, N.Y.), 2017-08, Vol.19 (8), p.606-616

2017

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HDAC inhibitors improve CRISPR-Cas9 mediated prime editing and base editing

Molecular therapy. Nucleic acids, 2022-12, Vol.30, p.173-173

2022

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Nuclear Factor Kappa B Signaling Initiates Early Differentiation of Neural Stem Cells

Stem cells (Dayton, Ohio), 2012-03, Vol.30 (3), p.510-524

2012

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Polymeric Nanomedicine for Combined Gene/Chemotherapy Elicits Enhanced Tumor Suppression

Molecular pharmaceutics, 2016-02, Vol.13 (2), p.663-676

2016

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Transdifferentiation of fast skeletal muscle into functional endothelium in vivo by transcription factor Etv2

PLoS biology, 2013-06, Vol.11 (6), p.e1001590-e1001590

2013

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Long-Term Metabolic Correction of Phenylketonuria by AAV-Delivered Phenylalanine Amino Lyase

Molecular therapy. Methods & clinical development, 2020-12, Vol.19, p.507-517

2020

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A universal strategy for AAV delivery of base editors to correct genetic point mutations in neonatal PKU mice

Molecular therapy. Methods & clinical development, 2022-03, Vol.24, p.230-240

2022

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DnaQ mediates directional spacer acquisition in the CRISPR-Cas system by a time-dependent mechanism

Innovation (New York, NY), 2023-09, Vol.4 (5), p.100495-100495, Article 100495

2023

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Long-Term Metabolic Correction of Phenylketonuria by AAV-Delivered Phenylalanine Amino Lyase

Molecular therapy. Methods & clinical development, 2022-09, Vol.26, p.95-95

2022

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A PCR based protocol for detecting indel mutations induced by TALENs and CRISPR/Cas9 in zebrafish

Artificial Virus Delivers CRISPR-Cas9 System for Genome Editing of Cells in Mice

Long Noncoding RNA LINC00092 Acts in Cancer-Associated Fibroblasts to Drive Glycolysis and Progression of Ovarian Cancer

Recent advances in therapeutic CRISPR-Cas9 genome editing: mechanisms and applications

CRISPR/Cas9-Mediated Genome Editing of Epigenetic Factors for Cancer Therapy

BE-PIGS: a base-editing tool with deaminases inlaid into Cas9 PI domain significantly expanded the editing scope

Case report: A case of delayed cutaneous metastases from signet-ring cell mixed-type gastric cancer

Enhancing prime editing via inhibition of mismatch repair pathway

sgBE: a structure-guided design of sgRNA architecture specifies base editing window and enables simultaneous conversion of cytosine and adenosine

HDAC inhibitors improve CRISPR-Cas9 mediated prime editing and base editing

Recent Advances in CRISPR/Cas9 Directed Base Editing

WT-PE: Prime editing with nuclease wild-type Cas9 enables versatile large-scale genome editing

Efficient Gene Targeting in Zebrafish Mediated by a Zebrafish-Codon- Optimized Cas9 and Evaluation of Off-Targeting Effect

The RNA binding protein SORBS2 suppresses metastatic colonization of ovarian cancer by stabilizing tumor-suppressive immunomodulatory transcripts

CRISPR/Cas9-mediated correction of human genetic disease

Dual-AAV split prime editor corrects the mutation and phenotype in mice with inherited retinal degeneration

Wolf–Hirschhorn Syndrome Candidate 1 (whsc1) Functions as a Tumor Suppressor by Governing Cell Differentiation

HDAC inhibitors improve CRISPR-Cas9 mediated prime editing and base editing

Nuclear Factor Kappa B Signaling Initiates Early Differentiation of Neural Stem Cells

Polymeric Nanomedicine for Combined Gene/Chemotherapy Elicits Enhanced Tumor Suppression

Transdifferentiation of fast skeletal muscle into functional endothelium in vivo by transcription factor Etv2

Long-Term Metabolic Correction of Phenylketonuria by AAV-Delivered Phenylalanine Amino Lyase

A universal strategy for AAV delivery of base editors to correct genetic point mutations in neonatal PKU mice

DnaQ mediates directional spacer acquisition in the CRISPR-Cas system by a time-dependent mechanism

Long-Term Metabolic Correction of Phenylketonuria by AAV-Delivered Phenylalanine Amino Lyase

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