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Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice

Cell, 2020-04, Vol.181 (3), p.590-603.e16

2020

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Lentiviral delivery of co-packaged Cas9 mRNA and a Vegfa-targeting guide RNA prevents wet age-related macular degeneration in mice

Nature biomedical engineering, 2021-02, Vol.5 (2), p.144-156

2021

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CRISPR/Cas9-mediated targeted chromosome elimination

Genome Biology, 2017-11, Vol.18 (1), p.224-18, Article 224

2017

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Homology-mediated end joining-based targeted integration using CRISPR/Cas9

Cell research, 2017-06, Vol.27 (6), p.801-814

2017

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In vivo simultaneous transcriptional activation of multiple genes in the brain using CRISPR–dCas9-activator transgenic mice

Nature neuroscience, 2018-03, Vol.21 (3), p.440-446

2018

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Tild-CRISPR Allows for Efficient and Precise Gene Knockin in Mouse and Human Cells

Developmental cell, 2018-05, Vol.45 (4), p.526-536.e5

2018

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One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAs

Cell research, 2017-07, Vol.27 (7), p.933-945

2017

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Base editing-mediated splicing correction therapy for spinal muscular atrophy

Cell research, 2020-06, Vol.30 (6), p.548-550

2020

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Endogenous promoter-driven sgRNA for monitoring the expression of low-abundance transcripts and lncRNAs

Nature cell biology, 2021-01, Vol.23 (1), p.99-108

2021

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CRISPR/Cas9 – Mediated Precise Targeted Integration In Vivo Using a Double Cut Donor with Short Homology Arms

EBioMedicine, 2017-06, Vol.20 (C), p.19-26

2017

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Morphological changes of radial glial cells during mouse embryonic development

Brain research, 2015-03, Vol.1599, p.57-66

2015

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Screened AAV variants permit efficient transduction access to supporting cells and hair cells

Cell discovery, 2019-10, Vol.5 (1), p.1-4, Article 49

2019

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Off-target RNA mutation induced by DNA base editing and its elimination by mutagenesis

Nature (London), 2019-07, Vol.571 (7764), p.275-278

2019

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Synthesis of porous carbon-doped g-C3N4 nanosheets with enhanced visible-light photocatalytic activity

Applied surface science, 2017-05, Vol.403, p.682-690

2017

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Advanced Fabrication of Chemically Bonded Graphene/TiO2 Continuous Fibers with Enhanced Broadband Photocatalytic Properties and Involved Mechanisms Exploration

Scientific reports, 2016-12, Vol.6 (1), p.38066-38066, Article 38066

2016

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Error Floor Estimation of Long LDPC Codes on Magnetic Recording Channels

IEEE transactions on magnetics, 2010-06, Vol.46 (6), p.1836-1839

2010

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Performance Evaluation of Partial Response Targets for Perpendicular Recording Using Field Programmable Gate Arrays

IEEE transactions on magnetics, 2007-06, Vol.43 (6), p.2259-2261

2007

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BaseLine Wander Compensation by Per-Survivor-Processing

IEEE transactions on magnetics, 2006-10, Vol.42 (10), p.2609-2611

2006

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Intelligent Recognition Model of Business English Translation Based on Improved GLR Algorithm

Computational intelligence and neuroscience, 2022, Vol.2022, p.4105942-8

2022

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The SH2 domain is crucial for function of Fyn in neuronal migration and cortical lamination

BMB Reports, 2015, 48(2), , pp.97-102

2015

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Decoding Behavior Study of LDPC Codes Under a Realistic Magnetic Recording Channel Model

IEEE transactions on magnetics, 2006-10, Vol.42 (10), p.2606-2608

2006

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Robust iterative tree-pruning detection and LDPCC decoding

IEEE journal on selected areas in communications, 2005-05, Vol.23 (5), p.1013-1025

2005

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Mouse Fyn induces pseudopodium formation in Chinese hamster ovary cells

Journal of Veterinary Science, 2014, 15(1), , pp.111-115

2014

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Treatment of autosomal recessive hearing loss via in vivo CRISPR/Cas9-mediated optimized homology-directed repair in mice

Cell research, 2022-07, Vol.32 (7), p.699-702

2022

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Abundant Focal Adhesion Kinase Causes Aberrant Neuronal Migration Via Its Phosphorylation at Tyr925

Journal of molecular neuroscience, 2018, Vol.64 (1), p.102-110

2018

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Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice

Lentiviral delivery of co-packaged Cas9 mRNA and a Vegfa-targeting guide RNA prevents wet age-related macular degeneration in mice

CRISPR/Cas9-mediated targeted chromosome elimination

Homology-mediated end joining-based targeted integration using CRISPR/Cas9

In vivo simultaneous transcriptional activation of multiple genes in the brain using CRISPR–dCas9-activator transgenic mice

Tild-CRISPR Allows for Efficient and Precise Gene Knockin in Mouse and Human Cells

One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAs

Base editing-mediated splicing correction therapy for spinal muscular atrophy

Endogenous promoter-driven sgRNA for monitoring the expression of low-abundance transcripts and lncRNAs

CRISPR/Cas9 – Mediated Precise Targeted Integration In Vivo Using a Double Cut Donor with Short Homology Arms

Morphological changes of radial glial cells during mouse embryonic development

Screened AAV variants permit efficient transduction access to supporting cells and hair cells

Off-target RNA mutation induced by DNA base editing and its elimination by mutagenesis

Synthesis of porous carbon-doped g-C3N4 nanosheets with enhanced visible-light photocatalytic activity

Advanced Fabrication of Chemically Bonded Graphene/TiO2 Continuous Fibers with Enhanced Broadband Photocatalytic Properties and Involved Mechanisms Exploration

Error Floor Estimation of Long LDPC Codes on Magnetic Recording Channels

Performance Evaluation of Partial Response Targets for Perpendicular Recording Using Field Programmable Gate Arrays

BaseLine Wander Compensation by Per-Survivor-Processing

Intelligent Recognition Model of Business English Translation Based on Improved GLR Algorithm

The SH2 domain is crucial for function of Fyn in neuronal migration and cortical lamination

Decoding Behavior Study of LDPC Codes Under a Realistic Magnetic Recording Channel Model

Robust iterative tree-pruning detection and LDPCC decoding

Mouse Fyn induces pseudopodium formation in Chinese hamster ovary cells

Treatment of autosomal recessive hearing loss via in vivo CRISPR/Cas9-mediated optimized homology-directed repair in mice

Abundant Focal Adhesion Kinase Causes Aberrant Neuronal Migration Via Its Phosphorylation at Tyr925

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