Search Results - "Tu, Zhuchi"
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Functional disruption of the dystrophin gene in rhesus monkey using CRISPR/Cas9
Published in Human molecular genetics (01-07-2015)“…CRISPR/Cas9 has been used to genetically modify genomes in a variety of species, including non-human primates. Unfortunately, this new technology does cause…”
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Promoting Cas9 degradation reduces mosaic mutations in non-human primate embryos
Published in Scientific reports (03-02-2017)“…CRISPR-Cas9 is a powerful new tool for genome editing, but this technique creates mosaic mutations that affect the efficiency and precision of its ability to…”
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CRISPR/Cas9-mediated PINK1 deletion leads to neurodegeneration in rhesus monkeys
Published in Cell research (01-04-2019)Get full text
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CRISPR/Cas9-mediated disruption of SHANK3 in monkey leads to drug-treatable autism-like symptoms
Published in Human molecular genetics (15-02-2019)“…Abstract Monogenic mutations in the SHANK3 gene, which encodes a postsynaptic scaffold protein, play a causative role in autism spectrum disorder (ASD)…”
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CRISPR/Cas9: a powerful genetic engineering tool for establishing large animal models of neurodegenerative diseases
Published in Molecular neurodegeneration (04-08-2015)“…Animal models are extremely valuable to help us understand the pathogenesis of neurodegenerative disorders and to find treatments for them. Since large animals…”
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Maternal valproic acid exposure leads to neurogenesis defects and autism-like behaviors in non-human primates
Published in Translational psychiatry (21-10-2019)“…Despite the substantial progress made in identifying genetic defects in autism spectrum disorder (ASD), the etiology for majority of ASD individuals remains…”
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PINK1 kinase dysfunction triggers neurodegeneration in the primate brain without impacting mitochondrial homeostasis
Published in Protein & cell (01-01-2022)“…In vitro studies have established the prevalent theory that the mitochondrial kinase PINK1 protects neurodegeneration by removing damaged mitochondria in…”
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Application of CRISPR/Cas9 System in Establishing Large Animal Models
Published in Frontiers in cell and developmental biology (17-05-2022)“…The foundation for investigating the mechanisms of human diseases is the establishment of animal models, which are also widely used in agricultural industry,…”
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A Specific Mini‐Intrabody Mediates Lysosome Degradation of Mutant Huntingtin
Published in Advanced science (01-11-2023)“…Abstract Accumulation of misfolded proteins leads to many neurodegenerative diseases that can be treated by lowering or removing mutant proteins. Huntington's…”
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Tauopathy promotes spinal cord-dependent production of toxic amyloid-beta in transgenic monkeys
Published in Signal transduction and targeted therapy (22-09-2023)“…Tauopathy, characterized by the hyperphosphorylation and accumulation of the microtubule-associated protein tau, and the accumulation of Aβ oligomers,…”
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Generation of inactivated IL2RG and RAG1 monkeys with severe combined immunodeficiency using base editing
Published in Signal transduction and targeted therapy (04-09-2023)“…Severe combined immunodeficiency (SCID) encompasses a range of inherited disorders that lead to a profound deterioration of the immune system. Among the…”
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Intravenous AAV9 administration results in safe and widespread distribution of transgene in the brain of mini-pig
Published in Frontiers in cell and developmental biology (24-01-2023)“…Animal models are important for understanding the pathogenesis of human diseases and for developing and testing new drugs. Pigs have been widely used in the…”
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CHD8 mutations increase gliogenesis to enlarge brain size in the nonhuman primate
Published in Cell discovery (07-03-2023)“…Autism spectrum disorder (ASD) is a complex neurodevelopmental condition that affects social interaction and behavior. Mutations in the gene encoding…”
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A Huntingtin Knockin Pig Model Recapitulates Features of Selective Neurodegeneration in Huntington’s Disease
Published in Cell (03-05-2018)“…Huntington’s disease (HD) is characterized by preferential loss of the medium spiny neurons in the striatum. Using CRISPR/Cas9 and somatic nuclear transfer…”
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Use of CRISPR/Cas9 to model brain diseases
Published in Progress in neuro-psychopharmacology & biological psychiatry (02-02-2018)“…•Genomic editing has been used to generate animal models of human diseases to mimic neurological symptoms and to study disease pathogenesis and treatments.•Of…”
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Altered neurogenesis and disrupted expression of synaptic proteins in prefrontal cortex of SHANK3-deficient non-human primate
Published in Cell research (01-10-2017)“…Dear Editor, Despite substantial progress made toward under- standing the molecular changes contributing to autism spectrum disorders (ASD), the…”
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TBN improves motor function and prolongs survival in a TDP-43M337V mouse model of ALS
Published in Human molecular genetics (28-07-2021)“…Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are serious neurodegenerative diseases. Although their pathogenesis is…”
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Large animal models for Huntington's disease research
Published in Dōngwùxué yánjiū (18-03-2024)“…Huntington's disease (HD) is a hereditary neurodegenerative disorder for which there is currently no effective treatment available. Consequently, the…”
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Deficiency of parkin causes neurodegeneration and accumulation of pathological α-synuclein in monkey models
Published in The Journal of clinical investigation (15-10-2024)“…Parkinson's disease (PD) is characterized by age-dependent neurodegeneration and the accumulation of toxic phosphorylated α-synuclein (pS129-α-syn). The…”
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Deficiency of parkin causes neurodegeneration and accumulation of pathological [alpha]-synuclein in monkey models
Published in The Journal of clinical investigation (15-10-2024)“…Parkinson's disease (PD) is characterized by age-dependent neurodegeneration and the accumulation of toxic phosphorylated [alpha]-synuclein…”
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