Search Results - "Gurumurthy, Channabasavaiah"

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    Easi-CRISPR for creating knock-in and conditional knockout mouse models using long ssDNA donors by Miura, Hiromi, Quadros, Rolen M, Gurumurthy, Channabasavaiah B, Ohtsuka, Masato

    Published in Nature protocols (01-01-2018)
    “…This protocol describes Easi -CRISPR, a method for creating knock-in, conditional knockout, and knockdown mouse models by CRISPR/Cas9-based genome engineering…”
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    Generating mouse models for biomedical research: technological advances by Gurumurthy, Channabasavaiah B, Lloyd, Kevin C Kent

    Published in Disease models & mechanisms (01-01-2019)
    “…Over the past decade, new methods and procedures have been developed to generate genetically engineered mouse models of human disease. This At a Glance article…”
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  3. 3

    Cross-contamination of CRISPR guides and other unrelated nucleotide sequences among commercial oligonucleotides by Arakawa, Hiroshi, Miura, Hiromi, Quadros, Rolen M, Ohtsuka, Masato, Gurumurthy, Channabasavaiah B

    Published in Nucleic acids research (12-04-2024)
    “…Custom oligonucleotides (oligos) are widely used reagents in biomedical research. Some common applications of oligos include polymerase chain reaction (PCR),…”
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    Arid1b haploinsufficiency disrupts cortical interneuron development and mouse behavior by Jung, Eui-Man, Moffat, Jeffrey Jay, Liu, Jinxu, Dravid, Shashank Manohar, Gurumurthy, Channabasavaiah Basavaraju, Kim, Woo-Yang

    Published in Nature neuroscience (01-12-2017)
    “…Haploinsufficiency of the AT-rich interactive domain 1B ( ARID1B ) gene causes autism spectrum disorder and intellectual disability; however, the…”
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    CRISPR/Cas9-based generation of knockdown mice by intronic insertion of artificial microRNA using longer single-stranded DNA by Miura, Hiromi, Gurumurthy, Channabasavaiah B, Sato, Takehito, Sato, Masahiro, Ohtsuka, Masato

    Published in Scientific reports (05-08-2015)
    “…Knockdown mouse models, where gene dosages can be modulated, provide valuable insights into gene function. Typically, such models are generated by embryonic…”
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    i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases by Ohtsuka, Masato, Sato, Masahiro, Miura, Hiromi, Takabayashi, Shuji, Matsuyama, Makoto, Koyano, Takayuki, Arifin, Naomi, Nakamura, Shingo, Wada, Kenta, Gurumurthy, Channabasavaiah B

    Published in Genome Biology (26-02-2018)
    “…We present a robust method called improved-Genome editing via Oviductal Nucleic Acids Delivery (i-GONAD) that delivers CRISPR ribonucleoproteins to E0.7…”
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    Prototype mouse models for researching SEND-based mRNA delivery and gene therapy by Gurumurthy, Channabasavaiah B., Quadros, Rolen M., Ohtsuka, Masato

    Published in Nature protocols (01-10-2022)
    “…One of the major challenges of gene therapy—an approach to treat diseases caused by faulty genes—is a lack of technologies that deliver healthy gene copies to…”
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    Creation of CRISPR-based germline-genome-engineered mice without ex vivo handling of zygotes by i-GONAD by Gurumurthy, Channabasavaiah B., Sato, Masahiro, Nakamura, Ayaka, Inui, Masafumi, Kawano, Natsuko, Islam, Md Atiqul, Ogiwara, Sanae, Takabayashi, Shuji, Matsuyama, Makoto, Nakagawa, Shinichi, Miura, Hiromi, Ohtsuka, Masato

    Published in Nature protocols (01-08-2019)
    “…Methods to create genetically engineered mice involve three major steps: harvesting embryos from one set of females, microinjection of reagents into embryos ex…”
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    Cleavage by Caspase 8 and Mitochondrial Membrane Association Activate the BH3-only Protein Bid during TRAIL-induced Apoptosis by Huang, Kai, Zhang, Jingjing, O’Neill, Katelyn L., Gurumurthy, Channabasavaiah B., Quadros, Rolen M., Tu, Yaping, Luo, Xu

    Published in The Journal of biological chemistry (27-05-2016)
    “…The BH3-only protein Bid is known as a critical mediator of the mitochondrial pathway of apoptosis following death receptor activation. However, since…”
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    GONAD: Genome-editing via Oviductal Nucleic Acids Delivery system: a novel microinjection independent genome engineering method in mice by Takahashi, Gou, Gurumurthy, Channabasavaiah B, Wada, Kenta, Miura, Hiromi, Sato, Masahiro, Ohtsuka, Masato

    Published in Scientific reports (22-06-2015)
    “…Microinjection is considered the gold standard technique for delivery of nucleic acids (NAs; transgenes or genome editing tools such as CRISPR/Cas9 systems)…”
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    Genetically modified mouse models to help fight COVID-19 by Gurumurthy, Channabasavaiah B., Quadros, Rolen M., Richardson, Guy P., Poluektova, Larisa Y., Mansour, Suzanne L., Ohtsuka, Masato

    Published in Nature protocols (01-12-2020)
    “…The research community is in a race to understand the molecular mechanisms of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, to…”
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    Precise and efficient nucleotide substitution near genomic nick via noncanonical homology-directed repair by Nakajima, Kazuhiro, Zhou, Yue, Tomita, Akiko, Hirade, Yoshihiro, Gurumurthy, Channabasavaiah B, Nakada, Shinichiro

    Published in Genome research (01-02-2018)
    “…CRISPR/Cas9, which generates DNA double-strand breaks (DSBs) at target loci, is a powerful tool for editing genomes when codelivered with a donor DNA template…”
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    Knock-in mouse models for studying somatostatin and cholecystokinin expressing cells by Balog, Marta, Anderson, Allison, Gurumurthy, Channabasavaiah B., Quadros, Rolen M., Korade, Zeljka, Mirnics, Karoly

    Published in Journal of neuroscience methods (01-11-2022)
    “…Somatostatin (SST) and cholecystokinin (CCK) are peptide hormones that regulate the endocrine system, cell proliferation and neurotransmission. We utilized the…”
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    Improved Genome Editing via Oviductal Nucleic Acids Delivery (i-GONAD): Protocol Steps and Additional Notes by Sato, Masahiro, Nakamura, Ayaka, Sekiguchi, Marie, Matsuwaki, Takashi, Miura, Hiromi, Gurumurthy, Channabasavaiah B, Kakuta, Shigeru, Ohtsuka, Masato

    “…The clustered regularly interspaced short palindromic repeats (CRISPR) technology has made it possible to produce genome-edited (GE) animals more easily and…”
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    Rescue of auditory function by a single administration of AAV-TMPRSS3 gene therapy in aged mice of human recessive deafness DFNB8 by Du, Wan, Ergin, Volkan, Loeb, Corena, Huang, Mingqian, Silver, Stewart, Armstrong, Ariel Miura, Huang, Zaohua, Gurumurthy, Channabasavaiah B., Staecker, Hinrich, Liu, Xuezhong, Chen, Zheng-Yi

    Published in Molecular therapy (06-09-2023)
    “…Patients with mutations in the TMPRSS3 gene suffer from recessive deafness DFNB8/DFNB10. For these patients, cochlear implantation is the only treatment…”
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