Search Results - "Gurumurthy, Channabasavaiah"
-
1
Easi-CRISPR for creating knock-in and conditional knockout mouse models using long ssDNA donors
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…”
Get full text
Journal Article -
2
Generating mouse models for biomedical research: technological advances
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…”
Get full text
Journal Article -
3
Cross-contamination of CRISPR guides and other unrelated nucleotide sequences among commercial oligonucleotides
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),…”
Get full text
Journal Article -
4
Diagnostics for SARS-CoV-2 infections
Published in Nature materials (01-05-2021)“…Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has spread to nearly every corner of the globe, causing societal instability. The resultant…”
Get full text
Journal Article -
5
Arid1b haploinsufficiency disrupts cortical interneuron development and mouse behavior
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…”
Get full text
Journal Article -
6
CRISPR/Cas9-based generation of knockdown mice by intronic insertion of artificial microRNA using longer single-stranded DNA
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…”
Get full text
Journal Article -
7
i-GONAD: a robust method for in situ germline genome engineering using CRISPR nucleases
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…”
Get full text
Journal Article -
8
Easi-CRISPR: a robust method for one-step generation of mice carrying conditional and insertion alleles using long ssDNA donors and CRISPR ribonucleoproteins
Published in Genome Biology (17-05-2017)“…Conditional knockout mice and transgenic mice expressing recombinases, reporters, and inducible transcriptional activators are key for many genetic studies and…”
Get full text
Journal Article -
9
Prototype mouse models for researching SEND-based mRNA delivery and gene therapy
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…”
Get full text
Journal Article -
10
Creation of CRISPR-based germline-genome-engineered mice without ex vivo handling of zygotes by i-GONAD
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…”
Get full text
Journal Article -
11
Cleavage by Caspase 8 and Mitochondrial Membrane Association Activate the BH3-only Protein Bid during TRAIL-induced Apoptosis
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…”
Get full text
Journal Article -
12
Human genome-edited hematopoietic stem cells phenotypically correct Mucopolysaccharidosis type I
Published in Nature communications (06-09-2019)“…Lysosomal enzyme deficiencies comprise a large group of genetic disorders that generally lack effective treatments. A potential treatment approach is to…”
Get full text
Journal Article -
13
GONAD: Genome-editing via Oviductal Nucleic Acids Delivery system: a novel microinjection independent genome engineering method in mice
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)…”
Get full text
Journal Article -
14
Genetically modified mouse models to help fight COVID-19
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…”
Get full text
Journal Article -
15
Precise and efficient nucleotide substitution near genomic nick via noncanonical homology-directed repair
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…”
Get full text
Journal Article -
16
CD4+ effector T cells accelerate Alzheimer's disease in mice
Published in Journal of neuroinflammation (19-11-2021)“…Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by pathological deposition of misfolded self-protein amyloid beta (Aβ) which…”
Get full text
Journal Article -
17
Simplified CRISPR tools for efficient genome editing and streamlined protocols for their delivery into mammalian cells and mouse zygotes
Published in Methods (San Diego, Calif.) (15-05-2017)“…[Display omitted] •Efficient genome editing using crRNA, tracrRNA and Cas9 ribonucleoproteins (ctRNPs).•Delivery of CRISPR ctRNPs into mammalian cells via…”
Get full text
Journal Article -
18
Knock-in mouse models for studying somatostatin and cholecystokinin expressing cells
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…”
Get full text
Journal Article -
19
Improved Genome Editing via Oviductal Nucleic Acids Delivery (i-GONAD): Protocol Steps and Additional Notes
Published in Methods in molecular biology (Clifton, N.J.) (2023)“…The clustered regularly interspaced short palindromic repeats (CRISPR) technology has made it possible to produce genome-edited (GE) animals more easily and…”
Get more information
Journal Article -
20
Rescue of auditory function by a single administration of AAV-TMPRSS3 gene therapy in aged mice of human recessive deafness DFNB8
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…”
Get full text
Journal Article