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British Journal of Pharmacology|April 29, 2010
High-throughput screening and small animal models, where are we?Jean Giacomotto, Laurent SégalatMolecular Psychiatry|November 16, 2020
Neurexins in autism and schizophrenia-a review of patient mutations, mouse models and potential future directionsAlisha Tromp, Bryan Mowry, Jean GiacomottoNeuroscience and Biobehavioral Reviews|May 23, 2026
Zebrafish Behavioral Phenotyping: Current Assays, Automated Platforms, and the Emerging Need for AI in Neuroscience, Drug Discovery and ToxicologyQuynh T N Nguyen, Jean GiacomottoNature Communications|June 9, 2015
Effective heritable gene knockdown in zebrafish using synthetic microRNAsJean Giacomotto, Silke Rinkwitz, Thomas S BeckerMethods (San Diego, Calif.)|November 2, 2011
Caenorhabditis elegans as a chemical screening tool for the study o f neuromuscular disorders. Manual and semi-automated methodsJean Giacomotto, Laurent Ségalat, Maïté Carre-Pierrat, et al.Communications Biology|June 26, 2021
Reduced C9orf72 function leads to defective synaptic vesicle release and neuromuscular dysfunction in zebrafishZoé Butti, Yingzhou Edward Pan, Jean Giacomotto, et al.Nucleic Acids Research|January 20, 2025
Cre-Lox miRNA-delivery technology optimized for inducible microRNA and gene-silencing studies in zebrafishFangfei Guo, Alisha Tromp, Haitao Wang, et al.Frontiers in Physiology|August 21, 2023
Optimising the zebrafish Cre/Lox toolbox. Codon improved iCre, new gateway tools, Cre protein and guidelinesAlisha Tromp, Haitao Wang, Thomas E Hall, et al.G3 (Bethesda, Md.)|September 9, 2021
Pipeline for generating stable large genomic deletions in zebrafish, from small domains to whole gene excisionsAlisha Tromp, Kate Robinson, Thomas E Hall, et al.Human Molecular Genetics|February 25, 2016
Tissue-specific models of spinal muscular atrophy confirm a critical role of SMN in motor neurons from embryonic to adult stagesAngela S Laird, Nikolce Mackovski, Silke Rinkwitz, et al.Pageof 4