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A CRISPR-Cas9-engineered mouse model for GPI-anchor deficiency mirrors human phenotypes and exhibits hippocampal synaptic dysfunctions.

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第一单位: Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.;Berlin-Brandenburg School for Regenerative Therapies, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.;Research Group Development and Disease, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.;Institute for Genomic Statistics and Bioinformatics, University of Bonn, 53127 Bonn, Germany.
作者单位: Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.;Berlin-Brandenburg School for Regenerative Therapies, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.;Research Group Development and Disease, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.;Institute for Genomic Statistics and Bioinformatics, University of Bonn, 53127 Bonn, Germany. [1] Animal Outcome Core Facility of the NeuroCure Center, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.;Institute of Cognitive Neurobiology, Humboldt University, 10117 Berlin, Germany. [2] Institute for Genomic Statistics and Bioinformatics, University of Bonn, 53127 Bonn, Germany.;Institute of Human Genetics, Faculty of Medicine, University Hospital Bonn, 53127 Bonn, Germany. [3] Neuroscience Research Center, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany. [4] Section for Translational Epilepsy Research, Department of Neuropathology, University Hospital Bonn, 53127 Bonn, Germany.;Department of Epileptology, University Hospital Bonn, 53127 Bonn, Germany. [5] Section for Translational Epilepsy Research, Department of Neuropathology, University Hospital Bonn, 53127 Bonn, Germany. [6] Anatomisches Institut, Anatomie und Zellbiologie, Faculty of Medicine, University of Bonn, 53115 Bonn, Germany. [7] Institute of Veterinary Pharmacology and Toxicology, University of Zürich (UZH), 8057 Zürich, Switzerland. [8] Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.;Research Group Development and Disease, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany. [9] Institute for Genomic Statistics and Bioinformatics, University of Bonn, 53127 Bonn, Germany. [10] Department Developmental Genetics, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany. [11] Sequencing Core Facility, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany. [12] The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032.;Institute for Systems Genomics, University of Connecticut, Farmington, CT 06032. [13] Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany. [14] Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, 13353 Berlin, Germany.;Research Group Development and Disease, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.;Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany. [15] Institute for Genomic Statistics and Bioinformatics, University of Bonn, 53127 Bonn, Germany; pkrawitz@uni-bonn.de. [16]
DOI 10.1073/pnas.2014481118
PMID 33402532
发布时间 2021-05-10
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Proceedings of the National Academy of Sciences of the United States of America

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