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A CRISPR-Cas9-engineered mouse model for GPI anchor deficiency mirrors human phenotype and shows hippocampal synaptic dysfunctions
View ORCID ProfileMiguel Rodríguez de los Santos, View ORCID ProfileMarion Rivalan, Friederike S. David, Alexej Knaus, Alexander Stumpf, Laura Moreno Velasquez, Anne Voigt, Daniele Mattei, Melissa Long, Guido Vogt, Lars Wittler, Bernd Timmermann, Peter N. Robinson, Denise Horn, Stefan Mundlos, Uwe Kornak, Dietmar Schmitz, York Winter, View ORCID ProfilePeter M. Krawitz
doi: https://doi.org/10.1101/2020.04.20.050591
Miguel Rodríguez de los Santos
1Institute for Medical Genetics and Human Genetics, Charité – Universitätsmedizin Berlin, Germany
2Berlin-Brandenburg School for Regenerative Therapies, Berlin, Germany
3Max-Planck-Institute for molecular Genetics, FG Development and Disease, Berlin, Germany
4Institute for Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany
Marion Rivalan
5Animal Outcome Core Facility of the NeuroCure Center, Charité – Universitätsmedizin Berlin, Germany and Institute of Cognitive Neurobiology, Humboldt University Berlin, Germany
Friederike S. David
4Institute for Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany
6Institute of Human Genetics, University of Bonn, Faculty of Medicine & University Hospital Bonn, Bonn, Germany
Alexej Knaus
4Institute for Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany
Alexander Stumpf
7Neuroscience Research Center, Charité - Universitätsmedizin, Berlin, Germany
Laura Moreno Velasquez
7Neuroscience Research Center, Charité - Universitätsmedizin, Berlin, Germany
Anne Voigt
7Neuroscience Research Center, Charité - Universitätsmedizin, Berlin, Germany
Daniele Mattei
8Institute of Veterinary Pharmacology and Toxicology, University of Zurich, UZH, Zürich, Switzerland
Melissa Long
5Animal Outcome Core Facility of the NeuroCure Center, Charité – Universitätsmedizin Berlin, Germany and Institute of Cognitive Neurobiology, Humboldt University Berlin, Germany
Guido Vogt
1Institute for Medical Genetics and Human Genetics, Charité – Universitätsmedizin Berlin, Germany
3Max-Planck-Institute for molecular Genetics, FG Development and Disease, Berlin, Germany
Lars Wittler
9Max-Planck-Institute for molecular Genetics, Department Developmental Genetics, Berlin, Germany
Bernd Timmermann
10Max Planck Institute for Molecular Genetics, Sequencing Core Facility, Berlin, Germany
Peter N. Robinson
11The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA
12Institute for Systems Genomics, University of Connecticut, Farmington, Connecticut, USA
Denise Horn
1Institute for Medical Genetics and Human Genetics, Charité – Universitätsmedizin Berlin, Germany
Stefan Mundlos
1Institute for Medical Genetics and Human Genetics, Charité – Universitätsmedizin Berlin, Germany
3Max-Planck-Institute for molecular Genetics, FG Development and Disease, Berlin, Germany
13BCRT-Berlin Institute of Health Center for Regenerative Therapies, Charité Universitätsmedizin, Berlin
Uwe Kornak
1Institute for Medical Genetics and Human Genetics, Charité – Universitätsmedizin Berlin, Germany
13BCRT-Berlin Institute of Health Center for Regenerative Therapies, Charité Universitätsmedizin, Berlin
Dietmar Schmitz
7Neuroscience Research Center, Charité - Universitätsmedizin, Berlin, Germany
York Winter
5Animal Outcome Core Facility of the NeuroCure Center, Charité – Universitätsmedizin Berlin, Germany and Institute of Cognitive Neurobiology, Humboldt University Berlin, Germany
Peter M. Krawitz
4Institute for Genomic Statistics and Bioinformatics, University of Bonn, Bonn, Germany
Posted April 21, 2020.
A CRISPR-Cas9-engineered mouse model for GPI anchor deficiency mirrors human phenotype and shows hippocampal synaptic dysfunctions
Miguel Rodríguez de los Santos, Marion Rivalan, Friederike S. David, Alexej Knaus, Alexander Stumpf, Laura Moreno Velasquez, Anne Voigt, Daniele Mattei, Melissa Long, Guido Vogt, Lars Wittler, Bernd Timmermann, Peter N. Robinson, Denise Horn, Stefan Mundlos, Uwe Kornak, Dietmar Schmitz, York Winter, Peter M. Krawitz
bioRxiv 2020.04.20.050591; doi: https://doi.org/10.1101/2020.04.20.050591
A CRISPR-Cas9-engineered mouse model for GPI anchor deficiency mirrors human phenotype and shows hippocampal synaptic dysfunctions
Miguel Rodríguez de los Santos, Marion Rivalan, Friederike S. David, Alexej Knaus, Alexander Stumpf, Laura Moreno Velasquez, Anne Voigt, Daniele Mattei, Melissa Long, Guido Vogt, Lars Wittler, Bernd Timmermann, Peter N. Robinson, Denise Horn, Stefan Mundlos, Uwe Kornak, Dietmar Schmitz, York Winter, Peter M. Krawitz
bioRxiv 2020.04.20.050591; doi: https://doi.org/10.1101/2020.04.20.050591
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