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Open Access
Peer-reviewed
Research Article
A Broad Phenotypic Screen Identifies Novel Phenotypes Driven by a Single Mutant Allele in Huntington’s Disease CAG Knock-In Mice
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Sabine M. Hölter ,
Contributed equally to this work with: Sabine M. Hölter, Mary Stromberg
Affiliation German Mouse Clinic, Institute of Developmental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Mary Stromberg ,
Contributed equally to this work with: Sabine M. Hölter, Mary Stromberg
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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Marina Kovalenko,
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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Lillian Garrett,
Affiliation German Mouse Clinic, Institute of Developmental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Lisa Glasl,
Affiliation German Mouse Clinic, Institute of Developmental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Edith Lopez,
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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Jolene Guide,
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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Alexander Götz,
Affiliation Comprehensive Pneumology Center, Institute of Lung Biology and Disease, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Wolfgang Hans,
Affiliation German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Lore Becker,
Affiliation German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Birgit Rathkolb,
Affiliation German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Jan Rozman,
Affiliation German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Anja Schrewed,
Affiliation Department of Medicine III, Division of Cardiology, University of Heidelberg, Heidelberg, Germany
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Martin Klingenspor,
Affiliation Molecular Nutritional Medicine, Else Kröner-Fresenius Center and ZIEL Research Center for Nutrition and Food Sciences, Technische Universität München, Munich, Germany
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Thomas Klopstock,
Affiliation Department of Neurology, Friedrich-Baur-Institute and German Center for Vertigo and Balance Disorders, Ludwig-Maximilians-Universität München, Munich, Germany
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Holger Schulz,
Affiliation Institute of Epidemiology I, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Eckhard Wolf,
Affiliation Chair for Molecular Animal Breeding and Biotechnology, Gene Center, Ludwig-Maximilians-Universität München, Munich, Germany
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Wolfgang Wursta,
Affiliations Max Planck Institute of Psychiatry, Munich, Germany, Deutsches Zentrum für Neurodegenerative Erkrankungen, Standort München, Munich, Germany
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Tammy Gillis,
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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Hiroko Wakimoto,
Affiliation Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America;
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Jonathan Seidman,
Affiliation Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America;
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Marcy E. MacDonald,
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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Susan Cotman,
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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Valérie Gailus-Durner,
Affiliation German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Helmut Fuchs,
Affiliation German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Martin Hrabě de Angelis,
Affiliation German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Neuherberg/Munich, Germany
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Jong-Min Lee,
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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Vanessa C. Wheeler
* E-mail: Wheeler@chgr.mgh.harvard.edu
Affiliation Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, United States of America
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A Broad Phenotypic Screen Identifies Novel Phenotypes Driven by a Single Mutant Allele in Huntington’s Disease CAG Knock-In Mice
- Sabine M. Hölter,
- Mary Stromberg,
- Marina Kovalenko,
- Lillian Garrett,
- Lisa Glasl,
- Edith Lopez,
- Jolene Guide,
- Alexander Götz,
- Wolfgang Hans,
- Lore Becker
- Published: November 22, 2013
- https://doi.org/10.1371/journal.pone.0080923