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NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
Affiliation:1. Department of Biochemistry and Molecular Pharmacology, New York University Langone School of Medicine, New York, NY 10016, USA;2. Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA;3. Center for Integrative Brain Research, Seattle Children’s Research Institute, Seattle, WA, USA;4. Ruiz Department of Ophthalmology and Visual Science, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, TX 77030, USA;5. National Eye Institute, NIH, Bethesda, MD 20892, USA;6. Struttura Semplice Dipartimentale di Genetica Medica, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy;7. Institute of Medical Genetics, University of Zürich, Zürich, Switzerland;8. Dipartimento di Medicina Molecolare, Università di Pavia, Pavia, Italy;9. Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Schwabachanlage 10, 91054 Erlangen, Germany;10. Carle Physicians Group, Section of Neurology, St. Christopher’s Hospital for Children, Urbana, IL, USA;11. Neurology, IASO Children’s Hospital, Athens, Greece;12. Comprehensive Epilepsy Program, Jane and John Justin Neuroscience Center, Cook Children’s Medical Center, Fort Worth, TX 76104, USA;13. Division of Genetics, Department of Pediatrics, University of Virginia Children’s Hospital, Charlottesville, VA, USA;14. GeneDx, Inc., Gaithersburg, MD, USA;15. Liverpool Women’s Hospital, Liverpool, UK;16. Manchester Centre for Genomic Medicine, Manchester, UK;17. Research and Development Institute, Transilvania University of Brasov, School of Medicine, Brasov, Romania;18. Department of Pediatrics (Genetic Medicine), University of Washington, Seattle, WA, USA;19. IRCCS Mondino Foundation, Pavia, Italy;20. Department of Human Genetics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland
Abstract:
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