Genome‐wide transcriptomic and proteomic studies of Rett syndrome mouse models identify common signaling pathways and cellular functions as potential therapeutic targets

Author:

Krishnaraj Rahul1,Haase Florencia2,Coorey Bronte2,Luca Edward J3,Wong Ingar2,Boyling Alexandra2,Ellaway Carolyn145,Christodoulou John1456ORCID,Gold Wendy A.1247ORCID

Affiliation:

1. Genetic Metabolic Disorders Research Unit, Western Sydney Genetics ProgramThe Children's Hospital at Westmead Sydney New South Wales Australia

2. Molecular Neurobiology Research Group, Kids ResearchSydney Children's Hospitals Network Westmead Australia

3. University LibraryThe University of Sydney Sydney New South Wales Australia

4. Discipline of Child and Adolescent HealthThe University of Sydney Sydney New South Wales Australia

5. Genetic Medicine, Sydney Medical SchoolThe University of Sydney Sydney New South Wales Australia

6. Brain and Mitochondrial Research Group, Murdoch Children's Research Institute, and Department of Paediatrics, Melbourne Medical SchoolUniversity of Melbourne Melbourne Victoria Australia

7. Kids Neuroscience CentreThe Children's Hospital at Westmead Kids Research Westmead NSW Australia

Funder

International Rett Syndrome Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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