Ontology highlight
ABSTRACT:
INSTRUMENT(S): Orbitrap Fusion Lumos
ORGANISM(S): Rattus Norvegicus (rat) Homo Sapiens (human)
TISSUE(S): Brain, Cerebrospinal Fluid
SUBMITTER: Aga Gambus
LAB HEAD: Victor Faunez
PROVIDER: PXD030426 | Pride | 2022-10-14
REPOSITORIES: pride
Items per page: 1 - 5 of 114 |
iScience 20220817 9
MECP2 loss-of-function mutations cause Rett syndrome, a neurodevelopmental disorder resulting from a disrupted brain transcriptome. How these transcriptional defects are decoded into a disease proteome remains unknown. We studied the proteome of Rett cerebrospinal fluid (CSF) to identify consensus Rett proteome and ontologies shared across three species. Rett CSF proteomes enriched proteins annotated to HDL lipoproteins, complement, mitochondria, citrate/pyruvate metabolism, synapse compartments ...[more]