Ontology highlight
ABSTRACT:
INSTRUMENT(S):
ORGANISM(S): Homo Sapiens (human) Mus Musculus (mouse)
TISSUE(S): Brain, Stem Cell
SUBMITTER:
Zhiping Wu
LAB HEAD: Junmin Peng
PROVIDER: PXD067156 | Pride | 2025-12-08
REPOSITORIES: Pride
| Action | DRS | |||
|---|---|---|---|---|
| 20240129_091540_11phos_yue_Report.tsv | Tabular | |||
| APP_KI_Batch01_f01.1.pepXML | Pepxml | |||
| APP_KI_Batch01_f01.raw | Raw | |||
| APP_KI_Batch01_f02.1.pepXML | Pepxml | |||
| APP_KI_Batch01_f02.raw | Raw |
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Nature communications 20251128 1
Human genomic studies have identified protein-truncating variants in AKAP11 associated with both bipolar disorder (BD) and schizophrenia (SCZ), implicating a shared disease mechanism driven by loss-of-function. AKAP11, a protein kinase A (PKA) adapter, plays a key role in degrading the PKA-RI complex through selective autophagy. However, the neuronal functions of AKAP11 and the impact of its loss-of-function remains largely uncharacterized. Through multi-omics approaches, cell biology, and elect ...[more]