Sort   by:  
 Page size 
UnknownLoss of nuclear activity of the FBXO7 protein in patients with parkinsonian-pyramidal syndrome (PARK15).
Not available
S-EPMC3037939 | biostudies-literature
UnknownPARK15/FBXO7 is dispensable for PINK1/Parkin mitophagy in iNeurons and HeLa cell systems.
Not available
S-EPMC10398645 | biostudies-literature
ProteomicsRole of Fbxo7 in dopaminergic neurons
Analysis of a conditional knockout of Fbxo7/Park15 expression in mouse brains.
ORGANISM(S): Mus musculus (Mouse) 
2019-08-28 | PXD011666 | Pride
Fbxo7/park15 Dopaminergic Parkinson's disease 
ProteomicsPARK15/FBXO7 is dispensable for PINK1/Parkin mitophagy in iNeurons and HeLa cell systems
The protein kinase PINK1 and ubiquitin ligase Parkin promote removal of damaged mitochondria via a feed-forward mechanism involving ubiquitin (Ub) phosphorylation (pUb), Parkin activation, and ubiquitylation of mitochondrial outer membrane proteins to support recruitment of mitophagy receptors. The ...
ORGANISM(S): Homo sapiens (Human) 
2023-06-19 | PXD037797 | Pride
Mitophagy Proteomics Ineurons Fbxo7 
UnknownPARK15/FBXO7 is dispensable for PINK1/Parkin-dependent mitophagy in iNeuron and HeLa cell systems
Not available
S-SCDT-10_15252-EMBR_202256399 | biostudies-other
UnknownDopaminergic neuronal loss and dopamine-dependent locomotor defects in Fbxo7-deficient zebrafish.
Not available
S-EPMC3487786 | biostudies-literature
UnknownPI31 expression is neuroprotective in a mouse model of early-onset parkinsonism.
Not available
S-EPMC12478140 | biostudies-literature
UnknownFBXO7/ntc and USP30 antagonistically set the ubiquitination threshold for basal mitophagy and provide a target for Pink1 phosphorylation in vivo.
Not available
S-EPMC10427020 | biostudies-literature
ProteomicsLoss of the parkinsonism-associated protein FBXO7 in glutamatergic forebrain neurons in mice leads to anormal motor behavior and synaptic defects
Mutations in PARK15, which encodes for the F-box protein FBXO7 have been associated with Parkinsonian Pyramidal syndrome, a rare and complex movement disorder with Parkinsonian symptoms, pyramidal tract signs and juvenile onset. Our previous study showed that systemic loss of Fbxo7 in mice causes mo...
ORGANISM(S): Mus musculus (Mouse) 
2023-09-18 | PXD044119 | Pride
Brain Lc-ms Mouse Synapse 
UnknownFBXO7 Y52C polymorphism as a potential protective factor in Parkinson's disease.
Not available
S-EPMC4100735 | biostudies-literature
Sort   by:  
 Page size