Sort   by:  
 Page size 
ProteomicsTBCK, PPP1R21, and C12orf4-interaction AP-MS
To indentify the interaction protein of TBCK, PPP1R21, and C12orf4 by purification of flagg-tagged ones coupled mass spectrum
ORGANISM(S): Homo sapiens (Human) 
2026-03-02 | PXD053078 | Pride
Tbck And c12orf4-interaction ap-ms Ppp1r21 
UnknownHomozygous boricua TBCK mutation causes neurodegeneration and aberrant autophagy.
Not available
S-EPMC5876123 | biostudies-literature
UnknownTBCK influences cell proliferation, cell size and mTOR signaling pathway.
Not available
S-EPMC3747267 | biostudies-literature
UnknownTBCK-deficiency leads to compartment-specific mRNA and lysosomal trafficking defects in patient-derived neurons.
Not available
S-EPMC11908138 | biostudies-literature
UnknownTBCK Deficiency Alters Ribosomal Function, RNA Splicing, and miRNA Networks: Insights from Multi-Omics Analyses.
Not available
S-EPMC12486131 | biostudies-literature
UnknownNeuroprogenitor Cells From Patients With TBCK Encephalopathy Suggest Deregulation of Early Secretory Vesicle Transport.
Not available
S-EPMC8793280 | biostudies-literature
UnknownMyopathic changes associated with psychomotor delay and seizures caused by a novel homozygous mutation in TBCK.
Not available
S-EPMC7369155 | biostudies-literature
UnknownGene fusions AHRR-NCOA2, NCOA2-ETV4, ETV4-AHRR, P4HA2-TBCK, and TBCK-P4HA2 resulting from the translocations t(5;8;17)(p15;q13;q21) and t(4;5)(q24;q31) in a soft tissue angiofibroma.
Not available
S-EPMC5055197 | biostudies-literature
UnknownLysosomal dysfunction impairs mitochondrial quality control and is associated with neurodegeneration in TBCK encephaloneuronopathy.
Not available
S-EPMC8603245 | biostudies-literature
UnknownA Novel Human TBCK- Neuronal Cell Model Results in Severe Neurodegeneration and Partial Rescue with Mitochondrial Fission Inhibition.
Not available
S-EPMC11565812 | biostudies-literature
Sort   by:  
 Page size