The node-based overlap between this network and other networks is calculated as the Szymkiewicz-Simpson coefficient of their respective nodes. Up to the top 10 are shown below.
|Inert and seed-competent tau monomers suggest structural origins of aggregation v1.0.0||50%|
|Tau Modifications v1.9.5||47%|
|Tau Trimers Are the Minimal Propagation Unit Spontaneously Internalized to Seed Intracellular Aggregation v1.0.0||45%|
|Tau in physiology and pathology v1.0.0||43%|
|Pseudophosphorylation of tau at S422 enhances SDS-stable dimer formation and impairs both anterograde and retrograde fast axonal transport. v1.0.0||40%|
|Tau oligomers-Cytotoxicity, propagation, and mitochondrial damage v1.0.0||37%|
|Estrogen receptor-α is localized to neurofibrillary tangles in Alzheimer's disease v1.0.0||33%|
|Identification of the Tau phosphorylation pattern that drives its aggregation v1.0.0||31%|
|Caenorhabditis elegans models of tauopathy v1.0.0||30%|
|Alzheimer's disease pathological lesions activate the spleen tyrosine kinase. v1.0.0||29%|
BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.
If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.