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Entity

Name
MARK4 isoform 2 (688 aa)
Namespace
HBP
Namespace Version
20181119
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/90e1cb9e5e882703380c9db8d4915ac6f3cba137/export/hbp-names.belns

Appears in Networks 1

Tau Modifications v1.9.5

Tau Modifications Sections of NESTOR

In-Edges 1

bp(GO:"neuron development") positiveCorrelation p(HBP:"MARK4 isoform 2 (688 aa)") View Subject | View Object

Human microtubule affinity-regulating kinase 4S (hMARK4S),undetectable in human neural progenitor cells (HNPCs) and NTera2 (NT2) cells, is up-regulated in both cell systems from the very early stages of neuronal differentiation, suggesting euronal commitment is marked by MARK4S up-regulation. PubMed:16973293

Appears in Networks:

Out-Edges 2

p(HBP:"MARK4 isoform 2 (688 aa)") positiveCorrelation bp(GO:"neuron development") View Subject | View Object

Human microtubule affinity-regulating kinase 4S (hMARK4S),undetectable in human neural progenitor cells (HNPCs) and NTera2 (NT2) cells, is up-regulated in both cell systems from the very early stages of neuronal differentiation, suggesting euronal commitment is marked by MARK4S up-regulation. PubMed:16973293

Appears in Networks:

About

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.