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Entity

Name
140621
Namespace
NCBIGENE
Namespace Version
None
Pattern
^\d+$

Appears in Networks 1

In-Edges 4

a(MESH:antalarmin) increases act(p(NCBIGENE:140621)) View Subject | View Object

However, embryos that recovered from heat shock in the presence of the CRF-R1 antagonist, antalarmin, experienced a greater increase in caspase-3 activity than embryos not given the antagonist PubMed:29807032

bp(MESH:"Heat-Shock Response") association act(p(NCBIGENE:140621)) View Subject | View Object

The endogenous response to heat shock was characterized by transient changes in caspase-3 activity and gene expression. PubMed:29807032

bp(MESH:"Heat-Shock Response") increases act(p(NCBIGENE:140621)) View Subject | View Object

For embryos heat shocked at 6 hpf, the induction of caspase-3 activity was dependent on recovery time (interaction of main variables P=0.007), with a significant increase over controls at 7 h and 10 h recovery (Table 1). PubMed:29807032

p(NCBIGENE:492507) decreases act(p(NCBIGENE:140621)) View Subject | View Object

CRF overexpression by mRNA microinjection reduced heat shock-induced caspase-3 activity by approximately 2-fold relative to control-injected embryos PubMed:29807032

Out-Edges 1

act(p(NCBIGENE:140621)) association bp(MESH:"Heat-Shock Response") View Subject | View Object

The endogenous response to heat shock was characterized by transient changes in caspase-3 activity and gene expression. PubMed:29807032

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.