"Hep G2 Cells" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A human liver tumor cell line used to study a variety of liver-specific metabolic functions.
Descriptor ID |
D056945
|
MeSH Number(s) |
A11.251.860.180.432 A11.436.348.500
|
Concept/Terms |
Hep G2 Cells- Hep G2 Cells
- Cell, Hep G2
- Cells, Hep G2
- Hep G2 Cell
- HepG2 Cells
- Cell, HepG2
- Cells, HepG2
- HepG2 Cell
- Hep G2 Cell Line
- Hepatoblastoma G2 Cell Line
- Cell Line, Hep G2
- Cell Line, Hepatoblastoma G2
|
Below are MeSH descriptors whose meaning is more general than "Hep G2 Cells".
Below are MeSH descriptors whose meaning is more specific than "Hep G2 Cells".
This graph shows the total number of publications written about "Hep G2 Cells" by people in this website by year, and whether "Hep G2 Cells" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2017 | 0 | 2 | 2 |
2019 | 0 | 2 | 2 |
2024 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Hep G2 Cells" by people in Profiles.
-
Identification and molecular mechanism of novel hypoglycemic peptide in ripened pu-erh tea: Molecular docking, dynamic simulation, and cell experiments. Food Res Int. 2024 Oct; 194:114930.
-
MDM2-NFAT1 dual inhibitor, MA242: Effective against hepatocellular carcinoma, independent of p53. Cancer Lett. 2019 09 10; 459:156-167.
-
pH-responsive controlled release of mesoporous silica nanoparticles capped with Schiff base copolymer gatekeepers: Experiment and molecular dynamics simulation. Colloids Surf B Biointerfaces. 2019 Apr 01; 176:394-403.
-
Poly(2-(diethylamino)ethyl methacrylate)-based, pH-responsive, copolymeric mixed micelles for targeting anticancer drug control release. Int J Nanomedicine. 2017; 12:6857-6870.
-
Structural and Molecular Mechanisms of Cytokine-Mediated Endocrine Resistance in Human Breast Cancer Cells. Mol Cell. 2017 Mar 16; 65(6):1122-1135.e5.