A multi-omics exploration of PPARG activation in colon cancer: kinases featuring a PPRE sequence within regulatory regions

These findings advance our understanding of PPARG's regulatory network and underscore its potential as a therapeutic target, establishing a robust framework for future research in PPARG-related pathways.

Authors

Institutions

Publication Details

Journal
Biology Direct
Published
2025-06-11
DOI
https://doi.org/10.1186/s13062-025-00654-7
Citations
3
Primary Topic
Peroxisome Proliferator-Activated Receptors
Type
article
Field-Weighted Citation Impact
2.42

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A multi-omics exploration of PPARG activation in colon cancer: kinases featuring a PPRE sequence within regulatory regions

Pritha Saha, Priti Talwar, Palaniyandi Ravanan
3 citations
Biology Direct
Peroxisome Proliferator-Activated Receptors
2.42
article

A multi-omics exploration of PPARG activation in colon cancer: kinases featuring a PPRE sequence within regulatory regions

Pritha Saha, Priti Talwar, Palaniyandi Ravanan
article en
3 citations

Abstract

These findings advance our understanding of PPARG's regulatory network and underscore its potential as a therapeutic target, establishing a robust framework for future research in PPARG-related pathways.

Biology DirectVol. 20(1)
Central University of Tamil Nadu (IN), Vellore Institute of Technology University (IN)
VIT University, Science and Engineering Research Board
Openalex Percentile: Top 11%
Peroxisome Proliferator-Activated Receptors
2.42
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.