Cell Signaling Technology

ZEB1 (E2G6Y) Rabbit Monoclonal Antibody

#70512 · $159

27
Citing papers
366
Combined citations
Supplier page Find this product

Research areas

Epigenetics and DNA Methylation3Pancreatic and Hepatic Oncology Research3MicroRNA in disease regulation3Cancer-related molecular mechanisms research2Cancer Cells and Metastasis2Cellular Mechanics and Interactions2Barrier Structure and Function Studies2RNA modifications and cancer2

Papers citing this product

1
Cucurbitacin B inhibits TGF-β1-induced epithelial–mesenchymal transition (EMT) in NSCLC through regulating ROS and PI3K/Akt/mTOR pathways
Chinese Medicine·2022·79 cit.·DOI
2
Long non-coding RNA LINC00665 promotes gemcitabine resistance of Cholangiocarcinoma cells via regulating EMT and stemness properties through miR-424-5p/BCL9L axis
Cell Death and Disease·2021·56 cit.·DOI
3
Targeting mitochondrial one-carbon enzyme MTHFD2 together with pemetrexed confers therapeutic advantages in lung adenocarcinoma
Cell Death Discovery·2022·44 cit.·DOI
4
Alleviation of liver fibrosis by inhibiting a non-canonical ATF4-regulated enhancer program in hepatic stellate cells
Nature Communications·2025·38 cit.·DOI
5
Mechanosensitive hormone signaling promotes mammary progenitor expansion and breast cancer risk
Cell stem cell·2024·29 cit.·DOI
6
LZTR1 deficiency exerts high metastatic potential by enhancing sensitivity to EMT induction and controlling KLHL12-mediated collagen secretion
Cell Death and Disease·2023·18 cit.·DOI
7
The miR-182-5p/NDRG1 Axis Controls Endometrial Receptivity through the NF-κB/ZEB1/E-Cadherin Pathway
International Journal of Molecular Sciences·2022·18 cit.·DOI
8
Multi-Omics Profiling of Human Endothelial Cells from the Coronary Artery and Internal Thoracic Artery Reveals Molecular but Not Functional Heterogeneity
International Journal of Molecular Sciences·2023·17 cit.·DOI
9
Enhanced Epithelial-to-Mesenchymal Transition and Chemoresistance in Advanced Retinoblastoma Tumors Is Driven by miR-181a
Cancers·2022·14 cit.·DOI
10
ZEB1 shapes AML immunological niches, suppressing CD8 T cell activity while fostering Th17 cell expansion
Cell Reports·2024·11 cit.·DOI

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