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EMT: 2016

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EMT and Dissemination Precede Pancreatic Tumor Formation

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Dependency of a therapy-resistant state of cancer cells on a lipid peroxidase pathway

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EMT in cancer

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Epithelial-to-mesenchymal transition is not required for lung metastasis but contributes to chemoresistance

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Role of Par-4 in EMT

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The expression of metastasis-related protein among Indonesian colorectal carcinoma patients: A preliminary clinical study

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MicroRNA-1205 promotes breast cancer cell metastasis by regulating epithelial-to-mesenchymal transition via targeting of CDK3

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P4HA1 regulates EMT to affect glioma invasion

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Protein arginine methyltransferase 5 promotes metastasis via enhancing EGFR transcription and modulating AKT1 activation by methylationPreprint

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Análise do grau histológico e marcadores imunohistoquímicos para a identificação de pacientes com câncer de mama luminal de alto risco

da Luz, F. A. C. (2022) · doi:10.14393/ufu.te.2022.272 · Cited by 2

The Role of Epithelial–Mesenchymal Transition Markers in the Prediction of Lymph Node Metastases in Colorectal Cancer

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Targeting Epithelial-to-Mesenchymal Transition for Breast Cancer Stem Cells Therapeutics

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Compatibility of Calycosin-Tanshinone IIA improves Ang II-induced renal artery endothelial cell dysfunction through lncRNA-mRNA co-expression network

Jiang, Y., Han, C., Xu, W., Li, Y., & Liu, Y. (2025) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-024-00990-4 · Cited by 1

Direct cell interactions potentially regulate transcriptional programmes that control the responses of high grade serous ovarian cancer patients to therapy

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A Robust Marine Collagen Peptide–Agarose 3D Culture System for In Vitro Modeling of Hepatocellular Carcinoma and Anti-Cancer Therapeutic Development

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PRRX1 Orchestrates Pericyte–Myofibroblast Transition in Pathological Retinal Fibrosis

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Unravelling the molecular crosstalk between Epithelial-Mesenchymal transition and human papillomavirus in oral cancer

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ZEB1 level in thyroid papillary carcinoma tissue, metastasis, blood mononuclear cells and plasma

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MDK Activates the PI3K/AKT Axis to Induce AP2A1 Expression and Epithelial–Mesenchymal Transition in Colorectal Cancer

Li, T., Xu, C., Guo, Y., Xu, Y., Chen, K., Cheng, Y., Kesavamoorthy, G., Zhang, J., & Lin, M. (2026) · Cancers · doi:10.3390/cancers18081311 · Cited by 1

Metabolic plasticity and optimal redox homeostasis are essential for efficient metastatic colonization

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Endothelial to mesenchymal transition (EndMT) in atherosclerosis: mechanisms, models, and therapies

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[SOX2-OT/SOX2 axis regulates lung cancer H520 cell migration via Gli1-mediated epithelial-mesenchymal transition].

Dong, H., Zeng, L., Wu, Y., Miao, S., Ni, N., Liu, N., Chen, W., & Du, J. (2022) · PubMed Central · doi:10.12122/j.issn.1673-4254.2022.10.01 · Cited by 1

Epithelial–Mesenchymal Transition of Breast Cancer Cells Induced by Activation of the Transcription Factor Snail1

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Role of Circular RNAs in Prostate Cancer

Chen, F., Zhang, F., Liu, Y., & Leng, Y. (2023) · Current Medicinal Chemistry · doi:10.2174/0929867330666230531095850 · Cited by 1

SH2D5 promotes lung adenocarcinoma cell metastasis and triggers EMT via activating AKT signaling pathway

Du, L., Ren, W., Liu, L., Zhu, H., Xu, K., & Zhou, Y. (2024) · PLoS ONE · doi:10.1371/journal.pone.0316432 · Cited by 1

Identification and regulation of EMT cells in vivo by laser stimulation

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[ZEB2 Regulates the Migration and Invasion of PANC-1 Pancreatic Cancer Cells: An Experimental Study].

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Glutathione Peroxidase 8 (GPX8)-IL6 axis is essential in maintaining breast cancer mesenchymal stem-like state and aggressive phenotypePreprint

Khatib, A., Solaimuthu, B., Yosef, M. B., Oren, G., Rmaileh, A. A., Frisch, M. S., Axelrod, J. H., Lichtenstein, M., & Shaul, Y. D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/818245 · Cited by 1

A “NOTCH” deeper into the EMT program in Breast cancerPreprint

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Structural Symmetry of DNA Nucleotides and Steroid HormonesPreprint

Schaper, C. D. (2020) · ChemRxiv · doi:10.26434/chemrxiv.11991567 · Cited by 1

Data from Functional Hierarchy and Cooperation of EMT Master Transcription Factors in Breast Cancer Metastasis

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ZEB1 is Required for NHEJ-Mediated DSB Repair in EuchromatinPreprint

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Direct Binding of Complementary Symmetric Ligands to DNA Nucleotide Pairs by Means of Transcription FactorsPreprint

Schaper, C. D. (2020) · Preprints.org · doi:10.20944/preprints202009.0300.v1

Peer Review #2 of "The regulatory roles and mechanisms of the transcription factor FOXF2 in human diseases (v0.1)"

(2021) · PeerJ · doi:10.7287/peerj.10845v0.1/reviews/2

Peer Review #2 of "The regulatory roles and mechanisms of the transcription factor FOXF2 in human diseases (v0.2)"

(2021) · PeerJ · doi:10.7287/peerj.10845v0.2/reviews/2

Peer Review #2 of "The regulatory roles and mechanisms of the transcription factor FOXF2 in human diseases (v0.3)"

(2021) · PeerJ · doi:10.7287/peerj.10845v0.3/reviews/2

Transcript Factors Associated with Disease Resistance in Plants and Their Potential for Crop Improvement

Kiranmai, B., & Vasantha, S. (2021)

Single-Cell Resolution of MET- and EMT-Like Programs in Osteoblasts During Zebrafish Fin RegenerationPreprint

Tang, W., Watson, C. J., Olmstead, T., Allan, C. H., & Kwon, R. Y. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3860386

Defining Epithelial-Mesenchymal Plasticity in Cancer Using Single-Cell Genomics

Cook, D. P. (2021) · uO Research (University of Ottawa) · doi:10.20381/ruor-26722

NPR3 Inhibits EMT and Tumour Metastasis of Human Osteosarcoma by Activating AKT/mTOR-Mediated AutophagyPreprint

Yao, Z., Yang, Y., Chen, J., Chen, T., Han, L., Li, D., Ye, L., Zhu, Y., Feng, Y., Wu, J., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-923877/v1

MicroRNA involvement in invasion and metastasis

Solé, C., Bielowski, A., & Lawrie, C. H. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822287-4.00005-0

Understanding and Therapeutically Targeting the Scleroderma Myofibroblast

Ocon, A. J., Lokineni, S., & Korman, B. D. (2022) · Current Treatment Options in Rheumatology · doi:10.1007/s40674-021-00189-8

Expression and clinical significance of VEGF and markers of EMT in gastric cancerPreprint

Zhang, Y., Wang, Y., Zhao, M., Mi, J., Li, X., Li, H., Tang, M., Geng, Z., Zuo, L., Song, X., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1535500/v1

MEK Inhibition Enhances Presentation of Targetable MHC-I Tumor Antigens in Mutant MelanomasPreprint

Stopfer, L. E., Rettko, N. J., Leddy, O. K., Mesfin, J. M., Brown, E. N., Winski, S. L., Bryson, B. D., Wells, J. A., & White, F. M. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4018615

Genomic and local microenvironment effects shaping epithelial-to-mesenchymal trajectories in cancerPreprint

Tagliazucchi, G. M., Wiecek, A. J., Withnell, E., & Secrier, M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.23.453584

Peer Review #1 of "The regulatory roles and mechanisms of the transcription factor FOXF2 in human diseases (v0.1)"

(2021) · PeerJ · doi:10.7287/peerj.10845v0.1/reviews/1

Peer Review #1 of "The regulatory roles and mechanisms of the transcription factor FOXF2 in human diseases (v0.3)"

(2021) · PeerJ · doi:10.7287/peerj.10845v0.3/reviews/1

Análise do secretoma de células de câncer de ovário Caov-3 induzidas ao processo de transição epitélio-mesenquimal por fator de crescimento EGF e sua associação com assinaturas de tumores de alto grau

Lanfredi, G. P. (2022) · doi:10.11606/t.17.2022.tde-08092022-152815

Understanding cellular and molecular mechanisms of zebrafish cardiomyocyte integrity and valve interstitial cell differentiation

Gentile, A. (2022) · doi:10.21248/gups.70220

Diallyl trisulfide inhibits the metastasis of anaplastic thyroid carcinoma cells by targeting TGF-β-Smad3-integrin α2β1 signaling pathway

Wang, Y., Xu, S., Cheng, X. F., Wu, J., Yu, H., Bao, J., Zhang, L., & Lu, R. (2022) · Process Biochemistry · doi:10.1016/j.procbio.2022.11.009

Association of Epithelial Mesenchymal Transition, Stemness and Inflammation in Colorectal Carcinoma. Doctoral Thesis

Briede, I. (2022) · doi:10.25143/prom-rsu_2022-13_dt

Dual role of CASP8AP2/FLASH in regulating epithelial-to-mesenchymal (EMT) plasticityPreprint

Catalanotto, M., Vaz, J. M., Abshire, C. F., Youngblood, R., Chu, M., Levine, H., Jolly, M. K., & Dragoi, A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.12.532282

Supplementary File 2 from Functional Hierarchy and Cooperation of EMT Master Transcription Factors in Breast Cancer Metastasis

Addison, J., Voronkova, M. A., Fugett, J. H., Lin, C., Linville, N. C., Trinh, B., Livengood, R. H., Smolkin, M. B., Schaller, M. D., Ruppert, J. M., et al. (2023) · doi:10.1158/1541-7786.22526843.v1

Data from Functional Hierarchy and Cooperation of EMT Master Transcription Factors in Breast Cancer Metastasis

Addison, J., Voronkova, M. A., Fugett, J. H., Lin, C., Linville, N. C., Trinh, B., Livengood, R. H., Smolkin, M. B., Schaller, M. D., Ruppert, J. M., et al. (2023) · doi:10.1158/1541-7786.c.6545231.v1

Targeting Snail1 by CRISPR/Cas9 System Inhibits the Proliferation and Migration of Human Gastric Cancer Cells

Zhang, P.-W., Chen, Z., & Shi, Z. (2023) · Journal of cancer research updates · doi:10.30683/1929-2279.2023.12.5

Unraveling the Complexity: Expression Patterns and Prognostic Value of Cell Adhesion Junction Regulatory Genes in Hepatocellular CarcinomaPreprint

Jin, Y., Zhang, Y., Xie, G., & Suo, Z. (2023) · Research Square · doi:10.21203/rs.3.rs-3220479/v1

A expressão dos marcadores de transição epitélio-mesenquimal SNAI1 e o ZEB1 resulta em alterações transcricionais para promover progressão tumoral e evasão imune no câncer de próstata

Chaves, L. P. (2023) · doi:10.11606/d.17.2023.tde-08082023-145937

Compatibility of Calycosin-Tanshinone IIA improves Ang II-induced renal artery endothelial cell dysfunction through lncRNA-mRNA coexpression networkPreprint

YanYun, J., Cong, H., WanLi, X., YuQiu, L., & Liu, Y. (2023) · Research Square · doi:10.21203/rs.3.rs-3205631/v1

LncRNA LINC01671/YY1 positive feedback loop induced EMT modulates CCL2 secretion in colorectal cancer to attract M2-like TAM infiltrationPreprint

Tan, Y. Q., Wei, C., Zhang, G., Ni, L., Chen, Y., Du, X., Zhu, M., Zhao, H., Cheng, Z., & Liu, Q. (2023) · Research Square · doi:10.21203/rs.3.rs-3321885/v1

Hypoxia and Epithelial-to-Mesenchymal Transition (EMT) in Cancer: A Non-coding RNA Perspective

Singh, A., Gupta, R., & Kulshreshtha, R. (2023) · RNA technologies · doi:10.1007/978-3-031-36390-0_21

Cancer stem cells, signalling pathways and chemopreventive effects of phytochemicals in androgen-regulated cancers

Varma, S., & Basak, S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-443-13212-4.00005-2

DNA damage-induced PARP/ALC1 activation leads to Epithelial-to-Mesenchymal transition stimulating homologous recombinationPreprint

Rajabi, F., Smith, R., Liu-Bordes, W.-Y., Schertzer, M. J., Huet, S., & Londoño‐Vallejo, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.16.575847

Additional file 3 of Pan-cancer quantitation of epithelial-mesenchymal transition dynamics using parallel reaction monitoring-based targeted proteomics approach

Jain, A., Sambath, J., Sathe, G. J., George, I. A., Pandey, A., Thompson, E. W., & Kumar, P. (2022) · Figshare · doi:10.6084/m9.figshare.19164407

Additional file 4 of Pan-cancer quantitation of epithelial-mesenchymal transition dynamics using parallel reaction monitoring-based targeted proteomics approach

Jain, A., Sambath, J., Sathe, G. J., George, I. A., Pandey, A., Thompson, E. W., & Kumar, P. (2022) · Figshare · doi:10.6084/m9.figshare.19164410

Additional file 2 of Pan-cancer quantitation of epithelial-mesenchymal transition dynamics using parallel reaction monitoring-based targeted proteomics approach

Jain, A., Sambath, J., Sathe, G. J., George, I. A., Pandey, A., Thompson, E. W., & Kumar, P. (2022) · Figshare · doi:10.6084/m9.figshare.19164404

Additional file 1 of Comprehensive analysis of EMT-related genes and lncRNAs in the prognosis, immunity, and drug treatment of colorectal cancer

Yang, Y., Feng, M., Bai, L., Liao, W., Zhou, K., Zhang, M., Wu, Q., Wen, F., Lei, W., Zhang, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16625488

Epithelial-mesenchymal transition of breast cancer cells activated by SNAIL1 transcription factor

Litovka, N. I., Zhitnyak, I. Y., & Gloushankova, N. A. (2023) · Biochemistry (Moscow) · doi:10.31857/s0320972523010025

Tumor evolution during chemotherapy

Garavaglia, B., Vallino, L., Ferraresi, A., Dhanasekaran, D. N., & Isidoro, C. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-824040-3.00012-1 · Cited by 1

In vitro effect of 1-methyltryptophan isomers on epithelial-mesenchymal transition transcription factors in tubular epithelial cells after ischemia-reperfusion injury

AliNejad Kasbakhi, N., Vavrincová-Yaghi, D., & Čepcová, D. (2024) · Archives of Razi Institute · doi:10.32592/ari.2024.79.2.307

Human Blood Serum Antagonizes Effects of EGFR/HER2-Targeted Drug Lapatinib on Squamous Carcinoma SK-BR-3 Cell Growth and Gene Expression

Shaban, N., Raevskiy, M., Захарова, Г. С., Shipunova, V. O., Deyev, S. M., Suntsova, M., Sorokin, M., Buzdin, A. A., & Kamashev, D. (2024) · Biochemistry (Moscow) · doi:10.31857/s0320972524030068

An ERRα-ZEB1 transcriptional signature predicts survival in triple-negative breast cancers

Shi, J., Poulard, C., Cerutti, C., Trédan, O., Romancer, M. L., Shi, T., & Vanacker, J.-M. (2026) · Molecular Medicine · doi:10.1186/s10020-026-01487-4 · Cited by 1

Single-nucleus multiple-organ chromatin accessibility mapping in the ratPreprint

Li, R., Yuan, Y., Duan, S., Deng, Q., Ma, W., Liu, C., Gao, P., Li, L., & Liu, C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.11.622900

Epithelial–Mesenchymal Transition Functions as a Driver for the Direct Conversion of Somatic Cells

Motohashi, T., Aoki, H., Kunisada, T., & Osawa, M. (2025) · Stem Cells and Development · doi:10.1089/scd.2024.0181

ERK2-mediated phosphorylation of ZEB1 at S322 enhances PD-L1 expression and EMT, leading to pancreatic cancer progression

Park, M. K., Lee, H. J., Sung, J. Y., Byun, H. J., Kim, H. J., Kim, E. J., Nguyen, T. M., Kang, G.-J., Oh, S. H., Shim, J. G., et al. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02182-3

The Impact of NF-κB-Mediated Cellular Plasticity Reprogramming on Anlotinib Sensitivity in Anaplastic Thyroid CarcinomaPreprint

Fu, K., Liang, J., Wu, J., Ding, L., Li, L., Lv, Z., Jiang, L., Tan, Z., & Wang, J. (2025) · Research Square · doi:10.21203/rs.3.rs-6600544/v1

WITHDRAWN: Mammalian longevity is associated with restricted epithelial plasticityPreprint

Zheng, Z. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.22.683248

Additional file 9 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981835

Additional file 15 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981856

Additional file 4 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981820

Additional file 14 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981853

Additional file 19 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981868

Additional file 1 of Pan-cancer quantitation of epithelial-mesenchymal transition dynamics using parallel reaction monitoring-based targeted proteomics approach

Jain, A., Sambath, J., Sathe, G. J., George, I. A., Pandey, A., Thompson, E. W., & Kumar, P. (2022) · Figshare · doi:10.6084/m9.figshare.19164401

Additional file 1 of EMP3 as a prognostic biomarker correlates with EMT in GBM

Li, L., Xia, S., Zhao, Z., Deng, L., Wang, H., Yang, D., Hu, Y., Ji, J., Huang, D., & Xin, T. (2024) · Figshare · doi:10.6084/m9.figshare.26668506

Additional file 11 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981844

Additional file 10 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981841

Additional file 1 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981811

Additional file 3 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981817

Additional file 17 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981862

Additional file 3 of EMP3 as a prognostic biomarker correlates with EMT in GBM

Li, L., Xia, S., Zhao, Z., Deng, L., Wang, H., Yang, D., Hu, Y., Ji, J., Huang, D., & Xin, T. (2024) · Figshare · doi:10.6084/m9.figshare.26668512

Additional file 2 of EMP3 as a prognostic biomarker correlates with EMT in GBM

Li, L., Xia, S., Zhao, Z., Deng, L., Wang, H., Yang, D., Hu, Y., Ji, J., Huang, D., & Xin, T. (2024) · Figshare · doi:10.6084/m9.figshare.26668509

Additional file 20 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981874

Additional file 13 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981850

Additional file 12 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981847

Additional file 7 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981829

Additional file 5 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981823

Additional file 16 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981859

Additional file 18 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981865

Additional file 6 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981826

Additional file 2 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981814

Additional file 1 of LINC01410 leads the migration, invasion and EMT of bladder cancer cells by modulating miR-4319 / Snail1

Guo, W., Gai, Q., Ma, Y., Shan, Z., & Wu, J. (2021) · Figshare · doi:10.6084/m9.figshare.15178935

Additional file 8 of Characteristics and transcriptional regulators of spontaneous epithelial–mesenchymal transition in genetically unperturbed patient-derived non-spindled breast carcinoma

Lien, H.-C., Yu, H.-C., Yu, W.-H., Lin, S.-F., Chen, T. W., Chen, I.-C., Hsiao, L.-P., Yeh, L.-C., Li, Y.-C., Lo, C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26981832

Additional file 1 of RAB4A GTPase regulates epithelial-to-mesenchymal transition by modulating RAC1 activation

Karthikeyan, S., Casey, P. J., & Wang, M. (2022) · Figshare · doi:10.6084/m9.figshare.21430854

Snail1 Induced Suppression of Proliferation via EGR1, FOXO1, and CEPBγ Creates a Vulnerability for Targeting Apoptotic and Cellular Senescence Pathways

Tran, J. D., Sundaram, S., Shivpuri, S., Khawaja, H., & Miranti, C. K. (2026) · Cancers · doi:10.3390/cancers18030510

EMT transcription factors in cancer development re-evaluated: Beyond EMT and MET

Goossens, S., Vandamme, N., Vlierberghe, P. V., & Berx, G. (2017) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2017.06.006 · Cited by 292

Understanding the Complex Milieu of Epithelial-Mesenchymal Transition in Cancer Metastasis: New Insight Into the Roles of Transcription Factors

Imodoye, S. O., Adedokun, K. A., Muhammed, A. O., Bello, I. O., Muhibi, M. A., Oduola, T., & Oyenike, M. A. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.762817 · Cited by 50

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