
OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
A dynamic in vivo model of epithelial-to-mesenchymal transitions in circulating tumor cells and metastases of breast cancer
Arnaud Bonnomet, Laïdya Syne, Anne Brysse, et al.
Oncogene (2011) Vol. 31, Iss. 33, pp. 3741-3753
Closed Access | Times Cited: 193
Arnaud Bonnomet, Laïdya Syne, Anne Brysse, et al.
Oncogene (2011) Vol. 31, Iss. 33, pp. 3741-3753
Closed Access | Times Cited: 193
Showing 1-25 of 193 citing articles:
Emerging Biological Principles of Metastasis
Arthur W. Lambert, Diwakar R. Pattabiraman, Robert A. Weinberg
Cell (2017) Vol. 168, Iss. 4, pp. 670-691
Open Access | Times Cited: 2667
Arthur W. Lambert, Diwakar R. Pattabiraman, Robert A. Weinberg
Cell (2017) Vol. 168, Iss. 4, pp. 670-691
Open Access | Times Cited: 2667
Epithelial Mesenchymal Transition in Tumor Metastasis
Vivek Mittal
Annual Review of Pathology Mechanisms of Disease (2018) Vol. 13, Iss. 1, pp. 395-412
Open Access | Times Cited: 1263
Vivek Mittal
Annual Review of Pathology Mechanisms of Disease (2018) Vol. 13, Iss. 1, pp. 395-412
Open Access | Times Cited: 1263
Epithelial–mesenchymal plasticity in carcinoma metastasis
Jeff H. Tsai, Jing Yang
Genes & Development (2013) Vol. 27, Iss. 20, pp. 2192-2206
Open Access | Times Cited: 1103
Jeff H. Tsai, Jing Yang
Genes & Development (2013) Vol. 27, Iss. 20, pp. 2192-2206
Open Access | Times Cited: 1103
EMT, cell plasticity and metastasis
Christine L. Chaffer, Beatriz P. San Juan, Elgene Lim, et al.
Cancer and Metastasis Reviews (2016) Vol. 35, Iss. 4, pp. 645-654
Closed Access | Times Cited: 769
Christine L. Chaffer, Beatriz P. San Juan, Elgene Lim, et al.
Cancer and Metastasis Reviews (2016) Vol. 35, Iss. 4, pp. 645-654
Closed Access | Times Cited: 769
EMT, MET, Plasticity, and Tumor Metastasis
Basil Bakir, Anna M. Chiarella, Jason R. Pitarresi, et al.
Trends in Cell Biology (2020) Vol. 30, Iss. 10, pp. 764-776
Open Access | Times Cited: 725
Basil Bakir, Anna M. Chiarella, Jason R. Pitarresi, et al.
Trends in Cell Biology (2020) Vol. 30, Iss. 10, pp. 764-776
Open Access | Times Cited: 725
Circulating tumour cells escape from EpCAM-based detection due to epithelial-to-mesenchymal transition
Tobias M. Gorges, Ingeborg Tinhofer, Michael Drosch, et al.
BMC Cancer (2012) Vol. 12, Iss. 1
Open Access | Times Cited: 520
Tobias M. Gorges, Ingeborg Tinhofer, Michael Drosch, et al.
BMC Cancer (2012) Vol. 12, Iss. 1
Open Access | Times Cited: 520
Mohit Kumar Jolly, Kathryn E. Ware, Shivee Gilja, et al.
Molecular Oncology (2017) Vol. 11, Iss. 7, pp. 755-769
Open Access | Times Cited: 340
Eribulin mesilate suppresses experimental metastasis of breast cancer cells by reversing phenotype from epithelial–mesenchymal transition (EMT) to mesenchymal–epithelial transition (MET) states
Takeshi Yoshida, Yoichi Ozawa, Takayuki Kimura, et al.
British Journal of Cancer (2014) Vol. 110, Iss. 6, pp. 1497-1505
Open Access | Times Cited: 338
Takeshi Yoshida, Yoichi Ozawa, Takayuki Kimura, et al.
British Journal of Cancer (2014) Vol. 110, Iss. 6, pp. 1497-1505
Open Access | Times Cited: 338
Mesenchymal–epithelial transition (MET) as a mechanism for metastatic colonisation in breast cancer
N. P. A. D. Gunasinghe, Alan Wells, Erik W. Thompson, et al.
Cancer and Metastasis Reviews (2012) Vol. 31, Iss. 3-4, pp. 469-478
Open Access | Times Cited: 321
N. P. A. D. Gunasinghe, Alan Wells, Erik W. Thompson, et al.
Cancer and Metastasis Reviews (2012) Vol. 31, Iss. 3-4, pp. 469-478
Open Access | Times Cited: 321
Targeting EMT in cancer: opportunities for pharmacological intervention
Felicity M. Davis, Teneale A. Stewart, Erik W. Thompson, et al.
Trends in Pharmacological Sciences (2014) Vol. 35, Iss. 9, pp. 479-488
Open Access | Times Cited: 314
Felicity M. Davis, Teneale A. Stewart, Erik W. Thompson, et al.
Trends in Pharmacological Sciences (2014) Vol. 35, Iss. 9, pp. 479-488
Open Access | Times Cited: 314
Induction of epithelial–mesenchymal transition (EMT) in breast cancer cells is calcium signal dependent
Felicity M. Davis, Iman Azimi, Richard Faville, et al.
Oncogene (2013) Vol. 33, Iss. 18, pp. 2307-2316
Open Access | Times Cited: 312
Felicity M. Davis, Iman Azimi, Richard Faville, et al.
Oncogene (2013) Vol. 33, Iss. 18, pp. 2307-2316
Open Access | Times Cited: 312
Microenvironmental Regulation of Epithelial–Mesenchymal Transitions in Cancer
Dingcheng Gao, Linda T. Vahdat, Stephen T.C. Wong, et al.
Cancer Research (2012) Vol. 72, Iss. 19, pp. 4883-4889
Open Access | Times Cited: 301
Dingcheng Gao, Linda T. Vahdat, Stephen T.C. Wong, et al.
Cancer Research (2012) Vol. 72, Iss. 19, pp. 4883-4889
Open Access | Times Cited: 301
Role of ErbB Receptors in Cancer Cell Migration and Invasion
Aline Appert-Collin, P. Hubert, Gérard Crémel, et al.
Frontiers in Pharmacology (2015) Vol. 6
Open Access | Times Cited: 286
Aline Appert-Collin, P. Hubert, Gérard Crémel, et al.
Frontiers in Pharmacology (2015) Vol. 6
Open Access | Times Cited: 286
The epithelial–mesenchymal transition under control: Global programs to regulate epithelial plasticity
M. Ángela Nieto, Amparo Cano
Seminars in Cancer Biology (2012) Vol. 22, Iss. 5-6, pp. 361-368
Closed Access | Times Cited: 256
M. Ángela Nieto, Amparo Cano
Seminars in Cancer Biology (2012) Vol. 22, Iss. 5-6, pp. 361-368
Closed Access | Times Cited: 256
Drug resistance in cancer: mechanisms and tackling strategies
Tanweer Haider, Vikas Pandey, Nagma Banjare, et al.
Pharmacological Reports (2020) Vol. 72, Iss. 5, pp. 1125-1151
Closed Access | Times Cited: 218
Tanweer Haider, Vikas Pandey, Nagma Banjare, et al.
Pharmacological Reports (2020) Vol. 72, Iss. 5, pp. 1125-1151
Closed Access | Times Cited: 218
Plasticity of disseminating cancer cells in patients with epithelial malignancies
Natalia Bednarz‐Knoll, Catherine Alix‐Panabières, Klaus Pantel
Cancer and Metastasis Reviews (2012) Vol. 31, Iss. 3-4, pp. 673-687
Closed Access | Times Cited: 214
Natalia Bednarz‐Knoll, Catherine Alix‐Panabières, Klaus Pantel
Cancer and Metastasis Reviews (2012) Vol. 31, Iss. 3-4, pp. 673-687
Closed Access | Times Cited: 214
Revisiting epithelial‐mesenchymal transition in cancer metastasis: the connection between epithelial plasticity and stemness
Tsai‐Tsen Liao, Muh‐Hwa Yang
Molecular Oncology (2017) Vol. 11, Iss. 7, pp. 792-804
Open Access | Times Cited: 211
Tsai‐Tsen Liao, Muh‐Hwa Yang
Molecular Oncology (2017) Vol. 11, Iss. 7, pp. 792-804
Open Access | Times Cited: 211
Circulating tumour cells: the evolving concept and the inadequacy of their enrichment by EpCAM-based methodology for basic and clinical cancer research
Phulwinder K. Grover, Adrian G. Cummins, Timothy Price, et al.
Annals of Oncology (2014) Vol. 25, Iss. 8, pp. 1506-1516
Open Access | Times Cited: 201
Phulwinder K. Grover, Adrian G. Cummins, Timothy Price, et al.
Annals of Oncology (2014) Vol. 25, Iss. 8, pp. 1506-1516
Open Access | Times Cited: 201
Cancer cell plasticity: Impact on tumor progression and therapy response
Victoria da Silva-Diz, Laura Lorenzo-Sanz, Adrià Bernat-Peguera, et al.
Seminars in Cancer Biology (2018) Vol. 53, pp. 48-58
Closed Access | Times Cited: 175
Victoria da Silva-Diz, Laura Lorenzo-Sanz, Adrià Bernat-Peguera, et al.
Seminars in Cancer Biology (2018) Vol. 53, pp. 48-58
Closed Access | Times Cited: 175
Update on Epithelial-Mesenchymal Plasticity in Cancer Progression
Rosa Fontana, Aida Mestre‐Farrera, Jing Yang
Annual Review of Pathology Mechanisms of Disease (2023) Vol. 19, Iss. 1, pp. 133-156
Open Access | Times Cited: 52
Rosa Fontana, Aida Mestre‐Farrera, Jing Yang
Annual Review of Pathology Mechanisms of Disease (2023) Vol. 19, Iss. 1, pp. 133-156
Open Access | Times Cited: 52
Antibody-independent isolation of circulating tumor cells by continuous-flow dielectrophoresis
Sangjo Shim, Katherine Stemke‐Hale, Apostolia M. Tsimberidou, et al.
Biomicrofluidics (2013) Vol. 7, Iss. 1
Open Access | Times Cited: 201
Sangjo Shim, Katherine Stemke‐Hale, Apostolia M. Tsimberidou, et al.
Biomicrofluidics (2013) Vol. 7, Iss. 1
Open Access | Times Cited: 201
Breast cancer stem cells: Multiple capacities in tumor metastasis
Shaoqing Geng, Aris T. Alexandrou, Jian Jian Li
Cancer Letters (2014) Vol. 349, Iss. 1, pp. 1-7
Open Access | Times Cited: 167
Shaoqing Geng, Aris T. Alexandrou, Jian Jian Li
Cancer Letters (2014) Vol. 349, Iss. 1, pp. 1-7
Open Access | Times Cited: 167
Beyond the Capture of Circulating Tumor Cells: Next‐Generation Devices and Materials
Brenda J. Green, Tina Saberi Safaei, Adam Mepham, et al.
Angewandte Chemie International Edition (2015) Vol. 55, Iss. 4, pp. 1252-1265
Closed Access | Times Cited: 149
Brenda J. Green, Tina Saberi Safaei, Adam Mepham, et al.
Angewandte Chemie International Edition (2015) Vol. 55, Iss. 4, pp. 1252-1265
Closed Access | Times Cited: 149
Loss of E-cadherin activates EGFR-MEK/ERK signaling, which promotes invasion via the ZEB1/MMP2 axis in non-small cell lung cancer
Gab-Yong Bae, So‐Jung Choi, Ji‐Seon Lee, et al.
Oncotarget (2013) Vol. 4, Iss. 12, pp. 2512-2522
Open Access | Times Cited: 143
Gab-Yong Bae, So‐Jung Choi, Ji‐Seon Lee, et al.
Oncotarget (2013) Vol. 4, Iss. 12, pp. 2512-2522
Open Access | Times Cited: 143
Neutralization of IL-8 decreases tumor PMN-MDSCs and reduces mesenchymalization of claudin-low triple-negative breast cancer
Charli Dominguez, Kristen K. McCampbell, Justin M. David, et al.
JCI Insight (2017) Vol. 2, Iss. 21
Open Access | Times Cited: 143
Charli Dominguez, Kristen K. McCampbell, Justin M. David, et al.
JCI Insight (2017) Vol. 2, Iss. 21
Open Access | Times Cited: 143