Molecules and Cells

Cited by CrossRef (33)

  1. Daphné Lehalle, Umut Altunoglu, Ange-Line Bruel, Eric Arnaud, Patricia Blanchet, Jong-Woo Choi, Julie Désir, Esra Kiliç, Damien Lederer, Lucile Pinson, Christel Thauvin-Robinet, Amihood Singer, Julien Thevenon, Patrick Callier, Hulya Kayserili, Laurence Faivre. Clinical delineation of a subtype of frontonasal dysplasia with creased nasal ridge and upper limb anomalies: Report of six unrelated patients. Am J Med Genet 2017;173:3136
    https://doi.org/10.1002/ajmg.a.38490
  2. Robert M. Hughes, Jitka A.I. Virag. Harnessing the Power of Eph/ephrin Biosemiotics for Theranostic Applications. Pharmaceuticals 2020;13:112
    https://doi.org/10.3390/ph13060112
  3. Lizandra Jimenez, Hui Yu, Andrew J. McKenzie, Jeffrey L. Franklin, James G. Patton, Qi Liu, Alissa M. Weaver. Quantitative Proteomic Analysis of Small and Large Extracellular Vesicles (EVs) Reveals Enrichment of Adhesion Proteins in Small EVs. J. Proteome Res. 2019;18:947
    https://doi.org/10.1021/acs.jproteome.8b00647
  4. Liangqun Lu, Bernie J. Daigle. Prognostic analysis of histopathological images using pre-trained convolutional neural networks: application to hepatocellular carcinoma. 2020;8:e8668
    https://doi.org/10.7717/peerj.8668
  5. Ryota Tamura, Hiroyuki Miyoshi, Kent Imaizumi, Masahiro Yo, Yoshitaka Kase, Tsukika Sato, Mizuto Sato, Yukina Morimoto, Oltea Sampetrean, Jun Kohyama, Munehisa Shinozaki, Atsushi Miyawaki, Kazunari Yoshida, Hideyuki Saya, Hideyuki Okano, Masahiro Toda. Gene therapy using genome‐edited iPS cells for targeting malignant glioma . Bioengineering & Transla Med 2022
    https://doi.org/10.1002/btm2.10406
  6. Polina Goichberg. Current Understanding of the Pathways Involved in Adult Stem and Progenitor Cell Migration for Tissue Homeostasis and Repair. Stem Cell Rev and Rep 2016;12:421
    https://doi.org/10.1007/s12015-016-9663-7
  7. Shinya Sato, Suhas Vasaikar, Adel Eskaros, Young Kim, James S. Lewis, Bing Zhang, Andries Zijlstra, Alissa M. Weaver. EPHB2 carried on small extracellular vesicles induces tumor angiogenesis via activation of ephrin reverse signaling. 2019;4
    https://doi.org/10.1172/jci.insight.132447
  8. Zhimin Huang, Simeng Liu, Anna Tang, Laith Al-Rabadi, Mark Henkemeyer, Patrice N. Mimche, Yufeng Huang. Key role for EphB2 receptor in kidney fibrosis. 2021;135:2127
    https://doi.org/10.1042/CS20210644
  9. M. Popović, A. Matana, V. Torlak, T. Boutin, D. Brdar, I. Gunjača, D. Kaličanin, I. Kolčić, V. Boraska Perica, A. Punda, O. Polašek, M. Barbalić, C. Hayward, T. Zemunik. Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone. J Endocrinol Invest 2019;42:1171
    https://doi.org/10.1007/s40618-019-01030-9
  10. Songyang Zheng, Fangling Sun, Xin Tian, Zixin Zhu, Yufeng Wang, Wenrong Zheng, Tingting Liu, Wen Wang. Roles of Eph/ephrin signaling pathway in repair and regeneration for ischemic cerebrovascular and cardiovascular diseases. Journal of Neurorestoratology 2023;11:100040
    https://doi.org/10.1016/j.jnrt.2022.100040
  11. Anna Haeger, Katarina Wolf, Mirjam M. Zegers, Peter Friedl. Collective cell migration: guidance principles and hierarchies. Trends in Cell Biology 2015;25:556
    https://doi.org/10.1016/j.tcb.2015.06.003
  12. Jianbo Wang, Joana Galvao, Krista M. Beach, Weijia Luo, Raul A. Urrutia, Jeffrey L. Goldberg, Deborah C. Otteson. Novel Roles and Mechanism for Krüppel-like Factor 16 (KLF16) Regulation of Neurite Outgrowth and Ephrin Receptor A5 (EphA5) Expression in Retinal Ganglion Cells. Journal of Biological Chemistry 2016;291:18084
    https://doi.org/10.1074/jbc.M116.732339
  13. Devargya Ganguly, Joshua Abby Thomas, Abid Ali, Rahul Kumar. Mechanistic and therapeutic implications of EphA‐4 receptor tyrosine kinase in the pathogenesis of Alzheimer's disease. Eur J of Neuroscience 2022;56:5532
    https://doi.org/10.1111/ejn.15591
  14. M. Ilcim Thestrup, Sara Caviglia, Jordi Cayuso, Ronja L. S. Heyne, Racha Ahmad, Wolfgang Hofmeister, Letizia Satriano, David G. Wilkinson, Jesper B. Andersen, Elke A. Ober. A morphogenetic EphB/EphrinB code controls hepatopancreatic duct formation. Nat Commun 2019;10
    https://doi.org/10.1038/s41467-019-13149-7
  15. Tingting Liu, Songyang Zheng, Fangling Sun, Xin Tian, Zixin Zhu, Wenrong Zheng, Yufeng Wang, Jianguo Xing, Wen Wang, Youhua Wang. Morroniside Regulates Endothelial Cell Function via the EphrinB Signaling Pathway after Oxygen-Glucose Deprivation In Vitro. Evidence-Based Complementary and Alternative Medicine 2022;2022:1
    https://doi.org/10.1155/2022/6875053
  16. Du Yang, Chunna Jin, Hong Ma, Mingyuan Huang, Guo-Ping Shi, Jianan Wang, Meixiang Xiang. EphrinB2/EphB4 pathway in postnatal angiogenesis: a potential therapeutic target for ischemic cardiovascular disease. Angiogenesis 2016;19:297
    https://doi.org/10.1007/s10456-016-9514-9
  17. Shu-Ting Liu, Shu-Min Zhong, Xue-Yan Li, Feng Gao, Fang Li, Meng-Lu Zhang, Ke Zhu, Xing-Huai Sun, Xin Wang, Yanying Miao, Xiong-Li Yang, Zhongfeng Wang. EphrinB/EphB forward signaling in Müller cells causes apoptosis of retinal ganglion cells by increasing tumor necrosis factor alpha production in rat experimental glaucomatous model. acta neuropathol commun 2018;6
    https://doi.org/10.1186/s40478-018-0618-x
  18. Hassan Ebrahim, Khalid El Sayed. Discovery of Novel Antiangiogenic Marine Natural Product Scaffolds. Marine Drugs 2016;14:57
    https://doi.org/10.3390/md14030057
  19. Ying Xiong, Kai‑Xue Li, Hong Wei, Lu Jiao, Shao‑Yong Yu, Li Zeng. Eph/ephrin signalling serves a bidirectional role in lipopolysaccharide‑induced intestinal injury. Mol Med Report 2018
    https://doi.org/10.3892/mmr.2018.9169
  20. Alanna Sedgwick, Crislyn D’Souza-Schorey. Wnt Signaling in Cell Motility and Invasion: Drawing Parallels between Development and Cancer. Cancers 2016;8:80
    https://doi.org/10.3390/cancers8090080
  21. Başak Kandemir, Ugur Dag, Burcu Bakir Gungor, İlknur Melis Durasi, Burcu Erdogan, Eray Sahin, Ugur Sezerman, Isil Aksan Kurnaz, Jinsong Zhang. In silico analyses and global transcriptional profiling reveal novel putative targets for Pea3 transcription factor related to its function in neurons. PLoS ONE 2017;12:e0170585
    https://doi.org/10.1371/journal.pone.0170585
  22. Sarah Mele, Travis K. Johnson. Receptor Tyrosine Kinases in Development: Insights from Drosophila. IJMS 2019;21:188
    https://doi.org/10.3390/ijms21010188
  23. Hongkui Wang, Hui Zhu, Qi Guo, Tianmei Qian, Ping Zhang, Shiying Li, Chengbin Xue, Xiaosong Gu. Overlapping Mechanisms of Peripheral Nerve Regeneration and Angiogenesis Following Sciatic Nerve Transection. Front. Cell. Neurosci. 2017;11
    https://doi.org/10.3389/fncel.2017.00323
  24. Ting Yu, Si Chu, Xingxing Liu, Junyi Li, Qianyun Chen, Meng Xu, Hui Wu, Mingyue Li, Yalan Dong, Feng Zhu, Haifeng Zhou, Desheng Hu, Heng Fan. Extracellular vesicles derived from EphB2-overexpressing bone marrow mesenchymal stem cells ameliorate DSS-induced colitis by modulating immune balance. Stem Cell Res Ther 2021;12
    https://doi.org/10.1186/s13287-021-02232-w
  25. Fumihiko Okumura, Akiko Joo-Okumura, Keisuke Obara, Alexander Petersen, Akihiko Nishikimi, Yoshinori Fukui, Kunio Nakatsukasa, Takumi Kamura, Jonathan Chernoff. Ubiquitin ligase SPSB4 diminishes cell repulsive responses mediated by EphB2. MBoC 2017;28:3532
    https://doi.org/10.1091/mbc.e17-07-0450
  26. Björn Becker, M. Reza Shaebani, Domenik Rammo, Tobias Bubel, Ludger Santen, Manfred J. Schmitt. Cargo binding promotes KDEL receptor clustering at the mammalian cell surface. Sci Rep 2016;6
    https://doi.org/10.1038/srep28940
  27. Katherine A. Young, Laura Biggins, Hayley J. Sharpe. Protein tyrosine phosphatases in cell adhesion. 2021;478:1061
    https://doi.org/10.1042/BCJ20200511
  28. Evelien G. G. Sprenkeler, Stefanie S. V. Henriet, Anton T. J. Tool, Iris C. Kreft, Ivo van der Bijl, Cathelijn E. M. Aarts, Michel van Houdt, Paul J. J. H. Verkuijlen, Koen van Aerde, Gerald Jaspers, Arno van Heijst, Wouter Koole, Thatjana Gardeitchik, Judy Geissler, Martin de Boer, Simon Tol, Christine W. Bruggeman, Floris P. J. van Alphen, Han J. M. P. Verhagen, Emile van den Akker, Hans Janssen, Robin van Bruggen, Timo K. van den Berg, Kian D. Liem, Taco W. Kuijpers. MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerization. 2020;135:2171
    https://doi.org/10.1182/blood.2019002633
  29. Rebecca S. G. Kong, Guanxiang Liang, Yanhong Chen, Paul Stothard, Le Luo Guan. Transcriptome profiling of the rumen epithelium of beef cattle differing in residual feed intake. BMC Genomics 2016;17
    https://doi.org/10.1186/s12864-016-2935-4
  30. Suk-young Lee, Yoo Jin Na, Yoon A Jeong, Jung Lim Kim, Sang Cheul Oh, Dae-Hee Lee. Upregulation of EphB3 in gastric cancer with acquired resistance to a FGFR inhibitor. The International Journal of Biochemistry & Cell Biology 2018;102:128
    https://doi.org/10.1016/j.biocel.2018.07.008
  31. Li Zeng, Kaixue Li, Hong Wei, Jingjing Hu, Lu Jiao, Shaoyong Yu, Ying Xiong. A Novel EphA2 Inhibitor Exerts Beneficial Effects in PI-IBS in Vivo and in Vitro Models via Nrf2 and NF-κB Signaling Pathways. Front. Pharmacol. 2018;9
    https://doi.org/10.3389/fphar.2018.00272
  32. Christabel X. Tan, Cagla Eroglu. Cell adhesion molecules regulating astrocyte–neuron interactions. Current Opinion in Neurobiology 2021;69:170
    https://doi.org/10.1016/j.conb.2021.03.015
  33. Jasper J Visser, Yolanda Cheng, Steven C Perry, Andrew Benjamin Chastain, Bayan Parsa, Shatha S Masri, Thomas A Ray, Jeremy N Kay, Woj M Wojtowicz. An extracellular biochemical screen reveals that FLRTs and Unc5s mediate neuronal subtype recognition in the retina. 2015;4
    https://doi.org/10.7554/eLife.08149