Molecules and Cells

Cited by CrossRef (12)

  1. Gianfranco Matrone, Kathryn S. Wilson, John J. Mullins, Carl S. Tucker, Martin A. Denvir. Temporal cohesion of the structural, functional and molecular characteristics of the developing zebrafish heart. Differentiation 2015;89:117
    https://doi.org/10.1016/j.diff.2015.05.001
  2. Antonia Germani, Eleonora Foglio, Maurizio C. Capogrossi, Matteo Antonio Russo, Federica Limana. Generation of cardiac progenitor cells through epicardial to mesenchymal transition. J Mol Med 2015;93:735
    https://doi.org/10.1007/s00109-015-1290-2
  3. Almudena Expósito-Villén, Amelia E. Aránega, Diego Franco. Functional Role of Non-Coding RNAs during Epithelial-To-Mesenchymal Transition. ncRNA 2018;4:14
    https://doi.org/10.3390/ncrna4020014
  4. Santiago Sánchez-Ramírez, Yessica Rico, Kristin H. Berry, Taylor Edwards, Alice E. Karl, Brian T. Henen, Robert W. Murphy. Landscape limits gene flow and drives population structure in Agassiz’s desert tortoise (Gopherus agassizii). Sci Rep 2018;8
    https://doi.org/10.1038/s41598-018-29395-6
  5. Rabea Hinkel, Katharina Klett, Andrea Bähr, Christian Kupatt. Thymosin β4-mediated protective effects in the heart. Expert Opinion on Biological Therapy 2018;18:121
    https://doi.org/10.1080/14712598.2018.1490409
  6. Kamal M. Kassem, Sonal Vaid, Hongmei Peng, Sarah Sarkar, Nour-Eddine Rhaleb. Tβ4–Ac-SDKP pathway: Any relevance for the cardiovascular system?. Can. J. Physiol. Pharmacol. 2019;97:589
    https://doi.org/10.1139/cjpp-2018-0570
  7. Klaudia Maar, Roland Hetenyi, Szabolcs Maar, Gabor Faskerti, Daniel Hanna, Balint Lippai, Aniko Takatsy, Ildiko Bock-Marquette. Utilizing Developmentally Essential Secreted Peptides Such as Thymosin Beta-4 to Remind the Adult Organs of Their Embryonic State—New Directions in Anti-Aging Regenerative Therapies. Cells 2021;10:1343
    https://doi.org/10.3390/cells10061343
  8. Dawn Bannerman, Simon Pascual-Gil, Marie Floryan, Milica Radisic. Bioengineering strategies to control epithelial-to-mesenchymal transition for studies of cardiac development and disease. APL Bioengineering 2021;5:021504
    https://doi.org/10.1063/5.0033710
  9. Yun Sun, Xiaojuan Chen, Yue Xu, Qiaohong Liu, Xue Jiang, Shifeng Wang, Weiliang Guo, Yongcan Zhou. Thymosin β4 is involved in the antimicrobial immune response of Golden pompano, Trachinotus ovatus. Fish & Shellfish Immunology 2017;69:90
    https://doi.org/10.1016/j.fsi.2017.08.006
  10. Lirong Bai, Wenyao He, Sigang Fan, Baosuo Liu, Tong Zhou, Dongling Zhang, Dianchang Zhang, Dahui Yu. Multiple functions of thymosin β4 in the pearl oyster Pinctada fucata suggest its multiple potential roles in artificial pearl culture. Fish & Shellfish Immunology 2020;103:23
    https://doi.org/10.1016/j.fsi.2020.04.040
  11. Camille Fédou, Ophélie Lescat, Guylène Feuillet, Marie Buléon, Eric Neau, Benjamin Breuil, Mélinda Alvès, Julie Batut, Patrick Blader, Stéphane Decramer, Jean Sébastien Saulnier-Blache, Julie Klein, Bénédicte Buffin-Meyer, Joost P. Schanstra. The low affinity p75 neurotrophin receptor is down-regulated in congenital anomalies of the kidney and the urinary tract: Possible involvement in early nephrogenesis. Biochemical and Biophysical Research Communications 2020;533:786
    https://doi.org/10.1016/j.bbrc.2020.09.084
  12. Song-Song Zou, Jing Wang, Bao-Xia Li, Gui-Wen Yang, Jie-Jie Sun, Hui-Ting Yang. Thymosin participates in antimicrobial immunity in zebrafish. Fish & Shellfish Immunology 2019;87:371
    https://doi.org/10.1016/j.fsi.2019.01.040