Zebrafish heart regeneration occurs by cardiomyocyte dedifferentiation and proliferation

Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation

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A Dynamic Epicardial Injury Response Supports Progenitor Cell Activity during Zebrafish Heart Regeneration

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Injury-induced fetal reprogramming imparts multipotency and reparative properties to pericardial adipose stem cells

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Epigenetic Regulation of Organ Regeneration in Zebrafish

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Oxygen as a key regulator of cardiomyocyte proliferation: New results about cell culture conditions!

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A Novel Zebrafish Larvae Hypoxia/Reoxygenation Model for Assessing Myocardial Ischemia/Reperfusion Injury

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The Diversity of Muscles and Their Regenerative Potential across Animals

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Extracellular Matrix and Cellular Plasticity in Musculoskeletal Development

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Adenoviral Mediated Delivery of OSKM Factors Induces Partial Reprogramming of Mouse Cardiac Cells In Vivo

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The use of transgenics in the laboratory axolotl

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May the best wound WIHN: the hallmarks of wound-induced hair neogenesis

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Brain Regeneration Resembles Brain Cancer at Its Early Wound Healing Stage and Diverges From Cancer Later at Its Proliferation and Differentiation Stages

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Mesentery AjFGF4–AjFGFR2–ERK pathway modulates intestinal regeneration via targeting cell cycle in echinoderms

Zeng, C., Guo, M. Z., Xiang, Y., Song, M., Xiao, K., & Li, C. (2022) · Cell Proliferation · doi:10.1111/cpr.13351 · Cited by 17

Metabolic reprogramming and membrane glycan remodeling as potential drivers of zebrafish heart regeneration

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Malat1 deficiency prevents neonatal heart regeneration by inducing cardiomyocyte binucleation

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Pharmacological Therapy in the Heart as an Alternative to Cellular Therapy: A Place for the Brain Natriuretic Peptide?

Rosenblatt‐Velin, N., Badoux, S., & Liaudet, L. (2016) · Stem Cells International · doi:10.1155/2016/5961342 · Cited by 17

ANGPTL8 reverses established adriamycin cardiomyopathy by stimulating adult cardiac progenitor cells

Chen, S., Chen, J., Meng, X., Shen, J.-S., Huang, J., Huang, P., Pu, Z., McNeill, N. H., & Grayburn, P. A. (2016) · Oncotarget · doi:10.18632/oncotarget.13061 · Cited by 17

Micro RNAs are involved in activation of epicardium during zebrafish heart regeneration

Ceci, M., Carlantoni, C., Missinato, M. A., Bonvissuto, D., Giacomo, B. D., Contu, R., & Romano, N. (2018) · Cell Death Discovery · doi:10.1038/s41420-018-0041-x · Cited by 17

Covering and Re-Covering the Heart: Development and Regeneration of the Epicardium

Cao, Y., & Cao, J. (2018) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd6010003 · Cited by 17

Single-cell transcriptome and epigenomic reprogramming of cardiomyocyte-derived cardiac progenitor cells

Chen, X., Chakravarty, T., Zhang, Y., Li, X., Zhong, J. F., & Wang, C. (2016) · Scientific Data · doi:10.1038/sdata.2016.79 · Cited by 17

Hypoxia and Tissue Regeneration: Adaptive Mechanisms and Therapeutic Opportunities

Vélez, I. C. V., Domínguez, C. M. C., Sánchez, M. J. F., & Garavito-Aguilar, Z. V. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199272 · Cited by 18

Oxidative phosphorylation is required for cardiomyocyte re-differentiation and long-term fish heart regeneration

Lekkos, K., Hu, Z., Nguyen, P. D., Honkoop, H., Sengul, E., Alonaizan, R., Koth, J., Ying, J., Lemieux, M. E., Kenward, A., et al. (2025) · Nature Cardiovascular Research · doi:10.1038/s44161-025-00718-x · Cited by 16

Cardiac stem cells for myocardial regeneration: promising but not ready for prime time

Lader, J. M., Stachel, M., & Bu, L. (2017) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2017.05.009 · Cited by 16

Role of Mononuclear Cardiomyocytes in Cardiac Turnover and Regeneration

Becker, C., & Hesse, M. (2020) · Current Cardiology Reports · doi:10.1007/s11886-020-01289-y · Cited by 16

Prolonged cardiac NR4A2 activation causes dilated cardiomyopathy in mice

Ashraf, S., Taegtmeyer, H., & Harmancey, R. (2022) · Basic Research in Cardiology · doi:10.1007/s00395-022-00942-7 · Cited by 16

The Promising Role of a Zebrafish Model Employed in Neural Regeneration Following a Spinal Cord Injury

Zeng, C., & Tsai, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241813938 · Cited by 16

Single-cell chromatin profiling reveals genetic programs activating proregenerative states in nonmyocyte cells

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Mechanisms of Cell Regeneration — From Differentiation to Maintenance of Cell Phenotype

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Zebrafish Cardiac Injury and Regeneration Models: A Noninvasive and Invasive In Vivo Model of Cardiac Regeneration

Dickover, M. S., Zhang, R., Han, P., & Chi, N. C. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-505-7_27 · Cited by 16

Update on the Pathogenic Implications and Clinical Potential of microRNAs in Cardiac Disease

Notari, M., Pulecio, J., & Raya, Á. (2015) · BioMed Research International · doi:10.1155/2015/105620 · Cited by 16

Choosing Cell Fate Through a Dynamic Cell Cycle

Chen, X., Hartman, A. A., & Guo, S. (2015) · Current Stem Cell Reports · doi:10.1007/s40778-015-0018-0 · Cited by 19

XGSA: A statistical method for cross-species gene set analysis

Djordjevic, D., Kusumi, K., & Ho, J. W. K. (2016) · Bioinformatics · doi:10.1093/bioinformatics/btw428 · Cited by 16

Myocardial infarction and the immune response - Scarring or regeneration? A comparative look at mammals and popular regenerating animal models

Dittrich, A., & Lauridsen, H. (2019) · Journal of Immunology and Regenerative Medicine · doi:10.1016/j.regen.2019.100016 · Cited by 16

High-Frequency Ultrasound Echocardiography to Assess Zebrafish Cardiac Function

Evangelisti, A., Schimmel, K., Joshi, S., Shah, K., Fisch, S., Alexander, K. M., Liao, R., & Morgado, I. M. (2020) · Journal of Visualized Experiments · doi:10.3791/60976 · Cited by 16

MiR-324/SOCS3 Axis Protects Against Hypoxia/Reoxygenation-Induced Cardiomyocyte Injury and Regulates Myocardial Ischemia via TNF/NF-κB Signaling Pathway

Han, X., Chen, X., Han, J., Zhong, Y., Li, Q., & An, Y. (2020) · International Heart Journal · doi:10.1536/ihj.19-687 · Cited by 16

A Roadmap to Heart Regeneration Through Conserved Mechanisms in Zebrafish and Mammals

Brezitski, K., Goff, A., DeBenedittis, P., & Karra, R. (2021) · Current Cardiology Reports · doi:10.1007/s11886-021-01459-6 · Cited by 18

Advances in protein glycosylation and its role in tissue repair and regeneration

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The (Real) Neurogenic/Gliogenic Potential of the Postnatal and Adult Brain Parenchyma

Bonfanti, L. (2013) · ISRN Neuroscience · doi:10.1155/2013/354136 · Cited by 18

KCTD10 is critical for heart and blood vessel development of zebrafish

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Injectable hydrogel as stem cell scaffolds from the thermosensitive terpolymer of NIPAAm/AAc/HEMAPCL

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Generating an In Vitro 3D Cell Culture Model from Zebrafish Larvae for Heart Research

Grunow, B., Mohamet, L., & Shiels, H. A. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.118224 · Cited by 16

Proliferation of embryonic cardiomyocytes in zebrafish requires the sodium channel scn5Lab

Bennett, J. S., Stroud, D. M., Becker, J. R., & Roden, D. M. (2013) · genesis · doi:10.1002/dvg.22400 · Cited by 16

Beyond the Mammalian Heart: Fish and Amphibians as a Model for Cardiac Repair and Regeneration

Jewhurst, K., & McLaughlin, K. A. (2015) · Journal of Developmental Biology · doi:10.3390/jdb4010001 · Cited by 16

Cell Lineages, Growth and Repair of the Mouse Heart

Lescroart, F., & Meilhac, S. M. (2012) · Results and problems in cell differentiation · doi:10.1007/978-3-642-30406-4_15 · Cited by 16

Zebrafish as a Versatile Model for Cardiovascular Research: Peering into the Heart of the Matter

Angom, R. S., Singh, M., Muhammad, H., Varanasi, S. M., & Mukhopadhyay, D. (2025) · Cells · doi:10.3390/cells14070531 · Cited by 17

Generating Conditional Mutations in Zebrafish Using Gene-trap Mutagenesis

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The stress responsive gene ankrd1a is dynamically regulated during skeletal muscle development and upregulated following cardiac injury in border zone cardiomyocytes in adult zebrafish

Boskovic, S., Marín‐Juez, R., Stamenković, N., Radojkovic, D. P., Stainier, D. Y. R., & Kojić, S. (2021) · Gene · doi:10.1016/j.gene.2021.145725 · Cited by 15

Endothelial Brg1 fine-tunes Notch signaling during zebrafish heart regeneration

Xiao, C., Hou, J., Wang, F., Song, Y., Zheng, J., Luo, L., Wang, J., Ding, W., Zhu, X., & Xiong, J. (2023) · npj Regenerative Medicine · doi:10.1038/s41536-023-00293-4 · Cited by 17

Cardiomyocyte Ploidy, Metabolic Reprogramming and Heart Repair

Elia, A., Mohsin, S., & Khan, M. (2023) · Cells · doi:10.3390/cells12121571 · Cited by 15

Fulfilling the Promise of RNA Therapies for Cardiac Repair and Regeneration

Giacca, M. (2023) · Stem Cells Translational Medicine · doi:10.1093/stcltm/szad038 · Cited by 15

Harnessing the regenerative potential of interleukin11 to enhance heart repair

Shin, K., Rodriguez, A., Kim, C., Silaban, I. M., Xia, Y., Sun, J., Dong, C., Keleş, S., Wang, J., Cao, J., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-54060-0 · Cited by 15

Is heart regeneration on the right track?

Mummery, C. L., & Lee, R. T. (2013) · Nature Medicine · doi:10.1038/nm.3158 · Cited by 15

Mammalian Cardiac Regeneration After Fetal Myocardial Infarction Requires Cardiac Progenitor Cell Recruitment

Allukian, M., Xu, J., Morris, M., Caskey, R. C., Dorsett‐Martin, W., Plappert, T. A., Griswold, M. E., Gorman, J. H., Gorman, R. C., & Liechty, K. W. (2013) · The Annals of Thoracic Surgery · doi:10.1016/j.athoracsur.2013.04.005 · Cited by 15

Galanin regulates blood glucose level in the zebrafish: a morphological and functional study

Podlasz, P., Jakimiuk, A., Chmielewska‐Krzesińska, M., Kasica, N., Nowik, N., & Kaleczyc, J. (2015) · Histochemistry and Cell Biology · doi:10.1007/s00418-015-1376-5 · Cited by 15

Use of Phage PhiC31 Integrase as a Tool for Zebrafish Genome Manipulation

Lister, J. A. (2011) · Methods in cell biology · doi:10.1016/b978-0-12-374814-0.00011-2 · Cited by 15

Cancer Stem Cells: Dynamic Entities in an Ever-Evolving Paradigm

López-Bertoni, H., Li, Y.-Q., & Laterra, J. (2015) · Biology and Medicine · doi:10.4172/0974-8369.1000s2-001 · Cited by 15

Isolation of Novel CreERT2-Driver Lines in Zebrafish Using an Unbiased Gene Trap Approach

Jungke, P., Hammer, J., Hans, S., & Brand, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129072 · Cited by 15

A systems mechanobiology model to predict cardiac reprogramming outcomes on different biomaterials

Kong, Y. P., Rioja, A. Y., Xue, X., Sun, Y., Fu, J., & Putnam, A. J. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.07.036 · Cited by 15

Multi-species comparisons of snakes identify coordinated signalling networks underlying post-feeding intestinal regeneration

Perry, B. W., Andrew, A. L., Kamal, A. H. M., Card, D. C., Schield, D. R., Pasquesi, G. I. M., Pellegrino, M. W., Mackessy, S. P., Chowdhury, S. M., Secor, S. M., et al. (2019) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2019.0910 · Cited by 15

Wound Healing Insights from Flies and FishPreprint

George, A., & Martin, P. B. (2022) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041217 · Cited by 15

Cryo‐injury procedure‐induced cardiac regeneration shows unique gene expression profiles in the newt Pleurodeles waltl

Uemasu, H., Ikuta, H., Igawa, T., Suzuki, M., Kyakuno, M., Iwata, Y., Tazawa, I., Ogino, H., Satoh, Y., Takeuchi, T., et al. (2021) · Developmental Dynamics · doi:10.1002/dvdy.450 · Cited by 14

A Role of Thyroid Hormones in Acute Myocardial Infarction: An Update

Jafar, T. H., Rasool, R., Unar, A., Chanihoon, G. Q., & Mubeen, B. (2022) · Current Cardiology Reviews · doi:10.2174/1573403x18666220428121431 · Cited by 14

Epicardial EMT and cardiac repair: an update

Foglio, E., D’Avorio, E., Nieri, R., Russo, M. A., & Limana, F. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-03823-z · Cited by 14

microRNA and Cardiac Regeneration

Gnecchi, M., Pisano, F., & Bariani, R. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-22380-3_7 · Cited by 14

Cardiomyocyte dedifferentiation and remodeling in 3D scaffolds to generate the cellular diversity of engineering cardiac tissues

Wang, C., Liu, W. Y., Shen, Y., Chen, J., Zhu, H., Yang, X., Jiang, X., Wang, Y., & Zhou, J. (2019) · Biomaterials Science · doi:10.1039/c9bm01003c · Cited by 14

MicroRNA roles in regeneration: Multiple lessons from zebrafish

Ribeiro, A. D. O., de Oliveira, A. C., Costa, J. M., Nachtigall, P. G., Herkenhoff, M. E., Campos, V. F., Delella, F. K., & Pinhal, D. (2021) · Developmental Dynamics · doi:10.1002/dvdy.421 · Cited by 14

Regulation of collagen deposition in the trout heart during thermal acclimation

Johnston, E. F., & Gillis, T. E. (2022) · Current Research in Physiology · doi:10.1016/j.crphys.2022.02.004 · Cited by 14

The Effects of Sesquiterpene Lactones on the Differentiation of Human or Animal Cells Cultured In-Vitro: A Critical Systematic Review

Fateh, S. T., Fateh, S. T., Shekari, F., Mahdavi, M., Aref, A. R., & Salehi-Najafabadi, A. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.862446 · Cited by 14

Spinal cord regeneration — the origins of progenitor cells for functional rebuilding

Walker, S. E., & Echeverri, K. (2022) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.101917 · Cited by 14

Mononuclear Cells from Dedifferentiation of Mouse Myotubes Display Remarkable Regenerative Capability

Yang, Z., Liu, Q., Mannix, R. J., Xu, X., Li, H., Ma, Z., Ingber, D. E., Allen, P. D., & Wang, Y. (2014) · Stem Cells · doi:10.1002/stem.1742 · Cited by 14

Regeneration potential of adult cardiac myocytes

Oyama, K., El‐Nachef, D., & MacLellan, W. R. (2013) · Cell Research · doi:10.1038/cr.2013.78 · Cited by 14

The Non-coding Road Towards Cardiac Regeneration

Hudson, J. E., & Porrello, E. R. (2013) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-013-9486-8 · Cited by 14

Cardiac Stem Cell Therapy

Ye, J., & Yeghiazarians, Y. (2013) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e318299ebc0 · Cited by 14

Mechanisms and Therapeutic Targets of Cardiac Regeneration: Closing the Age Gap

Castellan, R. F. P., & Meloni, M. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00007 · Cited by 14

Monitoring of Adult Zebrafish Heart Regeneration Using High-Frequency Ultrasound Spectral Doppler and Nakagami Imaging

Yeo, S., Yoon, C., Lien, C., Song, T., & Shung, K. K. (2019) · Sensors · doi:10.3390/s19194094 · Cited by 14

Progress Toward and Challenges Remaining for Thyroid Tissue Regeneration

Romitti, M., & Costagliola, S. (2023) · Endocrinology · doi:10.1210/endocr/bqad136 · Cited by 13

Characteristics of a gill resection – Regeneration model in freshwater laboratory-reared Atlantic salmon (Salmo salar)

Kazerouni, E. G., Wilson, J. M., Jones, S. R. M., & Brauner, C. J. (2023) · Aquaculture · doi:10.1016/j.aquaculture.2023.740210 · Cited by 13

Reactive oxygen species during heart regeneration in zebrafish: Lessons for future clinical therapies

Helston, O., & Amaya, E. (2021) · Wound Repair and Regeneration · doi:10.1111/wrr.12892 · Cited by 13

Carpaine Promotes Proliferation and Repair of H9c2 Cardiomyocytes after Oxidative Insults

Sudi, S. B., Chin, Y.-Z., Wasli, N. S., Fong, S. Y., Shimmi, S. C., How, S., & Sunggip, C. (2022) · Pharmaceuticals · doi:10.3390/ph15020230 · Cited by 13

Single-cell analysis reveals an Angpt4-initiated EPDC-EC-CM cellular coordination cascade during heart regeneration

Wu, Z., Shi, Y., Cui, Y., Xing, X., Zhang, L., Liu, D., Zhang, Y., Dong, J., Li, J., Pang, M., et al. (2022) · Protein & Cell · doi:10.1093/procel/pwac010 · Cited by 13

The regenerative response of cardiac interstitial cells

Rolland, L., Harrington, A., Faucherre, A., Abaroa, J. M., Gangatharan, G., Gamba, L., Séverac, D., Pratlong, M., Moore‐Morris, T., & Jopling, C. (2022) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjac059 · Cited by 13

Increased Fat Graft Survival by Promoting Adipocyte Dedifferentiation

Chai, Y., Jia, X., Zhu, J., Jiang, C., Yin, N., & Li, F. (2022) · Aesthetic Surgery Journal · doi:10.1093/asj/sjac296 · Cited by 13

miRNA Overexpression Induces Cardiomyocyte Proliferation In Vivo

Baker, A. H., & van Rooij, E. (2013) · Molecular Therapy · doi:10.1038/mt.2013.20 · Cited by 13

Tuning cell fate

Kami, D., & Gojo, S. (2014) · Organogenesis · doi:10.4161/org.28816 · Cited by 14

Small Solutions to Big Problems

Srivastava, D., & Heidersbach, A. J. (2013) · Circulation Research · doi:10.1161/circresaha.113.301409 · Cited by 13

Snai1 is important for avian epicardial cell transformation and motility

Tao, G., Miller, L. J., & Lincoln, J. (2013) · Developmental Dynamics · doi:10.1002/dvdy.23967 · Cited by 13

Prometheus’s heart: what lies beneath

Barile, L., & Lionetti, V. (2011) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2011.01487.x · Cited by 13

Is adult cardiac regeneration absent in Xenopus laevis yet present in Xenopus tropicalis?

Marshall, L., Girardot, F., DEMENEIX, B. A., & Coen, L. (2018) · Cell & Bioscience · doi:10.1186/s13578-018-0231-5 · Cited by 13

Leukocyte-Mediated Cardiac Repair after Myocardial Infarction in Non-Regenerative vs. Regenerative Systems

Peterson, E., Sun, J., & Wang, J. (2022) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd9020063 · Cited by 14

Magnetic Resonance Imaging of the Regenerating Neonatal Mouse Heart

Gunadasa-Rohling, M., Masters, M., Maguire, M. L., Smart, S., Schneider, J. E., & Riley, P. R. (2018) · Circulation · doi:10.1161/circulationaha.118.036086 · Cited by 13

The Regulatory Role of Oxygen Metabolism in Exercise-Induced Cardiomyocyte Regeneration

Bo, B., Li, S., Zhou, K., & Wei, J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.664527 · Cited by 12

Targeting cardiomyocyte proliferation as a key approach of promoting heart repair after injury

Li, S., Ma, W., & Cai, B. (2021) · Molecular Biomedicine · doi:10.1186/s43556-021-00047-y · Cited by 12

Hallmark Molecular and Pathological Features of POLG Disease are Recapitulated in Cerebral Organoids

Chen, A., Yangzom, T., Hong, Y., Lundberg, B. C., Sullivan, G. J., Tzoulis, C., Bindoff, L. A., & Liang, K. X. (2024) · Advanced Science · doi:10.1002/advs.202307136 · Cited by 12

Induced Cytokinesis Generates Highly Proliferative Mononuclear Cardiomyocytes at the Expense of Contractility

Lam, N. T., Nguyen, N. U. N., Elhelaly, W. M., Hsu, C.-C., Menendez-Montes, I., Xiao, F., Ali, S. R., Vo, N., Briard, N., El-Feky, L., et al. (2025) · Circulation · doi:10.1161/circulationaha.124.065763 · Cited by 12

Harnessing the Potential of Adult Cardiac Stem Cells: Lessons from Haematopoiesis, the Embryo and the Niche

Balmer, G. M., & Riley, P. R. (2012) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-012-9386-3 · Cited by 13

Studies of Ribonucleotide Reductase in Crucian Carp—An Oxygen Dependent Enzyme in an Anoxia Tolerant Vertebrate

Sandvik, G. K., Tomter, A. B., Bergan, J., Zoppellaro, G., Barra, A., Røhr, Å. K., Kolberg, M., Ellefsen, S., Andersson, K. K., & Nilsson, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042784 · Cited by 12

Dieldrin Augments mTOR Signaling and Regulates Genes Associated with Cardiovascular Disease in the Adult Zebrafish Heart (Danio rerio)

Slade, L., Cowie, A. M., Martyniuk, C. J., Kienesberger, P. C., & Pulinilkunnil, T. (2017) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.116.239806 · Cited by 12

Cardiac Preconditioning, Remodeling and Regeneration

Gillis, T. E., & Johnston, E. F. (2017) · Fish physiology · doi:10.1016/bs.fp.2017.09.004 · Cited by 12

Decoding the proregenerative competence of regulatory T cells through complex tissue regeneration in zebrafish

Gupta, S., Adhikary, S., & Hui, S. P. (2021) · Clinical & Experimental Immunology · doi:10.1111/cei.13661 · Cited by 12

Pulse Inversion Chirp Coded Tissue Harmonic Imaging (PI-CTHI) of Zebrafish Heart Using High Frame Rate Ultrasound Biomicroscopy

Park, J., Huang, Y., Chen, R., Lee, J.-W., Cummins, T. M., Zhou, Q., Lien, C., & Shung, K. K. (2012) · Annals of Biomedical Engineering · doi:10.1007/s10439-012-0636-y · Cited by 12

Transcriptional response to cardiac injury in the zebrafish: systematic identification of genes with highly concordant activity across in vivo models

Rodius, S., Nazarov, P. V., Nepomuceno-Chamorro, I. A., Jeanty, C., González‐Rosa, J. M., Ibberson, M. R., Costa, R., Xénarios, I., Mercader, N., & Azuaje, F. J. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-852 · Cited by 12

Long-term in vivo single-cell lineage tracing of deep structures using three-photon activation

Tekeli, I., Aujard, I., Trepat, X., Jullien, L., Raya, Á., & Zalvidea, D. (2016) · Light Science & Applications · doi:10.1038/lsa.2016.84 · Cited by 12

Primary contribution to zebrafish heart regeneration by gata4+ cardiomyocytes

Kikuchi, K., Holdway, J. E., Werdich, A. A., Anderson, R. M., Fang, Y., Egnaczyk, G. F., Evans, T., MacRae, C. A., Stainier, D. Y. R., & Poss, K. D. (2010) · Nature · doi:10.1038/nature08804 · Cited by 1,084

Zebrafish as a Model for Studying Cardiac Regeneration

Wu, C. C., & Weidinger, G. (2014) · Current Pathobiology Reports · doi:10.1007/s40139-014-0042-2 · Cited by 2

Cardiac Regeneration in Zebrafish

Wu, C. C., & Weidinger, G. (2016) · Springer eBooks · doi:10.1007/978-3-319-27583-3_10

Signals for cardiomyocyte proliferation during zebrafish heart regeneration

Pronobis, M. I., & Poss, K. D. (2020) · Current Opinion in Physiology · doi:10.1016/j.cophys.2020.02.002 · Cited by 29

Cardiac Regeneration in the Zebrafish Model System

Poss, K. D. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-381332-9.00040-2