Title: The Influence of the Nerve in Regeneration of the Amphibian Extremity
Abstract: Previous articleNext article No AccessThe Influence of the Nerve in Regeneration of the Amphibian ExtremityMarcus SingerMarcus Singer Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmail SectionsMoreDetailsFiguresReferencesCited by The Quarterly Review of Biology Volume 27, Number 2Jun., 1952 Published in association with Stony Brook University Article DOIhttps://doi.org/10.1086/398873 Views: 13Total views on this site Citations: 502Citations are reported from Crossref PDF download Crossref reports the following articles citing this article:Vaibhav P. Pai, Ben G. Cooper, Michael Levin Screening Biophysical Sensors and Neurite Outgrowth Actuators in Human Induced-Pluripotent-Stem-Cell-Derived Neurons, Cells 11, no.1616 (Aug 2022): 2470.https://doi.org/10.3390/cells11162470Daniel Osorio-Méndez, Andrew Miller, Ian J. Begeman, Andrew Kurth, Ryan Hagle, Daniela Rolph, Amy L. Dickson, Chen-Hui Chen, Mary Halloran, Kenneth D. Poss, Junsu Kang Voltage-gated sodium channel scn8a is required for innervation and regeneration of amputated adult zebrafish fins, Proceedings of the National Academy of Sciences 119, no.2828 (Jul 2022).https://doi.org/10.1073/pnas.2200342119Chiara Sinigaglia, Alba Almazán, Marie Lebel, Marie Sémon, Benjamin Gillet, Sandrine Hughes, Eric Edsinger, Michalis Averof, Mathilde Paris Distinct gene expression dynamics in developing and regenerating crustacean limbs, Proceedings of the National Academy of Sciences 119, no.2727 (Jul 2022).https://doi.org/10.1073/pnas.2119297119Fadi Sader, Stéphane Roy Tgf‐β superfamily and limb regeneration: Tgf‐β to start and Bmp to end, Developmental Dynamics 251, no.66 (Jun 2021): 973–987.https://doi.org/10.1002/dvdy.379Nicholas D. Leigh, Joshua D. Currie Rebuilding limbs, one cell at a time, Developmental Dynamics 55 (Mar 2022).https://doi.org/10.1002/dvdy.463Rui Gong, Zuke Jiang, Naufal Zagidullin, Tianyi Liu, Benzhi Cai Regulation of cardiomyocyte fate plasticity: a key strategy for cardiac regeneration, Signal Transduction and Targeted Therapy 6, no.11 (Jan 2021).https://doi.org/10.1038/s41392-020-00413-2Yanmei Liu, Wilson Pak-Kin Lou, Ji-Feng Fei The engine initiating tissue regeneration: does a common mechanism exist during evolution?, Cell Regeneration 10, no.11 (Apr 2021).https://doi.org/10.1186/s13619-020-00073-1Jun Ishikawa, Makoto Takeo, Ayako Iwadate, Junko Koya, Miho Kihira, Masamitsu Oshima, Yuki Suzuki, Kazushi Taniguchi, Ayaka Kobayashi, Takashi Tsuji Mechanical homeostasis of liver sinusoid is involved in the initiation and termination of liver regeneration, Communications Biology 4, no.11 (Apr 2021).https://doi.org/10.1038/s42003-021-01936-2Kaylee M Wells, Kristina Kelley, Mary Baumel, Warren A Vieira, Catherine D McCusker Neural control of growth and size in the axolotl limb regenerate, eLife 10 (Nov 2021).https://doi.org/10.7554/eLife.68584Warren A. Vieira, Kelsey Anderson, Lindsay Glass Campbell, Catherine D. McCusker Characterizing the regenerative capacity and growth patterns of the Texas blind salamander ( Eurycea rathbuni ), Developmental Dynamics 250, no.66 (Sep 2020): 880–895.https://doi.org/10.1002/dvdy.245Varun B. Dwaraka, S. Randal Voss Towards comparative analyses of salamander limb regeneration, Journal of Experimental Zoology Part B: Molecular and Developmental Evolution 336, no.22 (Oct 2019): 129–144.https://doi.org/10.1002/jez.b.22902Valentina Daponte, Przemko Tylzanowski, Antonella Forlino Appendage Regeneration in Vertebrates: What Makes This Possible?, Cells 10, no.22 (Jan 2021): 242.https://doi.org/10.3390/cells10020242Junta Imai Regulation of Adaptive Cell Proliferation by Vagal Nerve Signals for Maintenance of Whole-Body Homeostasis: Potential Therapeutic Target for Insulin-Deficient Diabetes, The Tohoku Journal of Experimental Medicine 254, no.44 (Jan 2021): 245–252.https://doi.org/10.1620/tjem.254.245Xiaoyan Chen, Caiqi Zhao, Cuiping Zhang, Qingmei Li, Jie Chen, Lianping Cheng, Jian Zhou, Xiao Su, Yuanlin Song Vagal-α7nAChR signaling promotes lung stem cells regeneration via fibroblast growth factor 10 during lung injury repair, Stem Cell Research & Therapy 11, no.11 (Jun 2020).https://doi.org/10.1186/s13287-020-01757-wMustafa Sibai, Ebru Altuntaş, Barış Ethem Süzek, Betül Şahin, Cüneyd Parlayan, Gürkan Öztürk, Ahmet Tarık Baykal, Turan Demircan Comparison of protein expression profile of limb regeneration between neotenic and metamorphic axolotl, Biochemical and Biophysical Research Communications 522, no.22 (Feb 2020): 428–434.https://doi.org/10.1016/j.bbrc.2019.11.118Julian U.G. Wagner, Stefanie Dimmeler Cellular cross-talks in the diseased and aging heart, Journal of Molecular and Cellular Cardiology 138 (Jan 2020): 136–146.https://doi.org/10.1016/j.yjmcc.2019.11.152Marietta R. Easterling, Kristin M. Engbrecht, Erica J. Crespi Endocrine regulation of regeneration: Linking global signals to local processes, General and Comparative Endocrinology 283 (Nov 2019): 113220.https://doi.org/10.1016/j.ygcen.2019.113220Warren A. Vieira, Kaylee M. Wells, Michael J. Raymond, Larissa De Souza, Erik Garcia, Catherine D. McCusker FGF, BMP, and RA signaling are sufficient for the induction of complete limb regeneration from non-regenerating wounds on Ambystoma mexicanum limbs, Developmental Biology 451, no.22 (Jul 2019): 146–157.https://doi.org/10.1016/j.ydbio.2019.04.008David L. Stocum Nerves and Proliferation of Progenitor Cells in Limb Regeneration, Developmental Neurobiology 79, no.55 (Oct 2018): 468–478.https://doi.org/10.1002/dneu.22643Judith R. Soper, S. Fiona Bonar, Dudley J. O’Sullivan, Janet McCredie, Hans-Georg Willert Thalidomide and neurotrophism, Skeletal Radiology 48, no.44 (Oct 2018): 517–525.https://doi.org/10.1007/s00256-018-3086-2Mu-Hui Wang, Cheng-Han Wu, Ting-Yu Huang, Hung-Wei Sung, Ling-Ling Chiou, Shau-Ping Lin, Hsuan-Shu Lee Nerve-mediated expression of histone deacetylases regulates limb regeneration in axolotls, Developmental Biology (Feb 2019).https://doi.org/10.1016/j.ydbio.2019.02.011Shunichi Morikawa, Haizea Iribar, Araika Gutiérrez-Rivera, Taichi Ezaki, Ander Izeta Pericytes in Cutaneous Wound Healing, (May 2019): 1–63.https://doi.org/10.1007/978-3-030-16908-4_1Yuichiro Suzuki, Jacquelyn Chou, Sarah L. Garvey, Victoria R. Wang, Katherine O. Yanes Evolution and Regulation of Limb Regeneration in Arthropods, (Oct 2019): 419–454.https://doi.org/10.1007/978-3-030-23459-1_17Nicholas D. Leigh, Garrett S. Dunlap, Kimberly Johnson, Rachelle Mariano, Rachel Oshiro, Alan Y. Wong, Donald M. Bryant, Bess M. Miller, Alex Ratner, Andy Chen, William W. Ye, Brian J. Haas, Jessica L. Whited Transcriptomic landscape of the blastema niche in regenerating adult axolotl limbs at single-cell resolution, Nature Communications 9, no.11 (Dec 2018).https://doi.org/10.1038/s41467-018-07604-0Tomohito Izumi, Junta Imai, Junpei Yamamoto, Yohei Kawana, Akira Endo, Hiroto Sugawara, Masato Kohata, Yoichiro Asai, Kei Takahashi, Shinjiro Kodama, Keizo Kaneko, Junhong Gao, Kenji Uno, Shojiro Sawada, Vladimir V. Kalinichenko, Yasushi Ishigaki, Tetsuya Yamada, Hideki Katagiri Vagus-macrophage-hepatocyte link promotes post-injury liver regeneration and whole-body survival through hepatic FoxM1 activation, Nature Communications 9, no.11 (Dec 2018).https://doi.org/10.1038/s41467-018-07747-0Neil Deochand, Mack S. Costello, Michelle E. Deochand Behavioral Research with Planaria, Perspectives on Behavior Science 41, no.22 (Nov 2018): 447–464.https://doi.org/10.1007/s40614-018-00176-wCelia Herrera-Rincon, Annie S. Golding, Kristine M. Moran, Christina Harrison, Christopher J. Martyniuk, Justin A. Guay, Julia Zaltsman, Hayley Carabello, David L. Kaplan, Michael Levin Brief Local Application of Progesterone via a Wearable Bioreactor Induces Long-Term Regenerative Response in Adult Xenopus Hindlimb, Cell Reports 25, no.66 (Nov 2018): 1593–1609.e7.https://doi.org/10.1016/j.celrep.2018.10.010Dana M. Cairns, Jodie E. Giordano, Sylvia Conte, Michael Levin, David L. Kaplan Ivermectin Promotes Peripheral Nerve Regeneration during Wound Healing, ACS Omega 3, no.1010 (Oct 2018): 12392–12402.https://doi.org/10.1021/acsomega.8b01451Sera M. Busse, Patrick T. McMillen, Michael Levin Cross-limb communication during Xenopus hindlimb regenerative response: non-local bioelectric injury signals, Development 145, no.1919 (Oct 2018).https://doi.org/10.1242/dev.164210Francesca Meda, Christine Rampon, Edmond Dupont, Carole Gauron, Aurélien Mourton, Isabelle Queguiner, Marion Thauvin, Michel Volovitch, Alain Joliot, Sophie Vriz Nerves, H2O2 and Shh: Three players in the game of regeneration, Seminars in Cell & Developmental Biology 80 (Aug 2018): 65–73.https://doi.org/10.1016/j.semcdb.2017.08.015Ricardo Londono, Aaron X. Sun, Rocky S. Tuan, Thomas P. Lozito Tissue Repair and Epimorphic Regeneration: an Overview, Current Pathobiology Reports 6, no.11 (Feb 2018): 61–69.https://doi.org/10.1007/s40139-018-0161-2Wan-Jin Lu, Randall K. Mann, Allison Nguyen, Tingting Bi, Max Silverstein, Jean Y. Tang, Xiaoke Chen, Philip A. Beachy Neuronal delivery of Hedgehog directs spatial patterning of taste organ regeneration, Proceedings of the National Academy of Sciences 115, no.22 (Dec 2017).https://doi.org/10.1073/pnas.1719109115Ashley W. Seifert, Ken Muneoka The blastema and epimorphic regeneration in mammals, Developmental Biology 433, no.22 (Jan 2018): 190–199.https://doi.org/10.1016/j.ydbio.2017.08.007Junta Imai Regulation of compensatory β-cell proliferation by inter-organ networks from the liver to pancreatic β-cells, Endocrine Journal 65, no.77 (Jan 2018): 677–684.https://doi.org/10.1507/endocrj.EJ18-0241Celia Herrera-Rincon, Vaibhav P. Pai, Kristine M. Moran, Joan M. Lemire, Michael Levin The brain is required for normal muscle and nerve patterning during early Xenopus development, Nature Communications 8, no.11 (Sep 2017).https://doi.org/10.1038/s41467-017-00597-2Junpei Yamamoto, Junta Imai, Tomohito Izumi, Hironori Takahashi, Yohei Kawana, Kei Takahashi, Shinjiro Kodama, Keizo Kaneko, Junhong Gao, Kenji Uno, Shojiro Sawada, Tomoichiro Asano, Vladimir V. Kalinichenko, Etsuo A. Susaki, Makoto Kanzaki, Hiroki R. Ueda, Yasushi Ishigaki, Tetsuya Yamada, Hideki Katagiri Neuronal signals regulate obesity induced β-cell proliferation by FoxM1 dependent mechanism, Nature Communications 8, no.11 (Dec 2017).https://doi.org/10.1038/s41467-017-01869-7David L. Stocum Mechanisms of urodele limb regeneration, Regeneration 4, no.44 (Dec 2017): 159–200.https://doi.org/10.1002/reg2.92Ken Muneoka, Eva Lai, Robert J. Christy, Jon E. Mogford Limb Regrowth and Tissue Engineering Alternatives, (Sep 2017): 213–236.https://doi.org/10.1007/978-1-4939-7247-0_12Anthony L. Mescher, Anton W. Neff, Michael W. King Inflammation and immunity in organ regeneration, Developmental & Comparative Immunology 66 (Jan 2017): 98–110.https://doi.org/10.1016/j.dci.2016.02.015Johanna E. Farkas, James R. Monaghan A brief history of the study of nerve dependent regeneration, Neurogenesis 4, no.11 (Apr 2017): e1302216.https://doi.org/10.1080/23262133.2017.1302216Ravi Karra, Kenneth D. Poss , Journal of Clinical Investigation 127, no.22 ( 2017): 427.https://doi.org/10.1172/JCI89786成浩 谢 The Progress of Research on the WNT/β-Catenin Pathway in Regeneration, Advances in Marine Sciences 04, no.0404 (Jan 2017): 1–7.https://doi.org/10.12677/AMS.2017.44016Frederike Alwes, Camille Enjolras, Michalis Averof Live imaging reveals the progenitors and cell dynamics of limb regeneration, eLife 5 (Oct 2016).https://doi.org/10.7554/eLife.19766Adam B. Cook, Ashley W. Seifert Beryllium nitrate inhibits fibroblast migration to disrupt epimorphic regeneration, Development 143, no.1919 (Aug 2016): 3491–3505.https://doi.org/10.1242/dev.134882Moran Neuhof, Michael Levin, Oded Rechavi Vertically- and horizontally-transmitted memories – the fading boundaries between regeneration and inheritance in planaria, Biology Open 5, no.99 (Aug 2016): 1177–1188.https://doi.org/10.1242/bio.020149Jingjing Li, Siwei Zhang, Enrique Amaya The cellular and molecular mechanisms of tissue repair and regeneration as revealed by studies in Xenopus, Regeneration 3, no.44 (Oct 2016): 198–208.https://doi.org/10.1002/reg2.69Johanna E. Farkas, Polina D. Freitas, Donald M. Bryant, Jessica L. Whited, James R. Monaghan Neuregulin-1 signaling is essential for nerve-dependent axolotl limb regeneration, Development 143, no.1515 (Jun 2016): 2724–2731.https://doi.org/10.1242/dev.133363František Baluška, Michael Levin On Having No Head: Cognition throughout Biological Systems, Frontiers in Psychology 7 (Jun 2016).https://doi.org/10.3389/fpsyg.2016.00902Miguel Torres Limb regrowth takes two, Nature 533, no.76037603 (Apr 2016): 328–330.https://doi.org/10.1038/nature17889Susan V. Bryant, David M. Gardiner The relationship between growth and pattern formation, Regeneration 3, no.22 (Apr 2016): 103–122.https://doi.org/10.1002/reg2.55Danielle M. de Jong, Elaine C. Seaver, Michael Schubert A Stable Thoracic Hox Code and Epimorphosis Characterize Posterior Regeneration in Capitella teleta, PLOS ONE 11, no.22 (Feb 2016): e0149724.https://doi.org/10.1371/journal.pone.0149724Christopher L Antos, Franziska Knopf, Michael Brand Regeneration of Organs and Appendages in Zebrafish: A Window into Underlying Control Mechanisms, (Feb 2016): 1–17.https://doi.org/10.1002/9780470015902.a0022101.pub2Johanna E. Farkas, Piril Erler, Polina D. Freitas, Alexandra E. Sweeney, James R. Monaghan Organ and Appendage Regeneration in the Axolotl, (Apr 2016): 223–247.https://doi.org/10.1007/978-3-319-27583-3_7Nicky Pirotte, Nathalie Leynen, Tom Artois, Karen Smeets Do you have the nerves to regenerate? The importance of neural signalling in the regeneration process, Developmental Biology 409, no.11 (Jan 2016): 4–15.https://doi.org/10.1016/j.ydbio.2015.09.025Ahmed I. Mahmoud, Caitlin C. O’Meara, Matthew Gemberling, Long Zhao, Donald M. Bryant, Ruimao Zheng, Joseph B. Gannon, Lei Cai, Wen-Yee Choi, Gregory F. Egnaczyk, Caroline E. Burns, C. Geoffrey Burns, Calum A. MacRae, Kenneth D. Poss, Richard T. Lee Nerves Regulate Cardiomyocyte Proliferation and Heart Regeneration, Developmental Cell 34, no.44 (Aug 2015): 387–399.https://doi.org/10.1016/j.devcel.2015.06.017Yuval Rinkevich, Zeshaan N. Maan, Graham G. Walmsley, Subhro K. Sen Injuries to appendage extremities and digit tips: A clinical and cellular update, Developmental Dynamics 244, no.55 (Apr 2015): 641–650.https://doi.org/10.1002/dvdy.24265Jeffrey Lehrberg, David M. Gardiner, Shree Ram Singh Regulation of Axolotl (Ambystoma mexicanum) Limb Blastema Cell Proliferation by Nerves and BMP2 in Organotypic Slice Culture, PLOS ONE 10, no.44 (Apr 2015): e0123186.https://doi.org/10.1371/journal.pone.0123186David L Stocum, Karen Crawford Regeneration of the Urodele Limb, (Apr 2015): 1–9.https://doi.org/10.1002/9780470015902.a0001100.pub4Catherine McCusker, Susan V. Bryant, David M. Gardiner The axolotl limb blastema: cellular and molecular mechanisms driving blastema formation and limb regeneration in tetrapods, Regeneration 2, no.22 (May 2015): 54–71.https://doi.org/10.1002/reg2.32Anoop Kumar, Jean Paul Delgado Generation of Aneurogenic Larvae by Parabiosis of Salamander Embryos, (Feb 2015): 147–157.https://doi.org/10.1007/978-1-4939-2495-0_12Aki Makanae, Kazumasa Mitogawa, Akira Satoh Co-operative Bmp- and Fgf-signaling inputs convert skin wound healing to limb formation in urodele amphibians, Developmental Biology 396, no.11 (Dec 2014): 57–66.https://doi.org/10.1016/j.ydbio.2014.09.021Mariana G Simões, Anabela Bensimon-Brito, Mariana Fonseca, Ana Farinho, Fábio Valério, Sara Sousa, Nuno Afonso, Anoop Kumar, Antonio Jacinto Denervation impairs regeneration of amputated zebrafish fins, BMC Developmental Biology 14, no.11 (Dec 2014).https://doi.org/10.1186/s12861-014-0049-2Yuval Rinkevich, Daniel T. Montoro, Ethan Muhonen, Graham G. Walmsley, David Lo, Masakazu Hasegawa, Michael Januszyk, Andrew J. Connolly, Irving L. Weissman, Michael T. Longaker Clonal analysis reveals nerve-dependent and independent roles on mammalian hind limb tissue maintenance and regeneration, Proceedings of the National Academy of Sciences 111, no.2727 (Jun 2014): 9846–9851.https://doi.org/10.1073/pnas.1410097111Ling Yu, Mingquan Yan, Jennifer Simkin, Paulina D. Ketcham, Eric Leininger, Manjong Han, Ken Muneoka Angiogenesis is inhibitory for mammalian digit regeneration, Regeneration 1, no.33 (Oct 2014): 33–46.https://doi.org/10.1002/reg2.24Antony Athippozhy, Jeffrey Lehrberg, James R. Monaghan, David M. Gardiner, S. Randal Voss Characterization of in vitro transcriptional responses of dorsal root ganglia cultured in the presence and absence of blastema cells from regenerating salamander limbs, Regeneration 1, no.22 (Jul 2014): 1–10.https://doi.org/10.1002/reg2.14T. Shomrat, M. Levin An automated training paradigm reveals long-term memory in planarians and its persistence through head regeneration, Journal of Experimental Biology 216, no.2020 (Jul 2013): 3799–3810.https://doi.org/10.1242/jeb.087809Catherine D. McCusker, David M. Gardiner, Panagiotis A Tsonis Positional Information Is Reprogrammed in Blastema Cells of the Regenerating Limb of the Axolotl (Ambystoma mexicanum), PLoS ONE 8, no.99 (Sep 2013): e77064.https://doi.org/10.1371/journal.pone.0077064David L. Stocum Urodele Limb Regeneration: Mechanisms of Blastema Formation and Growth, (Jul 2013): 107–117.https://doi.org/10.1007/978-1-4614-7696-2_7T. Harshani Peiris, Néstor J. Oviedo Gap junction proteins: Master regulators of the planarian stem cell response to tissue maintenance and injury, Biochimica et Biophysica Acta (BBA) - Biomembranes 1828, no.11 (Jan 2013): 109–117.https://doi.org/10.1016/j.bbamem.2012.03.005James R. Monaghan, Antony Athippozhy, Ashley W. Seifert, Sri Putta, Arnold J. Stromberg, Malcolm Maden, David M. Gardiner, S. Randal Voss Gene expression patterns specific to the regenerating limb of the Mexican axolotl, Biology Open 1, no.1010 (Jul 2012): 937–948.https://doi.org/10.1242/bio.20121594Gufa Lin, Ying Chen, Jonathan M.W. Slack Transgenic Analysis of Signaling Pathways Required for Xenopus Tadpole Spinal Cord and Muscle Regeneration, The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology 295, no.1010 (Aug 2012): 1532–1540.https://doi.org/10.1002/ar.22437Zhe Yuan, Hans-Uwe Dahms, Lu-Lu Han, Qiu-Ying Li, Qiao-Zhi Zhang, Rong-Jie Wu, Jian Tan, Xiang-Yang Zou, Lin Hou Cloning and characterization of a trypsin-like serine protease gene, a novel regeneration-related gene from Apostichopus japonicus, Gene 502, no.11 (Jul 2012): 46–52.https://doi.org/10.1016/j.gene.2012.04.026Akira Satoh, Susan V. Bryant, David M. Gardiner Nerve signaling regulates basal keratinocyte proliferation in the blastema apical epithelial cap in the axolotl (Ambystoma mexicanum), Developmental Biology 366, no.22 (Jun 2012): 374–381.https://doi.org/10.1016/j.ydbio.2012.03.022Ashley W. Seifert, James R. Monaghan, Matthew D. Smith, Bret Pasch, Adrian C. Stier, François Michonneau, Malcolm Maden The influence of fundamental traits on mechanisms controlling appendage regeneration, Biological Reviews 87, no.22 (Sep 2011): 330–345.https://doi.org/10.1111/j.1469-185X.2011.00199.xYutaka Toya, Yoshihiko Kumai, Ryosei Minoda, Eiji Yumoto Modulation of nerve fibers in the rat thyroarytenoid muscle following recurrent laryngeal nerve injury, Acta Oto-Laryngologica 132, no.33 (Dec 2011): 305–313.https://doi.org/10.3109/00016489.2011.637176David L. Stocum Regeneration of Appendages, (Jan 2012): 183–226.https://doi.org/10.1016/B978-0-12-384860-4.00008-3Gemma Buckley, Jason Wong, Anthony D. Metcalfe, Mark W. J. Ferguson Denervation affects regenerative responses in MRL/MpJ and repair in C57BL/6 ear wounds, Journal of Anatomy 220, no.11 (Nov 2011): 3–12.https://doi.org/10.1111/j.1469-7580.2011.01452.xNick R Love, Yaoyao Chen, Boyan Bonev, Michael J Gilchrist, Lynne Fairclough, Robert Lea, Timothy J Mohun, Roberto Paredes, Leo AH Zeef, Enrique Amaya Genome-wide analysis of gene expression during Xenopus tropicalis tadpole tail regeneration, BMC Developmental Biology 11, no.11 (Nov 2011).https://doi.org/10.1186/1471-213X-11-70Michael Levin The wisdom of the body: future techniques and approaches to morphogenetic fields in regenerative medicine, developmental biology and cancer, Regenerative Medicine 6, no.66 (Nov 2011): 667–673.https://doi.org/10.2217/rme.11.69David L. Stocum The role of peripheral nerves in urodele limb regeneration, European Journal of Neuroscience 34, no.66 (Sep 2011): 908–916.https://doi.org/10.1111/j.1460-9568.2011.07827.xAnoop Kumar, Jean-Paul Delgado, Phillip B. Gates, Graham Neville, Andrew Forge, Jeremy P. Brockes The aneurogenic limb identifies developmental cell interactions underlying vertebrate limb regeneration, Proceedings of the National Academy of Sciences 108, no.3333 (Aug 2011): 13588–13593.https://doi.org/10.1073/pnas.1108472108Hitoshi Yokoyama, Tamae Maruoka, Haruki Ochi, Akio Aruga, Shiro Ohgo, Hajime Ogino, Koji Tamura, Michael Klymkowsky Different Requirement for Wnt/β-Catenin Signaling in Limb Regeneration of Larval and Adult Xenopus, PLoS ONE 6, no.77 (Jul 2011): e21721.https://doi.org/10.1371/journal.pone.0021721Leah J. Campbell, Edna C. Suárez-Castillo, Humberto Ortiz-Zuazaga, Dunja Knapp, Elly M. Tanaka, Craig M. Crews Gene expression profile of the regeneration epithelium during axolotl limb regeneration, Developmental Dynamics 240, no.77 (Jun 2011): 1826–1840.https://doi.org/10.1002/dvdy.22669Susanna Fraguas, Sara Barberán, Francesc Cebrià EGFR signaling regulates cell proliferation, differentiation and morphogenesis during planarian regeneration and homeostasis, Developmental Biology 354, no.11 (Jun 2011): 87–101.https://doi.org/10.1016/j.ydbio.2011.03.023Sandra Rieger, Alvaro Sagasti, William A. Harris Hydrogen Peroxide Promotes Injury-Induced Peripheral Sensory Axon Regeneration in the Zebrafish Skin, PLoS Biology 9, no.55 (May 2011): e1000621.https://doi.org/10.1371/journal.pbio.1000621David L. Stocum, Jo Ann Cameron Looking proximally and distally: 100 years of limb regeneration and beyond, Developmental Dynamics 240, no.55 (Feb 2011): 943–968.https://doi.org/10.1002/dvdy.22553Tetsuya Bando, Taro Mito, Taro Nakamura, Hideyo Ohuchi, Sumihare Noji Regulation of leg size and shape: Involvement of the Dachsous-fat signaling pathway, Developmental Dynamics 240, no.55 (Feb 2011): 1028–1041.https://doi.org/10.1002/dvdy.22590Gemma Buckley, Anthony D. Metcalfe, Mark W. J. Ferguson Peripheral nerve regeneration in the MRL/MpJ ear wound model, Journal of Anatomy 218, no.22 (Oct 2010): 163–172.https://doi.org/10.1111/j.1469-7580.2010.01313.xR. A. Blassberg, A. Garza-Garcia, A. Janmohamed, P. B. Gates, J. P. Brockes Functional convergence of signalling by GPI-anchored and anchorless forms of a salamander protein implicated in limb regeneration, Journal of Cell Science 124, no.11 (Nov 2010): 47–56.https://doi.org/10.1242/jcs.076331A. Acely Garza-Garcia, Paul C. Driscoll, Jeremy P. Brockes Evidence for the Local Evolution of Mechanisms Underlying Limb Regeneration in Salamanders, Integrative and Comparative Biology 50, no.44 (Apr 2010): 528–535.https://doi.org/10.1093/icb/icq022Anoop Kumar, Graham Nevill, Jeremy P. Brockes, Andrew Forge A comparative study of gland cells implicated in the nerve dependence of salamander limb regeneration, Journal of Anatomy 217, no.11 (Apr 2010): 16–25.https://doi.org/10.1111/j.1469-7580.2010.01239.xAnthony L Mescher Nerve‐dependent Tissue and Organ Regeneration, (Apr 2010).https://doi.org/10.1002/9780470015902.a0001103.pub2Néstor J. Oviedo, Junji Morokuma, Peter Walentek, Ido P. Kema, Man Bock Gu, Joo-Myung Ahn, Jung Shan Hwang, Takashi Gojobori, Michael Levin Long-range neural and gap junction protein-mediated cues control polarity during planarian regeneration, Developmental Biology 339, no.11 (Mar 2010): 188–199.https://doi.org/10.1016/j.ydbio.2009.12.012Ling Yu, Manjong Han, Mingquan Yan, Eun-Chee Lee, Jangwoo Lee, Ken Muneoka BMP signaling induces digit regeneration in neonatal mice, Development 137, no.44 (Feb 2010): 551–559.https://doi.org/10.1242/dev.042424Christopher L. Antos, Elly M. Tanaka Vertebrates That Regenerate As Models For Guiding Stem Cels, (Jan 2010): 184–214.https://doi.org/10.1007/978-1-4419-7037-4_13James R Monaghan, Leonard G Epp, Srikrishna Putta, Robert B Page, John A Walker, Chris K Beachy, Wei Zhu, Gerald M Pao, Inder M Verma, Tony Hunter, Susan V Bryant, David M Gardiner, Tim T Harkins, S Randal Voss Microarray and cDNA sequence analysis of transcription during nerve-dependent limb regeneration, BMC Biology 7, no.11 (Jan 2009).https://doi.org/10.1186/1741-7007-7-1J McCredie History, heresy and radiology in scientific discovery, Journal of Medical Imaging and Radiation Oncology 53, no.55 (Oct 2009): 433–441.https://doi.org/10.1111/j.1754-9485.2009.02101.xDavid L Stocum Regeneration of the Urodele Limb, (Sep 2009).https://doi.org/10.1002/9780470015902.a0001100.pub3Michael Levin Regeneration: Recent advances, major puzzles, and biomedical opportunities, Seminars in Cell & Developmental Biology 20, no.55 (Jul 2009): 515–516.https://doi.org/10.1016/j.semcdb.2009.04.011Yoonsung Lee, Danyal Hami, Sarah De Val, Birgit Kagermeier-Schenk, Airon A. Wills, Brian L. Black, Gilbert Weidinger, Kenneth D. Poss Maintenance of blastemal proliferation by functionally diverse epidermis in regenerating zebrafish fins, Developmental Biology 331, no.22 (Jul 2009): 270–280.https://doi.org/10.1016/j.ydbio.2009.05.545Stéphane Roy, Samuel Gatien Regeneration in axolotls: a model to aim for!, Experimental Gerontology 43, no.1111 (Nov 2008): 968–973.https://doi.org/10.1016/j.exger.2008.09.003Jeremy P. Brockes, Anoop Kumar Comparative Aspects of Animal Regeneration, Annual Review of Cell and Developmental Biology 24, no.11 (Nov 2008): 525–549.https://doi.org/10.1146/annurev.cellbio.24.110707.175336Viravuth P Yin, Kenneth D Poss New regulators of vertebrate appendage regeneration, Current Opinion in Genetics & Development 18, no.44 (Aug 2008): 381–386.https://doi.org/10.1016/j.gde.2008.06.008A. Satoh, G.M.C. Graham, S.V. Bryant, D.M. Gardiner Neurotrophic regulation of epidermal dedifferentiation during wound healing and limb regeneration in the axolotl (Ambystoma mexicanum), Developmental Biology 319, no.22 (Jul 2008): 321–335.https://doi.org/10.1016/j.ydbio.2008.04.030Marcus Singer Penetration of Labelled Amino Acids into the Peripheral Nerve Fibre from Surrounding Body Fluidst, (May 2008): 200–219.https://doi.org/10.1002/9780470719633.ch12Bruce M. Carlson The Denervated Muscle : 45 years later, Neurological Research 30, no.22 (Jul 2013): 119–122.https://doi.org/10.1179/174313208X281127Teresa Adell, Maria Marsal, Emili Saló Planarian GSK3s are involved in neural regeneration, Development Genes and Evolution 218, no.22 (Jan 2008): 89–103.https://doi.org/10.1007/s00427-007-0199-3Yuka Taniguchi, Takuji Sugiura, Akira Tazaki, Kenji Watanabe, Makoto Mochii Spinal cord is required for proper regeneration of the tail in Xenopus tadpoles, Development, Growth & Differentiation 50, no.22 (Jan 2008): 109–120.https://doi.org/10.1111/j.1440-169X.2007.00981.xMalcolm Maden Axolotl/Newt, (Jan 2008): 467–480.https://doi.org/10.1007/978-1-60327-483-8_32Hitoshi Yokoyama Initiation of limb regeneration: The critical steps for regenerative capacity, Development, Growth & Differentiation 50, no.11 (Nov 2007): 13–22.https://doi.org/10.1111/j.1440-169X.2007.00973.xFrancesc Cebrià Regenerating the central nervous system: how easy for planarians!, Development Genes and Evolution 217, no.11-1211-12 (Nov 2007): 733–748.https://doi.org/10.1007/s00427-007-0188-6A. Kumar, J. W. Godwin, P. B. Gates, A. A. Garza-Garcia, J. P. Brockes Molecular Basis for the Nerve Dependence of Limb Regeneration in an Adult Vertebrate, Science 318, no.58515851 (Nov 2007): 772–777.https://doi.org/10.1126/science.1147710J. P. Quilang, Z. U. Basiao, R. C. Pagulayan, R. R. Roderos, E. B. Barrios Meristic and morphometric variation in the silver perch, Leiopotherapon plumbeus (Kner, 1864), from three lakes in the Philippines, Journal of Applied Ichthyology 23, no.55 (Oct 2007): 561–567.https://doi.org/10.1111/j.1439-0426.2007.00862.xFrancesc Cebrià, Phillip A. Newmark Morphogenesis defects are associated with abnormal nervous system regeneration following roboA RNAi in planarians, Development 134, no.55 (Mar 2007): 833–837.https://doi.org/10.1242/dev.02794D. S. Adams, A. Masi, M. Levin H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration, Development 134, no.77 (Feb 2007): 1323–1335.https://doi.org/10.1242/dev.02812Hideki Masaki, Hiroyuki Ide Regeneration potency of mouse limbs, Development, Growth & Differentiation 49, no.22 (Feb 2007): 89–98.https://doi.org/10.1111/j.1440-169X.2007.00909.xYuki Nakatani, Atsushi Kawakami, Akira Kudo Cellular and molecular processes of regeneration, with special emphasis on fish fins, Development, Growth & Differentiation 49, no.22 (Feb 2007): 145–154.https://doi.org/10.1111/j.1440-169X.2007.00917.x References, (Jan 2007): 325–369.https://doi.org/10.1016/B978-012369439-3/50018-0Ai-Sun Tseng, Dany S. Adams, Dayong Qiu, Punita Koustubhan, Michael Levin Apoptosis is required during early stages of tail regeneration in Xenopus laevis, Developmental Biology 301, no.11 (Jan 2007): 62–69.https://doi.org/10.1016/j.ydbio.2006.10.048Judith D. Salley-Guydon, Roy A. Tassava Timing the commitment to a wound-healing response o
Publication Year: 1952
Publication Date: 1952-06-01
Language: en
Type: review
Indexed In: ['crossref', 'pubmed']
Access and Citation
Cited By Count: 619
AI Researcher Chatbot
Get quick answers to your questions about the article from our AI researcher chatbot