The DOI matches its Crossref record; 401 of the 403 references it cites were found in a registry or an index.
DEVELOPMENT OF THE VERTEBRATE NEUROMUSCULAR JUNCTION
Abstract
▪ Abstract We describe the formation, maturation, elimination, maintenance, and regeneration of vertebrate neuromuscular junctions (NMJs), the best studied of all synapses. The NMJ forms in a series of steps that involve the exchange of signals among its three cellular components—nerve terminal, muscle fiber, and Schwann cell. Although essentially any motor axon can form NMJs with any muscle fiber, an additional set of cues biases synapse formation in favor of appropriate partners. The NMJ is functional at birth but undergoes numerous alterations postnatally. One step in maturation is the elimination of excess inputs, a competitive process in which the muscle is an intermediary. Once elimination is complete, the NMJ is maintained stably in a dynamic equilibrium that can be perturbed to initiate remodeling. NMJs regenerate following damage to nerve or muscle, but this process differs in fundamental ways from embryonic synaptogenesis. Finally, we consider the extent to which the NMJ is a suitable model for development of neuron-neuron synapses.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Synaptic pruning is an activity-dependent developmental program in which a large number of synapses that form in early development are eliminated while a subset of synapses are maintained and strengthened (Hua and Smith, 2004; Katz and Shatz, 1996; Sanes and Lichtman, 1999).”
From Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner (2012) · cites this paper as Sanes and Lichtman, 1999
In the citing paper
“Neuronal-specific Agrn isoforms containing the Z exons (32 and 33) are the most potent in promoting AChR aggregation74–77.”
From The neurogenetics of alternative splicing (2016) · cites this paper as [77]
Citations
Cites
1 retracted
Huang, C., Flucher, B. E., Schmidt, M. M., Stroud, S. K., & Schmidt, J. (1994) · Neuron · doi:10.1016/0896-6273(94)90467-7 · Cited by 43
RetractedThe Molecular Biology of Axon Guidance
Tessier‐Lavigne, M., & Goodman, C. S. (1996) · Science · doi:10.1126/science.274.5290.1123 · Cited by 3,311
The synaptic vesicle cycle: a cascade of protein–protein interactions
Südhof, T. C. (1995) · Nature · doi:10.1038/375645a0 · Cited by 1,991
Molecular diversity of myofibrillar proteins: gene regulation and functional significance
Schiaffino, S., & Reggiani, C. (1996) · Physiological Reviews · doi:10.1152/physrev.1996.76.2.371 · Cited by 1,545
Katz, B. (1966) · Medical Entomology and Zoology · Cited by 1,410
Multiple essential functions of neuregulin in development
Meyer, D., & Birchmeier, C. (1995) · Nature · doi:10.1038/378386a0 · Cited by 1,273
Molecular and cellular biology of cholinesterases
Massoulié, J., Pezzementi, L., Bon, S., Krejci, E., & Vallette, F.-M. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90040-y · Cited by 1,214
THE EPHRINS AND EPH RECEPTORS IN NEURAL DEVELOPMENT
Flanagan, J. G., & Vanderhaeghen, P. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.309 · Cited by 1,091
Molecular distinction between fetal and adult forms of muscle acetylcholine receptor
Mishina, M., Takai, T., Imoto, K., Noda, M., Takahashi, T., Numa, S., Methfessel, C., & Sakmann, B. J. (1986) · Nature · doi:10.1038/321406a0 · Cited by 1,000
Defective neuromuscular synaptogenesis in agrin-deficient mutant mice.
Gautam, M., Noakes, P., Moscoso, L. M., Rupp, F., Scheller, R., Merlie, J., & Sanes, J. (1996) · Cell · doi:10.1016/s0092-8674(00)81253-2 · Cited by 941
Self-citation
Research works printed but not linked: 10
- Aframian D, 1988, Puerto Rico Health Sci. J., 7, 80
- Bewick GS, 1996, J. Neurocytol., 25, 367
- Brand-Saberi B, 1996, Int. J. Dev. Biol., 40, 411
- Burgess RW, 1998, Neurosci. Abstr., 24, 1534
- Ganju P, 1995, Oncogene, 11, 281
- Laskowski MB, 1998, Neurosci. Abstr., 24, 791
- Martin D, 1996, Am. J. Physiol., 271, R1422
- Patton BL, 1995, Neurosci. Abstr., 20, 799
- Serpinskaya AS, 1997, Neurosci. Abstr., 23, 33
- Zhou H, 1998, Neurosci. Abstr., 24, 1534
Cited by
Sorted by citations
Items 801–900 of 1,001
Arqué, G., Casanovas, A., & Dierssen, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054285 · Cited by 26
The function of Shp2 tyrosine phosphatase in the dispersal of acetylcholine receptor clusters
Qian, Y. K., Chan, A. W. S., Madhavan, R., & Peng, H. B. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-70 · Cited by 25
Gordon, T., Ly, V. D. N., Hegedus, J., & Tyreman, N. (2008) · Neurological Research · doi:10.1179/174313208x332977 · Cited by 25
Xu, F., Hennessy, D. A., Lee, T. K. M., & Syed, N. I. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4682-08.2009 · Cited by 25
Tetruashvily, M. M., McDonald, M. A., Frietze, K. K., & Boulanger, L. M. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.01.008 · Cited by 27
CaM Kinase II-dependent Suppression of Nicotinic Acetylcholine Receptor δ-Subunit Promoter Activity
Tang, H., Sun, Z., & Goldman, D. J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101670200 · Cited by 25
Ponomareva, O. N., Ma, H., Vock, V. M., Ellerton, E. L., Moody, S. E., Dakour, R., Chodosh, L. A., & Rimer, M. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.10.004 · Cited by 26
Localizing synaptic mRNAs at the neuromuscular junction: It takes more than transcription
Chakkalakal, J. V., & Jasmin, B. J. (2002) · BioEssays · doi:10.1002/bies.10205 · Cited by 25
Cai, H., Xu, X., Lu, J., Lichtman, J. W., Yung, S. P., & Wong, S. T. C. (2008) · Medical Image Analysis · doi:10.1016/j.media.2008.03.002 · Cited by 25
Self-citationCASK and Dlg form a PDZ protein complex at the mammalian neuromuscular junction
Sanford, J. L., Mays, T. A., & Rafael‐Fortney, J. A. (2004) · Muscle & Nerve · doi:10.1002/mus.20073 · Cited by 25
Neuronal activity and the establishment of normal and epileptic circuits during brain development
Swann, J. W., Smith, K. L., & Lee, C. L. (2001) · International review of neurobiology · doi:10.1016/s0074-7742(01)45007-0 · Cited by 25
Duong, C. V., Geißen, M., & Rohrer, H. (2002) · Development · doi:10.1242/dev.129.6.1387 · Cited by 25
Simon, C. M., Blanco-Redondo, B., Buettner, J. M., Pagiazitis, J. G., Fletcher, E. V., Longang, J. K. S., & Mentis, G. Z. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2142-20.2020 · Cited by 24
Disassembly and Rewiring of a Mature Converging Excitatory Circuit Following Injury
Santina, L. D., Yu, A. K., Harris, S. C., Soliño, M., Ruiz, T. G., Most, J. A., Kuo, Y., Dunn, F. A., & Ou, Y. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109463 · Cited by 24
Transgenic Overexpression of Dystroglycan Does Not Inhibit Muscular Dystrophy in mdx Mice
Hoyte, K., Jayasinha, V., Xia, B., & Martin, P. T. (2004) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63158-6 · Cited by 25
Katz, E., & Elgoyhen, A. B. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00224 · Cited by 24
Tomàs, J. M., García, N., Lanuza, M. A., Santafé, M. M., Tomàs, M., Nadal, L., Hurtado, E., Simó, A., Cilleros‐Mañé, V., & Just‐Borràs, L. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00397 · Cited by 24
Kowalski, J. L., Nemanich, S. T., Nawshin, T., Chen, M., Peyton, C., Zorn, E., Hickey, M. K., Rao, R., Georgieff, M., Rudser, K. D., et al. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8081208 · Cited by 25
Developmental demands contribute to early neuromuscular degeneration in CMT2D mice
Sleigh, J. N., Mech, A. M., & Schiavo, G. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02798-y · Cited by 24
Shp2 Is Dispensable in the Formation and Maintenance of the Neuromuscular Junction
Dong, X., Li, X.-M., Gao, T.-M., Zhang, E. E., Feng, G., Xiong, W., & Mei, L. (2006) · Neurosignals · doi:10.1159/000094484 · Cited by 24
Postnatal development of 5-HT1A receptor expression in rat somatic motoneurons
Talley, E. M., & Bayliss, D. A. (2000) · Developmental Brain Research · doi:10.1016/s0165-3806(00)00036-5 · Cited by 24
Motor neurite outgrowth is selectively inhibited by cell surface MuSK and agrin
Dimitropoulou, A., & Bixby, J. L. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.09.013 · Cited by 24
Davis, G. W. (2000) · Neuron · doi:10.1016/s0896-6273(00)81190-3 · Cited by 24
Regulation of MuSK Expression by a Novel Signaling Pathway
Kim, C., Xiong, W., & Mei, L. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305058200 · Cited by 24
Conservation and Innovation: Versatile Roles for LRP4 in Nervous System Development
DePew, A. T., & Mosca, T. J. (2021) · Journal of Developmental Biology · doi:10.3390/jdb9010009 · Cited by 24
Zou, S., & Pan, B. (2022) · Cell & Bioscience · doi:10.1186/s13578-022-00829-z · Cited by 22
An Optimized Workflow to Generate and Characterize iPSC-Derived Motor Neuron (MN) Spheroids
Castellanos‐Montiel, M. J., Chaineau, M., Franco-Flores, A. K., Haghi, G., Valenzuela, D. C., Reintsch, W., Chen, C. X. ‐., & Durcan, T. M. (2023) · Cells · doi:10.3390/cells12040545 · Cited by 23
Tseng, C., Zhang, L., Cascio, M., & Wang, Z.-Z. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300282200 · Cited by 23
The Wnt and BMP Families of Signaling Morphogens at the Vertebrate Neuromuscular Junction
Henríquez, J. P., Krull, C. E., & Osses, N. (2011) · International Journal of Molecular Sciences · doi:10.3390/ijms12128924 · Cited by 23
Blocking p75NTR receptors alters polyinnervationz of neuromuscular synapses during development
García, N., Tomàs, M., Santafé, M. M., Lanuza, M. A., Besalduch, N., & Tomàs, J. M. (2011) · Journal of Neuroscience Research · doi:10.1002/jnr.22620 · Cited by 21
Animal models for studying motor axon terminal paralysis and recovery
Rigoni, M., & Montecucco, C. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.13956 · Cited by 23
Synapse Elimination Triggered by BMP4 Exocytosis and Presynaptic BMP Receptor Activation
Higashi, T., Tanaka, S., Iida, T., & Okabe, S. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.101 · Cited by 23
Meng, J. L., & Heckscher, E. S. (2020) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2020.11.010 · Cited by 26
The role of myostatin and bone morphogenetic proteins in muscular disorders
Tsuchida, K. (2006) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.6.2.147 · Cited by 23
R-Roscovitine Improves Motoneuron Function in Mouse Models for Spinal Muscular Atrophy
Tejero, R., Balk, S., Franco-Espín, J., Ojeda, J., Hennlein, L., Drexl, H., Dombert, B., Clausen, J.-D., Torres‐Benito, L., Saal-Bauernschubert, L., et al. (2020) · iScience · doi:10.1016/j.isci.2020.100826 · Cited by 23
Barradeau, S., Imaizumi‐Scherrer, T., Weiss, M. C., & Faust, D. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081393598 · Cited by 23
Lee, Y. I. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134724 · Cited by 23
Classic Major Histocompatibility Complex Class I Molecules: New Actors at the Neuromuscular Junction
Cullheim, S., & Thams, S. (2010) · The Neuroscientist · doi:10.1177/1073858410381534 · Cited by 24
Synaptic Functions of Invertebrate Varicosities: What Molecular Mechanisms Lie Beneath
Giachello, C. N., Montarolo, P. G., & Ghirardi, M. (2012) · Neural Plasticity · doi:10.1155/2012/670821 · Cited by 21
An Agonist of the CXCR4 Receptor Strongly Promotes Regeneration of Degenerated Motor Axon Terminals
Negro, S., Zanetti, G., Mattarei, A., Valentini, A., Megighian, A., Tombesi, G., Zugno, A., Dianin, V., Pirazzini, M., Fillo, S., et al. (2019) · Cells · doi:10.3390/cells8101183 · Cited by 22
Super-resolution microscopy for analyzing neuromuscular junctions and synapses
Badawi, Y., & Nishimune, H. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134644 · Cited by 22
Minatel, E., Neto, H. S., & Marques, M. J. (2003) · Muscle & Nerve · doi:10.1002/mus.10416 · Cited by 22
Motor Unit Abnormalities in Dystonia musculorum Mice
Repentigny, Y. D., Ferrier, A., Ryan, S. D., Sato, T., & Kothary, R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021093 · Cited by 22
Synapse Formation and Plasticity: The Roles of Local Protein Synthesis
Wiersma-Meems, R., van Minnen, J., & Syed, N. I. (2005) · The Neuroscientist · doi:10.1177/1073858404274110 · Cited by 22
In Vivo Regulation of Acetylcholinesterase Insertion at the Neuromuscular Junction
y Valenzuela, I. M.-P., Hume, R. I., Krejci, É., & Akaaboune, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502874200 · Cited by 22
Congenital myasthenic syndromes
Nogajski, J. H., Kiernan, M. C., Ouvrier, R., & Andrews, P. I. (2008) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2008.05.001 · Cited by 22
Stability and variability of synapses in the adult molluskan CNS
Magoski, N. S., & Bulloch, A. G. (2000) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(200003)42:4 · Cited by 8
Saint‐Amant, L., Sprague, S. M., Hirata, H., Li, Q., Cui, W. W., Zhou, W., Poudou, O., Hume, R. I., & Kuwada, J. Y. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20569 · Cited by 22
Meunier, F. A., Herreros, J., Schiavo, G., Poulain, B., & Molgó, J. (2002) · Humana Press eBooks · doi:10.1385/1-59259-132-9:305 · Cited by 26
Why so many forms of acetylcholinesterase?
Legay, C. (2000) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(20000401)49:1 · Cited by 90
Wang, C.-H., Huang, Y., Chen, P., Cheng, Y.-J., Kao, H.-H., Pi, H., & Chien, C. (2017) · eLife · doi:10.7554/elife.26886 · Cited by 20
An Overview of Neuromuscular Junction Aging Findings in Human and Animal Studies
Khosa, S., Trikamji, B., Khosa, G. S., Khanli, H. M., & Mishra, S. K. (2019) · Current Aging Science · doi:10.2174/1874609812666190603165746 · Cited by 21
Xing, G., Jing, H., Zheng, Y., Chen, P., Wang, H., Xiong, W., & Mei, L. (2021) · Neuron · doi:10.1016/j.neuron.2021.04.021 · Cited by 21
Basu, S., Sladecek, S., Pemble, H., Wittmann, T., Slotman, J. A., van Cappellen, W. A., Brenner, H.-R., & Galjart, N. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.589457 · Cited by 21
Elimination of Redundant Synaptic Inputs in the Absence of Synaptic Strengthening
Wang, H., Liu, H., & Zhang, Z. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4569-11.2011 · Cited by 20
Limits to the Development of Fast Neuromuscular Transmission in Zebrafish
Drapeau, P., Buss, R. R., Ali, D. W., Legendre, P., & Rotundo, R. L. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.6.2951 · Cited by 21
Nadal, L., García, N., Hurtado, E., Simó, A., Tomàs, M., Lanuza, M. A., Cilleros‐Mañé, V., & Tomàs, J. M. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00024 · Cited by 21
Escobar-Corona, C., Torres-Castillo, S., Rodríguez‐Torres, E. E., Segura‐Alegría, B., Jiménez‐Estrada, I., & Quiróz-González, S. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.02.008 · Cited by 21
Charoensook, S. N., Williams, D. J., Chakraborty, S., Leong, K. W., & Vunjak‐Novakovic, G. (2017) · Integrative Biology · doi:10.1039/c7ib00144d · Cited by 21
Glial cells maintain synapses by inhibiting an activity-dependent retrograde protease signal
Gould, T. W., Dominguez, B., de Winter, F., Yeo, G. W.-M., Liu, P., Sundararaman, B., Stark, T., Vu, A. Q., Degen, J. L., Lin, W., et al. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1007948 · Cited by 21
Oprişoreanu, A., Smith, H. L., Arya, S., Webster, R. G., Zhong, Z., Eaton-Hart, C., Wehner, D., Cardozo, M. J., Becker, T., Talbot, K., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.033 · Cited by 21
Nerve, Muscle, and Synaptogenesis
Swenarchuk, L. E. (2019) · Cells · doi:10.3390/cells8111448 · Cited by 25
Motoneuron Replacement for Reinnervation of Skeletal Muscle in Adult Rats
Grumbles, R. M., Almeida, V. W., Casella, G. T., Wood, P. M., Hemstapat, R., & Thomas, C. K. (2012) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31826cf69a · Cited by 21
Boeri, J., Corronc, H. L., Lejeune, F., Bras, B. L., Mouffle, C., Angelim, M. K. S. C., Mangin, J., Branchereau, P., Legendre, P., & Czarnecki, A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3203-17.2018 · Cited by 21
Bittman, K. S., Panzer, J. A., & Balice‐Gordon, R. J. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20253 · Cited by 21
Wörl, J., & Neuhuber, W. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20436 · Cited by 21
ATP induces post-synaptic gene expressions in vertebrate skeletal neuromuscular junctions
Tsim, K. W. K., Choi, R. C. Y., Siow, N. L., Cheng, A. W. M., Ling, K., Jiang, J. X., Tung, E. K. K., Lee, H. H. C., Xie, H. Q., Simon, J., et al. (2003) · Journal of Neurocytology · doi:10.1023/b:neur.0000020613.25367.78 · Cited by 21
Phosphorylation of the nicotinic acetylcholine receptor in myotube‐cholinergic neuron cocultures
Lanuza, M. A., Gizaw, R., Viloria, A., González, C. M., Besalduch, N., Dunlap, V., Tomàs, J. M., & Nelson, P. G. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20848 · Cited by 21
Structure and Function of the Mammalian Neuromuscular Junction
Davis, L. A., Fogarty, M. J., Brown, A. D., & Sieck, G. C. (2022) · Comprehensive physiology · doi:10.1002/cphy.c210022 · Cited by 48
Disruption of Neuromuscular Junction Following Spinal Cord Injury and Motor Neuron Diseases
Nemeth, C., Banik, N. L., & Haque, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063520 · Cited by 20
Effects of thyroid hormones in skeletal muscle protein turnover
Nappi, A., Moriello, C., Morgante, M., Fusco, F., Crocetto, F., & Miro, C. (2024) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp-2024-0139 · Cited by 24
MacDonald, R., Barbat‐Artigas, S., Cho, C., Peng, H., Shang, J., Moustaine, A., Carbonetto, S., Robitaille, R., Chalifour, L. E., & Paudel, H. K. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00258 · Cited by 22
Schizophrenia: Complement Cleaning or Killing
Hogenaar, J. T. T., & van Bokhoven, H. (2021) · Genes · doi:10.3390/genes12020259 · Cited by 21
Negro, S., Lauria, F., Stazi, M., Tebaldi, T., D’Este, G., Pirazzini, M., Megighian, A., Lessi, F., Mazzanti, C. M., Sales, G., et al. (2022) · Acta Neuropathologica Communications · doi:10.1186/s40478-022-01495-5 · Cited by 20
Parisi, M. J., Aimino, M. A., & Mosca, T. J. (2023) · Cell Reports Methods · doi:10.1016/j.crmeth.2023.100477 · Cited by 20
Brugeaud, A., Tong, M., Luo, L., & Edge, A. S. B. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22136 · Cited by 21
Rodella, U., Negro, S., Scorzeto, M., Bergamin, E., Jalink, K., Montecucco, C., Yuki, N., & Rigoni, M. (2017) · Disease Models & Mechanisms · doi:10.1242/dmm.027870 · Cited by 20
Effects of disease-afflicted and aging neurons on the musculoskeletal system
Valdez, G. (2019) · Bone · doi:10.1016/j.bone.2019.01.023 · Cited by 22
Ohno, T., Maeda, H., & Sakurai, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3903-03.2004 · Cited by 20
Confortim, H. D., Jerônimo, L. C., Centenaro, L. A., Pinheiro, P. F. F., Brancalhão, R. M. C., Matheus, S. M. M., & Torrejais, M. M. (2015) · Micron · doi:10.1016/j.micron.2014.12.006 · Cited by 20
Musarella, M., Alcaraz, G., Caillol, G., Boudier, J., Couraud, F., & Autillo‐Touati, A. (2005) · Glia · doi:10.1002/glia.20252 · Cited by 20
Marques, M. J., Mendes, Z. T. R., Minatel, E., & Neto, H. S. (2005) · Journal of Neurocytology · doi:10.1007/s11068-006-8725-1 · Cited by 20
Critical period for activity-dependent elimination of corticospinal synapses in vitro
Ohno, T., & Sakurai, M. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.01.056 · Cited by 20
N‐cadherin regulates primary motor axon growth and branching during zebrafish embryonic development
Brusés, J. L. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22602 · Cited by 20
Gašperšič, R., Koritnik, B., Eržen, I., & Sketelj, J. (2001) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(01)00018-1 · Cited by 20
Morimoto, T., Nobechi, M., Komatsu, A., Miyakawa, H., & Nose, A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.11.059 · Cited by 19
Time Course Analysis of Skeletal Muscle Pathology of GDE5 Transgenic Mouse
Hashimoto, T., Yang, B., Okazaki, Y., Yoshizawa, I., Kajihara, K., Katô, N., Wada, M., & Yanaka, N. (2016) · PLoS ONE · doi:10.1371/journal.pone.0163299 · Cited by 19
Tumor necrosis factor alpha mediates neuromuscular synapse elimination
Fu, X.-Q., Peng, J., Wang, A., & Luo, Z. (2020) · Cell Discovery · doi:10.1038/s41421-020-0143-5 · Cited by 19
Engel, A. (2008) · Handbook of Clinical Neurology · doi:10.1016/s0072-9752(07)01503-5 · Cited by 54
Dissection of the Transversus Abdominis Muscle for Whole-mount Neuromuscular Junction Analysis
Murray, L. M., Gillingwater, T. H., & Kothary, R. (2014) · Journal of Visualized Experiments · doi:10.3791/51162 · Cited by 19
Mechanisms for axon maintenance and plasticity in motoneurons: alterations in motoneuron disease
Jablonka, S., Dombert, B., Asan, E., & Sendtner, M. (2013) · Journal of Anatomy · doi:10.1111/joa.12097 · Cited by 19
Fluorescence imaging of synapse dynamics in normal circuit maturation and in developmental disorders
Okabe, S. (2017) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.93.029 · Cited by 21
Miš, K., Grubič, Z., Lorenzon, P., Sciancalepore, M., Marš, T., & Pirkmajer, S. (2017) · Molecules · doi:10.3390/molecules22091418 · Cited by 19
Transmembrane Collagens in Neuromuscular Development and Disorders
Wakabayashi, T. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.635375 · Cited by 19
Rosenthal, J., Yin, J., Lei, J., Sathyamurthy, A., Short, J., Long, C., Spillman, E., Sheng, C., & Yuan, Q. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2004685118 · Cited by 19
Development of ionic currents of zebrafish slow and fast skeletal muscle fibers
Coutts, C. A., Patten, S. A., Balt, L. N., & Ali, D. W. (2005) · Journal of Neurobiology · doi:10.1002/neu.20214 · Cited by 19
Neural Agrin Changes the Electrical Properties of Developing Human Skeletal Muscle Cells
Jurdana, M., Fumagalli, G. F., Grubič, Z., Lorenzon, P., Marš, T., & Sciancalepore, M. (2008) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-008-9304-z · Cited by 19
Confortim, H. D., Jerônimo, L. C., Centenaro, L. A., Pinheiro, P. F. F., Matheus, S. M. M., & Torrejais, M. M. (2016) · Muscle & Nerve · doi:10.1002/mus.25187 · Cited by 19
Inhibition of MuSK Expression by CREB Interacting with a CRE-Like Element and MyoD
Kim, C., Xiong, W., & Mei, L. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.13.5329-5338.2005 · Cited by 19
Pre- and postsynaptic actions of L1-CAM in nicotinic pathways
Triana‐Baltzer, G., Liu, Z., & Berg, D. K. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.07.008 · Cited by 19
Metadata
- Authors
- Sanes, J. R., & Lichtman, J. W.
- Affiliations
- Washington University in St. Louis (US)
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 1999-03
- Volume
- 22
- Issue
- 1
- Pages
- 389-442
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- OpenAlex
- W2134505400
- Cited by
- 1,532
- References
- 403
- Citations by year
- 2026: 22 · 2025: 36 · 2024: 47 · 2023: 35 · 2022: 35 · 2021: 47 · 2020: 60 · 2019: 44 · 2018: 48 · 2017: 55 · 2016: 49 · 2015: 27 · 2014: 57 · 2013: 39 · 2012: 57
- FWCI
- 8.58
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Keywords
- neuromuscular junction, synaptogenesis, synapse maturation, synaptic pruning, synapse maintenance, synaptic remodeling, neuromuscular junction regeneration, motor axons, muscle fibers, Schwann cells, vertebrate development
- MeSH terms
- Animals, Glycoproteins, Nerve Regeneration, Neuromuscular Junction, Synapses, Transcription, Genetic, Vertebrates, Signal Transduction, Presynaptic Terminals, Neuregulins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review