The DOI matches its Crossref record; 96 of the 98 references it cites were found in a registry or an index.
Synaptic adhesion molecules
Abstract
Formation, differentiation and plasticity of synapses, the specialized cell-cell contacts through which neurons communicate, all require interactions between pre- and post-synaptic partners. Several synaptically localized adhesion molecules potentially capable of mediating these interactions have been identified recently. Functional studies suggest roles for some of them in target recognition (e.g. SYG-1 and sidekicks), formation and alignment of synaptic specializations (e.g. SynCAM, neuroligin and neurexin), and regulation of synaptic structure and function (e.g. cadherins and syndecan).
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
“Specific molecules, such as SYG-1 and sidekicks, are essential for cellular target recognition, while syndecans regulate synaptic structure and function [76].”
From Molecular Physiology of the Neuronal Synapse (2026) · cites this paper as [76]
Citations
Cites
Hynes (2002) · doi:10.1016/s0092-8674(02)00971-6 · Cited by 8,606
Gray, E. G., & Whittaker, V. P. (1962) · PubMed · Cited by 2,530
CHEMOAFFINITY IN THE ORDERLY GROWTH OF NERVE FIBER PATTERNS AND CONNECTIONS
Sperry, R. W. (1963) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.50.4.703 · Cited by 1,946
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
Study, P. A. R. I. S., Jamain, S., Quach, H., Betancur, C., Råstam, M., Colineaux, C., Gillberg, I. C., Soderstrom, H., Giros, B., Leboyer, M., et al. (2003) · Nature Genetics · doi:10.1038/ng1136 · Cited by 1,851
DEVELOPMENT OF THE VERTEBRATE NEUROMUSCULAR JUNCTION
Sanes, J. R., & Lichtman, J. W. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.389 · Cited by 1,532
Self-citationNeuroligin Expressed in Nonneuronal Cells Triggers Presynaptic Development in Contacting Axons
Scheiffele, P., Fan, J., Choih, J., Fetter, R., & Serafini, T. (2000) · Cell · doi:10.1016/s0092-8674(00)80877-6 · Cited by 1,218
PDZ Domains and the Organization of Supramolecular Complexes
Sheng, M., & Sala, C. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1 · Cited by 1,211
Mechanisms and functions of eph and ephrin signalling
Kullander, K., & Klein, R. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm856 · Cited by 1,158
SynCAM, a Synaptic Adhesion Molecule That Drives Synapse Assembly
Biederer, T., Sara, Y., Mozhayeva, M., Atasoy, D., Liu, X., Kavalali, E., & Südhof, T. (2002) · Science · doi:10.1126/science.1072356 · Cited by 834
Dendritic Spine Pathology: Cause or Consequence of Neurological Disorders?
Fiala, J. C., Spacek, J., & Harris, K. M. (2002) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00158-3 · Cited by 811
Research works printed but not linked: 2
- Südhof TC: The synaptic cleft and synaptic cell adhesion. In Synapses. Edited by Cowan WM, Südhof TC, Stevens CF. Baltimore: Johns Hopkins University Press; 2001:275-313.
- Gray, 1962, The isolation of nerve endings from brain, J. Anat., 96, 79
Cited by
Sorted by citations
Items 201–300 of 371
Cao, J., Dwyer, J. B., Mangold, J. E., Ju, W., Wei, J., Leslie, F. M., & Li, M. D. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710000179 · Cited by 26
Gordon, T., Ly, V. D. N., Hegedus, J., & Tyreman, N. (2008) · Neurological Research · doi:10.1179/174313208x332977 · Cited by 25
Molecular dynamics of photoreceptor synapse formation in the developing chick retina
Wahlin, K. J., Moreira, E. F., Hu, H., Yu, N., & Adler, R. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21582 · Cited by 25
Noh, K., Park, J.-C., Han, J., & Lee, S. J. (2020) · Experimental Neurobiology · doi:10.5607/en.2020.29.1.1 · Cited by 25
YTHDF1 Attenuates TBI-Induced Brain-Gut Axis Dysfunction in Mice
Huang, P., Liu, M., Zhang, J., Zhong, X., & Zhong, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24044240 · Cited by 24
Letellier, M., Willson, M. L., Gautheron, V., Mariani, J., & Lohof, A. M. (2008) · Developmental Neurobiology · doi:10.1002/dneu.20639 · Cited by 24
Rap2 and TNIK control Plexin-dependent tiled synaptic innervation in C. elegans
Chen, X., Shibata, A. C. E., Hendi, A., Kurashina, M., Fortes, E., Weilinger, N. L., MacVicar, B. A., Murakoshi, H., & Mizumoto, K. (2018) · eLife · doi:10.7554/elife.38801 · Cited by 24
Tuning synapses by proteolytic remodeling of the adhesive surface
Shinoe, T., & Goda, Y. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.08.005 · Cited by 23
Kumar, D., & Thakur, M. K. (2015) · AGE · doi:10.1007/s11357-015-9752-6 · Cited by 23
Letellier, M., Bailly, Y. J. R., Demais, V., Sherrard, R. M., Mariani, J., & Lohof, A. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0452-07.2007 · Cited by 23
Conditional deletion of Cadherin 13 perturbs Golgi cells and disrupts social and cognitive behaviors
Tantra, M., Guo, L., Kim, J., Zainolabidin, N., Eulenburg, V., Augustine, G. J., & Chen, A. I. (2018) · Genes Brain & Behavior · doi:10.1111/gbb.12466 · Cited by 24
Calahorro, F., & Ruiz‐Rubio, M. (2013) · Genes Brain & Behavior · doi:10.1111/gbb.12046 · Cited by 23
Structure and Functions of Sidekicks
Yamagata, M. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00139 · Cited by 22
Self-citationThinking about Visual Behavior; Learning about Photoreceptor Function
Choe, K., & Clandinin, T. R. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)69007-2 · Cited by 22
Li, T., Tian, Y., Li, Q., Chen, H., Lv, H., Xie, W., & Han, J. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.644583 · Cited by 24
Jovanova-Nešić, K., & Shoenfeld, Y. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.08.013 · Cited by 21
Ito, S., & Takeichi, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906653106 · Cited by 20
Naik, A. S., Lin, J. M., Taroc, E. Z. M., Katreddi, R. R., Frias, J. A., Lemus, A. A., Sammons, M. A., & Forni, P. E. (2020) · Development · doi:10.1242/dev.184036 · Cited by 21
Dash, B. P., Naumann, M., Sterneckert, J. L., & Hermann, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21186938 · Cited by 19
Weaving the neuronal net with target‐derived fibroblast growth factors
Umemori, H. (2009) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2008.01079.x · Cited by 17
Synaptic transmission is impaired at neuronal autonomic synapses in agrin‐null mice
Gingras, J., Rassadi, S., Cooper, E., & Ferns, M. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20304 · Cited by 18
The cell biology of synaptic specificity during development
Christensen, R. P., Shao, Z., & Colón‐Ramos, D. A. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.07.004 · Cited by 19
Cell adhesion molecules and sleep
O’Callaghan, E. K., Roig, M. N. B., & Mongrain, V. (2016) · Neuroscience Research · doi:10.1016/j.neures.2016.11.001 · Cited by 18
Gharib, A., Komaki, A., Manoochehri, H., Saidijam, M., Barkley, V., Sarihi, A., & Mirnajafi‐Zadeh, J. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.03.007 · Cited by 16
Trafficking and Activity of Glutamate and GABA Receptors: Regulation by Cell Adhesion Molecules
Keable, R., Leshchyns’ka, I., & Sytnyk, V. (2020) · The Neuroscientist · doi:10.1177/1073858420921117 · Cited by 16
Podestá, M. F., Yam, P. T., Codagnone, M. G., Uccelli, N. A., Colman, D., & Reinés, A. G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108921 · Cited by 16
Claudins in the brain: Unconventional functions in neurons
Tikiyani, V., & Babu, K. (2019) · Traffic · doi:10.1111/tra.12685 · Cited by 16
Lee, J. Y., Geng, J., Lee, J., Wang, A. R., & Chang, K. T. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3128-16.2017 · Cited by 15
Pharmacology of Cell Adhesion Molecules of the Nervous System
Kiryushko, D. V., Bock, E., & Berezin, V. (2007) · Current Neuropharmacology · doi:10.2174/157015907782793658 · Cited by 15
Role of neurexin2a in lead-induced locomotor defect in developing zebrafish
Tu, H., Peng, T., Liu, J., Chen, X., Fan, C., Huang, Z., Zhang, Y., Zou, F., & Meng, X. (2017) · Aquatic Toxicology · doi:10.1016/j.aquatox.2017.11.011 · Cited by 16
Shirogane, Y., Hashiguchi, T., & Yanagi, Y. (2019) · Journal of Virology · doi:10.1128/jvi.01727-19 · Cited by 16
Cell Adhesion Molecules of the Immunoglobulin Superfamily in the Nervous System
Walmod, P. S., Pedersen, M. V., Berezin, V., & Bock, E. (2007) · Springer eBooks · doi:10.1007/978-0-387-30379-6_2 · Cited by 16
Tikiyani, V., Li, L., Sharma, P., Liu, H., Hu, Z., & Babu, K. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.053 · Cited by 14
Seabold, G. K., Wang, P. Y., Petralia, R. S., Chang, K., Zhou, A., McDermott, M. I., Wang, Y., Milgram, S. L., & Wenthold, R. J. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.279661 · Cited by 15
Neurotrophic Factors and Their Receptors
(1995) · Nature Biotechnology · doi:10.1038/nbt1195-1170 · Cited by 15
An insight into the TAM system in Alzheimer’s disease
Zhou, S., Li, Y., Zhang, Z., & Yuan, Y. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109791 · Cited by 14
Transmitter-receptor mismatch in GABAergic synapses in the absence of activity
Cesa, R., Morando, L., & Strata, P. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806979105 · Cited by 14
Csk‐homologous kinase interacts with SHPS‐1 and enhances neurite outgrowth of PC12 cells
Mitsuhashi, H., Futai, E., Sasagawa, N., Hayashi, Y. K., Nishino, I., & Ishiura, S. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05121.x · Cited by 13
Cell Adhesion Molecules at Synapses
Reichardt, L. F., & Lee, S.-H. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00355-7 · Cited by 13
Ligand-receptor interactions: A key to understanding microglia and astrocyte roles in epilepsy
Thergarajan, P., O'Brien, T. J., Jones, N. C., & Ali, I. Y. (2024) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2024.110219 · Cited by 13
Zhang, Z., Zhou, W., Fan, J., Ren, Y., & Yin, G. (2013) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2013.01.006 · Cited by 12
Matthäus, F., Smith, V. A., Fogtman, A., Sommer, W. H., Leonardi‐Essmann, F., Lourdusamy, A., Reimers, M. A., Spanagel, R., & Gebicke‐Haerter, P. J. (2009) · Pharmacopsychiatry · doi:10.1055/s-0029-1216348 · Cited by 12
Cadm1 Expression and Function in the Mouse Lens
María, A., Shi, Y., Luo, X., van der Weyden, L., & Bassnett, S. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-6677 · Cited by 11
Chen, H., Luo, R., Gong, S., Matta, S. G., & Sharp, B. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086214 · Cited by 11
Tóth, M., & Zupan, B. (2007) · Wiley eBooks · doi:10.1002/9780470101001.hcn023 · Cited by 12
Nickel reduces calcium dependent dimerization in neural cadherin
Dukes, M. P., Rowe, R. K., Harvey, T., Rangel, W., & Pedigo, S. (2018) · Metallomics · doi:10.1039/c8mt00349a · Cited by 10
Zhang, Z., Hou, M., Ou, H., Wang, D., Li, Z., Zhang, H., & Lu, J. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1067529 · Cited by 9
Parent, A., & Thinakaran, G. (2010) · International Journal of Alzheimer s Disease · doi:10.4061/2010/825918 · Cited by 10
Why we need more synaptogenic cell-adhesion proteins
Brose, N. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300505110 · Cited by 9
Calahorro, F., Holden-Dye, L. M., & O'Connor, V. M. (2015) · Gene Expression Patterns · doi:10.1016/j.gep.2015.02.002 · Cited by 9
The cell adhesion protein CAR is a negative regulator of synaptic transmission
Wrackmeyer, U., Kaldrack, J., Jüttner, R., Pannasch, U., Gimber, N., Freiberg, F., Purfürst, B., Kainmueller, D., Schmitz, D., Haucke, V., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-43150-5 · Cited by 11
Dystonin/BPAG1 modulates diabetes and Alzheimer’s disease cross-talk: a meta-analysis
Cheng, J., Liu, H., Hwang, S., Hsu, L., Lin, W., & Tsai, F. (2019) · Neurological Sciences · doi:10.1007/s10072-019-03879-3 · Cited by 10
Portillo, F., & Moreno‐López, B. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02165-9 · Cited by 8
Taste arbor structural variability analyzed across taste regions
Ohman, L. C., Hanbali, L. B., & Krimm, R. F. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25459 · Cited by 8
Mechanical computation in neurons
Laishram, J., Avossa, D., Shahapure, R. B., & Torre, V. (2009) · Developmental Neurobiology · doi:10.1002/dneu.20733 · Cited by 8
Nishimune, H. (2011) · Channels · doi:10.4161/chan.5.5.16472 · Cited by 7
Structural and Functional Organization of the Postsynaptic Density
Verpelli, C., Heise, C., & Sala, C. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00004-3 · Cited by 7
Rhoades, R. E., Henry, B., Pritchett, D. L., Fang, Y., & Teng, S. (2022) · Genes · doi:10.3390/genes13050789 · Cited by 7
Dyhrfort, P., Wettervik, T. S., Clausen, F., Enblad, P., Hillered, L., & Lewén, A. (2023) · Neurotrauma Reports · doi:10.1089/neur.2022.0067 · Cited by 7
How are neurons wired to form functional and plastic circuits?
Stoeckli, E. T., & Zou, Y. (2009) · EMBO Reports · doi:10.1038/embor.2009.47 · Cited by 7
Molecular Physiology of the Neuronal Synapse
Ramírez-Expósito, M. J., Cueto-Ureña, C., & Martínez-Martos, J. M. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48010088 · Cited by 6
“Specific molecules, such as SYG-1 and sidekicks, are essential for cellular target recognition, while syndecans regulate synaptic structure and function [76].”
Ochsner, S. A., & McKenna, N. J. (2020) · Thyroid · doi:10.1089/thy.2019.0307 · Cited by 6
Structural basis of SALM3 dimerization and synaptic adhesion complex formation with PTPσ
Karki, S., Shkumatov, A. V., Bae, S., Kim, H., Ko, J., & Kajander, T. (2020) · Scientific Reports · doi:10.1038/s41598-020-68502-4 · Cited by 6
Post-translational modifications of the ligands: Requirement for TAM receptor activation
Geng, K. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2020.09.002 · Cited by 7
Protocadherins and Synapse Development
Weiner, J. A. (2006) · Springer eBooks · doi:10.1007/978-0-387-32562-0_10 · Cited by 6
Self-citationNeuroligins Determine Synapse Maturation and Function
Aramuni, G. (2007) · doi:10.53846/goediss-216 · Cited by 5
Temporal Dysynchrony in brain connectivity gene expression following hypoxia
Milash, B. A., Gao, J., Stevenson, T. J., Son, J., Dahl, T. M., & Bonkowsky, J. L. (2016) · BMC Genomics · doi:10.1186/s12864-016-2638-x · Cited by 5
Glial Control of Synaptogenesis
Allen, N. J. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199794591.003.0031 · Cited by 4
Up-regulated serum levels of TAM receptor tyrosine kinases in a group of Egyptian autistic children
Mostafa, G. A., ElGebaly, H. H., Shehab, A. A. S., & Mohamed, M. A. E. H. (2022) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2022.577811 · Cited by 6
Wang, Z., Hu, T., Feng, D., & Chen, G. (2012) · Neurological Sciences · doi:10.1007/s10072-012-1240-5 · Cited by 5
Con-nectin axons and dendrites
Beaudoin, G. M. J. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200606024 · Cited by 5
Synaptic Patterning by Morphogen Signaling
Williamson, W. R., & Hiesinger, P. R. (2008) · Science Signaling · doi:10.1126/stke.118pe20 · Cited by 4
Targeting AXL in mesothelioma: From functional characterization to clinical implication
Bhadresha, K. P., Mirza, S., Penny, C. B., & Mughal, M. J. (2023) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2023.104043 · Cited by 4
Neurosteroids alter glutamate-induced changes in neurite morphology of NG108-15 cells
Johansson, T., Elfverson, M., Birgner, C., Frändberg, P., Nyberg, F., & Grevès, P. L. (2007) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2007.03.024 · Cited by 4
CD226 deficiency improves cognitive functions and ameliorates anxiety‐like behaviors in mice
Fang, L., Jin, J., Chen, P., Wang, N., Zeng, H., Jin, B., Li, H., & Chen, L. (2017) · Brain and Behavior · doi:10.1002/brb3.871 · Cited by 4
Axl and EGFR Dual-Specific Binding Affibody for Targeted Therapy in Nasopharyngeal Carcinoma
Kamara, S., He, W., Guo, Y., Liu, Y., Liu, L., Du, W., Chen, J., Zhu, S., & Zhang, L. (2024) · Cells · doi:10.3390/cells13221823 · Cited by 3
Synapse formation and function
Sanes, D. H., Reh, T. A., & Harris, W. A. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374539-2.00012-4 · Cited by 3
The influence of NRXN1 on systemizing and the brain structure in healthy adults
Shiota, Y., Matsudaira, I. Y., Takeuchi, H., Ono, C., Tomita, H., Kawashima, R., & Taki, Y. (2021) · Brain Imaging and Behavior · doi:10.1007/s11682-021-00530-8 · Cited by 3
Neuroligin 2 governs synaptic morphology and function through RACK1-cofilin signaling in Drosophila
Sun, Y., Li, M., Geng, J., Meng, S., Tu, R., Zhuang, Y., Sun, M., Rui, M., Ou, M., Xing, G., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-05428-3 · Cited by 4
Genetic Analysis of Synaptogenesis
Lu, C. S., & Vactor, D. V. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00104-6 · Cited by 3
Actualités sur la génétique des retards mentaux liés au chromosome X
Bahi‐Buisson, N., Chelly, J., & Portes, V. D. (2006) · Revue Neurologique · doi:10.1016/s0035-3787(06)75105-0 · Cited by 3
Zhang, T., Xu, Z., Chen, L. H., Zhang, X. H., Wang, D. L., Zhao, Z., Deng, J., Li, W. X., Zhang, Y., Xu, X. S., et al. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.07.074 · Cited by 3
In vivo imaging of long-term changes in the Drosophila neuromuscular junction
Rasse, T. M. (2005) · doi:10.53846/goediss-309 · Cited by 3
Control of Synaptic Specificity by Limiting Promiscuous Synapse FormationPreprint
Xu, C., Theisen, E. K., Rumbaut, E., Shum, B., Peng, J., Tarnogorska, D., Borycz, J. A., Tan, L., Courgeon, M., Meinertzhagen, I. A., et al. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3244754 · Cited by 3
AXL in cardiovascular diseases: Pathophysiological insights and clinical perspectives
Cheng, Q., Wang, C., & Liu, F. (2025) · Pathology - Research and Practice · doi:10.1016/j.prp.2025.156120 · Cited by 2
Signal Transduction Mechanisms
Miftahof, R. N. (2017) · Springer eBooks · doi:10.1007/978-3-319-59677-8_7 · Cited by 2
The Power of Diversity in Neuroscience Research Models
Banerjee, A., Froudarakis, E., Rapti, G., Genzel, L., & Konstantinides, N. (2026) · European Journal of Neuroscience · doi:10.1111/ejn.70384 · Cited by 2
Extracellular neuroligin-ICAM5 coupling drives dendritic growth via actin remodeling
Geyskens, C., Raux, B., Apóstolo, N., Boonen, E., Vandensteen, J., Marques, B., Machado, J., Kumru, L., Nys, J., Creemers, E., et al. (2026) · iScience · doi:10.2139/ssrn.6506752 · Cited by 2
Models of Synaptic Transmission and Regulation
Miftahof, R. N., & Nam, H. G. (2011) · Springer eBooks · doi:10.1007/978-3-642-21473-8_7 · Cited by 1
Xie, H., Liu, S., Fu, Y., Cheng, Q., Wang, P., Bi, C., Wang, R., Chen, M., & Fang, M. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.12.030 · Cited by 2
The Architecture of the Presynaptic Release Site
Zhai, R. G. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-34229-5_1 · Cited by 1
Li, Z., Ge, B.-Y., Li, H., Huang, C., Ji, Y., Schachner, M., Yin, S., Li, S., & Zhao, J. (2025) · Biomolecules · doi:10.3390/biom15071032 · Cited by 1
Role of Receptor Tyrosine Kinase AXL in Cancer
Kumar, R., Tanwar, P., Bhatia, D. D., & Solanki, R. (2025) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-031-93894-8_4 · Cited by 1
Afadin sorts different retinal neuron types into accurate cellular layersPreprint
Lum, M. R., Patel, S. H., Graham, H. K., Zhao, M., Yi, Y., Li, L., Yao, M., Torre, A. L., Santina, L. D., Han, Y., et al. (2025) · eLife · doi:10.7554/elife.105575.2 · Cited by 2
Synaptic Cell Adhesion: A Structural Perspective
Bandekar, S. J., Kordon, S. P., & Araç, D. (2026) · Advances in neurobiology · doi:10.1007/978-3-032-12594-1_6 · Cited by 1
Microglia in Epilepsy: From Molecular Mechanism to Therapeutic Strategy
Paudel, Y. N., Angelopoulou, E., Kulkarni, S., Blair, R. E., & Deshpande, L. S. (2026) · Cells · doi:10.3390/cells15090835 · Cited by 1
Synapse Formation in the Mammalian Central Nervous System
Yasuda, M., & Umemori, H. (2009) · Springer eBooks · doi:10.1007/978-0-387-92708-4_4 · Cited by 1
Adhesion Molecules at the Synapse
El-Husseini, A. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_7 · Cited by 1
Mutations in Synaptic Adhesion Molecules
Ko, J., Montani, C., Kim, E., & Sala, C. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800109-7.00011-x · Cited by 1
Stasi, R. D., Rosa, L. D., Izzi, G., & D’Andrea, L. D. (2024) · Molecules · doi:10.3390/molecules29020521 · Cited by 1
Metadata
- Authors
- Yamagata, M., Sanes, J. R., & Weiner, J. A.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Yamagata, Masahito
- Sanes, Joshua R
- Weiner, Joshua A
- Venue
- Current Opinion in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2003-10
- Volume
- 15
- Issue
- 5
- Pages
- 621-632
- ISSN
- 0955-0674 (ISSN-L)
- OpenAlex
- W2067561211
- Cited by
- 374
- References
- 98
- Citations by year
- 2026: 12 · 2025: 10 · 2024: 4 · 2023: 9 · 2022: 7 · 2021: 4 · 2020: 17 · 2019: 12 · 2018: 8 · 2017: 6 · 2016: 16 · 2015: 12 · 2014: 13 · 2013: 17 · 2012: 11
- FWCI
- 2.64
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Current Opinion in Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- synaptic adhesion molecules, synaptogenesis, synaptic plasticity, target recognition, side kick, neuroligins, neurexin, cadherins, syndecans, synaptic specializations
- MeSH terms
- Amino Acid Sequence, Animals, Axons, Cytoskeleton, Immunoglobulins, Nerve Tissue Proteins, Synaptic Transmission, Synapses, Synaptic Vesicles, Cell Adhesion Molecules, Cadherins, Protein Structure, Tertiary, Neural Cell Adhesion Molecules, GTP-Binding Proteins, Caenorhabditis elegans Proteins
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