The DOI matches its Crossref record; 78 of the 78 references it cites were found in a registry or an index.
Aberrant Rac1-cofilin signaling mediates defects in dendritic spines, synaptic function, and sensory perception in fragile X syndrome
Open accessAbstract
Inhibiting Rac1-PAK-LIMK signaling may restore synaptic function and sensory processing in patients with fragile X syndrome.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The cited source says what the claim attributes to it.
In the citing paper
“Rac1 has been identified as a converging factor downstream of numerous proteins encoded by high-risk ASD genes, such as SHANK 4–6, FMR1 (fragile X mental retardation-1) 7, 8, NRXN 9, and AUTS2 10.”
From Autism-like social deficit generated by Dock4 deficiency is rescued by restoration of Rac1 activity and NMDA receptor function. (2021) · cites this paper as [7]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951
Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase
Arber, S., Barbayannis, F. A., Hanser, H., Schneider, C., Stanyon, C. A., Bernard, O., & Caroni, P. (1998) · Nature · doi:10.1038/31729 · Cited by 1,426
Cofilin phosphorylation by LIM-kinase 1 and its role in Rac-mediated actin reorganization
Yang, N., Higuchi, O., Ohashi, K., Nagata, K., Wada, A., Kangawa, K., Nishida, E., & Mizuno, K. (1998) · Nature · doi:10.1038/31735 · Cited by 1,296
Actin in action: the interplay between the actin cytoskeleton and synaptic efficacy.
Cingolani, L. A., & Goda, Y. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2373 · Cited by 831
Actin in dendritic spines: connecting dynamics to function
Hotulainen, P., & Hoogenraad, C. C. (2010) · Journal of Cell Biology · doi:10.1083/jcb.201003008 · Cited by 815
Niwa, R., Nagata-Ohashi, K., Takeichi, M., Mizuno, K., & Uemura, T. (2002) · Cell · doi:10.1016/s0092-8674(01)00638-9 · Cited by 694
A critical period for long-term potentiation at thalamocortical synapses
Crair, M. C., & Malenka, R. C. (1995) · Nature · doi:10.1038/375325a0 · Cited by 691
Lüscher, C., & Huber, K. M. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.016 · Cited by 627
Rogers, S. J., Hepburn, S., & Wehner, E. (2003) · Journal of Autism and Developmental Disorders · doi:10.1023/b:jadd.0000006000.38991.a7 · Cited by 609
Abnormal Development of Dendritic Spines in FMR1 Knock-Out Mice
Nimchinsky, E. A., Oberlander, A. M., & Svoboda, K. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05139.2001 · Cited by 560
Cited by
Sorted by citations
A synaptic perspective of fragile X syndrome and autism spectrum Disorders.
Bagni, C., & Zukin, R. S. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.041 · Cited by 326
Self-citationActivation of autophagy rescues synaptic and cognitive deficits in fragile X mice
Yan, J., Porch, M. W., Court-Vazquez, B. L., Bennett, M. V. L., & Zukin, R. S. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1808247115 · Cited by 146
Self-citationSawicka, K., Hale, C. R., Park, C. Y., Fak, J. J., Gresack, J. E., Driesche, S. J. V., Kang, J. J., Darnell, J. C., & Darnell, R. B. (2019) · eLife · doi:10.7554/elife.46919 · Cited by 118
ATP Synthase c-Subunit Leak Causes Aberrant Cellular Metabolism in Fragile X Syndrome
Licznerski, P., Park, H., Rolyan, H., Chen, R., Mnatsakanyan, N., Miranda, P., Graham, M. M., Wu, J., Cruz-Reyes, N., Mehta, N. A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.07.008 · Cited by 119
Banerjee, A., Ifrim, M. F., Valdez‐Sinon, A. N., Raj, N., & Bassell, G. J. (2018) · Brain Research · doi:10.1016/j.brainres.2018.04.008 · Cited by 111
Guo, D., Peng, Y., Wang, L., Sun, X., Wang, X., Liang, C., Yang, X., Li, S., Xu, J., Ye, W.-C., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-019-0472-7 · Cited by 102
Plasticity of dendritic spines: Molecular function and dysfunction in neurodevelopmental disorders
Nishiyama, J. (2019) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12899 · Cited by 96
Rho GTPases in Intellectual Disability: From Genetics to Therapeutic Opportunities
Zamboni, V., Jones, R., Umbach, A., Ammoni, A., Passafaro, M., Hirsch, E., & Merlo, G. R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061821 · Cited by 83
The Role of ADF/Cofilin in Synaptic Physiology and Alzheimer’s Disease
Zablah, Y. B., Merovitch, N., & Jia, Z. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.594998 · Cited by 73
Rho Signaling in Synaptic Plasticity, Memory, and Brain Disorders
Zhang, H., Zablah, Y. B., Zhang, H., & Jia, Z. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.729076 · Cited by 70
The Role of p21-Activated Kinases in Cancer and Beyond: Where Are We Heading?
Liu, H., Liu, K., & Dong, Z. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.641381 · Cited by 69
Modeling Fragile X Syndrome in Drosophila
Drozd, M. M., Bardoni, B., & Capovilla, M. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00124 · Cited by 70
Zhang, Z., Ye, M., Li, Q., You, Y., Yu, H., Ma, Y., Mei, L., Sun, X., Wang, L., Yue, W., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.091 · Cited by 67
The Role of Rac GTPase in Dendritic Spine Morphogenesis and Memory
Costa, J. F., Dines, M., & Lamprecht, R. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00012 · Cited by 58
The p21-activated kinases in neural cytoskeletal remodeling and related neurological disorders
Zhang, K., Wang, Y., Fan, T., Zeng, C., & Sun, Z. S. (2020) · Protein & Cell · doi:10.1007/s13238-020-00812-9 · Cited by 60
Villalonga-Rosso, E., Mosrin-Huaman, C., Normand, T., Girardin, C., Serrano, A., Žunar, B., Doudeau, M., Godin, F., Bénédetti, H., & Vallée, B. (2023) · Cells · doi:10.3390/cells12050805 · Cited by 64
Modulators of Kv3 Potassium Channels Rescue the Auditory Function of Fragile X Mice
El‐Hassar, L., Song, L., Tan, W. J. T., Large, C., Alvaro, G. S., Santos-Sacchi, J., & Kaczmarek, L. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0839-18.2019 · Cited by 60
LIM-Kinases in Synaptic Plasticity, Memory, and Brain Diseases
Zablah, Y. B., Zhang, H., Gugustea, R., & Jia, Z. (2021) · Cells · doi:10.3390/cells10082079 · Cited by 58
De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures
Horn, S., Au, M., Basel‐Vanagaite, L., Bayrak‐Toydemir, P., Chapin, A., Cohen, L., Elting, M. W., Graham, J. M., Gonzaga-Jauregui, C. G., Konen, O., et al. (2019) · Brain · doi:10.1093/brain/awz264 · Cited by 53
Lo, L. H.-Y., Dong, R., Lyu, Q., & Lai, K. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107744 · Cited by 51
Han, Z., Dong, Y., Lu, J., Yang, F., Zheng, Y., & Yang, H. (2021) · PubMed Central · Cited by 45
Roles of palmitoylation in structural long-term synaptic plasticity
Ji, B., & Skup, M. (2021) · Molecular Brain · doi:10.1186/s13041-020-00717-y · Cited by 44
D’Arrigo, G., Gabrielli, M., Scaroni, F., Swuec, P., Amin, L., Pegoraro, A., Adinolfi, E., Virgilio, F. D., Cojoc, D., Legname, G., et al. (2021) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12114 · Cited by 44
CXCL12-induced rescue of cortical dendritic spines and cognitive flexibility
Festa, L. K., Irollo, E., Platt, B. J., Tian, Y., Floresco, S., & Meucci, O. (2020) · eLife · doi:10.7554/elife.49717 · Cited by 41
SUMOylation of synaptic and synapse‐associated proteins: An update
Henley, J. M., Seager, R., Nakamura, Y., Talandyte, K., Nair, J. D., & Wilkinson, K. A. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15103 · Cited by 40
Sculpting Dendritic Spines during Initiation and Maintenance of Neuropathic Pain
Stratton, H. J., & Khanna, R. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1664-20.2020 · Cited by 44
Mercaldo, V., Vidimova, B., Gastaldo, D., Fernández, E., Lo, A. C., Cencelli, G., Pedini, G., Rubeis, S. D., Longo, F., Klann, E., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.008 · Cited by 32
Vigli, D., Rusconi, L., Valenti, D., Montanara, P. L., Cosentino, L., Lacivita, E., Leopoldo, M., Amendola, E., Gross, C. T., Landsberger, N., et al. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.10.018 · Cited by 33
Kulasiri, D., Khan, R., & Samarasinghe, S. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.300331 · Cited by 34
Rac-maninoff and Rho-vel: The symphony of Rho-GTPase signaling at excitatory synapses
Duman, J. G., Blanco, F. A., Cronkite, C. A., Ru, Q., Erikson, K., Mulherkar, S. A., Saifullah, A. B., Firozi, K., & Tolias, K. F. (2021) · Small GTPases · doi:10.1080/21541248.2021.1885264 · Cited by 35
Circuit-level theories for sensory dysfunction in autism: convergence across mouse models
Monday, H. R., Wang, H. C., & Feldman, D. E. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1254297 · Cited by 31
Sears, J. C., Choi, W. J., & Broadie, K. S. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.02.004 · Cited by 30
Stress-Sensitive Protein Rac1 and Its Involvement in Neurodevelopmental Disorders
Wang, X., Liu, D., Wei, F., Li, Y., Wang, X., Li, L., Wang, G., Zhang, S., & Zhang, L. (2020) · Neural Plasticity · doi:10.1155/2020/8894372 · Cited by 33
D’Incal, C., Broos, J., Torfs, T., Kooy, R. F., & Vanden Berghe, W. (2022) · Cells · doi:10.3390/cells11081325 · Cited by 29
Feuge, J., Scharkowski, F., Michaelsen‐Preusse, K., & Körte, M. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz059 · Cited by 28
Mouse models of fragile X-related disorders
Willemsen, R., & Kooy, R. F. (2023) · Disease Models & Mechanisms · doi:10.1242/dmm.049485 · Cited by 30
Pennucci, R., Gucciardi, I., & de Curtis, I. (2019) · PLoS ONE · doi:10.1371/journal.pone.0220496 · Cited by 27
Barnes, J., Salas, F., Mokhtari, R., Dolstra, H., Pedrosa, E., & Lachman, H. M. (2018) · Molecular Autism · doi:10.1186/s13229-018-0227-3 · Cited by 31
Yang, C.-Y., Yu, T.-H., Wen, W.-L., Ling, P., & Hsu, K. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2395-18.2019 · Cited by 26
Local Translation in Nervous System Pathologies
Gamarra, M., de la Cruz, A., Blanco‐Urrejola, M., & Baleriola, J. (2021) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2021.689208 · Cited by 30
Heinze, A., Schuldt, C., Khudayberdiev, S., van Bommel, B., Hacker, D., Schulz, T. G., Stringhi, R., Marcello, E., Mikhaylova, M., & Rust, M. B. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04593-8 · Cited by 24
Molosh, A. I., & Shekhar, A. (2018) · Progress in brain research · doi:10.1016/bs.pbr.2018.09.014 · Cited by 24
Sungur, A. Ö., Stemmler, L., Wöhr, M., & Rust, M. B. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00025 · Cited by 22
mTOR-Dependent Spine Dynamics in Autism
Chaudry, S., & Vasudevan, N. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.877609 · Cited by 23
Chen, Y.-S., Zhang, S., Tan, W., Zhu, Q., Yue, C., Xiang, P., Li, J., Wei, Z., & Zeng, Y. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03226-w · Cited by 19
Hlushchenko, I., Khanal, P., Abouelezz, A., Paavilainen, V. O., & Hotulainen, P. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00217 · Cited by 22
Lian, B., Liu, M., Lan, Z., Sun, T., Meng, Z., Chang, Q., Liu, Z., Zhang, J., & Zhao, C. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112503 · Cited by 19
Sun, W., Yang, J., Hong, Y., Yuan, H., Wang, J., Zhang, Y., Lu, X., Jin, C., Wu, S., & Cai, Y. (2019) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-019-00748-7 · Cited by 19
Transgenerational Effects of Prenatal Ethanol Exposure in Prepubescent Mice
Bottom, R. T., Kozanian, O. O., Rohac, D. J., Erickson, M. A., & Huffman, K. J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.812429 · Cited by 19
Chen, S.-J., Gao, C., Lv, Q., Zhao, M.-Q., Qin, X., & Liao, H. (2021) · Acta Pharmacologica Sinica · doi:10.1038/s41401-021-00823-0 · Cited by 18
LIMK1/2 in the mPFC Plays a Role in Chronic Stress-Induced Depressive-Like Effects in Mice
Gao, T., Wang, Y., Liu, L., Wang, J., Wang, Y., Guan, W., Chen, T., Zhao, J., & Jiang, B. (2020) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyaa067 · Cited by 17
Zhou, F., Ouyang, L., Xie, J., Liu, S., Li, Q., Yang, S., Li, J., Su, R., Rao, S., Yan, L., et al. (2023) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2023.115425 · Cited by 19
Destabilization of fear memory by Rac1-driven engram-microglia communication in hippocampus
Chen, R., Wang, Z., Lin, Q., Hou, X., Jiang, Y., Le, Q., Liu, X., Ma, L., & Wang, F. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.04.024 · Cited by 17
Chen, Z., Zhang, S., Nie, B., Huang, J., Han, Z., Chen, X. F., Bai, X., & Ouyang, H. (2020) · The Journal of Physiology · doi:10.1113/jp279525 · Cited by 16
Ma, B., Shan, X., Yu, J., Zhu, T., Ren, L., Lv, H., Cheng, H., Zhang, T., Wang, L., Wei, F., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111722 · Cited by 15
Longatti, A., Ponzoni, L., Moretto, E., Giansante, G., Lattuada, N., Colombo, M. N., Francolini, M., Sala, M., Murru, L., & Passafaro, M. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02502-x · Cited by 14
Kim, J.-E., Lee, D.-S., Kim, T.-H., Park, H., Kim, M.-J., & Kang, T. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02788-9 · Cited by 14
Roles of Rac1-Dependent Intrinsic Forgetting in Memory-Related Brain Disorders: Demon or Angel
Wang, W., Wang, Z., Cao, J., Dong, Y., & Chen, Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310736 · Cited by 14
Scorrano, G., D’Onofrio, G., Accogli, A., Severino, M., Buchert, R., Kotzaeridou, U., Iapadre, G., Farello, G., Iacomino, M., Dono, F., et al. (2023) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2023.09.005 · Cited by 13
Takabatake, M., Goshima, Y., & Sasaki, Y. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00005 · Cited by 14
Loss of CC2D1A in Glutamatergic Neurons Results in Autistic-Like Features in Mice
Yang, C.-Y., Hung, Y.-C., Cheng, K., Ling, P., & Hsu, K. (2021) · Neurotherapeutics · doi:10.1007/s13311-021-01072-z · Cited by 14
Nash, B., Festa, L. K., Lin, C., & Meucci, O. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146409 · Cited by 14
Qualmann, B., & Kessels, M. M. (2021) · Cells · doi:10.3390/cells10051079 · Cited by 14
Borreca, A., Luca, M. D., Ferrante, A., Boussadia, Z., Pignataro, A., Martire, A., & Ammassari‐Teule, M. (2023) · Scientific Reports · doi:10.1038/s41598-023-27991-9 · Cited by 14
Mitochondrial leak metabolism induces the Spemann-Mangold Organizer via Hif-1α in Xenopus
Garfinkel, A. M., Mnatsakanyan, N., Patel, J. H., Wills, A. E., Shteyman, A., Smith, P. J., Alavian, K. N., Jonas, E. A., & Khokha, M. K. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.08.015 · Cited by 13
Role of Cyclins and Cytoskeletal Proteins in Endometriosis: Insights into Pathophysiology
Szymański, M., Bonowicz, K., Antosik, P., Jerka, D., Głowacka, M., Soroka, M., Steinbrink, K., Kleszczyński, K., & Gagat, M. (2024) · Cancers · doi:10.3390/cancers16040836 · Cited by 13
Yang, X., Cao, Z., Zhang, J., Shao, B., Song, M., Han, Y., & Li, Y. (2018) · Environmental Pollution · doi:10.1016/j.envpol.2018.09.145 · Cited by 15
Byeon, S., Werner, B., Falter, R., Davidsen, K., Snyder, C., Ong, S., & Yadav, S. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.836746 · Cited by 12
Rac1/PAK1 signaling contributes to bone cancer pain by Regulation dendritic spine remodeling in rats
Xu, L., Yang, L., Wu, Y., Wan, X., Tang, X., Xu, Y., Chen, Q., Liu, Y., & Liu, S. (2023) · Molecular Pain · doi:10.1177/17448069231161031 · Cited by 13
Tactile sensory processing deficits in genetic mouse models of autism spectrum disorder
Falcão, M., Monteiro, P., & Jacinto, L. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16135 · Cited by 14
Cytoskeletal regulation of synaptogenesis in a model of human fetal brain development
Wilson, E. S., Rudisill, T., Kirk, B., Johnson, C., Kemper, P., & Litwa, K. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24692 · Cited by 12
Vallejo, D., Lindsay, C., González-Billault, C., & Inestrosa, N. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15448 · Cited by 10
Sechi, S., Karimpour-Ghahnavieh, A., Frappaolo, A., Francesco, L. D., Piergentili, R., Schininà, E., D’Avino, P. P., & Giansanti, M. G. (2021) · Cells · doi:10.3390/cells10092336 · Cited by 11
Alteration of synaptic protein composition during developmental synapse maturation
Kaizuka, T., & Takumi, T. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16304 · Cited by 13
Walkley, S. U., Abbeduto, L., Batshaw, M. L., Bhattacharyya, A., Bookheimer, S. Y., Christian, B. T., Constantino, J. N., de Vellis, J., Doherty, D., Nelson, D. L., et al. (2019) · Annals of Neurology · doi:10.1002/ana.25531 · Cited by 11
Infantile spasms-linked Nedd4-2 mediates hippocampal plasticity and learning via cofilin signaling
Lee, K. Y., Zhu, J., Cutia, C. A., Christian, C. A., Rhodes, J. S., & Tsai, N. (2021) · EMBO Reports · doi:10.15252/embr.202152645 · Cited by 10
Liu, X., & Wang, J. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.07.017 · Cited by 10
FLNA regulates neuronal maturation by modulating RAC1-Cofilin activity in the developing cortex
Falace, A., Corbières, L., Palminha, C., Guarnieri, F. C., Schaller, F., Buhler, E., Carlo, C. T. D. S., Montheil, A., Watrin, F., Manent, J., et al. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106558 · Cited by 9
Conditional Astrocyte Rac1KO Attenuates Hyperreflexia after Spinal Cord Injury
Benson, C. A., Olson, K., Patwa, S., Kauer, S. D., King, J. F., Waxman, S. G., & Tan, A. M. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1670-22.2023 · Cited by 9
Remodeling of the postsynaptic proteome in male mice and marmosets during synapse development
Kaizuka, T., Suzuki, T., Kishi, N., Tamada, K., Kilimann, M. W., Ueyama, T., Watanabe, M., Shimogori, T., Okano, H., Dohmae, N., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46529-9 · Cited by 9
Inhibitors of the p21 Activated Kinases
Sampat, N., & Minden, A. (2018) · Current Pharmacology Reports · doi:10.1007/s40495-018-0132-7 · Cited by 9
Hou, K., & Zheng, X. (2024) · Genes · doi:10.3390/genes15091118 · Cited by 12
Dysfunctions of cellular context-sensitivity in neurodevelopmental learning disabilities
Granato, A., Phillips, W. A., Schulz, J. M., Mototaka Suzuki, A., & Larkum, M. E. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105688 · Cited by 8
Wilson, A., Barakat, R., Mu, R., Karush, L. L., Gao, Y., Hartigan, K. A., Chen, J., Shu, H., Turner, T. N., Maloney, S. E., et al. (2023) · Human Molecular Genetics · doi:10.1093/hmg/ddad155 · Cited by 7
Discovery of MDI-114215: A Potent and Selective LIMK Inhibitor To Treat Fragile X Syndrome
Baldwin, A. G., Foley, D., Collins, R. J., Lee, H.-A., Jones, D. H., Wahab, B., Waters, L., Pedder, J., Paine, M., Feng, G. J., et al. (2024) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.4c02694 · Cited by 7
Altered hippocampal dendritic spine maturation after hypoxia-induced seizures in neonatal rats
Bell, J. J. L., Handy, M., Nieder, C., Getzfread, M., & Jensen, F. E. (2021) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2021.103629 · Cited by 8
Inka2, a novel Pak4 inhibitor, regulates actin dynamics in neuronal development
Yamada, S., Mizukoshi, T., Tokunaga, A., & Sakakibara, S. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010438 · Cited by 7
Dong, R., Li, X., Flores, A. D., & Lai, K. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105029 · Cited by 7
The small GTPase Arf6 is dysregulated in a mouse model for fragile X syndrome
Briševac, D., Scholz, R., Du, D., Elagabani, M. N., Köhr, G., & Kornau, H. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15230 · Cited by 7
Stress Elicits Contrasting Effects on Rac1-Cofilin Signaling in the Hippocampus and Amygdala
Bose, M., Nawaz, M. S., Pal, R., & Chattarji, S. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.880382 · Cited by 7
Ren, B., Wang, L., Yang, N., Liu, T., Zhao, L., Ma, H., Li, J., Zhang, Y., & Ren, X. (2021) · Future Oncology · doi:10.2217/fon-2021-0116 · Cited by 6
Reaction–Diffusion Model-Based Research on Formation Mechanism of Neuron Dendritic Spine Patterns
Jia, Y., Zhao, Q., Yin, H., Guo, S., Sun, M., Yang, Z. R., & Zhao, X. (2021) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2021.563682 · Cited by 5
Schuldt, C., Khudayberdiev, S., Chandra, B., Linne, U., & Rust, M. B. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05393-y · Cited by 5
Design decisions for incorporating spatial and mechanical aspects in models of signaling networks
Bell, M. K., & Rangamani, P. (2021) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2021.03.004 · Cited by 4
Chang, J., Chen, C., Li, W., & Abumaria, N. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01045-6 · Cited by 4
PAK1 inhibition with Romidepsin attenuates H‐reflex hyperexcitability after spinal cord injury
Kauer, S. D., Benson, C. A., Carrara, J., Tarafder, A. A., Ibrahim, Y. H., Estacion, M. A., Waxman, S. G., & Tan, A. M. (2024) · The Journal of Physiology · doi:10.1113/jp284976 · Cited by 4
Wang, X., Wang, L., Bu, Q., Xiao, Y., Zhao, Y., Jiang, L., Dai, Y., Li, H., Liu, H., Chen, Y., et al. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1867-24.2025 · Cited by 3
Gao, J., Shen, J., Gao, L., Yan, D., Wang, Y., Meng, J., Chen, D., Li, H., & Wu, J. (2025) · NeuroToxicology · doi:10.1016/j.neuro.2025.103331 · Cited by 3
Tetrahydropyrazolopyridinones as a Novel Class of Potent and Highly Selective LIMK Inhibitors
Baldwin, A. G., Foley, D., Jones, D. H., Lee, H.-A., Collins, R. J., Wahab, B., Pedder, J. H., Waters, L., Paine, M., Schino, L., et al. (2025) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c00974 · Cited by 3
Altered auditory feature discrimination in a rat model of Fragile X Syndrome
Gauthier, D. W., James, N., & Auerbach, B. D. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003248 · Cited by 2
Metadata
- Authors
- Pyronneau, A., He, Q., Hwang, J.-Y., Porch, M., Contractor, A., & Zukin, R. S.
- Affiliations
- Albert Einstein College of Medicine (US)
- Northwestern University (US)
- Corresponding author
- Zukin, R. Suzanne
- Venue
- Science Signaling
- Published
- 2017-11-07
- Volume
- 10
- Issue
- 504
- ISSN
- 1937-9145 (ISSN-L)
- 1945-0877
- PMC
- PMC5988355
- OpenAlex
- W2767737184
- Cited by
- 122
- References
- 78
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 14 · 2023: 17 · 2022: 10 · 2021: 24 · 2020: 17 · 2019: 14 · 2018: 11 · 2017: 1
- FWCI
- 7.81
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science Signaling (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (award304400, MH092877, award304548, NS45693, award304549, HD083828, award304565, GM007288)
- National Institute of Mental Health (award304564, MH108362, award308817, R21MH104808)
- Brain and Behavior Research Foundation (award304558, Distinguished Investigator Grant, award304563, Young Investigator Grant)
- McKnight Foundation (award304550)
- National Institute of General Medical Sciences (award316793, T32-GM007822)
- American Heart Association (award304562, Scientist Development Grant)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- fragile X syndrome, Rac1, cofilin, PAK1, dendritic spines, synaptic function, sensory perception, layer 5 pyramidal neurons, small molecule inhibitors, spine density, FMRP
- MeSH terms
- Actins, Animals, Disease Models, Animal, Fragile X Syndrome, Neuropeptides, Perception, Phosphorylation, Pyridones, Pyrimidines, Somatosensory Cortex, Synapses, Pyramidal Cells, Mice, Knockout, rac1 GTP-Binding Protein, Dendritic Spines, Cofilin 1, Mice, p21-Activated Kinases
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