Translational Control in Synaptic Plasticity and Cognitive Dysfunction

mTOR Signaling in Growth Control and Disease

Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509

Long‐lasting potentiation of synaptic transmission in the dentate area of the unanaesthetized rabbit following stimulation of the perforant path

Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424

TOR signaling in growth and metabolism

Wullschleger, S., Loewith, R., & Hall, M. N. (2006) · Cell · doi:10.1016/j.cell.2006.01.016 · Cited by 5,787

Genome-wide atlas of gene expression in the adult mouse brain

Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., Boe, A. F., Boguski, M. S., Brockway, K. S., Byrnes, E. J., et al. (2007) · Nature · doi:10.1038/nature05453 · Cited by 5,572

Memory - A century of consolidation

McGaugh, J. L. (2000) · Science · doi:10.1126/science.287.5451.248 · Cited by 4,250

Upstream and downstream of mTOR

Hay, N., & Sonenberg, N. (2004) · Genes & Development · doi:10.1101/gad.1212704 · Cited by 4,181

LTP and LTD

Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968

The molecular biology of memory storage: a dialogue between genes and synapses

Kandel, E. R. (2001) · Science · doi:10.1126/science.1067020 · Cited by 3,917

Genome-Wide Analysis in Vivo of Translation with Nucleotide Resolution Using Ribosome Profiling

Ingolia, N. T., Ghaemmaghami, S., Newman, J. R. S., & Weissman, J. S. (2009) · Science · doi:10.1126/science.1168978 · Cited by 3,853

Regulation of Translation Initiation in Eukaryotes: Mechanisms and Biological Targets

Sonenberg, N., & Hinnebusch, A. G. (2009) · Cell · doi:10.1016/j.cell.2009.01.042 · Cited by 3,304

Rheb mediates neuronal-activity-induced mitochondrial energetics through mTORC1-independent PDH activation

Yang, W., Pang, D., Chen, M., Du, C., Jia, L., Wang, L., He, Y., Jiang, W., Luo, L., Yu, Z., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.02.022 · Cited by 47

Shifting patterns of polyribosome accumulation at synapses over the course of hippocampal long‐term potentiation

Ostroff, L. E., Watson, D. J., Cao, G., Parker, P. H., Smith, H., & Harris, K. M. (2018) · Hippocampus · doi:10.1002/hipo.22841 · Cited by 42

Metformin treatment improves the spatial memory of aged mice in an APOE genotype–dependent manner

Zhang, J., Lin, Y., Dai, X., Fang, W., Wu, X., & Chen, X. (2019) · The FASEB Journal · doi:10.1096/fj.201802718r · Cited by 44

Quercetin Regulates the Integrated Stress Response to Improve Memory

Nakagawa, T., & Ohta, K. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112761 · Cited by 44

Rapamycin restores BDNF-LTP and the persistence of long-term memory in a model of Down's syndrome

Andrade‐Talavera, Y., Benito, I., Casañas, J. J., Moreno, A. R., & Montesinos, M. L. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.09.005 · Cited by 42

Comprehensive behavioral analysis of RNG105 (Caprin1) heterozygous mice: Reduced social interaction and attenuated response to novelty

Ohashi, R., Takao, K., Miyakawa, T., & Shiina, N. (2016) · Scientific Reports · doi:10.1038/srep20775 · Cited by 45

Arc Regulates Transcription of Genes for Plasticity, Excitability and Alzheimer’s Disease

Leung, H.-W., Foo, G., & VanDongen, A. M. J. (2022) · Biomedicines · doi:10.3390/biomedicines10081946 · Cited by 41

eIF2-dependent translation initiation: Memory consolidation and disruption in Alzheimer’s disease

Oliveira, M. M., & Klann, E. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.07.009 · Cited by 43

Stress-induced inhibition of translation independently of eIF2α phosphorylation

Knutsen, J. H. J., Rødland, G. E., Bøe, C. A., Håland, T. W., Sunnerhagen, P., Grallert, B., & Boye, E. (2015) · Journal of Cell Science · doi:10.1242/jcs.176545 · Cited by 40

Region specific activation of the AKT and mTORC1 pathway in response to excessive alcohol intake in rodents

Laguesse, S., Morisot, N., Phamluong, K., & Dorit Ron, A. (2016) · Addiction Biology · doi:10.1111/adb.12464 · Cited by 40

Targeting the intracellular signaling “STOP” and “GO” pathways for the treatment of alcohol use disorders

Dorit Ron, A., & Berger, A. L. (2018) · Psychopharmacology · doi:10.1007/s00213-018-4882-z · Cited by 37

mTOR-dependent alterations of Kv1.1 subunit expression in the neuronal subset-specific Pten knockout mouse model of cortical dysplasia with epilepsy

Nguyen, L. H., & Anderson, A. E. (2018) · Scientific Reports · doi:10.1038/s41598-018-21656-8 · Cited by 39

eIF2α-mediated translational control regulates the persistence of cocaine-induced LTP in midbrain dopamine neurons

Placzek, A. N., Prisco, G. V. D., Khatiwada, S., Sgritta, M., Huang, W., Krnjević, K., Kaufman, R. J., Dani, J. A., Walter, P., & Costa‐Mattioli, M. (2016) · eLife · doi:10.7554/elife.17517 · Cited by 35

Molecular mechanisms controlling protein synthesis in memory reconsolidation

Roesler, R. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.04.015 · Cited by 37

IRE1α RIDD activity induced under ER stress drives neuronal death by the degradation of 14-3-3 θ mRNA in cortical neurons during glucose deprivation

Gómora‐García, J. C., Gerónimo‐Olvera, C., Pérez-Martínez, X., & Massieu, L. (2021) · Cell Death Discovery · doi:10.1038/s41420-021-00518-9 · Cited by 39

Convergent Neuronal Plasticity and Metaplasticity Mechanisms of Stress, Nicotine, and Alcohol

Ostroumov, A., & Dani, J. A. (2017) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010617-052735 · Cited by 36

Accumulation of Polyribosomes in Dendritic Spine Heads, But Not Bases and Necks, during Memory Consolidation Depends on Cap-Dependent Translation Initiation

Ostroff, L. E., Botsford, B. W., Gindina, S., Cowansage, K. K., LeDoux, J. E., Klann, E., & Hoeffer, C. A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3301-16.2017 · Cited by 37

Rescue of Learning and Memory Deficits in the Human Nonsyndromic Intellectual Disability Cereblon Knock-Out Mouse Model by Targeting the AMP-Activated Protein Kinase–mTORC1 Translational Pathway

Bavley, C. C., Rice, R. C., Fischer, D. K., Fakira, A. K., Byrne, M., Kosovsky, M., Rizzo, B. K., Prete, D. D., Alaedini, A., Morón, J. A., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0599-17.2018 · Cited by 36

TAR DNA-Binding Protein 43 and Disrupted in Schizophrenia 1 Coaggregation Disrupts Dendritic Local Translation and Mental Function in Frontotemporal Lobar Degeneration

Endo, R., Takashima, N., Nekooki-Machida, Y., Komi, Y., Hui, K. K., Takao, M., Akatsu, H., Murayama, S., Sawa, A., & Tanaka, M. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.03.008 · Cited by 35

Stress Responses in Down Syndrome Neurodegeneration: State of the Art and Therapeutic Molecules

Lanzillotta, C., & Domenico, F. D. (2021) · Biomolecules · doi:10.3390/biom11020266 · Cited by 36

A Functional Dissection of the mRNA and Locally Synthesized Protein Population in Neuronal Dendrites and Axons

Perez, J. D., Fusco, C. M., & Schuman, E. M. (2021) · Annual Review of Genetics · doi:10.1146/annurev-genet-030321-054851 · Cited by 36

mTORC1 in the orbitofrontal cortex promotes habitual alcohol seeking

Morisot, N., Berger, A. L., Phamluong, K., Laguesse, S., Moffat, J. J., & Dorit Ron, A. (2019) · eLife · doi:10.7554/elife.51333 · Cited by 31

A Novel Selective PKR Inhibitor Restores Cognitive Deficits and Neurodegeneration in Alzheimer Disease Experimental Models

Lopez‐Grancha, M., Bernardelli, P., Moindrot, N., Genet, E., Vincent, C., Roudières, V., Krick, A., Sabuco, J.-F., Machnik, D., Ibghi, D., et al. (2021) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.121.000590 · Cited by 34

Proteostasis and RNA Binding Proteins in Synaptic Plasticity and in the Pathogenesis of Neuropsychiatric Disorders

Klein, M. E., Monday, H. R., & Jordan, B. A. (2016) · Neural Plasticity · doi:10.1155/2016/3857934 · Cited by 37

Integrator loss leads to dsRNA formation that triggers the integrated stress response

Baluapuri, A., Zhao, N. C., Marina, R. J., Huang, K.-L., Kuzkina, A., Amodeo, M. E., Stein, C. B., Ahn, L., Farr, J. S., Schaffer, A. E., et al. (2025) · Cell · doi:10.1016/j.cell.2025.03.025 · Cited by 39

Long-Term Memory Formation inDrosophilaRequires Training-Dependent Glial Transcription

Matsuno, M., Horiuchi, J., Yuasa, Y., Ofusa, K., Miyashita, T., Masuda, T., & Saitoe, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3865-14.2015 · Cited by 34

Forebrain-specific, conditional silencing of Staufen2 alters synaptic plasticity, learning, and memory in rats

Berger, S. M., Fernández‐Lamo, I., Schönig, K., Moya, S. M. F., Ehses, J., Schieweck, R., Clementi, S., Enkel, T., Grothe, S., Halbach, O. V. B. U., et al. (2017) · Genome biology · doi:10.1186/s13059-017-1350-8 · Cited by 34

Translation Regulation by eIF2α Phosphorylation and mTORC1 Signaling Pathways in Non-Communicable Diseases (NCDs)

Rios-Fuller, T. J., Mahé, M., Walters, B., Abbadi, D., Pérez-Baos, S., Gadi, A., Andrews, J. J., Katsara, O., Vincent, C. T., & Schneider, R. J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155301 · Cited by 34

Maternal High-Fat Diet Multigenerationally Impairs Hippocampal Synaptic Plasticity and Memory in Male Rat Offspring

Lin, C., Lin, Y., Yu, J., Yu, J., Cheng, Y., Wu, X., Lin, Y., & Lin, Y. (2020) · Endocrinology · doi:10.1210/endocr/bqaa214 · Cited by 33

Dysregulation of Translation in TDP-43 Proteinopathies: Deficits in the RNA Supply Chain and Local Protein Production

Bjork, R. T., Mortimore, N. P., Loganathan, S., & Zarnescu, D. C. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.840357 · Cited by 36

Molecular targets for modulating the protein translation vital to proteostasis and neuron degeneration in Parkinson’s disease

Zhou, Z., Selvaratnam, T., Lee, J. C. T., Chao, Y., & Tan, E. (2019) · Translational Neurodegeneration · doi:10.1186/s40035-019-0145-0 · Cited by 33

Spatial organization of the transcriptome in individual neuronsPreprint

Wang, G., Ang, C. E., Fan, J., Wang, A., Moffitt, J. R., & Zhuang, X. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.07.414060 · Cited by 33

Role of CPEB3 protein in learning and memory: new insights from synaptic plasticity

Qu, W., Sun, Q. H., Liu, Q. Q., Jin, H. J., Cui, R., Yang, W., Song, D. B., & Li, B. J. (2020) · Aging · doi:10.18632/aging.103404 · Cited by 31

Monitoring Astrocytic Proteome Dynamics by Cell Type-Specific Protein Labeling

Müller, A., Stellmacher, A., Freitag, C. E., Landgraf, P., & Dieterich, D. C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0145451 · Cited by 31

Dynamic landscape of the local translation at activated synapses

Khlebodarova, T. M., Kogai, V. V., Trifonova, E. A., & Likhoshvai, V. A. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.245 · Cited by 33

Molecular mechanisms for targeted ASD treatments

Basilico, B., Morandell, J., & Novarino, G. (2020) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2020.06.004 · Cited by 30

Translational control in brain pathologies: biological significance and therapeutic opportunities

Delaidelli, A., Jan, A., Herms, J. W., & Sorensen, P. H. B. (2019) · Acta Neuropathologica · doi:10.1007/s00401-019-01971-8 · Cited by 31

Inactivation of BRD7 results in impaired cognitive behavior and reduced synaptic plasticity of the medial prefrontal cortex

Xu, Y., Cao, W., Zhou, M., Li, C.-Q., Luo, Y., Wang, H., Zhao, R., Jiang, S., Yang, J., Liu, Y., et al. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.02.031 · Cited by 30

Age-dependent shift in the de novo proteome accompanies pathogenesis in an Alzheimer’s disease mouse model

Elder, M. K., Erdjument‐Bromage, H., Oliveira, M. M., Mamcarz, M., Neubert, T. A., & Klann, E. (2021) · Communications Biology · doi:10.1038/s42003-021-02324-6 · Cited by 33

5'-UTR SNP of FGF13 causes translational defect and intellectual disability

Pan, X., Zhao, J., Zhou, Z., Chen, J., Yang, Z., Wu, Y., Bai, M., Jiao, Y., Yang, Y., Hu, X., et al. (2021) · eLife · doi:10.7554/elife.63021 · Cited by 30

Positive Allosteric Modulation of mGlu1 Reverses Cocaine-Induced Behavioral and Synaptic Plasticity Through the Integrated Stress Response and Oligophrenin-1

Kawa, A. B., Hwang, E.-K., Funke, J. R., Zhou, H., Costa‐Mattioli, M., & Wolf, M. E. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.05.008 · Cited by 29

Chronic Mild Stress-Induced Alterations of Local Protein Synthesis: A Role for Cognitive Impairment

Calabrese, F., Brivio, P., Gruca, P., Łasoń, M., Papp, M., & Riva, M. A. (2017) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00392 · Cited by 30

M(en)TORship lessons on life and death by the integrated stress response

Koromilas, A. E. (2018) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2018.12.009 · Cited by 28

Mechanistic target of rapamycin (mTOR) signaling in status epilepticus

Crino, P. B. (2019) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2019.106550 · Cited by 29

Akt activation ameliorates deficits in hippocampal-dependent memory and activity-dependent synaptic protein synthesis in an Alzheimer’s disease mouse model

Kommaddi, R. P., Gowaikar, R., Haseena, P. A., Diwakar, L., Singh, K. P., & Mondal, A. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105619 · Cited by 29

Inhibition of LTP-Induced Translation by IL-1β Reduces the Level of Newly Synthesized Proteins in Hippocampal Dendrites

Prieto, G. A., Smith, E. D., Tong, L., Nguyen, M., & Cotman, C. W. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00511 · Cited by 30

Low-Level Brain Somatic Mutations Are Implicated in Schizophrenia

Kim, M.-H., Kim, I. B., Lee, J., Cha, D. H., Park, S. M., Kim, J. H., Kim, R., Park, J. S., An, Y., Kim, K., et al. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.01.014 · Cited by 28

Biological implications of genetic variations in autism spectrum disorders from genomics studies

Zhang, Y., Liu, X., Guo, R., Xu, W., Guo, Q. J., Hao, C., Ni, X., & Li, W. (2021) · Bioscience Reports · doi:10.1042/bsr20210593 · Cited by 33

Combined exposure of lead and high-fat diet enhanced cognitive decline via interacting with CREB-BDNF signaling in male rats

Liu, R., Bai, L., Liu, M., Wang, R., Wu, Y., Li, Q., Ba, Y., Zhang, H., Zhou, G., Yu, F., et al. (2022) · Environmental Pollution · doi:10.1016/j.envpol.2022.119200 · Cited by 27

Quantitative Subcellular Proteomics of the Orbitofrontal Cortex of Schizophrenia Patients

Velásquez, E., Martins‐de‐Souza, D., Velásquez, I., Carneiro, G. R. A., Schmitt, A., Falkai, P., Domont, G. B., & Nogueira, F. C. S. (2019) · Journal of Proteome Research · doi:10.1021/acs.jproteome.9b00398 · Cited by 28

FMRP and CYFIP1 at the Synapse and Their Role in Psychiatric Vulnerability

Clifton, N. E., Thomas, K. L., Wilkinson, L. S., Hall, J., & Trent, S. (2020) · Complex Psychiatry · doi:10.1159/000506858 · Cited by 28

Cell Adhesion Molecules and Protein Synthesis Regulation in Neurons

Kozlova, I., Sah, S. K., Keable, R., Leshchyns’ka, I., Janitz, M., & Sytnyk, V. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.592126 · Cited by 27

Synaptic crosstalk conferred by a zone of differentially regulated Ca 2+ signaling in the dendritic shaft adjoining a potentiated spine

Dittmer, P. J., Dell’Acqua, M. L., & Sather, W. A. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902461116 · Cited by 27

Therapeutic effects of extinction learning as a model of exposure therapy in rats

Fucich, E. A., Paredes, D., & Morilak, D. A. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.127 · Cited by 24

Signaling Pathways for Long-Term Memory Formation in the Cricket

Matsumoto, Y., Matsumoto, C. S., & Mizunami, M. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.01014 · Cited by 27

De Novo Protein Synthesis Mediated by the Eukaryotic Elongation Factor 2 Is Required for the Anxiolytic Effect of Oxytocin

Martinetz, S., Meinung, C.-P., Jurek, B., von Schack, D., van den Burg, E. H., Slattery, D. A., & Neumann, I. D. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.01.010 · Cited by 25

The Role of Acupuncture Improving Cognitive Deficits due to Alzheimer’s Disease or Vascular Diseases through Regulating Neuroplasticity

Ji, S., Duan, J., Hou, X., Zhou, L., Qin, W., Niu, H., Luo, S., Zhang, Y., Chan, P., & Jin, X. (2021) · Neural Plasticity · doi:10.1155/2021/8868447 · Cited by 28

Emerging roles of endoplasmic reticulum proteostasis in brain development

Vásquez, G. E., Medinas, D. B., Urra, H., & Hetz, C. A. (2022) · Cells and Development · doi:10.1016/j.cdev.2022.203781 · Cited by 29

CNTNAP2 intracellular domain (CICD) generated by γ-secretase cleavage improves autism-related behaviors

Zhang, J., Cai, F., Lu, R., Xing, X., Xu, L., Wu, K., Gong, Z., Zhang, Q., Zhang, Y., Xing, M., et al. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01431-6 · Cited by 27

A unique binding mode of the eukaryotic translation initiation factor 4E for guiding the design of novel peptide inhibitors

Marino, D. D., D’Annessa, I., Tancredi, H., Bagni, C., & Gallicchio, E. (2015) · Protein Science · doi:10.1002/pro.2708 · Cited by 28

Fragile X syndrome: Are signaling lipids the missing culprits?

Tabet, R., Vitale, N., & Moine, H. (2016) · Biochimie · doi:10.1016/j.biochi.2016.09.002 · Cited by 27

PTEN Activity Defines an Axis for Plasticity at Cortico-Amygdala Synapses and Influences Social Behavior

Sánchez‐Puelles, C., Calleja-Felipe, M., Ouro, A., Bougamra, G., Arroyo, A., Diez, I. P., Erramuzpe, A., Cortés, J. M., Hernández, J. M., Luján, R., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz103 · Cited by 26

Corticosterone-mediated microglia activation affects dendritic spine plasticity and motor learning functions in minimal hepatic encephalopathy

Sun, X., Han, R., Cheng, T., Zheng, Y., Xiao, J., So, K., & Zhang, L. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.08.184 · Cited by 25

Historical perspective and progress on protein ubiquitination at glutamatergic synapses

Mabb, A. M. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108690 · Cited by 24

Control of circadian rhythm on cortical excitability and synaptic plasticity

Lodovichi, C., & Ratto, G. M. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1099598 · Cited by 23

Human umbilical cord-derived mesenchymal stem cells ameliorate perioperative neurocognitive disorder by inhibiting inflammatory responses and activating BDNF/TrkB/CREB signaling pathway in aged mice

Wei, P., Jia, M., Kong, X., Lyu, W., Feng, H., Sun, X., Li, J., & Yang, J. (2023) · Stem Cell Research & Therapy · doi:10.1186/s13287-023-03499-x · Cited by 25

Genes known to escape X chromosome inactivation predict co‐morbid chronic musculoskeletal pain and posttraumatic stress symptom development in women following trauma exposure

Yu, S., Chen, C., Pan, Y., Kurz, M. C., Datner, E. M., Hendry, P. L., Velilla, M., Lewandowski, C., Pearson, C., Domeier, R. M., et al. (2018) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32706 · Cited by 22

Developmental lead (Pb)-induced deficits in hippocampal protein translation at the synapses are ameliorated by ascorbate supplementation

Ahmad, F., Salahuddin, M., Alsamman, K., AlMulla, A. A., & Salama, K. F. (2018) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s174083 · Cited by 23

A Yeast System for Discovering Optogenetic Inhibitors of Eukaryotic Translation Initiation

Lu, H., Mazumder, M., Jaikaran, A. S. I., Kumar, A., Leis, E. K., Xu, X., Altmann, M., Cochrane, A., & Woolley, G. A. (2019) · ACS Synthetic Biology · doi:10.1021/acssynbio.8b00386 · Cited by 23

Germinated Brown Rice Attenuates Cell Death in Vascular Cognitive Impaired Mice and Glutamate-Induced Toxicity In HT22 Cells

Oo, E. M., Ruamyod, K., Khowawisetsut, L., Turbpaiboon, C., Chaisuksunt, V., Uawithya, P., Pholphana, N., Rangkadilok, N., & Chompoopong, S. (2020) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b07957 · Cited by 22

Ferroptosis and cognitive impairment: Unraveling the link and potential therapeutic targets

Naderi, S., Khodagholi, F., Janahmadi, M., Motamedi, F., Torabi, A., Batool, Z., Heydarabadi, M. F., & Pourbadie, H. G. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.110210 · Cited by 23

Exome array analysis suggests an increased variant burden in families with schizophrenia

McCarthy, N. S., Melton, P. E., Ward, S. V., Allan, S. M., Dragović, M., Clark, M. L., Morar, B., Rubio, J. P., Blangero, J., Badcock, J. C., et al. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2016.12.007 · Cited by 21

Repeated Exposure to D-Amphetamine Decreases Global Protein Synthesis and Regulates the Translation of a Subset of mRNAs in the Striatum

Biever, A., Boubaker-Vitre, J., Cutando, L., Gracia‐Rubio, I., Costa‐Mattioli, M., Puighermanal, E., & Valjent, E. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00165 · Cited by 23

Mammalian target of rapamycin complex 1 and its downstream effector collapsin response mediator protein‐2 drive reinstatement of alcohol reward seeking

Hamida, S. B., Laguesse, S., Morisot, N., Park, J., Phuamluong, K., Berger, A. L., Park, K. D., & Dorit Ron, A. (2018) · Addiction Biology · doi:10.1111/adb.12653 · Cited by 21

Selective role of the translin/trax RNase complex in hippocampal synaptic plasticity

Park, A. J., Shetty, M. S., Baraban, J. M., & Abel, T. G. (2020) · Molecular Brain · doi:10.1186/s13041-020-00691-5 · Cited by 20

mRNA Trafficking in the Nervous System: A Key Mechanism of the Involvement of Activity-Regulated Cytoskeleton-Associated Protein (Arc) in Synaptic Plasticity

Fila, M., Diaz, L., Szczepańska, J., Pawłowska, E., & Błasiak, J. (2021) · Neural Plasticity · doi:10.1155/2021/3468795 · Cited by 20

Brain-specific inhibition of mTORC1 eliminates side effects resulting from mTORC1 blockade in the periphery and reduces alcohol intake in mice

Ehinger, Y., Zhang, Z., Phamluong, K., Soneja, D., Shokat, K. M., & Dorit Ron, A. (2021) · Nature Communications · doi:10.1038/s41467-021-24567-x · Cited by 18

Translational control by ketamine and its implications for comorbid cognitive deficits in depressive disorders

Lewis, V., Rodrigue, B., Arsenault, E., Zhang, M., Taghavi‐Abkuh, F., Silva, W. C. C., Myers, M., Matta‐Camacho, E., & Aguilar‐Valles, A. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15652 · Cited by 21

Pharming for Genes in Neurotransmission: Combining Chemical and Genetic Approaches in Caenorhabditis elegans

Blazie, S. M., & Jin, Y. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.7b00509 · Cited by 19

Anatomical correlates of rapid eye movement sleep-dependent plasticity in the developing cortex

Renouard, L., Bridi, M., Coleman, T., Arckens, L., & Frank, M. G. (2018) · SLEEP · doi:10.1093/sleep/zsy124 · Cited by 19

Inhibitors of eIF4G1–eIF1 uncover its regulatory role of ER/UPR stress-response genes independent of eIF2α-phosphorylation

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