The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
HDAC inhibition modulates hippocampus-dependent long-term memory for object location in a CBP-dependent manner
Open accessAbstract
Transcription of genes required for long-term memory not only involves transcription factors, but also enzymatic protein complexes that modify chromatin structure. Chromatin-modifying enzymes, such as the histone acetyltransferase (HAT) CREB (cyclic-AMP response element binding) binding protein (CBP), are pivotal for the transcriptional regulation required for long-term memory. Several studies have shown that CBP and histone acetylation are necessary for hippocampus-dependent long-term memory and hippocampal long-term potentiation (LTP). Importantly, every genetically modified Cbp mutant mouse exhibits long-term memory impairments in object recognition. However, the role of the hippocampus in object recognition is controversial. To better understand how chromatin-modifying enzymes modulate long-term memory for object recognition, we first examined the role of the hippocampus in retrieval of long-term memory for object recognition or object location. Muscimol inactivation of the dorsal hippocampus prior to retrieval had no effect on long-term memory for object recognition, but completely blocked long-term memory for object location. This was consistent with experiments showing that muscimol inactivation of the hippocampus had no effect on long-term memory for the object itself, supporting the idea that the hippocampus encodes spatial information about an object (such as location or context), whereas cortical areas (such as the perirhinal or insular cortex) encode information about the object itself. Using location-dependent object recognition tasks that engage the hippocampus, we demonstrate that CBP is essential for the modulation of long-term memory via HDAC inhibition. Together, these results indicate that HDAC inhibition modulates memory in the hippocampus via CBP and that different brain regions utilize different chromatin-modifying enzymes to regulate learning and memory.
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?
In the citing paper
“Pre-test muscimol microinjections into the dorsal hippocampus was reported to impair (Cohen et al., 2013; Stackman et al., 2016) or not affect (Haettig et al., 2011) NOP memory in mice.”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Haettig et al., 2011
In the citing paper
“Post-sample intra-hippocampus infusion of muscimol impaired long-term NOP (24 hours) memory (Cohen et al., 2013; Haettig et al., 2011), but see (Oliveira et al., 2010).”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Haettig et al., 2011
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
Chromatin modifications and their function
Kouzarides, T. (2007) · Cell · doi:10.1016/j.cell.2007.02.005 · Cited by 10,883
HDAC2 negatively regulates memory formation and synaptic plasticity
Guan, J.-S., Haggarty, S. J., Giacometti, E., Dannenberg, J.-H., Joseph, N., Gao, J., Nieland, T. J. F., Zhou, Y., Wang, X., Mazitschek, R., et al. (2009) · Nature · doi:10.1038/nature07925 · Cited by 1,644
Taverna, S. D., Li, H., Ruthenburg, A. J., Allis, C. D., & Patel, D. J. (2007) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1338 · Cited by 1,476
Regulation of histone acetylation during memory formation in the hippocampus
Levenson, J. M., O'Riordan, K. J., Brown, K. D., Trinh, M. A., Molfese, D. L., & Sweatt, J. D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m402229200 · Cited by 1,131
Spatial memory, recognition memory, and the hippocampus
Broadbent, N. J., Squire, L. R., & Clark, R. E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406344101 · Cited by 985
Chromatin Acetylation, Memory, and LTP Are Impaired in CBP+/− Mice
Alarcón, J. M., Malleret, G., Touzani, K., Vronskaya, S., Ishii, S., Kandel, E. R., & Barco, A. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.021 · Cited by 892
Vecsey, C. G., Hawk, J. D., Lattal, K. M., Stein, J. M., Fabian, S., Attner, M. A., Cabrera, S. M., McDonough, C. B., Brindle, P. K., Abel, T. G., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0296-07.2007 · Cited by 854
CBP Histone Acetyltransferase Activity Is a Critical Component of Memory Consolidation
Korzus, E., Rosenfeld, M. G., & Mayford, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.002 · Cited by 823
Rampon, C., Tang, Y.-P., Goodhouse, J., Shimizu, E., Kyin, M., & Tsien, J. Z. (2000) · Nature Neuroscience · doi:10.1038/72945 · Cited by 755 · cited 1×
“Many studies have found that hippocampal damage impairs memory (Clark et al. 2000; Rampon et al. 2000; Baker and Kim 2002; Gould et al. 2002; Gaskin et al. 2003; Broadbent et al. 2004; Hammond et al. 2004; Prusky et al. 2004; Ainge et al. 2006; de Lima et al. 2006; Rossato et al. 2007), whereas…”
BackgroundImpaired Recognition Memory in Rats after Damage to the Hippocampus
Clark, R. E., Zola, S. M., & Squire, L. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-23-08853.2000 · Cited by 740
Cited by
Sorted by citations
The neuropharmacology of butyrate: the bread and butter of the microbiota-gut-brain axis
Stilling, R. M., van de Wouw, M., Clarke, G., Stanton, C., Dinan, T. G., & Cryan, J. F. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.06.011 · Cited by 891
Histone acetylation: molecular mnemonics on the chromatin
Gräff, J., & Tsai, L.-H. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3427 · Cited by 680
Examining Object Location and Object Recognition Memory in Mice
Vogel‐Ciernia, A., & Wood, M. A. (2014) · Current Protocols in Neuroscience · doi:10.1002/0471142301.ns0831s69 · Cited by 342
HDAC3-selective inhibitor enhances extinction of cocaine-seeking behavior in a persistent manner
Malvaez, M., McQuown, S. C., Rogge, G. A., Astarabadi, M., Jacques, V., Carreiro, S. T., Rusche, J. R., & Wood, M. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1213364110 · Cited by 409
Epigenetic regulation of memory formation and maintenancePreprint
Zovkic, I. B., Karlsson, M. G., & Sweatt, J. D. (2013) · Learning & Memory · doi:10.1101/lm.026575.112 · Cited by 371
The Role of Histone Acetylation in Memory Formation and Cognitive Impairments
Peixoto, L., & Abel, T. G. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.86 · Cited by 353
The Potential of HDAC Inhibitors as Cognitive Enhancers
Gräff, J., & Tsai, L. (2013) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-011112-140216 · Cited by 306
Barrett, R. M., Malvaez, M., Kramar, E., Matheos, D. P., Arrizon, A., Cabrera, S. M., Lynch, G., Greene, R. W., & Wood, M. A. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.61 · Cited by 243
An epigenetic framework for neurodevelopmental disorders: From pathogenesis to potential therapy
Millan, M. J. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.11.015 · Cited by 229
Gupta, S., Franklin, A. V., DeRamus, T. P., Wheelock, M. D., Davis, R. L., McMahon, L. L., & Lubin, F. D. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0147-12.2012 · Cited by 231
Neurocognitive Aging and the Hippocampus across Species
Leal, S. L., & Yassa, M. A. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.10.003 · Cited by 221
How the epigenome integrates information and reshapes the synapse
Campbell, R. R., & Wood, M. A. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0121-9 · Cited by 185
Kumar, A. (2011) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2011.00007 · Cited by 175
Kwapis, J. L., Alaghband, Y., Kramár, E. A., López, A. J., Ciernia, A. V., White, A. O., Shu, G., Rhee, D., Michael, C. M., Montellier, E., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05868-0 · Cited by 175
Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158
Hopkins, M. E., Nitecki, R., & Bucci, D. J. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.07.071 · Cited by 160
Ganai, S. A., Ramadoss, M., & Mahadevan, V. (2015) · Current Neuropharmacology · doi:10.2174/1570159x13666151021111609 · Cited by 161
Neuronal circuitry for recognition memory of object and place in rodent models
Chao, O. Y.-H., Nikolaus, S., Yang, Y., & Huston, J. P. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104855 · Cited by 171
Tcf4 Regulates Synaptic Plasticity, DNA Methylation, and Memory Function
Kennedy, A. J., Rahn, E. J., Paulukaitis, B. S., Savell, K. E., Kordasiewicz, H. B., Wang, J., Lewis, J. W., Posey, J. L., Strange, S. K., Karlsson, M. G., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.004 · Cited by 153
Regulation of object recognition and object placement by ovarian sex steroid hormones
Tuscher, J. J., Fortress, A. M., Kim, J., & Frick, K. M. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.08.001 · Cited by 142
HDAC3 Is a Negative Regulator of Cocaine-Context-Associated Memory Formation
Rogge, G. A., Singh, H., Dang, R., & Wood, M. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4472-12.2013 · Cited by 127
Snigdha, S., Prieto, G. A., Petrosyan, A., Loertscher, B. M., Dieskau, A. P., Overman, L. E., & Cotman, C. W. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2693-15.2016 · Cited by 125
HDAC3 and the molecular brake pad hypothesis
McQuown, S. C., & Wood, M. A. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.04.005 · Cited by 126
Differential roles for Nr4a1 and Nr4a2 in object location vs. object recognition long-term memory
McNulty, S. E., Barrett, R. M., Vogel-Ciernia, A., Malvaez, M., Hernandez, N., Davatolhagh, M. F., Matheos, D. P., Schiffman, A., & Wood, M. A. (2012) · Learning & Memory · doi:10.1101/lm.026385.112 · Cited by 117
Dharmalingam, P., Gopinath, K., & Sudhandiran, G. (2013) · NeuroMolecular Medicine · doi:10.1007/s12017-012-8210-1 · Cited by 122
Zhao, Z., Fan, L., Fortress, A. M., Boulware, M. I., & Frick, K. M. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5819-11.2012 · Cited by 115
Epigenetic mechanisms of memory formation and reconsolidation
Jarome, T. J., & Lubin, F. D. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.08.002 · Cited by 116
Benoit, J. D., RAKIC, P. T., & Frick, K. M. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.12.001 · Cited by 119
Insights into neuroepigenetics through human histone deacetylase PET imaging
Wey, H., Gilbert, T. M., Zürcher, N. R., She, A., Bhanot, A., Taillon, B. D., Schroeder, F. A., Wang, C., Haggarty, S. J., & Hooker, J. M. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf7551 · Cited by 108
Yu, C., Chang, P., Hsin, L., & Chern, J. (2013) · Journal of Medicinal Chemistry · doi:10.1021/jm400564j · Cited by 106
Hernandez, M. X., Jiang, S., Cole, T. A., Chu, S., Fonseca, M. I., Fang, M. J., Hohsfield, L. A., Torres, M. D., Green, K. N., Wetsel, R. A., et al. (2017) · Molecular Neurodegeneration · doi:10.1186/s13024-017-0210-z · Cited by 104
Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
Van‐Gils, J., Magdinier, F., Fergelot, P., & Lacombe, D. (2021) · Genes · doi:10.3390/genes12070968 · Cited by 103
HippoBellum: Acute Cerebellar Modulation Alters Hippocampal Dynamics and Function
Zeidler, Z., Hoffmann, K., & Krook-Magnuson, E. I. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0763-20.2020 · Cited by 102
Reolon, G. K., Maurmann, N., Werenicz, A., Garcia, V. A., Schröder, N., Wood, M. A., & Roesler, R. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.03.033 · Cited by 101
Integrin Dynamics Produce a Delayed Stage of Long-Term Potentiation and Memory Consolidation
Babayan, A. H., Kramár, E. A., Barrett, R. M., Jafari, M., Häettig, J., Chen, L. Y., Rex, C. S., Lauterborn, J. C., Wood, M. A., Gall, C. M., et al. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.2024-12.2012 · Cited by 93
Hawk, J. D., Florian, C., & Abel, T. (2011) · Learning & Memory · doi:10.1101/lm.2097411 · Cited by 98
Tuscher, J. J., Taxier, L. R., Fortress, A. M., & Frick, K. M. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.11.002 · Cited by 88
Understanding Epigenetics in the Neurodegeneration of Alzheimer’s Disease: SAMP8 Mouse Model
Griñán‐Ferré, C., Corpas, R., Puigoriol‐Illamola, D., Palomera‐Ávalos, V., Sanfeliu, C., & Pallàs, M. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-170664 · Cited by 86
Welbat, J. U., Naewla, S., Pannangrong, W., Sirichoat, A., Aranarochana, A., & Wigmore, P. M. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.114083 · Cited by 87
Zeidler, Z., Brandt-Fontaine, M., Leintz, C., Krook-Magnuson, C., Netoff, T. I., & Krook-Magnuson, E. I. (2018) · eNeuro · doi:10.1523/eneuro.0158-18.2018 · Cited by 83
López, A. J., Kramár, E. A., Matheos, D. P., White, A. O., Kwapis, J. L., Ciernia, A. V., Sakata, K., Espinoza, M. E., & Wood, M. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3682-15.2016 · Cited by 80
How Our Other Genome Controls Our Epi-Genome
Celluzzi, A., & Masotti, A. (2016) · Trends in Microbiology · doi:10.1016/j.tim.2016.05.005 · Cited by 81
Castellano, J. F., Fletcher, B. R., Kelley-Bell, B., Kim, D. H., Gallagher, M., & Rapp, P. R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033249 · Cited by 84
Fortress, A. M., Kim, J., Poole, R. L., Gould, T. J., & Frick, K. M. (2014) · Learning & Memory · doi:10.1101/lm.034033.113 · Cited by 79
Wang, W., Pan, Y.-W., Zou, J., Li, T., Abel, G. M., Palmiter, R. D., Storm, D. R., & Xia, Z. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3324-13.2014 · Cited by 76
Genes and epigenetic processes as prospective pain targets
Crow, M., Denk, F., & McMahon, S. B. (2013) · Genome Medicine · doi:10.1186/gm416 · Cited by 73
Federman, N., de la Fuente, V., Zalcman, G., Corbi, N., Onori, A., Passananti, C., & Romano, A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.4181-12.2013 · Cited by 73
Role of nucleosome remodeling in neurodevelopmental and intellectual disability disorders
López, A. J., & Wood, M. A. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00100 · Cited by 74
Audrain, M., Haure-Mirande, J.-V., Wang, M., Kim, S. H., Fanutza, T., Chakrabarty, P., Fraser, P., St George-Hyslop, P. H., Golde, T. E., Blitzer, R. D., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-018-0258-3 · Cited by 68
Cognition-Enhancing Vagus Nerve Stimulation Alters the Epigenetic Landscape
Sanders, T. H., Weiss, J. B., Hogewood, L., Chen, L., Paton, C., McMahan, R. L., & Sweatt, J. D. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2407-18.2019 · Cited by 71
Frick, K. M. (2012) · Behavioral Neuroscience · doi:10.1037/a0026660 · Cited by 68
The NR4A orphan nuclear receptors mediate transcription-dependent hippocampal synaptic plasticity
Bridi, M. S., & Abel, T. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.06.020 · Cited by 66
Griñán‐Ferré, C., Puigoriol‐Illamola, D., Palomera‐Ávalos, V., Pérez-Cáceres, D., Companys‐Alemany, J., Camins, A., Ortuño‐Sahagún, D., Rodrigo, T., & Pallàs, M. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00241 · Cited by 67
Epigenetics of Memory and Plasticity
Woldemichael, B. T., Bohacek, J., Gapp, K., & Mansuy, I. M. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00011-8 · Cited by 66
Krishna, K., Behnisch, T., & Sajikumar, S. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-150838 · Cited by 64
Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
Park, E., Kim, Y., Ryu, H., Kowall, N. W., Lee, J., & Ryu, H. (2014) · NeuroMolecular Medicine · doi:10.1007/s12017-013-8285-3 · Cited by 63
Fujita, Y., Morinobu, S., Takei, S., Fuchikami, M., Matsumoto, T., Yamamoto, S., & Yamawaki, S. (2012) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2012.01.026 · Cited by 66
Naewla, S., Sirichoat, A., Pannangrong, W., Chaisawang, P., Wigmore, P. M., & Welbat, J. U. (2019) · Nutrients · doi:10.3390/nu11040936 · Cited by 63
Epigenetic regulation of estrogen-dependent memory
Fortress, A. M., & Frick, K. M. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.05.001 · Cited by 64
Seese, R. R., Maske, A. R., LYNCH, G. S., & Gall, C. M. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.13 · Cited by 62
Epigenetic Mechanisms in Experience-Driven Memory Formation and Behavior
Puckett, R. E., & Lubin, F. D. (2011) · Epigenomics · doi:10.2217/epi.11.86 · Cited by 67
Hou, N., Ren, L., Gong, M., Bi, Y., Gu, Y., Dong, Z., Liu, Y., Chen, J., & Li, T. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8741-6 · Cited by 61
Klotho regulates postnatal neurogenesis and protects against age-related spatial memory loss
Laszczyk, A. M., Fox, S. N., Vo, H. T., Nettles, D., Pugh, P. C., Overstreet‐Wadiche, L., & King, G. D. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.07.008 · Cited by 61
Sharma, B., & Sharma, P. (2013) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2013.07.017 · Cited by 59
Pharmacological Activators of the NR4A Nuclear Receptors Enhance LTP in a CREB/CBP-Dependent Manner
Bridi, M. S., Hawk, J. D., Chatterjee, S., Safe, S. H., & Abel, T. G. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.253 · Cited by 61
Sorial, M. E. S., & Sayed, N. S. E. (2017) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-017-1357-4 · Cited by 58
da Silva, P. F., Garcia, V. A., Dornelles, A. D. S., da Silva, V. K., Maurmann, N., Portal, B. C. D., Ferreira, R. D. P., Piazza, F. C., Roesler, R., & Schröder, N. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.10.038 · Cited by 59
Pérez-García, G., Guzmán‐Quevedo, O., Aragão, R. D. S., & Bolaños‐Jiménez, F. (2016) · Scientific Reports · doi:10.1038/srep21275 · Cited by 59
Spaced training rescues memory and ERK1/2 signaling in fragile X syndrome model mice
Seese, R. R., Wang, K., Yao, Y. Q., Lynch, G., & Gall, C. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1413335111 · Cited by 52
Postsynaptic GABABReceptor Activity Regulates Excitatory Neuronal Architecture and Spatial Memory
Terunuma, M., Revilla-Sanchez, R., Quadros, I. M., Deng, Q., Deeb, T. Z., Lumb, M. J., Siciński, P., Haydon, P. G., Pangalos, M. N., & Moss, S. J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3320-13.2013 · Cited by 57
Anterior retrosplenial cortex is required for long-term object recognition memory
de Landeta, A. B., Pereyra, M., Medina, J. H., & Katche, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-60937-z · Cited by 55
Jarome, T. J., Perez, G., Webb, W. M., Hatch, K. M., Navabpour, S., Musaus, M., Farrell, K., Hauser, R. M., McFadden, T., Martin, K., et al. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.12.029 · Cited by 52
Tu, F., Pang, Q., Huang, T., Zhao, Y., Liu, M., & Chen, X. '. (2017) · Medical Science Monitor · doi:10.12659/msm.902770 · Cited by 54
Age-associated gut microbiota impairs hippocampus-dependent memory in a vagus-dependent manner
Rei, D., Saha, S., Haddad, M., Rubio, A. H., Perlaza, B. L., Berard, M., Ungeheuer, M., Sokol, H., & Lledo, P. (2022) · JCI Insight · doi:10.1172/jci.insight.147700 · Cited by 51
Kumar, D. B. U., Aggarwal, M., Kaas, G. A., Lewis, J., Wang, J., Ross, D. L., Zhong, C., Kennedy, A. J., Song, H., & Sweatt, J. D. (2015) · Neuroepigenetics · doi:10.1016/j.nepig.2015.10.002 · Cited by 49
Koss, W. A., & Frick, K. M. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.01.002 · Cited by 47
Haettig, J., Sun, Y., Wood, M. A., & Xu, X. (2013) · Learning & Memory · doi:10.1101/lm.027847.112 · Cited by 41
FGF-23 Deficiency Impairs Hippocampal-Dependent Cognitive Function
Laszczyk, A. M., Nettles, D., Pollock, T. A., Fox, S. N., Garcia, M. L., Wang, J., Quarles, L. D., & King, G. D. (2019) · eNeuro · doi:10.1523/eneuro.0469-18.2019 · Cited by 46
From Circuits to Chromatin: The Emerging Role of Epigenetics in Mental Health
Mews, P., Calipari, E. S., Day, J. J., Lobo, M. K., Bredy, T. W., & Abel, T. G. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1649-20.2020 · Cited by 42
Li, D., Jing, D., Liu, Z., Chen, Y., Huang, F., & Behnisch, T. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00133 · Cited by 43
Beldjoud, H., Barsegyan, A., & Roozendaal, B. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00108 · Cited by 44
Novelty and Novel Objects Increase c-Fos Immunoreactivity in Mossy Cells in the Mouse Dentate Gyrus
Bernstein, H. L., Lu, Y.-L., Botterill, J. J., & Scharfman, H. E. (2019) · Neural Plasticity · doi:10.1155/2019/1815371 · Cited by 44
Therapeutic Potential of Isoform Selective Hdac Inhibitors for the Treatment of Schizophrenia
Weïwer, M., Lewis, M. C., Wagner, F. F., & Holson, E. B. (2013) · Future Medicinal Chemistry · doi:10.4155/fmc.13.141 · Cited by 42
Ciernia, A. V., Pride, M. C., Durbin-Johnson, B. P., Noronha, A. B., Chang, A., Yasui, D. H., Crawley, J. N., & LaSalle, J. M. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx087 · Cited by 39
Blank, M., Dornelles, A. D. S., Werenicz, A., Velho, L. A., Pinto, D. F., Fedi, A. C., Schröder, N., & Roesler, R. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.02.009 · Cited by 40
Critical aspects of neurodevelopment
Chakraborty, R., Kumar, M., & Clement, J. P. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107415 · Cited by 41
Epigenetic Factors in Intellectual Disability
López‐Atalaya, J. P., Valor, L. M., & Barco, Á. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-800977-2.00006-1 · Cited by 44
Rossetti, F., Furtado, M. D. A., Pak, T. K., Bailey, K., Shields, M. C., Chanda, S., Addis, M., Robertson, B. D., Moffett, M. C., Lumley, L. A., et al. (2012) · NeuroToxicology · doi:10.1016/j.neuro.2012.02.010 · Cited by 38
Epigenetic contributions to cognitive aging: disentangling mindspan and lifespanPreprint
Spiegel, A. M., Sewal, A. S., & Rapp, P. R. (2014) · Learning & Memory · doi:10.1101/lm.033506.113 · Cited by 38
TIP60 in aging and neurodegeneration
Li, Z., & Rasmussen, L. J. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101195 · Cited by 37
Upadhya, D., Kodali, M., Gitaí, D. L. G., de Castro, O. W., Zanirati, G., Upadhya, R., Attaluri, S., Mitra, E., Shuai, B., Hattiangady, B., et al. (2019) · Aging and Disease · doi:10.14336/ad.2019.0720 · Cited by 38
Jia, M., Liu, W., Sun, H.-L., Chang, Y.-Q., Yang, J., Ji, M.-H., Yang, J.-J., & Feng, C. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00052 · Cited by 36
Epigenetics, Oestradiol and Hippocampal Memory Consolidation
Frick, K. M. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12106 · Cited by 39
Zhong, T., Guo, Q., Zou, W., Zhu, X., Song, Z., Sun, B., He, X., & Yang, Y. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125815 · Cited by 37
Aging mice show impaired memory updating in the novel OUL updating paradigm
Kwapis, J. L., Alaghband, Y., Keiser, A. A., Dong, T. N., Michael, C. M., Rhee, D., Shu, G., Dang, R., Matheos, D. P., & Wood, M. A. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0438-0 · Cited by 43
HDAC Inhibition Facilitates the Switch between Memory Systems in Young But Not Aged Mice
Dagnas, M., Guillou, J., Prévot, T. D., & Mons, N. E. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3453-12.2013 · Cited by 42
Faillace, M. P., Pisera-Fuster, A., Medrano, M. P., Bejarano, A., & Bernabeu, R. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4532-x · Cited by 35
Epigenetic Regulation of the Molecular Clockwork
Eckel‐Mahan, K. L., & Sassone‐Corsi, P. (2013) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-396971-2.00002-6 · Cited by 35
New innovations: Therapeutic opportunities for intellectual disabilities
Picker, J. D., & Walsh, C. A. (2013) · Annals of Neurology · doi:10.1002/ana.24002 · Cited by 38
Alaghband, Y., Kwapis, J. L., López, A. J., White, A. O., Aimiuwu, O. V., Al-Kachak, A., Bodinayake, K. K., Oparaugo, N. C., Dang, R., Astarabadi, M., et al. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.09.001 · Cited by 34
Metadata
- Authors
- Haettig, J., Stefanko, D. P., Multani, M. L., Figueroa, D. X., McQuown, S. C., & Wood, M. A.
- Affiliations
- University of California, Irvine (US)
- Venue
- Learning & Memory
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2011-01-11
- Volume
- 18
- Issue
- 2
- Pages
- 71-79
- ISSN
- 1072-0502 (ISSN-L)
- 1549-5485
- PMC
- PMC3032579
- OpenAlex
- W2159726740
- Cited by
- 211
- References
- 38
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 5 · 2023: 5 · 2022: 15 · 2021: 12 · 2020: 16 · 2019: 20 · 2018: 12 · 2017: 18 · 2016: 21 · 2015: 9 · 2014: 21 · 2013: 25 · 2012: 13
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Learning & Memory (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Whitehall Foundation
- National Institute of Mental Health (R01MH081004)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Histone Deacetylase Inhibitors Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- histone deacetylase inhibition, CBP, CREB-binding protein, hippocampal-dependent memory, object location memory, object recognition memory, long-term memory, chromatin modification, histone acetylation, muscimol inactivation, spatial memory, memory retrieval, hippocampal long-term potentiation
- MeSH terms
- Animals, Hippocampus, Histone Deacetylases, Immunohistochemistry, Learning, Male, Mice, Inbred C57BL, Mice, Mutant Strains, Muscimol, CREB-Binding Protein, Mice, Gene Knock-In Techniques, Histone Deacetylase Inhibitors, Memory, Long-Term, GABA-A Receptor Agonists
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