Stimulus-Transcription Coupling in the Nervous System: Involvement of the Inducible Proto-Oncogenes fos and jun

The Leucine Zipper: A Hypothetical Structure Common to a New Class of DNA Binding Proteins

Landschulz, W. H., Johnson, P. F., & McKnight, S. L. (1988) · Science · doi:10.1126/science.3289117 · Cited by 3,443

Expression of c- fos Protein in Brain: Metabolic Mapping at the Cellular Level

Sagar, S. M., Sharp, F. R., & Curran, T. (1988) · Science · doi:10.1126/science.3131879 · Cited by 1,925

DNA related to the transforming gene(s) of avian sarcoma viruses is present in normal avian DNA

STEHELIN, D., VARMUS, H. E., BISHOP, J. M., & VOGT, P. K. (1976) · Nature · doi:10.1038/260170a0 · Cited by 1,321

Human Proto-Oncogene c- jun Encodes a DNA Binding Protein with Structural and Functional Properties of Transcription Factor AP-1

Bohmann, D., Bos, T. J., Admon, A., Nishimura, T., Vogt, P. K., & Tjian, R. (1987) · Science · doi:10.1126/science.2825349 · Cited by 1,321

Stimulus-transcription coupling in neurons: role of cellular immediate-early genes

Morgan, J. I., & Curran, T. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90096-9 · Cited by 969

Identification of a set of genes expressed during the G0/G1 transition of cultured mouse cells.

Lau, L. F., & Nathans, D. (1985) · The EMBO Journal · doi:10.1002/j.1460-2075.1985.tb04057.x · Cited by 567

Regulation of the Hypothalamic-Pituitary-Adrenal Axis by Cytokines: Actions and Mechanisms of Action

TURNBULL, A. V., & RIVIER, C. L. (1999) · Physiological Reviews · doi:10.1152/physrev.1999.79.1.1 · Cited by 1,297

Cell type-specific loss of BDNF signaling mimics optogenetic control of cocaine reward

Lobo, M. K., Covington, H. E., Chaudhury, D., Friedman, A. K., Sun, H., Damez-Werno, D., Dietz, D. M., Zaman, S., Koo, J. W., Kennedy, P. J., et al. (2010) · Science · doi:10.1126/science.1188472 · Cited by 880

Neurobiology of relapse to heroin and cocaine seeking: a review

Shalev, U., Grimm, J. W., & Shaham, Y. (2002) · Pharmacological Reviews · doi:10.1124/pr.54.1.1 · Cited by 880

Multiple promoters direct tissue-specific expression of the rat BDNF gene

Timmusk, T., Palm, K., Metsis, M., Reintam, T., Paalme, V., Saarma, M., & Persson, H. (1993) · Neuron · doi:10.1016/0896-6273(93)90335-o · Cited by 858

Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality.

Chae, T., Kwon, Y. T., Bronson, R., Dikkes, P., Li, E., & Tsai, L.-H. (1997) · Neuron · doi:10.1016/s0896-6273(01)80044-1 · Cited by 715

Identification and characterization of Ref‐1, a nuclear protein that facilitates AP‐1 DNA‐binding activity.

Xanthoudakis, S., & Curran, T. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05097.x · Cited by 708

C/EBP is an immediate-early gene required for the consolidation of long-term facilitation in Aplysia

Alberini, C. M., Ghirardl, M., Metz, R., & Kandel, E. R. (1994) · Cell · doi:10.1016/0092-8674(94)90386-7 · Cited by 523

Activation of Corticotropin-Releasing Factor in the Limbic System During Cannabinoid Withdrawal

Rodrı́guez de Fonseca, F., Carrera, M. R. A., Navarro, M., Koob, G. F., & Weiss, F. (1997) · Science · doi:10.1126/science.276.5321.2050 · Cited by 499

Normally occurring environmental and behavioral influences on gene activity: From central dogma to probabilistic epigenesis

Gottlieb, G. (1998) · Psychological Review · doi:10.1037/0033-295x.105.4.792-802 · Cited by 489

Type 1 interleukin‐1 receptor in the rat brain: Distribution, regulation, and relationship to sites of IL‐1–induced cellular activation

Ericsson, A., Liu, C., Hart, R. P., & Sawchenko, P. E. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903610410 · Cited by 471

Lhx6 delineates a pathway mediating innate reproductive behaviors from the amygdala to the hypothalamus

Choi, G. B., Dong, H.-W., Murphy, A. J., Valenzuela, D. M., Yancopoulos, G. D., Swanson, L. W., & Anderson, D. J. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.011 · Cited by 462

Gene regulation in the immediate-early response process

Bahrami, S., & Drabløs, F. (2016) · Advances in Biological Regulation · doi:10.1016/j.jbior.2016.05.001 · Cited by 465

BDNF and epilepsy: too much of a good thing?

Binder, D. K., Croll, S. D., Gall, C. M., & Scharfman, H. E. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01682-9 · Cited by 454

Nuclear RNA-seq of single neurons reveals molecular signatures of activation

Lacar, B., Linker, S. B., Jaeger, B. N., Krishnaswami, S. R., Barron, J. J., Kelder, M. J. E., Parylak, S. L., Paquola, A. C. M., Venepally, P., Novotny, M., et al. (2016) · Nature Communications · doi:10.1038/ncomms11022 · Cited by 405

Activity-dependent regulation of conductances in model neurons

LeMasson, G., Marder, E., & Abbott, L. F. (1993) · Science · doi:10.1126/science.8456317 · Cited by 323

The Genomic Action Potential

Clayton, D. F. (2000) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2000.3967 · Cited by 322

Sequence of stress-induced alterations in indices of synaptic and transcriptional activation in parvocellular neurosecretory neurons

Kovacs, K., & Sawchenko, P. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-01-00262.1996 · Cited by 310

Stress History and Pubertal Development Interact to Shape Hypothalamic-Pituitary-Adrenal Axis Plasticity

Romeo, R. D., Bellani, R., Karatsoreos, I. N., Chhua, N., Vernov, M., Conrad, C. D., & McEwen, B. S. (2006) · Endocrinology · doi:10.1210/en.2005-1432 · Cited by 304

Augmentation of drug reward by chronic food restriction

Carr, K. D. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00759-x · Cited by 300

Developmental programming of hypothalamic feeding circuits

Bouret, S., & Simerly, R. (2006) · Clinical Genetics · doi:10.1111/j.1399-0004.2006.00684.x · Cited by 227

Minireview: Leptin and Development of Hypothalamic Feeding Circuits

Bouret, S. G., & Simerly, R. B. (2004) · Endocrinology · doi:10.1210/en.2004-0231 · Cited by 210

Cannabidiol inhibits the hyperlocomotion induced by psychotomimetic drugs in mice

Moreira, F. A., & Guimarães, F. S. (2005) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2005.02.040 · Cited by 206

Neural activation following sexual behavior in the male and female rat brain

Veening, J. G., & Coolen, L. M. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00190-3 · Cited by 200

Identification of an immune-responsive mesolimbocortical serotonergic system: potential role in regulation of emotional behavior

Lowry, C. A., Hollis, J. H., de Vries, A., Pan, B., Brunet, L. R., Hunt, J. R. F., Paton, J. F. R., van Kampen, E., Knight, D. M., Evans, A. K., et al. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.01.067 · Cited by 199

Striatal Fos expression is indicative of dopamine D1/D2 synergism and receptor supersensitivity.

LaHoste, G. J., Yu, J., & Marshall, J. F. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.16.7451 · Cited by 182

Role of Tumor Necrosis Factor-α in Methamphetamine-Induced Drug Dependence and Neurotoxicity

Nakajima, A., Yamada, K., Nagai, T., Uchiyama, T., Miyamoto, Y., Mamiya, T., He, J., Nitta, A., Mizuno, M., Tran, M. H., et al. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.4847-03.2004 · Cited by 176

Glucocorticoid Negative Feedback Selectively Targets Vasopressin Transcription in Parvocellular Neurosecretory Neurons

Kovács, K. J., Földes, A., & Sawchenko, P. E. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-10-03843.2000 · Cited by 172

The anterior insular cortex→central amygdala glutamatergic pathway is critical to relapse after contingency management

Venniro, M., Caprioli, D., Zhang, M., Whitaker, L. R., Zhang, S., Warren, B. L., Cifani, C., Marchant, N. J., Yizhar, O., Bossert, J. M., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.024 · Cited by 162

A Brief Introduction to the Transduction of Neural Activity into Fos Signal

Chung, L. (2015) · Development & Reproduction · doi:10.12717/dr.2015.19.2.061 · Cited by 164

A non-canonical pathway from cochlea to brain signals tissue-damaging noise

Flores, E. N., Duggan, A., Madathany, T., Hogan, A. K., Márquez, F. G., Kumar, G., Seal, R. P., Edwards, R. H., Liberman, M. C., & García-Añoveros, J. (2015) · Current Biology · doi:10.1016/j.cub.2015.01.009 · Cited by 161

Functional organisation of central cardiovascular pathways: studies using c-fos gene expression

Dampney, R. A. L., & Horiuchi, J. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.11.001 · Cited by 157

Projections of the suprachiasmatic nucleus to stress-related areas in the rat hypothalamus: A light and electron microscopic study

Buijs, R. M., Markman, M., Nunes‐Cardoso, B., Hou, Y., & Shinn, S. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903350104 · Cited by 153

Puberty and the maturation of the male brain and sexual behavior: recasting a behavioral potential

Romeo, R. D., Richardson, H. N., & Sisk, C. L. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00009-x · Cited by 152

Losing Control: Excessive Alcohol Seeking after Selective Inactivation of Cue-Responsive Neurons in the Infralimbic Cortex

Pfarr, S., Meinhardt, M. W., Klee, M. L., Hansson, A. C., Vengeliene, V., Schonig, K., Bartsch, D., Hope, B. T., Spanagel, R., & Sommer, W. H. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0684-15.2015 · Cited by 143

Vasopressinergic regulation of the hypothalamic pituitary adrenal axis and stress adaptation

Volpi, S., Rabadan-Diehl, C., & Aguilera, G. (2004) · Stress · doi:10.1080/10253890410001733535 · Cited by 136

Tissue inhibitor of metalloproteinases-1 (TIMP-1) is differentially induced in neurons and astrocytes after seizures: evidence for developmental, immediate early gene, and lesion response.

Rivera, S., Tremblay, E., Timsit, S., Canals, O., Ben-Ari, Y., & Khrestchatisky, M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04223.1997 · Cited by 135

Interleukin-6-Induced STAT3 and AP-1 Amplify Hepatocyte Nuclear Factor 1-Mediated Transactivation of Hepatic Genes, an Adaptive Response to Liver Injury

Leu, J. I., Crissey, M. A. S., Leu, J. P., Ciliberto, G., & Taub, R. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.2.414-424.2001 · Cited by 134

In situ hybridization analysis of vasopressin gene transcription in the paraventricular and supraoptic nuclei of the rat: Regulation by stress and glucocorticoids

Herman, J. P. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903630103 · Cited by 129

Neuronal Activity Increases the Phosphorylation of the Transcription Factor cAMP Response Element-binding Protein (CREB) in Rat Hippocampus and Cortex

Moore, A. N., Waxham, M. N., & Dash, P. K. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.24.14214 · Cited by 126

Differential psychostimulant-induced activation of neural circuits in dopamine transporter knockout and wild type mice

Trinh, J. V., Nehrenberg, D. L., Jacobsen, J. P. R., Caron, M. G., & Wetsel, W. C. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00165-9 · Cited by 113

Dietary Therapy Mitigates Persistent Wake Deficits Caused by Mild Traumatic Brain Injury

Lim, M. M., Elkind, J., Xiong, G., Galante, R., Zhu, J., Zhang, L., Lian, J., Rodin, J., Kuzma, N. N., Pack, A. I., et al. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3007092 · Cited by 113

The neuropharmacology of relapse to food seeking: Methodology, main findings, and comparison with relapse to drug seeking

Nair, S. G., Adams-Deutsch, T., Epstein, D. H., & Shaham, Y. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.05.003 · Cited by 112

Acute amygdaloid response to systemic inflammation.

Engler, H., Doenlen, R., Engler, A., Riether, C., Prager, G., Niemi, M.-B., Pacheco-López, G., Krügel, U., & Schedlowski, M. (2011) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2011.04.005 · Cited by 108

Activity-dependent current distributions in model neurons

Siegel, M., Marder, E., & Abbott, L. F. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.24.11308 · Cited by 91

Integration of vestibular and emetic gastrointestinal signals that produce nausea and vomiting: potential contributions to motion sickness

Yates, B. J., Catanzaro, M. F., Miller, D. J., & McCall, A. A. (2014) · Experimental Brain Research · doi:10.1007/s00221-014-3937-6 · Cited by 90

Distinct Tissue-Specific Roles for Thyroid Hormone Receptors β and α1 in Regulation of Type 1 Deiodinase Expression

Amma, L. L., Campos-Barros, A., Wang, Z., Vennström, B., & Forrest, D. (2001) · Molecular Endocrinology · doi:10.1210/mend.15.3.0605 · Cited by 94

Role of central amygdala neuronal ensembles in incubation of nicotine craving

Funk, D., Coen, K., Tamadon, S., Hope, B. T., Shaham, Y., & Lê, A. D. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1505-16.2016 · Cited by 87

Prevention of Cannabinoid Withdrawal Syndrome by Lithium: Involvement of Oxytocinergic Neuronal Activation

Cui, S.-S., Bowen, R. C., Gu, G.-B., Hannesson, D. K., Yu, P. H., & Zhang, X. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09867.2001 · Cited by 84

Cellular activation in limbic brain systems during social play behaviour in rats

van Kerkhof, L. W. M., Trezza, V., Mulder, T., Gao, P., Voorn, P., & Vanderschuren, L. J. M. J. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0558-y · Cited by 83

Brain-derived neurotrophic factor induces matrix metalloproteinase 9 expression in neurons via the serum response factor/c-Fos pathway

Kuzniewska, B., Rejmak, E., Malik, A. R., Jaworski, J., Kaczmarek, L., & Kalita, K. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.00008-13 · Cited by 82

Tuberoinfundibular peptide of 39 residues is activated during lactation and participates in the suckling-induced prolactin release in rat

Cservenák, M., Bodnár, I., Usdin, T. B., Palkovits, M., Nagy, G. M., & Dobolyi, A. (2010) · Endocrinology · doi:10.1210/en.2010-0767 · Cited by 82

Brain activation following peripheral administration of the GLP-1 receptor agonist exendin-4

Baraboi, E.-D., St-Pierre, D. H., Shooner, J., Timofeeva, E., & Richard, D. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00424.2010 · Cited by 79

Identification of Brain Nuclei Implicated in Cocaine-Primed Reinstatement of Conditioned Place Preference: A Behaviour Dissociable from Sensitization

Brown, R. M., Short, J. L., & Lawrence, A. J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015889 · Cited by 69

Redox Regulation of Ap-1

Xanthoudakis, S., & Curran, T. (1996) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4757-9480-9_10 · Cited by 63

Neural Circuits Controlling Cardiorespiratory Responses: Baroreceptor And Somatic Afferents In The Nucleus Tractus Solitarius

Potts, J. T. (2002) · Clinical and Experimental Pharmacology and Physiology · doi:10.1046/j.1440-1681.2002.03613.x · Cited by 60

Proto-Oncogenes of the fos/jun Family of Transcription Factors are Positive Regulators of Myeloid Differentiation

Lord, K. A., Abdollahi, A., Hoffman-Liebermann, B., & Liebermann, D. A. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.2.841-851.1993 · Cited by 54

Insensitivity of the hippocampus to environmental stimulation during postnatal development

Waters, N. S., Klintsova, A. Y., & Foster, T. C. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-20-07967.1997 · Cited by 46

Neuroimmune stress responses: reciprocal connections between the hypothalamus and the brainstem

Buller, K. M. (2003) · Stress · doi:10.1080/1025389031000092313 · Cited by 41

Gene expression in learning processes

Kaczmarek, L. (2000) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2000-1361 · Cited by 44

Vagus nerve stimulation inhibits heroin-seeking behavior induced by heroin priming or heroin-associated cues in rats

Liu, H., Liu, Y., Yu, J., Lai, M., Zhu, H., Sun, A., Chen, W., & Zhou, W. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.02.059 · Cited by 40

Unacylated-Ghrelin Impairs Hippocampal Neurogenesis and Memory in Mice and Is Altered in Parkinson’s Dementia in Humans

Hornsby, A. K. E., Buntwal, L., Carisi, M. C., Santos, V. V., Johnston, F., Roberts, L. D., Sassi, M., Mequinion, M., Stark, R., Reichenbach, A., et al. (2020) · Cell Reports Medicine · doi:10.1016/j.xcrm.2020.100120 · Cited by 35

Widespread expression of functional D1-dopamine receptors in fetal rat brain

Shearman, L. P., Zeitzer, J., & Weaver, D. R. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00091-6 · Cited by 35

Characterization and phosphorylation of CREB-like proteins in Aplysia central nervous system

Dash, P. K., & Moore, A. N. (1996) · Molecular Brain Research · doi:10.1016/0169-328x(95)00350-2 · Cited by 27

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Salin (1998) · doi:10.1002/(sici)1096-9861(19980720)397:1<41::aid-cne4>3.0.co;2-i

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Herman (2000) · doi:10.1002/1096-9861(20000703)422:3<352::aid-cne3>3.0.co;2-f

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(2002) · doi:10.14670/hh-17.1137