The addicted synapse: mechanisms of synaptic and structural plasticity in nucleus accumbens

Long-Term Potentiation--A Decade of Progress?

Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729

Structural basis of long-term potentiation in single dendritic spines

Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483

Dopamine reward circuitry: Two projection systems from the ventral midbrain to the nucleus accumbens–olfactory tubercle complex

Ikemoto, S. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.05.004 · Cited by 1,477

The many faces of CREB

Carlezon, W. A., Duman, R. S., & Nestler, E. J. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.06.005 · Cited by 1,382

Changing subunit composition of heteromeric NMDA receptors during development of rat cortex

Sheng, M., Cummings, J., Roldan, L. A., Jan, Y. N., & Jan, L. Y. (1994) · Nature · doi:10.1038/368144a0 · Cited by 1,377

A translational profiling approach for the molecular characterization of CNS cell types

Heiman, M., Schaefer, A., Gong, S., Peterson, J. D., Day, M., Ramsey, K. E., Suárez-Fariñas, M., Schwarz, C., Stephan, D. A., Surmeier, D. J., et al. (2008) · Cell · doi:10.1016/j.cell.2008.10.028 · Cited by 1,134

Transient and persistent dendritic spines in the neocortex in vivo

Holtmaat, A. J. G. D., Trachtenberg, J. T., Wilbrecht, L., Shepherd, G. M., Zhang, X., Knott, G. W., & Svoboda, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.003 · Cited by 1,131

Structural plasticity associated with exposure to drugs of abuse

Robinson, T. E., & Kolb, B. E. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.06.025 · Cited by 1,130

Molecular mechanisms of drug addiction

Nestler, E. J. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.06.031 · Cited by 1,108

Three-dimensional structure of dendritic spines and synapses in rat hippocampus (CA1) at postnatal day 15 and adult ages: implications for the maturation of synaptic physiology and long-term potentiation [published erratum appears in J Neurosci 1992 Aug;12(8):following table of contents]

Harris, K. M., Jensen, F. E., & Tsao, B. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-07-02685.1992 · Cited by 1,036

Cdc42 signaling regulated by dopamine D2 receptor correlatively links specific brain regions of hippocampus to cocaine addiction

Li, J., Wu, Y. H., Xue, T., He, J., Zhang, L., Liu, Y., Zhao, J., Chen, Z., Xie, M., Xiao, B., et al. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2022.166569 · Cited by 4

Accumulation of NMDA receptors in accumbal neuronal ensembles mediates increased conditioned place preference for cocaine after prolonged withdrawal

Huai, Z., Huang, B. Y., He, G., Li, H., Liu, Y., Le, Q., Wang, F., Lan, M., & Liu, X. (2024) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2024.102573 · Cited by 4

Solving the Global Opioid Crisis: Incorporating Genetic Addiction Risk Assessment with Personalized Dopaminergic Homeostatic Therapy and Awareness Integration Therapy

(2024) · Journal of Addiction Psychiatry · doi:10.17756/jap.2024-045 · Cited by 3

Auditory cortical neurons are recruited to encode fear signals and anxiety by neuroligin-3-mediated synapse formation

Zhang, Y., Chen, B., Li, J., Wang, L., Xu, Y., & Wang, J. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03357-9 · Cited by 3

Epigenetics, behavior and early nicotine

Maldonado, R. J., & Martín, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4330 · Cited by 3

Cocaine preexposure enhances sexual conditioning and increases resistance to extinction in male Japanese quail

Akins, C. K., Bolin, B. L., & Gill, K. E. (2017) · Learning & Behavior · doi:10.3758/s13420-017-0274-1 · Cited by 3

Structural Plasticity and Cortical Connectivity

Kehayas, V., & Holtmaat, A. J. D. G. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803784-3.00001-9 · Cited by 3

The Individualized Powerhouse: Mitofusin-2 Regulates Nucleus Accumbens Mitochondrial Influence on Individual Differences in Trait Anxiety

Calarco, C. A., & Lobo, M. K. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.03.031 · Cited by 3

Neurobiological theories of addiction

Koob, G. F., Arends, M. A., McCracken, M. L., & Moal, M. L. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816863-9.00003-0 · Cited by 3

Sensory Reinforced Corticostriatal Plasticity

Vautrelle, N., Coizet, V., Leriche, M., Dahan, L., Schulz, J. M., Zhang, Y.-F., Zeghbib, A., Overton, P. G., Bracci, E., Redgrave, P., et al. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230801110359 · Cited by 3

[Impairment of social interaction, coordination disorder, and hypersensitivity in Asperger's syndrome].

Asai, T. T., & Sugiyam, T. (2007) · PubMed · Cited by 3

Disrupting heroin-associated memory reconsolidation through actin polymerization inhibition in the nucleus accumbens core

Zhao, H., Li, H., Li, M., Du, P., Mo, X., Gong, M., Chen, J., & Liao, Y. (2024) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyae065 · Cited by 2

Endogenous regulator of G protein signaling 14 (RGS14) blunts cocaine-induced emotionally motivated behaviors in female mice

Bramlett, S. N., Foster, S. L., Weinshenker, D., & Hepler, J. R. (2025) · Addiction Neuroscience · doi:10.1016/j.addicn.2025.100203 · Cited by 3

Initial exposure to addictive drugs activates polysialylated NCAM-mediated hippocampal memory-associated synaptic plasticity in the rat prior to the emergence of dependence behaviour

Rombach, N., Fedriani, R., Scully, D., O'Sullivan, J., Mulvany, S. K., & Murphy, K. J. (2025) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2025.111395 · Cited by 2

Unveiling the therapeutic potential of octreotide in treating morphine dependence

Shabani, M., Pirmoradi, Z., Razavinasab, M., Hassanshahi, A., Naderi, R., Esmaili, Z., Ebrahimi, M. N., Ilaghi, M., Langarizadeh, M. A., Moqaddari, A. H., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-12761-6 · Cited by 2

Repeated Morphine Exposure Reversibly Impairs Spike Generation and Repetitive Firing in a Functionally Distinct Subpopulation of Orexin Neurons

Berry, E. A., Huhulea, E. N., Ishibashi, M., McGregor, R., Siegel, J. M., & Leonard, C. S. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0563-25.2025 · Cited by 3

Acetazolamide inhibition of carbonic anhydrase 4 reverses opioid-induced synaptic rearrangements in nucleus accumbens and reduces drug-seeking behavior

Gupta, S. C., Taugher, R. J., Ghobbeh, A., Jahnke, M. T., Fan, R., LaLumiere, R. T., & Wemmie, J. A. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-025-02319-5 · Cited by 4

Epigenetic Mechanisms of Drug Addiction Vulnerability

Wenderski, W., & Maze, I. S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-417114-5.00021-8 · Cited by 2

Regulation and Modulation of Depression-Related Behaviours: Role of Dopaminergic Neurons

Radwan, B., Liu, H., & Chaudhury, D. (2016) · Springer eBooks · doi:10.1007/978-3-319-46437-4_8 · Cited by 2

Reduced dopamine release in Dcc haploinsufficiency male mice abolishes the rewarding effects of cocaine but not those of morphine and ethanol

Darcq, E., Nouel, D., Hernández, G., Pokinko, M., Ash, P., Moquin, L., Gratton, A. P., Kieffer, B. L., & Flores, C. (2022) · Psychopharmacology · doi:10.1007/s00213-022-06288-1 · Cited by 2

Characterization of GEXP15 as a Potential Regulator of Protein Phosphatase 1 in Plasmodium falciparum

Mansour, H., Cabezas‐Cruz, A., Peucelle, V., Farce, A., Salomé‐Desnoulez, S., Metatla, I., Guerrera, I. C., Hollin, T., & Khalife, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612647 · Cited by 2

Tmod2is a regulator of cocaine responses through control of striatal and cortical excitability, and drug-induced plasticity

Mitra, A., Deats, S., Dickson, P. E., Zhu, J., Gardin, J., Nieman, B. J., Henkelman, R. M., Tsai, N., Chesler, E. J., Zhang, Z., et al. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1389-23.2024 · Cited by 2

miR-181a expressed in the dorsal hippocampus regulates the reinstatement of cocaine CPP by targeting PRKAA1

Zhu, J. W., Hou, Y., Li, W., Wang, X., Li, F. R., Li, N., Hu, Y., Wang, X., & Ge, S.-N. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.115097 · Cited by 2

Cofilin linked to GluN2B subunits of NMDA receptors is required for behavioral sensitization by changing the dendritic spines of neurons in the caudate and putamen after repeated nicotine exposure

Kim, S., Sohn, S., & Choe, E. S. (2024) · Behavioral and Brain Functions · doi:10.1186/s12993-024-00253-y · Cited by 2

Early developmental changes in GABAA receptor expression in nucleus accumbens medium spiny neurons

Wang, Z., Folorunso, O. O., Morris, K., Berretta, S., & Engin, E. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1445162 · Cited by 2

IBKinaseRegulatesSocialDefeatStress-InducedSynaptic andBehavioralPlasticity

Christoffel, D. J., Janssen, W., & FranciscaAhn, H. (2011) · Cited by 2

Ionotropic Glutamate Receptors in the Basal Ganglia

Jones, S., Brothwell, S., Huang‐Doran, I., & Hallett, J. (2011) · Frontiers in neuroscience · doi:10.1201/b11284-3 · Cited by 2

Effect of Spine Density on Excitability in Accumbal Medium Spiny Neurons-A Computational Approach

Rane, M., & Manchanda, R. (2017) · Journal of Addiction Research & Therapy · doi:10.4172/2155-6105.1000337 · Cited by 2

Fos-Expressing Neuronal Ensembles in Addiction Research

Hope, B. T. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812202-0.00006-3 · Cited by 2

What Have We Learned (or Expect to) From Analysis of Murine Genetic Models Related to Substance Use Disorders?

Peltz, G., & Tan, Y. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.793961 · Cited by 2

Neuroadaptive Changes that Result from Chronic Drug Exposure

Becker, H. C., Griffin, W. C., & Lopez, M. F. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-398335-0.00018-2 · Cited by 2

Sex experience increases delta FosB in male and female hamsters, but facilitates sex behavior only in females.

Acaba, L. A., Sidibe, D. K., Thygesen, J., Kloot, H. V. D., & Been, L. E. (2019) · Behavioral Neuroscience · doi:10.1037/bne0000313 · Cited by 2

Heroin self-administration and extinction increases prelimbic cortical astroglia-synapse proximity and alters dendritic spine morphometrics that are reversed by N-acetylcysteinePreprint

Siemsen, B. M., Denton, A., Hooker, K. N., Carpenter, E., Prescot, M. E., Brock, A., Leath, M., McFaddin, J. A., McGinty, J. F., & Scofield, M. D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.21.108530 · Cited by 2

Uncovering the link between synaptic density and mental illness through in vivo imaging

Smart, K. A., & Boileau, I. (2023) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.230033 · Cited by 2

Carbonic anhydrase 4 disruption and pharmacological inhibition reduce synaptic and behavioral adaptations following oxycodone withdrawalPreprint

Gupta, S. C., Taugher, R. J., Ghobbeh, A., Jahnke, M. T., Fan, R., LaLumiere, R. T., & Wemmie, J. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.23.634619 · Cited by 2

Novel Targets for Drug Treatment in Psychiatry

Kurita, M., García‐Bea, A., & González‐Maeso, J. (2016) · Springer eBooks · doi:10.1007/978-1-4939-2528-5_30 · Cited by 1

Neurobiology of Addiction

Bourin, M. (2024) · Springer eBooks · doi:10.1007/978-3-031-72219-6_14 · Cited by 1

The mesolimbic reward pathway is necessary for disruptions in cocaine-seeking behavior following mediated devaluation

Mo, B., Fex, V., McQueney, A., Olekanma, D. I., Reeves, C. A., Voutour, L. S., Simmons, S. C., Robison, A. J., Arguello, A. A., & Johnson, A. W. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02119-x · Cited by 1

Roles of Glia in Synapse Nano-organization

Choi, Y., & Chung, W. (2026) · Advances in neurobiology · doi:10.1007/978-3-032-12594-1_11 · Cited by 1

Proteomic Insights into Heroin Use: Links to Neurodegeneration

Sürmen, M. G., Pençe, S., Sürmen, S., Büyük, Y., Kuraş, S., Elibol, B., & Pençe, H. H. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05757-4 · Cited by 1

Basic research Chronic alcohol exposure increases ganglia endogenous morphine levels

Zhu, W. M., Li, Y., Kream, R. M., & Stefano, G. B. (2010) · Archives of Medical Science · doi:10.5114/aoms.2010.14249 · Cited by 1

Drug Use and Its Consequences

Madras, B. K. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418679-8.00001-0 · Cited by 1

Tipping the Scales Toward Addiction

Wright, W. J., & Dong, Y. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.02.009 · Cited by 1

Molecular Mechanisms of Drug-Induced Plasticity

Oliver, R. J., & Perrone‐Bizzozero, N. I. (2017) · InTech eBooks · doi:10.5772/67289 · Cited by 1

Regulatory Roles of MicroRNAs in Addictions and Other Psychiatric Diseases

Li, M. D. (2018) · Springer eBooks · doi:10.1007/978-981-10-7530-8_14 · Cited by 1

Pharmacological Inactivation of Medial Prefrontal Cortex Does Not Support Dichotomous “Go/Stop” Roles for Dorsal and Ventral Subdivisions in Natural Reward Seeking in Rats

Carney, R. S. E. (2020) · eNeuro · doi:10.1523/eneuro.0246-20.2020 · Cited by 1

Epigenetic Mechanisms of Drug Addiction

Maze, I. S., & Nestler, E. J. (2012) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-27913-3_12 · Cited by 1

Learning to become addicted, one synapse at a time

Attardo, A., & Cambridge, S. B. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.379046 · Cited by 1

Neurobiology of Addiction

Koob, G. F., Kandel, D. B., Baler, R., & Volkow, N. D. (2024) · Springer eBooks · doi:10.1007/978-3-030-51366-5_29 · Cited by 1

Addiction

Wolf, M. E. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374947-5.00061-4 · Cited by 1

Amphetamine Alters the Circadian Locomotor Activity Pattern of Adult WKY Female Rats

Jones, C. G., Yang, P. B., Wilcox, V. T., & Dafny, N. (2014) · Journal of Behavioral and Brain Science · doi:10.4236/jbbs.2014.45022 · Cited by 1

Cocaine sensitization does not alter SP effects on locomotion or excitatory synaptic transmission in the NAc of rats

Kombian, S. B., Ananthalakshmi, K. V. V., Zidichouski, J. A., & Saleh, T. M. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.09.008 · Cited by 1

Regulation of Corticostriatal Synaptic Plasticity in Physiological and Pathological Conditions

Filippo, M. D., & Calabresi, P. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00023-4 · Cited by 2

Single dose ketamine injection affects activation of cells in the nucleus accumbens of prenatally stressed rats

Çorumlu, E. P., Aydın, O. Ö., & Ulupınar, E. (2017) · Anatomy (International Journal of Experimental and Clinical Anatomy) · doi:10.2399/ana.17.035 · Cited by 1

Obesity and Stress: The Melanocortin Connection

Singhal, S., & Hill, J. W. (2018) · Springer eBooks · doi:10.1007/978-3-319-89506-2_11 · Cited by 1

Animal Models of Addiction

Evans, C. J., Kieffer, B. L., Jentsch, D., & Maldonado, R. J. (2017) · Oxford University Press eBooks · doi:10.1093/med/9780190681425.003.0043 · Cited by 1

Perception and action in nicotine addiction : fMRI and behavioral studies of sensorimotor and multisensory processes in smokers and non-smokers

Yalachkov, Y. (2011) · Research Publications (Maastricht University) · doi:10.26481/dis.20110317yy · Cited by 1

Neural mechanisms of MK-801 induced sensitisation

Lefevre, E. M. (2016) · The University of Queensland · doi:10.14264/uql.2016.911 · Cited by 1

3D SYNAPTIC ORGANIZATION OF THE RAT CA1 AND ALTERATIONS INDUCED BY COCAINE SELF-ADMINISTRATIONPreprint

Blázquez‐Llorca, L., Miguéns, M., Montero‐Crespo, M., Selvas, A., González‐Soriano, J., Ambrosio, E., & DeFelipe, J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.23.050575 · Cited by 1

Drug self-administration in head-restrained mice for simultaneous multiphoton imagingPreprint

Vollmer, K. M., Doncheck, E. M., Grant, R. I., Winston, K. T., Romanova, E. V., Bowen, C. W., Siegler, P. N., Bobadilla, A., Trujillo‐Pisanty, I., Kalivas, P. W., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.25.354209 · Cited by 1

The Collaborative Cross strains and their founders vary widely in cocaine-induced behavioral sensitizationPreprint

Schoenrock, S. A., Gagnon, L., Olson, A., Leonardo, M., Philip, V. M., He, H., Jentsch, J. D., Chesler, E. J., & Tarantino, L. M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.01.478694 · Cited by 1

Characterization of GEXP15 as a potential regulator of Protein Phosphatase 1 and partner of ribosomal complex in Plasmodium falciparumPreprint

Mansour, H., Cabezas‐Cruz, A., Peucelle, V., Farce, A., Salomé‐Desnoulez, S., Metatla, I., Guerrera, I. C., Hollin, T., & Khalife, J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.04.547663 · Cited by 1

Predict key biomarkers of Alcohol Dependence in Nucleus accumbens by Weighted gene co-expression network analysisPreprint

Shi, X., Xu, B., He, T., Shi, J., & Zhang, L. (2024) · Research Square · doi:10.21203/rs.3.rs-4201908/v1 · Cited by 1

Endogenous Regulator of G protein Signaling 14 (RGS14) suppresses cocaine-induced emotionally motivated behaviors in female micePreprint

Bramlett, S. N., Foster, S. L., Weinshenker, D., & Hepler, J. R. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.12.612719 · Cited by 1

DUSP5 Downregulation in Nucleus Accumbens Core Correlates with Synaptic Plasticity and Cue-Induced Cocaine ReinstatementPreprint

Taborda-Bejarano, J. P., Meyerink, M. E., Crans, D. C., Ramchandran, R., & García‐Keller, C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.19.677422 · Cited by 1

Examining the role of ASIC1A in mouse models of addiction and CO2-evoked panic-like behaviors

Kreple, C. J., Wemmie, J. A., Lee, A., Anderson, M. G., Richerson, G. B., Benson, C. J., & Harata, N. C. (2015) · doi:10.17077/etd.elc54pws

Behavioral responses to methylphenidate: correlations with neuronal activity in the caudate nucleus

Claussen, C. M. (2013) · Digital Commons-TMC (Texas Medical Center)

SUBTLE HETEROGENEITY OF HIGH-AFFINITY CHOLINE TRANSPORTER EXPRESSION AND LOCALIZATION IN LIMBIC PROJECTIONS OF THE CHOLINERGIC BRAINSTEM TEGMENTUM

Holmstrand, E. C. (2011) · D-Scholarship@Pitt (University of Pittsburgh)

HIV-1 AND COCAINE: MOTIVATION AND SYNAPTIC FUNCTION

Bertrand, S. J. (2015) · Scholar Commons (University of South Carolina)

Mesocorticolimbic adaptations in synaptic plasticity underlie the development of alcohol dependence

Jeanes, Z. M. (2012) · Texas ScholarWorks (Texas Digital Library)

COPI polices nicotine-mediated up-regulation of nicotinic receptors

Anand, R. (2013) · The Journal of General Physiology · doi:10.1085/jgp.201311136

Methods for treating neurological conditions (WO2011159945)

Meissner, W. G. (2012) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.2012.699524

Appetite regulating neuropeptides in alcohol addiction : focus on melanin concentrating hormone and its mch1-receptor

Karlsson, C. (2015) · Figshare

INTRINSIC MEMBRANE ADAPTATIONS TO COCAINE EXPOSURE AND SLEEP DEPRIVATION

Winters, B. D. (2012) · Research Exchange (Washington State University)

Evaluación de la eficacia de medicamentos empleados en el tratamiento de la dependencia de cocaína: Revisión sistemática y metaanálisis de los fármacos antiepilépticos y antipsicóticos

García, Y. Á. (2015) · TDX (Tesis Doctorals en Xarxa)

On nogo receptors, plasticity and lasting memories

Karlsson, T. E. (2012) · Figshare

Plenary lecture II The neurobiology of food intake in an obesogenic environment

Berthoud, H. (2012)

Impaired Behavioral and Pathological Outcomes Following Blast Neurotrauma

Sajja, V. S. S. S. (2013) · VTechWorks (Virginia Tech)

Transcriptional Effects of Heroin and Methamphetamine in the Striatum

Przewłocki, R., Korostyński, M., & Piechota, M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800213-1.00087-0

Title The Addicted Self: A Neuroscientific Perspective

Macmillan, P. P. (2016)

Full Title: Constitutive knockout of Kalirin-7 leads to increased rates of cocaine self- administration

Kiraly, D. D., Nemirovsky, N. E., LaRese, T. P., Tomek, S. E., Olive, M. F., Eipper, B. A., & Mains, R. E. (2013)

Section summary and perspectives: Translational medicine in psychiatry

Coyle, J. T. (2012) · Cambridge University Press eBooks · doi:10.1017/cbo9780511980053.007

Od mušica do ljudi: Cirkadijalni geni u neurogenetici ovisnosti

Waldowski, R. A. (2016) · Psihologijske teme

The role of cellular and chemical signaling within the nucleus accumbens in value-based decision making behaviors

Sugam, J. A. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/dc4f-dk30

Neuronal Signaling: an introduction

Sullivan, A. M. (2016) · Neuronal Signaling · doi:10.1042/ns20160025

Optogenetics to Study Reward Learning and Addiction

Gutman, A. L., & LaLumiere, R. T. (2017) · Cambridge University Press eBooks · doi:10.1017/9781107281875.019

Prenatal Cocaine-Induced Alterations in Dendritic Spine Density and Glutamate Neurotransmission

Frankfurt, M., Otkins, J., & Bakshi, K. P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803750-8.00025-7

Understanding Mood Disorders Using Electrophysiology and Circuit Breaking

Liu, H., & Chaudhury, D. (2017) · Springer eBooks · doi:10.1007/978-3-319-57363-2_14

Circadian Mechanisms Underlying

Neurophysiology, R.-R., & McClung, C. A. (2016)

Neuropeptide Receptors as Treatment Targets in Alcohol Use Disorders

Aziz, A. M. A. (2017) · Linköping University medical dissertations · doi:10.3384/diss.diva-139884

The Effects of Binge-Like Sucrose Consumption on the Mesolimbic Reward Pathway in the Brain

Shariff, M. R. (2017) · Queensland University of Technology · doi:10.5204/thesis.eprints.107900

Conditional Modulation of Sensitization of the Stimulant Effects of Cocaine by Wheel Running

Diaz, L. R. (2017) · Spectrum Research Repository (Concordia University)

Post-Transcriptional Regulation of Addiction-Related Behaviors: Opposing Roles of Nucleus Accumbens miR-495 and HuD

Oliver, & Robert, J. (2017) · UNM’s Digital Repository (University of New Mexico)

Mechanisms of Motivation in the Nucleus Accumbens

Cole, S. L. (2017) · Deep Blue (University of Michigan)

Motivating Change in Addiction via Modulation of the Dark Side

Koob, G. F. (2018) · Nebraska Symposium on Motivation/The Nebraska symposium on motivation · doi:10.1007/978-3-319-96920-6_1

Repression of Dlx1/2 Signaling by Nolz-1/Znf503 is Essential for Parcellation of the Striatal Complex into Dorsal and Ventral StriatumPreprint

Lu, K.-M., Chen, S.-Y., Ko, H.-A., Huang, T.-H., Hao, J. H.-J., Yan, Y., Chang, S. L., Evans, S. Μ., & Liu, F.-C. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/463398

The Neurobiology of Gambling Disorder: Neuroscientific Studies and Computational Perspectives

Genauck, A., & Romanczuk‐Seiferth, N. (2019) · Springer eBooks · doi:10.1007/978-3-030-03060-5_7 · Cited by 1

Neuronal mRNA Translation in Addiction

Puighermanal, E., & Valjent, E. (2018) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190686307.013.19

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