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For: Galvan A, Caiola MJ, Albaugh DL. Advances in optogenetic and chemogenetic methods to study brain circuits in non-human primates. J Neural Transm (Vienna) 2018;125:547-63. [PMID: 28238201 DOI: 10.1007/s00702-017-1697-8] [Cited by in Crossref: 40] [Cited by in F6Publishing: 42] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
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2 Karami S, Doroodmand MM, Mootabi-Alavi A. In Vivo Chemogenetic Biocompatibility of Mercury as a Specific Hypercalcemia Actuator in Snail's Spinal Cord Cell Manipulation: An Extracellular Field Potential Biosensor. ACS Appl Bio Mater 2022. [PMID: 35830462 DOI: 10.1021/acsabm.1c01064] [Reference Citation Analysis]
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5 Kostick-quenet K, Kalwani L, Koenig B, Torgerson L, Sanchez C, Munoz K, Hsu RL, Sierra-mercado D, Robinson JO, Outram S, Pereira S, Mcguire A, Zuk P, Lazaro-munoz G. Researchers’ Ethical Concerns About Using Adaptive Deep Brain Stimulation for Enhancement. Front Hum Neurosci 2022;16:813922. [DOI: 10.3389/fnhum.2022.813922] [Reference Citation Analysis]
6 Raper J, Galvan A. Applications of chemogenetics in non-human primates. Current Opinion in Pharmacology 2022. [DOI: 10.1016/j.coph.2022.102204] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Li L, Lu L, Ren Y, Tang G, Zhao Y, Cai X, Shi Z, Ding H, Liu C, Cheng D, Xie Y, Wang H, Fu X, Yin L, Luo M, Sheng X. Colocalized, bidirectional optogenetic modulations in freely behaving mice with a wireless dual-color optoelectronic probe. Nat Commun 2022;13:839. [PMID: 35149715 DOI: 10.1038/s41467-022-28539-7] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
8 Hirabayashi T, Nagai Y, Hori Y, Inoue KI, Aoki I, Takada M, Suhara T, Higuchi M, Minamimoto T. Chemogenetic sensory fMRI reveals behaviorally relevant bidirectional changes in primate somatosensory network. Neuron 2021;109:3312-3322.e5. [PMID: 34672984 DOI: 10.1016/j.neuron.2021.08.032] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
9 Wong WLE, Dawe GS, Young AH. The putative role of the relaxin-3/RXFP3 system in clinical depression and anxiety: A systematic literature review. Neurosci Biobehav Rev 2021;131:429-50. [PMID: 34537263 DOI: 10.1016/j.neubiorev.2021.09.028] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
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11 Wu S, Li H, Wang D, Zhao L, Qiao X, Zhang X, Liu W, Wang C, Zhou J. Genetically magnetic control of neural system via TRPV4 activation with magnetic nanoparticles. Nano Today 2021;39:101187. [DOI: 10.1016/j.nantod.2021.101187] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
12 Perry BAL, Lomi E, Mitchell AS. Thalamocortical interactions in cognition and disease: the mediodorsal and anterior thalamic nuclei. Neurosci Biobehav Rev 2021:S0149-7634(21)00294-3. [PMID: 34216651 DOI: 10.1016/j.neubiorev.2021.05.032] [Cited by in F6Publishing: 8] [Reference Citation Analysis]
13 Fiorenzano A, Sozzi E, Parmar M, Storm P. Dopamine Neuron Diversity: Recent Advances and Current Challenges in Human Stem Cell Models and Single Cell Sequencing. Cells 2021;10:1366. [PMID: 34206038 DOI: 10.3390/cells10061366] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
14 Galvan A, Petkau TL, Hill AM, Korecki AJ, Lu G, Choi D, Rahman K, Simpson EM, Leavitt BR, Smith Y. Intracerebroventricular Administration of AAV9-PHP.B SYN1-EmGFP Induces Widespread Transgene Expression in the Mouse and Monkey Central Nervous System. Hum Gene Ther 2021;32:599-615. [PMID: 33860682 DOI: 10.1089/hum.2020.301] [Cited by in Crossref: 1] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
15 Mantas I, Saarinen M, Xu ZD, Svenningsson P. Update on GPCR-based targets for the development of novel antidepressants. Mol Psychiatry 2021. [PMID: 33589739 DOI: 10.1038/s41380-021-01040-1] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 8.0] [Reference Citation Analysis]
16 Rook N, Tuff JM, Isparta S, Masseck OA, Herlitze S, Güntürkün O, Pusch R. AAV1 is the optimal viral vector for optogenetic experiments in pigeons (Columba livia). Commun Biol 2021;4:100. [PMID: 33483632 DOI: 10.1038/s42003-020-01595-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
17 Oh TJ, Fan H, Skeeters SS, Zhang K. Steering Molecular Activity with Optogenetics: Recent Advances and Perspectives. Adv Biol (Weinh) 2021;5:e2000180. [PMID: 34028216 DOI: 10.1002/adbi.202000180] [Cited by in Crossref: 2] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
18 Mitchell AS, Hartig R, Basso MA, Jarrett W, Kastner S, Poirier C. International primate neuroscience research regulation, public engagement and transparency opportunities. Neuroimage 2021;229:117700. [PMID: 33418072 DOI: 10.1016/j.neuroimage.2020.117700] [Cited by in Crossref: 2] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
19 Albaugh DL, Smith Y, Galvan A. Comparative analyses of transgene expression patterns after intra-striatal injections of rAAV2-retro in rats and rhesus monkeys: A light and electron microscopic study. Eur J Neurosci 2020;52:4824-39. [PMID: 33113247 DOI: 10.1111/ejn.15027] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
20 Bohlen MO, McCown TJ, Powell SK, El-Nahal HG, Daw T, Basso MA, Sommer MA, Samulski RJ. Adeno-Associated Virus Capsid-Promoter Interactions in the Brain Translate from Rat to the Nonhuman Primate. Hum Gene Ther 2020;31:1155-68. [PMID: 32940068 DOI: 10.1089/hum.2020.196] [Cited by in Crossref: 5] [Cited by in F6Publishing: 11] [Article Influence: 2.5] [Reference Citation Analysis]
21 Tremblay S, Acker L, Afraz A, Albaugh DL, Amita H, Andrei AR, Angelucci A, Aschner A, Balan PF, Basso MA, Benvenuti G, Bohlen MO, Caiola MJ, Calcedo R, Cavanaugh J, Chen Y, Chen S, Chernov MM, Clark AM, Dai J, Debes SR, Deisseroth K, Desimone R, Dragoi V, Egger SW, Eldridge MAG, El-Nahal HG, Fabbrini F, Federer F, Fetsch CR, Fortuna MG, Friedman RM, Fujii N, Gail A, Galvan A, Ghosh S, Gieselmann MA, Gulli RA, Hikosaka O, Hosseini EA, Hu X, Hüer J, Inoue KI, Janz R, Jazayeri M, Jiang R, Ju N, Kar K, Klein C, Kohn A, Komatsu M, Maeda K, Martinez-Trujillo JC, Matsumoto M, Maunsell JHR, Mendoza-Halliday D, Monosov IE, Muers RS, Nurminen L, Ortiz-Rios M, O'Shea DJ, Palfi S, Petkov CI, Pojoga S, Rajalingham R, Ramakrishnan C, Remington ED, Revsine C, Roe AW, Sabes PN, Saunders RC, Scherberger H, Schmid MC, Schultz W, Seidemann E, Senova YS, Shadlen MN, Sheinberg DL, Siu C, Smith Y, Solomon SS, Sommer MA, Spudich JL, Stauffer WR, Takada M, Tang S, Thiele A, Treue S, Vanduffel W, Vogels R, Whitmire MP, Wichmann T, Wurtz RH, Xu H, Yazdan-Shahmorad A, Shenoy KV, DiCarlo JJ, Platt ML. An Open Resource for Non-human Primate Optogenetics. Neuron 2020;108:1075-1090.e6. [PMID: 33080229 DOI: 10.1016/j.neuron.2020.09.027] [Cited by in Crossref: 13] [Cited by in F6Publishing: 20] [Article Influence: 6.5] [Reference Citation Analysis]
22 Amundsen Huffmaster SL, MacKinnon CD. Illuminating Cortical Control of Movement in Nonhuman Primates. Mov Disord 2020;35:1956. [PMID: 33463763 DOI: 10.1002/mds.28331] [Reference Citation Analysis]
23 Kelberman M, Keilholz S, Weinshenker D. What's That (Blue) Spot on my MRI? Multimodal Neuroimaging of the Locus Coeruleus in Neurodegenerative Disease. Front Neurosci 2020;14:583421. [PMID: 33122996 DOI: 10.3389/fnins.2020.583421] [Cited by in Crossref: 3] [Cited by in F6Publishing: 16] [Article Influence: 1.5] [Reference Citation Analysis]
24 Lawrence A, Chang HHV. Minimally invasive neural stimulation with a novel ultra-sensitive step function opsin: implications and future directions. J Neurophysiol 2020;124:1312-4. [PMID: 32997585 DOI: 10.1152/jn.00472.2020] [Reference Citation Analysis]
25 Kenwood MM, Kalin NH. Nonhuman Primate Models to Explore Mechanisms Underlying Early-Life Temperamental Anxiety. Biol Psychiatry 2021;89:659-71. [PMID: 33229035 DOI: 10.1016/j.biopsych.2020.08.028] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
26 Sun K, Xiao L, Wu Y, Zuo D, Zhang C, Liu S, He Z, Rong S, Wang F, Sun T. GABAergic neurons in the insular cortex play an important role in cue-morphine reward memory reconsolidation. Life Sciences 2020;254:117655. [DOI: 10.1016/j.lfs.2020.117655] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
27 Ojemann WKS, Griggs DJ, Ip Z, Caballero O, Jahanian H, Martinez-Conde S, Macknik S, Yazdan-Shahmorad A. A MRI-Based Toolbox for Neurosurgical Planning in Nonhuman Primates. J Vis Exp 2020. [PMID: 32744531 DOI: 10.3791/61098] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Cushnie AK, El-Nahal HG, Bohlen MO, May PJ, Basso MA, Grimaldi P, Wang MZ, de Velasco Ezequiel MF, Sommer MA, Heilbronner SR. Using rAAV2-retro in rhesus macaques: Promise and caveats for circuit manipulation. J Neurosci Methods 2020;345:108859. [PMID: 32668316 DOI: 10.1016/j.jneumeth.2020.108859] [Cited by in Crossref: 6] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
29 Fortuna MG, Hüer J, Guo H, Gruber J, Gruber-Dujardin E, Staiger JF, Scherberger H, Treue S, Gail A. Histological assessment of optogenetic tools to study fronto-visual and fronto-parietal cortical networks in the rhesus macaque. Sci Rep 2020;10:11051. [PMID: 32632196 DOI: 10.1038/s41598-020-67752-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
30 Deffains M, Nguyen TH, Orignac H, Biendon N, Dovero S, Bezard E, Boraud T. In vivo electrophysiological validation of DREADD‐based modulation of pallidal neurons in the non‐human primate. Eur J Neurosci 2021;53:2192-204. [DOI: 10.1111/ejn.14746] [Cited by in Crossref: 1] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
31 Gong X, Mendoza-Halliday D, Ting JT, Kaiser T, Sun X, Bastos AM, Wimmer RD, Guo B, Chen Q, Zhou Y, Pruner M, Wu CW, Park D, Deisseroth K, Barak B, Boyden ES, Miller EK, Halassa MM, Fu Z, Bi G, Desimone R, Feng G. An Ultra-Sensitive Step-Function Opsin for Minimally Invasive Optogenetic Stimulation in Mice and Macaques. Neuron 2020;107:38-51.e8. [PMID: 32353253 DOI: 10.1016/j.neuron.2020.03.032] [Cited by in Crossref: 28] [Cited by in F6Publishing: 43] [Article Influence: 14.0] [Reference Citation Analysis]
32 Fredericks JM, Dash KE, Jaskot EM, Bennett TW, Lerchner W, Dold G, Ide D, Cummins AC, Der Minassian VH, Turchi JN, Richmond BJ, Eldridge MAG. Methods for mechanical delivery of viral vectors into rhesus monkey brain. J Neurosci Methods 2020;339:108730. [PMID: 32302596 DOI: 10.1016/j.jneumeth.2020.108730] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
33 Jerusalem A, Al-Rekabi Z, Chen H, Ercole A, Malboubi M, Tamayo-Elizalde M, Verhagen L, Contera S. Electrophysiological-mechanical coupling in the neuronal membrane and its role in ultrasound neuromodulation and general anaesthesia. Acta Biomater 2019;97:116-40. [PMID: 31357005 DOI: 10.1016/j.actbio.2019.07.041] [Cited by in Crossref: 28] [Cited by in F6Publishing: 26] [Article Influence: 9.3] [Reference Citation Analysis]
34 Smith Y, Galvan A. Non-human primate research of basal ganglia and movement disorders: advances and challenges. J Neural Transm (Vienna) 2018;125:275-8. [PMID: 29423879 DOI: 10.1007/s00702-018-1849-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
35 Bohlen MO, El-Nahal HG, Sommer MA. Transduction of Craniofacial Motoneurons Following Intramuscular Injections of Canine Adenovirus Type-2 (CAV-2) in Rhesus Macaques. Front Neuroanat 2019;13:84. [PMID: 31619971 DOI: 10.3389/fnana.2019.00084] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.7] [Reference Citation Analysis]
36 Fomicheva A, Zhou C, Sun QQ, Gomelsky M. Engineering Adenylate Cyclase Activated by Near-Infrared Window Light for Mammalian Optogenetic Applications. ACS Synth Biol 2019;8:1314-24. [PMID: 31145854 DOI: 10.1021/acssynbio.8b00528] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 4.3] [Reference Citation Analysis]
37 Verhagen L, Gallea C, Folloni D, Constans C, Jensen DE, Ahnine H, Roumazeilles L, Santin M, Ahmed B, Lehericy S, Klein-Flügge MC, Krug K, Mars RB, Rushworth MF, Pouget P, Aubry JF, Sallet J. Offline impact of transcranial focused ultrasound on cortical activation in primates. Elife 2019;8:e40541. [PMID: 30747105 DOI: 10.7554/eLife.40541] [Cited by in Crossref: 80] [Cited by in F6Publishing: 83] [Article Influence: 26.7] [Reference Citation Analysis]
38 Allen DC, Carlson TL, Xiong Y, Jin J, Grant KA, Cuzon Carlson VC. A Comparative Study of the Pharmacokinetics of Clozapine N-Oxide and Clozapine N-Oxide Hydrochloride Salt in Rhesus Macaques. J Pharmacol Exp Ther 2019;368:199-207. [PMID: 30523062 DOI: 10.1124/jpet.118.252031] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
39 Snyder AZ, Bauer AQ. Mapping Structure-Function Relationships in the Brain. Biol Psychiatry Cogn Neurosci Neuroimaging 2019;4:510-21. [PMID: 30528965 DOI: 10.1016/j.bpsc.2018.10.005] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
40 Galvan A, Stauffer WR, Acker L, El-Shamayleh Y, Inoue KI, Ohayon S, Schmid MC. Nonhuman Primate Optogenetics: Recent Advances and Future Directions. J Neurosci 2017;37:10894-903. [PMID: 29118219 DOI: 10.1523/JNEUROSCI.1839-17.2017] [Cited by in F6Publishing: 52] [Reference Citation Analysis]
41 Alikaya A, Rack-Wildner M, Stauffer WR. Reward and value coding by dopamine neurons in non-human primates. J Neural Transm (Vienna) 2018;125:565-74. [PMID: 29076112 DOI: 10.1007/s00702-017-1793-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
42 Vuong J, Devergnas A. The role of the basal ganglia in the control of seizure. J Neural Transm (Vienna) 2018;125:531-45. [PMID: 28766041 DOI: 10.1007/s00702-017-1768-x] [Cited by in Crossref: 22] [Cited by in F6Publishing: 23] [Article Influence: 4.4] [Reference Citation Analysis]