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For: Wang Z, Maunze B, Wang Y, Tsoulfas P, Blackmore MG. Global Connectivity and Function of Descending Spinal Input Revealed by 3D Microscopy and Retrograde Transduction. J Neurosci 2018;38:10566-81. [PMID: 30341180 DOI: 10.1523/JNEUROSCI.1196-18.2018] [Cited by in Crossref: 26] [Cited by in F6Publishing: 14] [Article Influence: 6.5] [Reference Citation Analysis]
Number Citing Articles
1 Venkatesh I, Mehra V, Wang Z, Simpson MT, Eastwood E, Chakraborty A, Beine Z, Gross D, Cabahug M, Olson G, Blackmore MG. Co-occupancy identifies transcription factor co-operation for axon growth. Nat Commun 2021;12:2555. [PMID: 33953205 DOI: 10.1038/s41467-021-22828-3] [Reference Citation Analysis]
2 Chen Z, Fan G, Li A, Yuan J, Xu T. rAAV2-Retro Enables Extensive and High-Efficient Transduction of Lower Motor Neurons following Intramuscular Injection. Mol Ther Methods Clin Dev 2020;17:21-33. [PMID: 31890738 DOI: 10.1016/j.omtm.2019.11.006] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
3 Lu T, Shinozaki M, Nagoshi N, Nakamura M, Okano H. 3D imaging of supraspinal inputs to the thoracic and lumbar spinal cord mapped by retrograde tracing and light-sheet microscopy. J Neurochem 2022. [PMID: 35674500 DOI: 10.1111/jnc.15653] [Reference Citation Analysis]
4 Aizawa S, Okada T, Keino-Masu K, Doan TH, Koganezawa T, Akiyama M, Tamaoka A, Masu M. Abnormal Pyramidal Decussation and Bilateral Projection of the Corticospinal Tract Axons in Mice Lacking the Heparan Sulfate Endosulfatases, Sulf1 and Sulf2. Front Mol Neurosci 2019;12:333. [PMID: 32038163 DOI: 10.3389/fnmol.2019.00333] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
5 Campbell BC, Nabel EM, Murdock MH, Lao-Peregrin C, Tsoulfas P, Blackmore MG, Lee FS, Liston C, Morishita H, Petsko GA. mGreenLantern: a bright monomeric fluorescent protein with rapid expression and cell filling properties for neuronal imaging. Proc Natl Acad Sci U S A 2020;117:30710-21. [PMID: 33208539 DOI: 10.1073/pnas.2000942117] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
6 Sahni V, Itoh Y, Shnider SJ, Macklis JD. Crim1 and Kelch-like 14 exert complementary dual-directional developmental control over segmentally specific corticospinal axon projection targeting. Cell Rep 2021;37:109842. [PMID: 34686337 DOI: 10.1016/j.celrep.2021.109842] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Steward O, Yee KM, Metcalfe M, Willenberg R, Luo J, Azevedo R, Martin-Thompson JH, Gandhi SP. Rostro-Caudal Specificity of Corticospinal Tract Projections in Mice. Cereb Cortex 2021;31:2322-44. [PMID: 33350438 DOI: 10.1093/cercor/bhaa338] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Lin K, Zhong X, Li L, Ying M, Yang T, Zhang Z, He X, Xu F. AAV9-Retro mediates efficient transduction with axon terminal absorption and blood-brain barrier transportation. Mol Brain 2020;13:138. [PMID: 33054827 DOI: 10.1186/s13041-020-00679-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
9 Golan N, Cafferty WB. Dissociation of intact adult mouse cortical projection neurons for single-cell RNA-seq. STAR Protoc 2021;2:100941. [PMID: 34877546 DOI: 10.1016/j.xpro.2021.100941] [Reference Citation Analysis]
10 Ganley RP, Werder K, Wildner H, Zeilhofer HU. Spinally projecting noradrenergic neurons of the locus coeruleus display resistance to AAV2retro-mediated transduction. Mol Pain 2021;17:17448069211037887. [PMID: 34344259 DOI: 10.1177/17448069211037887] [Reference Citation Analysis]
11 Basista MJ, Yoshida Y. Corticospinal Pathways and Interactions Underpinning Dexterous Forelimb Movement of the Rodent. Neuroscience 2020;450:184-91. [PMID: 32512136 DOI: 10.1016/j.neuroscience.2020.05.050] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Nieuwenhuis B, Haenzi B, Hilton S, Carnicer-Lombarte A, Hobo B, Verhaagen J, Fawcett JW. Optimization of adeno-associated viral vector-mediated transduction of the corticospinal tract: comparison of four promoters. Gene Ther 2021;28:56-74. [PMID: 32576975 DOI: 10.1038/s41434-020-0169-1] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
13 Nakanishi K, Shinozaki M, Nagoshi N, Nakamura M, Okano H. biPACT: A method for three-dimensional visualization of mouse spinal cord circuits of long segments with high resolution. J Neurosci Methods 2022;379:109672. [PMID: 35843371 DOI: 10.1016/j.jneumeth.2022.109672] [Reference Citation Analysis]
14 Dumas L, Clavreul S, Michon F, Loulier K. Multicolor strategies for investigating clonal expansion and tissue plasticity. Cell Mol Life Sci 2022;79. [DOI: 10.1007/s00018-021-04077-1] [Reference Citation Analysis]
15 Rosenberg JB, Chen A, De BP, Dyke JP, Ballon DJ, Monette S, Ricart Arbona RJ, Kaminsky SM, Crystal RG, Sondhi D. Safety of Direct Intraparenchymal AAVrh.10-Mediated Central Nervous System Gene Therapy for Metachromatic Leukodystrophy. Hum Gene Ther 2021;32:563-80. [PMID: 33380277 DOI: 10.1089/hum.2020.269] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
16 McCreedy DA, Jalufka FL, Platt ME, Min SW, Kirchhoff MA, Pritchard AL, Reid SK, Manlapaz R, Mihaly E, Butts JC, Iyer NR, Sakiyama-Elbert SE, Crone SA, McDevitt TC. Passive Clearing and 3D Lightsheet Imaging of the Intact and Injured Spinal Cord in Mice. Front Cell Neurosci 2021;15:684792. [PMID: 34408627 DOI: 10.3389/fncel.2021.684792] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Sahni V, Shnider SJ, Jabaudon D, Song JHT, Itoh Y, Greig LC, Macklis JD. Corticospinal neuron subpopulation-specific developmental genes prospectively indicate mature segmentally specific axon projection targeting. Cell Rep 2021;37:109843. [PMID: 34686320 DOI: 10.1016/j.celrep.2021.109843] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Sathyamurthy A, Barik A, Dobrott CI, Matson KJE, Stoica S, Pursley R, Chesler AT, Levine AJ. Cerebellospinal Neurons Regulate Motor Performance and Motor Learning. Cell Rep 2020;31:107595. [PMID: 32402292 DOI: 10.1016/j.celrep.2020.107595] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 14.0] [Reference Citation Analysis]
19 Frezel N, Platonova E, Voigt FF, Mateos JM, Kastli R, Ziegler U, Karayannis T, Helmchen F, Wildner H, Zeilhofer HU. In-Depth Characterization of Layer 5 Output Neurons of the Primary Somatosensory Cortex Innervating the Mouse Dorsal Spinal Cord. Cereb Cortex Commun 2020;1:tgaa052. [PMID: 34296117 DOI: 10.1093/texcom/tgaa052] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
20 Pantazis CB, James MH, O'Connor S, Shin N, Aston-Jones G. Orexin-1 receptor signaling in ventral tegmental area mediates cue-driven demand for cocaine. Neuropsychopharmacology 2021. [PMID: 34635803 DOI: 10.1038/s41386-021-01173-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 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: 6] [Article Influence: 3.0] [Reference Citation Analysis]
22 Metcalfe M, Yee KM, Luo J, Martin-Thompson JH, Gandhi SP, Steward O. Harnessing rAAV-retro for gene manipulations in multiple pathways that are interrupted after spinal cord injury. Exp Neurol 2021;:113965. [PMID: 34973965 DOI: 10.1016/j.expneurol.2021.113965] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]