The LIM homeobox gene Isl1 is required for the correct development of the striatonigral pathway in the mouse
Open accessAbstract
Significance: The basal ganglia process cortical information that controls purposeful movements and appropriate behavior via the striatopallidal and striatonigral pathways. Despite their importance, little is known about the developmental mechanisms that control the formation of these pathways. We show here that telencephalic progenitors expressing the transcription factor Islet1 give rise to striatonigral neurons and that this factor is required for normal development of the striatonigral pathway. Moreover, Islet1 mouse mutants exhibit hyperactivity and a paradoxical response to psychostimulants. Given that the underlying causes of basal ganglia disorders such as attention deficit hyperactivity disorder (ADHD) are unknown, these findings may implicate possible alterations in neural circuitry.
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
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?
Isl1 is widely expressed in hypothalamus and CNU, and more highly in GABAergic than glutamatergic cell types.
“Isl1 is widely expressed in hypothalamus and CNU, and more highly in GABAergic than glutamatergic cell types115.”
From A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain (2023) · cites this paper as [115]
The Results (page unavailable) report Isl1 expression in a subpopulation of developing striatal neurons and in adult neurons of the rTh and zona incerta; fate-mapped striatal neurons have characteristics of GABAergic projection neurons. The paper does not establish widespread expression across the hypothalamus and CNU or compare Isl1 expression levels in GABAergic and glutamatergic cell types. (LLM, conf=0.83)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The functional anatomy of basal ganglia disorders
Albin, R. L., Young, A. B., & Penney, J. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90074-x · Cited by 5,353 · see citing works
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121 · see citing works
Gerfen, C. R., Engber, T. M., Mahan, L. C., Susel, Z., Chase, T. N., Monsma, F. J., & Sibley, D. R. (1990) · Science · doi:10.1126/science.2147780 · Cited by 2,967 · see citing works
Reversal of experimental parkinsonism by lesions of the subthalamic nucleus.
Bergman, H., Wichmann, T., & Delong, M. (1990) · Science · doi:10.1126/science.2402638 · Cited by 2,003 · see citing works
Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry
Kravitz, A. V., Freeze, B. S., Parker, P. R. L., Kay, K., Thwin, M. T., Deisseroth, K., & Kreitzer, A. C. (2010) · Nature · doi:10.1038/nature09159 · Cited by 1,885 · see citing works
Modulation of Striatal Projection Systems by Dopamine
Gerfen, C. R., & Surmeier, D. J. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113641 · Cited by 1,700 · see citing works
Neuronal subtype specification in the cerebral cortex
Molyneaux, B. J., Arlotta, P., Menezes, J. R. L., & Macklis, J. D. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2151 · Cited by 1,632 · see citing works
The neostriatal mosaic: multiple levels of compartmental organization
Gerfen, C. R. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90355-c · Cited by 1,471 · see citing works
Sussel, L., Marin, O., Kimura, S., & Rubenstein, J. L. R. (1999) · Development · doi:10.1242/dev.126.15.3359 · Cited by 873 · see citing works
Kawaguchi, Y. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-11-04908.1993 · Cited by 814 · see citing works
Pfaff, S., Mendelsohn, M., Stewart, C., Edlund, T., & Jessell, T. (1996) · Cell · doi:10.1016/s0092-8674(00)80985-x · Cited by 801 · see citing works
Wichterle, H., Turnbull, D. H., Nery, S., Fishell, G., & Alvarez-Buylla, A. (2001) · Development · doi:10.1242/dev.128.19.3759 · Cited by 722 · see citing works
Gerfen, C. R., & Scott Young, W. (1988) · Brain Research · doi:10.1016/0006-8993(88)91217-6 · Cited by 658 · see citing works
Gerfen, C. R., Baimbridge, K. G., & Miller, J. J. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.24.8780 · Cited by 636 · see citing works
Origin and Molecular Specification of Striatal Interneurons
Marín, Ó., Anderson, S. A., & Rubenstein, J. L. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-16-06063.2000 · Cited by 627 · see citing works
NIGG, J. T., & CASEY, B. J. (2005) · Development and Psychopathology · doi:10.1017/s0954579405050376 · Cited by 593 · see citing works
Hikida, T., Kimura, K., Wada, N., Funabiki, K., & Nakanishi, S. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.011 · Cited by 592 · see citing works
Herkenham, M. A., & Pert, C. B. (1981) · Nature · doi:10.1038/291415a0 · Cited by 544 · see citing works
Semaphorin 3E and Plexin-D1 Control Vascular Pattern Independently of Neuropilins
Gu, C., Yoshida, Y., Livet, J., Reimert, D. V., Mann, F., Merte, J., Henderson, C. E., Jessell, T. M., Kolodkin, A. L., & Ginty, D. D. (2004) · Science · doi:10.1126/science.1105416 · Cited by 543 · see citing works
Self-citationEarly restriction of peripheral and proximal cell lineages during formation of the lung
Perl, A. T., Wert, S. E., Nagy, A., Lobe, C. G., & Whitsett, J. A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152238499 · Cited by 525 · see citing works
Stenman, J. M., Toresson, H., & Campbell, K. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00167.2003 · Cited by 508 · see citing works
Self-citationFezl Is Required for the Birth and Specification of Corticospinal Motor Neurons
Molyneaux, B. J., Arlotta, P., Hirata, T., Hibi, M., & Macklis, J. D. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.030 · Cited by 481 · see citing works
Gsh2 and Pax6 play complementary roles in dorsoventral patterning of the mammalian telencephalon
Yun, K., Potter, S., & Rubenstein, J. L. R. (2001) · Development · doi:10.1242/dev.128.2.193 · Cited by 449 · see citing works
FACS-array profiling of striatal projection neuron subtypes in juvenile and adult mouse brains
Lobo, M. K., Karsten, S. L., Gray, M., Geschwind, D. H., & Yang, X. W. (2006) · Nature Neuroscience · doi:10.1038/nn1654 · Cited by 411 · see citing works
Semaphorin Regulation of Cellular Morphology
Tran, T. S., Kolodkin, A. L., & Bharadwaj, R. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010605.093554 · Cited by 388 · see citing works
Genetic control of dorsal-ventral identity in the telencephalon: opposing roles for Pax6 and Gsh2
Toresson, H., Potter, S. S., & Campbell, K. (2000) · Development · doi:10.1242/dev.127.20.4361 · Cited by 387 · see citing works
Self-citationKawaguchi, Y., Wilson, C. J., & Emson, P. C. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.62.5.1052 · Cited by 368 · see citing works
Kita, H., & Kitai, S. T. (1988) · Brain Research · doi:10.1016/0006-8993(88)91138-9 · Cited by 367 · see citing works
Xu, M., Hu, X.-T., Cooper, D. C., Moratalla, R., Graybiel, A., White, F. J., & Tonegawa, S. (1994) · Cell · doi:10.1016/0092-8674(94)90026-4 · Cited by 347 · see citing works
Nakamura, T., Colbert, M. C., & Robbins, J. M. (2006) · Circulation Research · doi:10.1161/01.res.0000227505.19472.69 · Cited by 343 · see citing works
Thor, S., Ericson, J., Brännström, T., & Edlund, H. (1991) · Neuron · doi:10.1016/0896-6273(91)90334-v · Cited by 333 · see citing works
Chauvet, S., Cohen, S., Yoshida, Y., Fekrane, L., Livet, J., Gayet, O., Ségu, L., Buhot, M.-C., Jessell, T. M., Henderson, C. E., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.019 · Cited by 251 · see citing works
Self-citationWaclaw, R. R., Allen, Z. J., Bell, S. M., Erdélyi, F., Szabó, G., Potter, S. S., & Campbell, K. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.018 · Cited by 237 · see citing works
Self-citationThe neostriatal mosaic: multiple levels of compartmental organization
Gerfen, C. R. (1992) · Springer eBooks · doi:10.1007/978-3-7091-9211-5_4 · Cited by 232 · see citing works
Zhao, Y., Marín, O., Hermesz, E., Powell, A., Flames, N., Palkovits, M., Rubenstein, J. L. R., & Westphal, H. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1537759100 · Cited by 227 · see citing works
Deacon, T. W., Pakzaban, P., & Isacson, O. (1994) · Brain Research · doi:10.1016/0006-8993(94)90526-6 · Cited by 224 · see citing works
Sun, Y.-F., Dykes, I. M., Liang, X.-Q., Eng, S., Evans, S. M., & Turner, E. (2008) · Nature Neuroscience · doi:10.1038/nn.2209 · Cited by 211 · see citing works
Toresson, H., de Urquiza, A. M., Fagerstrom, C., Perlmann, T., & Campbell, K. (1999) · Development · doi:10.1242/dev.126.6.1317 · Cited by 203 · see citing works
Self-citationHanashima, C., Shen, L., Li, S. C., & Lai, E. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06526.2002 · Cited by 194 · see citing works
Ebf1 controls early cell differentiation in the embryonic striatum
Garel, S., Marı́n, F., Grosschedl, R., & Charnay, P. (1999) · Development · doi:10.1242/dev.126.23.5285 · Cited by 193 · see citing works
Olsson, M. A., Björklund, A., & Campbell, K. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00532-0 · Cited by 177 · see citing works
Self-citationA role forGsh1in the developing striatum and olfactory bulb ofGsh2mutant mice
Toresson, H., & Campbell, K. (2001) · Development · doi:10.1242/dev.128.23.4769 · Cited by 171 · see citing works
Self-citationMu, X., Fu, X., Beremand, P. D., Thomas, T. L., & Klein, W. H. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802627105 · Cited by 167 · see citing works
Self-citationAnderson, K. D., & Reiner, A. J. (1991) · Brain Research · doi:10.1016/0006-8993(91)91403-n · Cited by 161 · see citing works
Long, J. E., Swan, C. H., Liang, W. S., Cobos, I., Potter, G. B., & Rubenstein, J. L. R. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21854 · Cited by 156 · see citing works
Yun, K., Garel, S., Fischman, S., & Rubenstein, J. L. R. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10685 · Cited by 156 · see citing works
Olsson, M. A., Campbell, K., Wictorin, K., & Björklund, A. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00325-d · Cited by 155 · see citing works
Self-citationNeurobiology of animal models of attention-deficit hyperactivity disorder
Russell, V. A. (2006) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2006.12.005 · Cited by 145 · see citing works
Drago, J., Gerfen, C. R., Westphal, H., & Steiner, H. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00145-5 · Cited by 145 · see citing works
Xu, M., Guo, Y. H., Vorhees, C. V., & Zhang, J. (2000) · Brain Research · doi:10.1016/s0006-8993(99)02258-1 · Cited by 144 · see citing works
Self-citationFragkouli, A., van Wijk, N. V., Lopes, R., Kessaris, N., & Pachnis, V. (2009) · Development · doi:10.1242/dev.038083 · Cited by 135 · see citing works
Developmental Origin of the Neuronal Subtypes That Comprise the Amygdalar Fear Circuit in the Mouse
Waclaw, R. R., Ehrman, L. A., Pierani, A., & Campbell, K. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5772-09.2010 · Cited by 130 · see citing works
Self-citationFoster, G. A., Schultzberg, M., Hökfelt, T. G. M., Goldstein, M., Hemmings, H. C., Ouimet, C. C., Walaas, S. I., & Greengard, P. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-07-01994.1987 · Cited by 125 · see citing works
Rubin, J. E., McIntyre, C. C., Turner, R. S., & Wichmann, T. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08108.x · Cited by 123 · see citing works
Semaphorin 3E–Plexin-D1 signaling controls pathway-specific synapse formation in the striatum
Ding, J., Oh, W., Sabatini, B. L., & Gu, C. (2011) · Nature Neuroscience · doi:10.1038/nn.3003 · Cited by 110 · see citing works
Foxp1 gene expression in projection neurons of the mouse striatum
Tamura, S., Morikawa, Y., Iwanishi, H., Hisaoka, T., & Senba, E. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.11.036 · Cited by 92 · see citing works
Pharmacologic Treatment of Attention Deficit Hyperactivity Disorder
Greenhill, L. L. (1992) · Psychiatric Clinics of North America · doi:10.1016/s0193-953x(18)30255-7 · Cited by 91 · see citing works
Ephrin-A Binding and EphA Receptor Expression Delineate the Matrix Compartment of the Striatum
Janis, L. S., Cassidy, R. M., & Kromer, L. F. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-12-04962.1999 · Cited by 90 · see citing works
Loss of Gsx1 and Gsx2 function rescues distinct phenotypes in Dlx1/2 mutants
Wang, B., Long, J. E., Flandin, P., Pla, R., Waclaw, R. R., Campbell, K., & Rubenstein, J. L. R. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23242 · Cited by 85 · see citing works
Self-citationKarasinska, J. M., George, S. R., Cheng, R., & O’Dowd, B. F. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04353.x · Cited by 83 · see citing works
Wang, H.-F., & Liu, F. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00590-x · Cited by 82 · see citing works
Elshatory, Y. M., & Gan, L. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5730-07.2008 · Cited by 80 · see citing works
Ascl1 is a required downstream effector of Gsx gene function in the embryonic mouse telencephalon
Wang, B., Waclaw, R. R., Allen, Z. J., Guillemot, F., & Campbell, K. (2009) · Neural Development · doi:10.1186/1749-8104-4-5 · Cited by 77 · see citing works
Self-citationZhou, L., Dey, C. R., Wert, S. E., Yan, C., Costa, R. H., & Whitsett, J. A. (1997) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(199711)210:3 · Cited by 72 · see citing works
Lobo, M. K., Yeh, C., & Yang, X. W. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21666 · Cited by 66 · see citing works
Passante, L., Gaspard, N., Degraeve, M., Frisén, J., Kullander, K., Maertelaer, V. D., & Vanderhaeghen, P. (2008) · Development · doi:10.1242/dev.024778 · Cited by 56 · see citing works
Chen, L., Chatterjee, M., & Li, J. Y. H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3742-10.2010 · Cited by 54 · see citing works
Mega, T., Lupia, M., Amodio, N., Horton, S. J., Mesuraca, M., Pelaggi, D., Agosti, V., Grieco, M., Chiarella, E., Spina, R., et al. (2011) · Cell Cycle · doi:10.4161/cc.10.13.16045 · Cited by 53 · see citing works
Dlx6 regulates molecular properties of the striatum and central nucleus of the amygdala
Wang, B., Lufkin, T., & Rubenstein, J. L. R. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22618 · Cited by 44 · see citing works
Lopes, R., van Wijk, N. V., Neves, G., & Pachnis, V. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109251109 · Cited by 42 · see citing works
Martín‐Ibáñez, R., Crespo, E., Urbán, N., Sergent‐Tanguy, S., Herranz, C., Jaumot, M., Valiente, M., Long, J. E., Pineda, J. R., Andreu, C., et al. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22215 · Cited by 39 · see citing works
IKAROS IS EXPRESSED IN DEVELOPING STRIATAL NEURONS AND INVOLVED IN ENKEPHALINERGIC DIFFERENTIATION
Ágoston, D. V., Szemes, M., Dobi, A., Palkovits, M., Georgopoulos, K., Gyorgy, A. B., & Ring, M. A. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04653.x · Cited by 37 · see citing works
Mice lacking p35 display hyperactivity and paradoxical response to psychostimulants
Krapacher, F. A., Mlewski, E. C., Ferreras, S., Pisano, V., Paolorossi, M., Hansen, C., & Paglini, M. G. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06748.x · Cited by 29 · see citing works
Martín‐Ibáñez, R., Crespo, E., Esgleas, M., Urbán, N., Wang, B., Waclaw, R. R., Georgopoulos, K., Martı́nez, S., Campbell, K., Vicario‐Abejón, C., et al. (2011) · Stem Cells and Development · doi:10.1089/scd.2011.0607 · Cited by 29 · see citing works
Self-citationCastelli, M., Federici, M., Rossi, S., Chiara, V. D., Napolitano, F., Studer, V., Motta, C., Sacchetti, L., Romano, R., Musella, A., et al. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07876.x · Cited by 28 · see citing works
Niwa‐Kawakita, M., Abramowski, V., Kalamarides, M., Thomas, G. D., & Giovannini, M. (2000) · genesis · doi:10.1002/(sici)1526-968x(200002)26:2 · Cited by 22 · see citing works
Tics and Tourette syndrome: An adult perspective
Fernandez, H. H., Gálvez-Jiménez, N., & Gálvez-Jiménez, N. (2012) · Cleveland Clinic Journal of Medicine · doi:10.3949/ccjm.79.s2a.07 · Cited by 22 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [63]Furuta Y, Lagutin O, Hogan BL, Oliver GC. Retina- and ventral forebrain-specific Cre recombinase activity in transgenic mice. Genesis. 2000;26(2):130–132. [PubMed] [Google Scholar]
Cited by
Sorted by citations
A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain
Yao, Z., van Velthoven, C. T. J., Kunst, M., Zhang, M., McMillen, D., Lee, C., Jung, W., Goldy, J., Abdelhak, A., Aitken, M., et al. (2023) · Nature · doi:10.1038/s41586-023-06812-z · Cited by 1,194 · see citing works
Cellular Taxonomy of the Mouse Striatum as Revealed by Single-Cell RNA-Seq
Gokce, O., Stanley, G. M., Treutlein, B., Neff, N. F., Camp, J. G., Malenka, R. C., Rothwell, P. E., Fuccillo, M. V., Südhof, T. C., & Quake, S. R. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.06.059 · Cited by 430 · see citing works
Continuous and Discrete Neuron Types of the Adult Murine Striatum
Stanley, G., Gokce, O., Malenka, R. C., Südhof, T. C., & Quake, S. R. (2020) · Neuron · doi:10.1016/j.neuron.2019.11.004 · Cited by 158 · see citing works
Carullo, N. V. N., Phillips, R. A., III, Simon, R. C., Soto, S. A. R., Hinds, J. E., Salisbury, A. J., Revanna, J. S., Bunner, K. D., Ianov, L., Sultan, F. A., et al. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa671 · Cited by 128 · see citing works
Nasif, S., de Souza, F. S. J., González, L. E., Yamashita, M., Orquera, D. P., Low, M. J., & Rubinstein, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1500672112 · Cited by 83 · see citing works
Xu, Z., Liang, Q., Song, X., Zhang, Z., Lindtner, S., Li, Z., Wen, Y. F., Liu, G., Guo, T., Qi, D., et al. (2018) · Development · doi:10.1242/dev.165456 · Cited by 69 · see citing works
Zhang, Q., Zhang, Y., Wang, C., Xu, Z., Liang, Q., An, L., Li, J., Liu, Z., You, Y., He, M., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.06.090 · Cited by 68 · see citing works
Molecular anatomy of the thalamic complex and the underlying transcription factors
Nagalski, A., Puelles, L., Dąbrowski, M., Węgierski, T., Kuźnicki, J., & Wisniewska, M. B. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1052-5 · Cited by 64 · see citing works
Single-Cell Analysis of Foxp1-Driven Mechanisms Essential for Striatal Development
Anderson, A. G., Kulkarni, A., Harper, M. J., & Konopka, G. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.02.030 · Cited by 54 · see citing works
Rataj-Baniowska, M., Niewiadomska-Cimicka, A., Paschaki, M., Szyszka-Niagolov, M., Carramolino, L., Torres, M., Dollé, P., & Krężel, W. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1278-15.2015 · Cited by 54 · see citing works
Active intermixing of indirect and direct neurons builds the striatal mosaic
Tinterri, A., Ménardy, F., Diana, M. A., Lokmane, L., Keita, M., Coulpier, F., Lemoine, S., Mailhes‐Hamon, C., Mathieu, B., Merchán, P., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07171-4 · Cited by 47 · see citing works
Self-citationKrajeski, R. N., Macey-Dare, A. D. B., van Heusden, F., Ebrahimjee, F., & Ellender, T. J. (2019) · The Journal of Physiology · doi:10.1113/jp278416 · Cited by 46 · see citing works
From Progenitors to Progeny: Shaping Striatal Circuit Development and Function
Knowles, R., Dehorter, N., & Ellender, T. J. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0620-21.2021 · Cited by 45 · see citing works
Guo, T., Liu, G., Du, H., Wen, Y. F., Wei, S., Li, Z., Tao, G., Shang, Z., Song, X., Zhang, Z., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz018 · Cited by 43 · see citing works
Dlx1/2- dependent expression of Meis2 promotes neuronal fate determination in the mammalian striatum
Su, Z., Wang, Z., Lindtner, S., Yang, L., Shang, Z., Tian, Y., Guo, R., You, Y., Zhou, W., Rubenstein, J. L. R., et al. (2022) · Development · doi:10.1242/dev.200035 · Cited by 40 · see citing works
Orquera, D. P., Tavella, M. B., de Souza, F. S. J., Nasif, S., Low, M. J., & Rubinstein, M. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2924-18.2019 · Cited by 43 · see citing works
Striatal circuit development and its alterations in Huntington's disease
Lebouc, M., Richard, Q., Garret, M., & Baufreton, J. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105076 · Cited by 42 · see citing works
Terry, N. A., Walp, E. R., Lee, R. A., Kaestner, K. H., & May, C. L. (2014) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00390.2013 · Cited by 42 · see citing works
Burk, K., Mire, E., Bellon, A., Hocine, M., Guillot, J., Moraes, F., Yoshida, Y., Simons, M., Chauvet, S., & Mann, F. (2017) · Nature Communications · doi:10.1038/ncomms14508 · Cited by 42 · see citing works
Self-citationCelsr3 and Fzd3 Organize a Pioneer Neuron Scaffold to Steer Growing Thalamocortical Axons
Feng, J., Xian, Q., Guan, T., Hu, J., Wang, M., Huang, Y., So, K., Evans, S. Μ., Chai, G., Goffinet, A. M., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw132 · Cited by 41 · see citing works
Neuronal cell types, projections, and spatial organization of the central amygdala
O’Leary, T. P., Kendrick, R. M., Bristow, B. N., Sullivan, K. E., Wang, L., Clements, J., Lemire, A. L., & Cembrowski, M. S. (2022) · iScience · doi:10.1016/j.isci.2022.105497 · Cited by 38 · see citing works
Desmaris, E., Keruzoré, M., Saulnier, A., Ratié, L., Assimacopoulos, S., Clercq, S. D., Nan, X., Roychoudhury, K., Qin, S., Kricha, S., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0375-18.2018 · Cited by 39 · see citing works
Self-citationChen, X., Saiyin, H., Liu, Y., Wang, Y., Li, X., Ji, R., & Ma, L. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001868 · Cited by 37 · see citing works
Parcellation of the striatal complex into dorsal and ventral districts
Chen, S., Lu, K.-M., Ko, H.-A., Huang, T.-H., Hao, J. H.-J., Yan, Y., Chang, S. L., Evans, S. Μ., & Liu, F. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1921007117 · Cited by 32 · see citing works
Yang, L., Su, Z., Wang, Z., Li, Z., Shang, Z., Du, H., Liu, G., Qi, D., Yang, Z., Xu, Z., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03552-8 · Cited by 36 · see citing works
Comella-Bolla, A., Orlandi, J. G., Miguez, A., Straccia, M., Garcı́a-Bravo, M., Bombau, G., Galofré, M., Sanders, P., Carrere-Molina, J., Segovia, J. C., et al. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-01907-4 · Cited by 33 · see citing works
Zfhx3 is required for the differentiation of late born D1-type medium spiny neurons
Zhang, Z., Wei, S., Du, H., Su, Z., Wen, Y. F., Shang, Z., Song, X., Xu, Z., You, Y., & Yang, Z. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113055 · Cited by 27 · see citing works
Frizzled3 Controls Axonal Polarity and Intermediate Target Entry during Striatal Pathway Development
Morello, F., Prasad, A. A., Rehberg, K., de Sá, R. V., Antón-Bolaños, N., Leyva‐Díaz, E., Adolfs, Y., Tissir, F., López‐Bendito, G., & Pasterkamp, R. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1840-15.2015 · Cited by 28 · see citing works
Newman, H., Liu, F., & Graybiel, A. M. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23725 · Cited by 27 · see citing works
Waclaw, R. R., Ehrman, L. A., Merchán, P., Kohli, V., Nardini, D., & Campbell, K. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.02.003 · Cited by 24 · see citing works
Self-citationHomeobox Gene Six3 is Required for the Differentiation of D2-Type Medium Spiny Neurons
Song, X., Chen, H., Shang, Z., Du, H., Li, Z., Wen, Y. F., Liu, G., Qi, D., You, Y., Yang, Z., et al. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00698-5 · Cited by 24 · see citing works
Merchán, P., Nardini, D., Waclaw, R. R., & Campbell, K. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24232 · Cited by 25 · see citing works
Self-citationMoreno, N., López, J. M., Morona, R., Lozano, D. D., Jiménez, S., & González, A. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00042 · Cited by 24 · see citing works
Konno, D., Kishida, C., Maehara, K., Ohkawa, Y., Kiyonari, H., Okada, S., & Matsuzaki, F. (2019) · Development · doi:10.1242/dev.174243 · Cited by 23 · see citing works
Helios expression coordinates the development of a subset of striatopallidal medium spiny neurons
Martín‐Ibáñez, R., Pardo, M., Giralt, A., Miguez, A., Guardia, I., Marion‐Poll, L., Herranz, C., Esgleas, M., Barriga, G. G.-D., Edel, M. J., et al. (2017) · Development · doi:10.1242/dev.138248 · Cited by 19 · see citing works
Cirnaru, M., Song, S., Tshilenge, K., Corwin, C., Mleczko, J., Aguirre, C. G., Benlhabib, H., Bendl, J. M., Apontes, P., Fullard, J. F., et al. (2021) · eLife · doi:10.7554/elife.65979 · Cited by 18 · see citing works
A role for sustained MAPK activity in the mouse ventral telencephalon
Talley, M. J., Nardini, D., Qin, S., Prada, C. E., Ehrman, L. A., & Waclaw, R. R. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2021.03.019 · Cited by 17 · see citing works
Self-citationPhillips, R. A., Wan, E., Tuscher, J. J., Reid, D., Drake, O. R., Ianov, L., & Day, J. J. (2023) · eLife · doi:10.7554/elife.89993 · Cited by 15 · see citing works
Nolz1 expression is required in dopaminergic axon guidance and striatal innervation
Soleilhavoup, C., Travaglio, M., Patrick, K., Garção, P., Boobalan, E., Adolfs, Y., Spriggs, R. V., Moles-Garcia, E., Dhiraj, D., Oosterveen, T., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16947-6 · Cited by 13 · see citing works
Wen, Y. F., Su, Z., Wang, Z., Yang, L., Liu, G., Shang, Z., Duan, Y., Du, H., Li, Z., You, Y., et al. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02378-x · Cited by 14 · see citing works
Ehrman, J. M., Merchan-Sala, P., Ehrman, L. A., Chen, B., Lim, H.-W., Waclaw, R. R., & Campbell, K. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.2291-21.2022 · Cited by 14 · see citing works
Self-citationKoh, Y., Park, I. H., Sun, C.-H., Lee, S., Yun, H., Park, C.-K., Park, S., Park, J. K., & Lee, S.-H. (2015) · Translational Oncology · doi:10.1016/j.tranon.2015.05.003 · Cited by 13 · see citing works
Tangential migration of corridor guidepost neurons contributes to anxiety circuits
Tinterri, A., Deck, M., Keita, M., Mailhes‐Hamon, C., Rubin, A. N., Kessaris, N., Lokmane, L., Bielle, F., & Garel, S. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24330 · Cited by 12 · see citing works
Clegg, J. M., Li, Z., Molinek, M., Caballero, I. M., Manuel, M. N., & Price, D. J. (2015) · Neural Development · doi:10.1186/s13064-015-0053-7 · Cited by 13 · see citing works
The transcription factor Zfp503 promotes the D1 MSN identity and represses the D2 MSN identity
Shang, Z., Shang, Z., Wang, Z., Wang, Z., Tian, Y., Gao, Y., Su, Z., Guo, R., Liu, G., Li, X., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.948331 · Cited by 12 · see citing works
The autism-associated Meis2 gene is necessary for cardiac baroreflex regulation in mice
Roussel, J., Larcher, R., Sicard, P., Bideaux, P., Richard, S., Marmigère, F., & Thireau, J. (2022) · Scientific Reports · doi:10.1038/s41598-022-24616-5 · Cited by 12 · see citing works
Kuerbitz, J., Madhavan, M., Ehrman, L. A., Kohli, V., Waclaw, R. R., & Campbell, K. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa323 · Cited by 10 · see citing works
Self-citationTranscription factor Sp9 is a negative regulator of D1-type MSN development
Li, Z., Shang, Z., Sun, M., Jiang, X., Tian, Y., Yang, L., Wang, Z., Su, Z., Liu, G., Li, X., et al. (2022) · Cell Death Discovery · doi:10.1038/s41420-022-01088-0 · Cited by 12 · see citing works
Kohli, V., Nardini, D., Ehrman, L. A., & Waclaw, R. R. (2017) · Developmental Dynamics · doi:10.1002/dvdy.24556 · Cited by 11 · see citing works
Self-citationLópez, J. M., Jiménez, S., Morona, R., Lozano, D. D., & Moreno, N. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25249 · Cited by 11 · see citing works
Pax2-Islet1 Transgenic Mice Are Hyperactive and Have Altered Cerebellar Foliation
Bohuslavová, R., Dodd, N., Macová, I., Chumak, T., Hořák, M., Syka, J., Fritzsch, B., & Pavlínková, G. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9716-6 · Cited by 10 · see citing works
Kim, N., Li, Y., Yu, R., Kwon, H.-S., Song, A., Jun, M.-H., Jeong, J.-Y., Lee, J. H., Lim, H., Kim, M. J., et al. (2024) · eLife · doi:10.7554/elife.96891 · Cited by 9 · see citing works
Sato, D. X., Inoue, Y., Kuga, N., Hattori, S., Nomoto, K., Morimoto, Y., Sala, G., Hagihara, H., Kikusui, T., Sasaki, T., et al. (2022) · iScience · doi:10.1016/j.isci.2022.104800 · Cited by 8 · see citing works
Zhang, Y., Zhao, W., Han, H., Li, S., Chen, D., & Zhang, Z. (2017) · Oncotarget · doi:10.18632/oncotarget.21140 · Cited by 7 · see citing works
Neurogenesis in the basal ganglia
Rubenstein, J. L. R., & Campbell, K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00018-7 · Cited by 7 · see citing works
Self-citationLozano, D. D., Moreno, N., Jiménez, S., Chinarro, A., Morona, R., & López, J. M. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25484 · Cited by 6 · see citing works
Epigenomic profiling of mouse nucleus accumbens at single-cell resolution
Bhatia, P., Yang, L., Luo, J. X. J., Xu, M., & Renthal, W. (2023) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2023.103857 · Cited by 5 · see citing works
Islet1 Precursors Contribute to Mature Interneuron Subtypes in Mouse Neocortex
Siddiqi, F., Trakimas, A. L., Joseph, D. J., Lippincott, M. L., Marsh, E. D., & Wolfe, J. H. N. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab152 · Cited by 5 · see citing works
Enhancer RNAs are necessary and sufficient for activity-dependent neuronal gene transcriptionPreprint
Carullo, N. V. N., Simon, R. C., Salisbury, A. J., Revanna, J. S., Bunner, K. D., Savell, K. E., Sultan, F. A., Ca, G., & Day, J. (2019) · IUScholarWorks Open (Indiana University) · doi:10.1101/270967 · Cited by 6 · see citing works
Biswas, S., Chan, C. S., Rubenstein, J. L. R., & Gan, L. (2023) · Developmental Biology · doi:10.1016/j.ydbio.2023.07.007 · Cited by 3 · see citing works
Phillips, R. A., Wan, E., Tuscher, J. J., Reid, D., Drake, O. R., Ianov, L., & Day, J. J. (2023) · eLife · doi:10.7554/elife.89993.3 · Cited by 2 · see citing works
Striatal circuit development and synapse maturation
Peixoto, R. T., & Kozorovitskiy, Y. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00021-1 · Cited by 2 · see citing works
Phillips, R. A., Wan, E., Tuscher, J. J., Reid, D., Drake, O. R., Ianov, L., & Day, J. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.02.543489 · Cited by 2 · see citing works
Tweedie, L., Riccetti, M., Cain, B., Qin, S., Salomone, J. R., Webb, J. A., Riesenberg, A. N., Ehrman, L. A., Waclaw, R. R., Kovall, R. A., et al. (2025) · Disease Models & Mechanisms · doi:10.1242/dmm.052110 · Cited by 1 · see citing works
Self-citationNguyen, Q., Tran, H., & Jeong, Y. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05523-6 · Cited by 1 · see citing works
Neuropilin-Dependent Signaling and Neuropilin-Independent Signaling of the Guidance Molecule Sema3E
Mann, F., & Chauvet, S. (2017) · Springer eBooks · doi:10.1007/978-3-319-48824-0_5
NKX2.1 is critical for melanocortin neuron identity, hypothalamic Pomc expression and body weightPreprint
Orquera, D. P., Tavella, M. B., de Souza, F. S. J., Nasif, S., Low, M. J., & Rubinstein, M. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/460501
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
Intestinal Enteroendocrine Disorders in the Fetus and Neonate
Yang, J. S., Jonnakuti, V. S., Stanescu, D. E., & León, D. D. D. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814823-5.00047-7
Sato, D. X., Inoue, Y., Morimoto, Y., Inoue, T., Kuga, N., Sasaki, T., Ikegaya, Y., Nomoto, K., Kikusui, T., Hattori, S., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.18.444749
Biswas, S., Chan, C. S., Rubenstein, J. L. R., & Gan, L. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.24.493171
Expression of the transcription factor Isl1 in dopaminergic neurons of the mouse forebrainPreprint
Camarano, A. C., Rubinstein, M., & de Souza, F. S. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.27.573451
Fjodorova, M., Prapaiwongs, P., Petter, O., Morella, I., Li, Z., Hall, J. H., Vinh, N., Davies, S., Green, J., Hall, J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.26.640425
Reevaluating the role of Pou3f1 in striatal development: Evidence from transgenic mouse models
Song, X., Zhang, F., Han, D., Yu, J., Ren, Q., Xin, X., Guo, R., & Le, W. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111302
Intestinal Enteroendocrine Disorders in the Fetus and Neonate
Rubenstein, A., & León, D. D. D. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-23940-3.00028-4
Hisamatsu, D., Hasegawa, H., Naka-Kaneda, H., Nakajima, K., Okano, H., & Shimazaki, T. (2026) · Developmental Biology · doi:10.1016/j.ydbio.2026.04.003
- Authors
- Ehrman, L. A., Mu, X., Waclaw, R. R., Yoshida, Y., Vorhees, C. V., Klein, W. H., & Campbell, K.
- Affiliations
- Cincinnati Children's Hospital Medical Center (US)
- The University of Texas MD Anderson Cancer Center (US)
- University of Cincinnati (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2013-09-30
- Volume
- 110
- Issue
- 42
- Pages
- E4026-35
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3801072
- OpenAlex
- W2081021881
- Cited by
- 79
- References
- 77
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 2 · 2023: 9 · 2022: 9 · 2021: 10 · 2020: 9 · 2019: 9 · 2018: 6 · 2017: 8 · 2016: 4 · 2015: 6 · 2014: 2
- FWCI
- 1.48
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (R01MH090740, MH090740)
- National Eye Institute (R01EY011930, P30EY010608, EY020545, EY010608-139005, EY011930, R01EY020545)
- National Cancer Institute (CA 016672, P30CA016672)
- National Institute of Environmental Health Sciences (T32ES007051)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Keywords
- Isl1, LIM homeobox genes, striatonigral pathway, striatal development, basal ganglia, substantia nigra, striatopallidal pathway, diencephalon, internal capsule, PlexinD1, semaphorin 3E, axon guidance, conditional gene inactivation, hyperlocomotion, fate mapping
- MeSH terms
- Animals, Behavior, Animal, Corpus Striatum, Cytoskeletal Proteins, Glycoproteins, Membrane Glycoproteins, Membrane Proteins, Nerve Tissue Proteins, Substantia Nigra, Transcription Factors, Signal Transduction, Cell Adhesion Molecules, Neuronal, Mice, Knockout, Semaphorins, Intracellular Signaling Peptides and Proteins, Mice, LIM-Homeodomain Proteins
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