The DOI matches its Crossref record; 102 of the 104 references it cites were found in a registry or an index.
Neuronal specification in the spinal cord: inductive signals and transcriptional codes
Abstract
Neural circuits are assembled with remarkable precision during embryonic development, and the selectivity inherent in their formation helps to define the behavioural repertoire of the mature organism. In the vertebrate central nervous system, this developmental program begins with the differentiation of distinct classes of neurons from progenitor cells located at defined positions within the neural tube. The mechanisms that specify the identity of neural cells have been examined in many regions of the nervous system and reveal a high degree of conservation in the specification of cell fate by key signalling molecules.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“the MGE can be further subdivided into dorsal, intermediate and ventrocaudal domains”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Jessell, 2000
In the citing paper
“Second, driven by the transcription factor network, each type of neural progenitors generates a series of neuronal cell types.”
From What is a cell type and how to define it? (2022) · cites this paper as Jessell, 2000
In the citing paper
“The generation and patterning of mouse cortex and spinal cord cell types are two example systems where extensive historical studies have uncovered several common principles (Cadwell et al., 2019; Catela et al., 2015; Jessell, 2000; O’Leary et al., 2007; Osseward and Pfaff, 2019; Sagner and Briscoe, 2019).”
From What is a cell type and how to define it? (2022) · cites this paper as Jessell, 2000
In the citing paper
“The set of cell type-defining transcription factors in a progenitor or a daughter cell can change with time, such that different neuronal types emanate from the same progenitor in a precisely timed “birth order”.”
From What is a cell type and how to define it? (2022) · cites this paper as Jessell, 2000
In the citing paper
“Third, specific sets of cell adhesion molecules provide guidance cues for axon path finding and synapse formation, leading to the assembly of region- and cell type-specific local and global circuit networks.”
From What is a cell type and how to define it? (2022) · cites this paper as Jessell, 2000
In the citing paper
“Later in development, the same neural progenitors also generate non-neuronal cell types such as astrocytes and oligodendrocytes.”
From What is a cell type and how to define it? (2022) · cites this paper as Jessell, 2000
In the citing paper
“First, opposing morphogen gradients establish the basic plan for cortex (anterior-posterior) or spinal cord (dorsal-ventral) patterning and provide instructive signals for the expression of complementary sets of transcription factor activators and repressors, which in turn define distinct neural progenitor domains within cortex or spinal cord.”
From What is a cell type and how to define it? (2022) · cites this paper as Jessell, 2000
In the citing paper
“Specification of the progenitor domains in the hindbrain and spinal cord relies on signaling molecules like WNT and retinoic acid (RA) secreted along the rostro-caudal axis, and sonic hedgehog (SHH) along the dorso-ventral axis”
From Generation of Functional Human 3D Cortico-Motor Assembloids (2020) · cites this paper as Jessell, 2000
In the citing paper
“The gene expression programme of each progenitor domain determines the neuronal cell type it generates”
From Single cell transcriptomics reveals spatial and temporal dynamics of gene expression in the developing mouse spinal cord (2019) · cites this paper as Jessell, 2000
In the citing paper
“This is directed by signals that emanate from the dorsal and ventral poles of the neural tube that partition progenitors into 13 transcriptionally distinct domains that are ordered along the dorsal ventral axis”
From Single cell transcriptomics reveals spatial and temporal dynamics of gene expression in the developing mouse spinal cord (2019) · cites this paper as Jessell, 2000
In the citing paper
“After their generation, MNs diversify and organise into distinct columns and pools along the anterior-posterior axis of the spinal cord”
From Single cell transcriptomics reveals spatial and temporal dynamics of gene expression in the developing mouse spinal cord (2019) · cites this paper as Jessell, 2000
Citations
Cites
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
Chiang, C. C., Litingtung, Y., Lee, E., Young, K. E., Corden, J. L., Westphal, H., & Beachy, P. A. (1996) · Nature · doi:10.1038/383407a0 · Cited by 3,062
Patterning the Vertebrate Neuraxis
Lumsden, A., & Krumlauf, R. K. (1996) · Science · doi:10.1126/science.274.5290.1109 · Cited by 1,142
Embryonic retinoic acid synthesis is essential for early mouse post-implantation development
Niederreither, K., Subbarayan, V., Dollé, P., & Chambon, P. (1999) · Nature Genetics · doi:10.1038/7788 · Cited by 1,111
Briscoe, J., Pierani, A., Jessell, T. M., & Ericson, J. (2000) · Cell · doi:10.1016/s0092-8674(00)80853-3 · Cited by 1,111
Self-citationThe tumour-suppressor gene patched encodes a candidate receptor for Sonic hedgehog
Stone, D. M., Hynes, M., Armanini, M. P., Swanson, T. A., Gu, Q., Johnson, R. L., Scott, M. P., Pennica, D., Goddard, A. D., PHILLIPS, H. S., et al. (1996) · Nature · doi:10.1038/384129a0 · Cited by 1,104
Pax6 Controls Progenitor Cell Identity and Neuronal Fate in Response to Graded Shh Signaling
Ericson, J., Rashbass, P., Schedl, A., Brenner‐Morton, S., Kawakami, A., van Heyningen, V., Jessell, T. M., & Briscoe, J. (1997) · Cell · doi:10.1016/s0092-8674(00)80323-2 · Cited by 1,044
Self-citationWang, B., Fallon, J. F., & Beachy, P. A. (2000) · Cell · doi:10.1016/s0092-8674(00)80678-9 · Cited by 1,014
Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes
Tsuchida, T., Ensini, M., Brenner‐Morton, S., Baldassare, M., Edlund, H., Jessell, T. M., & Pfaff, S. L. (1994) · Cell · doi:10.1016/0092-8674(94)90027-2 · Cited by 997
Self-citationRoelink, H., Porter, J. A., Chiang, C. C., Tanabe, Y., Chang, D. T., Beachy, P. A., & Jessell, T. M. (1995) · Cell · doi:10.1016/0092-8674(95)90397-6 · Cited by 888
Self-citationEricson, J., Brenner‐Morton, S., Kawakami, A., Roelink, H., & Jessell, T. M. (1996) · Cell · doi:10.1016/s0092-8674(00)81386-0 · Cited by 870
Self-citation
Flagged first, then by citations
2 of the 104 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 801–900 of 1,007
Sonic hedgehog signaling directs patterned cell remodeling during cranial neural tube closure
Brooks, E., Islam, M. T., Anderson, K. V., & Zallen, J. A. (2020) · eLife · doi:10.7554/elife.60234 · Cited by 57
Mauti, O., Sadhu, R., Gemayel, J., Gesemann, M., & Stoeckli, E. T. (2006) · BMC Developmental Biology · doi:10.1186/1471-213x-6-32 · Cited by 54
Morphogenetic action through flux-limited spreading
Verbeni, M., Sánchez, Ó., Mollica, E., Siegl‐Cachedenier, I., Carleton, A., Guerrero, I., Altaba, A. R. I., & Soler, J. (2013) · Physics of Life Reviews · doi:10.1016/j.plrev.2013.06.004 · Cited by 52
SUMOylation by Pias1 Regulates the Activity of the Hedgehog Dependent Gli Transcription Factors
Cox, B., Briscoe, J., & Ulloa, F. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011996 · Cited by 52
Evolution of Patterning Systems and Circuit Elements for Locomotion
Jung, H., & Dasen, J. S. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.01.008 · Cited by 51
The Composition, Development, and Regeneration of Neuromuscular Junctions
Liu, W., & Chakkalakal, J. V. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.08.005 · Cited by 55
Kriks, S., Lanuza, G. M., Mizuguchi, R., Nakafuku, M., & Goulding, M. (2005) · Development · doi:10.1242/dev.01878 · Cited by 52
Morphogens in motion: Growth control of the neural tube
Cayuso, J., & Martı́, E. (2005) · Journal of Neurobiology · doi:10.1002/neu.20169 · Cited by 52
Lazzari, G., Colleoni, S., Giannelli, S. G., Brunetti, D., Colombo, E. V., Lagutina, I., Galli, C., & Broccoli, V. (2006) · Stem Cells · doi:10.1634/stemcells.2006-0149 · Cited by 52
Coexpression of SCL and GATA3 in the V2 interneurons of the developing mouse spinal cord
Smith, E., Hargrave, M. R., Yamada, T., Begley, C. G., & Little, M. H. (2002) · Developmental Dynamics · doi:10.1002/dvdy.10093 · Cited by 52
Seifert‐Held, T., Bauer, J., Weissert, R., Fazekas, F., & Storch, M. K. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/64.5.404 · Cited by 54
Peyre, E., Silva, C. G., & Nguyen, L. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00129 · Cited by 51
Diverse Functions of MicroRNAs in Nervous System Development
Cochella, L., & Hobert, O. (2012) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-387038-4.00005-7 · Cited by 54
Binary fate decisions in differentiating neurons
Jukam, D., & Desplan, C. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.11.002 · Cited by 52
Jordan, P. M., Ojeda, L., Thonhoff, J. R., Gao, J.-L., Boehning, D., Yu, Y.-J., & Wu, P. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.21856 · Cited by 54
Sibilla, S., & Ballerini, L. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.06.001 · Cited by 50
In the swim of things: recent insights to neurogenetic disorders from zebrafish
Kabashi, E., Champagne, N., Brustein, E., & Drapeau, P. (2010) · Trends in Genetics · doi:10.1016/j.tig.2010.05.004 · Cited by 57
Khalil, O. S., Pisar, M., Forrest, C. M., Vincenten, M. C. J., Darlington, L. G., & Stone, T. W. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12535 · Cited by 51
Vue, T. Y., Kim, E. J., Parras, C. M., Guillemot, F., & Johnson, J. E. B. (2014) · Development · doi:10.1242/dev.105270 · Cited by 49
Generation of diverse cortical inhibitory interneurons
Sultan, K. T., & Shi, S. (2017) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.306 · Cited by 57
Spinal Inhibitory Interneurons: Gatekeepers of Sensorimotor Pathways
Stachowski, N. J., & Dougherty, K. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052667 · Cited by 56
Salie, R., Niederkofler, V., & Arber, S. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.002 · Cited by 51
Polycomb repressive complex 1 activities determine the columnar organization of motor neuronsPreprint
Golden, M. G., & Dasen, J. S. (2012) · Genes & Development · doi:10.1101/gad.199133.112 · Cited by 51
Homeodomain transcription factors in the development of subsets of hindbrain reticulospinal neurons
Cepeda-Nieto, A. C., Pfaff, S. L., & Varela-Echavarría, A. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.06.016 · Cited by 50
Origin and Evolution of the Brain
Barbieri, M. (2011) · Biosemiotics · doi:10.1007/s12304-011-9125-1 · Cited by 51
Transcriptional regulation of neuronal phenotype in mammals
Ma, Q. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.113449 · Cited by 50
Kang, K., Lee, D., Hong, S., Park, S., & Song, M. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.398263 · Cited by 50
The Full-length Unprocessed Hedgehog Protein Is an Active Signaling Molecule
Tokhunts, R. A., Singh, S., Chu, T., D’Angelo, G., Baubet, V., Goetz, J. A., Huang, Z. J., Yuan, Z., Ascano, M., Zavros, Y. L., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.078626 · Cited by 50
Lowry, N. A., Goderie, S. K., Adamo, M. A., Lederman, P., Charniga, C. J., Gill, J., Silver, J., & Temple, S. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.09.031 · Cited by 50
Giorgianni, M. W., & Mann, R. S. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.03.017 · Cited by 50
Yi, S., Jo, A.-Y., Park, C., Koh, H.-C., Park, R.-H., Suh‐Kim, H., Shin, I., Lee, Y., Kim, J., & Lee, S. (2008) · Molecular Therapy · doi:10.1038/mt.2008.189 · Cited by 50
Coulon, P., Bras, H., & Vinay, L. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22717 · Cited by 50
Holz, A., Kollmus, H., Ryge, J., Niederkofler, V., Dias, J. M. M., Ericson, J., Stoeckli, E. T., Kiehn, O., & Arnold, H.-H. (2010) · Development · doi:10.1242/dev.053819 · Cited by 50
Scaling Pattern to Variations in Size during Development of the Vertebrate Neural Tube
Uygur, A., Young, J. J., Huycke, T. R., Koska, M., Briscoe, J., & Tabin, C. J. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.03.024 · Cited by 50
New perspectives on the mechanisms establishing the dorsal-ventral axis of the spinal cord
Andrews, M. G., Kong, J. H., Novitch, B. G., & Butler, S. J. (2018) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2018.12.010 · Cited by 54
Osterfield, M., Kirschner, M. W., & Flanagan, J. G. (2003) · Cell · doi:10.1016/s0092-8674(03)00359-3 · Cited by 50
Tsuda, H., Sasai, N., Matsuo‐Takasaki, M., Sakuragi, M., Murakami, Y., & Sasai, Y. (2002) · Neuron · doi:10.1016/s0896-6273(02)00590-1 · Cited by 50
Asli, N. S., & Kessel, M. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.06.003 · Cited by 49
Generation of functional neurons and glia from multipotent adult mouse germ-line stem cells
Streckfuß‐Bömeke, K., Vlasov, A., Hülsmann, S., Yin, D., Nayernia, K., Engel, W., Hasenfuss, G. P., & Guan, K. (2008) · Stem Cell Research · doi:10.1016/j.scr.2008.09.001 · Cited by 49
Direct conversion of human pluripotent stem cells into cranial motor neurons using a piggyBac vector
Santis, R. D., Garone, M. G., Pagani, F., de Turris, V., Angelantonio, S. D., & Rosa, A. (2018) · Stem Cell Research · doi:10.1016/j.scr.2018.04.012 · Cited by 45
Glover, J. C. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00562-7 · Cited by 49
Takahashi, H., & Liu, F. (2006) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20077 · Cited by 51
Dorsal–ventral patterning: a view from the top
Zhuang, B., & Sockanathan, S. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.11.001 · Cited by 48
STAT3 promotes motor neuron differentiation by collaborating with motor neuron-specific LIM complex
Lee, S., Shen, R., Cho, H.-H., Kwon, R.-J., Seo, S. Y., Lee, J. W., & Lee, S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302676110 · Cited by 48
Bonito, M. D., & Studer, M. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00018 · Cited by 48
Ribeiro, A., Monteiro, J. F., Certal, A. C., Cristóvão, A. M., & Saúde, L. (2017) · Open Biology · doi:10.1098/rsob.170139 · Cited by 48
Chang, W., Pedroni, A., Bertuzzi, M., Kızıl, Ç., Simon, A., & Ampatzis, K. (2021) · Nature Communications · doi:10.1038/s41467-021-25052-1 · Cited by 48
Tarchini, B., Huynh, T. H. N., Cox, G. A., & Duboule, D. (2005) · Genes & Development · doi:10.1101/gad.351105 · Cited by 48
Delàs, M. J., Kalaitzis, C. M., Fawzi, T., Demuth, M., Zhang, I., Stuart, H. T., Costantini, E., Ivanovitch, K., Tanaka, E. M., & Briscoe, J. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.11.016 · Cited by 42
Sasakura, Y., Mita, K., Ogura, Y., & Horie, T. (2012) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2012.01343.x · Cited by 46
Du, Z., Li, X.-J., Nguyen, G. D., & Zhang, S.-C. (2006) · Molecular and cellular neurosciences · doi:10.1016/j.mcn.2006.08.007 · Cited by 51
Oustah, A. A., Danesin, C., Khouri‐Farah, N., Farreny, M.-A., Escalas, N., Cochard, P., Glise, B., & Soula, C. (2014) · Development · doi:10.1242/dev.101717 · Cited by 52
Lowry, N. A., Goderie, S. K., Lederman, P., Charniga, C. J., Gooch, M. R., Gracey, K. D., Banerjee, A., Punyani, S., Silver, J., Kane, R. S., et al. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2011.12.048 · Cited by 47
Neural stem cells and cell replacement therapy: making the right cells
Bithell, A., & Williams, B. P. (2004) · Clinical Science · doi:10.1042/cs20040276 · Cited by 46
A global genomic transcriptional code associated with CNS-expressed genes
Bailey, P. J., Klos, J. M., Andersson, E., Karlén, M., Källström, M., Ponjavic, J., Muhr, J., Lenhard, B., Sandelin, A., & Ericson, J. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.06.017 · Cited by 47
Shahbazi, E., Kiani, S., Gourabi, H., & Baharvand, H. (2011) · Tissue Engineering Part A · doi:10.1089/ten.tea.2011.0121 · Cited by 46
A Functionally Conserved Gene Regulatory Network Module Governing Olfactory Neuron Diversity
Li, Q., Barish, S., Okuwa, S., Maciejewski, A. J., Brandt, A., Reinhold, D., Jones, C. D., & Volkan, P. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1005780 · Cited by 43
Control of neuronal phenotype: what targets tell the cell bodies
Hippenmeyer, S., Krämer, I., & Arber, S. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.05.012 · Cited by 46
Coordination of cell cycle exit and differentiation of neuronal progenitors
Politis, P. K., Thomaidou, D., & Matsas, R. (2008) · Cell Cycle · doi:10.4161/cc.7.6.5550 · Cited by 47
Axonin-1/TAG-1 is required for pathfinding of granule cell axons in the developing cerebellum
Baeriswyl, T., & Stoeckli, E. T. (2008) · Neural Development · doi:10.1186/1749-8104-3-7 · Cited by 45
Marichal, N., García, G., Radmilovich, M., Trujillo-Cenóz, O., & Russo, R. E. (2012) · Stem Cells · doi:10.1002/stem.1175 · Cited by 45
Pisar, M., Forrest, C., Khalil, O. S., McNair, K., Vincenten, M. C., Qasem, S., Darlington, L., & Stone, T. W. (2014) · Brain Research · doi:10.1016/j.brainres.2014.06.016 · Cited by 45
Rnf220 cooperates with Zc4h2 to specify spinal progenitor domains
Kim, J., Choi, T.-I., Park, S., Kim, M., Kim, C.-H., & Lee, S. (2018) · Development · doi:10.1242/dev.165340 · Cited by 35
NAGASE, T., Nagase, M., Machida, M., & YAMAGISHI, M. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1389.029 · Cited by 45
Blacklaws, J., Deska‐Gauthier, D., Jones, C. T., Petracca, Y. L., Liu, M., Zhang, H., Fawcett, J. P., Glover, J. C., Lanuza, G. M., & Zhang, Y. (2015) · Developmental Neurobiology · doi:10.1002/dneu.22266 · Cited by 44
Detailed Expression Analysis of Regulatory Genes in the Early Developing Human Neural Tube
Marklund, U., Alekseenko, Z., Andersson, E., Falci, S. P., Westgren, M., Perlmann, T., Graham, A., Sundström, E., & Ericson, J. (2013) · Stem Cells and Development · doi:10.1089/scd.2013.0309 · Cited by 42
Rnf165/Ark2C Enhances BMP-Smad Signaling to Mediate Motor Axon Extension
Kelly, C. E., Thymiakou, E., Dixon, J. E., Tanaka, S., Godwin, J., & Episkopou, V. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001538 · Cited by 44
Wang, H., Lei, Q., Oosterveen, T., Ericson, J., & Matise, M. P. (2011) · Development · doi:10.1242/dev.068270 · Cited by 44
Luxenhofer, G., Helmbrecht, M. S., Langhoff, J., Giusti, S. A., Refojo, D., & Huber, A. B. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.12.023 · Cited by 42
Midbrain dopaminergic neuron fate specification: Of mice and embryonic stem cells
Gale, E. A., & Li, M. (2008) · Molecular Brain · doi:10.1186/1756-6606-1-8 · Cited by 47
Loss of ATF2 Function Leads to Cranial Motoneuron Degeneration during Embryonic Mouse Development
Ackermann, J., Ashton, G., Lyons, S., James, D. I., Hornung, J., Jones, N., & Breitwieser, W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019090 · Cited by 44
Horner, V. L., & Caspary, T. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.04.019 · Cited by 44
Origin of oligodendrocytes in mammalian forebrains: a revised perspective
Naruse, M., Ishizaki, Y., Ikenaka, K., Tanaka, A., & Hitoshi, S. (2016) · The Journal of Physiological Sciences · doi:10.1007/s12576-016-0479-7 · Cited by 43
E3 Ubiquitin Ligases in Neurological Diseases: Focus on Gigaxonin and Autophagy
Lescouzères, L., & Bomont, P. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.01022 · Cited by 43
Akay, T., & Murray, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031467 · Cited by 47
Genetic Regulation of Vertebrate Forebrain Development by Homeobox Genes
Leung, R. F., George, A. M., Roussel, E., Faux, M. C., Wigle, J. T., & Eisenstat, D. D. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.843794 · Cited by 40
Wightman, B., Ebert, B., Carmean, N., Weber, K. P., & Clever, S. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.08.032 · Cited by 44
Takemura, N. U. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.04.033 · Cited by 44
Specification of midbrain territory
Prakash, N., & Wurst, W. (2004) · Cell and Tissue Research · doi:10.1007/s00441-004-0955-x · Cited by 44
Generation of V2a Interneurons from Mouse Embryonic Stem Cells
Brown, C. R., Butts, J. C., McCreedy, D. A., & Sakiyama‐Elbert, S. E. (2014) · Stem Cells and Development · doi:10.1089/scd.2013.0628 · Cited by 42
Dorsoventral Patterning of the Brain: A Comparative Approach
Urbach, R., & Technau, G. M. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-78261-4_3 · Cited by 43
Rochtus, A. M., Izzi, B., Vangeel, E. B., Louwette, S., Wittevrongel, C., Lambrechts, D., Moreau, Y., Winand, R., Verpoorten, C., Jansen, K., et al. (2015) · Epigenetics · doi:10.1080/15592294.2014.998531 · Cited by 44
Synaptic Homeostasis Is Consolidated by the Cell Fate Gene gooseberry, a Drosophila pax3/7 Homolog
Marie, B., Pym, E. C. G., Bergquist, S. H., & Davis, G. W. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5467-09.2010 · Cited by 47
What can pluripotent stem cells teach us about neurodegenerative diseases?
Wichterle, H., & Przedborski, S. (2010) · Nature Neuroscience · doi:10.1038/nn.2577 · Cited by 42
Osteopontin is an alpha motor neuron marker in the mouse spinal cord
Misawa, H., Hara, M., Tanabe, S., Niikura, M., Moriwaki, Y., & Okuda, T. (2011) · Journal of Neuroscience Research · doi:10.1002/jnr.22813 · Cited by 43
Arbeille, E., Reynaud, F., Sanyas, I., Bozon, M., Kindbeiter, K., Causeret, F., Pierani, A., Falk, J., Moret, F., & Castellani, V. (2015) · Nature Communications · doi:10.1038/ncomms7366 · Cited by 43
Regulation of ventral midbrain patterning by Hedgehog signaling
Bayly, R. D., Ngo, M. C., Aglyamova, G. V., & Agarwala, S. (2007) · Development · doi:10.1242/dev.02850 · Cited by 43
Ji, S., Zhuang, B., Falco, C., Schneider, A., Schuster-Gossler, K., Gossler, A., & Sockanathan, S. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.05.015 · Cited by 43
New paradigms for the Hedgehog signaling network in mammary gland development and breast Cancer
Monkkonen, T., & Lewis, M. T. (2017) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2017.06.003 · Cited by 43
Hox genes and region‐specific sensorimotor circuit formation in the hindbrain and spinal cord
Bonito, M. D., Glover, J. C., & Studer, M. (2013) · Developmental Dynamics · doi:10.1002/dvdy.24055 · Cited by 42
Functions of BarH transcription factors during embryonic development
Reig, G., Cabrejos, M. E., & Concha, M. L. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.10.008 · Cited by 43
A Universal Property of Axonal and Dendritic Arbors
Snider, J., Pillai, A., & Stevens, C. F. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.013 · Cited by 44
SONIC HEDGEHOG mutations causing human holoprosencephaly impair neural patterning activity
Schell-Apacik, C., Rivero, M., Knepper, J. L., Roessler, E., Muenke, M., & Ming, J. E. (2003) · Human Genetics · doi:10.1007/s00439-003-0950-4 · Cited by 43
Arcuate Plan of Chick Midbrain Development
Sanders, T. A., Lumsden, A., & Ragsdale, C. W. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-24-10742.2002 · Cited by 43
A LIM-homeodomain code for development and evolution of forebrain connectivity
Bachy, I., Failli, V., & Rétaux, S. (2002) · Neuroreport · doi:10.1097/00001756-200202110-00002 · Cited by 43
Xue, W., Li, B., Liu, H., Xiao, Y., Li, B., Ren, L., Li, H., & Shao, Z. (2022) · iScience · doi:10.1016/j.isci.2022.105898 · Cited by 45
Pluripotent Stem Cells for Schwann Cell Engineering
Ma, M., Boddeke, E., & Copray, S. C. V. M. (2014) · Stem Cell Reviews and Reports · doi:10.1007/s12015-014-9577-1 · Cited by 42
Sensory gating of an embryonic zebrafish interneuron during spontaneous motor behaviors
Knogler, L. D., & Drapeau, P. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00121 · Cited by 42
Kanjhan, R., Noakes, P. G., & Bellingham, M. C. (2015) · Neural Plasticity · doi:10.1155/2016/3423267 · Cited by 42
Fine-Tuning of Shh/Gli Signaling Gradient by Non-proteolytic Ubiquitination during Neural Patterning
Ma, P., Song, N., Li, Y., Zhang, Q., Zhang, L., Zhang, L., Kong, Q., Ma, L., Yang, X., Ren, B., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.017 · Cited by 40
Metadata
- Authors
- Jessell, T. M.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Jessell, Thomas M.
- Venue
- Nature Reviews Genetics
- Published
- 2000-10
- Volume
- 1
- Issue
- 1
- Pages
- 20-29
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2081235375
- Cited by
- 2,089
- References
- 104
- Citations by year
- 2026: 36 · 2025: 46 · 2024: 41 · 2023: 45 · 2022: 64 · 2021: 57 · 2020: 88 · 2019: 64 · 2018: 64 · 2017: 62 · 2016: 76 · 2015: 80 · 2014: 80 · 2013: 103 · 2012: 100
- FWCI
- 5.90
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- neuronal specification, spinal cord development, neural tube, cell fate determination, transcriptional regulation, neural progenitor cells, neural circuit formation, signaling molecules, vertebrate central nervous system
- MeSH terms
- Animals, Neurons, Spinal Cord, Transcription, Genetic, Cell Lineage
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
