The late and dual origin of cerebrospinal fluid-contacting neurons in the mouse spinal cord
Open accessAbstract
Considerable progress has been made in understanding the mechanisms that control the production of specialized neuronal types. However, how the timing of differentiation contributes to neuronal diversity in the developing spinal cord is still a pending question. In this study, we show that CerebroSpinal Fluid-contacting Neurons (CSF-cNs), an anatomically discrete cell type of the ependymal area, originate from surprisingly late neurogenic events in the ventral spinal cord. CSF-cNs are identified by the expression of the transcription factors Gata2 and Gata3, and the ionic channels PKD2L1 and PKD1L2. Contrasting with Gata2/3+ V2b interneurons, CSF-cNs differentiation is independent of Foxn4 and takes place during advanced developmental stages previously assumed to be exclusively gliogenic. CSF-cNs are produced from two distinct dorso-ventral regions of the mouse spinal cord. Most CSF-cNs derive from progenitors circumscribed to the late-p2 and the oligodendrogenic (pOL) domains, whereas a second subset of CSF-cNs arises from cells bordering the floor plate. The development of these two subgroups of CSF-cNs is differentially controlled by Pax6, they adopt separate locations around the postnatal central canal and display electrophysiological differences. Our results highlight that spatio-temporal mechanisms are instrumental in creating neural cell diversity in the ventral spinal cord to produce distinct classes of interneurons, motoneurons, CSF-cNs, glial and ependymal cells.
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We identified central canal neurons (SCINH11), known as cerebrospinal fluid-contacting neurons, which expressed Gata2 and Gata3.
“In addition, here we identified central canal neurons (SCINH11), known as cerebrospinal fluid-contacting neurons, which expressed transcription factors Gata2 and Gata3 (Figure S7) (Petracca et al., 2016).”
From Molecular Architecture of the Mouse Nervous System (2018) · cites this paper as Petracca et al., 2016
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A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907 · see citing works
Neuronal specification in the spinal cord: inductive signals and transcriptional codes
Jessell, T. M. (2000) · Nature Reviews Genetics · doi:10.1038/35049541 · Cited by 2,089 · see citing works
A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex
Taniguchi, H., He, M., Wu, P., Kim, S., Paik, R., Sugino, K., Kvitsani, D., Fu, Y., Lu, J., Lin, Y., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.026 · Cited by 1,828 · see citing works
The development of neural stem cells
Temple, S. (2001) · Nature · doi:10.1038/35102174 · Cited by 1,494 · see citing works
Tamamaki, N., Yanagawa, Y., Tomioka, R., Miyazaki, J., Obata, K., & Kaneko, T. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10905 · Cited by 1,277 · see citing works
Briscoe, J., Pierani, A., Jessell, T. M., & Ericson, J. (2000) · Cell · doi:10.1016/s0092-8674(00)80853-3 · Cited by 1,111 · see citing works
Lu, Q. R., Sun, T., Zhu, Z.-M., Ma, N., García, M., Stiles, C., & Rowitch, D. (2002) · Cell · doi:10.1016/s0092-8674(02)00678-5 · Cited by 1,064 · see citing works
The bHLH Transcription Factors OLIG2 and OLIG1 Couple Neuronal and Glial Subtype Specification
Zhou, Q., & Anderson, D. J. (2002) · Cell · doi:10.1016/s0092-8674(02)00677-3 · Cited by 1,059 · see citing works
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 · see citing works
Vertebrate neurogenesis is counteracted by Sox1–3 activity
Bylund, M., Andersson, E., Novitch, B. G., & Muhr, J. (2003) · Nature Neuroscience · doi:10.1038/nn1131 · Cited by 825 · see citing works
The cells and logic for mammalian sour taste detection
Huang, A. L., Chen, X., Hoon, M. A., Chandrashekar, J. V., Guo, W., Tränkner, D., Ryba, N. J. P., & Zuker, C. S. (2006) · Nature · doi:10.1038/nature05084 · Cited by 814 · see citing works
Homeobox gene Nkx2.2 and specification of neuronal identity by graded Sonic hedgehog signalling
Briscoe, J., Sussel, L., Serup, P., Hartigan-O'Connor, D., Jessell, T., Rubenstein, J., & Ericson, J. (1999) · Nature · doi:10.1038/19315 · Cited by 807 · see citing works
Circuits controlling vertebrate locomotion: moving in a new direction
Goulding, M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2608 · Cited by 777 · cited 1× · see citing works
“These dorsoventrally restricted progenitors produce distinct corresponding early-born classes of postmitotic neurons (motoneurons and V0-V3 interneurons) identified by the expression of specific sets of transcription factors (Jessell, 2000; Briscoe and Novitch, 2008; Goulding, 2009; Francius et al., 2013).”
BackgroundAdult Ependymal Cells Are Postmitotic and Are Derived from Radial Glial Cells during Embryogenesis
Spassky, N., Merkle, F. T., Flames, N., Tramontin, A. D., García-Verdugo, J. M., & Alvarez-Buylla, A. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1108-04.2005 · Cited by 717 · see citing works
Developmental genetics of vertebrate glial–cell specification
Rowitch, D., & Kriegstein, A. (2010) · Nature · doi:10.1038/nature09611 · Cited by 685 · see citing works
Neuronal differentiation in the adult hippocampus recapitulates embryonic development
Espósito, M. S., Piatti, V. C., Laplagne, D. A., Morgenstern, N. A., Ferrari, C. C., Pitossi, F. J., & Schinder, A. F. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3114-05.2005 · Cited by 679 · see citing works
Self-citationSpinal Cord Injury Reveals Multilineage Differentiation of Ependymal Cells
Meletis, K., Barnabé‐Heider, F., Carlén, M., Evergren, E., Tomilin, N. V., Shupliakov, O., & Frisén, J. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060182 · Cited by 667 · see citing works
Regional Astrocyte Allocation Regulates CNS Synaptogenesis and Repair
Tsai, H., Li, H., Fuentealba, L. C., Molofsky, A. V., Taveira‐Marques, R., Zhuang, H., Tenney, A., Murnen, A. T., Fancy, S. P. J., Merkle, F. T., et al. (2012) · Science · doi:10.1126/science.1222381 · Cited by 529 · see citing works
The Development of the Rat Spinal Cord
Altman, J., & Bayer, S. A. (1984) · Advances in anatomy, embryology and cell biology · doi:10.1007/978-3-642-69537-7 · Cited by 509 · see citing works
Transient receptor potential family members PKD1L3 and PKD2L1 form a candidate sour taste receptor
Ishimaru, Y., Inada, H., Kubota, M., Zhuang, H., Tominaga, M., & Matsunami, H. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602702103 · Cited by 497 · see citing works
Balaskas, N., Ribeiro, A., Panovska, J., Dessaud, E., Sasai, N., Page, K., Briscoe, J., & Ribes, V. (2012) · Cell · doi:10.1016/j.cell.2011.10.047 · Cited by 468 · see citing works
Heterochrony: The Evolution of Ontogeny
McKinney, M. L., & McNamara, K. J. (1991) · Medical Entomology and Zoology · Cited by 451 · see citing works
Multiple origins of Cajal-Retzius cells at the borders of the developing pallium
Bielle, F., Griveau, A., Narboux‐Nême, N., Vigneau, S., Sigrist, M., Arber, S., Wassef, M., & Pierani, A. (2005) · Nature Neuroscience · doi:10.1038/nn1511 · Cited by 450 · see citing works
Lanuza, G. M., Gosgnach, S., Pierani, A., Jessell, T. M., & Goulding, M. (2004) · Neuron · doi:10.1016/s0896-6273(04)00249-1 · Cited by 450 · see citing works
Self-citationMcKinney, M. L., & McNamara, K. J. (1991) · Springer eBooks · doi:10.1007/978-1-4757-0773-1 · Cited by 441 · see citing works
Glial specification in the vertebrate neural tube
Rowitch, D. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1389 · Cited by 432 · see citing works
GATA-3 Is Involved in the Development of Serotonergic Neurons in the Caudal Raphe Nuclei
van Doorninck, J. H., van der Wees, J., Karis, A., Sabel-Goedknegt, E., Coesmans, M., Rutteman, M., Grosveld, F. G., & Zeeuw, C. I. D. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-12-j0002.1999 · Cited by 416 · see citing works
Optogenetic dissection of a behavioural module in the vertebrate spinal cord
Wyart, C., Bene, F. D., Warp, E., Scott, E. K., Trauner, D., Baier, H., & Isacoff, E. Y. (2009) · Nature · doi:10.1038/nature08323 · Cited by 409 · see citing works
V1 spinal neurons regulate the speed of vertebrate locomotor outputs
Gosgnach, S., Lanuza, G. M., Butt, S. J. B., Saueressig, H., Zhang, Y., Velasquez, T., Riethmacher, D., Callaway, E. M., Kiehn, O., & Goulding, M. (2006) · Nature · doi:10.1038/nature04545 · Cited by 405 · see citing works
Self-citationLbx1 specifies somatosensory association interneurons in the dorsal spinal cord
Gross, M. K., Dottori, M., & Goulding, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00690-6 · Cited by 396 · see citing works
Kirby, B. B., Takada, N., Latimer, A. J., Shin, J., Carney, T. J., Kelsh, R. N., & Appel, B. (2006) · Nature Neuroscience · doi:10.1038/nn1803 · Cited by 394 · see citing works
Control of Interneuron Fate in the Developing Spinal Cord by the Progenitor Homeodomain Protein Dbx1
Pierani, A., Moran-Rivard, L., Sunshine, M. J., Littman, D. R., Goulding, M., & Jessell, T. M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00212-4 · Cited by 379 · see citing works
Altman, J., & Bayer, S. A. (1984) · Advances in anatomy, embryology and cell biology · doi:10.1007/978-3-642-69537-7_1 · Cited by 378 · see citing works
Crone, S. A., Quinlan, K. A., Zagoraiou, L., Droho, S., Restrepo, C. E., Lundfald, L., Endo, T., Setlak, J., Jessell, T. M., Kiehn, O., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.009 · Cited by 358 · see citing works
V3 Spinal Neurons Establish a Robust and Balanced Locomotor Rhythm during Walking
Zhang, Y., Narayan, S., Geiman, E. J., Lanuza, G. M., Velasquez, T., Shanks, B., Akay, T., Dyck, J. R. B., Pearson, K. G., Gosgnach, S., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.027 · Cited by 350 · see citing works
Self-citationTlx3 and Tlx1 are post-mitotic selector genes determining glutamatergic over GABAergic cell fates
Cheng, L., Arata, A., Mizuguchi, R., Qian, Y., Karunaratne, A., Gray, P. A., Arata, S., Shirasawa, S., Bouchard, M., Luo, P., et al. (2004) · Nature Neuroscience · doi:10.1038/nn1221 · Cited by 350 · see citing works
Multiple dorsoventral origins of oligodendrocyte generation in the spinal cord and hindbrain.
Vallstedt, A., Klos, J. M., & Ericson, J. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.026 · Cited by 346 · see citing works
Hochstim, C., Deneen, B., Lukaszewicz, A., Zhou, Q., & Anderson, D. J. (2008) · Cell · doi:10.1016/j.cell.2008.02.046 · Cited by 331 · see citing works
Direct recording and molecular identification of the calcium channel of primary cilia
DeCaen, P. G., Delling, M., Vien, T. N., & Clapham, D. E. (2013) · Nature · doi:10.1038/nature12832 · Cited by 306 · see citing works
Activation of EGFP expression by Cre-mediated excision in a new ROSA26 reporter mouse strain
Mao, X., Fujiwara, Y., Chapdelaine-Williams, A. M., Yang, H., & Orkin, S. H. (2001) · Blood · doi:10.1182/blood.v97.1.324 · Cited by 291 · see citing works
The cytoarchitecture of gabaergic neurons in rat spinal cord
Barber, R. P., Vaughn, J. E., & Roberts, E. (1982) · Brain Research · doi:10.1016/0006-8993(82)90107-x · Cited by 255 · see citing works
Foxn4 Controls the Genesis of Amacrine and Horizontal Cells by Retinal Progenitors
Li, S., Mo, Z., Yang, X., Price, S. M., Shen, M. M., & Xiang, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.041 · Cited by 252 · see citing works
Zhang, J., Lanuza, G. M., Britz, O., Wang, Z., Siembab, V. C., Zhang, Y., Velasquez, T., Alvarez, F. J., Frank, E., & Goulding, M. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.013 · Cited by 233 · see citing works
Self-citationLocomotor rhythm generation linked to the output of spinal Shox2 excitatory interneurons
Dougherty, K. J., Zagoraiou, L., Satoh, D., Rozani, I., Doobar, S., Arber, S., Jessell, T. M., & Kiehn, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.015 · Cited by 229 · see citing works
Béla, V. I. G. H., Silva, M. J. M. E., Frank, C. L., Vincze, C., Czirok, S., Szabó, A., Lukáts, Á., & Szél, Á. (2004) · PubMed · doi:10.14670/hh-19.607 · Cited by 219 · see citing works
Zhang, Z. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00855.2003 · Cited by 210 · see citing works
Dessaud, E., Ribes, V., Balaskas, N., Yang, L. L., Pierani, A., Kicheva, A., Novitch, B. G., Briscoe, J., & Sasai, N. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000382 · Cited by 203 · see citing works
Pax6 and Engrailed 1 Regulate Two Distinct Aspects of Renshaw Cell Development
Sapir, T., Geiman, E. J., Wang, Z., Velasquez, T., Mitsui, S., Yoshihara, Y., Frank, E., Álvarez, F. J., & Goulding, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3187-03.2004 · Cited by 189 · see citing works
Time's arrow: heterochrony and the evolution of development
Smith, K. K. (2003) · The International Journal of Developmental Biology · doi:10.1387/ijdb.14756337 · Cited by 184 · see citing works
Kimura, Y., Satou, C., & Higashijima, S. (2008) · Development · doi:10.1242/dev.024802 · Cited by 182 · see citing works
Spatial and temporal regulation of ventral spinal cord precursor specification by Hedgehog signaling
Park, H.-C., Shin, J., & Appel, B. (2004) · Development · doi:10.1242/dev.01456 · Cited by 180 · see citing works
Notch and MAML Signaling Drives Scl-Dependent Interneuron Diversity in the Spinal Cord
Peng, C., Yajima, H., Burns, C. E., Zon, L. I., Sisodia, S. S., Pfaff, S. L., & Sharma, K. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.019 · Cited by 178 · see citing works
Lundfald, L., Restrepo, C. E., Butt, S. J. B., Peng, C., Droho, S., Endo, T., Zeilhofer, H. U., Sharma, K., & Kiehn, O. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05906.x · Cited by 172 · see citing works
Briscoe, J., & Novitch, B. G. (2008) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2006.2012 · Cited by 162 · see citing works
Actual problems of the cerebrospinal fluid-contacting neurons
Béla, V. I. G. H., & Vigh‐Teichmann, I. (1998) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19980401)41:1 · Cited by 151 · see citing works
GATA2 is required for the generation of V2 interneurons
Zhou, Y., Yamamoto, M. P., & Engel, J. D. (2000) · Development · doi:10.1242/dev.127.17.3829 · Cited by 133 · see citing works
Djenoune, L., Khabou, H., Joubert, F., Quan, F. B., Figueiredo, S. N., Bodineau, L., Bene, F. D., Burcklé, C., Tostivint, H., & Wyart, C. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00026 · Cited by 125 · see citing works
Barrio, M. G. D., Taveira‐Marques, R., Muroyama, Y., Yuk, D., Li, S., Wines-Samuelson, M., Shen, J., Smith, H. K., Xiang, M., Rowitch, D. H., et al. (2007) · Development · doi:10.1242/dev.005868 · Cited by 123 · see citing works
Dale, N., Roberts, A., Ottersen, O. P., & Storm‐Mathisen, J. (1987) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1987.0068 · Cited by 122 · see citing works
Chen, J.-A., Huang, Y.-P., Mazzoni, E. O., Tan, G. C., Zavadil, J., & Wichterle, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.01.014 · Cited by 121 · see citing works
Stam, F. J., Hendricks, T. J., Zhang, J., Geiman, E. J., Francius, C., Labosky, P. A., Clotman, F., & Goulding, M. (2012) · Development · doi:10.1242/dev.071134 · Cited by 115 · cited 2× · see citing works
“Although other cases have been reported in which the temporal component contributes to neuronal diversity in the spinal cord (Gross et al., 2002; Stam et al., 2012), we provide robust evidence of neuronal differentiation occurring in what has been classically termed the gliogenic phase, proving that neurogenic potenti…”
BackgroundCell Depletion Due to Diphtheria Toxin Fragment A after Cre-Mediated Recombination
Brockschnieder, D., Lappe-Siefke, C., Goebbels, S., Boesl, M. R., Nave, K., & Riethmacher, D. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.17.7636-7642.2004 · Cited by 114 · see citing works
Sabourin, J.-C., Ackema, K. B., Ohayon, D., Guichet, P., Perrin, F. E., Garcès, A., Ripoll, C., Charité, J., Simonneau, L., Kettenmann, H., et al. (2009) · Stem Cells · doi:10.1002/stem.226 · Cited by 112 · see citing works
State-Dependent Modulation of Locomotion by GABAergic Spinal Sensory Neurons
Fidelin, K., Djenoune, L., Stokes, C. C. A., Prendergast, A. E., Gómez, J., Baradel, A., Bene, F. D., & Wyart, C. (2015) · Current Biology · doi:10.1016/j.cub.2015.09.070 · Cited by 108 · see citing works
GATA Proteins Identify a Novel Ventral Interneuron Subclass in the Developing Chick Spinal Cord
Karunaratne, A., Hargrave, M. R., Poh, A. M., & Yamada, T. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0754 · Cited by 107 · see citing works
Combinatorial Gata2 and Sca1 expression defines hematopoietic stem cells in the bone marrow niche
Suzuki, N., Ohneda, O., Minegishi, N., Nishikawa, M., Ohta, T., Takahashi, S., Engel, J. D., & Yamamoto, M. P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508928103 · Cited by 107 · see citing works
Francius, C., Harris, A., Rucchin, V., Hendricks, T. J., Stam, F. J., Barber, M., Kurek, D., Grosveld, F. G., Pierani, A., Goulding, M., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0070325 · Cited by 97 · see citing works
Enigmatic Central Canal Contacting Cells: Immature Neurons in “Standby Mode”?
Marichal, N., García, G., Radmilovich, M., Trujillo-Cenóz, O., & Russo, R. E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6183-08.2009 · Cited by 96 · see citing works
Stoeckel, M. E., Uhl‐Bronner, S., Hugel, S., Veinante, P., Klein, M. J., Mutterer, J., Freund‐Mercier, M. J., & Schlichter, R. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10565 · Cited by 95 · see citing works
Fu, H. Q., Qi, Y. B., Tan, M. H., Cai, J., Hu, X., Liu, Z., Jensen, J. N., & Qiu, M. S. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10481 · Cited by 93 · see citing works
Yu, K., McGlynn, S., & Matise, M. P. (2013) · Development · doi:10.1242/dev.090845 · Cited by 93 · see citing works
Vertebrate floor-plate specification: variations on common themes
Strähle, U., Lam, C. S., Ertzer, R., & Rastegar, S. (2004) · Trends in Genetics · doi:10.1016/j.tig.2004.01.002 · Cited by 90 · see citing works
Lek, M., Dias, J. M., Marklund, U., Uhde, C. W., Kurdija, S., Lei, Q., Sussel, L., Rubenstein, J., Matise, M., Arnold, H., et al. (2010) · Development · doi:10.1242/dev.054288 · Cited by 90 · see citing works
Attenuation of Notch and Hedgehog Signaling Is Required for Fate Specification in the Spinal Cord
Huang, P., Xiong, F., Megason, S. G., & Schier, A. F. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002762 · Cited by 90 · see citing works
Shin, J., Poling, J., Park, H., & Appel, B. (2007) · Development · doi:10.1242/dev.001602 · Cited by 87 · see citing works
Li, S., Misra, K., Matise, M. P., & Xiang, M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504799102 · Cited by 84 · see citing works
Batista, M. F., Jacobstein, J., & Lewis, K. E. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.07.015 · Cited by 82 · see citing works
LMO4 Controls the Balance between Excitatory and Inhibitory Spinal V2 Interneurons
Joshi, K., Lee, S., Lee, J. W., Lee, S., & Lee, S. (2009) · Neuron · doi:10.1016/j.neuron.2009.02.011 · Cited by 80 · see citing works
Electrical properties of motoneurons in the spinal cord of rat embryos
Ziskind‐Conhaim, L. (1988) · Developmental Biology · doi:10.1016/0012-1606(88)90262-x · Cited by 80 · see citing works
Orts-Del’Immagine, A., Wanaverbecq, N., Tardivel, C., Tillement, V., Dallaporta, M., & Trouslard, J. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.227959 · Cited by 78 · see citing works
Regulatory interactions specifying Kolmer-Agduhr interneurons
Yang, L., Rastegar, S., & Strähle, U. (2010) · Development · doi:10.1242/dev.048470 · Cited by 77 · see citing works
Panayi, H., Panayiotou, E., Orford, M., Genethliou, N., Mean, R. J., Lapathitis, G., Li, S., Xiang, M., Kessaris, N., Richardson, W. D., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2402-10.2010 · Cited by 76 · see citing works
Engineering of a polymeric bacterial protein as a scaffold for the multiple display of peptides
Laplagne, D. A., Zylberman, V., Ainciart, N., Steward, M. W., Sciutto, E., Fossati, C. A., & Goldbaum, F. A. (2004) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.20248 · Cited by 70 · see citing works
Rocha, S. F., Lopes, S. S., Gossler, A., & Henrique, D. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.01.011 · Cited by 66 · see citing works
Béla, V. I. G. H., Vigh‐Teichmann, I., & Aros, B. (1977) · Cell and Tissue Research · doi:10.1007/bf00225666 · Cited by 65 · see citing works
Yeo, S., & Chitnis, A. B. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607062104 · Cited by 64 · see citing works
Dale, N., Roberts, A., Ottersen, O. P., & Storm‐Mathisen, J. (1987) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1987.0069 · Cited by 61 · see citing works
Orts-Del’Immagine, A., Kästner, A., Tillement, V., Tardivel, C., Trouslard, J., & Wanaverbecq, N. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087748 · Cited by 59 · see citing works
Jalalvand, E., Robertson, B., Wallén, P., Hill, R. H., & Grillner, S. E. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23542 · Cited by 58 · see citing works
Orts-Del’Immagine, A., Seddik, R., Tell, F., Airault, C., Er-Raoui, G., Najimi, M., Trouslard, J., & Wanaverbecq, N. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.07.030 · Cited by 57 · see citing works
Béla, V. I. G. H., Vigh‐Teichmann, I., Silva, M. J. M. E., & van den Pol, A. N. (1983) · Cell and Tissue Research · doi:10.1007/bf00218119 · Cited by 51 · see citing works
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 · see citing works
The TRPP Subfamily and Polycystin-1 Proteins
Semmo, M., Köttgen, M., & Hofherr, A. (2014) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-54215-2_27 · Cited by 48 · see citing works
Marichal, N., García, G., Radmilovich, M., Trujillo-Cenóz, O., & Russo, R. E. (2012) · Stem Cells · doi:10.1002/stem.1175 · Cited by 45 · see citing works
Discontinuous organization and specification of the lateral floor plate in zebrafish
Schäfer, M., Kinzel, D., & Winkler, C. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.09.018 · Cited by 41 · see citing works
Neurogenin3 Restricts Serotonergic Neuron Differentiation to the Hindbrain
Carcagno, A. L., Bella, D. J. D., Goulding, M., Guillemot, F., & Lanuza, G. M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3403-14.2014 · Cited by 35 · see citing works
Self-citationKútna, V., Ševc, J., Gombalová, Z. T., Matiašová, A. A., & Daxnerová, Z. (2013) · Acta Histochemica · doi:10.1016/j.acthis.2013.08.004 · Cited by 33 · see citing works
Structure of the medullo-spinal liquor-contacting neuronal system.
Béla, V. I. G. H., & Vigh‐Teichmann, I. (1971) · PubMed · Cited by 31 · see citing works
GABAergic signalling in a neurogenic niche of the turtle spinal cord
Reali, C., Fernández, A. S., Radmilovich, M., Trujillo-Cenóz, O., & Russo, R. E. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.214312 · Cited by 27 · see citing works
Lovász, L. (1971) · Acta Mathematica Academiae Scientiarum Hungaricae · doi:10.1007/bf01896014 · Cited by 16 · see citing works
Pax6 is expressed in subsets of V0 and V2 interneurons in the ventral spinal cord in mice
Panayiotou, E., Panayi, E., Lapathitis, G., Francius, C., Clotman, F., Kessaris, N., Richardson, W. D., & Malas, S. (2013) · Gene Expression Patterns · doi:10.1016/j.gep.2013.06.004 · Cited by 13 · see citing works
Flagged first, then by citations
2 of the 103 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Vigh, B. and Vigh-Teichmann, I. (1998). Actual problems of the cerebrospinal fluid- contacting neurons. Microsc. Res. Tech. 41, 57-83. · DOI
Cited by
Sorted by citations
Molecular Architecture of the Mouse Nervous System
Zeisel, A., Hochgerner, H., Lönnerberg, P., Johnsson, A., Memic, F., van der Zwan, J., Häring, M., Braun, E., Borm, L. E., La Manno, G., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.021 · Cited by 2,995 · see citing works
Single-cell profiling of the developing mouse brain and spinal cord with split-pool barcoding
Rosenberg, A. B., Roco, C. M., Muscat, R. A., Kuchina, A., Sample, P., Yao, Z., Graybuck, L. T., Peeler, D. J., Mukherjee, S., Chen, W., et al. (2018) · Science · doi:10.1126/science.aam8999 · Cited by 1,422 · see citing works
A harmonized atlas of mouse spinal cord cell types and their spatial organization
Russ, D. E., Cross, R. B. P., Li, L., Koch, S. C., Matson, K. J. E., Yadav, A., Alkaslasi, M. R., Lee, D. I., Le Pichon, C. E., Menon, V., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25125-1 · Cited by 255 · see citing works
Sternberg, J. R., Prendergast, A. E., Brosse, L., Cantaut-Belarif, Y., Thouvenin, O., Orts-Del’Immagine, A., Castillo, L., Djenoune, L., Kurisu, S., McDearmid, J. R., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06225-x · Cited by 148 · see citing works
Single-cell and spatial atlases of spinal cord injury in the Tabulae Paralytica
Skinnider, M. A., Gautier, M., Teo, A. Y. Y., Kathe, C., Hutson, T. H., Laskaratos, A., de Coucy, A., Regazzi, N., Aureli, V., James, N. D., et al. (2024) · Nature · doi:10.1038/s41586-024-07504-y · Cited by 131 · see citing works
The role of motile cilia in the development and physiology of the nervous system
Ringers, C., Olstad, E. W., & Jurisch‐Yaksi, N. (2019) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0156 · Cited by 120 · see citing works
Delineating the Diversity of Spinal Interneurons in Locomotor Circuits
Gosgnach, S., Bikoff, J. B., Dougherty, K. J., Manira, A. E., Lanuza, G. M., & Zhang, Y. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1829-17.2017 · Cited by 100 · see citing works
Self-citationVergara, H. M., Bertucci, P. Y., Hantz, P., Tosches, M. A., Achim, K., Vopálenský, P., & Arendt, D. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610602114 · Cited by 84 · see citing works
Regulating Endogenous Neural Stem Cell Activation to Promote Spinal Cord Injury Repair
Gilbert, E. A. B., Lakshman, N., Lau, K. S. K., & Morshead, C. M. (2022) · Cells · doi:10.3390/cells11050846 · Cited by 80 · see citing works
Orts-Del’Immagine, A., Cantaut-Belarif, Y., Thouvenin, O., Roussel, J., Baskaran, A., Langui, D., Koëth, F., Bivas, P., Lejeune, F., Bardet, P., et al. (2020) · Current Biology · doi:10.1016/j.cub.2019.12.071 · Cited by 81 · see citing works
The spinal ependymal zone as a source of endogenous repair cells across vertebrates
Becker, C. G., Becker, T., & Hugnot, J. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.04.002 · Cited by 80 · see citing works
Djenoune, L., Desban, L., Gomez, J., Sternberg, J. R., Prendergast, A., Langui, D., Quan, F. B., Marnas, H., Auer, T. O., Rio, J.-P., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-00350-1 · Cited by 65 · see citing works
Cerebrospinal fluid-contacting neurons: multimodal cells with diverse roles in the CNS
Wyart, C., Tano, M. C., Cantaut-Belarif, Y., Orts-Del’Immagine, A., & Böhm, U. L. (2023) · Nature reviews. Neuroscience · doi:10.1038/s41583-023-00723-8 · Cited by 65 · see citing works
Spinal V2b neurons reveal a role for ipsilateral inhibition in speed control
Callahan, R. A., Roberts, R., Sengupta, M., Kimura, Y., Higashijima, S.-I., & Bagnall, M. W. (2019) · eLife · doi:10.7554/elife.47837 · Cited by 57 · see citing works
Walking with Salamanders: From Molecules to Biorobotics
Ryczko, D., Simon, A., & Ijspeert, A. J. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.08.006 · Cited by 52 · see citing works
Spinal sensory neurons project onto the hindbrain to stabilize posture and enhance locomotor speed
Wu, M., Tano, M. C., Mirat, O., Lejeune, F., Roussel, J., Quan, F. B., Fidelin, K., & Wyart, C. (2021) · Current Biology · doi:10.1016/j.cub.2021.05.042 · Cited by 54 · see citing works
Andrzejczuk, L., Banerjee, S., England, S. J., Voufo, C., Kamara, K. O., & Lewis, K. E. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00170 · Cited by 44 · see citing works
Ghazale, H., Ripoll, C., Leventoux, N., Jacob, L., Azar, S., Mamaeva, D. V., Glasson, Y., Calvo, C., Thomas, J., Meneceur, S., et al. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.04.001 · Cited by 42 · see citing works
Nakamura, Y., Kurabe, M., Matsumoto, M., Sato, T., Miyashita, S., Hoshina, K., Kamiya, Y., Tainaka, K., Matsuzawa, H., Ohno, N., et al. (2023) · eLife · doi:10.7554/elife.83108 · Cited by 47 · see citing works
Prendergast, A. E., Jim, K. K., Marnas, H., Desban, L., Quan, F. B., Djenoune, L., Laghi, V., Hocquemiller, A., Lunsford, E. T., Roussel, J., et al. (2023) · Current Biology · doi:10.1016/j.cub.2023.01.039 · Cited by 39 · see citing works
Ependymal cells in the spinal cord as neuronal progenitors
Moreno‐Manzano, V. (2019) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2019.11.008 · Cited by 34 · see citing works
Deska‐Gauthier, D., Borowska-Fielding, J., Jones, C. T., & Zhang, Y. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1518-19.2019 · Cited by 33 · see citing works
Ascl1 Balances Neuronal versus Ependymal Fate in the Spinal Cord Central Canal.
Bella, D. J. D., Carcagno, A. L., Bartolomeu, M., Pardi, M. B., Löhr, H., Siegel, N., Hammerschmidt, M., Marin-Burgin, A., & Lanuza, G. M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.07.087 · Cited by 19 · see citing works
Self-citationDesban, L., Prendergast, A. E., Roussel, J., Rosello, M., Gény, D., Wyart, C., & Bardet, P. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000235 · Cited by 31 · see citing works
Identification and Expression Analysis of the Complete Family of Zebrafish pkd Genes
England, S. J., Campbell, P. C., Banerjee, S., Swanson, A. J., & Lewis, K. E. (2017) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2017.00005 · Cited by 31 · see citing works
Spinal Cord Stem Cells In Their Microenvironment: The Ependyma as a Stem Cell Niche
Marichal, N., Reali, C., Trujillo-Cenóz, O., & Russo, R. E. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-69194-7_5 · Cited by 31 · see citing works
Gilbert, E. A. B., & Vickaryous, M. K. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24335 · Cited by 30 · see citing works
Cañizares, M. A., Albors, A. R., Singer, G. A., Suttie, N., Gorkic, M., Felts, P. A., & Storey, K. G. (2019) · Journal of Anatomy · doi:10.1111/joa.13094 · Cited by 29 · see citing works
Postnatal maturation of mouse medullo-spinal cerebrospinal fluid-contacting neurons
Orts-Del’Immagine, A., Trouslard, J., Airault, C., Hugnot, J., Cordier, B., Doan, T., Kästner, A., & Wanaverbecq, N. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.11.028 · Cited by 28 · see citing works
Li, Y., Tzatzalos, E., Kwan, K. Y., Grumet, M., & Cai, L. (2016) · Scientific Reports · doi:10.1038/srep38665 · Cited by 27 · see citing works
Song, S., Li, Y.-H., Bao, C.-Y., Li, Y., Yin, P.-C., Hong, J. W., Li, W.-L., Shi, Y., & Zhang, L. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00047 · Cited by 21 · see citing works
Jurčić, N., Michelle, C., Trouslard, J., Wanaverbecq, N., & Kästner, A. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15342 · Cited by 20 · see citing works
Temporal cell fate determination in the spinal cord is mediated by the duration of Notch signalling
Jacobs, C. T., Kejriwal, A., Kocha, K. M., Jin, K. Y., & Huang, P. (2022) · Developmental Biology · doi:10.1016/j.ydbio.2022.05.010 · Cited by 20 · see citing works
The GPCR properties of polycystin-1- A new paradigm
Maser, R. L., Calvet, J. P., & Parnell, S. C. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.1035507 · Cited by 20 · see citing works
Somatostatin 1.1 contributes to the innate exploration of zebrafish larva
Quan, F. B., Desban, L., Mirat, O., Kermarquer, M., Roussel, J., Koëth, F., Marnas, H., Djenoune, L., Lejeune, F., Tostivint, H., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-72039-x · Cited by 19 · see citing works
Floor plate descendants in the ependyma of the adult mouse Central Nervous System
Khazanov, S., Paz, Y., Hefetz, A., Gonzales, B. J., Netser, Y., Mansour, A. A., & Ben‐Arie, N. (2016) · The International Journal of Developmental Biology · doi:10.1387/ijdb.160232nb · Cited by 17 · see citing works
Interneuron diversity and function in the spinal motor system
Bikoff, J. B. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2018.12.013 · Cited by 17 · see citing works
The Genetic Programs Specifying Kolmer–Agduhr Interneurons
Yang, L., Wang, F., & Strähle, U. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.577879 · Cited by 16 · see citing works
Gombalová, Z. T., Košuth, J., Matiašová, A. A., Zrubáková, J., Žežula, I., Giallongo, T., Giulio, A. M. D., Carelli, S., Tomašková, L., Daxnerová, Z., et al. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24909 · Cited by 15 · see citing works
The Neural Stem Cell Properties of PKD2L1+ Cerebrospinal Fluid-Contacting Neurons in vitro
Wang, S., He, Y., Zhang, H., Chen, L., Cao, L., Yang, L., Wang, C., Pan, Y., Tang, Q., Tan, W. H., et al. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.630882 · Cited by 14 · see citing works
Edwards‐Faret, G., Cebrián‐Silla, A., Méndez‐Olivos, E. E., González‐Pinto, K., García‐Verdugo, J. M., & Larraı́n, J. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24441 · Cited by 13 · see citing works
The neural stem cell properties of Pkd2l1+ cerebrospinal fluid-contacting neurons in vivo
Cao, L., Huang, M., Zhang, Q., Luo, Z.-R., Zhang, Y., An, P.-J., Yang, L., Tan, W. H., Wang, C., Dou, X., et al. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.992520 · Cited by 13 · see citing works
Bellegarda, C., Zavard, G., Moisan, L., Gray, R. S., Brochard-Wyart, F., Joanny, J., Cantaut-Belarif, Y., & Wyart, C. (2023) · eLife · doi:10.7554/elife.86175 · Cited by 12 · see citing works
The Temporal Mechanisms Guiding Interneuron Differentiation in the Spinal Cord
Deska‐Gauthier, D., & Zhang, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158025 · Cited by 11 · see citing works
A GABAergic Maf-expressing interneuron subset regulates the speed of locomotion in Drosophila
Babski, H., Jovanic, T., Surel, C., Yoshikawa, S., Zwart, M., Valmier, J., Thomas, J. B., Enriquez, J., Carroll, P., & Garcès, A. (2019) · Nature Communications · doi:10.1038/s41467-019-12693-6 · Cited by 11 · see citing works
Spinal sensory circuits in motion
Böhm, U. L., & Wyart, C. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.07.007 · Cited by 10 · see citing works
Matiašová, A. A., Ševc, J., Tomori, Z., Gombalová, Z. T., Gedrová, Š., & Daxnerová, Z. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24091 · Cited by 10 · see citing works
Alibardi, L. (2019) · Journal of Morphology · doi:10.1002/jmor.21031 · Cited by 10 · see citing works
Mukaigasa, K., Sakuma, C., & Yaginuma, H. (2021) · Development Growth & Differentiation · doi:10.1111/dgd.12750 · Cited by 5 · see citing works
Donato, S., & Vickaryous, M. K. (2022) · Journal of Developmental Biology · doi:10.3390/jdb10020021 · Cited by 5 · see citing works
Pasquini, J. M., Barrantes, F. J., & Quintá, H. R. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24243 · Cited by 5 · see citing works
Zhang, Y., Cao, L., Yan, H., Luo, Z., Chen, C., Shangguan, Z., Li, Q., Shi, X., Yang, L., Tan, W. H., et al. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02492-y · Cited by 4 · see citing works
Xiong, Y.-X., Pi, W., Wang, Z., Shi, W., Yan, W., Yang, H., Zhou, Y., Li, Q., & Yang, L. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1426395 · Cited by 4 · see citing works
Riondel, P., Jurčić, N., Mounien, L., Ibrahim, S., Ramírez‐Franco, J., Stefanovic, S., Trouslard, J., Wanaverbecq, N., & Seddik, R. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.2289-22.2024 · Cited by 4 · see citing works
He, Y., Shi, X., Chen, L., Zhao, W.-B., Shan, J., Lin, Z.-L., Yang, L., & Li, Q. (2020) · International Journal of Neuroscience · doi:10.1080/00207454.2020.1750396 · Cited by 4 · see citing works
Elysa, C., Blasco, E., Ramírez‐Franco, J., Riondel, P., Jurčić, N., Seddik, R., Michelle, C., Trouslard, J., & Wanaverbecq, N. (2025) · Communications Biology · doi:10.1038/s42003-025-08559-x · Cited by 3 · see citing works
Cucun, G., Köhler, M., Pfitsch, S., & Rastegar, S. (2023) · FEBS Journal · doi:10.1111/febs.16913 · Cited by 3 · see citing works
Kästner, A., & Wanaverbecq, N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.29.534787 · Cited by 3 · see citing works
The Tabulae Paralytica: Multimodal single-cell and spatial atlases of spinal cord injuryPreprint
Skinnider, M. A., Gautier, M., Teo, A. Y. Y., Kathe, C., Hutson, T. H., Laskaratos, A., de Coucy, A., Regazzi, N., Aureli, V., James, N. D., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.23.544348 · Cited by 3 · see citing works
Cao, L., Yan, W., Pi, W., Zhang, Y., Xiong, Y.-X., Yong, V. W., Xue, M., Li, Q., Zheng, C., & Yang, L. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111217 · Cited by 2 · see citing works
Luo, Z., Shangguan, Z., Cao, L., Zhang, Y., Li, Q., Shi, X., Fu, J., Wang, C., Dou, X., Tan, W. H., et al. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1549194 · Cited by 2 · see citing works
Culture of cerebrospinal fluid-contacting neurons from neonatal mouse spinal cord
Cao, L., Zhang, H., He, Y., An, P.-J., Yang, L., Tan, W. H., Liu, G., Wang, C., Dou, X., & Li, Q. (2023) · Cell and Tissue Banking · doi:10.1007/s10561-023-10098-w · Cited by 2 · see citing works
Li, Y., Hou, W., Jia, Y., Wen, X., Rao, C., Xu, X., Wei, Z., Bai, L., & Tan, H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.30.927509 · Cited by 2 · see citing works
The neuronal cell types of the spinal cord
Koch, S. C., & Levine, A. J. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-819260-3.00005-6 · Cited by 2 · see citing works
Sacher, F., Berki, B., Fages, A., Gavrilov, L., Klar, A., Luxey, M., & Tschopp, P. (2026) · iScience · doi:10.1016/j.isci.2026.115196 · Cited by 1 · see citing works
Development of the Spinal Cord
Ševc, J., Matiašová, A. A., & Daxnerová, Z. (2023) · Springer eBooks · doi:10.1007/978-3-031-39558-1_3 · Cited by 1 · see citing works
The Role of Ciliated Cells of the Spinal Canal
Esmaeli, M., Dehabadi, M. D., Barazesh, M., & Ghanbari, A. (2025) · Cell and Tissue Biology · doi:10.1134/s1990519x24600595 · Cited by 1 · see citing works
Early and late stages of Developmental Biology in Argentina
Sánchez, S. S., & Honoré, S. M. (2020) · The International Journal of Developmental Biology · doi:10.1387/ijdb.200024ss · Cited by 1 · see citing works
GABA excitatory actions in cerebrospinal-fluid contacting neurones of adult mouse spinal cordPreprint
Riondel, P., Jurčić, N., Trouslard, J., Wanaverbecq, N., & Seddik, R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.14.520067 · Cited by 1 · see citing works
Kalcheim, C. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735638130.793562488
Meng, X.-T., Song, S., Li, Y., Peng, S., & Zhang, L. (2024) · Research Square · doi:10.21203/rs.3.rs-4258857/v1
Elysa, C., Blasco, E., Ramírez‐Franco, J., Riondel, P., Jurčić, N., Seddik, R., Michelle, C., Trouslard, J., & Wanaverbecq, N. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.10.617653
Vitar, M., Prieto, D., Malas, S., Russo, R. E., & Trigo, F. F. (2026) · eLife · doi:10.7554/elife.109372.4
Vitar, M., Prieto, D., Malas, S., Russo, R. E., & Trigo, F. F. (2026) · eLife · doi:10.7554/elife.109372.1
Vitar, M., Prieto, D., Malas, S., Russo, R. E., & Trigo, F. F. (2026) · eLife · doi:10.7554/elife.109372
Neuronal populations underlying locomotion in zebrafish
Sternberg, J. R. (2016) · theses.fr (ABES) · doi:10.70675/4672b940zaeefz4dc4zadc5z91d95b993c6f
Investigation of neuropeptides in spinal circuits with special emphasis on somatostatin
Quan, F. B. (2020) · theses.fr (ABES) · doi:10.70675/bf43ed2azb519z404ez9000z923c31db3a40
Verran, E., Moizan, L., Tocquer, L., Quan, F. B., & Wyart, C. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.14.718607
Verran, E., Moizan, L., Tocquer, L., Quan, F. B., & Wyart, C. (2026) · eLife · doi:10.7554/elife.111150
Verran, E., Moizan, L., Tocquer, L., Quan, F. B., & Wyart, C. (2026) · eLife · doi:10.7554/elife.111150.1
Vitar, M., Prieto, D., Malas, S., Russo, R. E., & Trigo, F. F. (2026) · eLife · doi:10.7554/elife.109372.3
- Authors
- Petracca, Y. L., Sartoretti, M. M., Di Bella, D. J., Marin-Burgin, A., Carcagno, A. L., Schinder, A. F., & Lanuza, G. M.
- Affiliations
- Consejo Nacional de Investigaciones Científicas y Técnicas (AR)
- Developmental Neurobiology Lab, Instituto Leloir and Consejo Nacional de Investigaciones Científicas y Técnicas (IIBBA-CONICET). Av. Patricias Argentinas 435. Buenos Aires 1405, Argentina
- Neuronal Plasticity Lab, Instituto Leloir and Consejo Nacional de Investigaciones Científicas y Técnicas (IIBBA-CONICET). Av. Patricias Argentinas 435. Buenos Aires 1405, Argentina
- Corresponding author
- Lanuza, Guillermo M.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2016-01-01
- Volume
- 143
- Issue
- 5
- Pages
- 880-91
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- PMC
- PMC4813337
- OpenAlex
- W2263649084
- Cited by
- 90
- References
- 103
- Citations by year
- 2026: 8 · 2025: 5 · 2024: 5 · 2023: 11 · 2022: 7 · 2021: 7 · 2020: 11 · 2019: 15 · 2018: 6 · 2017: 7 · 2016: 8
- FWCI
- 6.13
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Development (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Americanae (AECID Library) (submittedVersion, cc-by-nc-sa)
- HighWire Press Open Archive (submittedVersion)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, cc-by-nc-sa)
- Funders
- Agencia Nacional de Promoci?n Cient?fica y Tecnol?gica of Argentina (PICT2011-1350, PRH-PICT09-116)
- Fogarty International Center, National Institutes of Health (1 R03 TW008026)
- International Brain Research Organization (IBRO Return Home Award)
- 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 › Cerebrospinal fluid and hydrocephalus
- Keywords
- cerebrospinal fluid-contacting neurons, spinal cord development, ependymal cells, GATA2, GATA3, PKD2L1, floor plate, Pax6, Foxn4, neuronal heterogeneity, central canal, mice
- MeSH terms
- Animals, Cell Differentiation, Cerebrospinal Fluid, Electrophysiology, Eye Proteins, Female, Genotype, Immunohistochemistry, Interneurons, Motor Neurons, Neurons, Spinal Cord, Stem Cells, In Situ Hybridization, Cell Lineage, GATA2 Transcription Factor, Mice, Forkhead Transcription Factors
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 ›
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