The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Genetic Ablation of V2a Ipsilateral Interneurons Disrupts Left-Right Locomotor Coordination in Mammalian Spinal Cord
Open accessOverview
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
Verification
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.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
Self-citationV1 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
Self-citationKimura, Y., Okamura, Y., & Higashijima, S.-I. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4993-05.2006 · Cited by 302
Initiation of locomotion in mammals
JORDAN, L. M. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb09040.x · Cited by 289
Cited by
Decoding the organization of spinal circuits that control locomotion
Kiehn, O. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.9 · Cited by 742
Self-citationCircuits controlling vertebrate locomotion: moving in a new direction
Goulding, M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2608 · Cited by 777
Current principles of motor control, with special reference to vertebrate locomotion
Grillner, S., & El Manira, A. (2020) · Physiological Reviews · doi:10.1152/physrev.00015.2019 · Cited by 560
Sathyamurthy, A., Johnson, K. R., Matson, K. J. E., Dobrott, C. I., Li, L., Ryba, A. R., Bergman, T. B., Kelly, M. C., Kelley, M. W., & Levine, A. J. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.02.003 · Cited by 370
In mice lacking V2a interneurons, gait depends on speed of locomotion
Crone, S. A., Zhong, G., Harris-Warrick, R., & Sharma, K. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1206-09.2009 · Cited by 263
Self-citationCell type prioritization in single-cell data
Skinnider, M. A., Squair, J. W., Kathe, C., Anderson, M. A., Gautier, M., Matson, K. J. E., Milano, M., Hutson, T. H., Barraud, Q., Phillips, A. A., et al. (2021) · Nature Biotechnology · doi:10.1038/s41587-020-0605-1 · Cited by 274
Bellardita, C., & Kiehn, O. (2015) · Current Biology · doi:10.1016/j.cub.2015.04.005 · Cited by 263
“Excitatory ipsilaterally projecting subsets of Chx10 expressing V2a neurons are known to be critically involved in left-right alternation [5–10] particularly at high locomotor speeds [6].”
Self-citationDescending command neurons in the brainstem that halt locomotion
Bouvier, J., Caggiano, V., Leiras, R., Caldeira, V., Bellardita, C., Balueva, K., Fuchs, A., & Kiehn, O. (2015) · Cell · doi:10.1016/j.cell.2015.10.074 · Cited by 259
Self-citationZhang, 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
Locomotor 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
Self-citationMaking sense out of spinal cord somatosensory development
Lai, H. C., Seal, R. P., & Johnson, J. E. (2016) · Development · doi:10.1242/dev.139592 · Cited by 188
Hayashi, M., Hinckley, C. A., Driscoll, S. P., Moore, N. J., Levine, A. J., Hilde, K. L., Sharma, K., & Pfaff, S. L. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.023 · Cited by 188
Ampatzis, K., Song, J., Ausborn, J., & El Manira, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.018 · Cited by 186
Zhong, G., Droho, S., Crone, S. A., Dietz, S., Kwan, A. C., Webb, W. W., Sharma, K., & Harris-Warrick, R. M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4849-09.2010 · Cited by 159
Self-citationFiring and Cellular Properties of V2a Interneurons in the Rodent Spinal Cord
Dougherty, K. J., & Kiehn, O. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4821-09.2010 · Cited by 138
Self-citationA Functional Topographic Map for Spinal Sensorimotor Reflexes
Gatto, G., Bourane, S., Ren, X., Di Costanzo, S., Fenton, P. K., Halder, P., Seal, R. P., & Goulding, M. D. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.003 · Cited by 92
Origin of excitation underlying locomotion in the spinal circuit of zebrafish
Eklöf-Ljunggren, E., Haupt, S., Ausborn, J., Dehnisch, I., Uhlén, P., Higashijima, S.-I., & El Manira, A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1115377109 · Cited by 95
The late and dual origin of cerebrospinal fluid-contacting neurons in the mouse spinal cord
Petracca, Y. L., Sartoretti, M. M., Di Bella, D. J., Marin-Burgin, A., Carcagno, A. L., Schinder, A. F., & Lanuza, G. M. (2016) · Development · doi:10.1242/dev.129254 · Cited by 90
Song, J., Pallucchi, I., Ausborn, J., Ampatzis, K., Bertuzzi, M., Fontanel, P., Picton, L. D., & El Manira, A. (2020) · Neuron · doi:10.1016/j.neuron.2019.12.030 · Cited by 84
Brainstem Circuits Controlling Action Diversification
Ruder, L., & Arber, S. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050201 · Cited by 69
Assembly and function of spinal circuits for motor control
Catela, C., Shin, M. M., & Dasen, J. S. (2015) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100814-125155 · Cited by 77
Motor control of Drosophila feeding behavior
Schwarz, O., Bohra, A. A., Liu, X., Reichert, H., VijayRaghavan, K., & Pielage, J. (2017) · eLife · doi:10.7554/elife.19892 · Cited by 62
Functional organization of V2a‐related locomotor circuits in the rodent spinal cord
Dougherty, K. J., & Kiehn, O. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05502.x · Cited by 75
Self-citationSpinal V3 interneurons and Left-Right coordination in mammalian locomotion
Danner, S. M., Zhang, H., Shevtsova, N. A., Borowska-Fielding, J., Deska-Gauthier, D., Rybak, I. A., & Zhang, Y. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00516 · Cited by 71
Dual midbrain and forebrain origins of thalamic inhibitory interneurons
Jager, P., Moore, G., Calpin, P., Durmishi, X., Salgarella, I., Menage, L., Kita, Y., Wang, Y., Kim, D. W., Blackshaw, S., et al. (2021) · eLife · doi:10.7554/elife.59272 · Cited by 61
Dorsally derived spinal interneurons in locomotor circuits
Vallstedt, A., & Kullander, K. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06801.x · Cited by 64
Song, J., Dahlberg, E., & El Manira, A. (2018) · Nature Communications · doi:10.1038/s41467-018-05827-9 · Cited by 64
Characterization of Foxp2-expressing cells in the developing spinal cord
Morikawa, Y., Hisaoka, T., & Senba, E. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.05.022 · Cited by 33
Spinal V1 neurons inhibit motor targets locally and sensory targets distally
Sengupta, M., Daliparthi, V., Roussel, Y., Bui, T. V., & Bagnall, M. W. (2021) · Current Biology · doi:10.1016/j.cub.2021.06.053 · Cited by 30
Decoding cell type diversity within the spinal cord
Dobrott, C. I., Sathyamurthy, A., & Levine, A. J. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2018.11.006 · Cited by 26
The Brain and Spinal Cord Networks Controlling Locomotion
Jordan, L. M., & Sławińska, U. (2014) · Neuronal Networks in Brain Function, CNS Disorders, and Therapeutics · doi:10.1016/b978-0-12-415804-7.00017-4 · Cited by 9
Harris, A., Masgutova, G., Collin, A., Toch, M., Hidalgo-Figueroa, M., Jacob, B., Corcoran, L. M., Francius, C., & Clotman, F. (2018) · doi:10.1101/413054 · Cited by 2
Metadata
- Authors
- Crone, S. A., Quinlan, K. A., Zagoraiou, L., Droho, S., Restrepo, C. E., Lundfald, L., Endo, T., Setlak, J., Jessell, T. M., Kiehn, O., & Sharma, K.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2008-10
- Volume
- 60
- Issue
- 1
- Pages
- 70-83
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2034951262
- Cited by
- 358
- References
- 4
- FWCI
- 8.03
- Type
- journal article
- Language
- en
- Open access
- bronze
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
