The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Descending projections of the songbird nucleus robustus archistriatalis
Abstract
The descending, efferent projections of nucleus robustus archistriatalis were investigated in male zebra finches and greenfinches with injections of either biotinylated dextran amine or cholera toxin B‐chain conjugated to horseradish peroxidase. The results show that in addition to the well‐known projections to the tracheosyringeal motor nucleus and the dorsomedial nucleus of the intercollicular complex, there are other projections of comparable density to the ipsilateral nucleus ambiguus and nucleus retroambigualis. Within nucleus ambiguus, robustus axons terminate in close proximity to laryngeal motoneurons which were retrogradely labelled in the same bird by injections of cholera B‐chain into the laryngeal muscles; and within nucleus retroambigualis robustus axons terminate in relation to bulbospinal neurons previously shown to project to regions of spinal cord containing motoneurons innervating abdominal expiratory muscles (J.M. Wild, Brain Res. 606:119–124, 1993). These projections of nucleus robustus thus seem well placed to coordinate syringeal, laryngeal, and expiratory muscle activity during vocalization. Other relatively sparse, but distinct, projections of nucleus robustus were found to nucleus dorsolateralis anterior thalami, pars medialis, to a narrow region between the superior olivary nucleus and the spinal lemniscus, and to the rostral ventrolateral medulla. Neurons in these last two locations were retrogradely labelled bilaterally following injections of cholera B‐chain into nucleus retroambigualis of one side. Together with sparse contralateral projections of nucleus robustus to all brainstem targets receiving ipsilateral projections, potential pathways are thus identified by which the respiratory‐vocal activity controlled by one side of the lower medulla can be influenced by the nucleus robustus of either side, thereby possibly bringing about bilateral coordination of respiratory‐vocal output. © 1993 Wiley‐Liss, Inc.
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Cites
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Central control of song in the canary, Serinus canarius
Nottebohm, F., Stokes, T. M., & Leonard, C. M. (1976) · Journal of Comparative Neurology · doi:10.1002/cne.901650405 · Cited by 1,643
Biotinylated dextran amine as an anterograde tracer for single- and double-labeling studies
Veenman, C. L., Reiner, A., & Honig, M. G. (1992) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(92)90089-v · Cited by 608
Connections of vocal control nuclei in the canary telencephalon
Nottebohm, F., Paton, J. A., & Kelley, D. B. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902070406 · Cited by 526
Stokes, T. M., Leonard, C. M., & Nottebohm, F. (1974) · Journal of Comparative Neurology · doi:10.1002/cne.901560305 · Cited by 448
The archistriatum of the pigeon: Organization of afferent and efferent connections
Zeier, H., & Karten, H. J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90185-5 · Cited by 438
Neurophysiology of Breathing in Mammals
Feldman, J. L. (1986) · Comprehensive Physiology · doi:10.1002/cphy.cp010409 · Cited by 400
Brain pathways for learned and unlearned vocalizations differ in zebra finches
Simpson, H., & Vicario, D. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-05-01541.1990 · Cited by 387
Hormonal control of cell form and number in the zebra finch song system
Gurney, M. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-06-00658.1981 · Cited by 363
Axonal connections of a forebrain nucleus involved with vocal learning in zebra finches
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Cited by
Revised nomenclature for avian telencephalon and some related brainstem nuclei
Reiner, A., Perkel, D. J., Bruce, L. L., Butler, A. B., Csillag, A., Kuenzel, W., Medina, L., Paxinos, G., Shimizu, T., Striedter, G., et al. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.20118 · Cited by 1,148
An ultra-sparse code underliesthe generation of neural sequences in a songbird
Hahnloser, R. H. R., Kozhevnikov, A. A., & Fee, M. S. (2002) · Nature · doi:10.1038/nature00974 · Cited by 986
Avian brains and a new understanding of vertebrate brain evolution
Jarvis, E. D., Güntürkün, O., Bruce, L., Csillag, A., Karten, H., Kuenzel, W., Medina, L., Paxinos, G., Perkel, D. J., Shimizu, T., et al. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1606 · Cited by 984
Self-citationDo birds possess homologues of mammalian primary visual, somatosensory and motor cortices?
Medina, L., & Reiner, A. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01486-1 · Cited by 375
Relapse to drug-seeking: neural and molecular mechanisms
Self, D. W., & Nestler, E. J. (1998) · Drug and Alcohol Dependence · doi:10.1016/s0376-8716(98)00065-9 · Cited by 295
Metadata
- Authors
- Wild, J. M.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1993-12-08
- Volume
- 338
- Issue
- 2
- Pages
- 225-241
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2126957719
- Cited by
- 294
- References
- 24
- FWCI
- 9.77
- Type
- journal article
- Language
- en
- Open access
- closed
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