Cited by 171Neurogenesis and neuroplasticity mechanismsNeuroscience and Neuropharmacology ResearchDevelopmental Biology and Gene Regulation

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Cogeneration of retrogradely labeled corticocortical projection and GABA-immunoreactive local circuit neurons in cerebral cortex

Miller, Michael W.·1985·Developmental Brain Research

DOI 10.1016/0165-3806(85)90040-9

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Abstract

The times of origin of cortico-cortical projection neurons and local circuit neurons in rat visual cortex were determined. The birthdates of the projection neurons were assessed using a technique that combined retrograde labeling with lectin-bound horseradish peroxidase and tritiated thymidine autoradiography. The birthdates of some cortical local circuit neurons were determined by combining GABA immunocytochemistry with [3H]thymidine autoradiography. Double-labeled neurons (those with retrograde or immunoreactive label in their perikarya and autoradiographic silver grains over their nuclei) were born during the third week of gestation. Projection and local circuit neurons born on gestational day 14, 15, 17, 19 or 20 were located primarily in layer VIb, VIa, V, III or II, respectively. Thus, both populations of neurons are generated by parallel and concurrent inside-to-outside patterns.

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Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.
Hsu, S. M., Raine, L., & Fanger, H. (1981) · Journal of Histochemistry & Cytochemistry · doi:10.1177/29.4.6166661 · Cited by 14,075
The autoradiographic demonstration of axonal connections in the central nervous system
Cowan, W. M., Gottlieb, D. I., Hendrickson, A. E., Price, J. L., & Woolsey, T. A. (1972) · Brain Research · doi:10.1016/0006-8993(72)90344-7 · Cited by 1,610
Autoradiographic Study of Cell Migration during Histogenesis of Cerebral Cortex in the Mouse
ANGEVINE, J. B., & SIDMAN, R. L. (1961) · Nature · doi:10.1038/192766b0 · Cited by 1,530
Developmental Neurobiology
Jacobson, M. (1978) · Springer eBooks · doi:10.1007/978-1-4757-4951-9 · Cited by 1,218
Clustered intrinsic connections in cat visual cortex
Gilbert, C., & Wiesel, T. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-05-01116.1983 · Cited by 1,016
Morphology and intracortical projections of functionally characterised neurones in the cat visual cortex
Gilbert, C. D., & Wiesel, T. N. (1979) · Nature · doi:10.1038/280120a0 · Cited by 1,016
Technical considerations on the use of horseradish peroxidase as a neuronal marker
Adams, J. C. (1977) · Neuroscience · doi:10.1016/0306-4522(77)90074-4 · Cited by 914
The migration of neuroblasts in the developing cerebral cortex.
Berry, M., & Rogers, A. W. (1965) · PubMed · Cited by 674
Varieties and distribution of non‐pyramidal cells in the somatic sensory cortex of the squirrel monkey
Jones, E. G. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901600204 · Cited by 593
Aspinous and sparsely-spinous stellate neurons in the visual cortex of rats contain glutamic acid decarboxylase
Ribak, C. E. (1978) · Journal of Neurocytology · doi:10.1007/bf01173991 · Cited by 551

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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Authors: Miller, M. W.
Affiliations: Tulane University (US)
Corresponding author: Miller, Michael W.
ORCID: Miller, Michael W.
Venue: Developmental Brain Research
Publisher: Elsevier BV
Published: 1985-12
Volume: 23
Issue: 2
Pages: 187-192
ISSN: 0165-3806 (ISSN-L)
DOI: 10.1016/0165-3806(85)90040-9
OpenAlex: W2105681070
Cited by: 171
References: 32
Citations by year: 2025: 1 · 2024: 2 · 2022: 3 · 2021: 3 · 2020: 2 · 2019: 1 · 2018: 3 · 2017: 2 · 2016: 2 · 2015: 5 · 2014: 3 · 2013: 6 · 2012: 4
FWCI: 2.75
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Developmental Brain Research (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute on Alcohol Abuse and Alcoholism (AA 05912)
National Eye Institute (EY05003)
Topics: Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Keywords: local circuit neurons, neuronal birthdate, cortical development, visual cortex, GABA immunoreactivity, retrograde tracing, 3H-thymidine autoradiography, cortical layers, gestational age
MeSH terms: Animals, Cell Movement, gamma-Aminobutyric Acid, Immunoenzyme Techniques, Mitosis, Neural Pathways, Visual Cortex, Rats

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Cogeneration of retrogradely labeled corticocortical projection and GABA-immunoreactive local circuit neurons in cerebral cortex

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