The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.
Entorhinal cortex of the monkey: V. Projections to the dentate gyrus, hippocampus, and subicular complex
Abstract
The topographic and laminar organization of entorhinal projections to the dentate gyrus, hippocampus, and subicular complex was investigated in the Macaca, fascicularis monkey. Injections of 3 H‐amino acids were placed at various positions within the entorhinal cortex and the distribution of anterogradely labeled fibers and terminals within the other fields of the hippocampal formation was determined. Injections of the retrograde tracers Fast blue, Diamidino yellow, and wheat germ agglutinin‐horseradish peroxidase (WGA‐HRP) were also placed into the dentate gyrus, hippocampus, and subicular complex, and the distribution of retrogradely labeled cells in the entorhinal cortex was plotted using a computer‐aided digitizing system. The entorhinal cortex gave rise to projections that terminated in the subiculum, in the CA1, CA2, and CA3 fields of the hippocampus, and in the dentate gyrus. Projections to the dentate gyrus, and fields CA3 and CA2 of the hippocampus, originated preferentially in layers II and VI of the entorhinal cortex whereas projections to CA1 and to the subiculum originated mainly in layers III and V. Anterograde tracing experiments demonstrated that all regions of the entorhinal cortex project to the outer two‐thirds of the molecular layer of the dentate gyrus and to much of the radial extent of the stratum lacunosum‐moleculare of CA3 and CA2. While the terminal distributions of entorhinal projections to the dentate gyrus, CA3, and CA2 were not as clearly laminated as in the rat, projections from rostral levels of the entorhinal cortex preferentially innervated the outer portion of the molecular layer and stratum lacunosum‐moleculare, whereas more caudal levels of the entorhinal cortex projected relatively more heavily to the deeper portions of the entorhinal terminal zones. The entorhinal projection to the CA1 field of the hippocampus and to the subiculum followed a transverse rather than radial gradient of distribution. Rostral levels of the entorhinal cortex terminated most heavily at the border of CA1 and the subiculum. More caudal levels of the entorhinal cortex projected to progressively more distal portions of the subiculum (towards the presubiculum) and more proximal portions of CA1 (towards CA2). Lateral portions of the entorhinal cortex projected to caudal levels of the recipient fields and more medial parts of the entorhinal cortex projected to progressively more rostral portions of the fields.
Overview
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
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 1,611
Functional organization of the extrinsic and intrinsic circuitry of the parahippocampal region
Witter, M. P., Groenewegen, H. J., Lopes da Silva, F. H., & Lohman, A. H. M. (1989) · Progress in Neurobiology · doi:10.1016/0301-0082(89)90009-9 · Cited by 918
Self-citationSteward, O. (1976) · Journal of Comparative Neurology · doi:10.1002/cne.901670303 · Cited by 880
Cells of origin of entorhinal cortical afferents to the hippocampus and fascia dentata of the rat
Steward, O., & Scoville, S. A. (1976) · Journal of Comparative Neurology · doi:10.1002/cne.901690306 · Cited by 834
The entorhinal cortex of the monkey: II. Cortical afferents
Insausti, R., Amaral, D. G., & Cowan, W. M. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902640306 · Cited by 833
Self-citationVan Hoesen, G. W., Pandya, D. N., & Butters, N. (1975) · Brain Research · doi:10.1016/0006-8993(75)90205-x · Cited by 692
Origin and termination of the hippocampal perforant path in the rat studied by silver impregnation
Hjorth‐Simonsen, A., & Jeune, B. (1972) · Journal of Comparative Neurology · doi:10.1002/cne.901440206 · Cited by 679
Mesulam, M. M. (1976) · Journal of Histochemistry & Cytochemistry · doi:10.1177/24.12.63512 · Cited by 658
Van Hoesen, G. W., & Pandya, D. N. (1975) · Brain Research · doi:10.1016/0006-8993(75)90204-8 · Cited by 493
A stereotaxic atlas of the brain of the cynomolgus monkey (Macaca fascicularis)
Szabo, J., & Cowan, W. M. (1984) · Journal of Comparative Neurology · doi:10.1002/cne.902220208 · Cited by 412
Cited by
Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358
Episodic memory, amnesia, and the hippocampal–anterior thalamic axis
Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879
Functional differentiation in the hippocampus
Moser, M.-B., & Moser, E. I. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:6<608::aid-hipo3>3.0.co;2-7 · Cited by 1,346
Limbic connections of the orbital and medial prefrontal cortex in macaque monkeys
Carmichael, S. T., & Price, J. L. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903630408 · Cited by 1,197
Hippocampal synaptic loss in early Alzheimer's disease and mild cognitive impairment
Scheff, S. W., Price, D. A., Schmitt, F. A., & Mufson, E. J. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.09.012 · Cited by 1,017
Metadata
- Authors
- Witter, M. P., & Amaral, D. G.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1991-05-15
- Volume
- 307
- Issue
- 3
- Pages
- 437-459
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2074157272
- Cited by
- 480
- References
- 28
- FWCI
- 5.89
- Type
- journal article
- Language
- en
- Open access
- closed
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
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Entorhinal cortex of the monkey: V. Projections to the dentate gyrus, hippocampus, and subicular complex. https://app.cochat.ai/papers/10.1002/cne.903070308
- The paper
- Witter, M. P., & Amaral, D. G. (1991). Entorhinal cortex of the monkey: V. Projections to the dentate gyrus, hippocampus, and subicular complex. Journal of Comparative Neurology. https://doi.org/10.1002/cne.903070308
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.