ArticleCellular and molecular neurobiology1995
A golgi study of cell types in the dentate gyrus of the adult human brain.
Article in Cellular and molecular neurobiology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Selective alterations in GABAA receptor subtypes in human temporal lobe epilepsy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000Trial
- Contributions of Adult-Generated Granule Cells to Hippocampal Pathology in Temporal Lobe Epilepsy: A Neuronal Bestiary.Brain plasticity (Amsterdam, Netherlands) · 2018Review
- Hippocampal granule cell pathology in epilepsy - a possible structural basis for comorbidities of epilepsy?Epilepsy & behavior : E&B · 2014Review
- Synaptic input to dentate granule cell basal dendrites in a rat model of temporal lobe epilepsy.The Journal of comparative neurology · 2008Article
- Pilocarpine-induced seizures cause selective time-dependent changes to adult-generated hippocampal dentate granule cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007Article
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2 authors.
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Abstract
1. The morphology of neurons in the dentate gyrus of the adult human brain was analyzed with two variants of Golgi technique. 2. About 20 neuronal types and subtypes were observed in the dentate gyrus of the adult human, several of which has not previously been described in the human. The human dentate gyrus harbors 4 types of neurons in the molecular layer, 3 types within the granule cell layer, and at least 10 types in the hilus. 3. Compared to the granule neurons in the rat brain, human granule neurons show a much greater variability. Many of these human neurons have basal dendrites and/or axonal spines. Also, there are significant differences among these neurons regarding the density of their dendritic trees and dendritic spines. In contrast to the rat, human hilar neurons with complex spines have complex spines not only on their dendrites but also on their cell bodies. 4. This study opens the door for further morphological studies involving specific diseases such as Alzheimer's disease and epilepsy.
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