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Sandra E. Dos Santos

Researcher at Vanderbilt University

Publications -  6
Citations -  604

Sandra E. Dos Santos is an academic researcher from Vanderbilt University. The author has contributed to research in topics: Brain size & Evolution of mammals. The author has an hindex of 5, co-authored 6 publications receiving 142 citations. Previous affiliations of Sandra E. Dos Santos include Federal University of Rio de Janeiro.

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Cellular Scaling Rules for the Brains of Marsupials: Not as “Primitive” as Expected

TL;DR: The results suggest that Australasian marsupials have diverged from the ancestral Theria neuronal scaling rules, and support the suggestion that the scaling of average neuronal cell size with increasing numbers of neurons varies in evolution independently of the allocation of neurons across structures.
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A community-based transcriptomics classification and nomenclature of neocortical cell types

Rafael Yuste, +71 more
- 24 Aug 2020 - 
TL;DR: This work proposes the adoption of a transcriptome-based taxonomy of cell types for mammalian neocortex that should be hierarchical and use a standardized nomenclature, and could serve as an example for cell type atlases in other parts of the body.
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Similar microglial cell densities across brain structures and mammalian species: Implications for brain tissue function

TL;DR: The addition of microglial cells to mammalian brains is governed by mechanisms that constrain the size of these cells and have remained conserved over 200 million years of mammalian evolution, suggesting that microglia-dependent functional recovery may be particularly difficult in those brain structures and species with high neuronal densities and therefore fewer microglian cells per neuron.
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You Do Not Mess with the Glia

TL;DR: This paper showed that the restricted variation in size and distribution of glial cells has important consequences for neural tissue function that is aligned with their many fundamental roles being uncovered, and pointed to the possibility that this constraint is related to the late differentiation of the various glial cell types.