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M

M. Shinohara

Researcher at National Institutes of Health

Publications -  11
Citations -  7028

M. Shinohara is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Ocular dominance column & Orientation column. The author has an hindex of 11, co-authored 11 publications receiving 6920 citations.

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The [14C]deoxyglucose method for the measurement of local cerebral glucose utilization: theory, procedure, and normal values in the conscious and anesthetized albino rat.

TL;DR: The method can be applied to most laboratory animals in the conscious state and is based on the use of 2‐deoxy‐D‐[14C]glucose as a tracer for the exchange of glucose between plasma and brain and its phosphorylation by hexokinase in the tissues.
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Metabolic mapping of the primary visual system of the monkey by means of the autoradiographic [14C]deoxyglucose technique

TL;DR: An autoradiographic technique that employs 2-[14-C]deoxyglucose to measure the local rates of glucose utilization within the brain has been applied to the binocular visual system of the Macaque monkey.
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Cerebral glucose utilization: local changes during and after recovery from spreading cortical depression

TL;DR: Cerebral glucose utilization is markedly increased in most areas of the cerebral cortex and reduced in many subcortical structures during spreading cortical depression and during recovery, but the increased metabolic activity is distributed in columns running perpendicularly through the cortex.
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Mapping the primate visual system with [2-14C]deoxyglucose

TL;DR: The [2-14C]deoxyglucose method was used to identify the cerebral areas related to vision in the rhesus monkey (Macaca mulatta) and reveal the full extent of those pathways and their points of contact with limbic, striatal, and diencephalic structures.
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The lumped constant of the deoxyglucose method in hypoglycemia: effects of moderate hypoglycemia on local cerebral glucose utilization in the rat.

TL;DR: The weighted average rate of glucose utilization for the brain as a whole was significantly depressed by 14% in the hypoglycemic animals, suggesting that glucose delivery and transport to the tissue became rate-limiting first in those structures with the greatest metabolic demands for glucose.