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Measuring the Maturity of the Fast-Spiking Interneuron Transcriptional Program in Autism, Schizophrenia, and Bipolar Disorder

Overview of attention for article published in PLOS ONE, August 2012
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Title
Measuring the Maturity of the Fast-Spiking Interneuron Transcriptional Program in Autism, Schizophrenia, and Bipolar Disorder
Published in
PLOS ONE, August 2012
DOI 10.1371/journal.pone.0041215
Pubmed ID
Authors

Michael J. Gandal, Addie May Nesbitt, Richard M. McCurdy, Mark D. Alter

Abstract

Emerging evidence suggests that fast-spiking (FS) interneurons are disrupted in multiple neuropsychiatric disorders including autism, schizophrenia, and bipolar disorder. FS cells, which are the primary source of synaptic inhibition, are critical for temporally organizing brain activity, regulating brain maturation, and modulating critical developmental periods in multiple cortical systems. Reduced expression of parvalbumin, a marker of mature FS cells, has been reported in individuals with schizophrenia and bipolar disorder and in mouse models of schizophrenia and autism. Although these results suggest that FS cells may be immature in neuropsychiatric disease, this possibility had not previously been formally assessed.

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Mendeley readers

The data shown below were compiled from readership statistics for 95 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 2%
Brazil 1 1%
Unknown 92 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 21 22%
Researcher 17 18%
Student > Master 10 11%
Student > Bachelor 9 9%
Professor > Associate Professor 5 5%
Other 14 15%
Unknown 19 20%
Readers by discipline Count As %
Neuroscience 24 25%
Agricultural and Biological Sciences 21 22%
Medicine and Dentistry 9 9%
Psychology 8 8%
Pharmacology, Toxicology and Pharmaceutical Science 2 2%
Other 9 9%
Unknown 22 23%