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CRMP-2 peptide mediated decrease of high and low voltage-activated calcium channels, attenuation of nociceptor excitability, and anti-nociception in a model of AIDS therapy-induced painful peripheral…

Overview of attention for article published in Molecular Pain, July 2012
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Title
CRMP-2 peptide mediated decrease of high and low voltage-activated calcium channels, attenuation of nociceptor excitability, and anti-nociception in a model of AIDS therapy-induced painful peripheral neuropathy
Published in
Molecular Pain, July 2012
DOI 10.1186/1744-8069-8-54
Pubmed ID
Authors

Andrew D Piekarz, Michael R Due, May Khanna, Bo Wang, Matthew S Ripsch, Ruizhong Wang, Samy O Meroueh, Michael R Vasko, Fletcher A White, Rajesh Khanna

Abstract

The ubiquity of protein-protein interactions in biological signaling offers ample opportunities for therapeutic intervention. We previously identified a peptide, designated CBD3, that suppressed inflammatory and neuropathic behavioral hypersensitivity in rodents by inhibiting the ability of collapsin response mediator protein 2 (CRMP-2) to bind to N-type voltage-activated calcium channels (CaV2.2) [Brittain et al. Nature Medicine 17:822-829 (2011)].

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 28 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 28 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 6 21%
Student > Ph. D. Student 6 21%
Professor 3 11%
Researcher 3 11%
Student > Bachelor 2 7%
Other 2 7%
Unknown 6 21%
Readers by discipline Count As %
Agricultural and Biological Sciences 8 29%
Medicine and Dentistry 5 18%
Chemistry 3 11%
Neuroscience 2 7%
Psychology 1 4%
Other 2 7%
Unknown 7 25%