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Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody

Overview of attention for article published in PLOS ONE, April 2013
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Title
Fluorescent Affibody Peptide Penetration in Glioma Margin Is Superior to Full Antibody
Published in
PLOS ONE, April 2013
DOI 10.1371/journal.pone.0060390
Pubmed ID
Authors

Kristian Sexton, Kenneth Tichauer, Kimberley S. Samkoe, Jason Gunn, P. Jack Hoopes, Brian W. Pogue

Abstract

Fluorescence imaging has the potential to significantly improve neurosurgical resection of oncologic lesions through improved differentiation between normal and cancerous tissue at the tumor margins. In order to successfully mark glioma tissue a fluorescent tracer must have the ability to penetrate through the blood brain barrier (BBB) and provide delineation in the tumor periphery where heterogeneously intact BBB may exist. In this study it was hypothesized that, due to its smaller size, fluorescently labeled anti-EGFR Affibody protein (∼7 kDa) would provide a more clear delineation of the tumor margin than would fluorescently labeled cetuximab, a full antibody (∼150 kDa) to the epidermal growth factor receptor (EGFR).

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 60 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 2%
Unknown 59 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 15 25%
Student > Master 10 17%
Student > Bachelor 6 10%
Researcher 5 8%
Professor > Associate Professor 4 7%
Other 9 15%
Unknown 11 18%
Readers by discipline Count As %
Medicine and Dentistry 9 15%
Agricultural and Biological Sciences 9 15%
Chemistry 8 13%
Biochemistry, Genetics and Molecular Biology 7 12%
Engineering 6 10%
Other 8 13%
Unknown 13 22%