MALDI imaging mass spectrometry to investigate endogenous peptides in an animal model of Usher's disease
Author:
Affiliation:
1. Institute of Toxicology; Hannover Medical School; Hannover Germany
2. Institute of Laboratory Animal Science; Hannover Medical School; Hannover Germany
Publisher
Wiley
Subject
Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pmic.201300558/fullpdf
Reference50 articles.
1. Usher syndrome (sensorineural deafness and Retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches;Bonnet;Curr. Opin. Neurol.,2012
2. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with Retinitis pigmentosa and sensorineural hearing loss;Ebermann;Hum. Genet.,2007
3. A mutation in Myo15 leads to Usher-like symptoms in LEW/Ztm-ci2 rats;Held;PLoS One,2011
4. Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin;Aller;Mol. Vis.,2010
5. Molecular imaging of biological samples: localization of peptides and proteins using MALDI-TOF MS;Caprioli;Anal. Chem.,1997
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