Article ID Journal Published Year Pages File Type
5511472 The International Journal of Biochemistry & Cell Biology 2016 10 Pages PDF
Abstract
The present work describes not only the proteomic profile in RTT fibroblasts, but also identifies the modified proteins by 4-HNE and nitrotyrosine. Of note, for the first time, it appears that a dysregulation of NO pathway can be associated to RTT pathophysiology. In conclusion, the evidence of a wide range of proteins able to forms adducts with 4-HNE, Nitrotyrosine or with both confirms the possible alteration of several aspects of cellular functions that well correlates to the complex clinical features of RTT patients.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
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