Barth Syndrome (BTHS) is an early onset, lethal X-linked disorder caused by a mutation in tafazzin (TAFAZZIN), a mitochondrial acyltransferase that remodels monolysocardiolipin (MLCL) to mature cardiolipin (CL) and is essential for normal mitochondrial, cardiac, and skeletal muscle function. Current gene therapies in preclinical development require high levels of transduction. We tested whether TAFAZZIN gene therapy could be enhanced with the addition of a cell-penetrating peptide, penetratin (Antp).
View Article and Find Full Text PDFIntroduction: Osteochondroma is a long bone benign tumor presenting at the metaphysis. Most of the occurrences are isolated lesions with very rare intra-articular extensions. Some occur as part of multiple hereditary exostoses.
View Article and Find Full Text PDFBackground: Feature selection is a vital process in data mining and machine learning approaches by determining which characteristics, out of the available features, are most appropriate for categorization or knowledge representation. However, the challenging task is finding a chosen subset of elements from a given set of features to represent or extract knowledge from raw data. The number of features selected should be appropriately limited and substantial to prevent results from deviating from accuracy.
View Article and Find Full Text PDFRecent Adv Drug Deliv Formul
June 2024
Using skin patches to deliver drugs is dependable and doesn't have the same issues as permeation enhancers, which help drugs get through the skin but struggle because of the skin's natural barrier. Strategies are required to increase topical bioavailability to enhance drug absorption. Natural compounds offer a promising solution by temporarily reducing skin barrier resistance and improving drug absorption.
View Article and Find Full Text PDF