Laying the Foundation for Cystic Fibrosis Therapy: An Interview with Michael Boyle
نویسندگان
چکیده
منابع مشابه
Clinical Practice Guidelines From the Cystic Fibrosis Foundation for Preschoolers With Cystic Fibrosis.
Cystic fibrosis (CF) clinical care guidelines exist for the care of infants up to age 2 years and for individuals ≥6 years of age. An important gap exists for preschool children between the ages of 2 and 5 years. This period marks a time of growth and development that is critical to achieve optimal nutritional status and maintain lung health. Given that disease often progresses in a clinically ...
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This project aims to develop a new framework which enables compilers to adapt with and exploit the exponential growth in hardware performance. This is achieved by systematically describing the program optimisation space and by developing new approaches to explore this space in a manner independent of application or underlying architecture. Furthermore, by transcending the distinction between co...
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Cystic fibrosis (CF) is an autosomal recessive disorder caused by mutations in CFTR genes that affect chloride ion channel. The CF is a good nominee for gene therapy as the asymptomatic carriers are phenotypically normal, and the desired cells are accessible for vector delivery. Gene therapy shows promising effects involving the correction of gene or replacement of the mutant gene with the func...
متن کاملEnteral tube feeding for individuals with cystic fibrosis: Cystic Fibrosis Foundation evidence-informed guidelines.
Nutrition is integral to the care of individuals with cystic fibrosis (CF). Better nutritional status is associated with improved pulmonary function. In some individuals with CF, enteral tube feeding can be useful in achieving optimal nutritional status. Current nutrition guidelines do not include detailed recommendations for enteral tube feeding. The Cystic Fibrosis Foundation convened an expe...
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ژورنال
عنوان ژورنال: Human Gene Therapy
سال: 2020
ISSN: 1043-0342,1557-7422
DOI: 10.1089/hum.2020.29134.int