The fatty acid imbalance of cystic fibrosis exists at birth independent of feeding in pig and ferret models

Persons with cystic fibrosis (CF) exhibit a unique alteration of fatty acid composition, marked especially among polyunsaturates by relative deficiency of linoleic acid and excess of Mead acid. Relative deficiency of docosahexaenoic acid is variably found. However, the initial development of these a...

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Detalles Bibliográficos
Autores principales: Uc, Aliye, Strandvik, Birgitta, Yao, Jianrong, Liu, Xiaoming, Yi, Yaling, Sun, Xingshen, Welti, Ruth, Engelhardt, John F., Norris, Andrew W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2022
Materias:
Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747517/
https://www.ncbi.nlm.nih.gov/pubmed/36416119
http://dx.doi.org/10.1042/CS20220450

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