Validation of Knock-Out Caco-2 TC7 Cells as Models of Enterocytes of Patients with Familial Genetic Hypobetalipoproteinemias

Abetalipoproteinemia (FHBL-SD1) and chylomicron retention disease (FHBL-SD3) are rare recessive disorders of lipoprotein metabolism due to mutations in MTTP and SAR1B genes, respectively, which lead to defective chylomicron formation and secretion. This results in lipid and fat-soluble vitamin malab...

Descripción completa

Detalles Bibliográficos
Autores principales: Bordat, Claire, Vairo, Donato, Cuerq, Charlotte, Halimi, Charlotte, Peiretti, Franck, Penhoat, Armelle, Vieille-Marchiset, Aurélie, Gonzalez, Teresa, Michalski, Marie-Caroline, Nowicki, Marion, Peretti, Noël, Reboul, Emmanuelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9921550/
https://www.ncbi.nlm.nih.gov/pubmed/36771214
http://dx.doi.org/10.3390/nu15030505

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9921550/
https://www.ncbi.nlm.nih.gov/pubmed/36771214
http://dx.doi.org/10.3390/nu15030505

Ejemplares similares