A functional CFTR assay using primary cystic fibrosis intestinal organoids-Reference-Cited by-同舟云学术

A functional CFTR assay using primary cystic fibrosis intestinal organoids

Published:2013-06-02 Issue:7 Volume:19 Page:939-945
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Dekkers Johanna F,Wiegerinck Caroline L,de Jonge Hugo R,Bronsveld Inez,Janssens Hettie M,de Winter-de Groot Karin M,Brandsma Arianne M,de Jong Nienke W M,Bijvelds Marcel J C,Scholte Bob J,Nieuwenhuis Edward E S,van den Brink Stieneke,Clevers Hans,van der Ent Cornelis K,Middendorp Sabine,Beekman Jeffrey M

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.3201.pdf

Reference49 articles.

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2. Rommens, J.M. et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 245, 1059–1065 (1989).

3. Kerem, B. et al. Identification of the cystic fibrosis gene: genetic analysis. Science 245, 1073–1080 (1989).

4. Ratjen, F. & Döring, G. Cystic fibrosis. Lancet 361, 681–689 (2003).

5. Cheng, S.H. et al. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis. Cell 63, 827–834 (1990).

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