Genetic deletion of keratin 8 corrects the altered bone formation and osteopenia in a mouse model of cystic fibrosis-Reference-Cited by-同舟云学术

Genetic deletion of keratin 8 corrects the altered bone formation and osteopenia in a mouse model of cystic fibrosis

Published:2016-01-13 Issue:7 Volume:25 Page:1281-1293
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Le Henaff Carole,Faria Da Cunha Mélanie,Hatton Aurélie,Tondelier Danielle,Marty Caroline,Collet Corinne,Zarka Mylène,Geoffroy Valérie,Zatloukal Kurt,Laplantine Emmanuel,Edelman Aleksander,Sermet-Gaudelus Isabelle,Marie Pierre J.

Funder

Inserm, University Paris Diderot Sorbonne Paris Cité, the Associations Prévention and Traitement des Décalcifications and Rhumatisme et Travail

French Research Agency, ANR CORCF, Vaincre La Mucoviscidose

Mucoviscidose-ABCF2

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/25/7/1281/18527189/ddw009.pdf

Reference41 articles.

1. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

2. Twenty years after cystic fibrosis gene identification: Where are we and what are we up to?

3. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

4. The ΔF508-CFTR mutation inhibits wild-type CFTR processing and function when co-expressed in human airway epithelia and in mouse nasal mucosa

5. CFTR: folding, misfolding and correcting the ΔF508 conformational defect

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