miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR ‐101 that regulate WISP1 expression-Reference-Cited by-同舟云学术

miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR ‐101 that regulate WISP1 expression

Published:2020-11-26 Issue:2 Volume:253 Page:186-197
ISSN:0022-3417
Container-title:The Journal of Pathology
language:en
Short-container-title:J. Pathol.

Author:

Pommier Alexandra¹,Varilh Jessica¹,Bleuse Solenne¹,Delétang Karine¹,Bonini Jennifer¹,Bergougnoux Anne¹²,Brochiero Emmanuelle³⁴^ORCID,Koenig Michel¹²,Claustres Mireille¹,Taulan‐Cadars Magali¹^ORCID

Affiliation:

1. Université de Montpellier, Laboratoire de Génétique de Maladies Rares EA7402 Montpellier France

2. CHU de Montpellier, Laboratoire de Génétique Moléculaire Montpellier France

3. Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM) Montréal QC Canada

4. Département de Médecine Université de Montréal Montréal QC Canada

Funder

Association Vaincre la Mucoviscidose

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/path.5571

Reference44 articles.

1. Regulation of Cystic Fibrosis Transmembrane Conductance Regulator by MicroRNA-145, -223, and -494 Is Altered in ΔF508 Cystic Fibrosis Airway Epithelium

2. miRNA-221 is elevated in cystic fibrosis airway epithelial cells and regulates expression of ATF6

3. Early origins and evolution of microRNAs and Piwi-interacting RNAs in animals

4. A challenge for miRNA: multiple isomiRs in miRNAomics

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