Up-regulation of miR-34b/c by JNK and FOXO3 protects from liver fibrosis.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
09 03 2021
Historique:
entrez: 2 3 2021
pubmed: 3 3 2021
medline: 17 8 2021
Statut: ppublish

Résumé

α1-Antitrypsin (AAT) deficiency is a common genetic disease presenting with lung and liver diseases. AAT deficiency results from pathogenic variants in the

Identifiants

pubmed: 33649241
pii: 2025242118
doi: 10.1073/pnas.2025242118
pmc: PMC7958360
pii:
doi:

Substances chimiques

Forkhead Box Protein O3 0
FoxO3 protein, mouse 0
MIRN34b microRNA, mouse 0
MIRN34c microRNA, mouse 0
MicroRNAs 0
Serpina1a protein, mouse 0
alpha 1-Antitrypsin 0
MAP Kinase Kinase 4 EC 2.7.12.2

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001453
Pays : United States

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Pasquale Piccolo (P)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy; piccolo@tigem.it brunetti@tigem.it.
Department of Translational Medicine, Federico II University, 80131 Naples, Italy.

Rosa Ferriero (R)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.

Anna Barbato (A)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.

Sergio Attanasio (S)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.

Marcello Monti (M)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.

Claudia Perna (C)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.

Florie Borel (F)

Department of Pediatrics, University of Massachusetts Medical School, Worcester, MA 01655.
Horae Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA 01655.

Patrizia Annunziata (P)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.

Annamaria Carissimo (A)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.

Rossella De Cegli (R)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.

Luca Quagliata (L)

Molecular Pathology Division, Institute of Pathology, University Hospital of Basel, University of Basel, 4003 Basel, Switzerland.

Luigi M Terracciano (LM)

Molecular Pathology Division, Institute of Pathology, University Hospital of Basel, University of Basel, 4003 Basel, Switzerland.

Chantal Housset (C)

Centre de Recherche Saint-Antoine, Sorbonne Université, INSERM, 75012 Paris, France.
Department of Hepatology, Reference Center for Inflammatory Biliary Diseases and Autoimmune Hepatitis, Saint-Antoine Hospital, Assistance Publique-Hôpitaux de Paris, 75012 Paris, France.

Jeffrey H Teckman (JH)

Cardinal Glennon Children's Medical Center, St. Louis University School of Medicine, St. Louis, MO 63104.

Christian Mueller (C)

Department of Pediatrics, University of Massachusetts Medical School, Worcester, MA 01655.
Horae Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA 01655.

Nicola Brunetti-Pierri (N)

Telethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy; piccolo@tigem.it brunetti@tigem.it.
Department of Translational Medicine, Federico II University, 80131 Naples, Italy.

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Classifications MeSH