A missense mutation in the proprotein convertase gene <i>furinb</i> causes hepatic cystogenesis during liver development in zebrafish-Reference-Cited by-同舟云学术

A missense mutation in the proprotein convertase gene furinb causes hepatic cystogenesis during liver development in zebrafish

Published:2022-08-26 Issue:11 Volume:6 Page:3083-3097
ISSN:2471-254X
Container-title:Hepatology Communications
language:en
Short-container-title:Hepatology Communications

Author:

Ellis Jillian L.¹,Evason Kimberley J.²³,Zhang Changwen¹,Fourman Makenzie N.¹,Liu Jiandong²⁴,Ninov Nikolay²⁵⁶,Delous Marion²⁷,Vanhollebeke Benoit²⁸,Fiddes Ian²,Otis Jessica P.⁹¹⁰¹¹,Houvras Yariv¹²,Farber Steven A.⁹¹⁰,Xu Xiaolei¹³,Lin Xueying¹³,Stainier Didier Y. R.²¹⁴,Yin Chunyue¹²¹⁵^ORCID

Affiliation:

1. Division of Gastroenterology, Hepatology, and Nutrition Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

2. Department of Biochemistry and Biophysics Program in Developmental and Stem Cell Biology Liver Center and Diabetes Center University of California, San Francisco San Francisco California USA

3. Huntsman Cancer Institute and Department of Pathology University of Utah Salt Lake City Utah USA

4. McAllister Heart Institute Department of Pathology and Laboratory Medicine School of Medicine The University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

5. Center for Regenerative Therapies TU Dresden Dresden Germany

6. Paul Langerhans Institute Dresden of the Helmholtz Center Munich at the University Hospital Carl Gustav Carus of TU Dresden German Center for Diabetes Research Dresden Germany

7. Equipe GENDEV Centre de Recherche en Neurosciences de Lyon Inserm U1028 CNRS UMR5292 Universite Lyon 1 Universite St Etienne Lyon France

8. Laboratory of Neurovascular Signaling Department of Molecular Biology ULB Neuroscience Institute Universite Libre de Bruxelles Gosselies Belgium

9. Department of Embryology Carnegie Institution for Science Baltimore Maryland USA

10. Department of Biology Johns Hopkins University Baltimore Maryland USA

11. Department of Molecular and Cellular Biology and Biochemistry Brown University Providence Rhode Island USA

12. Weill Cornell Medical College and New York Presbyterian Hospital New York New York USA

13. Department of Biochemistry and Molecular Biology Department of Cardiovascular Medicine Mayo Clinic Rochester Minnesota USA

14. Department of Developmental Genetics Max Planck Institute for Heart and Lung Research Bad Nauheim Germany

15. Division of Developmental Biology Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

Funder

Damon Runyon Cancer Research Foundation

Liver Center, University of California, San Francisco

National Cancer Institute

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute on Alcohol Abuse and Alcoholism

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hep4.2038

Reference50 articles.

1. An updated review of cystic hepatic lesions

2. Medical and surgical treatment options for polycystic liver disease1

3. Polycystic Liver Disease: The Benefits of Targeting cAMP

4. Pathobiology of inherited biliary diseases: a roadmap to understand acquired liver diseases

5. Proliferation-Independent Initiation of Biliary Cysts in Polycystic Liver Diseases

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1. Forward genetics combined with unsupervised classifications identified zebrafish mutants affecting biliary system formation;Developmental Biology;2024-08

2. Unfolded Protein Response Signaling in Liver Disorders: A 2023 Updated Review;International Journal of Molecular Sciences;2023-09-14

3. A TGFβ-ECM-integrin signaling axis drives structural reconfiguration of the bile duct to promote polycystic liver disease;Science Translational Medicine;2023-09-13