Erythroferrone structure, function, and physiology: Iron homeostasis and beyond-Reference-Cited by-同舟云学术

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Erythroferrone structure, function, and physiology: Iron homeostasis and beyond

Published:2020-12-28 Issue:7 Volume:236 Page:4888-4901
ISSN:0021-9541
Container-title:Journal of Cellular Physiology
language:en
Short-container-title:J Cell Physiol

Author:

Srole Daniel N¹^ORCID,Ganz Tomas²^ORCID

Affiliation:

1. Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA University of California Los Angeles California USA

2. Department of Medicine, David Geffen School of Medicine at UCLA University of California Los Angeles California USA

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcp.30247

Reference58 articles.

1. The BMP‐SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE‐A260S variant

2. KDIGO clinical practice guideline for anemia in chronic kidney disease;Anemia Work Group;Kidney International Supplements,2012

3. Antibodies against the erythroferrone N-terminal domain prevent hepcidin suppression and ameliorate murine thalassemia

4. Erythroferrone inhibits the induction of hepcidin by BMP6

5. Erythroferrone and matriptase‐2 independently regulate hepcidin expression

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