FADD phosphorylation contributes to development of renal fibrosis by accelerating epithelial-mesenchymal transition-Reference-Cited by-同舟云学术

FADD phosphorylation contributes to development of renal fibrosis by accelerating epithelial-mesenchymal transition

Published:2022-10-24 Issue:5 Volume:22 Page:580-595
ISSN:1538-4101
Container-title:Cell Cycle
language:en
Short-container-title:Cell Cycle

Author:

Lin Yan¹^ORCID,Cai Fangfang¹²^ORCID,Wang Xiaoyang¹^ORCID,Yang Yunwen¹^ORCID,Ren Yongzhe¹^ORCID,Yao Chun¹,Yin Xiaoxing³^ORCID,Zhuang Hongqin¹^ORCID,Hua Zichun¹²⁴^ORCID

Affiliation:

1. The State Key Laboratory of Pharmaceutical Biotechnology, College of Life Sciences, Nanjing University, Nanjing, P. R. China

2. School of Biopharmacy, China Pharmaceutical University, Nanjing, China

3. Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou medical university, Xuzhou, China

4. Changzhou High-Tech Research Institute of Nanjing University and Jiangsu TargetPharma Laboratories Inc., Changzhou, P. R. China

Funder

National Key R&D Research Program by Ministry of Science and Technology of China

the Chinese National Natural Sciences Foundation

Publisher

Informa UK Limited

Subject

Cell Biology,Developmental Biology,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/15384101.2022.2136463

Reference35 articles.

1. FADD, a novel death domain-containing protein, interacts with the death domain of fas and initiates apoptosis

2. A mouse Fas-associated protein with homology to the human Mort1/FADD protein is essential for Fas-induced apoptosis

3. The roles of FADD in extrinsic apoptosis and necroptosis

4. FADD prevents RIP3-mediated epithelial cell necrosis and chronic intestinal inflammation

5. The Adaptor Protein FADD Protects Epidermal Keratinocytes from Necroptosis In Vivo and Prevents Skin Inflammation

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