CHIP control degradation of mutant ETF : QO through ubiquitylation in late‐onset multiple acyl‐CoA dehydrogenase deficiency-Reference-Cited by-同舟云学术

CHIP control degradation of mutant ETF : QO through ubiquitylation in late‐onset multiple acyl‐CoA dehydrogenase deficiency

Published:2021-01-25 Issue:2 Volume:44 Page:450-468
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J of Inher Metab Disea

Author:

Liu Xin‐Yi¹,Chen Xue‐Jiao¹²,Zhao Miao¹,Wang Zhi‐qiang¹³,Chen Hai‐zhu¹,Li Hong‐Fu⁴,Wang Chen‐Ji⁵,Wu Shi‐Fei⁶,Peng Chao⁶,Yin Yue⁶,Fu Hong‐Xia¹,Lin Min‐Ting¹,Yu Long⁵,Xiong Zhi‐Qi⁷,Wu Zhi‐Ying⁴,Wang Ning¹³

Affiliation:

1. Department of Neurology Fujian Institute of Neurology, the First Affiliated Hospital, Fujian Medical University Fuzhou Fujian China

2. Department of Neurology Zhangzhou Affiliated Hospital of Fujian Medical University Zhangzhou Fujian China

3. Fujian Key Laboratory of Molecular Neurology Fujian Medical University Fuzhou Fujian China

4. Department of Neurology and Research Center of Neurology in the Second Affiliated Hospital and the Collaborative Innovation Center for Brain Science, Zhejiang University School of Medicine Hangzhou Zhejiang China

5. State Key Laboratory of Genetic Engineering Fudan University Shanghai China

6. National Facility for Protein Science in Shanghai Zhangjiang Lab, Shanghai Advanced Research Institute, Chinese Academy of Science Shanghai China

7. Institute of Neuroscience State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences Shanghai China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12361

Reference46 articles.

1. Newborn screening for glutaric aciduria‐II: the New England experience;Sahai I;JIMD Rep,2014

2. Newly Identified Forms of Electron Transfer Flavoprotein Deficiency in Two Patients with Glutaric Aciduria Type II

3. Acyl-CoA dehydrogenases. A mechanistic overview

4. Riboflavin therapy

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2. Enolase 1 Regulates Gastric Cancer Progression through the Electron Transfer Flavoprotein Dehydrogenase Gene;J BIOL REG HOMEOS AG;2023

3. Novel variant of ETFDH leading to multiple acyl-CoA dehydrogenase deficiency by promoting protein degradation via ubiquitin proteasome pathway;Clinica Chimica Acta;2022-05

4. Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series;Frontiers in Neurology;2021-11-08