The association between LIN28A gene rare variants and Parkinson’s disease in Chinese population-Reference-Cited by-同舟云学术

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The association between LIN28A gene rare variants and Parkinson’s disease in Chinese population

Published:2022-06 Issue: Volume:829 Page:146515
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Huang Xiurong,Zhao Yuwen,Pan Hongxu,Wang Yige,Liu Zhenhua,Xu Qian,Sun Qiying,Tan Jieqiong,Yan Xinxiang,Li Jinchen,Tang Beisha,Guo Jifeng

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference44 articles.

1. LIN28 alters cell fate succession and acts independently of the let-7 microRNA during neurogliogenesis in vitro;Balzer;Development,2010

2. Expression of exogenous LIN28 contributes to proliferation and survival of mouse primary cortical neurons in vitro;Bhuiyan;Neuroscience,2013

3. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism;Bonifati;Science,2003

4. LIN28A loss of function is associated with Parkinson's disease pathogenesis;Chang;Embo J,2019

5. LIN28A is a suppressor of ER-associated translation in embryonic stem cells;Cho;Cell,2012

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Analysis of LIN28A variants in patients with Parkinson’s disease;Journal of Human Genetics;2023-01-19

2. Association of rare PPARGC1A variants with Parkinson’s disease risk;Journal of Human Genetics;2022-08-22

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