Liu X - Search Results

1

hTBK1-c.978T>A mutation promotes the ferroptosis in NSC-34 cells via mediation of KEAP1/NRF2/p62 signaling.

Zhang Y, Fan D, Liu X, Liu X, He J, Zhang N, Tang L. Zhang Y, et al. Among authors: liu x. Am J Transl Res. 2020 Nov 15;12(11):7386-7394. eCollection 2020. Am J Transl Res. 2020. PMID: 33312375 Free PMC article.

2

A novel mutation of the glycyl-tRNA synthetase (GARS) gene associated with Charcot-Marie-Tooth type 2D in a Chinese family.

Sun A, Liu X, Zheng M, Sun Q, Huang Y, Fan D. Sun A, et al. Among authors: liu x. Neurol Res. 2015 Sep;37(9):782-7. doi: 10.1179/1743132815Y.0000000055. Epub 2015 May 22. Neurol Res. 2015. PMID: 26000875

3

[Clinical and electrophysiological characteristics and therapeutic analysis of 9 patients with Lewis-Sumner syndrome].

Sun A, Zhang Y, Liu X, Chen L, Sun Q, Zhang S, Fan D. Sun A, et al. Among authors: liu x. Zhonghua Yi Xue Za Zhi. 2016 Mar 22;96(11):859-62. doi: 10.3760/cma.j.issn.0376-2491.2016.11.007. Zhonghua Yi Xue Za Zhi. 2016. PMID: 27045647 Chinese.

4

DCTN1 gene analysis in Chinese patients with sporadic amyotrophic lateral sclerosis.

Liu X, Yang L, Tang L, Chen L, Liu X, Fan D. Liu X, et al. PLoS One. 2017 Aug 8;12(8):e0182572. doi: 10.1371/journal.pone.0182572. eCollection 2017. PLoS One. 2017. PMID: 28792508 Free PMC article.

5

Two rare variants of the ANXA11 gene identified in Chinese patients with amyotrophic lateral sclerosis.

Liu X, Wu C, He J, Zhang N, Fan D. Liu X, et al. Neurobiol Aging. 2019 Feb;74:235.e9-235.e12. doi: 10.1016/j.neurobiolaging.2018.09.020. Epub 2018 Sep 22. Neurobiol Aging. 2019. PMID: 30337194

6

A novel MYH7 mutation resulting in Laing distal myopathy in a Chinese family.

Liu XY, Zhang YS, Sun AP, Zhong YF, Zheng DF, Fan DS. Liu XY, et al. Chin Med J (Engl). 2019 Apr 5;132(7):856-859. doi: 10.1097/CM9.0000000000000148. Chin Med J (Engl). 2019. PMID: 30897599 Free PMC article. No abstract available.

7

A case of de novo dynamin 2 (DNM2)-related centronuclear myopathy with electrical but not clinical myotonia.

Huang X, Liu XY, Chen L, Sun AP, Zhang YS, Zheng DF, Zhong YF, Fan DS. Huang X, et al. Among authors: liu xy. Chin Med J (Engl). 2020 Aug 18;133(24):3023-3024. doi: 10.1097/CM9.0000000000000974. Chin Med J (Engl). 2020. PMID: 32826616 Free PMC article. No abstract available.

8

TBK1 variants in Chinese patients with amyotrophic lateral sclerosis.

Liu X, He J, Chen L, Zhang N, Tang L, Liu X, Ma Y, Fan D. Liu X, et al. Neurobiol Aging. 2021 Jan;97:149.e9-149.e15. doi: 10.1016/j.neurobiolaging.2020.07.028. Epub 2020 Aug 4. Neurobiol Aging. 2021. PMID: 32893041

9

[Rare variants of HSPB1 are probably associated with amyotrophic lateral sclerosis].

Chen J, Liu X, Xu Y, Fan D. Chen J, et al. Among authors: liu x. Nan Fang Yi Ke Da Xue Xue Bao. 2021 Jan 30;41(1):75-78. doi: 10.12122/j.issn.1673-4254.2021.01.10. Nan Fang Yi Ke Da Xue Xue Bao. 2021. PMID: 33509756 Free PMC article. Chinese.

10

GLT8D1 may not be significant in Chinese sporadic amyotrophic lateral sclerosis patients.

Yilihamu M, He J, Liu X, Tian J, Fan D. Yilihamu M, et al. Among authors: liu x. Neurobiol Aging. 2021 Jun;102:224.e1-224.e3. doi: 10.1016/j.neurobiolaging.2021.01.028. Epub 2021 Feb 7. Neurobiol Aging. 2021. PMID: 33714647

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

137,225 results

Search Page

Filters