Lin XH - Search Results

1

Loss of function of CMPK2 causes mitochondria deficiency and brain calcification.

Zhao M, Su HZ, Zeng YH, Sun Y, Guo XX, Li YL, Wang C, Zhao ZY, Huang XJ, Lin KJ, Ye ZL, Lin BW, Hong S, Zheng J, Liu YB, Yao XP, Yang D, Lu YQ, Chen HZ, Zuo E, Yang G, Wang HT, Huang CW, Lin XH, Cen Z, Lai LL, Zhang YK, Li X, Lai T, Lin J, Zuo DD, Lin MT, Liou CW, Kong QX, Yan CZ, Xiong ZQ, Wang N, Luo W, Zhao CP, Cheng X, Chen WJ. Zhao M, et al. Among authors: lin bw, lin mt, lin j, lin xh, lin kj. Cell Discov. 2022 Nov 29;8(1):128. doi: 10.1038/s41421-022-00475-2. Cell Discov. 2022. PMID: 36443312 Free PMC article.

2

Knockdown of myorg leads to brain calcification in zebrafish.

Zhao M, Lin XH, Zeng YH, Su HZ, Wang C, Yang K, Chen YK, Lin BW, Yao XP, Chen WJ. Zhao M, et al. Among authors: lin bw, lin xh. Mol Brain. 2022 Jul 23;15(1):65. doi: 10.1186/s13041-022-00953-4. Mol Brain. 2022. PMID: 35870928 Free PMC article.

3

Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China.

Dong EL, Wang C, Wu S, Lu YQ, Lin XH, Su HZ, Zhao M, He J, Ma LX, Wang N, Chen WJ, Lin X. Dong EL, et al. Among authors: lin xh, lin x. Mol Neurodegener. 2018 Jul 6;13(1):36. doi: 10.1186/s13024-018-0269-1. Mol Neurodegener. 2018. PMID: 29980238 Free PMC article.

4

Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76).

Lu YQ, Dong EL, Yang WQ, Lai LL, Lin XH, Ma LX, Chen WJ, Wang N, Lin X. Lu YQ, et al. Among authors: lin xh, lin x. Stem Cell Res. 2019 Jan;34:101354. doi: 10.1016/j.scr.2018.11.015. Epub 2018 Nov 27. Stem Cell Res. 2019. PMID: 30611022 Free article.

5

Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia.

Lin X, Su HZ, Dong EL, Lin XH, Zhao M, Yang C, Wang C, Wang J, Chen YJ, Yu H, Xu J, Ma LX, Xiong ZQ, Wang N, Chen WJ. Lin X, et al. Among authors: lin xh. Brain. 2019 Aug 1;142(8):2238-2252. doi: 10.1093/brain/awz158. Brain. 2019. PMID: 31203368

6

Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia.

Lai LL, Chen YJ, Li YL, Lin XH, Wang MW, Dong EL, Wang N, Chen WJ, Lin X. Lai LL, et al. Among authors: lin xh, lin x. Ann Clin Transl Neurol. 2020 Oct;7(10):1862-1869. doi: 10.1002/acn3.51169. Epub 2020 Aug 29. Ann Clin Transl Neurol. 2020. PMID: 32860341 Free PMC article.

7

Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia.

Zhao M, Chen YJ, Wang MW, Lin XH, Dong EL, Chen WJ, Wang N, Lin X. Zhao M, et al. Among authors: lin xh, lin x. Mol Diagn Ther. 2019 Dec;23(6):781-789. doi: 10.1007/s40291-019-00426-w. Mol Diagn Ther. 2019. PMID: 31630374

8

Higher Concentration of Plasma Glial Fibrillary Acidic Protein in Wilson Disease Patients with Neurological Manifestations.

Lin J, Zheng Y, Liu Y, Lin Y, Wang Q, Lin XH, Zhu W, Lin WH, Wang N, Chen WJ, Fu Y. Lin J, et al. Among authors: lin wh, lin y, lin xh. Mov Disord. 2021 Jun;36(6):1446-1450. doi: 10.1002/mds.28509. Epub 2021 Jan 27. Mov Disord. 2021. PMID: 33502774 Free PMC article.

9

Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort study.

Qiu YS, Zeng YH, Yuan RY, Ye ZX, Bi J, Lin XH, Chen YJ, Wang MW, Liu Y, Yao SB, Chen YK, Jiang JY, Lin Y, Lin X, Wang N, Fu Y, Chen WJ. Qiu YS, et al. Among authors: lin y, lin xh, lin x. BMJ Open. 2022 Jan 11;12(1):e054011. doi: 10.1136/bmjopen-2021-054011. BMJ Open. 2022. PMID: 35017251 Free PMC article.

10

Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia.

Chen YJ, Wang MW, Dong EL, Lin XH, Wang N, Zhang ZQ, Lin X, Chen WJ. Chen YJ, et al. Among authors: lin xh, lin x. Parkinsonism Relat Disord. 2019 Aug;65:256-260. doi: 10.1016/j.parkreldis.2019.06.008. Epub 2019 Jun 9. Parkinsonism Relat Disord. 2019. PMID: 31227335

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