Liu XY - Search Results

1

Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.

Chen WJ, Lin QF, Zhang QJ, He J, Liu XY, Lin MT, Murong SX, Liou CW, Wang N. Chen WJ, et al. Among authors: liu xy. Clin Chim Acta. 2013 Aug 23;423:35-8. doi: 10.1016/j.cca.2013.04.006. Epub 2013 Apr 13. Clin Chim Acta. 2013. PMID: 23588064

2

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.

Chen WJ, Yao XP, Zhang QJ, Ni W, He J, Li HF, Liu XY, Zhao GX, Murong SX, Wang N, Wu ZY. Chen WJ, et al. Among authors: liu xy. Gene. 2013 Oct 15;529(1):159-62. doi: 10.1016/j.gene.2013.07.071. Epub 2013 Aug 11. Gene. 2013. PMID: 23939468

3

A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency.

Liu XY, Wang ZQ, Wang DN, Lin MT, Wang N. Liu XY, et al. Chin Med J (Engl). 2016 Jan 20;129(2):142-6. doi: 10.4103/0366-6999.173438. Chin Med J (Engl). 2016. PMID: 26830983 Free PMC article.

4

Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Fu HX, Liu XY, Wang ZQ, Jin M, Wang DN, He JJ, Lin MT, Wang N. Fu HX, et al. Among authors: liu xy. Neurol Sci. 2016 Jul;37(7):1099-105. doi: 10.1007/s10072-016-2549-2. Epub 2016 Mar 21. Neurol Sci. 2016. PMID: 27000805

5

Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations.

Liu XY, Jin M, Wang ZQ, Wang DN, He JJ, Lin MT, Fu HX, Wang N. Liu XY, et al. Chin Med J (Engl). 2016 Jun 20;129(12):1425-31. doi: 10.4103/0366-6999.183423. Chin Med J (Engl). 2016. PMID: 27270537 Free PMC article.

6

Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency.

Chen HZ, Jin M, Cai NQ, Lin XD, Liu XY, Xu LQ, Lin MT, Lin F, Wang N, Wang ZQ, Xu GR. Chen HZ, et al. Among authors: liu xy. Chin Med J (Engl). 2019 Jul 5;132(13):1615-1618. doi: 10.1097/CM9.0000000000000288. Chin Med J (Engl). 2019. PMID: 31058673 Free PMC article.

7

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

Liu XY, Chen XJ, Zhao M, Wang ZQ, Chen HZ, Li HF, Wang CJ, Wu SF, Peng C, Yin Y, Fu HX, Lin MT, Yu L, Xiong ZQ, Wu ZY, Wang N. Liu XY, et al. J Inherit Metab Dis. 2021 Mar;44(2):450-468. doi: 10.1002/jimd.12361. Epub 2021 Jan 25. J Inherit Metab Dis. 2021. PMID: 33438237

8

Bioinformatic Analysis to Identify and Cellular Experiments to Validate Autophagy-related Genes in Psoriasis.

Bai R, Wu S, Liu X, Xing Z, Luo R, Zhang W, Liu M, Ma X, Lei H, Wang N, Zheng Y. Bai R, et al. Comb Chem High Throughput Screen. 2024;27(9):1318-1328. doi: 10.2174/0113862073238968230920054712. Comb Chem High Throughput Screen. 2024. PMID: 37881076

9

Comprehensive Proteomic Analysis of Dysferlinopathy Unveiling Molecular Mechanisms and Biomarkers Linked to Pathological Progression.

Wang D, Liu XY, He QF, Zheng FZ, Chen L, Zheng Y, Zeng MH, Lin YH, Lin X, Chen HZ, Lin MT, Wang N, Wang ZQ, Lin F. Wang D, et al. Among authors: liu xy. CNS Neurosci Ther. 2024 Oct;30(10):e70065. doi: 10.1111/cns.70065. CNS Neurosci Ther. 2024. PMID: 39350328 Free PMC article.

10

Genetic association between asthma and alopecia areata: A two-sample Mendelian randomization study.

Du W, He K, Liu X, Yin T, Xiao S, Zheng Y. Du W, et al. Skin Res Technol. 2024 Jul;30(7):e13844. doi: 10.1111/srt.13844. Skin Res Technol. 2024. PMID: 38965800 Free PMC article.

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