Lin XF - Search Results

1

Analysis of low-density lipoprotein receptor gene mutations in a family with familial hypercholesterolemia.

Hu YN, Wu M, Yu HP, Wu QY, Chen Y, Zhang JH, Ruan DD, Zhang YP, Zou J, Zhang L, Lin XF, Fang ZT, Liao LS, Lin F, Li H, Luo JW. Hu YN, et al. Among authors: lin xf. PLoS One. 2024 Oct 11;19(10):e0310547. doi: 10.1371/journal.pone.0310547. eCollection 2024. PLoS One. 2024. PMID: 39392848 Free PMC article.

2

SGLT2 inhibitors ameliorate NAFLD in mice via downregulating PFKFB3, suppressing glycolysis and modulating macrophage polarization.

Lin XF, Cui XN, Yang J, Jiang YF, Wei TJ, Xia L, Liao XY, Li F, Wang DD, Li J, Wu Q, Yin DS, Le YY, Yang K, Wei R, Hong TP. Lin XF, et al. Acta Pharmacol Sin. 2024 Dec;45(12):2579-2597. doi: 10.1038/s41401-024-01389-3. Epub 2024 Sep 18. Acta Pharmacol Sin. 2024. PMID: 39294445 Free PMC article.

3

Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.

Ruan DD, Ruan XL, Wang RL, Lin XF, Zhang YP, Lin B, Li SJ, Wu M, Chen Q, Zhang JH, Cheng Q, Zhang YW, Lin F, Luo JW, Zheng Z, Li YF. Ruan DD, et al. Among authors: lin xf. Sci Rep. 2024 Sep 10;14(1):21122. doi: 10.1038/s41598-024-72293-3. Sci Rep. 2024. PMID: 39256586 Free PMC article. No abstract available.

4

A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemia.

He KY, Yu HP, Zou J, Chen X, Chen L, Ruan DD, Chen T, Chen Q, Zhang L, Gao MZ, Lin XF, Li H, Fang ZT, Wu J, Luo JW, Liao LS. He KY, et al. Among authors: lin xf. Clin Chim Acta. 2025 Jan 1;564:119930. doi: 10.1016/j.cca.2024.119930. Epub 2024 Aug 16. Clin Chim Acta. 2025. PMID: 39154701

5

In vitro study of ATP1A3 p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism.

Ruan DD, Zou J, Liao LS, Ji MD, Wang RL, Zhang JH, Zhang L, Gao MZ, Chen Q, Yu HP, Wei W, Li YF, Li H, Lin F, Luo JW, Lin XF. Ruan DD, et al. Among authors: lin xf. Front Neurosci. 2024 Jul 31;18:1415576. doi: 10.3389/fnins.2024.1415576. eCollection 2024. Front Neurosci. 2024. PMID: 39145297 Free PMC article.

6

Risk prediction and prognostic analysis of post-implantation syndrome after thoracic endovascular aortic repair.

Xie LF, Lin XF, Wu QS, Xie YL, Zhang ZF, Qiu ZH, Chen LW. Xie LF, et al. Among authors: lin xf. Sci Rep. 2024 Jul 29;14(1):17376. doi: 10.1038/s41598-024-65877-6. Sci Rep. 2024. PMID: 39075074 Free PMC article.

7

ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy.

Hu YY, Song W, Liu ZG, Ye XG, Zhang HW, Li X, Luo JX, Wang PY, Wang J, Lin XF, Zhu HL, Liao WP, Li B, Chen XQ. Hu YY, et al. Among authors: lin xf. World J Pediatr. 2024 Aug;20(8):859-867. doi: 10.1007/s12519-024-00830-1. Epub 2024 Jul 26. World J Pediatr. 2024. PMID: 39060771 No abstract available.

8

Development of a machine learning-based model to predict major adverse events after surgery for type A aortic dissection complicated by malnutrition.

Xie LF, Lin XF, Xie YL, Wu QS, Qiu ZH, Lan Q, Chen LW. Xie LF, et al. Among authors: lin xf. Front Nutr. 2024 Jul 4;11:1428532. doi: 10.3389/fnut.2024.1428532. eCollection 2024. Front Nutr. 2024. PMID: 39027660 Free PMC article.

9

A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification.

Yao XJ, Chen Q, Yu HP, Ruan DD, Li SJ, Wu M, Liao LS, Lin XF, Fang ZT, Luo JW, Xie BS. Yao XJ, et al. Among authors: lin xf. BMC Pulm Med. 2024 Jul 16;24(1):343. doi: 10.1186/s12890-024-03164-w. BMC Pulm Med. 2024. PMID: 39014333 Free PMC article.

10

Effect of endoscopic full-thickness resection assisted by distal serosal turnover with floss traction for gastric submucosal masses.

Liu TW, Lin XF, Wen ST, Xu JY, Fu ZL, Qin SM. Liu TW, et al. Among authors: lin xf. World J Clin Cases. 2024 Jun 6;12(16):2738-2744. doi: 10.12998/wjcc.v12.i16.2738. World J Clin Cases. 2024. PMID: 38899293 Free PMC article.

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