Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Lin, Xiang  [Clear All Filters]
2023
Lin X, Jiang J-Y, Hong D-J, Lin K-J, Li J-J, Chen Y-J, Qiu Y-S, Wang Z, Liao Y-C, Yang K, et al. Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization. Mov Disord. 2023.
2022
Jin M, Wang D, Li G, Lin J, Lin X, Wang N. Generation and characterization of an induced pluripotent stem cell line (FJMUNi001-A) from a patient with Duchenne muscular dystrophy carrying c.4518 + 512 T > A variant in the DMD gene. Stem Cell Res. 2022;60:102718.
2021
Das S, Feng Q, Balasubramanian I, Lin X, Liu H, Pellόn-Cardenas O, Yu S, Zhang X, Liu Y, Wei Z, et al. Colonic healing requires WNT produced by epithelium as well as Tagln+ and Acta2+ stromal cells. Development. 2021.
2019
Liu Q, Bai W, Huang F, Tang J, Lin X. Downregulation of microRNA-196a inhibits stem cell self-renewal ability and stemness in non-small-cell lung cancer through upregulating GPX3 expression. Int J Biochem Cell Biol. 2019:105571.
2018
Lu Y-Q, Dong E-L, Yang W-Q, Lai L-L, Lin X-H, Ma L-X, Chen W-J, Wang N, Lin X. 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). Stem Cell Res. 2018;34:101354.
2016
Wang Q, Yang J, Lin X, Huang Z, Xie C, Fan H. Spot14/Spot14R expression may be involved in MSC adipogenic differentiation in patients with adolescent idiopathic scoliosis. Mol Med Rep. 2016.