代表性论文
1.Tian Y, Wang L, Chen R, Miao Y, Liu Y, Huang W, Fang L, Liu S, Luo J, Sun X, Zhang Y, Ye D. Self-Assembled Triple-Targeted Radiosensitizer Enhances Hypoxic Tumor Targeting and Radio-Immunotherapy Efficacy. Angew Chem Int Ed Engl. 2025 Apr 25;64(18):e202500645.(通讯作者)
2.Chen L, Wang HL, Zhu YB, Jin Z, Huang JB, Lin XF, Luo JW, Fang ZT. Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene. Cell Death Dis. 2020 Mar 2;11(3):159.(通讯作者)
3.Chen T, Ruan DD, Zhang JH, Wang HL, Wu M, Wu QY, Zhang YP, Wu JB, Ye Y, Chou GX, Luo JW. Eucarbwenstols A-H, eight novel compounds from Eucalyptus robusta prevents MPC-5 injury via ROS modulation and regulation of mitochondrial membrane potential. Bioorg Chem. 2022 Dec;129:106159.(通讯作者)
4.Gan YM, Zhang YP, Ruan DD, Huang JB, Zhu YB, Lin XF, Xiao XP, Cheng Q, Geng ZB, Liao LS, Tang FQ, Luo JW. Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription. Cell Death Dis. 2022 Jun 2;13(6):518.(通讯作者)
5.Zhang YP, Lin B, Ji YY, Hu YN, Lin XF, Tang Y, Zhang JH, Wu SJ, Cai SL, Zhou YF, Chen T, Fang ZT, Luo JW. A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1. Thromb J. 2021 Sep 8;19(1):64. (通讯作者)
6.Wang RL, Ruan DD, Hu YN, Gan YM, Lin XF, Fang ZT, Liao LS, Tang FQ, He WB, Luo JW. Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant. Front Pediatr. 2022 May 6;10:878172.(通讯作者)
7.Pan HH, Ruan DD, Wu M, Chen T, Lu T, Gan YM, Wang C, Liao LS, Lin XF, Chen X, Zhu YB, Fang ZT, Yu QH, Yang GK, Ye LF, Luo JW. Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome. J Med Genet. 2023 Nov 27;60(12):1210-1214.(通讯作者)
8.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. Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation. Sci Rep. 2024 Apr 1;14(1):7638.(通讯作者)
9.Gao MZ, Zeng JY, Chen XJ, Shi L, Hong FY, Lin M, Luo JW, Chen H. Dimethyl fumarate ameliorates oxidative stress-induced acute kidney injury after traumatic brain injury by activating Keap1-Nrf2/HO-1 signaling pathway. Heliyon. 2024 Jun 4;10(11):e32377.(通讯作者)
10.Zhang JH, Liu J, Chen Q, Ruan DD, Liao LS, Lin KP, Zheng XL, Luo JW, Zhang L. A rare concurrence of monoclonal gammopathies in an older adult with tubulointerstitial nephritis and uveitis syndrome. BMC Geriatr. 2025 Jul 2;25(1):472.(通讯作者)
