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Chen C, Zuo Y, Hu H, Shao Y, Dong S, Zeng J, Huang L, Liu Z, Shen Q, Liu F, Liao X, Cao Z, Zhong Z, Lu H*, Bi Y*, Chen J*. Cysteamine hydrochloride affects ocular development and triggers associated inflammation in zebrafish. J Hazard Mater. 2023 Oct 5;459:132175.
Sun S, Li X, Zhang L, Zhong Z, Chen C, Zuo Y, Chen Y, Hu H, Liu F, Xiong G, Lu H*, Chen J*, Dai J*. Hexafluoropropylene oxide trimer acid (HFPO-TA) disturbs embryonic liver and biliary system development in zebrafish. Sci Total Environ. 2023 Feb 10;859(Pt 1):160087.
Hu H, Su M, Ba H, Chen G, Luo J, Liu F, Liao X, Cao Z, Zeng J, Lu H, Xiong G*, Chen J*. ZIF-8 nanoparticles induce neurobehavioral disorders through the regulation of ROS-mediated oxidative stress in zebrafish embryos. Chemosphere. 2022 Oct;305:135453.
Chen C, Zheng Y, Li X, Zhang L, Liu K, Sun S, Zhong Z, Hu H, Liu F, Xiong G, Liao X, Lu H, Bi Y*, Chen J*, Cao Z*. Cysteamine affects skeletal development and impairs motor behavior in zebrafish. Frontiers in Pharmacology. 2022 Aug 19;13:966710.
Zhong Z, Wu Z, Zhang J*, Chen J*. A novel BLOC1S5-related HPS-11 patient and zebrafish with bloc1s5 disruption. Pigment Cell Melanoma Res. 2021 Nov;34(6):1112-1119.
Han S#, Chen J#, Hua J#, Hu X, Jian S, Zheng G, Wang J, Li H, Yang J, Hejtmancik JF, Qu J*, Ma X*, Hou L. MITF protects against oxidative damage-induced retinal degeneration by regulating the NRF2 pathway in the retinal pigment epithelium. Redox Biology, 2020 Jul;34:101537.
Zhong Z, Gu L, Zheng X, Ma N, Wu Z, Duan J, Zhang J*, Chen J*. Comprehensive analysis of spectral distribution of a large cohort of Chinese patients with non-syndromic oculocutaneous albinism facilitates genetic diagnosis. Pigment Cell Melanoma Res. 2019 Sep;32(5):672-686.
Gao Y#, Ren RJ#, Zhong ZL#, Dammer E, Zhao QH, Shan S, Zhou Z, Li X, Zhang YQ, Cui HL, Hu YB, Chen SD, Chen JJ*, Guo QH*, Wang G*. Mutation Profile of APP, PSEN1, and PSEN2 in Chinese Familial Alzheimer
Chen J# , Wang Q#, Cabrera PE, Zhong Z, Sun W, Jiao X, Chen Y, Govindarajan G, Naeem MA, Khan SN, Ali MH, Assir MZ, Rahman FU, Qazi ZA, Riazuddin S, Akram J, Riazuddin SA, Hejtmancik JF*. Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening. Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2207-2217. doi: 10.1167/iovs.17-21469.
Chen J, Smaoui N, Hammer MB, Jiao X, Riazuddin SA, Harper S, Katsanis N, Riazuddin S, Chaabouni H, Berson EL, Hejtmancik JF*. Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genes. Invest Ophthalmol Vis Sci. 2011 Jul 18;52(8):5317-24. doi: 10.1167/iovs.11-7554.
Chen J#, Ma Z#,, Jiao X, Fariss R, Kantorow WL, Kantorow M, Pras E, Frydman M, Pras E, Riazuddin S, Riazuddin SA, Hejtmancik JF*. Mutations in FYCO1 cause autosomal-recessive congenital cataracts. Am J Hum Genet. 2011 Jun 10;88(6):827-838. doi: 10.1016/j.ajhg.2011.05.008.
Chen J, Wildhardt G, Zhong Z, R?th R, Weiss B, Steinberger D, Decker J, Blum WF, Rappold G*. Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain. J Med Genet. 2009 Dec;46(12):834-9. doi: 10.1136/jmg.2009.067785. Epub 2009 Jul 2.
Chen JJ#, Liang YH#, Zhou FS, Yang S, Wang J, Wang PG, Du WH, Xu SJ, Huang W, Zhang XJ*. The gene for a rare autosomal dominant form of pompholyx maps to chromosome 18q22.1-18q22.3. J Invest Dermatol. 2006 Feb;126(2):300-4.
Chen JJ#, Huang W#, Gui JP, Yang S, Zhou FS, Xiong QG, Wu HB, Cui Y, Gao M, Li W, Li JX, Yan KL, Yuan WT, Xu SJ, Liu JJ, Zhang XJ*. A novel linkage to generalized vitiligo on 4q13-q21 identified in a genomewide linkage analysis of Chinese families. Am J Hum Genet. 2005 Jun;76(6):1057-65. Epub 2005 Apr 4
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