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Showing results for gao xia fan
Search for Gaoxia Fan instead (1 results)
Biomarkers of ageing of humans and non-human primates.
Wu Z, Qu J, Zhang W; Aging Biomarker Consortium; Liu GH. Wu Z, et al. Nat Rev Mol Cell Biol. 2025 Nov;26(11):826-847. doi: 10.1038/s41580-025-00883-8. Epub 2025 Sep 11. Nat Rev Mol Cell Biol. 2025. PMID: 40935898 Review.
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials.
Fan X, Gao Z, Zhong J, Chen Y, Chen X, Landegger LD, Moser T, Zeng FG, Sun Y, Jin X, Nash R, Chien WW, Jiang D, Greinwald JH, Bance M, Rodríguez MM, Lee SY, Feng G, Yang H, Wu CC, Xu L, Yuan W, Feng Y, Zhao Y, Vona B, Strenzke N, Beutner D, Amin N, Arwyn-Jones J, Chandrasekeharan D, Shi D, Zhang D, Yang J, Qi J, Wang Q, Yin Y, Cheng YF, Tao Y, Yu Y, Wang D, Jiang L, Guo L, Chen L, Cheng X, Cui C, Lv J, Han S, Wang W, Li Y, Gao X, Liu XZ, Zha D, Shi H, Chen B, Wang Q, Yuan H, Yang S, Yin S, Wu H, Wang Z, Li H, Rubinstein JT, Lustig LR, Chai R, Chen ZY, Shu Y. Fan X, et al. Among authors: gao x. Med. 2026 Jan 9;7(1):100886. doi: 10.1016/j.medj.2025.100886. Epub 2025 Oct 23. Med. 2026. PMID: 41135524 Free article.
Expert consensus on the off-label use of drugs for pediatric rare diseases in China (2025 edition).
Mo X, Deng H, Yang J, Li J, Ouyang S, Chen F, Cui Y, Gao X, Jiang H, Li X, Liu L, Liu J, Qiu L, Rong X, Wen Z, Wang J, Zeng P, Zhang W, Zhao X, Zhou J, Chen J, Chen P, Chen W, Chen Z, Fang R, Fan X, Jia Y, Li Z, Li X, Li X, Lin Y, Liu M, Mai H, Miao J, Wang X, Wang Y, Wang J, Wei L, Wu J, Yu S, Zeng L, Zhang B, Zhang H, Zheng Z, Chen X, Xia S, Zhou W, Sun J, Li Y; Rare Disease Expert Committee of Guangdong Pharmaceutical Association. Mo X, et al. Among authors: gao x. Transl Pediatr. 2025 Nov 30;14(11):3094-3124. doi: 10.21037/tp-2025-521. Epub 2025 Nov 26. Transl Pediatr. 2025. PMID: 41367530 Free PMC article. Review.
Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy.
Tang X, Liu C, Liu X, Chen J, Fan X, Liu J, Ma D, Cao G, Chen Z, Xu D, Zhu Y, Jiang X, Cheng L, Wu Y, Hou L, Li Y, Shao X, Zheng S, Zhang A, Zheng B, Jian S, Rong Z, Su Q, Gao X, Rao J, Shen Q, Xu H; Chinese Children Genetic Kidney Disease Database (CCGKDD); “Internet Plus” Nephrology Alliance of the National Center for Children’s Care. Tang X, et al. Among authors: gao x. J Med Genet. 2022 Feb;59(2):147-154. doi: 10.1136/jmedgenet-2020-107184. Epub 2020 Dec 15. J Med Genet. 2022. PMID: 33323469
27 results