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ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
Zhang Y, Huang H, Zhao G, Yokoyama T, Vega H, Huang Y, Sood R, Bishop K, Maduro V, Accardi J, Toro C, Boerkoel CF, Lyons K, Gahl WA, Duan X, Malicdan MC, Lin S. Zhang Y, et al. Among authors: duan x. PLoS Genet. 2017 Feb 3;13(2):e1006481. doi: 10.1371/journal.pgen.1006481. eCollection 2017 Feb. PLoS Genet. 2017. PMID: 28158191 Free PMC article.
Hereditary dentin defects with systemic diseases.
Su T, Zhu Y, Wang X, Zhu Q, Duan X. Su T, et al. Among authors: duan x. Oral Dis. 2023 Sep;29(6):2376-2393. doi: 10.1111/odi.14589. Epub 2023 Apr 24. Oral Dis. 2023. PMID: 37094075 Review.
[Expert consensus on the biobank development of oral genetic diseases and rare diseases and storage codes of related biological samples from craniofacial and oral region].
Ruan WY, Zhang YL, Zheng SG, Sun Y, Fan ZP, Song YL, Sun HC, Wang WM, Dai JW, Zhao ZJ, Zhang TT, Chen D, Pan YC, Jiang YG, Wang XD, Zheng LW, Zhu QL, He M, Xu BS, Jia ZL, Han D, Duan XH. Ruan WY, et al. Among authors: duan xh. Zhonghua Kou Qiang Yi Xue Za Zhi. 2023 Aug 9;58(8):749-758. doi: 10.3760/cma.j.cn112144-20230523-00210. Zhonghua Kou Qiang Yi Xue Za Zhi. 2023. PMID: 37550034 Chinese.
7,935 results