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Cited by in F6Publishing
For: Chen X, Deng S, Xia H, Yuan L, Xu H, Tang S, Deng H. Identification of a CCDC114 variant in a Han-Chinese patient with situs inversus. Exp Ther Med 2020;20:3336-42. [PMID: 32855706 DOI: 10.3892/etm.2020.9059] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Yu X, Yuan L, Deng S, Xia H, Tu X, Deng X, Huang X, Cao X, Deng H. Identification of DNAH17 Variants in Han-Chinese Patients With Left–Right Asymmetry Disorders. Front Genet 2022;13:862292. [DOI: 10.3389/fgene.2022.862292] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Gui M, Farley H, Anujan P, Anderson JR, Maxwell DW, Whitchurch JB, Botsch JJ, Qiu T, Meleppattu S, Singh SK, Zhang Q, Thompson J, Lucas JS, Bingle CD, Norris DP, Roy S, Brown A. De novo identification of mammalian ciliary motility proteins using cryo-EM. Cell 2021;184:5791-5806.e19. [PMID: 34715025 DOI: 10.1016/j.cell.2021.10.007] [Cited by in F6Publishing: 8] [Reference Citation Analysis]
3 Xiong Y, Xia H, Yuan L, Deng S, Ding Z, Deng H. Identification of compound heterozygous DNAH11 variants in a Han-Chinese family with primary ciliary dyskinesia. J Cell Mol Med 2021;25:9028-37. [PMID: 34405951 DOI: 10.1111/jcmm.16866] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Xia H, Huang X, Deng S, Xu H, Yang Y, Liu X, Yuan L, Deng H. DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease. PLoS One 2021;16:e0252786. [PMID: 34133440 DOI: 10.1371/journal.pone.0252786] [Cited by in F6Publishing: 2] [Reference Citation Analysis]