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Structural insight into the mechanisms of enveloped virus tethering by tetherin.
Yang H, Wang J, Jia X, McNatt MW, Zang T, Pan B, Meng W, Wang HW, Bieniasz PD, Xiong Y. Yang H, et al. Among authors: xiong y. Proc Natl Acad Sci U S A. 2010 Oct 26;107(43):18428-32. doi: 10.1073/pnas.1011485107. Epub 2010 Oct 12. Proc Natl Acad Sci U S A. 2010. PMID: 20940320 Free PMC article.
Structural insight into HIV-1 capsid recognition by rhesus TRIM5α.
Yang H, Ji X, Zhao G, Ning J, Zhao Q, Aiken C, Gronenborn AM, Zhang P, Xiong Y. Yang H, et al. Among authors: xiong y. Proc Natl Acad Sci U S A. 2012 Nov 6;109(45):18372-7. doi: 10.1073/pnas.1210903109. Epub 2012 Oct 22. Proc Natl Acad Sci U S A. 2012. PMID: 23091002 Free PMC article.
Mechanism of allosteric activation of SAMHD1 by dGTP.
Ji X, Wu Y, Yan J, Mehrens J, Yang H, DeLucia M, Hao C, Gronenborn AM, Skowronski J, Ahn J, Xiong Y. Ji X, et al. Among authors: xiong y. Nat Struct Mol Biol. 2013 Nov;20(11):1304-9. doi: 10.1038/nsmb.2692. Epub 2013 Oct 20. Nat Struct Mol Biol. 2013. PMID: 24141705 Free PMC article.
Mutations in ASPH cause facial dysmorphism, lens dislocation, anterior-segment abnormalities, and spontaneous filtering blebs, or Traboulsi syndrome.
Patel N, Khan AO, Mansour A, Mohamed JY, Al-Assiri A, Haddad R, Jia X, Xiong Y, Mégarbané A, Traboulsi EI, Alkuraya FS. Patel N, et al. Among authors: xiong y. Am J Hum Genet. 2014 May 1;94(5):755-9. doi: 10.1016/j.ajhg.2014.04.002. Epub 2014 Apr 24. Am J Hum Genet. 2014. PMID: 24768550 Free PMC article.
Neu-Laxova syndrome, an inborn error of serine metabolism, is caused by mutations in PHGDH.
Shaheen R, Rahbeeni Z, Alhashem A, Faqeih E, Zhao Q, Xiong Y, Almoisheer A, Al-Qattan SM, Almadani HA, Al-Onazi N, Al-Baqawi BS, Saleh MA, Alkuraya FS. Shaheen R, et al. Among authors: xiong y. Am J Hum Genet. 2014 Jun 5;94(6):898-904. doi: 10.1016/j.ajhg.2014.04.015. Epub 2014 May 15. Am J Hum Genet. 2014. PMID: 24836451 Free PMC article.
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