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GLP-1R Signaling and Functional Molecules in Incretin Therapy.
Wan W, Qin Q, Xie L, Zhang H, Wu F, Stevens RC, Liu Y. Wan W, et al. Among authors: liu y. Molecules. 2023 Jan 11;28(2):751. doi: 10.3390/molecules28020751. Molecules. 2023. PMID: 36677809 Free PMC article. Review.
Critical role of spectrin in hearing development and deafness.
Liu Y, Qi J, Chen X, Tang M, Chu C, Zhu W, Li H, Tian C, Yang G, Zhong C, Zhang Y, Ni G, He S, Chai R, Zhong G. Liu Y, et al. Sci Adv. 2019 Apr 17;5(4):eaav7803. doi: 10.1126/sciadv.aav7803. eCollection 2019 Apr. Sci Adv. 2019. PMID: 31001589 Free PMC article.
Deficits in human trisomy 21 iPSCs and neurons.
Weick JP, Held DL, Bonadurer GF 3rd, Doers ME, Liu Y, Maguire C, Clark A, Knackert JA, Molinarolo K, Musser M, Yao L, Yin Y, Lu J, Zhang X, Zhang SC, Bhattacharyya A. Weick JP, et al. Among authors: liu y. Proc Natl Acad Sci U S A. 2013 Jun 11;110(24):9962-7. doi: 10.1073/pnas.1216575110. Epub 2013 May 28. Proc Natl Acad Sci U S A. 2013. PMID: 23716668 Free PMC article.
A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.
Chan B, Clasquin M, Smolen GA, Histen G, Powe J, Chen Y, Lin Z, Lu C, Liu Y, Cang Y, Yan Z, Xia Y, Thompson R, Singleton C, Dorsch M, Silverman L, Su SM, Freeze HH, Jin S. Chan B, et al. Among authors: liu y. Hum Mol Genet. 2016 Jun 1;25(11):2182-2193. doi: 10.1093/hmg/ddw085. Epub 2016 Apr 5. Hum Mol Genet. 2016. PMID: 27053713 Free PMC article.
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