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Page 1
Neuronal defects in a human cellular model of 22q11.2 deletion syndrome.
Khan TA, Revah O, Gordon A, Yoon SJ, Krawisz AK, Goold C, Sun Y, Kim CH, Tian Y, Li MY, Schaepe JM, Ikeda K, Amin ND, Sakai N, Yazawa M, Kushan L, Nishino S, Porteus MH, Rapoport JL, Bernstein JA, O'Hara R, Bearden CE, Hallmayer JF, Huguenard JR, Geschwind DH, Dolmetsch RE, Paşca SP. Khan TA, et al. Among authors: sun y. Nat Med. 2020 Dec;26(12):1888-1898. doi: 10.1038/s41591-020-1043-9. Epub 2020 Sep 28. Nat Med. 2020. PMID: 32989314 Free PMC article.
Patient Brain Organoids Identify a Link between the 16p11.2 Copy Number Variant and the RBFOX1 Gene.
Kostic M, Raymond JJ, Freyre CAC, Henry B, Tumkaya T, Khlghatyan J, Dvornik J, Li J, Hsiao JS, Cheon SH, Chung J, Sun Y, Dolmetsch RE, Worringer KA, Ihry RJ. Kostic M, et al. Among authors: sun y. ACS Chem Neurosci. 2023 Nov 15;14(22):3993-4012. doi: 10.1021/acschemneuro.3c00442. Epub 2023 Oct 30. ACS Chem Neurosci. 2023. PMID: 37903506 Free PMC article.
Alpha-actinin-2, a cytoskeletal protein, binds to angiogenin.
Hu H, Gao X, Sun Y, Zhou J, Yang M, Xu Z. Hu H, et al. Among authors: sun y. Biochem Biophys Res Commun. 2005 Apr 8;329(2):661-7. doi: 10.1016/j.bbrc.2005.01.158. Biochem Biophys Res Commun. 2005. PMID: 15737636
25 results