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A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.
Tsai MH, Kuo PW, Myers CT, Li SW, Lin WC, Fu TY, Chang HY, Mefford HC, Chang YC, Tsai JW. Tsai MH, et al. Among authors: chang hy, chang yc. Eur J Paediatr Neurol. 2016 Sep;20(5):788-94. doi: 10.1016/j.ejpn.2016.05.010. Epub 2016 May 30. Eur J Paediatr Neurol. 2016. PMID: 27292316
Identification of genes associated with cortical malformation using a transposon-mediated somatic mutagenesis screen in mice.
Lu IL, Chen C, Tung CY, Chen HH, Pan JP, Chang CH, Cheng JS, Chen YA, Wang CH, Huang CW, Kang YN, Chang HY, Li LL, Chang KP, Shih YH, Lin CH, Kwan SY, Tsai JW. Lu IL, et al. Among authors: chang hy, chang ch, chang kp. Nat Commun. 2018 Jun 27;9(1):2498. doi: 10.1038/s41467-018-04880-8. Nat Commun. 2018. PMID: 29950674 Free PMC article.
The CD8+ T cell tolerance checkpoint triggers a distinct differentiation state defined by protein translation defects.
Van Der Byl W, Nüssing S, Peters TJ, Ahn A, Li H, Ledergor G, David E, Koh AS, Wagle MV, Deguit CDT, de Menezes MN, Travers A, Sampurno S, Ramsbottom KM, Li R, Kallies A, Beavis PA, Jungmann R, Bastings MMC, Belz GT, Goel S, Trapani JA, Crabtree GR, Chang HY, Amit I, Goodnow CC, Luciani F, Parish IA. Van Der Byl W, et al. Among authors: chang hy. Immunity. 2024 May 16:S1074-7613(24)00231-0. doi: 10.1016/j.immuni.2024.04.026. Online ahead of print. Immunity. 2024. PMID: 38776918
Pathways for macrophage uptake of cell-free circular RNAs.
Amaya L, Abe B, Liu J, Zhao F, Zhang WL, Chen R, Li R, Wang S, Kamber RA, Tsai MC, Bassik MC, Majeti R, Chang HY. Amaya L, et al. Among authors: chang hy. Mol Cell. 2024 May 10:S1097-2765(24)00388-5. doi: 10.1016/j.molcel.2024.04.022. Online ahead of print. Mol Cell. 2024. PMID: 38761795 Free article.
2,108 results