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Showing results for chen chun an
Search for Chunchun An instead (2 results)
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.
Pérez Baca MDR, Jacobs EZ, Vantomme L, Leblanc P, Bogaert E, Dheedene A, De Cock L, Haghshenas S, Foroutan A, Levy MA, Kerkhof J, McConkey H, Chen CA, Batzir NA, Wang X, Palomares M, Carels M; ZFHX3 consortium; Dermaut B, Sadikovic B, Menten B, Yuan B, Vergult S, Callewaert B. Pérez Baca MDR, et al. Among authors: chen ca. Am J Hum Genet. 2024 Mar 7;111(3):509-528. doi: 10.1016/j.ajhg.2024.01.013. Epub 2024 Feb 26. Am J Hum Genet. 2024. PMID: 38412861
Tunable Single-Photon Emission with Wafer-Scale Plasmonic Array.
Chen CA, Chen PH, Zheng YX, Chen CH, Hsu MK, Hsu KC, Lai YY, Chuu CS, Deng H, Lee YH. Chen CA, et al. Nano Lett. 2024 Mar 20;24(11):3395-3403. doi: 10.1021/acs.nanolett.3c05155. Epub 2024 Feb 15. Nano Lett. 2024. PMID: 38359157 Free PMC article.
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene.
Del Rocío Pérez Baca M, Jacobs EZ, Vantomme L, Leblanc P, Bogaert E, Dheedene A, De Cock L, Haghshenas S, Foroutan A, Levy MA, Kerkhof J, McConkey H, Chen CA, Batzir NA, Wang X, Palomares M, Carels M; ZFHX3 consortium; Demaut B, Sadikovic B, Menten B, Yuan B, Vergult S, Callewaert B. Del Rocío Pérez Baca M, et al. Among authors: chen ca. medRxiv [Preprint]. 2023 May 24:2023.05.22.23289895. doi: 10.1101/2023.05.22.23289895. medRxiv. 2023. PMID: 37292950 Free PMC article. Preprint.
Passivated Interfacial Traps of Monolayer MoS2 with Bipolar Electrical Pulse.
Chen PH, Chen CA, Lin YT, Hsieh PY, Chuang MH, Liu X, Hsieh TY, Shen CH, Shieh JM, Wu MC, Chen YF, Yang CC, Lee YH. Chen PH, et al. Among authors: chen ca. ACS Appl Mater Interfaces. 2023 Mar 1;15(8):10812-10819. doi: 10.1021/acsami.2c19705. Epub 2023 Feb 20. ACS Appl Mater Interfaces. 2023. PMID: 36802479
179 results