Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ken Xiong"'
Autor:
Bettina van Lengerich, Lihong Zhan, Dan Xia, Darren Chan, David Joy, Joshua I. Park, David Tatarakis, Meredith Calvert, Selina Hummel, Steve Lianoglou, Michelle E. Pizzo, Rachel Prorok, Elliot Thomsen, Laura M. Bartos, Philipp Beumers, Anja Capell, Sonnet S. Davis, Lis de Weerd, Jason C. Dugas, Joseph Duque, Timothy Earr, Kapil Gadkar, Tina Giese, Audrey Gill, Johannes Gnörich, Connie Ha, Malavika Kannuswamy, Do Jin Kim, Sebastian T. Kunte, Lea H. Kunze, Diana Lac, Kendra Lechtenberg, Amy Wing-Sze Leung, Chun-Chi Liang, Isabel Lopez, Paul McQuade, Anuja Modi, Vanessa O. Torres, Hoang N. Nguyen, Ida Pesämaa, Nicholas Propson, Marvin Reich, Yaneth Robles-Colmenares, Kai Schlepckow, Luna Slemann, Hilda Solanoy, Jung H. Suh, Robert G. Thorne, Chandler Vieira, Karin Wind-Mark, Ken Xiong, Y. Joy Yu Zuchero, Dolo Diaz, Mark S. Dennis, Fen Huang, Kimberly Scearce-Levie, Ryan J. Watts, Christian Haass, Joseph W. Lewcock, Gilbert Di Paolo, Matthias Brendel, Pascal E. Sanchez, Kathryn M. Monroe
Publikováno v:
Nature neuroscience 26, 416-429 (2023). doi:10.1038/s41593-022-01240-0
Loss-of-function variants of TREM2 are associated with increased risk of Alzheimer’s disease (AD), suggesting that activation of this innate immune receptor may be a useful therapeutic strategy. Here we describe a high-affinity human TREM2-activati
Autor:
Yuqing Deng, Ken Xiong, Xun Xu, Zhiwei Huang, Dan Jiang, Ying Gu, Xie Lin, Hui Jiang, Pan Jianchang, Wei Wang, Kang Xiongbin, Jun Xia, Zhu Zhu, Jing Li, Radoje Drmanac, Liqiong Luo, Snezana Drmanac, Amulya Nanisetti, Chao Liu, Lars Bolund, Jia Sophie Liu, Zhangzhang Lan, Fang Chen, Xiuqing Zhang, Ping Liu, Qiu Yong, Qianyu Shi
Publikováno v:
Chen, F, Liu, P, Gu, Y, Zhu, Z, Nanisetti, A, Lan, Z, Huang, Z, Liu, J S, Kang, X, Deng, Y, Luo, L, Jiang, D, Qiu, Y, Pan, J, Xia, J, Xiong, K, Liu, C, Xie, L, Shi, Q, Li, J, Zhang, X, Wang, W, Drmanac, S, Bolund, L, Jiang, H, Drmanac, R & Xu, X 2017, ' Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non-invasive prenatal testing ', Prenatal Diagnosis, vol. 37, no. 13, pp. 1311-1321 . https://doi.org/10.1002/pd.5186
Objective: The purpose of this study were to develop a methodology of isolating fetal cells from maternal blood and use deep sequence demonstrating the promise for complete and accurate genetic screening compared to other non-invasive prenatal testin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d0d9e72bfeecc57bc116f328fcc9ae5
https://pure.au.dk/portal/da/publications/isolation-and-whole-genome-sequencing-of-fetal-cells-from-maternal-blood-towards-the-ultimate-noninvasive-prenatal-testing(bb8d5767-ab87-4a6d-982a-c7e26cbb4a12).html
https://pure.au.dk/portal/da/publications/isolation-and-whole-genome-sequencing-of-fetal-cells-from-maternal-blood-towards-the-ultimate-noninvasive-prenatal-testing(bb8d5767-ab87-4a6d-982a-c7e26cbb4a12).html