Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Shuxi Liu"'
Autor:
Xiaoyan Zhou, Hongtao Wang, Shuxi Liu, Hao Wang, John You En Chan, Cheng-Feng Pan, Daomu Zhao, Joel K. W. Yang, Cheng-Wei Qiu
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract Caustics occur in diverse physical systems, spanning the nano-scale in electron microscopy to astronomical-scale in gravitational lensing. As envelopes of rays, optical caustics result in sharp edges or extended networks. Caustics in structu
Externí odkaz:
https://doaj.org/article/6a55d53e118049f5af4a52abbc207ac4
Autor:
Shuxi Liu, Ziyi Yan, Yuan Peng, Yunqiu Liu, Yiling Li, Daxiang Xu, Yuying Gong, Zeyu Cui, Yongshui Wu, Yumei Zhang, Dahui Wang, Wei Pan, Xiaoying Yang
Publikováno v:
Parasites & Vectors, Vol 16, Iss 1, Pp 1-18 (2023)
Abstract Background Toxoplasma gondii (T. gondii) is increasingly considered a risk factor for neurodegenerative diseases. However, there is only limited information on the development of drugs for T. gondii infection. Lentinan from Lentinula edodes
Externí odkaz:
https://doaj.org/article/74096d88c0a641c59ca188f97a961909
Autor:
Zeyu Cui, Yuying Gong, Xiaotong Luo, Niuyi Zheng, Shimin Tan, Shuxi Liu, Youwei Li, Qingling Wang, Fenfen Sun, Minmin Hu, Wei Pan, Xiaoying Yang
Publikováno v:
Parasites & Vectors, Vol 16, Iss 1, Pp 1-15 (2023)
Abstract Background Toxoplasma gondii (T. gondii) is a neuroinvasive parasite causing neuroinflammation, which in turn is associated with a higher risk for several psycho-behavioral disorders. There is an urgent need to identify drugs capable of impr
Externí odkaz:
https://doaj.org/article/b5e854b332cc4d74ba143c6b9428d39f
Autor:
Ganka Douglas, Jeanne Meck, Lindsay Havens Dyer, Rhonda Brandon, Lisa Dyer, Patricia Fernandez Ferri, Mingjuan Liao, Shuxi Liu, Ludmila Matyakhina, Evica Rajcan-Separovic, Laura Sack, May Sanyoura, Wei Wang, Paul Kruszka
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100500- (2023)
Externí odkaz:
https://doaj.org/article/d954158160c74fa187360331d5abe6cb
Publikováno v:
Optics Express.
Autor:
Zeyu Cui, Yuying Gong, Xiaotong Luo, Niuyi Zheng, Shimin Tan, Shuxi Liu, Youwei Li, Qingling Wang, Fenfen Sun, Minmin Hu, Wei Pan, Xiaoying Yang Yang
Background Toxoplasma gondii (T. gondii) is a neuroinvasive parasite causing neuroinflammation, which is associated with a higher risk for several psycho-behavioral disorders. There is an urgent need to identify drugs capable of improving cognitive d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fc4d6d10eead58cbad00e1d386c36c9
https://doi.org/10.21203/rs.3.rs-2109273/v1
https://doi.org/10.21203/rs.3.rs-2109273/v1
Autor:
Zeyu Cui, Yuying Gong, Xiaotong Luo, Niuyi Zheng, Shimin Tan, Shuxi Liu, Youwei Li, Qingling Wang, Fenfen Sun, Minmin Hu, Wei Pan, Xiaoying Yang
Toxoplasma gondii (T. gondii) is a neuroinvasive parasite closely associated with a higher risk for several psycho-behavioral disorders. β-glucan is an immunomodulating ingredient extracted from mushrooms. In this study, we evaluated the effect of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a935b308b6bfa919d635c2183026283f
https://doi.org/10.21203/rs.3.rs-2041961/v1
https://doi.org/10.21203/rs.3.rs-2041961/v1
Autor:
Daxiang Xu, Ziyi Yan, Yuying Zhou, Yan He, Shuxi Liu, Zixuan Gao, Xiyue Zhang, Xiaohui Ding, Yinghua Yu, Xiaoying Yang, Wei Pan
Publikováno v:
Parasitology research. 121(12)
Chronic Toxoplasma gondii (T. gondii) infection has been revealed to be a risk factor for neuropsychiatric diseases, including anxiety. However, there is no intervention strategy. The present study aimed to investigate the protective effect of β-glu
Autor:
James W. Wheless, Thierry Frebourg, Robert Olaso, Rosemarie Smith, Kelly Nori, François Lecoquierre, Delphine Héron, Roseline Caumes, Anne Boland, Ange-Line Bruel, Candy Kumps, Gaël Nicolas, Sarah Stewart, Sophie Rondeau, Diane Doummar, Marlène Rio, Giulia Barcia, Anne-Marie Guerrot, Gwenaël Le Guyader, Alexandra Afenjar, Sarah Vergult, Karine Poirier, Juliette Coursimault, Jennifer Morrison, Amy Kritzer, Anne-Sophie Alaix, Rebecca Hernan, Anne-Sophie Denommé-Pichon, Sabine Sigaudy, Christine Coubes, Pascale Saugier-Veber, Francisca Millan Zamora, Austin Larson, Michelle M. Morrow, Christine Poitou, Björn Menten, Mathilde Nizon, Thomas Smol, Elise Schaefer, Bénédicte Gérard, Charles Coutton, Salima El Chehadeh, Fanggeng Zou, Stéphanie Valence, Anita Shanmugham, Wendy K. Chung, Bert Callewaert, Christina Kresge, Arnold Munnich, Beth A. Pletcher, Laurence Faivre, Estelle Colin, Laurence Colleaux, Patricia G Wheeler, Annelies Dheedene, Frédéric Tran Mau-Them, Jean-François Deleuze, Claude Houdayer, Jeanne Amiel, Frédéric Bilan, Marine Tessarech, Bertrand Isidor, Guillaume Jouret, Cyril Mignot, Benjamin Cogné, Shuxi Liu, Boris Keren, Françoise Devillard, Catherine Schramm, Margaret Helm
Publikováno v:
Human Genetics
Human Genetics, 2022, 141 (1), pp.65-80. ⟨10.1007/s00439-021-02383-z⟩
Human Genetics, Springer Verlag, 2021, ⟨10.1007/s00439-021-02383-z⟩
Human Genetics, 2021, ⟨10.1007/s00439-021-02383-z⟩
Human Genetics, 2022, 141 (1), pp.65-80. ⟨10.1007/s00439-021-02383-z⟩
Human Genetics, Springer Verlag, 2021, ⟨10.1007/s00439-021-02383-z⟩
Human Genetics, 2021, ⟨10.1007/s00439-021-02383-z⟩
International audience; Pathogenic variants of the myelin transcription factor-1 like (MYT1L) gene include heterozygous missense, truncating variants and 2p25.3 microdeletions and cause a syndromic neurodevelopmental disorder (OMIM#616,521). Despite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d62d99917d3e3b78e73c61b6c495303
https://hal.science/hal-03820933
https://hal.science/hal-03820933
Autor:
Kyle Retterer, Carlos Borroto, Erin Beaver, Jane Juusola, Lorne A. Clarke, Kevin Galens, Zhancheng Zhang, Shuxi Liu, Jennifer Heeley, Kevin J. Arvai, Rebecca I. Torene, Jagdeep S. Walia, Julie Scuffins, Danna Hull, Bethany Friedman, Hana Sroka, Sarah Neil
Publikováno v:
Genetics in Medicine
Purpose Exome sequencing (ES) is increasingly used for the diagnosis of rare genetic disease. However, some pathogenic sequence variants within the exome go undetected due to the technical difficulty of identifying them. Mobile element insertions (ME