Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Shiyi Xiong"'
Autor:
Jinjiao Dong, Wenjun Wang, Guodong Zheng, Nansheng Wu, Jingjing Xie, Shiyi Xiong, Panting Tian, Jingen Li
Publikováno v:
Current Research in Food Science, Vol 8, Iss , Pp 100760- (2024)
Choerospondias axillaris fruit has attracted more and more attention due to its various pharmacological activities, which are rich in polysaccharides. This study investigated the in vitro saliva-gastrointestinal digestion and fecal fermentation behav
Externí odkaz:
https://doaj.org/article/9704f245cbb74c0d9cb7bf8931c32c60
Autor:
Tong Zhao, Yuchen Zhu, Rui Zhao, Shiyi Xiong, Jing Sun, Juntao Zhang, Daidi Fan, Jianjun Deng, Haixia Yang
Publikováno v:
Pharmacological Research, Vol 193, Iss , Pp 106820- (2023)
Nuciferine aporphine alkaloid mainly exists in Nelumbo nucifera Gaertn and is a beneficial to human health, such as anti-obesity, lowering blood lipid, prevention of diabetes and cancer, closely associated with inflammation. Importantly, nuciferine m
Externí odkaz:
https://doaj.org/article/17ce9a5e76674f259a4f20d83cbbf305
Autor:
Charlotte Gehin, Museer A. Lone, Winston Lee, Laura Capolupo, Sylvia Ho, Adekemi M. Adeyemi, Erica H. Gerkes, Alexander P.A. Stegmann, Estrella López-Martín, Eva Bermejo-Sánchez, Beatriz Martínez-Delgado, Christiane Zweier, Cornelia Kraus, Bernt Popp, Vincent Strehlow, Daniel Gräfe, Ina Knerr, Eppie R. Jones, Stefano Zamuner, Luciano A. Abriata, Vidya Kunnathully, Brandon E. Moeller, Anthony Vocat, Samuel Rommelaere, Jean-Philippe Bocquete, Evelyne Ruchti, Greta Limoni, Marine Van Campenhoudt, Samuel Bourgeat, Petra Henklein, Christian Gilissen, Bregje W. van Bon, Rolph Pfundt, Marjolein H. Willemsen, Jolanda H. Schieving, Emanuela Leonardi, Fiorenza Soli, Alessandra Murgia, Hui Guo, Qiumeng Zhang, Kun Xia, Christina R. Fagerberg, Christoph P. Beier, Martin J. Larsen, Irene Valenzuela, Paula Fernández-Álvarez, Shiyi Xiong, Robert Śmigiel, Vanesa López-González, Lluís Armengol, Manuela Morleo, Angelo Selicorni, Annalaura Torella, Moira Blyth, Nicola S. Cooper, Valerie Wilson, Renske Oegema, Yvan Herenger, Aurore Garde, Ange-Line Bruel, Frederic Tran Mau-Them, Alexis B.R. Maddocks, Jennifer M. Bain, Musadiq A. Bhat, Gregory Costain, Peter Kannu, Ashish Marwaha, Neena L. Champaigne, Michael J. Friez, Ellen B. Richardson, Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, Yask Gupta, Tze Y. Lim, Simone Sanna-Cherchi, Bruno Lemaitre, Toshiyuki Yamaji, Kentaro Hanada, John E. Burke, Ana Marjia Jakšić, Brian D. McCabe, Paolo De Los Rios, Thorsten Hornemann, Giovanni D’Angelo, Vincenzo A. Gennarino
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 10 (2023)
Neural differentiation, synaptic transmission, and action potential propagation depend on membrane sphingolipids, whose metabolism is tightly regulated. Mutations in the ceramide transporter CERT (CERT1), which is involved in sphingolipid biosynthesi
Externí odkaz:
https://doaj.org/article/47a113198d5649e88315ddec99f2067f
Publikováno v:
Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-10 (2022)
Abstract Background With the introduction of genetic tests such as chromosomal microarray analysis (CMA) and exome sequencing (ES) into fetal medical practices, genotype–phenotype correlations in intrauterine-onset disorders have substantially impr
Externí odkaz:
https://doaj.org/article/e2a7ac055023429c9594b0691e7743e2
Autor:
Dong Dong, Shiyi Xiong, Elena Nichini, Xiaoqiong Chen, Binjuan Liu, Liling Zhu, Faustina Fu Yip, Luming Sun, Jianfeng Zhu
Publikováno v:
Frontiers in Medicine, Vol 9 (2023)
ObjectiveDue to the changing medical demands in the healthcare system, there is a need for a standardized and professionalized curriculum for genetic counselors. This mixed-method study will observe and evaluate the first Peer Experiential and Recipr
Externí odkaz:
https://doaj.org/article/68ba39e732874899ab8a1820b870109a
Publikováno v:
Stem Cell Research, Vol 61, Iss , Pp 102777- (2022)
We generated a human induced pluripotent stem cell (iPSC) line, FMUPDCi001-A, from peripheral blood mononuclear cells of a patient with mental retardation, autosomal recessive 36 (MRT36), and compound heterozygous c.219dupA and c.587C > T variants in
Externí odkaz:
https://doaj.org/article/ef553713e01d4499946170de198bad2f
Autor:
Niu Li, Yirou Wang, Yu Yang, Pengpeng Wang, Hui Huang, Shiyi Xiong, Luming Sun, Min Cheng, Cui Song, Xinran Cheng, Yu Ding, Guoying Chang, Yao Chen, Yufei Xu, Tingting Yu, Ru-en Yao, Yiping Shen, Xiumin Wang, Jian Wang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-13 (2018)
Abstract Background Wiedemann–Steiner syndrome (WDSTS) is a rare genetic disorder characterized by facial gestalt, neurodevelopmental delay, skeletal anomalies and growth retardation, which is caused by variation of KMT2A gene. To date, only 2 Chin
Externí odkaz:
https://doaj.org/article/f0d6669fbafe4102b8661ff152c7c733
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract Background Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterized by the development of hamartomas in multiple organs, including the brain, heart, skin, kidney, lung and retina. A diagnosis of TSC is establi
Externí odkaz:
https://doaj.org/article/0d564d2e50394463aa95ae1e35920a1b
Publikováno v:
Maternal-Fetal Medicine. 4:286-289
Autor:
Xing Wei, Xinyao Zhou, Jia Zhou, Gang Zou, Yingjun Yang, Fenhe Zhou, Shiyi Xiong, Jianping Chen, Luming Sun
Publikováno v:
Fetal Diagnosis and Therapy. 49:138-144
Objective: We aimed to study the value of exome sequencing (ES) in severe pleural effusion with nonimmune hydrops fetalis (NIHF) that underwent thoracoamniotic shunt (TAS). Methods: It was a retrospective study of NIHF that underwent TAS between 2012