Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Peixiang Wang"'
Autor:
Yishuo Wu, Guangyang Shang, Cong Ma, Yingjie Shi, Zhexu Song, Peixiang Wang, Yanzi Gao, Qian Wang, Meina Yu, Jiumei Xiao, Cheng Zou
Publikováno v:
Polymers, Vol 16, Iss 17, p 2446 (2024)
Stepwise photopolymerization is a miraculous strategy modulating the polymer skeleton and electro-optical properties of light modulators based on liquid crystal/polymer composites. However, owing to the indistinct polymerization mechanism and curing
Externí odkaz:
https://doaj.org/article/2fbf034ffb1f4e1b87853bb6374c8b3c
Publikováno v:
Arabian Journal of Chemistry, Vol 16, Iss 9, Pp 105048- (2023)
In this study, the degradation of salicylhydroxamic acid (SHA) in industrial beneficiation wastewater was investigated using dielectric barrier discharge (DBD) and La-Fe3O4-doped activated carbon (La-Fe3O4/AC). The physical and chemical properties of
Externí odkaz:
https://doaj.org/article/c1b01a09d57e489f9595e4d9c4c9a1b3
Autor:
Sharmistha Mitra, Baozhi Chen, Peixiang Wang, Erin E. Chown, Mathew Dear, Dikran R. Guisso, Ummay Mariam, Jun Wu, Emrah Gumusgoz, Berge A. Minassian
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 1 (2023)
Externí odkaz:
https://doaj.org/article/24f6a47e51664198bbbbbe98bb91751b
Autor:
Erin E. Chown, Peixiang Wang, Xiaochu Zhao, Justin J. Crowder, Jordan W. Strober, Mitchell A. Sullivan, Yunlin Xue, Cody S. Bennett, Ami M. Perri, Bret M. Evers, Peter J. Roach, Anna A. Depaoli‐Roach, H. Orhan Akman, Bartholomew A. Pederson, Berge A. Minassian
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 11, Pp 2186-2198 (2020)
Abstract Objective Adult polyglucosan body disease (APBD) is an adult‐onset neurological variant of glycogen storage disease type IV. APBD is caused by recessive mutations in the glycogen branching enzyme gene, and the consequent accumulation of po
Externí odkaz:
https://doaj.org/article/17d8578f86794d68bd05a48ab3d0c12b
Autor:
Saija Ahonen, Ian Seath, Clare Rusbridge, Susan Holt, Gill Key, Travis Wang, Peixiang Wang, Berge A. Minassian
Publikováno v:
Canine Medicine and Genetics, Vol 8, Iss 1, Pp 1-2 (2021)
Externí odkaz:
https://doaj.org/article/47688ab0d4f541f38d2204172f4213b7
Autor:
Jinghu Gao, Linyue Zhao, Qian Luo, Shuyao Liu, Ziyang Lin, Peixiang Wang, Xin Fu, Juan Chen, Hongjie Zhang, Long Lin, Anbing Shi
Publikováno v:
PLoS Genetics, Vol 16, Iss 5, p e1008763 (2020)
The ACK family tyrosine kinase SID-3 is involved in the endocytic uptake of double-stranded RNA. Here we identified SID-3 as a previously unappreciated recycling regulator in the Caenorhabditis elegans intestine. The RAB-10 effector EHBP-1 is require
Externí odkaz:
https://doaj.org/article/a7f518378bc2432f8e084853fcd1e5a6
Autor:
Saija Ahonen, Ian Seath, Clare Rusbridge, Susan Holt, Gill Key, Travis Wang, Peixiang Wang, Berge A. Minassian
Publikováno v:
Canine Genetics and Epidemiology, Vol 5, Iss 1, Pp 1-9 (2018)
Abstract Background Canine DNA-testing has become an important tool in purebred dog breeding and many breeders use genetic testing results when planning their breeding strategies. In addition, information obtained from testing of hundreds dogs in one
Externí odkaz:
https://doaj.org/article/ded1efa9f95e4e6b8e3ce12f4f77a2b9
Autor:
Thilo von Klopmann, Saija Ahonen, Irene Espadas-Santiuste, Kaspar Matiasek, Daniel Sanchez-Masian, Stefan Rupp, Helene Vandenberghe, Jeremy Rose, Travis Wang, Peixiang Wang, Berge Arakel Minassian, Clare Rusbridge
Publikováno v:
Life, Vol 11, Iss 7, p 689 (2021)
Canine Lafora disease is a recessively inherited, rapidly progressing neurodegenerative disease caused by the accumulation of abnormally constructed insoluble glycogen Lafora bodies in the brain and other tissues due to the loss of NHL repeat contain
Externí odkaz:
https://doaj.org/article/571134d3e5474292a3df9d9d222b80e8
Autor:
Felix Nitschke, Mitchell A Sullivan, Peixiang Wang, Xiaochu Zhao, Erin E Chown, Ami M Perri, Lori Israelian, Lucia Juana‐López, Paola Bovolenta, Santiago Rodríguez de Córdoba, Martin Steup, Berge A Minassian
Publikováno v:
EMBO Molecular Medicine, Vol 9, Iss 7, Pp 906-917 (2017)
Abstract Lafora disease (LD) is a fatal progressive epilepsy essentially caused by loss‐of‐function mutations in the glycogen phosphatase laforin or the ubiquitin E3 ligase malin. Glycogen in LD is hyperphosphorylated and poorly hydrosoluble. It
Externí odkaz:
https://doaj.org/article/a2b1331cf25e4a71adbb2ac75bba0a1b
Autor:
Mitchell A. Sullivan, Silvia Nitschke, Evan P. Skwara, Peixiang Wang, Xiaochu Zhao, Xiao S. Pan, Erin E. Chown, Travis Wang, Ami M. Perri, Jennifer P.Y. Lee, Francisco Vilaplana, Berge A. Minassian, Felix Nitschke
Publikováno v:
Cell Reports, Vol 27, Iss 5, Pp 1334-1344.e6 (2019)
Summary: Lafora disease (LD) and adult polyglucosan body disease (APBD) are glycogen storage diseases characterized by a pathogenic buildup of insoluble glycogen. Mechanisms causing glycogen insolubility are poorly understood. Here, in two mouse mode
Externí odkaz:
https://doaj.org/article/93cbd4080dd64d3b94ee2bdd6691b639