Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Bin Xiao"'
Autor:
Dan-Dan Li, Dong-Hao Bai, Jee H. Jung, Bin Xiao, Ying Wang, Na Zhao, Shang-Wu Jin, Li-Dong Sun, Eun La Kim
Publikováno v:
Biomolecules & Therapeutics
In a search for effective PPAR-γ agonists, 110 clinical drugs were screened via molecular docking, and 9 drugs, including parecoxib, were selected for subsequent biological evaluation. Molecular docking of parecoxib to the ligand-binding domain of P
Autor:
Ke-Yu Chen, Xiao-Ming Zhang, Pan Li, Zhu Jiang, Zhi-Yang Xia, Chengyi Shen, Qian Xia, Tao Cheng, Chunrong Zhu, Lei Zhong, Bin Xiao, Changqiang Wu
Publikováno v:
Journal of medicinal chemistry. 64(13)
Liver-specific contrast agents (CAs) can improve the Magnetic resonance imaging (MRI) detection of focal and diffuse liver lesions by increasing the lesion-to-liver contrast. A novel Mn(II) complex, Mn-BnO-TyrEDTA, with a lipophilic group-modified et
Publikováno v:
European journal of medicinal chemistry. 202
Celiac disease affects approximately 1% of the population and is a major public health problem worldwide. It is trigged by gluten-derived peptides, which have unusually high proline-glutamine motif content and are highly resistant to proteolysis by d
Publikováno v:
Journal of molecular medicine (Berlin, Germany). 96(7)
The cystic fibrosis transmembrane conductance regulator (CFTR) is linked to cell apoptosis and abundantly expressed in brain tissue. Mitochondrial oxidative stress plays a key role in activating apoptotic pathway following cerebral ischemia reperfusi
Autor:
Pei Juan Lu, Xiao Xiao, Chunping Qiao, Lei Xu, Qi Long Lu, Chi Hsien Wang, Derek J. Blake, Bin Xiao, Elizabeth Keramaris
Publikováno v:
Molecular Therapy. 21(10):1832-1840
Mutations in the FKRP gene are associated with a wide range of muscular dystrophies from mild limb-girdle muscular dystrophy (LGMD) 2I to severe Walker–Warburg syndrome and muscle-eye-brain disease. The characteristic biochemical feature of these d
Autor:
Hong Bin Xiao, Xiao Ni Liu, Ying Chen, Wei Yan Cai, Ya Jie Wang, Yan Guo, Xiao Gang Weng, Xi Chen, Yu Jie Li, Xiao Xin Zhu, He Fei Huang, Qi Li, Xiao Xi Kan, Qing Yang
Publikováno v:
Drug Design, Development and Therapy
Ya Jie Wang,1 Qi Li,1 Hong Bin Xiao,1 Yu Jie Li,1 Qing Yang,1 Xiao Xi Kan,1 Ying Chen,1 Xiao Ni Liu,2 Xiao Gang Weng,1 Xi Chen,1 Wei Yan Cai,1 Yan Guo,1 He Fei Huang,1 Xiao Xin Zhu11Institute of Chinese Materia Medica, China Academy of Chinese Medica
Autor:
Chuanxi Cai, Zhenhua Yuan, Ruhang Tang, Juan Li, Bo He, Bin Xiao, Noah Weisleder, Chunping Qiao, Hua Zhu, Xiao Xiao, Christina Mayer, Jianbin Li, Jianjie Ma, Pei-Hui Lin
Publikováno v:
Molecular therapy : the journal of the American Society of Gene Therapy. 20(4)
Muscular dystrophies (MDs) are caused by genetic mutations in over 30 different genes, many of which encode for proteins essential for the integrity of muscle cell structure and membrane. Their deficiencies cause the muscle vulnerable to mechanical a
Autor:
Bo Wu, Mona Shaban, Caryn Cloer, Xiao Xiao, Kanneboyina Nagaraju, Qi Long Lu, Peijuan Lu, Juan Li, Arpana Sali, Bin Xiao
Antisense therapy has been successful to skip targeted dystrophin exon with correction of frameshift and nonsense mutations of Duchenne muscular dystrophy (DMD). Systemic production of truncated but functional dystrophin proteins has been achieved in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02017fc3f7438f44c6f3b3d950b33791
https://europepmc.org/articles/PMC3048192/
https://europepmc.org/articles/PMC3048192/