Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Yuyu FENG"'
Publikováno v:
Frontiers in Plant Science, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/e2066d4525344740a11e80c772494457
Autor:
Yonglan Huang, Xiaobing Wu, Sichi Liu, Wenhao Ma, Yuyu Feng, Yan Zhang, Xuefang Jia, Chengfang Tang, Fang Tang
Publikováno v:
Current Gene Therapy. 22:352-365
Background: GM1 gangliosidosis (GM1) is an autosomal recessive disorder characterized by the deficiency of beta-galactosidase (β-gal), a ubiquitous lysosomal enzyme that catalyzes the hydrolysis of GM1 ganglioside. Objective: The study aims to explo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caebd629881e586689b14e8286f41539
https://doi.org/10.2174/1566523222666220304092732
https://doi.org/10.2174/1566523222666220304092732
Autor:
Hui Niu, Yuyu Feng, Jie Ding, Wei Zhang, Chenxing Hu, Qingxiang Zhang, Chen Zhang, Cuiqing Li
Publikováno v:
Korean Journal of Chemical Engineering. 39:1936-1945
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27e6defddc5910ecadc9a54dd8b2f689
https://doi.org/10.1007/s11814-022-1114-3
https://doi.org/10.1007/s11814-022-1114-3
Publikováno v:
Drug Discovery Today. 27:838-847
Nucleic acid (NA)–ligand interactions have crucial roles in many cellular processes and, thus, are increasingly attracting therapeutic interest in drug discovery. Molecular docking is a valuable tool for studying molecular interactions. However, be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae4443a76b456715453a2ba0750b8e3
https://doi.org/10.1016/j.drudis.2021.10.013
https://doi.org/10.1016/j.drudis.2021.10.013
Publikováno v:
Journal of Chemical Information and Modeling. 61:4771-4782
Nucleic acid-ligand interactions play an important role in numerous cellular processes such as gene function expression and regulation. Therefore, nucleic acids such as RNAs have become more and more important drug targets, where the structural deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65551b0055ddd0980a20e1949f3821e9
https://doi.org/10.1021/acs.jcim.1c00341
https://doi.org/10.1021/acs.jcim.1c00341
Autor:
Ting XIE, Minyi TAN, Xiang JIANG, Yuyu FENG, Qianyu CHEN, Huifen MEI, Yanying CAI, Hongmei ZOU, Yonglan HUANG
Publikováno v:
Zhejiang Da Xue Xue Bao Yi Xue Ban
OBJECTIVE: To investigate the clinical features and outcomes of children with congenital hypothyroidism (CH) missed by neonatal screening. METHODS: The clinical and laboratory date of 31 children with CH missed by neonatal screening from February 201
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d7c85d1daeebda89ed20308061a6ba5
https://pubmed.ncbi.nlm.nih.gov/36207837
https://pubmed.ncbi.nlm.nih.gov/36207837
Publikováno v:
Proteins: Structure, Function, and Bioinformatics
Protein-protein docking plays an important role in the computational prediction of the complex structure between two proteins. For years, a variety of docking algorithms have been developed, as witnessed by the critical assessment of prediction inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282fb86029dc0fff53e105c69ab1a00d
Publikováno v:
Communications in Theoretical Physics. 75:055601
Defective structures, such as DNA mismatches, occur in DNA with a high frequency in some biological processes. They are difficult to identify and have recently become the focus of single-molecule investigations. Three single-molecule experiments were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74eeabe5751de9f03d6614b4889ab094
https://doi.org/10.1088/1572-9494/acc64c
https://doi.org/10.1088/1572-9494/acc64c
Autor:
Jian Sun, Xin Wang, Xiaobin Ma, Yuyu Feng, Yajun Wang, Junren Wang, Shujuan Jiang, Chunyan Xing
Background: Asthma is a chronic inflammatory disorder of the airway that requires long-term medication management. Objective: To describe the real-world prescribing patterns for asthma management in the Chinese population. Methods: A retrospective an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8168630c6c09fd9b089b80704ea8c211
https://doi.org/10.21203/rs.3.rs-1158031/v1
https://doi.org/10.21203/rs.3.rs-1158031/v1
Autor:
Fang Tang, Xiaoling Jiang, Li Liu, Chunhua Zeng, Sichi Liu, Chengfang Tang, Yonglan Huang, Yuyu Feng
Publikováno v:
Exp Biol Med (Maywood)
GM1 gangliosidosis is a rare lysosomal storage disease caused by a deficiency of β-galactosidase due to mutations in the GLB1 gene. We established a C57BL/6 mouse model with Glb1G455R mutation using CRISPR/Cas9 genome editing. The β-galactosidase e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08023058dcde91715cd9517690ef6b75
https://pubmed.ncbi.nlm.nih.gov/33583210
https://pubmed.ncbi.nlm.nih.gov/33583210