Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Qiaoli Yu"'
Publikováno v:
Antioxidants, Vol 12, Iss 5, p 1127 (2023)
Hydrogen sulfide (H2S) and its oxidation product zero-valent sulfur (S0) play important roles in animals, plants, and bacteria. Inside cells, S0 exists in various forms, including polysulfide and persulfide, which are collectively referred to as sulf
Externí odkaz:
https://doaj.org/article/0da8481de0b14a3d9478d761fab0d6c0
Autor:
Chunhua Zeng, Yunting Lin, Zhikun Lu, Zhen Chen, Xiaoling Jiang, Xiaojian Mao, Zongcai Liu, Xinshuo Lu, Kangdi Zhang, Qiaoli Yu, Xiaoya Wang, Yonglan Huang, Li Liu
Publikováno v:
BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Hajdu-Cheney syndrome (HCS) is a rare inherited skeletal disorder caused by pathogenic mutations in exon 34 of NOTCH2. Its highly variable phenotypes make early diagnosis challenging. In this paper, we report a case of early-onset
Externí odkaz:
https://doaj.org/article/9f9a422efae44b2d84b2cec34b49442e
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
Escherichia coli recA− strains are usually used for cloning to prevent insert instability via RecA-dependent recombination. Here, we report that E. coli BW25113 (recA+) competent cells prepared by using a previously reported transformation and stor
Externí odkaz:
https://doaj.org/article/dafa76d7748749a89faa0cef64c8b916
Autor:
Xiaojian Mao, Sichi Liu, Yunting Lin, Zhen Chen, Yongxian Shao, Qiaoli Yu, Haiying Liu, Zhikun Lu, Huiyin Sheng, Xinshuo Lu, Yonglan Huang, Li Liu, Chunhua Zeng
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-8 (2019)
Abstract Objective Hypophosphatasia (HPP) is an inherited disorder of defective skeletal mineralization caused by mutations in the ALPL gene that encodes the Tissue Non-specific Alkaline Phosphatase (TNSALP). It is subdivided into six forms depending
Externí odkaz:
https://doaj.org/article/b4cf500806954da68416cc9d14501a32
Publikováno v:
Antioxidants, Vol 11, Iss 7, p 1292 (2022)
Sulfane sulfur is a class of compounds containing zero-valent sulfur. Most sulfane sulfur compounds are reactive and play important signaling roles. Key enzymes involved in the production and metabolism of sulfane sulfur have been characterized; howe
Externí odkaz:
https://doaj.org/article/00760e229ad244b0abafa643fefd01e6
Autor:
Li Wang, Fengying Yuan, Qiaoli Yuan, Guidong Dai, Xiaofei Lu, Li Zhou, Yurong Zheng, Yunzhu Wu, Maohua Wang, Guangxiang Chen
Publikováno v:
Heliyon, Vol 10, Iss 23, Pp e40428- (2024)
Background: Several clinical neuroimaging studies have reported structural and functional brain abnormalities associated with peripheral inflammatory cytokines or kynurenine pathway metabolites in patients with depression. However, it is not clear wh
Externí odkaz:
https://doaj.org/article/485a8d1149014759b6e06e47eb29e179
Autor:
Zongcai Liu, Li Liu, Zhen Chen, Chunhua Zeng, Qiaoli Yu, Kangdi Zhang, Xiaojian Mao, Yunting Lin, Xiaoling Jiang, Yonglan Huang, Xiaoya Wang, Zhikun Lu, Xinshuo Lu
Publikováno v:
BMC Musculoskeletal Disorders, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders
Background Hajdu-Cheney syndrome (HCS) is a rare inherited skeletal disorder caused by pathogenic mutations in exon 34 of NOTCH2. Its highly variable phenotypes make early diagnosis challenging. In this paper, we report a case of early-onset HCS with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95a71816dedbaea8e09348e4575f921a
http://link.springer.com/article/10.1186/s12891-020-3181-0
http://link.springer.com/article/10.1186/s12891-020-3181-0
Publikováno v:
Molecular microbiologyREFERENCES. 115(6)
The recombination of short homologous ends in Escherichia coli has been known for 30 years, and it is often used for both site-directed mutagenesis and in vivo cloning. For cloning, a plasmid and target DNA fragments were converted into linear DNA fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93c40bea7bf495b53da2aedd46956904
https://pubmed.ncbi.nlm.nih.gov/33372330
https://pubmed.ncbi.nlm.nih.gov/33372330
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract In this study, a gold nanoparticles colorimetric probe (AuNPs) with direct response to mercury ions (Hg2+) were developed using treated N-methylpyrrolidone (NMP) and chloroauric acid (HAuCl4) as precursors. NMP showed good reducibility after
Externí odkaz:
https://doaj.org/article/6c929dd6ed6943a392f484561cfe7fa4
Autor:
Qiaoli Yu, Xiaojian Mao, Haiying Liu, Yongxian Shao, Yunting Lin, Li Liu, Xinshuo Lu, Zhikun Lu, Huiyin Sheng, Sichi Liu, Zhen Chen, Yonglan Huang, Chunhua Zeng
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-8 (2019)
BMC Pediatrics
BMC Pediatrics
Objective Hypophosphatasia (HPP) is an inherited disorder of defective skeletal mineralization caused by mutations in the ALPL gene that encodes the Tissue Non-specific Alkaline Phosphatase (TNSALP). It is subdivided into six forms depending on the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1aca49672c0684adfeadade4520d2f01
https://doi.org/10.21203/rs.2.12359/v3
https://doi.org/10.21203/rs.2.12359/v3
