Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Bing-Bing Wu"'
Autor:
Qian Gao, Wei-Cheng Xu, Xuan Nie, Kang-Jie Bian, Hong-Rui Yuan, Wen Zhang, Bing-Bing Wu, Xi-Sheng Wang
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract The migratory insertion of metal-hydride into alkene has allowed regioselective access to organometallics, readily participating in subsequent functionalization as one conventional pathway of hydroalkylation, whereas analogous process with f
Externí odkaz:
https://doaj.org/article/090ce43e3ef145cf8ebe96f2910d0bcc
Autor:
Hong-Zhi Liu, Xiao-Xuan Shu, Mingjie Huang, Bing-Bing Wu, Jie-Jie Chen, Xi-Sheng Wang, Hui-Lin Li, Han-Qing Yu
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-11 (2024)
Abstract Polymerization-driven removal of pollutants in advanced oxidation processes (AOPs) offers a sustainable way for the simultaneous achievement of contamination abatement and resource recovery, supporting a low-carbon water purification approac
Externí odkaz:
https://doaj.org/article/78817344922940eba30f91f33a5339a9
Autor:
Ruo-Xing Jin, Bing-Bing Wu, Kang-Jie Bian, Jian-Liang Yu, Jing-Cheng Dai, Ya-Wen Zuo, Yi-Fan Zhang, Xi-Sheng Wang
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-8 (2022)
The efficient construction of trifluoromethylated alkanes bearing a CF3 chiral center is of great importance in organic synthesis. Here, the authors disclose the enantioselective syntheses of α-trifluoromethylated allylic alkanes via reductive trifl
Externí odkaz:
https://doaj.org/article/be493e5df7fa45cca79da39f622e55a4
Autor:
Yan Xu, Rui Zhao, Min Wang, Xin‐hua Wang, Yi Wang, Hao Li, Yang‐yang Ma, Bing‐bing Wu, Yuan‐feng Zhou
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Background Focal cortical dysplasia type 2 (FCD2) is a malformation of cortical development that constitutes a common cause of pediatric focal epilepsy. Germline or somatic variants in the mammalian target of rapamycin (mTOR) signaling pathw
Externí odkaz:
https://doaj.org/article/5fd12f31005740b4a04c293705b9d6ef
Autor:
Yan Xu, Ya-lan Dou, Xiang Chen, Xin-ran Dong, Xin-hua Wang, Bing-bing Wu, Guo-qiang Cheng, Yuan-feng Zhou
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-11 (2021)
Abstract Background The clinical features of KCNQ2-related disorders range from benign familial neonatal seizures 1 to early infantile epileptic encephalopathy 7. The genotype-phenotypic association is difficult to establish. Objective To explore pot
Externí odkaz:
https://doaj.org/article/59eac94279b14295a9380b666272da00
Autor:
Guo-min Li, Yi-fan Li, Qiao-qian Zeng, Xiao-mei Zhang, Hai-mei Liu, Jia-yan Feng, Yu Shi, Bing-bing Wu, Hong Xu, Li Sun
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Lupus podocytopathy is a glomerular lesion in systemic lupus erythematosus (SLE) characterized by diffuse podocyte foot process effacement (FPE) without immune complex (IC) deposition or with only mesangial IC deposition. It is rarely seen in childre
Externí odkaz:
https://doaj.org/article/dac9dab191bb4544a69fa2e0db3f47e9
Publikováno v:
Guangtongxin yanjiu, Iss 3, Pp 17-23,30 (2022)
Wavelength Division Multiplexing (WDM) system has been evolving and upgrading in the direction of high speed, long distance and large capacity. In recent years, with the maturity of high-speed optoelectronic devices, the research and application of b
Externí odkaz:
https://doaj.org/article/5eb3e1956c9e4da398cd5b12473399f2
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Background This article reports the effects of proenkephalin (PENK) on osteosarcoma (OS) cell migration. Methods A Gene Expression Omnibus (GEO) dataset was used to identify differentially expressed genes (DEGs) in OS tumor samples and norma
Externí odkaz:
https://doaj.org/article/72f5ba85cf4a48b989fa45ac3d465d11
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background The association between mutations in the TNFAIP3 gene and a new autoinflammatory disease (called A20 haploinsufficiency, HA20) has recently been recognized. Here, we describe four patients with HA20 from two unrelated Chinese fami
Externí odkaz:
https://doaj.org/article/3f4d3944825247fc837eac6786024abd
Publikováno v:
BMC Medical Genomics, Vol 11, Iss 1, Pp 1-5 (2018)
Abstract Background Verheij syndrome is a rare microdeletion syndrome of chromosome 8q24.3 that harbors PUF60, SCRIB, and NRBP2 genes. Subsequently, loss of function mutations in PUF60 have been found in children with clinical features significantly
Externí odkaz:
https://doaj.org/article/9d910014222e4651af6a5c3dafbef518