Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lixi Zhao"'
Publikováno v:
Journal of Materials Research and Technology, Vol 33, Iss , Pp 1130-1139 (2024)
Creep, as a long-term deformation characteristic of shotcrete, significantly influences the load-bearing performance and durability of tunnel support structures. This study conducted creep tests on shotcrete under varying stress levels. The results r
Externí odkaz:
https://doaj.org/article/04a746b898af401da1c0d7620a7e4e8c
Objective: To investigate the association between SNP in the BTNL2 gene region and the susceptibility to osteoarthritis of the knee. Methods: The blood samples of 103 knee osteoarthritis and 134 healthy subjects were collected. Four SNP in the BTNL2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5c16b2e7816d0d7a69289b52ba2cad09
https://europepmc.org/articles/PMC6949757/
https://europepmc.org/articles/PMC6949757/
Publikováno v:
Water Policy. 17:1033-1044
North China Plain is one of the most important grain-producing areas in China. Because of unevenly distributed precipitation in this semi-arid area, crop production largely relies on underground blue water (UBW) to irrigate, overexploitation of which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::458839c1a81c21bf3b47b6443f8a87d8
https://doi.org/10.2166/wp.2015.114
https://doi.org/10.2166/wp.2015.114
Autor:
Lixi Zhao, Jing Wang, Zhi Cheng, Longfei Cheng, Binbin Wang, Hong Pan, Wei Tian, Xu Ma, Xiaomei Zhu
Publikováno v:
Genetic Testing and Molecular Biomarkers. 17:840-843
Aim: Developmental dysplasia of the hip (DDH) is one of the most common hip deformities in children. Since the COL1A1 gene is located in the DDH relating region, we investigated the COL1A1 promoter variations in the development of DDH. Results: We co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0fd2061f5e80109bec35d349c90e4de
https://doi.org/10.1089/gtmb.2013.0179
https://doi.org/10.1089/gtmb.2013.0179
Autor:
Qiaolian Wen, Longfei Cheng, Hongjun Li, Lixi Zhao, Si Chen, Jing Wang, Binbin Wang, Jingwen Yang, Xinyu Zhang, Xu Ma, Han-Zhong Li
Publikováno v:
Journal of Cystic Fibrosis. 11:316-323
Background Genetic testing of the cystic fibrosis transmembrane conductance ( CFTR ) gene is currently performed in patients with congenital bilateral absence of vas deferens (CBAVD). This study was conducted to investigate the role of mutations in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0151c88746003a44b81afd150491723
https://doi.org/10.1016/j.jcf.2012.01.005
https://doi.org/10.1016/j.jcf.2012.01.005
Publikováno v:
Environmental toxicology and pharmacology. 42
Previous studies have shown that levo-dopamine (L-dopa) can improve the consciousness of certain patients with prolonged coma after cerebral ischemia-reperfusion injury, and promote cell growth in vivo. This study aimed to investigate whether L-dopa,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63a411e30ce343c25a7aa102e36982b2
https://pubmed.ncbi.nlm.nih.gov/26867202
https://pubmed.ncbi.nlm.nih.gov/26867202
Autor:
Lixi Zhao, Xu Ma, Hui Li, Binbin Wang, Xiaopeng Deng, Zhi Cheng, Hong Pan, Jing Wang, Longfei Cheng
Publikováno v:
Pediatric cardiology. 36(8)
The aim of this study was to investigate the possible genetic effect of sequence variations in TWIST1 on the pathogenesis of ventricular septal defect in humans. We examined the coding region of TWIST1 in a cohort of 196 Chinese people with non-syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f39e6e94ab8b9811744c5e53d21c2377
https://pubmed.ncbi.nlm.nih.gov/25981568
https://pubmed.ncbi.nlm.nih.gov/25981568
Publikováno v:
Science China Life Sciences. 56:1063-1065
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d78b57823155d0e43a318ba78a474d08
https://doi.org/10.1007/s11427-013-4514-0
https://doi.org/10.1007/s11427-013-4514-0
Autor:
Xiaopeng Deng, Longfei Cheng, Lixi Zhao, Binbin Wang, Xu Ma, Peisu Suo, Zhi Cheng, Jing Wang, Hui Li
Publikováno v:
World Journal of Pediatrics. 9:278-280
The hematopoietically expressed homeobox (HHEX) gene is an important determinant of mammalian heart development. This study aimed to identify the potential mutations of the gene in Chinese patients with congenital heart disease (CHD). We collected 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d31c801ec0fcda81fd30aa5a03d0bc7
https://doi.org/10.1007/s12519-013-0430-4
https://doi.org/10.1007/s12519-013-0430-4
Autor:
Wei Tian, Longfei Cheng, Zhi Cheng, Jian Jia, Jianmin Wang, Jing Wang, Shilian Kan, Binbin Wang, Peisu Suo, Lixi Zhao, Xu Ma
Publikováno v:
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders, Vol 13, Iss 1, p 59 (2012)
BMC Musculoskeletal Disorders, Vol 13, Iss 1, p 59 (2012)
BackgroundDevelopmental dysplasia of the hip (DDH) is a congenital or acquired deformation or misalignment of the hip joint which affects mainly females. We hypothesized thatHOXD9gene could be regulated in acetabular size or shape and related in DDH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb65844d17e19a2f4a5e5d7ab02f51b0
http://europepmc.org/articles/PMC3404944
http://europepmc.org/articles/PMC3404944