Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jiabao REN"'
Autor:
Jiabao Ren, Xing Zhang, SU Heiyan-Perhat, Po Yang, Helong Han, Yao Li, Jie Gao, Enpeng He, Yanhong Li
Publikováno v:
Plants, Vol 13, Iss 2, p 288 (2024)
Prunus cerasifera Ehrhart (P. cerasifera) flourishes uniquely in the arid landscapes of Xinjiang, China. Preliminary studies have revealed the therapeutic potential of its polyphenol extract (PPE) in mitigating liver lipid accumulation in mice fed a
Externí odkaz:
https://doaj.org/article/dc2c8c33185e4607ac0eefa067b9eed8
Autor:
Jiabao REN, Ya ZHAO, Yunyun YUAN, Jing ZHANG, Yulin DING, Meikang LI, Yilin AN, Wenjing CHEN, Li ZHANG, Boyu LIU, Shushen ZHENG, Wenjing SHEN
Publikováno v:
Journal of Applied Oral Science, Vol 31 (2023)
Abstract Studies have reported that >91.9% of non-syndromic tooth agenesis cases are caused by seven pathogenic genes. Objective To report novel heterozygous PAX9 variants in a Chinese family with non-syndromic oligodontia and summarize the reported
Externí odkaz:
https://doaj.org/article/5bbc761b58c74a63b6c4a4df879f135b
Autor:
Jiabao Ren, Sifang Gan, Shushen Zheng, Meikang Li, Yilin An, Shuo Yuan, Xiuge Gu, Li Zhang, Yan Hou, Qingqing Du, Guozhong Zhang, Wenjing Shen
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Non-syndromic oligodontia is characterized by the absence of six or more permanent teeth, excluding third molars, and can have aesthetic, masticatory, and psychological consequences. Previous studies have shown that PAX9 is associated wit
Externí odkaz:
https://doaj.org/article/d41daaf6a38a49449a7ade27fc49f919
Autor:
Hongyu Zhang, Xuanting Kong, Jiabao Ren, Shuo Yuan, Chunyan Liu, Yan Hou, Ye Liu, Lingqiang Meng, Guozhong Zhang, Qingqing Du, Wenjing Shen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Abstract Background Causative variants in genes of the EDA/EDAR/NF‐κB pathway, such as EDA and EDARADD, have been widely identified in patients with non‐syndromic tooth agenesis (NSTA). However, few cases of NSTA are due to ectodysplasin‐A rec
Externí odkaz:
https://doaj.org/article/d96da6fa5ba14613a7d76e38e733eb06
Autor:
Zhenzhen, Chen, Jiabao, Ren, Tingyu, Duan, Ke, Chen, Ruyi, Hou, Yimiao, Li, Leixiao, Zeng, Xiaoxuan, Meng, Yibo, Wu, Yu, Liu
Medication literacy is integral to health literacy, pivotal for medication safety and adherence. It denotes an individual's capacity to discern, comprehend, and convey medication-related information. Existing scales, however, are time-consuming and p
Externí odkaz:
http://arxiv.org/abs/2405.02853
Autor:
Wenjing Shen, Chunyan Liu, Xuanting Kong, Ye Liu, Hongyu Zhang, Lingqiang Meng, Guozhong Zhang, Yan Hou, Jiabao Ren, Qingqing Du, Shuo Yuan
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Background Causative variants in genes of the EDA/EDAR/NF‐κB pathway, such as EDA and EDARADD, have been widely identified in patients with non‐syndromic tooth agenesis (NSTA). However, few cases of NSTA are due to ectodysplasin‐A receptor (ED
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54324856a1c9ab721b459dbdcdfaa0d2
http://europepmc.org/articles/PMC8222839
http://europepmc.org/articles/PMC8222839
Publikováno v:
Advances in Social Science, Education and Humanities Research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4478fae486a633e9a7c85ab211e3d6c
https://doi.org/10.2991/assehr.k.211220.257
https://doi.org/10.2991/assehr.k.211220.257
Autor:
Xu Wang, Lingqiang Meng, Wenjing Chen, Qingqing Du, Zhiyu Zhang, Shuo Yuan, Dongru Yang, Jiabao Ren, Wenjing Shen, Jiuping Bai, Guozhong Zhang, Shushen Zheng, Hong Qu
Publikováno v:
Medicine
A mutation in the epithelial morphogen gene ectodysplasin-A1 (EDA1) is responsible for the disorder X-linked hypohidrotic ectodermal dysplasia (XLHED), the most common form of ectodermal dysplasia. XLHED is characterized by impaired development of ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b42d9b4f87a35a6b0920a5a805b0ae7
http://europepmc.org/articles/PMC7220389
http://europepmc.org/articles/PMC7220389
Autor:
Siying Sun, Jiabao Ren, Jiale Liu, Liang Rong, Hangli Wang, Yeyuan Xiao, Faqian Sun, Rongwei Mei, Chongjun Chen, Xiaomei Su
Publikováno v:
Journal of Environmental Management. 304:114290
The feasibility of pyrite as catalysts in the persulfate oxidation and electron donor for subsequent bacterial denitrification was investigated. The results demonstrated that pyrite-activated persulfate oxidation could efficiently degrade the organic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b3fcc650f55d008473dc7b247fc9510
https://doi.org/10.1016/j.jenvman.2021.114290
https://doi.org/10.1016/j.jenvman.2021.114290
Autor:
Liyuan Yang, Genqi Lu, Wenjing Shen, Shushen Zheng, Haiyan Lu, Shuo Yuan, Jiabao Ren, Guozhong Zhang, Wenjing Chen
Publikováno v:
Medicine
Cleidocranial dysplasia (CCD) is mainly attributable to a variant of runt-related transcription factor 2 (RUNX2) on chromosome 6p21. CCD is an autosomal dominant skeletal disorder characterized by open/delayed closure of fontanels, clavicular hypopla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b6bc302ceb0327e866866370bbad8a
https://doi.org/10.1097/md.0000000000027746
https://doi.org/10.1097/md.0000000000027746