Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Li-Jie Song"'
Autor:
Zhi-wei Chang, Yong-xu Jia, Wei-jie Zhang, Li-jie Song, Ming Gao, Ming-jun Li, Rui-hua Zhao, Jing Li, Ya-li Zhong, Qiao-zhi Sun, Yan-ru Qin
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 37, Iss 1, Pp 1-12 (2018)
Abstract Background This study aims to clarify the underlying mechanism for the tumor suppressive function of lnc TUSC7 in chemotherapy resistance of esophageal squamous cell carcinoma (ESCC). Methods TUSC7, miR-224 and DESC1 expressions in ESCC tiss
Externí odkaz:
https://doaj.org/article/a23fff6929f048fc8fb3f4b517d1bf7c
Publikováno v:
Environmental technology.
Chromium (Cr) pollution is the primary pollution problem of the soil in tannery. However, the effect of tanning chemicals on Cr migration in soil has not been clearly elucidated. Column leaching tests were designed in this study to reveal the transpo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2aa1e0cab4ad5240d6b3f7a26c71468
https://pubmed.ncbi.nlm.nih.gov/34739353
https://pubmed.ncbi.nlm.nih.gov/34739353
Publikováno v:
Translational Cancer Research. 7:353-362
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cd24ea6f4b0fc28aad27dfe3c265205
https://doi.org/10.21037/tcr.2018.03.13
https://doi.org/10.21037/tcr.2018.03.13
Publikováno v:
Chemosphere. 284:131413
Chromium (Cr) and tannin are two major pollutants in leather industry. However, little is known about the co-migration of leather tannins and Cr in soils. In this study, column experiments were conducted to estimate Cr leaching behavior from topsoil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::654925d92b55170e035ff76e727ae6ad
https://doi.org/10.1016/j.chemosphere.2021.131413
https://doi.org/10.1016/j.chemosphere.2021.131413
Publikováno v:
Journal of Applied Polymer Science. 138:50403
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::754e58da698f2cc7f9053ead5c127c6e
https://doi.org/10.1002/app.50403
https://doi.org/10.1002/app.50403
Autor:
Yi Liu, Ou Wang, Weibo Xia, Dou-dou Ma, Xiao-jie Xu, Yu-wen Song, Yan Jiang, Fang Lv, Xiaoping Xing, Li-jie Song, Mei Li, Jian-yi Wang, Asan
Publikováno v:
Clinica Chimica Acta. 461:172-180
Backgrounds Osteogenesis imperfecta (OI) is a rare inherited disease characterized by increased bone fragility and vulnerability to fractures. Recently, WNT1 is identified as a new candidate gene for OI, here we detect pathogenic mutations in WNT1 an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75018b8c1818c91275b5fb9ff9156409
https://doi.org/10.1016/j.cca.2016.07.012
https://doi.org/10.1016/j.cca.2016.07.012
Autor:
Xiao-jie Xu, Fang Lv, Ou Wang, Weibo Xia, Yi Liu, Yan Jiang, Mei Li, Jian-yi Wang, Dou-dou Ma, Jiawei Wang, Asan, Xiaoping Xing, Li-jie Song
Publikováno v:
Journal of Human Genetics. 62:205-211
Osteogenesis imperfecta (OI) is a group of hereditary disorders characterized by decreased bone mass and increased fracture risk. The majority of OI cases have an autosomal dominant pattern of inheritance and are usually caused by mutations in genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afa8fe357da4af210baa276d8332c03a
https://doi.org/10.1038/jhg.2016.109
https://doi.org/10.1038/jhg.2016.109
Autor:
Yu-wen Song, Yan Jiang, Ou Wang, Weibo Xia, Jian-yi Wang, Yi Liu, Li-jie Song, Mei Li, Jiawei Wang, Xiao-jie Xu, Fang Lv, Asan, Xiaoping Xing
Publikováno v:
Journal of Human Genetics. 61:539-545
Osteogenesis imperfecta (OI) is a group of clinically and genetically heterogeneous disorders characterized by decreased bone mass and recurrent bone fractures. Transmembrane protein 38B (TMEM38B) gene encodes trimeric intracellular cation channel ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2563cf943eb042e010b89c4dd915781
https://doi.org/10.1038/jhg.2016.11
https://doi.org/10.1038/jhg.2016.11
Autor:
Zi-ying Yang, Jian Wang, A. San, Wei-bo Xia, Li-jie Song, Xiao-ping Xing, Xiao-jie Xu, Fang Lv, Mei Li, Yan Jiang, Yi Liu, Huanming Yang, Jian-yi Wang, Ou Wang
Publikováno v:
Calcified tissue international. 100(1)
Osteogenesis imperfecta (OI) is a group of inherited disorders characterized by recurrent fragile fractures. Serpin peptidase inhibitor, clade F, member 1 (SERPINF1) is known to cause a distinct, extremely rare autosomal recessive form of type VI OI.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee3e967b43d121bae79a1febd8b098ab
https://pubmed.ncbi.nlm.nih.gov/27796462
https://pubmed.ncbi.nlm.nih.gov/27796462
Autor:
Yu-wen Song, Ou Wang, Weibo Xia, Xiao-jie Xu, Fang Lv, Li-jie Song, Yi Liu, Yan Jiang, Asan, Jian-yi Wang, Xiaoping Xing, Jiawei Wang, Mei Li
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 460
Background Osteogenesis imperfecta (OI) is a group of hereditary disorders characterized by low bone mass and recurrent fractures. Most OI cases follow an autosomal dominant pattern of inheritance and are attributed to mutations in genes encoding typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0a5d6b6516c3dffebe010ac8bbbf447
https://pubmed.ncbi.nlm.nih.gov/27312322
https://pubmed.ncbi.nlm.nih.gov/27312322