Zobrazeno 1 - 10
of 162
pro vyhledávání: '"XIN-YI XIA"'
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 7, Pp 814-820 (2021)
Abstract. Background:. Vitamin D deficiency has been reported to be associated with diabetic microvascular complications, but previous studies have only focused on the relationship between vitamin D and specific complications. Therefore, we aimed to
Externí odkaz:
https://doaj.org/article/25349f5b1be64d2aa5b2e464a056763e
Autor:
Li-Bo Zhang, Rong-Rong Pang, Qing-Hua Qiao, Zhi-Hua Wang, Xin-Yi Xia, Chang-Jun Wang, Xiao-Li Xu
Publikováno v:
Military Medical Research, Vol 7, Iss 1, Pp 1-6 (2020)
Abstract Background Gastrointestinal symptoms are not rare among coronavirus disease 2019 (COVID-19) patients, but there have been no reports regarding convalescent plasma therapy for the recovery of gastrointestinal problems in COVID-19 patients. Ca
Externí odkaz:
https://doaj.org/article/4a8a5a959f184dcba95f3dcab6670996
Autor:
Jian-Hong Liu, Xiu-Xiu Wei, Ang Li, Ying-Xia Cui, Xin-Yi Xia, Wei-Song Qin, Ming-Chao Zhang, Er-Zhi Gao, Jun Sun, Chun-Lin Gao, Feng-Xia Liu, Qiu-Yue Wu, Wei-Wei Li, Asan, Zhi-Hong Liu, Xiao-Jun Li
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177685 (2017)
Alport syndrome (AS) is a clinically and genetically heterogeneous, progressive nephropathy caused by mutations in COL4A3, COL4A4, and COL4A5, which encode type IV collagen. The large sizes of these genes and the absence of mutation hot spots have co
Externí odkaz:
https://doaj.org/article/5d8fd1cbfd01476ca700cca2280e75f4
Autor:
Na Li, Jian Yu, Xiang Cao, Qiu-Yue Wu, Wei-Wei Li, Tian-Fu Li, Cui Zhang, Ying-Xia Cui, Xiao-Jun Li, Zhi-Min Yin, Xin-Yi Xia
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e100505 (2014)
OBJECTIVE: Mutations in the type II collagen gene are associated with certain human disorders, collectively termed type II collagenopathies. They include Legg-Calvé-Perthes disease (LCPD) and avascular necrosis of the femoral head (ANFH). These two
Externí odkaz:
https://doaj.org/article/9aad098b8720415cacc0d284177eb348
Autor:
Ying-Xia Cui, Xin-Yi Xia, Yang Zhou, Lin Gao, Xue-Jun Shang, Tong Ni, Wei-Ping Wang, Xiao-Buo Fan, Hong-Lin Yin, Shao-Jun Jiang, Bing Yao, Yu-An Hu, Gang Wang, Xiao-Jun Li
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79808 (2013)
Dyschromatosis universalis hereditaria (DUH) is a rare heterogeneous pigmentary genodermatosis, which was first described in 1933. The genetic cause has recently been discovered by the discovery of mutations in ABCB6. Here we investigated a Chinese f
Externí odkaz:
https://doaj.org/article/83c4e3e9c5d24a77b836b2715c80cf36
Autor:
Yi-Ting Wang, Shao-Xiu Ji, Xin-Yi Xia, Ting-Jun Wan, Jia-Xi Zou, Bai-Xue Li, Qian-Nan Hu, Xin Chen, Jie Mu, Quan-Sheng Feng, Li Wen
Publikováno v:
Journal of Thoracic Disease. 15:1460-1472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a496e5550cadcb4b7569762edf2cfea2
https://doi.org/10.21037/jtd-23-322
https://doi.org/10.21037/jtd-23-322
Autor:
Wei Qin Li, Xiang-dong Zhou, Tao Luo, Cong Chen, Hua Rong Zhang, Chang Lin Yin, Hai Bo Wu, Qing Mao, Pei Pei Zhang, Tai Sheng Li, Shuyang Zhang, Xin Yi Xia, Xindong Liu, Lei Zhao, Yi Fang Ping, Zhi Cheng He, Heng Zhang, Ding Yu Zhang, Jun Cai, Rong Chen, Rui Jing, Chaofu Wang, Yan Wang, Dong Po Jiang, Ze Xuan Yan, Rui Tang, Xiao Hong Yao, Yu Shi, Xiu-Wu Bian, Yong Ren, Juan Wang, Zhenhua Liu, Wen Juan Fu, Yan Qing Ding, Heng Li, Xiao Chun Fei, Xue Quan Huang
Publikováno v:
Cell Research
Severe COVID-19 disease caused by SARS-CoV-2 is frequently accompanied by dysfunction of the lungs and extrapulmonary organs. However, the organotropism of SARS-CoV-2 and the port of virus entry for systemic dissemination remain largely unknown. We p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5124af9d1e1b6a79089e9a446ad428c5
https://doi.org/10.1038/s41422-021-00523-8
https://doi.org/10.1038/s41422-021-00523-8
Autor:
Shao‐Xiu Ji, Yan‐Feng Zheng, Xia Li, Bai‐Xue Li, Jia‐Xi Zou, Yi‐Ting Wang, Xin‐Yi Xia, Xin Chen, Qian‐Nan Hu, Ting‐Jun Wan, Li Wen, Quan‐Sheng Feng
Publikováno v:
Anatomical record (Hoboken, N.J. : 2007)REFERENCES.
HIV/AIDS pandemic remains the world's most severe public health challenge, especially for HIV/AIDS immunological nonresponders (HIV/AIDS-INRs), who tend to have higher mortality. Due to the advantages in promoting patients' immune reconstitution, Tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8561adf13c8718df8d1773e073befe4e
https://pubmed.ncbi.nlm.nih.gov/35775967
https://pubmed.ncbi.nlm.nih.gov/35775967
Publikováno v:
Computational and Structural Biotechnology Journal
Computational and Structural Biotechnology Journal, Vol 18, Iss, Pp 1891-1903 (2020)
Computational and Structural Biotechnology Journal, Vol 18, Iss, Pp 1891-1903 (2020)
Graphical abstract
The effective non-invasive diagnosis and prognosis are critical for cancer treatment. The plasma cell-free DNA (cfDNA) provides a good material for cancer liquid biopsy and its worth in this field is increasingly explored. Her
The effective non-invasive diagnosis and prognosis are critical for cancer treatment. The plasma cell-free DNA (cfDNA) provides a good material for cancer liquid biopsy and its worth in this field is increasingly explored. Her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e8e0518c4f41d3f98f19936a95baccd
http://europepmc.org/articles/PMC7387736
http://europepmc.org/articles/PMC7387736
Autor:
Yan-Ju, Guo, Yao-Man, Guo, Ying, Han, Qiu-Yue, Wu, Yang, Yang, Tao, Luo, Xiao-Feng, Xu, Xin-Yi, Xia
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 27(10)
To compare the efficiency of the target gene panel method and whole-exome sequencing (WES) in detecting idiopathic hypogonadotropic hypogonadism (IHH), and select a more suitable gene detection method.We selected 24 genes closely related to the molec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2e3d2c07c1a295af2a93e427901b8344
https://pubmed.ncbi.nlm.nih.gov/34914268
https://pubmed.ncbi.nlm.nih.gov/34914268