Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ri-Li Yu"'
Autor:
Yang Shen, Kai-Ming Duan, Sai-Ying Wang, An-Qi Ping, Ming-Hua Chen, Ri-Li Yu, Kai Gao, Shu-Ting Yang, Yong-Zhong Tang, Zhi-Hong Bai, Si-Qi Yang
Publikováno v:
Journal of affective disorders. 296
Preventive intervention can significantly reduce the human and economic costs of postpartum depression (PPD) compared with treatment post-diagnosis. However, identifying women with a high PPD risk and making a judgement as to the benefits of preventi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad7dcf553aeca103c94aa38054a5a202
https://pubmed.ncbi.nlm.nih.gov/34606808
https://pubmed.ncbi.nlm.nih.gov/34606808
Autor:
Qian Xu, Ya-qin Wang, Zhenhua Liu, Jifeng Guo, Kai Li, Xinxiang Yan, Qiying Sun, Ri-li Yu, Beisha Tang
Publikováno v:
Neuroscience Letters. 566:206-209
With the completion of the Human Genome Project, GWAS have been widely used in exploring the genetic studies of complex diseases. A meta-analysis of datasets from five Parkinson's disease GWAS from the USA and Europe found 11 loci that surpassed the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::053eedc2875b5755531c57c63a86def4
https://doi.org/10.1016/j.neulet.2014.03.007
https://doi.org/10.1016/j.neulet.2014.03.007
Autor:
Yacen Hu, Jifeng Guo, Sanxi Ai, Chun-rong Wang, Beisha Tang, Xinxiang Yan, Lu Shen, Cheng-yuan Song, Qian Xu, Ri-li Yu
Publikováno v:
Journal of the Neurological Sciences. 337:123-128
article i nfo SNCA is a pathogenic gene identified in rare familial PD, and over-expression of SNCA was suggested in the pathogenesis of familial and sporadic PD. Rep1 polymorphism of SNCA was associated with susceptibility to sporadic PD and SNCA ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f9775f574d49931d70b131873e343af
https://doi.org/10.1016/j.jns.2013.11.033
https://doi.org/10.1016/j.jns.2013.11.033
Publikováno v:
Neuroscience Letters. 552:58-61
Recent GWASs have implicated many novel SNPs in the development of Parkinson's disease (PD). Single nucleotide polymorphism (SNP) rs2046571 of the HSA2 (encoding hyaluronan synthase 2) was reported to have marginal association with PD. Herein, we con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4df58617d9f7aaa1c240772d1e8c9236
https://doi.org/10.1016/j.neulet.2013.07.031
https://doi.org/10.1016/j.neulet.2013.07.031
Autor:
Ri-li Yu, Zhan-yun Lv, Beisha Tang, Jifeng Guo, Kai Li, Xinxiang Yan, Jin-yong Tian, Qiying Sun
Publikováno v:
Parkinsonism & Related Disorders. 18:641-644
The PLA2G6 gene encodes a group VIA calcium-independent phospholipase A(2), and has been suggested as the causative gene for autosomal recessive dystonia-parkinsonism. We conducted a case-control study using 531 mainland Chinese Parkinson's disease (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::759a9a3c7da6ad075c62a119d5944ee9
https://doi.org/10.1016/j.parkreldis.2012.02.015
https://doi.org/10.1016/j.parkreldis.2012.02.015
Autor:
Ri-li Yu, Xinxiang Yan, Kai Li, Beisha Tang, Qiying Sun, Jifeng Guo, Kun Xia, Qian Li, Zhan-yun Lv
Publikováno v:
Neuroscience Letters. 517:56-59
a b s t r a c t Two novel single nucleotide polymorphisms (SNPs) (rs6812193 and rs11868035) were recently identified to be associated with Parkinson's disease (PD) in a Web Based Genome-Wide Association Study. Herein, we conducted a case-control stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9791b97b61bb997256d4284b3e8b6776
https://doi.org/10.1016/j.neulet.2012.04.024
https://doi.org/10.1016/j.neulet.2012.04.024
Autor:
Chang, Cheng-Yi1,2 (AUTHOR), Wu, Chih-Cheng3,4,5 (AUTHOR), Tzeng, Chung-Yuh6 (AUTHOR), Li, Jian-Ri7 (AUTHOR), Chen, Yu-Fang8 (AUTHOR), Chen, Wen-Ying2 (AUTHOR), Kuan, Yu-Hsiang9 (AUTHOR), Liao, Su-Lan10 (AUTHOR), Chen, Chun-Jung10,11 (AUTHOR) cjchen@vghtc.gov.tw
Publikováno v:
Journal of Neuroinflammation. 11/7/2024, Vol. 21 Issue 1, p1-20. 20p.
Autor:
Lu Shen, Zhan-yun Lv, Kai Li, Ri-li Yu, Chang-he Shi, Xinxiang Yan, Jifeng Guo, Jin-yong Tian, Beisha Tang
Publikováno v:
Neuroscience Letters. 514:156-158
Recent studies have shown that PLA2G6 is a causative gene for PARK14-linked autosomal recessive early-onset complicated dystonia-parkinsonism, early-onset parkinsonism with frontotemporal dementia and autosomal recessive early-onset Parkinsonism with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ff98e9a5939a9523893291f60caac8e
https://doi.org/10.1016/j.neulet.2012.02.078
https://doi.org/10.1016/j.neulet.2012.02.078
Autor:
Ri-li Yu, Hong Jiang, Lei Wang, Lin-zi Luo, Qi-Yin Sun, Xinxiang Yan, Zhan-yun Lv, Beisha Tang, Kun Xia, Lu Shen, Kai Li, Jifeng Guo, Ling-yan Yao, Yacen Hu, Qian Pan
Publikováno v:
Neurobiology of aging. 36(4)
It has been reported that some single-nucleotide polymorphisms (SNPs) are associated with the risk of Parkinson's disease (PD), but whether a combination of these SNPs would have a stronger association with PD than any individual SNP is unknown. Sixt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::217bab7b7cfa5577e7fa12c9407ad5f7
https://pubmed.ncbi.nlm.nih.gov/25623333
https://pubmed.ncbi.nlm.nih.gov/25623333
Autor:
Ya-qin Wang, Beisha Tang, Zhenhua Liu, Zhanfang Sun, Xinxiang Yan, L i Su, Ri-li Yu, Yuan Zhang, Jifeng Guo
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 22(6)
A recent meta-analysis of datasets from five of the published Parkinson’s disease (PD) genome-wide association studies implicated the single nucleotide polymorphism (SNP) rs12817488 in coiled-coil domain containing 62 (CCDC62)/huntingtin interactin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99af9a2bfd8e69a4b5ed2c9451be461c
https://pubmed.ncbi.nlm.nih.gov/25818163
https://pubmed.ncbi.nlm.nih.gov/25818163