Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Xian‑Xian Yu"'
Autor:
Yan-Jiao Lu, Wen-Wen Yu, Meng-Meng Cui, Xian-Xian Yu, Huan-Lei Song, Mei-Rong Bai, Wen-Jie Wu, Bei-Lin Gu, Jun Wang, Wei Cai, Xun Chu
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Hirschsprung disease (HSCR) has a higher incidence in children with Down syndrome (DS), which makes trisomy 21 a predisposing factor to HSCR. DSCAM and BACE2 are close together on the HSCR-associated critical region of chromosome 21. Common variants
Externí odkaz:
https://doaj.org/article/c8bb0480bb6747498aad1a84c6b175d2
Autor:
Wei-Bo Niu, Mei-Rong Bai, Huan-Lei Song, Yan-Jiao Lu, Wen-Jie Wu, Yi-Ming Gong, Xian-Xian Yu, Zhi-Liang Wei, Wen-Wen Yu, Bei-Lin Gu, Wei Cai, Xun Chu
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Background and Aims: Hirschsprung’s disease (HSCR) is a rare genetically heterogeneous congenital disorder. A recent study based on whole genome sequencing demonstrated that common variants at four novel loci, which contained two intronic variants
Externí odkaz:
https://doaj.org/article/6fd21b4b5aee46e98091bc3b4977cdd1
Autor:
Zhi-Liang Wei, Xian-Xian Yu, Xun Chu, Wenjie Wu, Bei-Lin Gu, Huan-Lei Song, Mei-Rong Bai, Yi-Ming Gong, Yan-Jiao Lu, Wei Cai
Publikováno v:
Journal of Pediatric Surgery. 55:2758-2765
Background Hirschsprung disease (HSCR) is a neurodevelopmental disorder with a strong genetic component. Common variants of NRG1 contributed to HSCR risk in Asians, and rare variants of ERBB2 and ITGB4 were found to be associated with HSCR. ERBB2 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ca2e5035aacfe14d17388fedcf3c328
https://doi.org/10.1016/j.jpedsurg.2020.04.008
https://doi.org/10.1016/j.jpedsurg.2020.04.008
Autor:
Zhi-Liang Wei, Ying Zhou, Wei-Bo Niu, Xun Chu, Wenjie Wu, Yi-Ming Gong, Xian-Xian Yu, Wen-Wen Yu, Bei-Lin Gu, Yan-Jiao Lu, Wei Cai, Mei-Rong Bai, Huan-Lei Song
Publikováno v:
Aging. 12:7163-7182
Biliary atresia (BA) is an idiopathic neonatal cholestatic disease. Recent genome-wide association study (GWAS) revealed that common variation of ADD3, GPC1, ARF6, and EFEMP1 gene was associated with BA susceptibility. We aimed to evaluate the associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b3096235dd5a426b65e2be2e6962e87
https://doi.org/10.18632/aging.103067
https://doi.org/10.18632/aging.103067
Autor:
Mei-Rong Bai, Yan-Jiao Lu, Bei-Lin Gu, Wei Cai, Yi-Ming Gong, Zhi-Liang Wei, Xian-Xian Yu, Huan-Lei Song, Wenjie Wu, Xun Chu
Publikováno v:
Pediatric research. 89(3)
Hirschsprung’s disease (HSCR) is the most common congenital cause of intestinal obstruction in children. Sotos syndrome (SoS) is an overgrowth disorder with constipation and sometimes accompanied by HSCR. NSD1 gene mutation is the main cause of SoS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0623caf9c90aa8bcf4cb4ad62eb9122
https://pubmed.ncbi.nlm.nih.gov/32380506
https://pubmed.ncbi.nlm.nih.gov/32380506
Autor:
Mei-Rong, Bai, Wei-Bo, Niu, Ying, Zhou, Yi-Ming, Gong, Yan-Jiao, Lu, Xian-Xian, Yu, Zhi-Liang, Wei, Wenjie, Wu, Huan-Lei, Song, Wen-Wen, Yu, Bei-Lin, Gu, Wei, Cai, Xun, Chu
Publikováno v:
Aging (Albany NY)
Biliary atresia (BA) is an idiopathic neonatal cholestatic disease. Recent genome-wide association study (GWAS) revealed that common variation of ADD3, GPC1, ARF6, and EFEMP1 gene was associated with BA susceptibility. We aimed to evaluate the associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46c66340adbb8c277331859ec74aea2d
https://pubmed.ncbi.nlm.nih.gov/32315284
https://pubmed.ncbi.nlm.nih.gov/32315284
The aim of the present study was to determine the effects of emodin, a natural compound with antioxidant properties, on oxidative stress and apoptosis induced by hypoxia/reoxygenation (H/R) in HK-2 human renal tubular cells. In HK-2 cells subjected t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::914c635bc351278945a084c44159507e
https://europepmc.org/articles/PMC5488603/
https://europepmc.org/articles/PMC5488603/
Autor:
Xian-Xian Yu, Yu Zhang, Hong-Wei Xue, Dun Wang, Wen-Hui Lin, Song-Hao Zu, Yan-Jie Zhang, Bao-Jun Yang
Publikováno v:
Scientific Reports
Brassinosteroids (BRs) play key roles in plant growth and development, and regulate various agricultural traits. Enhanced BR signaling leads to increased seed number and yield in Arabidopsis bzr1-1D (AtBZR1P234L, gain-of-function mutant of the import
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95a1a6b4f75a3a18921d56a436f13fa5
https://doi.org/10.1038/srep31134
https://doi.org/10.1038/srep31134
Autor:
Yan-Xiong Du, Zhen-Tao Liang, Yi-Chao Li, Xian-Xian Yue, Qing-Xian Lv, Wei Huang, Xi Chen, Hui Yan, Shi-Liang Zhu
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-7 (2016)
Stimulated Raman adiabatic passage is a robust approach to realize high-fidelity state transfer, but requires long operation. Here, the authors propose a shortcut-to-adiabatic protocol to speed up such approach by modifying the Raman pulses, and demo
Externí odkaz:
https://doaj.org/article/e383984e1fcb4631b4b72c628d8f6a06