Zobrazeno 1 - 10
of 244
pro vyhledávání: '"Xinran DONG"'
Autor:
Tiantian Xiao, Liyuan Hu, Huiyao Chen, Xinyue Gu, Jianguo Zhou, Yanping Zhu, Xiaoping Lei, Siyuan Jiang, Yulan Lu, Xinran Dong, Lizhong Du, Shoo K. Lee, Rong Ju, Wenhao Zhou, for the Chinese Neonatal Network
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background The occurrence of severe intraventricular hemorrhage (sIVH) was high in the very preterm infants (VPIs) in China. The management strategies significantly contributed to the occurrence of sIVH in VPIs. However, the status of the pe
Externí odkaz:
https://doaj.org/article/9f70fdd44f6a4a188f6009a45f0bfe88
Publikováno v:
Stem Cell Research, Vol 78, Iss , Pp 103451- (2024)
Hereditary fructose intolerance (HFI) is an autosomal recessive metabolic disease associated with a mutation in the aldolase B gene on chromosome 9q31. In this study, we generated a human-induced pluripotent stem cell (hiPSC) line, FDCHi015-A, from p
Externí odkaz:
https://doaj.org/article/fa8adbb01d1b43eea5c6651157e13d22
Autor:
Qi Ni, Meiling Tang, Xiang Chen, Yulan Lu, Bingbing Wu, Huijun Wang, Wenhao Zhou, Xinran Dong
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
ObjectiveFructose-1,6-bisphosphatase deficiency (FBP1D) is a rare inborn error due to mutations in the FBP1 gene. The genetic spectrum of FBP1D in China is unknown, also nonspecific manifestations confuse disease diagnosis. We systematically estimate
Externí odkaz:
https://doaj.org/article/c285b8ae1aa64b5ea23274f29c49c07b
Autor:
Fuqiang Yang, Ziqi Zhao, Dan Zhang, Yu Xiong, Xinran Dong, Yuchen Wang, Min Yang, Taotao Pan, Chuanyu Liu, Kaiyi Liu, Yifeng Lin, Yongjie Liu, Qiang Tu, Yashan Dang, Mingyang Xia, Da Mi, Wenhao Zhou, Zhiheng Xu
Publikováno v:
Cell Discovery, Vol 10, Iss 1, Pp 1-16 (2024)
Abstract Human cerebellum encompasses numerous neurons, exhibiting a distinct developmental paradigm from cerebrum. Here we conducted scRNA-seq, scATAC-seq and spatial transcriptomic analyses of fetal samples from gestational week (GW) 13 to 18 to ex
Externí odkaz:
https://doaj.org/article/04c54dfeb30e4aadb7fae935df16a2fc
Autor:
Hui Xiao, Huiyao Chen, Xiang Chen, Yulan Lu, Bingbing Wu, Huijun Wang, Yun Cao, Liyuan Hu, Xinran Dong, Wenhao Zhou, Lin Yang
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-15 (2023)
Abstract Background In China, ~1,072,100 small for gestational age (SGA) births occur annually. These SGA newborns are a high-risk population of developmental delay. Our study aimed to evaluate the genetic profile of SGA newborns in the newborn inten
Externí odkaz:
https://doaj.org/article/a13219e6102b4b708d625471812653ae
Autor:
Xiao Wang, Tiantian Xiao, Jin Wang, Bingbing Wu, Huijun Wang, Yulan Lu, Yaqiong Wang, Bin Chen, Liyuan Hu, Yun Cao, Rong Zhang, Guoqiang Cheng, Laishuan Wang, Zhihua Li, Xinran Dong, Lin Yang, Wenhao Zhou
Publikováno v:
Frontiers in Genetics, Vol 14 (2024)
Objective: We aimed to investigate the clinical and genetic risk factors associated with neonatal severe unconjugated hyperbilirubinemia.Methods: This was a retrospective, 1:1 matched, case–control study. We included 614 neonates diagnosed with sev
Externí odkaz:
https://doaj.org/article/a8b98f175f9444bf880fbabcf59dac07
Autor:
Xiaoshan Ji, Yanzhuang Ge, Qi Ni, Suhua Xu, Zhongmeng Xiong, Lin Yang, Liyuan Hu, Yun Cao, Yulan Lu, Qiufen Wei, Wenqing Kang, Deyi Zhuang, Wenhao Zhou, Xinran Dong
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Primary carnitine deficiency (PCD) caused by pathogenic variants in the solute carrier family 22 member 5 (SLC22A5) gene is a rare autosomal recessive disease that results in defective fatty acid oxidation. PCD can be detected through tandem mass spe
Externí odkaz:
https://doaj.org/article/5f3c68adea68453ea7eb5ba93262620c
Autor:
Xinran Dong, Liang Ding, Andrew Thrasher, Xinge Wang, Jingjing Liu, Qingfei Pan, Jordan Rash, Yogesh Dhungana, Xu Yang, Isabel Risch, Yuxin Li, Lei Yan, Michael Rusch, Clay McLeod, Koon-Kiu Yan, Junmin Peng, Hongbo Chi, Jinghui Zhang, Jiyang Yu
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-10 (2023)
Abstract Many signaling and other genes known as “hidden” drivers may not be genetically or epigenetically altered or differentially expressed at the mRNA or protein levels, but, rather, drive a phenotype such as tumorigenesis via post-translatio
Externí odkaz:
https://doaj.org/article/14c0f151bd884b528e374cdf295c69fb
Autor:
Xiang Chen, Yuxi Chen, Kai Yan, Huiyao Chen, Qian Qin, Lin Yang, Bo Liu, Guoqiang Cheng, Yun Cao, Bingbing Wu, Xinran Dong, Zhongwei Qiao, Wenhao Zhou, Jing Ni
Publikováno v:
Chinese Medical Journal, Vol 136, Iss 7, Pp 807-814 (2023)
Abstract. Background:. Significant brain volume deviation is an essential phenotype in children with neurodevelopmental delay (NDD), but its genetic basis has not been fully characterized. This study attempted to analyze the genetic factors associate
Externí odkaz:
https://doaj.org/article/643a34dfc89b4661a168c81801c284c5
Publikováno v:
Materials & Design, Vol 233, Iss , Pp 112285- (2023)
The ever-increasing demands for miniature integrated optics, mechanics, electronics, and biofluidics have generated great interest in high-performance glass components featuring functional micro/nanostructures. Focusing on micro/nanostructuring of op
Externí odkaz:
https://doaj.org/article/cb4598d9dc5e459bb47243db17ee6fc2