Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Chao-Sheng Lu"'
Autor:
Rong-Yue Sun, Yue Xu, Qing-Qing Huang, Si-Si Hu, Hua-Zhi Xu, Yan-Zhao Luo, Ting Zhu, Jun-Hui Sun, Yu-Jing Gong, Mian-Mian Zhu, Hong-Wei Wang, Jing-Ye Pan, Chao-Sheng Lu, Dan Wang
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-11 (2024)
Abstract Background Genetic variants in COL4A2 are less common than those of COL4A1 and their fetal clinical phenotype has not been well described to date. We present a fetus from China with an intronic variant in COL4A2 associated with a prenatal di
Externí odkaz:
https://doaj.org/article/c4abd43693c04e8c93bdd88b4df5e015
Autor:
Luca Valenti, Ming-Hua Zheng, Ting Zhu, Rong-Yue Sun, Mian-Mian Zhu, Ji-an Sun, Hong-Wei Wang, Chen-Yu Wu, Yu-Jing Gong, Chao-Sheng Lu, Luisa Ronzoni
Publikováno v:
eGastroenterology, Vol 2, Iss 1 (2024)
Background Dubin-Johnson syndrome (DJS), a rare autosomal recessive liver condition, is caused by biallelic loss-of-function mutations of the ABCC2 gene. This study aimed to investigate genetic variations in the drug efflux transporter ABCC2 (MRP2) g
Externí odkaz:
https://doaj.org/article/ea7c654919aa4da397c41a87b410cf0b
Autor:
Hua-Chun Weng, Xin-Yu Lu, Yu-Peng Xu, Yi-Hong Wang, Dan Wang, Yi-Ling Feng, Zhang Chi, Xiao-Qing Yan, Chao-Sheng Lu, Hong-Wei Wang
Publikováno v:
Molecular Medicine, Vol 27, Iss 1, Pp 1-18 (2021)
Abstract Background Patients with salt-sensitive hypertension are often accompanied with severe renal damage and accelerate to end-stage renal disease, which currently lacks effective treatment. Fibroblast growth factor 21 (FGF21) has been shown to s
Externí odkaz:
https://doaj.org/article/42f916f3a833486b840d8b7c6447bf5d
Autor:
Yi‐ming Chen, Wei Chen, Yue Xu, Chao‐sheng Lu, Mian‐mian Zhu, Rong‐yue Sun, Yihong Wang, Yuan Chen, Jiaming Shi, Dan Wang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 9, Pp n/a-n/a (2022)
Abstract Background Succinate‐CoA ligase/synthetase (SCS) deficiency is responsible for encephalomyopathy with mitochondrial DNA depletion and mild methylmalonic aciduria. Variants in SUCLG1, the nuclear gene encoding the alpha subunit of the SCS e
Externí odkaz:
https://doaj.org/article/5c46ad19e3ca4d9894bc80efdd6216bc
Autor:
Sun, Rong-Yue1 (AUTHOR), Xu, Yue1 (AUTHOR), Huang, Qing-Qing1 (AUTHOR), Hu, Si-Si1 (AUTHOR), Xu, Hua-Zhi2 (AUTHOR), Luo, Yan-Zhao3 (AUTHOR), Zhu, Ting1 (AUTHOR), Sun, Jun-Hui4 (AUTHOR), Gong, Yu-Jing1 (AUTHOR), Zhu, Mian-Mian1 (AUTHOR), Wang, Hong-Wei5 (AUTHOR), Pan, Jing-Ye6,7 (AUTHOR), Lu, Chao-Sheng1 (AUTHOR) lucs363@163.com, Wang, Dan1 (AUTHOR) wd608044@wmu.edu.cn
Publikováno v:
BMC Medical Genomics. 9/30/2024, Vol. 17 Issue 1, p1-11. 11p.
Novel compound heterozygous SUCLG1 variants may contribute to mitochondria DNA depletion syndrome‐9.
Autor:
Chen, Yi‐ming1 (AUTHOR), Chen, Wei2 (AUTHOR), Xu, Yue3 (AUTHOR), Lu, Chao‐sheng3 (AUTHOR), Zhu, Mian‐mian3 (AUTHOR), Sun, Rong‐yue3 (AUTHOR), Wang, Yihong3 (AUTHOR), Chen, Yuan3 (AUTHOR), Shi, Jiaming3 (AUTHOR), Wang, Dan3 (AUTHOR) wd608044@wmu.edu.cn
Publikováno v:
Molecular Genetics & Genomic Medicine. Sep2022, Vol. 10 Issue 9, p1-10. 10p.
Publikováno v:
Genomics & Genetics Weekly; 6/24/2024, p1249-1249, 1p
Autor:
TAK WING NG, DENNIS
Publikováno v:
Journal of World Christianity; 2017, Vol. 7 Issue 2, p101-122, 22p
Autor:
Benjamin A. Elman, Alexander Woodside
This comprehensive volume integrates the history of late imperial China with the history of education over three centuries, revealing the significance of education in Chinese social, political, and intellectual life. A collaboration between social an
