Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Weiying Ji"'
Autor:
Shruthi Mohan, Renee Geck, Shawn Fayer, Roseann Donnelly, Mary Relling, Tom Vulliamy, Kelly Caudle, Amber Waddell, Essence Kendall, Gonzalo Domingo, Angelo Minucci, Benedikt Ley, Cindy Chu, Cyrine Haidar, Howard McLeod, Josef Prchal, Mahmoud Sirdah, Vimla Aggarwal, Weiying Jiang, Emily Kyle, Meredith Weaver, Michelle Whirl-Carrillo, Andrew Stergachis
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100885- (2024)
Externí odkaz:
https://doaj.org/article/bea17b054abe4a83a7e7e16cc0023536
Autor:
Wei Xia, Shunqing Xu, Li Li, Yuanyuan Li, Youjie Wang, Shuna Jin, Yang Peng, Weiying Ji, Jianhua Gong, Bin Zhang, Chunhui Li, Ranran Song
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
The study aims to develop new birth weight prediction models for different gestational age stages using 2-dimensional (2D) ultrasound measurements in a Chinese population. 2D ultrasound was examined in pregnant women with normal singleton within 3 da
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Objective: Oculocutaneous albinism (OCA) is an autosomal recessive disorder caused by a variety of genomic variations. Our aim is to identify the molecular basis of OCA in two families and lay the foundation for prenatal diagnosis.Methods: Four types
Externí odkaz:
https://doaj.org/article/b146d25c758442fa8a432ab3d97f548c
Publikováno v:
Metabolites, Vol 13, Iss 6, p 761 (2023)
We aimed to explore the differential metabolites in amniotic fluid and its cells from fetuses with fetal growth restriction (FGR). A total of 28 specimens of amniotic fluid were collected, including 18 with FGR and 10 controls. Differential metabolit
Externí odkaz:
https://doaj.org/article/f183884d8e4f495d9c0bfe5da6a25639
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Abstract Background Isolated sulfite oxidase deficiency (ISOD) is a life‐threatening rare autosomal recessive disorder caused by pathogenic variants in SUOX (OMIM 606887) gene. The aim of our study was to establish a comprehensive genetic diagnosis
Externí odkaz:
https://doaj.org/article/33acfdf6853c40c0b80e0ef71569408e
Autor:
Hua Wang, Peiheng He, Hehai Pan, Jun long, Jianru Wang, Zemin Li, Hui Liu, Weiying Jiang, Zhaomin Zheng
Publikováno v:
Experimental and Molecular Medicine, Vol 50, Iss 4, Pp 1-14 (2018)
Spinal disease: Circular RNA linked to disc degeneration A circular RNA molecule helps protect against degenerative disc disease. Hua Wang and coworkers from Sun Yat-Sen University in Guangzhou, China, examined whether circular RNAs, regulatory molec
Externí odkaz:
https://doaj.org/article/250cfb643fb447ff8dedb3941ab86f45