Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Songchang Chen"'
Autor:
Wenman, Wu, Xuanyou, Zhou, Zhengwen, Jiang, Dazhi, Zhang, Feng, Yu, Lanlan, Zhang, Xuefeng, Wang, Songchang, Chen, Chenming, Xu
Publikováno v:
Human Genomics. 16
Background High-cost, time-consuming and complex processes of several current approaches limit the use of noninvasive prenatal diagnosis (NIPD) for monogenic disorders in clinical application. Thus, a more cost-effective and easily implementable appr
Autor:
Ye Liu, Xinzhu Li, Songchang Chen, Li Wang, Yajing Tan, Xiaocui Li, Lin Tang, Junyu Zhang, Dandan Wu, Yanting Wu, Xinmei Liu, Yimin Zhu, Jianzhong Sheng, Jiexue Pan, Li Jin, Hefeng Huang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
BackgroundAssisted reproductive technology (ART) might induce adverse pregnancy outcomes and increase the risk of metabolic diseases in offspring’ later life with unknown reasons. Here we evaluated the global methylation level and methylation profi
Autor:
Songchang Chen, Lanlan Zhang, Jiong Gao, Shuyuan Li, Chunxin Chang, Yiyao Chen, Hongjun Fei, Junyu Zhang, Yanlin Wang, Hefeng Huang, Chenming Xu, Daru Lu
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences
Non-invasive prenatal testing (NIPT) for common fetal trisomies is effective. However, the usefulness of cell-free DNA testing to detect other chromosomal abnormalities is poorly understood. We analyzed the positive rate at different read depths in n
Autor:
Songchang Chen, Jianmei Niu, Yanlin Wang, Mujin Ye, Yinghua Shen, Shuyuan Li, Xu Han, Chenming Xu
Publikováno v:
Prenatal diagnosisREFERENCES. 40(12)
Objective To evaluate whether chromosomal microarray (CMA) should be offered to fetuses with ultrasonographic soft markers (USMs) in the second trimester. Methods A prospective cohort study and meta-analysis were conducted. In the prospective cohort
Autor:
Shuyuan Li, Xu Han, Mujin Ye, Songchang Chen, Yinghua Shen, Jianmei Niu, Yanlin Wang, Chenming Xu
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Frontiers in Genetics
Frontiers in Genetics
Several recurrent microdeletions and microduplications in the proximal, central, and distal regions of chromosomal 22q11.2 have been identified. However, due to a limited number of patients reported in the literature, highly variable clinical phenoty
Autor:
Xu Han, Li Jin, Songchang Chen, Yanlin Wang, Jianmei Niu, Shuyuan Li, Zhaoxia Qian, Chenming Xu, Pin Li
Publikováno v:
Prenatal diagnosis. 39(3)
Objective To evaluate the usefulness and incremental diagnostic yield of chromosomal microarray analysis (CMA) compared with standard karyotyping in fetuses with congenital anomalies of the kidney and urinary tract (CAKUT). Methods A prospective coho