Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Bole Du"'
Autor:
Qing Lin, Chunya Liang, Bole Du, Lijiao Li, Hong Li, Xiaolan Mai, Sheng Li, Wenyu Xu, Cunzhen Wu, Mi Zeng
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-11 (2024)
Abstract Background Copy number variation (CNV) of X chromosome can lead to a variety of neonatal abnormalities, especially for male fetuses. In recent years, due to the high sensitivity and high specificity of NIPS, its application has gradually exp
Externí odkaz:
https://doaj.org/article/5037c4c1101e489cbbf3346f2d15e6ae
Autor:
Fuman Jiang, Weiqiang Liu, Longmei Zhang, Yulai Guo, Min Chen, Xiaojing Zeng, Yang Wang, Yufan Li, JiaJia Xian, BoLe Du, Yuhuan Xie, Shuming Ouyang, Sheng Li, Yinghong Yang, Chunsheng Zhang, Fei Luo, Xiaofang Sun
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Noninvasive prenatal testing (NIPT) for single gene disorders remains challenging. One approach that allows for accurate detection of the slight increase of the maternally inherited allele is the relative haplotype dosage (RHDO) analysis, wh
Externí odkaz:
https://doaj.org/article/a9e696309ee54b9796c8e78e93f38f86
Autor:
Haoxian Li, Bole Du, Fuman Jiang, Yulai Guo, Yang Wang, Chunsheng Zhang, Xiaojing Zeng, Yuhuan Xie, Shuming Ouyang, Yexing Xian, Min Chen, Weiqiang Liu, Xiaofang Sun
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 11, Pp n/a-n/a (2019)
Abstract Background β‐thalassemia is one of the most common monogenic diseases in the world. Southeast China is a highly infected area affected by four β‐thalassemia mutation types (HBB:c.‐78A>G, HBB:c.52A>T, HBB:c.126_129delCTTT, and HBB:c.3
Externí odkaz:
https://doaj.org/article/3471723885204fcfa8bd73521bf6d1cd
Feasibility Study of Semiconductor Sequencing for Noninvasive Prenatal Detection of Fetal Aneuploidy
Autor:
Feng Mu, Yu Liang, Wei Wang, Ling Yang, Jiucheng Liu, Sang Hua, Yuan Yuan, Kaiyan Feng, Xin Yi, Lili Ye, Caixia Liu, Bole Du, Yibin Hao, Fuman Jiang, Xinjie Huang
Publikováno v:
Clinical Chemistry. 59:846-849
BACKGROUND Noninvasive prenatal detection of common fetal aneuploidies with cell-free DNA from maternal plasma has been achieved with high-throughput next-generation sequencing platforms. Turnaround times for previously tested platforms are still uns
Autor:
Tze Kin Lau, Wei Wang, Yuying Yuan, Jun Wang, KaiKai Liao, Lijun Zhou, Zhonglin Chen, Fuman Jiang, Lijian Zhao, Zhongyi Zhu, Fang Chen, Ya Gao, Yi Zhou, Guo Yulai, Bole Du, Yumei Hou, Hongyun Zhang, Cong Yu
Publikováno v:
Reproductive sciences (Thousand Oaks, Calif.). 22(11)
To study factors that influence the concentration of cell-free fetal DNA (fetal fraction) using a large clinical data set of pregnancies with male fetus. A retrospective analysis of 23 067 pregnancies that received noninvasive prenatal testing from J
Autor:
Hao Zeng, Lijun Zhou, Xianghua Chai, Yicou Xu, Huiling Li, Zhiheng Lan, Meizhen Zhou, Ling Yang, Changjian Huang, Zhongyi Zhu, Bole Du, Wei Wang, Jun Wang, Fan Yang, Zhonglin Chen, Yuying Yuan, Guo Yulai, Fuman Jiang
Publikováno v:
Human immunology. 76(6)
Human leukocyte antigen (HLA) DNA typing is an essential part to identify a donor who may be a good match for the patients who need haematopoietic stem cells from bone marrow. Thus, fetching quickly high-resolution genotype is very important at prese
Autor:
P. Mailhe, F. Bole Du Chomont
Publikováno v:
La thermomécanique du crayon combustible.
Autor:
Yuan Yuan, Fuman Jiang, Sang Hua, Bole Du, Yibin Hao, Lili Ye, Jiucheng Liu, Kaiyan Feng, Xinjie Huang, Xin Yi, Wei Wang, Ling Yang, Feng Mu, Caixia Liu, Yu Liang
Publikováno v:
Clinical Chemistry; 2013, Vol. 59 Issue 5, p846-849, 4p, 1 Graph
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