Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Zhengwen, Jiang"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background Molecular analysis of the CYP21A2 gene is highly important for understanding the aetiology of 21-hydroxylase deficiency (21-OHD). The aim of this study was to use a novel approach named CNVplex, together with the SNaPshot assay an
Externí odkaz:
https://doaj.org/article/643376abb7dc4856a79b7bcafc8cb11c
Publikováno v:
地质科技通报, Vol 43, Iss 4, Pp 128-140 (2024)
Objective The composition and degradability of dissolved organic matter (DOM) play a critical role in evaluating biogenic gas production during shale gas exploration. A simple and effective method needs to be developed to assess the composition, func
Externí odkaz:
https://doaj.org/article/db948a9cb84243b3b45d4c39549e6b65
Autor:
Wenman Wu, Xuanyou Zhou, Zhengwen Jiang, Dazhi Zhang, Feng Yu, Lanlan Zhang, Xuefeng Wang, Songchang Chen, Chenming Xu
Publikováno v:
Human Genomics, Vol 16, Iss 1, Pp 1-15 (2022)
Abstract 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 implement
Externí odkaz:
https://doaj.org/article/10b73b04c3904bab9bfb2765c1d1ed85
Autor:
Xiafeng Yu, Yu Tao, Xu Liu, Feng Yu, Chuan Jiang, Yingying Xiao, Haibo Zhang, Yongrui He, Lincai Ye, Ying Wang, Chunxia Zhou, Jian Wang, Zhengwen Jiang, Haifa Hong
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundCopy number variations (CNVs) have been shown to be overrepresented in children with congenital heart disease (CHD). Genetic evaluation of CHD is currently underperformed in China. We sought to determine the occurrence of CNVs in CNV region
Externí odkaz:
https://doaj.org/article/e7e49f10ca3f4e1783cc2183a6e5c36d
Autor:
Xiaobin Chen, Yuxiang Lin, Zhengwen Jiang, Yan Li, Yihua Zhang, Ying Wang, Feng Yu, Wenhui Guo, Lili Chen, Minyan Chen, Wenzhe Zhang, Chuan Wang, Fangmeng Fu
Publikováno v:
Breast, Vol 62, Iss , Pp 114-122 (2022)
Background: The quantitative relationship between HER2 copy number and prognosis in HER2 positive adjuvant setting remain controversial, and few studies have focused on adjuvant setting to illustrate the potential clinical relevance of HER2 in cfDNA.
Externí odkaz:
https://doaj.org/article/e9743e39839a481da11b6e85c7b3f983
Publikováno v:
Plants, Vol 12, Iss 20, p 3529 (2023)
Sulfotransferases (SOTs) (EC 2.8.2.-) are sulfate regulatory proteins in a variety of organisms that have been previously shown to be involved in regulating a variety of physiological and biological processes, such as growth, development, adaptation
Externí odkaz:
https://doaj.org/article/f1eb12e302a3469ab1dd58f20e7e6db4
Autor:
Ping Hu, Jianxin Tan, Feng Yu, Binbin Shao, Fang Zhang, Jingjing Zhang, Yingchun Lin, Tao Tao, Lili Jiang, Zhengwen Jiang, Zhengfeng Xu
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-9 (2022)
Abstract Expanded carrier screening, a type of reproductive genetic testing for couples, has gained tremendous popularity for assessing the risk of passing on certain genetic conditions to offspring. Here, a carrier screening assay for 448 pathogenic
Externí odkaz:
https://doaj.org/article/0c93ffa8665e4f0aa146ea7abed09d05
Publikováno v:
Applied Sciences, Vol 12, Iss 4, p 2247 (2022)
The spatial distribution of elements can be regarded as a numerical field of concentration values with a continuous spatial coverage. An active area of research is to discover geologically meaningful relationships among elements from their spatial di
Externí odkaz:
https://doaj.org/article/3e7f29d9daf141aa8db04188de80b470
Autor:
Ping Hu, Jianxin Tan, Feng Yu, Binbin Shao, Fang Zhang, Jingjing Zhang, Yingchun Lin, Tao Tao, Lili Jiang, Zhengwen Jiang, Zhengfeng Xu
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/c21343329156449d85a679db3321199b
Autor:
Yuqing Zhu, Cuiping Zhang, Zhengfeng Xu, Ping Hu, Jianxin Tan, An Liu, Yingchun Lin, Zhengwen Jiang, Yan Wang, Fengchang Qiao, Jingjing Zhang, Binbin Shao, Tao Tao
Publikováno v:
Clinica Chimica Acta. 523:267-272
Background and aims Hyperphenylalaninemia (HPA) is a common autosomal recessive disorder of phenylalanine metabolism, mainly caused by the deficiency of phenylalanine hydroxylase gene (PAH). A simple, fast, and accurate assay to achieve early diagnos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d8a9be95f82bde8bc096496b955c7ba
https://doi.org/10.1016/j.cca.2021.10.009
https://doi.org/10.1016/j.cca.2021.10.009