Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Fenxia Li"'
Autor:
Min Zhang, Kun Li, Shoufang Qu, Zhiwei Guo, Yuanli Wang, Xu Yang, Junhua Zhou, Guojun Ouyang, Rongtao Weng, Fenxia Li, Yingsong Wu, Xuexi Yang
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-12 (2022)
Abstract Background Chromosomal aneuploidy is the most common birth defect. However, the developmental mechanism and gene expression profile of fetuses with chromosomal aneuploidy are relatively unknown, and the maternal immune changes induced by fet
Externí odkaz:
https://doaj.org/article/d5ae43a9500c41b08bad696e989acea9
Autor:
Siping Liu, Fang Yang, Qingxian Chang, Bei Jia, Yushuang Xu, Ruifeng Wu, Liyan Li, Weishan Chen, Ailan Yin, Fodi Huang, Suxin Feng, Fenxia Li
Publikováno v:
Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-8 (2022)
Abstract Objective Since 2011, noninvasive prenatal testing (NIPT) has undergone rapid expansion, with both utilization and coverage. However, conclusive data regarding the clinical validity and utility of this testing tool are lacking. Thus, there i
Externí odkaz:
https://doaj.org/article/0568344cf6934cd2b08b27dfcb46a221
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
The Kagami–Ogata syndrome (KOS) is a rare imprinting disorder with a distinct clinical phenotype. In KOS, polyhydramnios is associated with a small bell-shaped thorax and coat-hanger ribs. The genetic etiology of KOS includes paternal uniparental d
Externí odkaz:
https://doaj.org/article/6b42c6a957ab440397bac3db58772c4b
Molecular analysis of 76 Chinese hemophilia B pedigrees and the identification of 10 novel mutations
Autor:
Limin Huang, Liyan Li, Sheng Lin, Juanjuan Chen, Kun Li, Dongmei Fan, Wangjie Jin, Yihong Li, Xu Yang, Yufeng Xiong, Fenxia Li, Xuexi Yang, Ming Li, Qiang Li
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Abstract Background Hemophilia B (HB) is an X‐linked recessive inherited bleeding disorder caused by mutations in the F9 gene that lead to plasma factor IX deficiency. To identify the causative mutations in HB, a molecular analysis of HB pedigrees
Externí odkaz:
https://doaj.org/article/6b78fe3a4ae8428b917651c58001403a
Autor:
Junxiang Yan, Zixu Zhang, Hongdan Shi, Xinke Xue, Ang Li, Fenxia Liu, Peng Ding, Xi Guo, Boyang Cao
Publikováno v:
BMC Microbiology, Vol 24, Iss 1, Pp 1-12 (2024)
Abstract Background Plesiomonas shigelloides is a gram-negative opportunistic pathogen associated with gastrointestinal and extraintestinal diseases in humans. There have been reports of specific functional genes in the study of P. shigelloides, but
Externí odkaz:
https://doaj.org/article/af893a678c544d6ab5e31634db9a4365
Autor:
Siping Liu, Qingxian Chang, Fang Yang, Yushuang Xu, Bei Jia, Ruifeng Wu, Liyan Li, Ailan Yin, Weishan Chen, Fodi Huang, Xuexi Yang, Fenxia Li
Publikováno v:
Archives of Gynecology and Obstetrics.
This paper evaluated the clinical utility of massively parallel sequencing-based non-invasive prenatal testing (NIPT) for detecting trisomy 21 (T21), T18, T13, sex chromosome aneuploidies (SCA), and rare chromosome aneuploidies (RCA) among the data c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b607df2e5ec0649e4332d455a1e88127
https://doi.org/10.1007/s00404-022-06908-3
https://doi.org/10.1007/s00404-022-06908-3
Autor:
Fenxia Li, Siping Liu, Qingxian Chang, Fang Yang, Yushuang Xu, Bei Jia, Ruifeng Wu, Liyan Li, Ailan Yin, Weishan Chen, Fodi Huang
Background: This paper evaluated the clinical utility of massively parallel sequencing-based non-invasive prenatal testing (NIPT) for detecting trisomy 21 (T21), T18, T13, sex chromosome aneuploidies (SCA), and rare chromosome aneuploides (RCA) among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e4291350671861c58fa3a1e14c69146
https://doi.org/10.21203/rs.3.rs-1560689/v1
https://doi.org/10.21203/rs.3.rs-1560689/v1
Publikováno v:
International Journal of Engineering and Technology. :218-223
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1597af41ecb66155da0f587158e6c596
https://doi.org/10.7763/ijet.2019.v11.1150
https://doi.org/10.7763/ijet.2019.v11.1150
Publikováno v:
International Journal of Engineering and Technology. :1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fdee70db359b3517f04b39856f5d438
https://doi.org/10.7763/ijet.2019.v11.1113
https://doi.org/10.7763/ijet.2019.v11.1113