Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jiazi Xie"'
Autor:
Jiandong Shen, Taoli Ding, Xueping Sun, Ji Yang, Yue Zhang, Jing Wang, Mengdi Ge, Heng Xu, Jiazi Xie, Fei Wang, Feiyang Diao
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-10 (2024)
Abstract Background Dystrophinopathies are the most common X-linked inherited muscle diseases, and the disease-causing gene is DMD. Exonic duplications are a common type of pathogenic variants in the DMD gene, however, 5’ end exonic duplications co
Externí odkaz:
https://doaj.org/article/7c2e136828244e9d98c21c38f97d1f51
Autor:
Boxian Huang, Chunyan Jiang, Aiqin Chen, Yugui Cui, Jiazi Xie, Jiandong Shen, Juan Chen, Lingbo Cai, Tingting Liao, Song Ning, Shi-Wen Jiang, Guoping Fan, Lianju Qin, Jiayin Liu
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 54, Iss 5, Pp 505-511 (2015)
Objective: Human-embryonic-stem-cell (hESC) lines derived from chromosomally or genetically abnormal embryos obtained following preimplantation genetic diagnosis are valuable in investigating genetic disorders. Materials and methods: In this study, a
Externí odkaz:
https://doaj.org/article/6a31608e6df847d597e04ec7372d80d6
Publikováno v:
2022 IEEE 5th Advanced Information Management, Communicates, Electronic and Automation Control Conference (IMCEC).
Autor:
Jiandong, Shen, Yan, Gao, Wei, Wu, Jinyong, Liu, Xueping, Sun, Yawen, Peng, Jiazi, Xie, Daowu, Wang, Yugui, Cui, Jiayin, Liu, Feiyang, Diao
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(10)
To explore the genetic etiology of recurrent hydatidiform mole (RHM) and provide accurate guidance for reproduction.Peripheral venous blood samples of the probands with RHM and members from 5 unrelated pedigrees were collected. Genomic DNA was extrac
Publikováno v:
In Fertility and Sterility October 2024 122(4) Supplement:e336-e337
Autor:
Chuyu Li, Jiazi Xie, Juan Dong, Chao Gao, Meng Xia, Yuting Lin, Yugui Cui, Lianju Qin, Wei Wu
Background:Low-level mosaicism is a common trait of early human development. Although mosaic embryos may lead to healthy live births, the direct effects of mosaicism are unknown. While embryo self-correction was demonstrated in mouse models, humans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b0c02b1c7bf327acb83e15e992cf41e
https://doi.org/10.21203/rs.3.rs-1558669/v2
https://doi.org/10.21203/rs.3.rs-1558669/v2
Autor:
Xiang Ma, Jiazi Xie, Yan Gao, Feiyang Diao, Fangxi Sun, Dianyun Qu, Yugui Cui, Jiayin Liu, Jiandong Shen, Daowu Wang, Xueping Sun
Publikováno v:
J Assist Reprod Genet
PURPOSE: To identify the disease-causing genes of Chinese Han women with idiopathic premature ovarian insufficiency (POI). METHODS: Seventy-four Chinese Han women with idiopathic POI were collected to analyze the genetic etiology. Triplet repeat-prim
Autor:
X. Johné Liu, Long Ma, Jiazi Xie, Jiayin Liu, Yan Xing, Jing Wang, Lingbo Cai, Jiandong Shen, Yugui Cui, Meng-Ting Hu
Publikováno v:
Fertility and sterility. 114(2)
Objective To evaluate the effect of coenzyme Q10 (CoQ10) supplementation on oocyte maturation rates and postmeiotic aneuploidy rates during in vitro maturation (IVM) of human oocytes. Design Clinical laboratory observation. Setting Hospital and unive
Autor:
Jiazi Xie, Song Ning, Lianju Qin, Lingbo Cai, Ting-Ting Liao, Boxian Huang, Guoping Fan, Shi-Wen Jiang, Aiqin Chen, Juan Chen, Jiandong Shen, Chunyan Jiang, Y. Cui, Jiayin Liu
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 54, Iss 5, Pp 505-511 (2015)
Objective Human-embryonic-stem-cell (hESC) lines derived from chromosomally or genetically abnormal embryos obtained following preimplantation genetic diagnosis are valuable in investigating genetic disorders. Materials and methods In this study, a n
Autor:
Xueping, Sun, Jiandong, Shen, Wei, Wu, Jiazi, Xie, Chao, Gao, Lianju, Qin, Yugui, Cui, Jiayin, Liu
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 30(3)
To identify potential mutation of ectodysplasin A (EDA) gene in a Chinese family affected with X-linked hypohidrotic ectodermal dysplasia.Blood samples were collected from the affected male proband, his family members and 103 unrelated individuals. F