Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Yueping Zhang"'
Autor:
Yueping Zhang, Xiandong Peng, Jiangfeng Ye, Lu Li, Caixia Lei, Shuo Zhang, Guowu Chen, Jing Fu, Xiaoxi Sun, Yi-Lun Sui
Publikováno v:
Reproductive and Developmental Medicine, Vol 4, Iss 1, Pp 32-41 (2020)
Objective: To evaluate the effect of preimplantation genetic testing for aneuploidy (PGT-A) in infertile patients with recurrent pregnancy loss (RPL). Methods: A prospective randomized clinical trial was performed in a university-affiliated fertility
Autor:
Caixia Lei, Xiaoxi Sun, Shuo Zhang, Yu Liang, Yueping Zhang, Guoliang Yu, Xiao Luo, Congjian Xu, Jing Fu, Depeng Wang, Qi Yang, Junping Wu, Fan Liang, Daru Lu
Publikováno v:
Journal of Medical Genetics
BackgroundPreimplantation genetic testing (PGT) has already been applied in patients known to carry chromosomal structural variants to improve the clinical outcome of assisted reproduction. However, conventional molecular techniques are not capable o
Autor:
Shuo Zhang, Bo Liang, Yueping Zhang, Congjian Xu, Kong Lingyin, Yan Mao, Jun Zhang, Zhao Dingding, Xiaoxi Sun
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-10 (2019)
BMC Medical Genomics
BMC Medical Genomics
Background Preimplantation genetic testing (PGT) has already been applied in chromosomally balanced translocation carriers to improve the clinical outcome of assisted reproduction. However, traditional methods could not further distinguish embryos ca
Publikováno v:
Reproductive and Developmental Medicine, Vol 3, Iss 4, Pp 205-212 (2019)
Objective: To evaluate whether preimplantation genetic testing for aneuploidy (PGT-A) with comprehensive chromosome screening increases live birth rate (LBR) in normal karyotype couples with recurrent pregnancy loss (RPL). Methods: A retrospective co
Autor:
Min Xiao, Caixia Lei, Guangquan Chen, Yanping Xi, Junping Wu, Yueping Zhang, Shuo Zhang, Wenbi Zhang, Xiaoxi Sun
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 9, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Expanded carrier screening (ECS) has emerged as an effective approach to identify at‐risk couples (ARCs)—before they initiate attempts at reproduction—who possess a high probability of having a child affected by severe recessive dise
Autor:
Jing Zhou, Yijuan Sun, Yueping Zhang, Caixia Lei, Xiaoxi Sun, Jing Fu, Shuo Zhang, Saijuan Zhu, Junping Wu, Haiyan Sun
Publikováno v:
Reproductive and Developmental Medicine, Vol 2, Iss 1, Pp 30-37 (2018)
Background: Reciprocal translocation (RCP) causes male infertility and female recurrent pregnancy loss. Male and female carriers have different responses to meiotic disturbances. Gender difference in outcomes of the RCP couples undergoing preimplanta
Autor:
Haiyan, Sun, Caixia, Lei, Shuo, Zhang, Min, Xiao, Junping, Wu, Jialong, Wu, Saijuan, Zhu, Jing, Zhou, Yueping, Zhang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 35(3)
To report on prenatal diagnosis and follow up of two patients with paternal uniparental disomy of chromosome 6 (pUPD6).Fetal cells were subjected to in situ culturing and G-banded chromosomal analysis. DNA samples of the fetuses and their parents wer
Autor:
Haiyan Sun, Jing Fu, Xiaoxi Sun, Yijuan Sun, Jing Zhou, Shuo Zhang, Daru Lu, Yueping Zhang, Caixia Lei, Junping Wu
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 10, Iss 1, Pp 1-9 (2017)
BMC Medical Genomics, Vol 10, Iss 1, Pp 1-9 (2017)
Background Preimplantation genetic diagnosis (PGD) is now widely used to select embryos free of chromosomal copy number variations (CNV) from chromosome balanced translocation carriers. However, it remains a difficulty to distinguish in embryos betwe
Autor:
Shuo, Zhang, Caixia, Lei, Junping, Wu, Haiyan, Sun, Yuezhou, Yang, Yueping, Zhang, Xiaoxi, Sun
Publikováno v:
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine. 36(9)
The purpose of this study was to evaluate the diagnostic utility of karyotype analysis of amniotic fluid for fetuses with abnormal sonographic findings and to determine the detection rates of abnormal karyotypes.We conducted a retrospective study of
Publikováno v:
Bioscience trends. 10(2)
The aim of this study is to evaluate the pregnancy outcomes and prognoses for fetuses with ventriculomegaly. Two hundred and forty-one cases of fetuses with ventriculomegaly were included in this study. The subjects were divided into three groups acc