Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Fuyuan, Qiao"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background Fetal skeletal dysplasia is a diverse group of degenerative diseases of bone and cartilage disorders that can lead to movement disorder and even death. This study aims to evaluate the diagnostic yield of sonographic examination an
Externí odkaz:
https://doaj.org/article/05c65f408add497eb0ca4fc13cf7e533
Publikováno v:
Clinical Case Reports, Vol 10, Iss 9, Pp n/a-n/a (2022)
Abstract To identify the pathogenic gene variation in a Chinese family with Hereditary Multiple Exostoses (HME). By examining blood‐sourced DNA and clinical manifestations of the proband and his family members, the whole exome sequencing (WES) and
Externí odkaz:
https://doaj.org/article/3da96b9c111c4363ac0801a0b3ee8ed6
Autor:
Ying Zha, Haiyi Liu, Xingguang Lin, Long Yu, Peng Gao, Yuqi Li, Min Wu, Xun Gong, Xinyi Bian, Qi Kang, Pan Zhi, Xiaohe Dang, Jingyu Wang, Ling Feng, Fuyuan Qiao, Yafei Huang, Wanjiang Zeng
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The maternal-fetal immune disorder is considered to be an important factor of preterm birth (PTB); however, the underlying mechanism is still not fully understood. This study was designed to explore the innate and adaptive immune features in the deci
Externí odkaz:
https://doaj.org/article/86cd53601ded45bd988420ccf6679147
Autor:
Wanlu Liu, Xinwei Shi, Yuqi Li, Fuyuan Qiao, Suhua Chen, Ling Feng, Wanjiang Zeng, Dongrui Deng, Yuanyuan Wu
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: It is challenging to make an accurate prenatal diagnosis for congenital anomalies of the kidney and urinary tract (CAKUT) because of its pathologic diversity. This study aims to evaluate the performance of whole-exome sequencing (WES) com
Externí odkaz:
https://doaj.org/article/e3d983643d434aaf98dfdc754e6a5950
Autor:
Nan, Yu, Wenyuan, Hu, Beejadhursing, Rajluxmee, Qingling, Kang, Wanjiang, Zeng, Dongrui, Deng, Suhua, Chen, Ling, Feng, Fuyuan, Qiao, Xun, Gong
Publikováno v:
In European Journal of Obstetrics & Gynecology and Reproductive Biology March 2020 246:45-49
Publikováno v:
Clinical Case Reports, Vol 9, Iss 12, Pp n/a-n/a (2021)
Abstract The proband is a five‐year‐old boy diagnosed with Duchenne muscular dystrophy (DMD) by clinical manifestations and laboratory examination, but clinical phenotype of his parents is normal. In the study, his mother had a second pregnancy,
Externí odkaz:
https://doaj.org/article/9098f3db7e1e4cbdbac996e53a4cc3aa
Autor:
Ying Zhang, Hao Liu, Xinwei Shi, Fuyuan Qiao, Wanjiang Zeng, Ling Feng, Dongrui Deng, Haiyi Liu, Yuanyuan Wu
Publikováno v:
BMC Pregnancy and Childbirth, Vol 17, Iss 1, Pp 1-9 (2017)
Abstract Backgroud Widespread endothelial injury contributes to the occurrence of preeclampsia. Maspin, first identified as a tumor suppressor, plays a critical role in cell invasion and angiogenesis. Our previous studies found that the expression of
Externí odkaz:
https://doaj.org/article/66c0906e902045acbcebb9f947fb52a8
Autor:
yang xiao, Xinyi Bian, Xinwei Shi, Jianlin Ding, Hongju Tang, Peng Xu, Dongrui Deng, Wanjiang Zeng, Suhua Chen, Fuyuan Qiao, Ling Feng, Yuanyuan Wu
Publikováno v:
Archives of Gynecology and Obstetrics.
Objective To assess the clinical application value of copy number variation sequencing (CNV-seq) combined with karyotype analysis in prenatal diagnosis of fetuses with increased nuchal translucency. Methods 205 fetuses who were diagnosed with increas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1b87d204adda1fc272cd1b56937a9b1
https://doi.org/10.1007/s00404-022-06900-x
https://doi.org/10.1007/s00404-022-06900-x
Autor:
Xinyi Bian, Xiao Yang, Xinwei Shi, Wanjiang Zeng, Dongrui Deng, Suhua Chen, Fuyuan Qiao, Ling Feng, Yuanyuan Wu
Publikováno v:
Open Life Sciences. 18
This study introduced whole-exome sequencing (WES) in prenatal diagnosis of fetal bowel dilatation to improve the detection outcome when karyotype analysis and copy number variation sequencing (CNV-seq) were uninformative in detecting pathogenic vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92f8951797d805af8ef5175714d8cc03
https://doi.org/10.1515/biol-2022-0598
https://doi.org/10.1515/biol-2022-0598
Background Fetal skeletal dysplasia (FSD) is a diverse group of degenerative diseases of bone and cartilage disorders that can lead to movement disorder and even death. This study aims to deliver prenatal diagnosis through sonographic examination and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90e460505299311654fe06e4b4f7973b
https://doi.org/10.21203/rs.3.rs-2181067/v1
https://doi.org/10.21203/rs.3.rs-2181067/v1
