Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Qingxian Chang"'
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
Publikováno v:
Biomarkers in Medicine. 16:1171-1179
Aim: The CYP19A1 gene encodes the key aromatase for estrogen biosynthesis, and this study aimed to explore the relationship between CYP19A1 rs6493497 and rs936306 polymorphisms and depression risk. Methods: CYP19A1 rs6493497 and rs936306 genotyping w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53b6da3bc6bc1a1287ae888fa9c5db58
https://doi.org/10.2217/bmm-2022-0370
https://doi.org/10.2217/bmm-2022-0370
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
Autor:
Xujie Deng, Yu Lan, Siping Liu, Liyan Li, Ming Yang, Yanping Yang, Yixian Peng, Qingxian Chang
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 25
To systematically investigate chromosomal abnormalities and copy number variants (CNVs) in fetuses with different types of ventriculomegaly (VM) by karyotyping and/or chromosomal microarray analysis (CMA).This retrospective study included 312 fetuses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33ce3d9e1abb2a42960b116ba2594f69
https://pubmed.ncbi.nlm.nih.gov/32014392
https://pubmed.ncbi.nlm.nih.gov/32014392
Autor:
Qiuju Peng, Yanping Yang, Zhijian Zhou, Yanying Kong, Qingxian Chang, Yuguan Wen, Lebin Liu, Huacheng Yan
Publikováno v:
Neuroscience letters. 713
Estrogen plays a vital role in the pathogenesis of depression. The cytochrome p450 (CYP) 19A1 gene encodes aromatase, which is responsible for a key step in estrogen production. Previous studies suggested that CYP19A1 polymorphisms increase the risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51d98ae21f0623fc10f0818dc668b5a9
https://pubmed.ncbi.nlm.nih.gov/31518674
https://pubmed.ncbi.nlm.nih.gov/31518674
Autor:
Qingxian, Chang, Cuihua, Chen, Mei, Zhong, Yuwen, Qiu, Chaoqun, Xiao, Qitao, Huang, Yanhong, Yu
Publikováno v:
Nan fang yi ke da xue xue bao = Journal of Southern Medical University. 33(3)
To investigate the implications of a prenatal diagnosis of single umbilical artery (SUA) for chromosomal abnormalities and neonatal outcomes.From January, 2008 to June, 2012, color Doppler ultrasound identified 44 fetuses with SUA. Prenatal diagnoses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::39ecccd9aad78b6b94087ec27e9650b5
https://pubmed.ncbi.nlm.nih.gov/23529252
https://pubmed.ncbi.nlm.nih.gov/23529252
Publikováno v:
Neural Regeneration Research; May2011, Vol. 6 Issue 13, p1005-1009, 5p
Publikováno v:
Neural Regeneration Research; May2010, Vol. 5 Issue 9, p4-4, 1p