Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yinghui Dang"'
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-4 (2019)
Abstract Background Copy number variations (CNVs) involving the 17q12 region are associated with a broad range of clinical phenotypes. Deletion of the 17q12 chromosome results in structural or functional abnormalities in the kidney and urethra, type
Externí odkaz:
https://doaj.org/article/c16a20b7c28943f4acf698d9fcdf67bb
Autor:
Liang Jiang, Weiqiang Liu, Huizhen Guo, Yinghui Dang, Tingcai Cheng, Wanying Yang, Qiang Sun, Bingbing Wang, Yumei Wang, Enyu Xie, Qingyou Xia
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Peptidoglycan recognition protein (PGRP) is an important pattern recognition receptor in innate immunity that is vital for bacterial recognition and defense in insects. Few studies report the role of PGRP in viral infection. Here we cloned two forms
Externí odkaz:
https://doaj.org/article/6157830dde194e9bb79f6ffcffa53597
Autor:
Yunyun Zheng, Guihu Wang, Jianfang Zhang, Yinghui Dang, Jia Li, Shanning Wan, Miaomiao Tang, Hong Yang
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 253:278-284
Purpose The 12q terminal duplication is a chromosomal structural abnormality that has been rarely reported. The common clinical manifestations include intellectual disability and speech delay. We report two cases of patients with a duplication of chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f49c7dc2ba1f9034b9b95dddd64bd9f
https://doi.org/10.1016/j.ejogrb.2020.08.002
https://doi.org/10.1016/j.ejogrb.2020.08.002
Publikováno v:
Fetal and Pediatric Pathology. 39:269-276
Objective: There is scant information available about fetuses with 7q11.23 copy number variants (CNVs) found during pregnancy. We studied the clinical significance of 7q11.23 CNVs in prenatal diagnosis. Materials and methods: The amniocentesis was pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd0d596a289937d3f20d48607c8b3d6a
https://doi.org/10.1080/15513815.2019.1651802
https://doi.org/10.1080/15513815.2019.1651802
Autor:
Yunyun Zheng, Jianfang Zhang, Li Jia, Ying Xu, Yinghui Dang, Shanning Wan, Tingting Song, Yu Li, Jiao Zheng, Hong Yang
Publikováno v:
Journal of Clinical Laboratory Analysis
Background Central nervous system (CNS) abnormalities are a group of serious birth defects associated with high rates of stillbirths, infant death, or abnormal development, and various disease‐causing copy number variations play a much more importa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43f04596853502ea79cfc57a1caa462f
https://doi.org/10.1002/jcla.23434
https://doi.org/10.1002/jcla.23434
Publikováno v:
The Journal of Gene Medicine. 22
BACKGROUND The present study aimed to determine the accuracy (Z-value) of non-invasive prenatal testing (NIPT) results for sex chromosome aneuploidy (SCA) in routine clinical practice. METHODS Among a cohort of 12505 pregnant females, maternal plasma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0782487584f0a45a93d8ac7beffa6564
https://doi.org/10.1002/jgm.3199
https://doi.org/10.1002/jgm.3199
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-4 (2019)
Molecular Cytogenetics
Molecular Cytogenetics
Background Copy number variations (CNVs) involving the 17q12 region are associated with a broad range of clinical phenotypes. Deletion of the 17q12 chromosome results in structural or functional abnormalities in the kidney and urethra, type 5 diabete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7c33de6b6dac6dda426079df1b5da67
https://doi.org/10.1186/s13039-019-0431-7
https://doi.org/10.1186/s13039-019-0431-7
Publikováno v:
Ginekologia polska. 90(5)
Objectives: Cell-free fetal DNA has been widely used in prenatal genetic testing during recent years. We explored the feasibility of non-invasive prenatal testing (NIPT) for analysis of common fetal aneuploidies among pregnancies in northwest China.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4524f5b197fbabdb3e9207b501e33217
https://pubmed.ncbi.nlm.nih.gov/31165466
https://pubmed.ncbi.nlm.nih.gov/31165466
Autor:
Liang, Jiang, Weiqiang, Liu, Huizhen, Guo, Yinghui, Dang, Tingcai, Cheng, Wanying, Yang, Qiang, Sun, Bingbing, Wang, Yumei, Wang, Enyu, Xie, Qingyou, Xia
Publikováno v:
Frontiers in Immunology
Peptidoglycan recognition protein (PGRP) is an important pattern recognition receptor in innate immunity that is vital for bacterial recognition and defense in insects. Few studies report the role of PGRP in viral infection. Here we cloned two forms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::39ed1268a401845df250b2f47762706e
https://pubmed.ncbi.nlm.nih.gov/31031766
https://pubmed.ncbi.nlm.nih.gov/31031766
Autor:
Yunyun Zheng, Jianfang Zhang, Hui Xu, Yu Li, Tingting Song, Yinghui Dang, Biliang Chen, Shanning Wan
Publikováno v:
Journal of Clinical Laboratory Analysis
Background Non-invasive prenatal testing (NIPT) is extensively used in the detection of fetal trisomies 21, 18, and 13, which is promptly becoming a common clinical practice. Concerned about the clinical application of non-invasive detection of the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c241a998f84ae878cea315c536af3874
https://pubmed.ncbi.nlm.nih.gov/30666717
https://pubmed.ncbi.nlm.nih.gov/30666717