Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Chunxin Chang"'
Autor:
Songchang Chen, Lanlan Zhang, Jiong Gao, Shuyuan Li, Chunxin Chang, Yiyao Chen, Hongjun Fei, Junyu Zhang, Yanlin Wang, Hefeng Huang, Chenming Xu, Daru Lu
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Non-invasive prenatal testing (NIPT) for common fetal trisomies is effective. However, the usefulness of cell-free DNA testing to detect other chromosomal abnormalities is poorly understood. We analyzed the positive rate at different read depths in n
Externí odkaz:
https://doaj.org/article/f1aacf1656a24e4e915d33b9fb99ab8d
Autor:
Shuyuan Li, Xu Han, Liang Zhang, Yan Xu, Chunxin Chang, Li Gao, Jiahan Zhan, Renyi Hua, Aiping Mao, Yanlin Wang
Publikováno v:
Clinical Chemistry; Nov2023, Vol. 69 Issue 11, p1295-1306, 12p
Autor:
Songchang Chen, Weihui Shi, Yeqing Qian, Liya Wang, Junyu Zhang, Shuyuan Li, Yiyao Chen, Chunxin Chang, Hongjun Fei, Lanlan Zhang, Hefeng Huang, Chenming Xu
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundX-linked lymphoproliferative disease (XLP) is a rare primary immunodeficiency disorder. We performed experiments based on two strategies of preimplantation genetic testing (PGT) for a family with XLP caused by a mutation in SH2D1A (c.191G >
Externí odkaz:
https://doaj.org/article/4b486e43bedb4abc865c82d3696b314e
Autor:
Weihui Shi, Yiyao Chen, Songchang Chen, Shuyuan Li, Chunxin Chang, Lanlan Zhang, Hongjun Fei, Hefeng Huang, Junyu Zhang, Chenming Xu
Publikováno v:
Journal of Bio-X Research, Vol 1, Iss 3, Pp 140-146 (2018)
Abstract. Kabuki syndrome (KS) is a rare congenital mental retardation condition characterized by facial dysmorphia, visceral and skeletal malformations, and developmental delay. The integrated phenotype and genotype-based prioritization is critical
Externí odkaz:
https://doaj.org/article/d5526d18e4ab40a2860849aa732a4c7d
Autor:
Shuyuan Li, Xu Han, Yan Xu, Chunxin Chang, Li Gao, Jiaqi Li, Yulin Lu, Aiping Mao, Yanlin Wang
Publikováno v:
The Journal of Molecular Diagnostics. 24:1009-1020
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d722ff64ffc415139407ec02097210c6
https://doi.org/10.1016/j.jmoldx.2022.05.001
https://doi.org/10.1016/j.jmoldx.2022.05.001
Autor:
Bo Xu, Xiaojiao Chen, Zhilei Mao, Minjian Chen, Xiumei Han, Guizhen Du, Xiaoli Ji, Chunxin Chang, Virender K Rehan, Xinru Wang, Yankai Xia
Publikováno v:
PLoS ONE, Vol 14, Iss 8, p e0221486 (2019)
[This corrects the article DOI: 10.1371/journal.pone.0074968.].
Externí odkaz:
https://doaj.org/article/f713af4006dc42dc95e167b9c046256c
Autor:
Yiyao Chen, Chunxin Chang, Chenming Xu, Weihua Peng, Songchang Chen, Zhongwei Bao, Li Jin, Lanlan Zhang, Huanhuan Zhu, Qian Zhang, Shuyuan Li, Daru Lu, Lili Jiang, Liming Chu, Chen Xiaoyan, Chao Liu, Yu Feng, Zhengwen Jiang
Publikováno v:
Journal of Human Genetics. 67:107-114
Infertility affects about 15% of heterosexual couples and male factors account for ~45-50% of clinical cases. Genetic factors play an important role in male infertility and thus we try to develop a cost-effective method for screening the genetic fact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a827e09533c3ce77eda0564b1bc4f803
https://doi.org/10.1038/s10038-021-00973-3
https://doi.org/10.1038/s10038-021-00973-3
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(3)
To carry out prenatal diagnosis for families with high risk for spinal muscular atrophy (SMA) by using multiplex ligation-dependent probe amplification (MLPA).Twenty-one families were enrolled. MLPA was used to detect copy numbers of SMN1 and SMN2 ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::782dcf14d71cc0c3b72802afae550325
https://pubmed.ncbi.nlm.nih.gov/33751527
https://pubmed.ncbi.nlm.nih.gov/33751527
Autor:
Bo Xu, Xiaojiao Chen, Zhilei Mao, Minjian Chen, Xiumei Han, Guizhen Du, Xiaoli Ji, Chunxin Chang, Virender K Rehan, Xinru Wang, Yankai Xia
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e74968 (2013)
Perfluorooctane sulfonate (PFOS) poses potential risks to reproduction and development. Mouse embryonic stem cells (mESCs) are ideal models for developmental toxicity testing of environmental contaminants in vitro. However, the mechanism by which PFO
Externí odkaz:
https://doaj.org/article/7cc5714b15094d89b6d7ec90440f1f92
Autor:
Songchang, Chen, Qian, Zhang, Liming, Chu, Chunxin, Chang, Yiyao, Chen, Zhongwei, Bao, Weihua, Peng, Lanlan, Zhang, Shuyuan, Li, Chao, Liu, Huanhuan, Zhu, Feng, Yu, Xiaoyan, Chen, Lili, Jiang, Daru, Lu, Zhengwen, Jiang, Li, Jin, Chenming, Xu
Publikováno v:
Journal of human genetics. 67(2)
Infertility affects about 15% of heterosexual couples and male factors account for ~45-50% of clinical cases. Genetic factors play an important role in male infertility and thus we try to develop a cost-effective method for screening the genetic fact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8533fe5a638086473475bcc9a97b8463
https://pubmed.ncbi.nlm.nih.gov/34462535
https://pubmed.ncbi.nlm.nih.gov/34462535