Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jiangyang Xue"'
Publikováno v:
PeerJ, Vol 12, p e17142 (2024)
Background Genetic knockout-based studies conducted in mice provide a powerful means of assessing the significance of a gene for fertility. Forkhead-associated phosphopeptide binding domain 1 (FHAD1) contains a conserved FHA domain, that is present i
Externí odkaz:
https://doaj.org/article/b4c4ab581a61434ea4813ddb8a277ae5
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Balanced translocation (BT) carriers can produce imbalanced gametes and experience recurrent spontaneous abortions (RSAs) and even give birth to a child with complex chromosomal disorders. Here, we report a cryptic BT, t(5; 6) (p15.31; p2
Externí odkaz:
https://doaj.org/article/cee520446a1843b88d3fe36b33a0e055
Autor:
Baolu Shi, Jiangyang Xue, Hao Yin, Rui Guo, Mengcheng Luo, Lan Ye, Qinghua Shi, Xiaoyan Huang, Mingxi Liu, Jiahao Sha, P Jeremy Wang
Publikováno v:
PLoS Genetics, Vol 15, Iss 2, p e1007952 (2019)
Meiotic recombination permits exchange of genetic material between homologous chromosomes. The replication protein A (RPA) complex, the predominant ssDNA-binding complex, is required for nearly all aspects of DNA metabolism, but its role in mammalian
Externí odkaz:
https://doaj.org/article/164838f74e2645ec9d4de7ffd1f3ce3e
Publikováno v:
Journal of International Medical Research, Vol 46 (2018)
Objective To explore the etiology of human oocyte maturation arrest in two infertile Chinese sisters. Methods Clinical examination and genetic testing of all available family members were conducted, and the findings were used to create a pedigree. Mu
Externí odkaz:
https://doaj.org/article/bcca209fa64a4cfbbfb931b5d30f0362
Autor:
Baolu Shi, Jiangyang Xue, Jian Zhou, Seth D Kasowitz, Yuanwei Zhang, Guanxiang Liang, Yongjuan Guan, Qinghua Shi, Mingxi Liu, Jiahao Sha, Xiaoyan Huang, P Jeremy Wang
Publikováno v:
PLoS Genetics, Vol 14, Iss 1, p e1007175 (2018)
The microrchidia (MORC) family proteins are chromatin-remodelling factors and function in diverse biological processes such as DNA damage response and transposon silencing. Here, we report that mouse Morc2b encodes a functional germ cell-specific mem
Externí odkaz:
https://doaj.org/article/6cf2830a2caa47e9ada36b7ee582e7c1
Autor:
Yuxin Zhang, Lulu Yan, Min Xie, Jiangyang Xue, Xumian Yang, Yongming Xue, Liyun Tian, Haibo Li
Publikováno v:
American Journal of Medical Genetics Part A.
Autor:
Yuxin, Zhang, Jiangyang, Xue, Lulu, Yan, Yingwen, Liu, Danyan, Zhuang, Min, Xie, Yibo, Chen, Yu, An, Yiping, Shen, Haibo, Li
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(8)
Through a retrospective large sample analysis of copy number variants in single center, we explored the technical standards for the interpretation and reporting of constitutional copy-number variants (CNVs) jointly proposed by the American College of
Autor:
Lulu, Yan, Zhaier, Lu, Yingwen, Liu, Chunxiao, Han, Hongjun, Ying, Youwei, Bao, Jiangyang, Xue, Haibo, Li
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(3)
To explore the genetic basis for a fetus with dysgenesis of corpus callosum and other brain malformations.Whole exome sequencing was carried out for the fetus and its parents. Suspected pathogenic variants were verified by Sanger sequencing.A novel d
Publikováno v:
Transl Pediatr
BACKGROUND: Chromosomal 22q11.2 dosage changes in the recurrent region can lead to a series of clinically variable pediatric syndromes. This study conducted a retrospective analysis of microarray tested cases with 22q11.2 recurrent copy number variat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a67810b0bb9f99bce2af7dfb492e6aa
https://europepmc.org/articles/PMC8753460/
https://europepmc.org/articles/PMC8753460/
Autor:
Minjuan Liu, Songwen Ju, Zhihong Zhang, Yinghua Liu, Hongwei Ma, Ming Sun, Wei De, Min Xie, Jiangyang Xue, Tianshi Ma, Zhaoxia Wang
Publikováno v:
Cancer Letters. 443:67-79
Multiple studies have revealed that long non-coding RNAs (lncRNAs) extensively participate in human cancer malignant progression. The long intergenic non-protein coding RNA 707 (LINC00707), 3087 bp in length, was recently reported to be an essential