Zobrazeno 1 - 10
of 553
pro vyhledávání: '"Lin, Yang"'
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-6 (2024)
Abstract Background Bosma arhinia microphthalmia syndrome (BAMS; MIM603457) is a rare genetic disorder, predominantly autosomal dominant. It is a multi-system developmental disorder characterized by severe hypoplasia of the nose and eyes, and reprodu
Externí odkaz:
https://doaj.org/article/78350bcedb3e401d91503ceb7b133748
Autor:
Fei Chen, Yan Zhang, Pai Peng, Xiao-Ting Huang, Zi-Han Qiu, Bao-Cheng Liu, Tie-Lin Yang, Bo Yang, Yan Guo
Publikováno v:
Genes and Diseases, Vol 11, Iss 2, Pp 546-549 (2024)
Externí odkaz:
https://doaj.org/article/8b8aad09a9404c1c837c46746fabd975
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 9, Iss 2, Pp 257-261 (2024)
AbstractThe genome-level features are crucial genetic resources for species identification and phylogenetic analysis. Here, the complete mitochondrial genome of Aphidius colemani Viereck 1912 (Hymenoptera: Braconidae: Aphidiinae) was sequenced, deter
Externí odkaz:
https://doaj.org/article/51435933d03e49379ebaf6728931759a
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
ObjectiveTo explore the clinical value of echocardiography in detecting fetal cardiac axis abnormalities during middle pregnancy for diagnosing conus arteriosus malformation, and to compare and analyze the genetic diagnosis results, in order to provi
Externí odkaz:
https://doaj.org/article/1383a0afb53848798f74bc76010a6e73
Autor:
Hui Xiao, Huiyao Chen, Xiang Chen, Yulan Lu, Bingbing Wu, Huijun Wang, Yun Cao, Liyuan Hu, Xinran Dong, Wenhao Zhou, Lin Yang
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-15 (2023)
Abstract Background In China, ~1,072,100 small for gestational age (SGA) births occur annually. These SGA newborns are a high-risk population of developmental delay. Our study aimed to evaluate the genetic profile of SGA newborns in the newborn inten
Externí odkaz:
https://doaj.org/article/a13219e6102b4b708d625471812653ae
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Objectives: We explored the role and molecular mechanisms of RNA-binding proteins (RBPs) and their regulated alternative splicing events (RASEs) in the pathogenesis of atopic dermatitis (AD).Methods: We downloaded RNA-seq data (GSE121212) from 10 hea
Externí odkaz:
https://doaj.org/article/69479c20231c43a6a3cb0f0ee6a9d915
Autor:
Ning Jiang, Wanqing Ding, Xiaojuan Zhu, Jianshu Chen, Lin Yang, Xiaoping Yi, Yingping Zhuang, Jiangchao Qian, Jiaofang Huang
Publikováno v:
BioDesign Research, Vol 6 (2024)
Recently, there has been increasing interest in the use of bacteria for cancer therapy due to their ability to selectively target tumor sites and inhibit tumor growth. However, the complexity of the interaction between bacteria and tumor cells evokes
Externí odkaz:
https://doaj.org/article/d8bfe92943df44e3aeabe22a83b58a9c
Autor:
Xiao Wang, Tiantian Xiao, Jin Wang, Bingbing Wu, Huijun Wang, Yulan Lu, Yaqiong Wang, Bin Chen, Liyuan Hu, Yun Cao, Rong Zhang, Guoqiang Cheng, Laishuan Wang, Zhihua Li, Xinran Dong, Lin Yang, Wenhao Zhou
Publikováno v:
Frontiers in Genetics, Vol 14 (2024)
Objective: We aimed to investigate the clinical and genetic risk factors associated with neonatal severe unconjugated hyperbilirubinemia.Methods: This was a retrospective, 1:1 matched, case–control study. We included 614 neonates diagnosed with sev
Externí odkaz:
https://doaj.org/article/a8b98f175f9444bf880fbabcf59dac07
Autor:
Xiaoshan Ji, Yanzhuang Ge, Qi Ni, Suhua Xu, Zhongmeng Xiong, Lin Yang, Liyuan Hu, Yun Cao, Yulan Lu, Qiufen Wei, Wenqing Kang, Deyi Zhuang, Wenhao Zhou, Xinran Dong
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Primary carnitine deficiency (PCD) caused by pathogenic variants in the solute carrier family 22 member 5 (SLC22A5) gene is a rare autosomal recessive disease that results in defective fatty acid oxidation. PCD can be detected through tandem mass spe
Externí odkaz:
https://doaj.org/article/5f3c68adea68453ea7eb5ba93262620c
Autor:
Xiao Wang, Shuming Tian, Hao Wang, Lin Yang, Xiaoling Zou, Xavier-ravi Baskaran, Qiang Li, Haitao Xing, Hong-Lei Li
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 8, Iss 6, Pp 699-703 (2023)
Here, the complete chloroplast genome sequence of Zingiber teres is described using MGI paired-end sequencing. The genome is 163,428 bp in length and contains a small single-copy region (SSC) of 15,782 bp, a large single-copy region (LSC) of 88,142 b
Externí odkaz:
https://doaj.org/article/e010f9f447fa478cab997a74ca6adeeb