Zobrazeno 1 - 10
of 51
pro vyhledávání: '"JING‑BIN YAN"'
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
IntroductionDown syndrome (DS) is the most common genetic condition that causes intellectual disability in humans. The molecular mechanisms behind the DS phenotype remain unclear. Therefore, in this study, we present new findings on its molecular mec
Externí odkaz:
https://doaj.org/article/308e33a9d4774d1c8eeb5f443f808ea9
Publikováno v:
Cell Biology International. 45:1383-1392
Mental retardation is the main clinical manifestation of Down syndrome (DS), and neural abnormalities occur during the early embryonic period and continue throughout life. Tc1, a model mouse for DS, carries the majority part of the human chromosome 2
Publikováno v:
PLoS Computational Biology
RNA editing is a co- or post-transcriptional modification through which some cells can make discrete changes to specific nucleotide sequences within an RNA molecule after transcription. Previous studies found that RNA editing may be critically involv
Autor:
Bofeng Zhu, Li Wang, Shi‑Xiu Liao, Qian‑Nan Guo, Lin Liu, Qiao‑Fang Hou, Jing‑Bin Yan, Hui‑Ru Zhao, Wei‑Li Shi, Hong‑Dan Wang
Publikováno v:
Molecular Medicine Reports
The discovery of cell-free DNA fetal (cff DNA) in maternal plasma during pregnancy provides a novel perspective for the development of non-invasive prenatal diagnosis (NIPD). Against the background of maternal DNA, the use of the relatively low conce
Long non-coding RNA LINC01296 is a potential prognostic biomarker in patients with colorectal cancer
Autor:
Jing-bin Yan, Jia-jun Qiu
Publikováno v:
Tumor Biology. 36:7175-7183
Colorectal cancer (CRC), one of the most malignant cancers, is currently the fourth leading cause of cancer deaths worldwide. Recent studies indicated that long non-coding RNAs (lncRNAs) could be robust molecular prognostic biomarkers that can refine
Autor:
Qing-wen Ma, Min Huang, Quo-qin Zhang, Yu-Juan Huang, Jing-Bin Yan, Miao Xu, Li-ming Bao, Jian-yi Wang, Zai-wei Zhou
Publikováno v:
Pediatric Cardiology. 36:475-480
Vasovagal syncope (VVS) causes accidental harm for susceptible patients. However, pathophysiology of this disorder remains largely unknown. In an effort to understanding of molecular mechanism for VVS, genome-wide gene expression profiling analyses w
Publikováno v:
Biotechnology Letters. 36:1209-1216
Human transferrin (hTF) belongs to the iron-binding glycoprotein family. It plays an important role in iron transport throughout the body. Transgenic mice are a good model to study how to produce functional hTF on a large-scale. We have improved the
Autor:
Jing-Bin Yan1,2, Miao Xu1, Can Xiong1, Da-Wen Zhou1, Zhao-Rui Ren1, Ying Huang1,2, Mommersteeg, Monique3, van Beuningen, Rinie3, Ying-Tai Wang4, Shi-Xiu Liao4, Fanyi Zeng1,2,5, Ying Wu1,3 ying.wu@philips.com, Yi-Tao Zeng1,2 ytzeng@stn.sh.cn
Publikováno v:
BMC Medical Genetics. 2011, Vol. 12 Issue 1, p68-78. 11p.
Autor:
Zhao-Rui Ren, Xiaoyan Jiang, Juan Wang, Connie J. Eaves, Shu-Zhen Huang, Yves Chalandon, Hui Qian, Yan Ping Xiao, Jing-Bin Yan, Fanyi Zeng, Wei Hu, Ashley Ringrose, Zhijuan Gong, Allen C. Eaves, Don A. Baldwin, Mei-Jue Chen
Publikováno v:
Cell Research, Vol. 23, No 6 (2013) pp. 859-62
Long-term deregulated human hematopoiesis in goats transplanted in utero with BCR-ABL -transduced lin − CD34 + cord blood cells
Publikováno v:
Oncotarget
// Jia-jun Qiu 1 , Zhao-rui Ren 1, 2 , Jing-bin Yan 1, 2 1 Shanghai Children’s Hospital, Shanghai Institute of Medical Genetics, Shanghai Jiao Tong University School of Medicine, Shanghai 200040, China 2 Key Laboratory of Embryo Molecular Biology,