Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Dan Li"'
Autor:
Hui Zhang, Philipp Kapranov, Runsheng Chen, Hui Li, Ferhat Ay, Cong Wang, Zi Yan, Yudi Liu, Zhonghua Du, Dan Li, Andrew R. Hoffman, Ilkay Celik, Benzheng Jiao, Miguel A. Esteban, Naifei Chen, Wei Li, Shilin Zhang, Jingcheng Chen, Jiuwei Cui, Huiling Chen, Xue Wen, Lei Zhou, Zhuo Wang, Baoming Qin, Jianjun Luo, Günhan Gülsoy, Yichen Wang, Sujun Gao, Changhao Fu, Shanshan Liu, Lin Jia, Songling Zhang, Daniela Salgado Figueroa, Yajing Hao, Ji-Fan Hu, Wang Yang, Yanbo Zhu
Publikováno v:
Genome Biology, Vol 22, Iss 1, Pp 1-29 (2021)
Genome Biology
Genome Biology
Background A specific 3-dimensional intrachromosomal architecture of core stem cell factor genes is required to reprogram a somatic cell into pluripotency. As little is known about the epigenetic readers that orchestrate this architectural remodeling
Autor:
Jun Lin, Ya-Dan Li, Xiao-Li Zhang, Qiang Shu, Ming Yang, Xian Wang, Faliang Wang, Yongfang Yue, Hongchuan Jin
Publikováno v:
Infectious Agents and Cancer, Vol 16, Iss 1, Pp 1-14 (2021)
Infectious Agents and Cancer
Infectious Agents and Cancer
Background Despite extensive molecular epidemiological studies, the prevalence and characteristics of Mouse Mammary Tumor Virus-Like Virus (MMTV-LV) in Chinese women breast cancer are still unclear. Besides, the prevalence of MMTV-LV in women breast
Autor:
Wen-jing Yang, Feng-hua Lan, Xian-guo Fu, Yong-jun Xu, Juan Liao, Duo Zhang, Dan Li, Ai-zhen Yan, Xiao-yan Guo
Publikováno v:
BMC Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
BMC Genetics
BMC Genetics
Background The disease gene of fragile X syndrome, FMR1 gene, encodes fragile X mental retardation protein (FMRP). The alternative splicing (AS) of FMR1 can affect the structure and function of FMRP. However, the biological functions of alternatively
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Coagulation factor XIII (FXIII) plays an essential role in maintaining hemostasis by crosslinking fibrin. Deficiency in FXIII affects clot stability and increases the risk of severe bleeding. Congenital FXIII deficiency is a rare disease.
Autor:
Xiliang Wang, Dan-Dan Li, Xiaowen Huang, Dong-Xiao Guo, Weidong Zhang, Qinglin Zhao, Dankang Li, Xiao Wang, Jie-Bin Cao, Chengda Zhang
Publikováno v:
Malaria Journal, Vol 18, Iss 1, Pp 1-11 (2019)
Malaria Journal
Malaria Journal
BackgroundImported malaria has been an important challenge for China. Fatality rates from malaria increased in China, particularly in Henan Province, primarily due to malpractice and misdiagnoses in healthcare institutions, and the level of imported
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
BMC Medical Genetics
BMC Medical Genetics
Background Uniparental disomy (UPD) refers to the situation in which two copies of homologous chromosomes or part of a chromosome originate from the one parent and no copy is supplied by the other parent. Case presentation Here, we reported a woman w
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-8 (2019)
BMC Medical Genetics
BMC Medical Genetics
Background Mutations in more than 52 genes have been identified in isolated congenital cataracts, the majority of which are located in crystalline and connexin (gap junction) genes. An in-frame one amino acid deletion in the beta-crystalline gene CRY
Autor:
Dan Li, Wenjuan Hu, Zhaoyong Wu, Dongxing Guo, Baoping Xu, Xiujun Tian, Jingyi Li, Kunling Shen, Shaogang Li, Ran Wei, Deli Xin
Publikováno v:
BMC Infectious Diseases, Vol 19, Iss 1, Pp 1-9 (2019)
BMC Infectious Diseases
BMC Infectious Diseases
Background The point mutations in 23S rRNA gene of Mycoplasma pneumoniae (M. pneumoniae) can lead to high-level resistance to macrolides. This study aimed to evaluate allele-specific real-time PCR (ASPCR) to detect the resistance-related mutations lo
Publikováno v:
BMC Medical Genomics, Vol 11, Iss S5, Pp 99-107 (2018)
BMC Medical Genomics
BMC Medical Genomics
Background Breast cancer is the most common type of invasive cancer in woman. It accounts for approximately 18% of all cancer deaths worldwide. It is well known that somatic mutation plays an essential role in cancer development. Hence, we propose th
Autor:
Dan Li, Mary Qu Yang
Publikováno v:
BMC Bioinformatics, Vol 18, Iss S14, Pp 31-38 (2017)
Background Long noncoding RNAs (lncRNAs) are involved in diverse biological processes and play an essential role in various human diseases. The number of lncRNAs identified has increased rapidly in recent years owing to RNA sequencing (RNA-Seq) techn